From 2012.igem.org

(Difference between revisions)

Latest revision as of 11:27, 9 October 2012

Caution

We devided our team into 2 groups in order to achieve Flower Fairy E.coli, Florigen and Secretion group. Florigen aims to confirm expression of florigen in E.coli, activation of R9 peptide, and function of FT made by E.coli. Secretion group aims to make a secretion system without cell death and confirm function of tatABCD and the other proteins.

August 2

Mutation of FT

by Sato
FT gene has two BioBrick restriction enzyme sites, EcoR1 and Pst1 which is next to each other.
So we tried to delete both at once by using two primers with mutation.

Inverse PCR
10xBufer	2mM dNTPs	primer fwd	primer rev	template	polymerase	MilliQ	Total
5	5	1.5	1.5	0.5	1	35.5	50

94℃ 2min, (98℃ 10sec, 68℃ 4min)x4cycles, 4℃ Hold

Dpn1 Digestion
PCR product	Dpn1
50	2

37℃,1h incubate

Self-ligation
product	MilliQ	Ligase	T4 Kinase	Total
2	7	5	1	15

16℃, 1h incubate

Transformation
competent cell	DNA
20	2

Cells were stored on ice for 30min.
After 42℃ 60sec heat shock, cells were stored on ice for 2min.
Then cells were precultureed at 37℃ for 1hr, plated to Kanamycin plate.

August 13

Liquid culture

FT at 37°C, for overnight.

August 14

Miniprep of FT

by Sato, Takeuchi
The concentration was 81.5ng/uL

Restriction digestion and Electrophoresis

by Sato
To check wheter mutation was succeed, we did restriction enzyme digestion.

DNA(FT,80ng/uL)	10xBuferH	EcoR1	Pst1	MilliQ	Total
5	2	1	-	12	20
5	2	-	1	12	20

37°C 2h incubate
We did electrophoresis of three FT plasmids, non-cutted, EcoR1 cutted, Pst1 cutted.
However, we couldn't get any bands (data not shown.)

Liquid culture

FT (4mL)

August 15

Miniprep of FT

by Sato, Takeuchi, Hyungcheol
We couldn't get enough concentration of plasmids.

Electrophoresis

by Sato
We retried electrophoresis of three samples same as yesterday.
However, we couldn't get any bands as well.

August 16

Transformation

by Takeuchi, Ota

Name	Well	Sample	Competent Cells	Total	Plate	Colony
FT	-	1 µL	10	11	LB (Kan+)	×
pSB1C3	1-3-A	1	10	11	LB (CP+)	○
I719005	1-15-N	1	10	11	LB (Amp+)	○

August 17

Transformation

by Takeuchi

Name	Well	Sample	Competent Cells	MilliQ	Total	Plate	Colony
FT	-	2	2	18	22	LB (Kan+)	×

We found that mutation of FT was not successful.

August 20

We decided to do PCR using FT specific primers before mutation.

PCR of FT

by Sato

10xBufer	dNTPs	MgSO4	primer fwd	primer rev	template	polymerase	MilliQ	Total
5	5	3	1	1	1(130ng/µL)	1(KOD plus neo)	33	50

94°C 2min, (98°C 10sec, 68°C 15sec)x30cycles, 4°C Hold
After the ethanol precipitation, we diluted in 30µL of MilliQ.
The concentration was 203ng/µL.

Electrophoresis

Lane	Name	length(bp)
1	1kb ladder	-
2	FT	600

August 21

Restriction digestion

by Sato

DNA(FT,203ng/µL)	10xBuferM	Xba11	Pst1	MilliQ	Total
10	4	1	1	24	40

37°C, 5h incubate
After the ethanol precipitation, we diluted in 30µL of MilliQ.
The concentration was 54,9ng/µL.

Ligation

by Sato

Vector		Insert		Ligation High Ver.2
pSB1C3	1	FT	10	5.5

Liquid culture

T7 promoter, pSB1C3 (4mL)

August 22

Miniprep

by Sato

T7 promoter	pSB1C3
85.3ng/µL	82.93ng/µL

August 23

Ethanol Precipitation

diluted in 20µL 79.3ng/µL

August 24

Restriction enzyme processing

T7 promoter(85.3ng/µL)	Spel	Pstl	buffer M	MiliQ	Total
10	1	1	2	6	20

->purifying column 33.4ng/µL(dissolution 40µL)

pSB1C3(82.9ng/µL)	Xbal	Spel	buffer M	MiliQ	Total
20	1	1	4	14	40

->gene clean2 39.9ng/µL(dissolution 40µL)

Ligation

FT(600bp, 79.3ng/µL)	pSB1C3(2000bp,39.9ng/µL)	Ligation High Ver.2
3µL => 597fmol	2µL => 60fmol	2.5µL

FT(600bp, 79.3ng/µL)	T7(2100bp,33.4ng/µL)	Ligation High Ver.2
2.4µL => 478fmol	2µL => 48fmol	2.2µL

=> 16℃,1hr incubate

August 27

Colony PCR

2X Quick Tag	VF2	VR	MiliQ	Total
25	1	1	23	50

Lane1: 1kb ladder
Lane2~16: FT(pSB1C3) about 800bp

FT(TOPO) PCR(re)

buffer	dNTPs	MgSO4	primer f	primer r	Template(130ng/µL)	KODplus neo	MilliQ	Total
5	5	3	1	1	1	1	33	50

94℃	98℃	68℃	cycles
2min	10sec	15sec	30

Liquid culture

by Nobeyama
FT 4ml

August 28

Mutation of FT (re)

inverse PCR

MilliQ	buffer	dNTP	primer f	primer r	FT(130ng/µL)	KODplus	Total
35.5	5	5	1.5	1.5	0.5	1	50

94℃	98℃	68℃	cycles
2min	10sec	4min	18

Lane1: 1kb ladder
Lane2: FT

Miniprep FT(TOPO)

158ng/µL

Tranformation

competent cell: 20
BBa.I746902 : 2
(plate 316f)
(GFP generator of pBAD/araC-mut3 GFP:6His-DT)

August 29

Mutaion of FT(re;re)

Inverse PCR

first

MilliQ	buffer	dNTP	primer f	primer r	FT(130ng/µL)	KODplus	Total
35.5	5	5	1.5	1.5	0.5	1	50

second

MilliQ	buffer	dNTP	primer f	primer r	FT(52ng/µL)	KODplus	Total
35	5	5	1.5	1.5	1	1	50

94℃	98℃	68℃	cycles
2min	10sec	4min	30

Lane1: 1kb ladder
Lane2: first Template 130ng/µL
Lane3: second Template 53ng/µL

first sample	Dpnl	total
45µL	2µL	47µL

in 37℃, 1 hour

Self-Ligation

PCR products	MilliQ	Ligation High	T4 kinase	total
2µL	7µL	5µL	1µL	15µL

in 16℃, 1.5hour incubate
Transformation
competent cell: 20
DNA : 2

Liquid culture(I746902): 3mL

August 30

Liquid culture(FT) 4mL x2

August 31

Miniprep(FT)

(1) 64.9ng/µL
(2) 52.6ng/µL

Restriction enzyme processing (Mutation checking)

FT(52.6ng/µL)	bufferH	E.coli	Pst1	MilliQ	total
1µL	5µL	0.5µL	0.5µL	3.5µL	10µL

in 37℃,1.5hour

PCR(RBS primer)

buffer for KODplus neo	dNTPs	MgSO4	primer f	primer r	Template(52.6ng/µL)	KODplus neo	MilliQ	Total
5	5	3	1	1	1	1	33	50

94℃	98℃	68℃	cycles
2min	10sec	15sec	30

Lane1: 1kb ladder
Lane2: FT
Lane3: FT(E.coli)
Lane4: FT(Pst1)
Lane5: FT PCR

PCR(re)

buffer	dNTPs	MgSO4	primer f	primer r	Template	KOD neo	MilliQ	Total
5	5	3	1	1	1	1	33	50

94℃	98℃	68℃	cycles
2min	10sec	15sec	35

Lane1: 1kb ladder
Lane2: FT

PCR(re)

buffer	dNTPs	MgSO4	primer f	primer r	Template	KOD neo	MilliQ	Total
5	5	2	1	1	1	1	34	50

94℃	98℃	68℃	cycles
2min	10sec	10sec	30

September 2

PCR(re;re)

first

buffer	dNTPs	MgSO4	primer f	primer r	Template(1ng/µL)	KODplus neo	MilliQ	Total
5	5	3	1	1	1	1	33	50

second

buffer	dNTPs	MgSO4	primer f	primer r	Template(10ng/µL)	KODplus neo	MilliQ	Total
5	5	3	1	1	1	1	33	50

94℃	98℃	68℃	cycles
2min	10sec	10sec	25

Lane1: first Template 1ng
Lane2: second Template 10ng
Lane3: 1kb ladder
refine first Template => 132ng/µL

September 3

Restriction enzyme processing

FT(132ng/µL)	bufferM	EcoRI	SpeI	MilliQ	Total
10	2	1	1	6	20

37℃,overnight => refinement 31.6ng/µL (Elution 40µL)

Ligation
Insert(FT: 31.6ng/µL, 600bp ): 2µL = 26fmol
Vector(DT: 28.0ng/µL, 3300bp): 3µL = 240fmol
Ligation High ver.2 :2.5µL
=> 16℃, 2 hours

Transformation

competent cell	DNA	plate	colony
20µL	FT-DT 2µL	Amp	o
20µL	pT7-6His-R9 2µL	Amp	o
10µL	GFP generator 1µL	Amp	o

(BBa,I746915,pT7-6His-GFP)

September 4

Colony PCR

Quick Tag	VF2	VR	MilliQ	Total
25	1	1	23	50

94℃	98℃	55℃	68℃	cycles
2min	30sec	30sec	1min	25

Lane1: 1kb ladder
Lane2: FT-DT(about 700bp)

Liquid culture(4ml) 23:30 ~
GFP generator, FT-DT

September 5

Miniprep(FT-DT) by Sato
88.8ng/µL

Restriction enzyme processing

FT-DT(88.8ng/µL)	XbaI	PstI	bufferM	MiliiQ	total
20	1	1	4	14	40

at 37℃, 2 hours

Electrophoresis by Takeuchi

Restriction enzyme processingby Takeuchi

FT-DT(88.8ng/µL)	bufferM	XbaI/Spe	MiliiQ	total
4	1	0.5	4.5	10

FT-DT	bufferH	Pst/Eco	MiliiQ	total
4	1	0.5	4.5	10

at 37℃,1hour 10min

September 6

Western blotting(BBa,I746915)

Sample making
SOC(ampt) 50ml + pre culture 1ml x2
OD600 = 0.5~0.7 incubate at 37℃ (OD 0.642)
add IPTG final concentration is 1mM (negative control)
incubate at 37℃,4 hours

SDS-PAGE
Do spin down E.coli and make suspension put E.coli into 1mL 1x sample buffer
95℃,10min
electrophoresis at 500V, 30mA, 50min
Lane1: 10µL (IPTG -)
Lane2: 10µL (IPTG -)
Lane3: 10µL (IPTG +)
Lane4: 5µL (IPTG -)
Lane5: 5µL (IPTG +)
Lane6: 2µL (IPTG -)
Lane7: 2µL (IPTG +)

Blotting at 50V,100mA,30min Put into blocking buffer and vibrating 30min
Incubate with Anti GFP(1/1000) 10mL at RT,1h
Washing with 10mL TBST (vibrating 10min x2)
Incubate with Anti-mouseAP(1/1000) 10mL at RT, 30min
Washing with 10mL TBST (vibrating 10min x3)
Put NBT,BCIP into dye buffer

September 9

Mutaion of FT

MilliQ	buffer	dNTP	primer f	primer r	FT(52ng/µL)	KODplus	Total
35	5	5	1.5	1.5	1	1	50

94℃	98℃	68℃	cycles
2min	10sec	4min	20

→　GeneClean II　32.6ng/µL

Dpn1 processing

TA buffer	DNA	Dpn1	Total
3.3	31	2	36.3

Ligation

DNA	MiliiQ	Ligation high Ver.2	T4 kinase	Total
2	7	5	1	15

Transformation competent cell: 10
DNA : 1

September 10

Miniprep of FT ①116.9ng/µL
② 34.5ng/µL
Restriction enzyme processing(Mutation checking)

FT①/②	bufferHl	EcoRI	PstI	MiliQ	Total
4	1	0.5	0	4	10
4	1	0	0.5	4	10

PCR

Bufer	dNTPs	MgSO4	primer(+/-RBS)fwd	primer(+/-RBS)rev	template①/②	KOD plus neo	MilliQ	Total
5	5	3	1	1	1	1	33	50

94℃	98℃	68℃	cycles
2min	10sec	10sec	25

->purifying column 17.4ng/µL

Restriction enzyme processing

FT(RBS+)32.6ng/µL	Xbal	Pstl	buffer M	BSA	Total
30	1	1	4	4	40

T7-His:R9(62.6ng/µL)	SpeI	Pstl	MilliQ	buffer M	Total
15	0.5	0.5	2	2	20

incubate at 37℃, 3hours
->purifying column 17.4ng/µL

September 11

Ligation
Vector(T7: 33.4ng/µL, 2100bp): 1µL = 24fmol
Insert(FT: 17.4ng/µL, 600bp ): 5µL = 217fmol
Ligation High ver.2 : 3µL
=> 16℃, 1 hours

Transformation

competent cell	DNA
20µL	T7-FT 2µL

PCR(FT without RBS retry)

Bufer	dNTPs	MgSO4	primer(-RBS)fwd	primer(-RBS)rev	template	KOD plus	MilliQ	Total
5	5	3	1	1	1	1	33	50

94℃	98℃	65℃	68℃	cycles
2min	15sec	30sec	30sec	25

Lane1:FT(RBS-) 600bp
Lane2:Ladder 100bp
=>purifying column 34.6ng/µL

Restriction enzyme processing

FT(RBS-)	XbaI	PstI	bufferM	BSA	total
30	1	1	4	4	40

at 37℃, 2 hours
=> 6.2ng/μL

GFP-DT	XbaI	PstI	bufferM	BSA	MilliQ	total
15	1	1	3	3	7	30

at 37℃, 2 hours
=> 7.0ng/μL

Ligation
Vector(T7-6His-R9: 11.6ng/µL, 2100bp): 1µL = 9fmol
Insert(FT: 6.2ng/µL, 600bp ): 5µL = 79fmol
Ligation High ver.2 : 3µL
=> 16℃, 1 hours

Vector(T7-6His-R9: 11.6ng/µL, 2100bp): 1µL = 9fmol
Insert(GFP-DT: 7.0ng/µL, 1000bp ): 9µL = 95fmol
Ligation High ver.2 : 4µL
=> 16℃, 1 hours

September 12

Transformation

competent cell	DNA	plate
20µL	T7-R9-GFP-DT 2µL	Amp
20µL	T7-R9-FT 2µL	Amp
BL21CDE3 10µL	T7-FT 1µL	Amp

Miniprep (T7-FT)
37.1ng/µL

September 13

Miniprep
①T7-R9-GFP-DT 90ng/µL
②T7-R9-FT 160ng/μL

Restriction enzyme processing

T7-R9-GFP-DT (90ng/µL)	EcoRI	PstI	buffer H	MilliQ	total
20	1	1	3	5	30

at 37℃, 2 hours
=> 20.7ng/μL

T7-R9-FT (160ng/µL)	EcoRI	SpeI	buffer M	MilliQ	total
20	1	1	3	5	30

at 37℃, 2 hours
=> 20.1ng/μL

'Transformation

competent cell BL21(DE3)	DNA	plate
10µL	T7-R9-GFP-DT 1µL	Amp
10µL	T7-R9-FT 1µL	Amp

Restriction enzyme processing

Buffer H	BSA	EcoRI	PstI	DpnⅠ	MilliQ	total
5	5	0.5	0.5	0.5	13.5	25

=>We define this solution "2× Master Mix"

2× Master Mix	pSB1C3(Linerarized Plasmid Backbone)
4	4

at 37℃, 30 minutes
80℃, 30 minutes

PCR(Insert His-tag)

MilliQ	Buffer for iPCR	dNTPs	primer fwd	primer rev	template(T7-FT 37.1ng/μL)	KOD plus	Total
35	5	5	1.5	1.5	1	1	50

94℃	94℃	56℃	68℃	cycles
2min	15sec	30sec	2.5min	15

Lane1:Ladder 1kb
Lane2:T7-6His:FT about 2700bp

September 14

Ligation
Vector(pSB1C3: 12.5/µL, 2000bp) : 2µL = 19fmol
Insert(T7-R9-GFP-DT: 20.7ng/µL, 700bp ): 4µL = 180fmol
Ligation High ver.2 : 3µL
=> 16℃, 1 hours

Dpn1 processing

PCR products(9/13)	Dpn1	Total
45	2	47

=>37℃, 1 hour

Self Ligation

PCR products	Ligation High	T4 Kinase	MilliQ	Total
2	5	1	7	15

=>16℃, 1 hour

Ligation
Vector(DT: 17.1/µL, 2100bp) : 2µL = 12fmol
Insert(T7-R9-FT: 20.1ng/µL, 650bp ): 5µL = 496fmol
Ligation High ver.2 : 3.5µL
=> 16℃, 1 hours

September 15

Restriction enzyme processing

FT without RBS (34.6ng/µL)	EcoRI	PstI	10× buffer H	MilliQ	total
10	0.5	0.5	2	7	20

Colony PCR

Quick Tag	VF	VR	MilliQ	Total
25	1	1	23	50

94℃	94℃	55℃	68℃	cycles
2min	30sec	30sec	1min	25

Electrophoresis
Lane1: ladder
Lane2: T7-R9-GFP-DT
Lane3: T7-R9-GFP-DT

Lane4: T7-R9-FT-DT
Lane5: T7-R9-FT-DT
Lane6: T7-R9-FT-DT
Lane7: T7-R9-FT-DT
Lane8: T7-R9-FT-DT
A member of secretion group electrophoresed DNA from Lane9 to Lane12.

Lane13: T7-His:FT
Lane14: T7-His:FT
Lane15: T7-His:FT
Lane16: T7-His:FT
Lane17: ladder

Liquid culture(3ml) 3:30~
T7-R9-FT-DT×2, T7-His:FT×2, T7-His:FT

September 16

Miniprep
①T7-R9-FT-DT 150ng/µL
②T7-R9-FT-DT 139ng/μL
③T7-R9-GFP-DT 67ng/µL
④T7-His:FT 153ng/μL
⑤T7-His:FT 73ng/μL

September 17

Purifying column
=>FT without RBS :36.4ng/µL

Ligation
Vector(PSB1C3: 12.5/µL, 2000bp) : 3µL = 9fmol
Insert(FT without RBS: 36.4ng/µL, 600bp ): 3µL = 92fmol
Ligation High ver.2 : 3µL
=> 16℃, 1 hours

September 18

Transformation by NAKAGAWA

competent cell	DNA	plate
20µL	PSB1C3 FT without RBS 1µL	CP+

Verification of R9 function by TAKEUCHI

R9(20µg/µL)	0.9µL
GFP(1.2mg/mL)	2.23µL
RBS	16.85µL
total	20µL

X5

Method:
1. Peel cuticles on parafilm by using the head of pencil.(Menasha,wI,54952)
2. Put plant cells into GFP&R9 or GFP for 5~30min.
3. Put plant cells into PBS.
4. Hoechst dyeing.

	1	2	3	4	5	6
R9	o	o	o	x	o	o
cuticle	o	o	o	o	x	x
soak in GFP	5min	15min	30min	5min	5min	30min

September 19

Transformation(re) by NAKAGAWA,TAKEUCHI
competent cell:20µL
DNA(No RBS FT):1µL
plate :CP+

Transformation(re;re) by NAKAGAWA,TAKEUCHI
competent cell:10µL
DNA(No RBS FT):1µL
LB :100µL
plate :CP+

Adjusted GM Agar Medium making by TAKEUCHI

Ingredient of MS medium(SIGMA M5519): 0.88g
MES : 0.1g
ion exchanged water : 200mL
NaOH : 26µL(adjust to pH5.6)
Agar medium : 1.6g

Autoclave 120℃

Colony PCR(re)

gelA
Lane1: 100bp Ladder
Lane2: No RBS FT colony number 9
Lane3: No RBS FT colony number 10
Lane4: No RBS FT colony number 11
Lane5: No RBS FT colony number 12
Lane6: No RBS FT colony number 13
Lane7: empty
Lane8: empty

gelB

Lane1: 100bp Ladder
Lane2: No RBS FT colony number 14
Lane3: No RBS FT colony number 15
Lane4: No RBS FT colony number 16
Lane5: No RBS FT colony number 17
Lane6: No RBS FT colony number 18
Lane7: No RBS FT colony number 19
Lane8: empty

gelC

Lane1: 100bp Ladder
Lane2: No RBS FT colony number 20
Lane3: No RBS FT colony number 21
Lane4: No RBS FT colony number 22
Lane5: No RBS FT colony number 23
Lane6: No RBS FT colony number 24
Lane7: empty
Lane8: empty

September 20

Liquid culture by NAKAGAWA
No RBS FT x8 (by using September 18)
Plate: CP+

Colony PCR

No RBS FT by using September19

Lane1 : 100bp ladder
Lane2 : colony number 1
Lane3 : colony number 2
Lane4 : colony number 3
Lane5 : colony number 4
Lane6 : colony number 5
Lane7 : colony number 6
Lane8 : colony number 7
Lane9 : colony number 8
Lane10: empty
Lane11: empty
Lane12: 100bp ladder
Liquid culture
A-11, A-12

Miniprep No RBS FT(by using September20) 1.-10.4µg/mL
2.-4.7µg/mL
3.-3.6µg/mL
4.-7.6µg/mL
5.-4.5µg/mL
6.-8.4µg/mL
7. 1.8µg/mL(average)
8. 18.1µg/mL
Restriction enzyme processing

DNA(No RBS FT)x2	E.coli	BufferH	MilliQ	total
30µL	1µL	4µL	5µL	40µL

in 37℃,2hours

Electrophoresis
DNA(No RBS FT) sample7,8: 10µL
Loading Dye : 2µL

Lane1: 1kb ladder
Lane2: empty
Lane3: No RBS FT(E) sample7
Lane4: empty
Lane5: No RBS FT(E) sample8
Lane6: empty

Electrophoresis(re)

RNA Extraction
5 leaves: 100mg
ISOGEN : 1mL
Elution : 20µL

cDNA Synthesis(1/4)

gDNA wipeout buffer	template RNA	H2O	Total
1µL	0.5µL	5.5µL	7µL

at 42℃, 2min

Reverse Transcriptase	RT buffer	primer mix	template	Total
0.5µL	2µL	0.5µL	7µL	10µL

at 42℃, 2min and 95℃,3min

RT PCR

buffer	dNTPs	MgSO4	primer f	primer r	Template	KODplus	MilliQ	Total
5	5	2	1.5	1.5	1	1	34.5	50

94℃	94℃	54℃	68℃	cycles
2min	15sec	30sec	10sec	30

1.TUBULIN
2.FUL
3.SEP3
4.AP1

September 22

mRNA extraction
FT and R9
Arabidopsis thaliana's leaves : 200mg

R9	FT	total
1.575μL	33.425μL	35μL

R9	GFP
1.575	33.425	35

1. Strip cuticles on palafilm by the head of a pencil.
2. Soak plant cells in R9 & FT or R9 & GFP for 2 hours(19:45~).
3. Add PBS (21:45~)

Microscope
R9+GFP+Plant Cell ver.3
R9+

R9	GFP	PBS	total
0.9	2.25	16.85	20μL

R9-

R9	GFP	PBS	total
0	2.25	17.65	20

same as 9/20, only not on parafilm but on microscope slide from the start.

September 23

RNA Extraction
FT- (GFP+) FT+

ISOGEN	chloroform	elution	total
1	200	11	212

Reverce Transcription

gDNA wipeout buffer	RNA	total
1	6	7

at 42 degree, for 2min.

Reverce Transcriptase	RT buffer	primer mix	Template	total
0.5	2	0.5	7	10

at 42 degree, for 30min.
at 95 degree, for 3min.

RT-PCR

Buffer	dNTPs	MgSO4	primer	Template	KOD Plus	MilliQ	total
5	5	2	1.5	1	1	34.5

94℃, 2min
94℃, 15sec
54℃, 30sec
68℃, 10sec

1.NC TUBULIN
2. FUL
3. SEP3
4. AP1
5.FT TUBULIN
6. FUL
7. SEP3
8. AP1

September 24

ScreeningPCR & Electrophoresis

Lane
1. 100bp ladder
2. T7-His:FT ① 9.2ng/μL
3. T7-His:FT ② 11.7ng/μL
4. T7-His:FT ③ 23.6ng/μL
5. T7-His:FT ④ 21.6ng/μL
6. T7-His:FT ⑤ 30.6ng/μL
7. T7-His:FT ⑥ 51.5ng/μL
8. T7-His:FT ⑦ 47.1ng/μL
9. T7-His:FT(A4) 20.0ng/μL
10. T7-His:FT(B1) 18.8ng/μL
11. final2(by_Secretion_group)
12. blank

FT Introduce

FT	R9	PBS	total
50	2.88	11.12	64

GFP	R9	PBS	total
7.2	2.88	53.02	64

We took 1 leaf out of 6 individuals of Arabidopsis thaliana that grow three weeks one by one
Leaves 30mg
1.cut off leaves
2.Inject the juice（by terumo-syringe）（Center tip、tuberculin 1nl)
3.store 20 min, then add PBS 600μL

September 25

RNA extraction
FT- (GFP+) FT+
elution 6µL

Reverce Transcription

gDNA wipeout buffer	RNA	total
1	6	7

at 42 degree, for 2min.

Reverce Transcriptase	RT buffer	primer mix	Template	total
0.5	2	0.5	7	10

at 42 degree, for 30min.
at 95 degree, for 3min.

RT-PCR

Buffer	dNTPs	MgSO4	primer	Template	KOD Plus	MilliQ	total
5	5	2	1.5	1	1	34.5

94℃, 2min
94℃, 15sec
54℃, 30sec
68℃, 10sec

1.TUBULIN NC
2.TUBULIN FT
3.FUL NC
4.FUL FT
5.SEP3 NC
6.SEP3 FT
7.AP1 NC
8.AP1 FT

October 12

Transformation

BL21(DE3)	T7-His-FT	T7-His-GFP-DT	total
1μL	10μL		11μL
1μL		10μL	11μL

October 16

Liquid culture
T7-His-FT 3mL

Transformation (retry)

BL21(DE3)	T7-His-GFP-DT	total
1μL	10μL	11μL

October 17

Moved 1mL of Liquid culture of T7-His-FT in 100mL of SOC medium -> 2 samples
Added IPTG 100μL to the medium(final conc. is 1mM) when value of OD600 is 0.649
Incubated at 20℃ for 4 hours.
Collect bacterial cells and freeze-preserved.

October 20

Liquid culture
2mL (T7-His-GFP)

October 21

Collect bacterial cells same way described above(value of OD600 is 0.8, at 37℃, for 4 hour)

Purification of GFP

Lysis buffer	lysozyme	Triton X-100	Ni-NTA resin	Elution buffer
5mL	0.1mL	0.3mL	1mL	2.5mL

fraction1:31.5µM->After consentrating 47.4µM
fraction2:15.8µM->After consentrating 33.4µM
fraction3:20.1µM
(Extinction coefficient=21,890)
RNA Extraction
Added 3μL of IPTG to 3mL of E.coli and then incubated 2 hour.

ISOGEN	chloroform	isopropanol	Elution buffer
1mL	0.2mL	0.5mL	11μL

deluted to 250ng/μL

Reverce Transcription

RNA(250ng/μL)	gDNA wipe out buffer	dH2O	total
0.5μL	1μL	5.5μL	7μL

Template	RT buffer	Primer mix	RT	total
7μL	2μL	0.5μL	0.5μL	10μL

RT-PCR Template is 20 times deluted cDNA

buffer	dNTPs	MgSO4	primer	primer	Template	KOD-Plus	MilliQ	total
5	5	2	1.5(His-FT f)	1.5(FT sequence r)	1	1	33	50
5	5	2	1.5(GAPDH)		1	1	34.5	50

94℃ 2min
94℃ 15sec
55℃ 30sec
68℃ 30sec
for 30 cycles

lane_1 : GAPDH
lane_2 : FT
lane_3 : 100bp ladder

October 22

Restriction

T7-His-FT(A4, 20ng/μL)	T7-His-FT(B2, 73ng/μL)	bufferH	EcoR1	Pst1	MilliQ	total
10μL		2μL	0.5μL	0.5μL	7μL	20μL
	5μL	2μL	0.5μL	0.5μL	12μL	20μL

at 37℃ for 1 hour

lane1 : T7-His-FT(B2)
lane2 : T7-His-FT(B2, EcoR1/Pst1)
lane3 : T7-His-FT(A4)
lane4 : T7-His-FT(A4, EcoR1/Pst1)

Transformation

T7-His-FT(B2)	BL21(DE3)	total
1	10	11

October 23

RNA Extraction from plant cell

ISOGEN	chloroform	isopropanol	High salt solution	Elution buffer
1mL	0.25mL	0.25mL	0.25mL	11μL

notes: After the homogenization with ISOGEN, sample 1 was incubated at 50℃ for 10min.
Sample1. 855.8ng/µL
Sample2. 812.4ng/µLL

October 24

Collect bacterial cells(T7-6His:FT) same way described above(value of OD600 is 0.722, at 37℃, for 4 hour)
2mL of culture was used for RNA extraction.
Purification of FT

Lysis buffer	lysozyme	Triton X-100	Ni-NTA resin	Elution buffer
5mL	0.15mL	0.3mL	0.5mL	1.2mL

fraction1:65.1µM
fraction2:42.1µM
fraction3:10.9µM
fraction4:6.8µM
(Ectinction coefficient=21,430)

RNA extraction

ISOGEN	chloroform	isopropanol	Elution buffer
1mL	0.2mL	0.5mL	11μL

diluted to 250ng/μL

Reverce Transcription

RNA(250ng/μL)	gDNA wipe out buffer	dH2O	total
0.5μL	1μL	5.5μL	7μL

Template	RT buffer	Primer mix	RT	total
7μL	2μL	0.5μL	0.5μL	10μL

RT-PCR Template is 20 times deluted cDNA

buffer	dNTPs	MgSO4	primer	primer	Template	KOD-Plus	MilliQ	total
5	5	2	1.5(His-FT f)	1.5(FT sequence r)	1	1	33	50
5	5	2	1.5(GAPDH)		1	1	34.5	50

94℃ 2min
94℃ 15sec
55℃ 30sec
68℃ 30sec
for 30 cycles

lane_1 : 100bp ladder
lane_2 : GAPDH
lane_3 : FT

Assay of FT activation

protein-R9 solution mix	FT	GFP	R9	PBS
sample1 (FT-)	-	200µL	0.11mg	100µL
sample2 (FT+)	230µL	-	0.21mg	70µL

100mg of Arabidopsis thaliana leaves were harvested for each samples and injected the solution mix.
incubation at room temperature for 13h in dark

October 25

sample1

sample2

ISOGEN	chloroform	isopropanol	High salt solution	Elution buffer
1mL	0.25mL	0.25mL	0.25mL	11μL

Sample1. 682.7ng/µL
Sample2. 859.3ng/µLL

diluted to 250ng/μL

Reverce Transcription

RNA(250ng/μL)	gDNA wipe out buffer	dH2O	total
1μL	2μL	11μL	14μL

Template	RT buffer	Primer mix	RT	total
14μL	4μL	1μL	1μL	20μL

RT-PCR Template is 20 times diluted cDNA

buffer	dNTPs	MgSO4	primer	Template	KOD-Plus	MilliQ	total
5	5	2	1.5	1	1	34.5	50

94℃ 2min
94℃ 15sec
54℃ 30sec
68℃ 10sec

February 7

Preculture

We started preculture at 12:10.

February 8

Liquid culture

We start culturing with 300mL of LB medium.

time	OD600
12:00	start
14:10	0.019
14:45	0.154
15:05	0.267
15:21	0.64

Making Competent Cell

We made competent cells.

Transformation

pGEM_TAP
LacP (BBa_R0011)
DT (BBa_B0015)

Making Culture Medium Plates

We made 200mL of ampicillin culture, kanamycin culture, and chloramphenicol culture.

Transformation

GFP(BBa_E0040) in pSB1A2
DT(BBa_B0015) in pSB1AK3
ara(BBa_I0500) in pSB2K3
LacP(BBa_R0011) in pSB1A2

February 9

Transformation

BBa-E0040(GFP)(Mr.Fujita)

Liquid culture

DT, LacP colony transformed on February 8
colony of competent cell made on February 8
B0040 1.4k pSB1A2 B0034 1.2M pSB1A2(from iGEM parts plate)

Making Competent cells

We did preculture for overnight. We put 1.5mL of preculture on 150mL of LB culture.

time	OD600
11:45	start
13:30	0.048
14:30	0.168
15:03	0.256
15:20	0.405
15:35	0.459
at last	0.576

February 11

Checking Transformation efficiency

Conpetent cell's transformation efficiency is 1.3x10^4colonys/μg

February 13

Transformation

Const promoter J23110, J23109, J23100

DNA	Competent cell	Total
1μL	20	21

No colony was there on February 14

Liquid culture

LacP, DT, RBS(BBa_B0034),GFP
start at 20:00
in Plus grow with Ampicilin 3mL

February 14

Miniprep

DNA	concentration[μg/μL]
LacP3	39.6
LacP4	40.8
LacP5	28.9
RBS1	28.2
RBS2	57.4
RBS3	13.2
DT3	69.7
DT4	64.4
DT5	61.5
GFP1	64.0
GFP2	50.5
GFP3	66.0

Restrictive Digestion

Const promoter J23100

DNA	Spe1	Pst1	Buffer2	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

at 37℃ for overnight

February 15

Making gel

1% Agarose gel

Agarose	TAE
1.6g	160mL

Electrophoresis

No.1

Gel No.1

Restriction product	loading dye
5μL	1

The marker was 1kb ladder
It seemed that this restriction product was not cut.

No.2

Gel No.2
Lane1 : 1kb ladder
Lane2 : J23100 2μL + 6*Loading dye 1μL
Lane3 : J23100(Spe1,Pst1) 5μL
Lane4 : J23100(Spe1,Pst1) 2μL

There were bands on lane_2 and we cannot identify these bands because the sample of lane_2 was not cut with any restriction enzyme.
There must have been bands at 2100bp and 883bp on lane_3 and lane_4.

Testing whether restriction enzyme were deactivated or not

DNA(DT)	restriction enzyme	Buffer	BSA	MilliQ	Total
10	0.5	3	0.5	16	30

at 37℃ for Oveernight
Restriction enzyme means Spe1(1, 2) Pst1(1, 2, 3) in this time.

February 16

Electrophoresis

1. 1kb ladder
2. DT2
3. DT3
4. DT2 (Spe1-1)
5. DT2 (Spe1-2)
6. DT2 (Pst1-1)
7. DT2 (Pst1-2)
8. DT2 (Pst1-3)
9. DT3 (Pst1-4)
10. 1kb ladder

Pst1-1, Pst1-2, and Pst1-3 did not cut DNAs. They seemed to be deactivated.

Genomic PCR

10*Buffer for KOD Plus	2mM dNTPs	25mM MgSO4	10μM primer-f	10μM primer-r	158ng/μL Genomic DNA	KOD plus	MilliQ	Total
5	5	3	1.5	1.5	1	1	32	50

Electrophoresis

1. 1kb ladder
2. TatABCD (2.5kb)
3. TAMO reductase (2.7kb)
4. Negative control
We got bands of TatABCD but there were nonspecific amplification products.
We failed amplification of TAMO reductase.

Transformation

Constitutive promoter (BBa_J23107, BBA_J23117)
High copy plasmid (pSB1AT3)

DNA	competent cell
1μL	10μL

February 17

PCR

We did PCR to amplify products of PCR that we had done yesterday but we could not amplify TatABCD.

Genomic PCR

Buffer	dNTPs	MgSO4	primer-f	primer-r	genomic DNA	KOD plus	MilliQ	Total
2.5	2.5	5	0.75	0.75	0.5	0.5	16	50

Predenature 94℃, 2min
Denature 98℃, 10sec
Annealing 57℃, 30sec
Extension 68℃, 2.5min
(30cycles)

Electrophoresis

1. 1kb ladder
2. TAMO reductase
3. Negative control

Restrictive Digestion

J23100	Spe1	Pst1	Buffer2	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

Genomic PCR

	Buffer	dNTPs	MgSO4	primer-f	primer-r	genomic DNA	KOD plus	MilliQ	Total
TMAO reductase	2.5	2.5	3	0.75	0.75	0.5	0.5	15.5	25
TatABCD	2.5	2.5	2	0.75	0.75	0.5	0.5	15.5	25
TatABCD	2.5	2.5	2	0.75	0.75	5	0.5	10.5	25

Electrophoresis

1. 1kb ladder
2.3. TAMO reductase
4. TatABCD
5. TatABCD(10 times amount of genome)

Checking of restriction enzyme

DT	enzyme	Buffer	BSA	MilliQ	Total
2	0.5	3	0.5	24	30

at 37℃ for overnight
We checked EcoR1 and Xba1.

February 18

Miniprep

	μg/mL	260/280	230/260
JS3117-1	135	1.5	2.06
JS3117-2	75	1.6	1.63
JS3109-1	115	1.5	1.88
JS3109-2	75	1.65	1.71
pSB1AT3-1	70	1.66	1.83
pSB1AT3-2	100	1.52	1.54

diluted to 25 times

Making Competent cells

We put 3mL of preculture product on yesterday onto 300mL of LB medium

time	OD600
10:30	start
12:10	0.118
13:00	0.270
13:30	0.502

Transformation

pSB1AT3-2	competent cell	MilliQ	Total
0	20	10	30
2	20	8	30
10	20	0	30

Results(on Feb. 19)

pSB1AT3-2	number of colony
0	0
2	177
10	590

Transformation efficiency 7.4x10^4 colonys/μg

February 20

Restrictive Digestion

sample 1

DT plasmid	EcoR1	Xba1	Buffer	BSA	MilliQ	Total
7.5	0.5	0.5	3	0.5	18	30

sample2

GFP plasmid	EcoR1	Spe1	Buffer	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

Electrophoresis

sample1

a. sample1 2μL + MilliQ 3μL + 6×Loading Dye 1μL
b. sample1 5μL + 6×Loading Dye 1μL
lane1. 1kb ladder
lane2. a
lane3. b
lane4. a
lane5. b
lane6. a
lane7. b
lane8. 1kb ladder

sample2

c. sample2 2μL + MilliQ 3μL + 6×Loading Dye 1μL
d. sample2 5μL + 6×Loading Dye 1μL
lane1. 1kb ladder
lane2. c
lane3. d
lane4. 1kb ladder

PCR

	Buffer	dNTPs	MgSO4	primer-f	primer-r	genomic DNA	KOD plus	MilliQ	Total
TatABCD1	2.5	2.5	1.5	0.75	0.75	0.5	0.5	16	25
TatABCD2	2.5	2.5	1.5	0.75	0.75	0.5	0.5	16	25
TMAO reductase1	2.5	2.5	2	0.75	0.75	0.5	0.5	15.5	25
TMAO reductase2	2.5	2.5	2	0.75	0.75	5	0.5	10.5	25

Predenature 94℃ 2min
Denature 98℃ 10sec
Annealing 59℃ 30sec
Extension 68℃ 2.5min
→30cycles

	Buffer	dNTPs	MgSO4	primer-f	primer-r	PCR products	genomic DNA	KOD plus	MilliQ	Total
TatABCD1	2.5	2.5	1.5	0.75	0.75	0	0.5	0.5	16	25
TatABCD2	2.5	2.5	1.5	0.75	0.75	1	0	0.5	15.5	25
TMAO reductase1	2.5	2.5	2	0.75	0.75	0	0	0.5	16	25
TMAO reductase2	2.5	2.5	2	0.75	0.75	0	0	0.5	16	25

Predenature 94℃ 2min
Denature 98℃ 10sec
Annealing 59℃ 30sec
Extension 68℃ 2.5min
→35cycles

Electrophoresis

lane1.1kb ladder
lane2.TatABCD
lane3.TatABCD
lane4.TAMO1
lane5.TAMO2
lane6.1kb ladder

lane1.1kb ladder
lane2.TatABCD1
lane3.TatABCD2
lane4.TAMO
lane5.TAMO
lane6.1kb ladder

February 21

PCR (Advantage HF protocol)

	buffer	dNTPs	primer-f	primer-r	gDNA	PCR products	DW	polymerase	Total
TatABCD	2.5	2.5	0.75	0.75	1	0	17	0.5	25
TMAO	2.5	2.5	0.75	0.75	0	1	17	0.5	25

Predenature 94℃ 1min
Denature 94℃ 30sec
Annealing 58℃ 30sec
Extension 68℃ 3min
→25cycles

Electrophoresis

1. 1kb ladder 2μL
2. TatABCD 5μL + 6×Loading Buffer 1μL
3. TAMO 5μL + 6×Loading Buffer 1μL
4. 1kb ladder 2μL

Liquid culture

pSB3C5-1,2
pSB4K5-1,2

February 22

Gel extraction

lane 1 of the gel 45.0μg/mL

PCR purification

product 38.2μg/mL

PCR

TMAO reductase

	Buffer	dNTPs	MgSO4	prefix primer-f	suffix primer-r	product of gel extract	product of PCR purification(1ng/μL)	KOD plus	MilliQ	Total
1	5	5	4	1.5	1.5	0.5	0	1	32.5	50
2	5	5	4	1.5	1.5	1	0	1	32.5	50
3	5	5	4	1.5	1.5	0	0.5	1	32.5	50
4	5	5	4	1.5	1.5	0	1	1	32.5	50

94℃, 2min
98℃, 10sec
59℃, 30sec
68℃, 3min
→25cycles

Electrophoresis

1. 1kb ladder
2. TAMO1
3. TAMO2
4. TAMO3
5. TAMO4
6. constructive promoter 1-18C
7. constructive promoter Spe1
8. constructive promoter Pst1
9. 1kb ladder

PCR

	Buffer	dNTPs	MgSO4	prefix primer-f	suffix primer-r	product of PCR purification(1ng/μL)	KOD plus	MilliQ	Total
1	5	5	3	1.5	1.5	0.5	1	32.5	50
2	5	5	3	1.5	1.5	1	1	32	50
3	5	5	3	1.5	1.5	2	1	31	50
4	5	5	3	1.5	1.5	3	1	30	50
5	5	5	3	1.5	1.5	10	1	29	50
6	5	5	3	1.5	1.5	0	1	33	50

94℃, 2min
98℃, 10sec
59℃, 30sec
68℃, 3min
→25cycles

Electrophoresis

Checking Dpn1

Buffer	LacP(28.7ng/μL)	Dpn1	MilliQ	Total
2	10	0.5	7.5	20
2	10	0	5	17

February 23

Colony PCR

TatABCD(2 samples)

Buffer	dNTPs	MgSO4	primer-f	primer-r	KOD plus	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

Predenature 94℃ 1min
Denature 98℃ 10sec
Annealing 59℃ 30sec
Extension 68℃ 3min
→25cycles

Electrophoresis

1. 1kb ladder 2μL
2. TatABCD 1 5μL + 6×Loading Buffer 1μL
3. TatABCD 2 5μL + 6×Loading Buffer 1μL
4. 1kb ladder 2μL

Miniprep

pSB4K5 and pSB3C5
deluted it to 25 times and then measured it
pSB4K5 1 : 60.0 μg/ml 1.67(260/280) 1.98(260/230)
pSB4K5 2 : 55.0 μg/ml 1.49(260/280) 1.62(260/230)
pSB3C5-3 : 3.6 μg/ml 1.57(260/280) 3.00(260/230)
pSB3C5-4 : 1.3 μg/ml 1.44(260/280) 1.04(260/230)

Liquid culture

pSB3C5-3,4

Electrophoresis

1. 1kb ladder 2μL
2. pSB3C5-3 5μL, 6×loading dye 1μL
3. pSB3C5-4 5μL, 6×loading dye 1μL
4. 1kb ladder 2μL

February 27

Test of Dpn1

Buffer2	GFP2	BSA	MilliQ	Dpn1
3	3	0.3	23	1

Colony PCR

	buffer	dNTPs	MgSO4	Primer-f	Primer-r	MilliQ	KOD Plus	Total
Colony PCR(2 samples)	5	5	3	1.5	1.5	33	1	50
Negative control	5	5	3	1.5	1.5	34	0	50

Predenature 94℃ 2min
Denature 98℃ 10sec
Annealing 59℃ 30sec
Extension 68℃ 3min
→25cycles

Electrophoresis

lane	DNA	sample	Loading Dye	MilliQ
1	1kb ladder	2	0	0
2	product of PCR1	5	1	0
3	product of PCR2	5	1	0
4	product of PCR(Negative control)	5	1	0
5	product of PCR(2/23)	5	1	0
6	GFP2(DPN1)	10	2	0
7	GFP2	3	2	7
8	1kb ladder	2	0	0

Results of liquid culture

We measure this after dilute it to 10 times.

pSB3C5-5	pSB3C5-6	pSB3C5-5(1% glucose)	pSB3C5-6(1% glucose)
8.5[µg/ml]	-1.8	-17.9	-18.2

PCR

	buffer	dNTPs	MgSO4	Primer-f(prefix)	Primer-r(suffix)	PCR purification product(1ng/µL)	MilliQ	KOD Plus	Total
1	5	5	3	1.5	1.5	0.2	32.8	1	50
2	5	5	3	1.5	1.5	0.5	32.5	1	50

PCR purification product was that purification product(75ng/µL) of electrophoresis-3 deluted to 1ng/µL

Predenature 94℃,2min
Denature 98℃,10sec
Annealing 59℃,30sec
Extension 68℃,3min
→25cycles

February 28

Electrophoresis

1. 1kb ladder
2. PCR1 →Product of gel extraction : TatABCD with prefix and suffix 105[ng/µL]
3. PCR2

Restrictive Digestion

Buffer2	plasmid(?)	enzyme	MilliQ	Total
2	2	0.2	15.8	20

incubate 1 hour at 37℃

Electrophoresis

1. 1kb ladder
2. Control (without enzymes)
3. EcoR1
4. Xba1 (crystallized)
5. Xba1 (with seal)
6. Spe1
7. Pst1
8. 1kb ladder

PCR and Electrophoresis

Quick Taq Dye Mix	primer-f	primer-r	template	MilliQ	Total
25	1.0	1.0	0.5	22.5	50

Predenature 94℃,2min
Denature 94℃,30sec
Annealing 59℃,30sec
Extension 68℃,3min
→25cycles

Restrictive Digestion

BufferH	TatABCD	EcoR1	Spe1	MilliQ	Total
2	5	0.2	0.2	12.6	20

PCR purification

We eluted the product for 30µL MilliQ

Ligation

Insert(TatABCD)	Vector(pSB1C3)	Ligation High	Total
10	1	5	16

4℃, overnight

February 29

Transformation

TatABCD	competent cell	Total
1	10	11

Checking Restriction enzyme

plasmid seems to be 1-18C promoter	Enzyme	Buffer	MilliQ	Total
2	0.2	2	15.8	20

Checking TatABCD

TatABCD	Hind3	Buffer	MilliQ	Total
5	0.2	2	12.8	20

PCR

	buffer	dNTPs	MgSO4	Primer-f	Primer-r	ColE1(6.5ng/µL) / TMAO	MilliQ	KOD Plus Neo	Total
Kil	2.5	2.5	1.5	0.75	0.75	0.5	16	0.5	25
TMAO	2.5	2.5	1.5	0.75	0.75	0.5	16	0.5	25

Predenature 94℃,2min
Denature 98℃,10sec
Annealing 60℃,30sec
Extension 68℃,3min
→30cycles

Electrophoresis

1. 1kb ladder
2. Kil (649bp)
3. TMAO (2720bp)
4. TMAO (Quick Taq)
5. TatABCD (Quick Taq)
6. TatABCD (Hind3)
7. 1kb ladder

March 1

PCR

TMAO

Template is gDNA and product of colony PCR gel extraction

	Buffer	gNTPs	MgSO4	Primer-f	Primer-r	KOD Plus Neo	Template gDNA	product of gel extraction	DW	Total
1	2.5	2.5	1.5	0.75	0.75	0.5	0.5	0	16	25
2	2.5	2.5	1.5	0.75	0.75	0.5	0	2	14.5	25

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 1.5min
→25cycles

Kil

Buffer	dNTPs	MgSO4	primer-f	primer-r	colE1(6.5ng/µL)	KOD Plus Neo	MilliQ	Total
2.5	2.5	1.5	0.75	0.75	0.5	16	0.5	25

94℃, 2min
98℃, 10sec
61℃, 30sec
68℃, 1min
→20cycles

Electrophoresis

1. 1kb ladder
2. TMAO1 (gDNA)
3. TMAO2 (product of gel extraction)
4. Kil

PCR

kil

Buffer	dNTPs	MgSO4	primer-f	primer-r	Product of Purification	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	32	1	50

94℃, 2min
98℃, 10sec
61℃, 30sec
68℃, 30sec
20cycles
→Purification 230ng/µL

Restrictive Digestion

Kil	EcoR1	Spe1	BufferH	MilliQ	Total
5	0.2	0.2	2	12.6	20

incubate at 37℃, for 1.5 hours

PCR Purification

Ligation

Kil	pSB1C3	Ligation High	Total
5	1	3	9

at 4℃, for overnight

March 2

Ligation

Kil	pSB1C3	Ligation High Ver.2	Total
5	1	3	9

TatABCD	pSB1C3	Ligation	Total
10	1	5	16

at 16℃ for 1 hour

Transformation

Kil	Kil(3/1,Ligation)	TatABCD	competet cell	Total
1	0	0	10	11
0	1	0	10	11
0	0	1	10	11

PCR

Quick Taq	primer-r	primer-f	template	MilliQ	Total
25	1	1	0.5	22.5	50

Electrophoresis

Restrictive Digestion

pSB3C5-5	EcoR1	Pst1	BufferH	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

at 37℃, for 2 hour

Electrophoresis

1. 1kb ladder 2µL
2. pSB3C5 5µL + 6×Loading Buffer 1µL
・product of gel extraction(about 2700bp)
－30.9µg/mL

Restrictive Digestion

GFP1 ,2 ,3

GFP	EcoR1	Pst1	Buffer	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

at 37℃, for 2.5 hours

Restrictive Digestion

DT	EcoR1	Xba1	BufferM	BSA	MilliQ	Total
10	0.2	0.2	3	0.3	16.3	30

Constitutive Promoter	Spe1	Pst1	BufferM	BSA	MilliQ	Total
15	0.2	0.2	3	0.3	11.3	30

at 37℃, 2 hours

J23117-1:135ng/µL, J23107-1:115ng/µL
DT3→PCR Purification
Promoter→Gel Extraction

Checking TMAO

something seems to be TMAO	Buffer2	EcoR1	MilliQ	Total
10	2	0.5	7.5	20

at 37℃, for 1 hour

Electrophoresis

1. 1kb ladder
2. GFP1 that had been cut by restriction enzyme
3. GFP2 that had been cut by restriction enzyme
4. GFP3 that had been cut by restriction enzyme
5. GFP1
6. GFP2
7. GFP3
8. TMAO (control)
9. TMAO (EcoR1)
10. DT (control)
11. DT (EcoR1, Xba1)
12. 1kb ladder

Checking TatABCD

Quick Taq	primer-f	primer-r	MilliQ	Total
25	1	1	23	50

Electrophoresis

March 3

PCR

	template	buffer	dNTPs	MgSO4	VF	VR	KOD plus	MilliQ	Total
1	1	5	5	3	1.5	1.5	1	32	50
2	2	5	5	3	1.5	1.5	1	31	50

94℃, 2min
98℃, 10sec
50℃, 30sec
68℃, 1min
→30cycles

Miniprep

14.2µg/mL, 15.0µg/mL

March 4

Sequence of TatABCD

Quick Taq	primer-f	promer-r sequence	template	MilliQ	Total
25	1	1	1	23	50

Quick Taq	primer-f sequence	primer-r	template	MilliQ	Total
25	1	1	1	23	50

Colony PCR of TMAO

buffer	dNTPs	NgSO4	primer-f	primerr-r	KOD plus	MilliQ	Total
5	5	4	1.5	1.5	1	32	50

→ethanol precipitation
94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 2.5min
→25cycles

Electrophoresis

1. 1kb ladder
2. TatABCD1
3. TatABCD2
4. TMAO
5. 1kb ladder

Restrictive Digestion

TMAO	EcoR1	BufferH	BSA	MilliQ	Total
10	0.2	3	0.3	16.5	30

TMAO	Xba1	Pst1	BudderM	BSA	MilliQ	Total
10	0.2	0.2	3	0.3	16.3	30

at 37℃ for 1 hour

Electrophoresis

Transformation

pSB1C3	competent cell(made at 2/8)	Total
5	100	105

March 5

Restrictive Digestion

pSB1C3(Xba1, Spe1)	Pst1	BufferH	BSA	MilliQ	Total
10	0.2	2	0.2	7.6	20
pSB1C3(Xba1, Spe1)	EcoR1	BufferH	BSA	MilliQ	Total
10	0.2	2	0.2	7.6	20

at 37℃ for 1 hour
→Then we did ethanol precipitation

Ligation

Kil(EcoR1, Spe1)	pSB1C3(EcoR1)	Ligation High	Total
5	1	3	9

at 16℃ for 1 hour

Transformation

Kil	competent cell	Total
1	10	11

We used commercially available competent cells in this time.

PCR

TMAO

buffer	dNTPs	MgSO4	Primer-f	Primer-r	Template	KOD plus	MilliQ	Total
5	5	3	1.5	1.5	1	1	32	50

Electrophoresis

Restrictive Digestion

	LacP	pSB3C5	EcoR1	Pst1	BufferH	BSA	MilliQ	Total
1	20	0	0.5	0.5	3	0.5	5.5	30
2	0	20	0.5	0.5	3	0.5	5.5	30

at 37℃ for 1 hour
1→Ethanol precipitation　45.4µg/mL
2→Gel extraction　38.7µg/mL

Ligation

LacP	pSB3C5	Ligation High	Total
10	2	6	18

at 4℃ for overnight

Transformation

LacP+pSB3C5	competent cell	Total
1	10	11

on ice for 30 mins.
heat shock at 42℃ for 60secs
on ice for 2 mins.
After we incubate with 200µL of SOC culture for 1 hour, we did plating on LB culture with CP

Restrictive Digestion

GFP Plasmid	EcoR1	Spe1	Buffer2	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

at 37℃ for 2 hours

Electrophoresis

1. Ladder 2µL
2. GFP Plasmid (already restricted) 2µL + Loading Dye 2µL + MilliQ 8µL
3. Ladder 2µL

PCR

torA signal and pspA
We did Colony PCR to pspA

Buffer	dNTPs	MgSO4	Primer-f	Primer-r	template(TMAO)	KOD plus	MilliQ	Total
2.5	2.5	1.5	0.75	0.75	0.5	0.5	16	25

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 30sec

electrophoresis

1. 100bp Ladder
2. torA signal (272bp)
3. pspA (969bp)
4. 100bp Ladder

March 6

Restrictive Digestion

GFP	EcoR1	Spe1	BufferM	BSA	MilliQ	Total
12	0.5	0.5	3	0.5	13.5	30

We did incubate at 37℃ for 1.5hours.
And we did gel extraction on 3/7 and get 40.0μg/mL GFP.

PCR

buffer	dNTPs	MgSO4	Primer-f	Primer-r	template	KOD plus neo	MilliQ	Total
5	5	3	1.5	1.5	0.5	1	32.5	50

94℃　2min
98℃　10sec
60℃　30sec
68℃　(torA 10sec / pspA 30sec) 25 cycles
We used product of PCR on 3/5 of torA and pspA as template.

Restrictive Digestion

Kil	EcoR1	Spe1	BufferM	BSA	MilliQ	Total
10	0.3	0.3	3	0.3	16.1	30

DT	EcoR1	Xba1	Buffer2	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

at 37℃ for 2 hours
→ purification 37.7ng/μL

Ligation

Kil	pSB1C3	Ligation High Ver.2	Total
4	2	3	9

Kil : 350fmol
pSB1C3 : 29fmol

at 16℃ for overnight

March 7

Electrophoresis

1. 1kb ladder 2µL
2. pspA (PCR product)2.5µL + Loading Dye 0.5µL
3. GFP 30µL + Loading Dye 6µL
4. 1kb ladder 2µL

The GFP was gel extracted on 3/6 and concentrated by Vacuum in 150µg/mL

Ligation

VectorDNA	GFP	Ligation High Ver.2	Total
5	15	10	30

Restrictive Digestion

torA	EcoR1	Spe1	bufferM	BSA	MilliQ	Total
10	0.3	0.3	3	0.3	16.1	30

pspA	EcoR1	Spe1	bufferM	BSA	MilliQ	Total
5	0.3	0.3	3	0.3	21.1	30

at 37℃ for 1.5 hours

Purification

torA→31.8ng/µL
pspA→49.3ng/µL

Ligation

torA	pSB1C3	Ligation High Ver.2	Total
3	3	3	9

pspA	pSB1C3	Ligation High Ver.2	Total
4	2	3	9

at 4℃, for overnight

torA→31.8ng/µL×3µL=95.4ng=0.529pmol
pSB1C3→19.4ng/µL×3µL=58.2ng=0.042pmol
pspA→49.3ng/µL×4µL=197.2ng=0.308pmol
pSB1C3→19.4ng/µL×2µL=38.8ng=0.029pmol

March 8

Restrictive Digestion

pSB4K5	EcoR1	Spe1	BufferM	BSA	MilliQ	Total
20	0.2	0.2	3	0.2	6.4	30

at 37℃ for 1 hour.
→Purification : 36.6ng/µL

Ligation

Kil	pSB4K5	Ligation High Ver.2	Total
10	1	5	16

at 4℃ for overnight

Kil→37.7ng/µL×10µL=377ng=879fmol
pSB4K5→36.6ng/µL×1µL=36.6ng=86fmol

Liquid culture

LacP + pSB3C5 -1, 2

Transformation

torA	pspA	competent cell	Total
1	0	10	11
0	1	10	11

We use commercially available competent cells in this time.

March 9

Restrictive Digestion

TatABCD	Xba1	Pst1	BufferM	BSA	MilliQ	Total
10	0.2	0.2	3	0.3	16.3	30

at 37℃ for 1hour
→purification : 75.0μg/mL (1.11 260/280 , 0.81 260/230)

Miniprep

LacP + pSB3C5 1 80.5μg/mL (1.78 260/280 , 2.00 260/230)
LacP + pSB3C5 2 107.2μg/mL (1.83 260/280 , 1.90 260/230)

Colony PCR

Quick Taq	VF	VR	MilliQ	Total
25	1	1	23	50

94℃ 2min
94℃ 30sec
55℃ 30sec
68℃ 6sec
25cycles

Ligation

TatABCD	constP J23107	Ligation High Ver.2	Total
5	1	3	9

TatABCD : 227fmol
constP J23107 : 21fmol

Transformation

	pspA	torA	Kil	competent cell
1	1	0	0	10
2	0	1	0	10
3	0	0	1	10

Miniprep

4mL of plusgrow which had been cultured for overnight.
pSB4K5 : 80.5μg/mL

March 10

Screening PCR

Quick Taq	VF	VR	MilliQ	Total
25	1	1	23	50

Then we did electrophoresis to confirm.
1. 1kb ladder
2. kil (649bp)
3. 4. 5. pspA (969bp)
6. 1kb ladder

1. 100bp ladder
2. 3. 4. torA signal

Restrictive Digestion

LacP-pSB3C5	Spe1	Pst1	BufferM	BSA	MilliQ	Total
10	0.2	0.2	2	0.2	7.4	20

for 2.5 hours at 37℃
→purification 29.0ng/μL

torA	Xba1	Pst1	BufferM	BSA	MilliQ	Total
10	0.2	0.2	2	0.2	7.4	20

for 2.5 hours at 37℃
→purification 91.8ng/μL

Ligation

torA	LacP-pSB3C5	Ligation High Ver.2	Total
4	2	3	9

torA : 929fmol
LacP-pSB3C5 : 284fmol
for overnight at 4℃

March 11

Miniprep

We used 3μL of plus grow that we had cultured for overnight.
torA : 62.8ng/μL

Screening PCR

Quick Taq	VF	VR	MilliQ	Total
25	1	1	23	50

Electrophoresis

1. 1kb ladder
2〜11. pspA (969bp)
12. 1kb ladder

The results were shown as photograph in the right.

It seemed that there were shorter sample than expected sample, so we did electrophoresis with pspA which was product of PCR and pspA which had already cut with EcoR1 and Spe1.

1.1kb ladder
2. pspA (PCR product)
3, pspA (Eco, Spe)
4〜6, pspA (colony PCR)
7,1kb ladder

The results were shown as photograph in the right.

March 12

Transformation

DT(1ng/μL)	DT(0.1ng/μL)	Kil	LacP-torA	MilliQ	competent cell	Total
1	0	0	0	0	20	21
0	1	0	0	0	20	21
0	0	5	0	0	50	51
0	0	0	5	0	50	51
0	0	0	0	1	20	21

Restrictive Digestion

pspA	EcoR1	Spe1	BufferM	BSA	MilliQ	Total
10	0.5	0.5	3	0.3	15.7	30

at 37℃ for 4 hours
→ We did purification and got 48.3ng/μL pspA.

Ligation

pspA	pSB1C3	MilliQ	Ligation High Ver.2	Total
4	2	0	3	9
2	2	0	2	6
0	2	2	2	6

March 13

Miniprep

pSB1C3 74.2µg/mL 1.65 (260/280) 1.31 (260/230)

March 14

Restrictive Digestion

pSB1C3	EcoR1	Spe1	BufferM	BSA	MilliQ	Total
20	0.2	0.2	4	0.4	15.2	40

We did gel extraction and got 47.2ng/µL pSB1C3 but we did not cut out RFP.

Ligation

torA	pSB1C3	Ligation High Ver.2	Total
4	2	3	9
MilliQ	pSB1C3	Ligation High Ver.2	Total
4	2	3	9

at 16℃, for 1 hour

torA : 0.707pmol
pSB1C3 : 0.068pmol

Liquid culture

We cultured LacP-pSB3C5 1,2,3,4,5 (CP tolerance)on culture with Amp.
→Only 4 which did not be cultured succeeded.

March 15

Liquid culture

We cultured LacP-pSB3C5 6,7,8,9,10 on culture with ampicillin.
→6,8,9,10 were succeeded.

Restrictive Digestion

GFP	EcoR1	Spe1	Buffer2	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

DT	EcoR1	Xba1	Buffer2	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

for 2 hours at 37℃.

Miniprep

pspA (pSB1C3) 40.5ng/µL

Ligation

pspA	DT	Ligation High Ver.2	Total
5	1.5	3	9.5

pspA : 385fmol
DT : 36fmol

Transformation

J23107-TatABCD	DT (0.1ng/µL)	DT (0.01ng/µL)	pspA-DT	competent cells on 3/15	Total
2	0	0	0	20	22
0	2	0	0	20	22
0	0	2	0	20	22
0	0	0	2	20	22

Screening PCR

Kil, pspA and torA

Quick Taq	Primer-r	Primer-f	MilliQ	Total
25	1	1	23	50

March 16

Miniprep

torA (pSB1C3) 68.8ng/µL
Kil (pSB4K5) 92.7ng/µL
torA was red for some reason. We do not know why.

Colony PCR

Quick Taq	Primer-r	Primer-f	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 6sec
→25cycles

Electrophoresis

The results were shown as photograph in the right.

Checking Transformation Efficiency

competent cells that were made on March 15.
DNA : 0.02ng → 668 colonies Transformation Efficiency : 3.3×10^7
DNA : 0.2ng → 1739 colonies Transformation Efficiency : 8.7×10^6

Restrictive Digestion

pSB1C3	EcoR1	Spe1	BSA	BufferM	BufferH	MilliQ	Total
20	0.2	0.2	0.3	3	0	6.3	30
5	0.2	0	0.2	0	2	12.6	20

at 37℃, for 2 hours.
We did gel extraction for product with EcoR1, Spe1. We got 46.1ng/µL pSB1C3.

Kil(pSB4K5)	EcoR1	Pst1	BSA	BufferH	MilliQ	Total
5	0.2	0.2	0.2	2	12.4	20
5	0.2	0	0.2	2	12.6	20

for overnight at 37℃.
We did this to confirm.

pspA (pSB1C3)	EcoR1	Pst1	BSA	BufferH	MilliQ	Total
5	0.2	0.2	0.2	2	12.4	20
5	0.2	0	0.2	2	12.6	20

for overnight at 37℃.
We did this to confirm.

Ligation

torA	pSB1C3	Ligation High Ver.2	Total
4	2	3	9

MilliQ	pSB1C3	Ligation High Ver.2	Total
4	2	3	9

at 16℃, for overnight

torA→767fmol
pSB1C3→68fmol

March 17

Miniprep

J23107-TatABCD 72.7ng/µL
pspA-DT 50.5ng/µL

Checking the Insert

J21037-TatABCD	EcoR1	Pst1	BSA	BufferH	MilliQ	Total
5	0.2	0.2	0.2	2	12.4	20
5	0.2	0	0.2	2	12.6	20

Success.

pspA-DT	EcoR1	Pst1	BSA	BufferH	MilliQ	Total
5	0.2	0.2	0.2	2	12.4	20
5	0.2	0	0.2	2	12.6	20

Failed.

March 19

Restrictive Digestion

DT	EcoR1	Xba1	BSA	BufferM	MilliQ	Total
10	0.2	0.2	0.3	3	16.3	30

We did Gel extraction and got 17.2ng/µL of DT.

Ligation

Kil	DT	Ligation High Ver.2	Total
10	2	6	18

We did this for an hour at 16℃.

Restrictive Digestion

GFP	EcoR1	Spe1	BSA	BufferM	MilliQ	Total
10	0.5	0.5	0.5	3	15.5	30

We did this for 4 hours at 37℃

Ligation

pspA	DT	Ligation High Ver.2	Total
5	5	5	15

pspA	pSB1C3	Ligation High Ver.2	Total
4	1	3	8

We did these for an hour at 16℃.

pspA (5µL)→377fmol
DT→39fmol
pspA (4µL)→339fmol
pSB1C3→34fmol

Transformation

pspA-DT, pspA (pSB1C3), torA (pSB1C3) and GFP-DT

March 20

Screaning PCR

Quick Taq	Primer-R	Primer-F	MilliQ	Total
25	1	1	23	50

pspA→○
pspA-DT→○
GFP-DT→○
torA→×
Kil-DT 6 of 8 sumples→○

Quick Taq	VR	VF	MilliQ	Total
25	1	1	23	50

pspA→○
pspA-DT→×

Restrictive Digestion

torA	EcoR1	Spe1	BSA	BufferM	MilliQ	Total
10	0.3	0.3	0.3	3	16.1	30

DT	EcoR1	Xba1	BSA	BufferM	MilliQ	Total
10	0.2	0.2	0.3	3	16.3	30

We did this for overnight at 37℃. And we did purification.
torA 34.2ng/µL
DT 28.0ng/µL

March 21

Miniprep

GFP-DT-1 : 77.7ng/µL
GFP-DT-2 : 67.6ng/µL

Restrictive Digestion

pSB1C3	EcoR1	Spe1	BSA	BufferM	MilliQ	Total
10	0.2	0.2	0.3	3	16.3	30
5	0.2	0	0.2	2	12.6	20

We did this for 3 hours at 37℃, and then we did gel extraction. We got 25.1ng/µL pSB1C3

GFP-DT	EcoR1	Pst1	Xba1	BSA	BufferM	MilliQ	Total
5	0.2	0.2	0	0.2	2	12.4	20
5	0.2	0	0	0.2	2	12.6	20
10	0.2	0	0.2	0.3	3	16.3	30

We did this for 3 hours at 37℃, and then we did Purification. We got 30.7ng/µL GFP-DT.

Ligation

	torA	pSB1C3	pspA	DT	GFP-DT	Ligation High Ver.2	Total
1	4	1	0	0	0	3	8
2	0	1	7	0	0	4	12
3	0	0	5	3	0	4	12
4	3	0	0	0	5	4	12

We did this for an hour at16℃.

March 22

PCR

We did PCR to amplify torA_signal that was product of PCR at March 5 with redesigned primers.

Buffer	dNTPs	MgSO4	Primer-F	Primer-R	Template	MilliQ	KOD plus neo	Total
5	5	3	1.5	1.5	0.5	32.5	1	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 10sec
→30cycles
→Purification 110.7ng/µL

Restrictive Digestion

torA	EcoR1	Spe1	BSA	BufferM	MilliQ	Total
10	0.2	0.2	0.3	3	16.3	30

Ligation

	torA	pSSB1C3	pspA	DT	GFP-DT	Ligation high	Total
1	4	3	0	0	0	4	11
2	3	0	0	0	3	3	9
3	0	0	5	5	0	5	15

torA (4µL)→512fmol
pSB1C3→54fmol
torA (3µL)→384fmol
GFP-DT→36fmol
pspA→377fmol
DT→65fmol

March 23

Screening PCR

torA (pSB1C3), torA-GFP-DT and pspA-DT

Quick Taq	VF	VR	MilliQ	Total
25	1	1	23	50

E.coli in liquid culture that had pspA(pSB1C3) also expressed RFP.

Restrictive Digestion

pspA	EcoR1	Spe1	BufferM	BSA	MilliQ	Total
5	0.3	0.3	3	0.3	21.1	30

And then we did ethanol precipitation

Ethanol precipitation

pspA 11.5ng/µL.

Miniprep

LacP+pSB3C5-8 77.9µg/mL
LacP+pSB3C5-10 69.0µg/mL
Kil+DT-4 58.0µg/mL
Kil+DT-7 15.2µg/mL

Restrictive Digestion

LacP+pSB3C5-8	Spe1	Pst1	Buffer2	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

Kil+DT-4	Xba1	Pst1	Buffer2	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

at 37℃ for 1.5 hours
And then we did Gel extraction.

Gel Extraction

LacP+pSB3C5-8 40.4µg/mL
Kil+DT-4 26.8µg/mL

March 26

Miniprep

torA(pSB1C3) 18.5[ng/µL]
torA-GFP-DT 20.0[ng/µL]

Restrictive Digestion

torA(pSB1C3)	EcoR1	Pst1	BufferH	BSA	MilliQ	Total
5	0.2	0.2	2	0.2	12.4	20
5	0.2	0	2	0.2	12.6	20

torA-GFP-DT	EcoR1	Xba1	Pst1	BufferH	BufferM	BSA	MilliQ	Total
5	0.2	0	0.2	2	0	0.2	12.4	20
5	0.2	0	0	2	0	0.2	12.6	20
20	0	0.2	0.2	0	3	0.3	6.3	30

We did Gel extraction and then got ??? 28.7[ng/µL]

Ligation

LacP (pSB3C5)	torA-GFP-DT	Ligation High Ver.2	Total
1	5	3	9

LacP : 22fmol
torA-GFP-DT : 197fmol

pspA	pSB1C3	Ligation High Ver.2	Total
10	1	5	16

pspA	DT	Ligation High Ver.2	Total
10	1	5	16

pspA : 180fmol
pSB1C3 : 18fmol
DT : 16fmol

LacP(pSB3C5)	Kil-DT	Ligation High Ver.2	Total
1	5	3	9

for 2 hours at 16℃

Transformation

LacP-Kil-DT	competent cell	Total
1	10	11

March 27

Miniprep

We retryed miniprep of torA(pSB1C3).
We got torA and its concentration was 39.3[ng/µL].

Transformation

Name	Well	Sample	Competent Cells	Total	Plate	Colony
BBa_K117004	14J(2011 plate2)	5	20	?	?	?

We added 100[µL] of culture medium before we started culturing the E.coli.

Screening PCR

Quick Taq	VF2	VR	MilliQ	Total
25	1	1	23	50

LacP-torA-GFP-DT 1, 3, 5, 6, 8, 9 was successful.
pspA-DT was failed.
E.coli that had pspA(pSB1C3) did not make any colony.
LacP-Kil-DT 1,2,3,4,5,6,7,8 was failed.

Liquid culture

LacP-torA-GFP-DT

July 23

Transformation

DT(64.4ng/μl)	Competent cell	Plating in SOC medium	Total
1	20	100	121

July 24

Plating in SOC medium

July 25

Transformation

BBa_J23113 from iGEM Kit
LacP from iGEM Kit

July 27

Restrictive Digestion

Kil +DT (44.0 ng/μl)	10xBuffer2	BSA	Xbal	MilliQ	Total
13.6	3.0	0.5	0.5	11.9	30.0

LacP(28.7ng/μl)	10xBuffer2	BSA	Spe1	Pst1	Total
20.9	3.0	0.5	0.5	4.6	30.0

July 30

Ligation

kil+DT(Xba1,Pst1)	LacP(Spe1,Pst1)	Ligation High	Total
30	6	36	72

July 31

Restriction Enzyme Processing

torA-GFP+DT	10×M Buffer	BSA	MilliQ	Xba1	Pst1	Total
2.5	3.0	0.5	23.4	0.3	0.3	30.0

Liquid Culture

J23113(backbone J61002)

August 1

Restrictive Digestion

LacP+kil+DT	BSA	10×H Buffer	EcoR1	Pst1	MilliQ	Total
5.0	0.5	3.0	0.5	0.5	20.5	30.0

37℃ 2h

LacP middle copy	BSA	10×H Buffer	EcoR1	Pst1	MilliQ	Total
10.0	0.5	3.0	0.5	0.5	15.5	30.0

37℃ 2h

MIniprep

J23113(backbone J61002)

Liquid culture

J23113(backboneJ61002) Three test tubes of 4 mL LB medium with ampicillin 37℃ overnight

August 3

Restrictive Digestion

pSB4K5	BSA	10×H Buffer	EcoR1	Pst1	MilliQ	Total
8.0	0.5	3.0	0.5	0.5	17.5	30.0

B0034	BSA	10×H Buffer	Spe1	Pst1	MilliQ	Total
12.0	0.5	3.0	0.5	0.5	13.5	30.0

37℃ 2h

DNA purification

Ligation

LacP+kil+DT	pSB4K5	ligation high	Total
15	15	15	45

16℃ 1h

Miniprep

J23113(backbone J61002) 218.0μg/mL
J23113(backbone J61002) 252.5μg/mL
J23113(backbone J61002) 201.0μg/mL
pSB3C5 45.0μg/ml 1.60 260/280 1.80 260/230
pSB4C5 213.0μg/mL 1.77 260/280 4.40 260/230

August 10

Ligation

B0034 Spe1 Pst1	GFP+DT Xba1 Pst1	ligation high	Total
2	3	4	9

16℃ 1h

Transformation

RBS+GFP+DT
LacP+kil+DT
RBS（for control）

To put 2ng DNA in 20μL competent cell and leave it on ice for 30min

Heat shock for 60s at 42℃

To leave on ice for 2min

To spread on ampicillin LB plate

August 13

Liquid culture

B0034 3mL ×3 　　　

37℃　overnight

August 14

Miniprep

B0034 0μg/mL

B0034 235.5μg/mL

B0034 76.5μg/mL

Colony PCR

LacP+kil+DT ×5

2×Quick Taq	VF	VF	MilliQ	Total
25	1	1	23	50

25cycles
pspA

10×Buffer for KOD-Plus-Ver2	2mM dNTPs	25mM MgSO4	Primer PsPA f-p	Primer PsPA r-s	KOD-Plus-	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

August 15

Colony PCR

pspA

2×Quick Taq	pspA r-s	pspA f-p	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
56℃, 30sec
68℃, 1min
→35cycles

August 16

Electrophoresis

positive control(GFP+DT)
negative control(MilliQ)
① ～⑥ colony PCR LacP+kil+DT

①1kb ladder
②Positive control (GFP+DT)
③Negative control (MilliQ)
④～⑨LacP+kil+DT　①～⑥
⑩～⑫pspA 10μL ,6×buffer 2μL
⑬1kb ladder

August 17

Colony PCR

pspA

10×Buffer for KOD-Plus-Ver2	2mM dNTPs	25mM MgSO4	Primer PsPA f	Primer PsPA r	KOD-Plus-	MilliQ	Total
5	3	3	1.5	1.5	1	35	50
5	3	5	1.5	1.5	1	33	50

negative control(MilliQ 50μL) 94℃, 2min
94℃, 15sec
55℃, 30sec
68℃, 1min
→35cycles

Electrophoresis

① 1kb ladder
②, ③ MgSO4 3μL, pspA
④, ⑤ MgSO4 5μL, pspA
⑥ negative control(MilliQ)
⑧ 1kb ladder

August 20

Restrictive Digestion

J23113(201.0ng/μL)	Xba1	Pst1	BufferM	BSA	MilliQ	Total
10	1	1	3	0.5	14.5	30

August 21

Colony PCR

pspA

10×Buffer	2mM dNTPs	25mM MgSO4	Primer PsPA f	Primer PsPA r	KOD Plus Neo	MilliQ	Total
5	3	5	1.5	1.5	1	33	50
5	3	7	1.5	1.5	1	31	50
5	3	10	1.5	1.5	1	28	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 30sec
→25cycles

Restrictive Digestion

J23113(218ng/μL)	Spe1	Pst1	BufferH	BSA	MilliQ	Total
10	1	1	3	0.5	14.5	30

torA-GFP-DT(20ng/μL)	Xba1	Pst1	BufferM	BSA	MilliQ	Total
5	0.6	0.6	3	0.5	20.3	30

Electrophoresis

① 1kb ladder
②, ③　torA-GFP-DT(Xba1,Pst1)
④, ⑤　J23113(Spe1,Pst1)

Transformation

LacP-torA-GFP-DT(Backbone pSB3C5)
BBa_K11704(Backbone pSB1A2)

Electrophoresis

laneA-C. pspA
laneD. pspA(without primer)

Colony PCR

pspA

10×Buffer	2mM dNTPs	25mM MgSO4	Primer PsPA f	Primer PsPA r	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

negative control for pspA

10×Buffer	2mM dNTPs	25mM MgSO4	Primer PsPA f-p	Primer PsPA r-s	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

GFP-DT(positive control)

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 30sec

Transformation

LacP-torA-GFP-DT(Backbone pSB3C5)
J23107-TatABCD

PCR

kil, torA-GFP

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	DNA	Total
5	5	3	1.5	1.5	1	32	1	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 30sec
→25cycles

August 22

Restrictive Digestion

pSB3C5	EcoR1	Pst1	BufferH	BSA	MilliQ	Total
13.3	0.5	0.5	3	0.5	12.2	30

Gel extraction

pSB3C5(EcoR1, Pst1)
27.2μg/mL

Transformation(the second time)

LacP-torA-GFP-DT(Backbone pSB3C5)
J23107-TatABCD

Electrophoresis

See "August 21 -Colony PCR-"
1. 1kb ladder
2. pspA(Primer pspA f&r)
3. negative control for 2
4. GFP-DT
5. pspA(Primer pspA f-p&r-s)
6. pspA(Primer pspA f-p&r-s)
7. negative control for 5&6

PCR

LacP-GFP-DT(a kit of biological parts)

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	DNA	Total
5	5	3	1.5	1.5	1	32	1	50

Colony PCR

pspA

10×Buffer	2mM dNTPs	25mM MgSO4	Primer pspA f	Primer pspA r	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

10×Buffer	2mM dNTPs	25mM MgSO4	Primer pspA f-p	Primer pspA r-s	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 30sec
→30cycles

Electrophoresis

1. 1kb ladder
2. pspA(Primer pspA f&r)
3. pspA(Primer pspA f-p&r-s)
4. negative control for pspA(Primer pspA f&r)
5. negative control for pspA(Primer pspA f-p&r-s)

Transformation

Kil

August 23

Colony PCR

J23107-TatABCD
VF and VR were used for amplifying approximately 2800bp

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	DNA	Total
5	5	3	1.5	1.5	1	32.5	0.5	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 90sec
→25cycles

August 24

Purification of PCR products

pspA(Primer pspA f-p&r-s)
84.1μg/mL
→See "August 22 -Colony PCR-"

Restrictive Digestion

pspA	EcoR1	Pst1	BufferH	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

pspA	Xba1	Pst1	BufferM	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

at 37℃ for 1h

Gel extraction

pspA(EcoR1, Pst1) 30.7μg/mL
pspA(Xba1, Pst1) 44.0μg/mL

Restrictive Digestion

pSB1C3(82.9μg/mL)	EcoR1	Pst1	BufferH	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

→Gel extraction

Electrophoresis

1. 1kb ladder
2. J23107-TatABCD →See "August 23 -PCR-"
3. negative control for J23107-TatABCD
4. pSB1C3(EcoR1, Pst1)

Ligation

pSB3C5(EcoR1, Pst1)	pspA(EcoR1, Pst1)	Ligation High Ver.2	Total
1	5	3	9

16℃, overnight

August 25

August 26

August 27

Ligation

pSB1C3(EcoR1, Pst1)	pspA(EcoR1, Pst1)	Ligation High Ver.2	Total
1	5	3	9

16℃, overnight

Colony PCR

Kil (1-7)

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 30sec
→30cycles

Purification of PCR products

torA-GFP →See "August 21 -PCR-"

Restrictive Digestion

LacP(Backbone:pSB3C5)	Spe1	Pst1	BufferH	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

at 37℃ for 1h
→Gel extraction

torA-GFP	Xba1	Pst1	BufferM	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

at 37℃ for 1h
→Purification

Purification of PCR products

J23107-TatABCD
42.0μg/mL
→See "August 23 -PCR-"

Restrictive Digestion

J23107-TatABCD	Spe1	EcoR1	BufferM	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

August 28

Colony PCR

Kil (1-16)

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

Transformation

pspA-pSB1C3
pspA-pSB3C5

Liquid culture

Kil-3 →Miniprep 100.4μg/mL
Kil-6
Kil-7 →Miniprep 77.7μg/mL
LacP-torA-GFP-1 →Miniprep 88.3μg/mL
LacP-torA-GFP-2 →Miniprep 85.0μg/mL
LacP-torA-GFP-3 →Miniprep +++

August 29

Kil assay

After culturing for 18hr at 37℃, we eliminated the supernatant using a centrifuge, and diluted it until OD600=0.1. Then we dispensed it. The dispense volume was 3mL. We added 0/0.001/0.01/0.1/1mM IPTG to each. While culturing again at 37℃, we measured OD600.

IPTG	0	0.001mM	0.01mM	0.1mM	1mM
0.5h	0.202	0.207	0.201	0.207	0.200
1h	0.406	0.428	0.424	0.402	0.421
1.5h	0.796	0.813	0.779	0.751	0.802
2h	1.107	1.129	1.141	1.092	1.124
2.5h	1.546	1.565	1.541	1.532	1.578
3h	1.912	1.933	1.890	1.883	1.940
3.5h	2.300	2.295	2.238	2.247	2.259
4h	2.546	2.545	2.528	2.490	2.520
4.5h	2.688	2.663	2.603	2.633	2.666
5h	2.699	2.826	2.787	2.593	2.673
5.5h	2.863	2.742	2.754	2.741	2.756
6h	2.831	2.876	2.758	2.759	2.728
20h	2.671	2.706	2.680	2.606	2.619

Liquid culture

pspA-pSB1C3(1-3)
pspA-pSB3C5(1-3)

Restrictive Digestion

LacP-Kil-DT(134.7ng/μL)	EcoR1	Spe1	BufferM	MilliQ	Total
10	1	1	3	15	30

37℃, overnight

Colony PCR

LacP-torA-GFP-DT (1-5)
pspA-pSB1C3 (1-5)
pspA-pSB3C5 (1-6)

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 40sec
→30cycles

Gel extraction

J23107-TatABCD(EcoR1, Pst1) -5.9μg/mL

August 30

Ligation

J23107-TatABCD(EcoR1, Spe1)22.2μg/mL	DT(EcoR1, Xba1)37.5μg/mL	Ligation High Ver.2	Total
10	1	9	20

at 16℃ for 1h

Transformation

J23107-TatABCD-DT (Amp resistance)

Electrophoresis

1. LacP-torA-GFP-DT-1
2. LacP-torA-GFP-DT-2
3. LacP-torA-GFP-DT-3
4. LacP-torA-GFP-DT-4
5. LacP-torA-GFP-DT-5
6. pspA-pSB1C3-1
7. pspA-pSB1C3-2
8. pspA-pSB1C3-3
9. pspA-pSB1C3-4
10.pspA-pSB1C3-5
11.pspA-pSB3C5-1
12.pspA-pSB3C5-2
13.pspA-pSB3C5-3
14.pspA-pSB3C5-4
15.pspA-pSB3C5-5
16.pspA-pSB3C5-6

Miniprep

pspA-pSB3C5-1 176μg/mL
pspA-pSB3C5-2 214μg/mL
pspA-pSB3C5-3 461μg/mL
pspA-pSB1C3-2 79μg/mL

Colony PCR

LacP-torA-GFP-DT (6-13)

2×Quick Taq	VF	VR	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
56℃, 30sec
68℃, 1min
→30cycles

Restrictive Digestion

pspA-pSB1C3	EcoR1	Spe1	BufferM	BSA	MilliQ	Total
15	0.5	0.5	5	0.5	28.5	50

at 37℃ for 1h

Electrophoresis

1. 1kb ladder
3. pspA-pSB1C3(EcoR1, Spe1)

August 31

Gel extraction

pspA-pSB1C3(EcoR1, Spe1) 8.0μg/mL

Purification

LacP-GFP-DT -0.7μg/mL

Ligation

pspA(EcoR1, Spe1)	DT(EcoR1, Xba1)	Ligation High Ver.2	Total
25	1	13	39

at 16℃ for 1h

Transformation

pspA-DT (Amp resistance)

September 2

Colony PCR

J23107-TatABCD-DT (1-8)

2×Quick Taq	VF	VR	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 3min
→25cycles

pspA-DT (2-8)

2×Quick Taq	VF	VR	MilliQ	Total
25	1	1	23	50

Extension, 10sec
→25cycles

Restrictive Digestion

LacP-torA-GFP-DT	EcoR1	Spe1	BufferH	MilliQ	Total
10	1	1	2	6	20

at 4℃ for overnight

Electrophoresis

1. 1kb ladder
3. J23107-TatABCD-DT-1
4. J23107-TatABCD-DT-3
5. J23107-TatABCD-DT-4
6. J23107-TatABCD-DT-5
7. J23107-TatABCD-DT-6
8. J23107-TatABCD-DT-7
9. J23107-TatABCD-DT-8

1. 1kb ladder
3. J23107-TatABCD-DT-1
4. J23107-TatABCD-DT-3
5. J23107-TatABCD-DT-4
6. J23107-TatABCD-DT-5
7. J23107-TatABCD-DT-6
8. J23107-TatABCD-DT-7
9. J23107-TatABCD-DT-8
11. LacP-pSB3C5(Spe1, Pst1)

1. 1kb ladder
3. pspA-DT-2
4. pspA-DT-3
5. pspA-DT-4
6. pspA-DT-5
7. pspA-DT-6
8. pspA-DT-7
9. pspA-DT-8

September 3

PCR

TatABCD-DT

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	DNA	Total
5	5	3	1.5	1.5	1	32	1	50

Gel extraction

LacP-torA-GFP-DT →See "September 5 -Gel extraction-"

Restrictive Digestion

torA-GFP-DT	Xba1	Pst1	BufferM	MilliQ	Total
20	2	2	4	12	40

Purification

J23107-TatABCD 29.6μg/mL 1.56(260/280) 1.60(260/230)

Electrophoresis

1. 1kb ladder
2. J23107-TatABCD

Liquid culture

LacP-kil-DT(1)
pspA-DT(4, 7)

PCR

J23107-TatABCD

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	DNA	Total
5	5	3	1.5	1.5	1	29	4	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 10sec
→30cycles

Gel extraction

LacP-torA-GFP-DT 31μg/mL 1.28(260/280) 0.49(260/230)
LacP-torA-GFP-DT 8μg/mL 1.32(260/280) 0.83(260/230)

Transformation

J23107-TatABCD (Amp resistance)
J23113-kil-DT (Amp resistance)
J23100-kil-DT (CP resistance)
J23101-kil-DT (CP resistance)
J23106-kil-DT (CP resistance)
J23115-kil-DT (CP resistance)→We didn't transform because of lack of culture medium.
J23105-kil-DT (CP resistance)→We didn't transform because of lack of culture medium.

Electrophoresis

1. 1kb ladder
2-7. LacP-torA-GFP-DT

Colony PCR

LacP-torA-GFP-DT (14-21) J23113-kil-DT (Amp resistance, 1-4) J23113-kil-DT (CP resistance, 1-4)

2×Quick Taq	primer-f	primer-r	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 1min
→25cycles

September 4

Liquid culture

LacP-kil-DT(4, 5)(Amp resistance)
pspA-DT(3, 6, 7)(Amp resistance)

PCR

We did PCR 10 more cycles to amplify products of PCR that we had done yesterday because we could not amplify J23107-TatABCD on September 3.
94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 1.5min
→30cycles

Electrophoresis

1-8. LacP-torA-GFP-DT

1-4. J23113-kil-DT (Amp resistance)
5-8. J23113-kil-DT (CP resistance)

Liquid culture

LacP-torA-GFP-DT
J23113-kil-DT
LacP-kil-DT(with IPTG)
LacP-kil-DT(without IPTG)

After 20 hour, we quantified OD600.

plasmid	OD600
LacP-kil-DT(with IPTG)	2.116
LacP-kil-DT(without IPTG)	2.320

We cultured CP tolerance plasmid and give an antibiotic(Amp or Kan or none) after 2 hours. We quantify OD600.

time	1	2	3
2hours	0.131	0.100	0.606
add an antibiotic	Amp	Kan	none
7hours	0.491	0.988	2.634
19hours	2.253	0.815	2.742

September 5

Colony PCR

J23107-TatABCD (1-7)

buffer	2mM dNTPs	25mM MgSO4	primer-f	primer-r	KOD Plus Neo	DW	Total
5	5	3	1.5	1.5	1	33	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 1.25min
→30cycles

Gel extraction

by Kato
See "September 3 -Gel extraction-" LacP-torA-GFP-DT 15.9μg/mL 1.29(260/280) 0.38(260/230) LacP-torA-GFP-DT 17.2μg/mL 1.23(260/280) 0.48(260/230)

Miniprep

J23113-kil-DT 85.7μg/mL 1.76(260/280) 1.97(260/230)
LacP-torA-GFP-DT 126.6μg/mL 1.81(260/280) 2.09(260/230)
LacP-kil-DT-4 62.5μg/mL 1.79(260/280) 1.99(260/230)
LacP-kil-DT-5 56.0μg/mL 1.79(260/280) 2.01(260/230)
pspA-DT-3 322μg/mL 1.45(260/280) 1.42(260/230)
pspA-DT-6 147.6μg/mL 1.25(260/280) 1.37(260/230)
pspA-DT-7 145.5μg/mL 1.24(260/280) 1.27(260/230)

Restrictive Digestion

pspA-DT-6	Xba1	Pst1	BufferM	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

at 37℃ for 1h

Electrophoresis

J23107-TatABCD (1-7)

Colony PCR

J23107-TatABCD (8-23)

2×Quick Taq	VF2	VR	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 1.5min
→30cycles

Gel extraction

pspA-DT 10.2μg/mL 1.42(260/280) 0.76(260/230)

Ligation

pspA-DT(Xba1, Pst1)	LacP(pSB3C5)(Spe1, Pst1)	Ligation High Ver.2	Total
5	1	3	9

at 16℃

Electrophoresis

LacP-torA-GFP-DT(8-15)

LacP-torA-GFP-DT(9-23)

Ligation

LacP-torA-GFP-DT(EcoR1, Spe1)	DT 17.2μg/mL(Xba1, Pst1)	Ligation High Ver.2	Total
15	25	20	60

Liquid culture

J23107-TatABCD-8
J23107-TatABCD-20
LacP-torA-GFP-DT-21

September 6

Miniprep

J23107-TatABCD-8 82.4μg/mL 2.06(260/280) 2.95(260/230)
J23107-TatABCD-20 102.9μg/mL 2.04(260/280) 2.94(260/230)

Restrictive Digestion

J23107-TatABCD 102.9μg/mL	Spe1	Pst1	BufferH	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

at 37℃ for 1h

Transformation

LacP-pspA-DT(pSB3C5)

DNA	Competent cell	Total
2	20	22

Gel extraction

J23107-TatABCD(Spe1, Pst1)
→We failed gel extraction because we mistook steps of experiment.

Electrophoresis

LacP-torA-GFP-DT-pspA-DT

Restrictive Digestion

by Terasaka

J23107-TatABCD	Spe1	Pst1	BufferH	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

Gel extraction

J23107-TatABCD(Spe1, Pst1)
→See "September 7 -Gel extraction-"

September 7

Liquid culture

LacP-torA-GFP-DT-1 (CP resistance)
LacP-torA-GFP-DT-21 (CP resistance)

preculture for 1 hour

Colony PCR

LacP-torA-GFP-DT (1-8) LacP-pspA-DT (1-8)

2×Quick Taq	VF2	VR	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 1.5min
→30cycles

Restrictive Digestion

by Terasaka

J23107-TatABCD	EcoR1	Spe1	BufferM	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

GFP-DT	Xba1	Pst1	BufferM	BSA	MilliQ	Total
15	0.5	0.5	3	0.5	10.5	30

Electrophoresis

① -⑧. LacP-pspA-DT
1-8. LacP-torA-GFP-DT

Gel extraction

J23107-TatABCD(EcoR1, Spe1)
J23107-TatABCD(Pst1, Spe1) ①57.6μg/mL ②23.4μg/mL
GFP-DT(Xba1, Pst1)

Restrictive Digestion

pspA-DT(145.5μg/mL)	Xba1	Pst1	BufferM	BSA	MilliQ	Total
20	0.5	0.5	3	0.5	5.5	30

37℃, overnight

Liquid culture

LacP-torA-GFP-DT-7 (LB 2mL)

+IPTG 0mM, 0.05mM, 0.1mM, 0.15mM, 0.2mM, 0.3mM

LacP-torA-GFP-DT-7 (LB 5mL)

September 8

Check the effect of Amp

We used 5mL of the liquid culture medium with LacP-torA-GFP-DT-7.
→See "September 7 -Liquid culture-"
We diluted it with LB until OD600=0.444, and dispensed it.
The dispense volume was 1.3mL.
We added 0/13/130μL of Amp(50mg/mL) to it.

5.5h after incubating at 37℃

Amp	0μL	13μL	130μL
OD600	2.457	2.696	0.310

Observation through a confocal microscope

We used the liquid culture media with LacP-torA-GFP-DT + 13μL of Amp(50mg/mL) + IPTG 0/0.1/0.15mM.
Their OD600 was 0.47.
3h after incubating at 37℃, we eliminated each supernatant using a centrifuge, and diluted them with LB to which Amp was added.
2.5h after incubating at 37℃, we observed them through a confocal microscope.
We failed to observe it.

Gel extraction

pspA-DT -5.5μg/mL

Restrictive Digestion

pspA-DT-3(322μg/mL)	Xba1	Pst1	BufferM	BSA	MilliQ	Total
10	1	1	3	3	12	30

at 37℃ for 1h

September 9

Restrictive Digestion

J23107-TatABCD(102.9μg/mL)	EcoR1	Spe1	BufferM	MilliQ	Total
10	1	1	3	15	30

Electrophoresis

1. J23107-TatABCD(EcoR1, Spe1)
2. J23107-TatABCD(before restriction)
3. pspA-DT(Xba1, Pst1)
4. pspA-DT(before restriction)

Gel extraction

J23107-TatABCD(EcoR1, Spe1) 26μg/mL
pspA-DT(Xba1, Pst1) 199μg/mL

Liquid culture

J23100/J23101/J23106-1
pspA-DT-5 ×2
LacP-torA-GFP-DT-21
GFP generator-2
LacP-pspA-DT-6

September 10

Miniprep

J23100-1 105.5μg/mL
J23101-1 76.0μg/mL
J23106-1 90.9μg/mL
pspA-DT-5 ①104.1μg/mL ②80.0μg/mL
LacP-torA-GFP-DT-21 79.6μg/mL
GFP generator-2 84.1μg/mL
LacP-pspA-DT-6 99.8μg/mL

Ligation

J23107-TatABCD-DT

J23107-TatABCD(EcoR1, Spe1)	DT(EcoR1, Xba1)	Ligation High Ver.2	Total
10	5	7.5	22.5

Negative control for J23107-TatABCD-DT

DT(EcoR1, Xba1)	Ligation High Ver.2	Total
5	5	10

J23107-TatABCD-pspA-DT

J23107-TatABCD(Spe1, Pst1)	pspA-DT(Xba1, Pst1)	Ligation High Ver.2	Total
3	6	9	18

Negative control for J23107-TatABCD-pspA-DT

J23107-TatABCD(Spe1, Pst1)	Ligation High Ver.2	Total
3	3	6

Restrictive Digestion

DNA	Spe1	Pst1	BufferH	MilliQ	Total
15	1	1	3	10	30

DNA=J23100(105.5μg/mL), J23101(76.0μg/mL), J23106(90.9μg/mL)
at 37℃

Gel extraction

J23100 27.1μg/mL
J23101 50.2μg/mL
J23106 16.1μg/mL

Ligation

J23100/J23101/J23106-kil-DT

J23100/J23101/J23106(Spe1, Pst1)	kil-DT(Xba1, Pst1)	Ligation High Ver.2	Total
1	5	3	9

Negative control for J23100/J23101/J23106-kil-DT

J23100/J23101/J23106(Spe1, Pst1)	MilliQ	Ligation High Ver.2	Total
1	5	3	9

Transformation

J23100/J23101/J23106-kil-DT

September 11

Colony PCR

J23107-TatABCD-DT (1-8)
J23107-TatABCD-pspA-DT (1-8)

2×Quick Taq	VF2	VR	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 3.5min
→30cycles

Electrophoresis

J23107-TatABCD-DT (1-8)

J23107-TatABCD-pspA-DT (1-8)

Restrictive Digestion

GFP generator(84.1μg/mL)	Xba1	Pst1	BufferM	BSA	MilliQ	Total
15	1	1	3	3	7	30

LacP-torA-GFP-DT(85.0μg/mL)	Spe1	Pst1	BufferH	MilliQ	Total
15	1	1	3	10	30

LacP-pspA-DT(99.8μg/mL)	Xba1	Pst1	BufferM	BSA	MilliQ	Total
15	1	1	3	3	7	30

Liquid culture

pSB1C3(self-ligation) ×5 in LB 3mLCP 3μL
When OD600=approximately 0.6, we added 0/30/60/150/300μL of Amp(50mg/mL) to each liquid culture medium.
1h and 5h after incubating at 37℃, we measured OD600.

	1h	5h
0	-0.020	0.403
30	-0.046	0.544
60	0.263	0.007
150	0.061	0.839
300	0.093	1.441

Ligation

pSB3C5(EcoR1, Pst1)	pspA-DT(Xba1, Pst1)	J23107-TatABCD(EcoR1, Spe1)	Ligation High Ver.2	Total
1	3	5	4.5	13.5

4℃, overnight

Colony PCR

J23100-kil-DT (1-6)
J23101-kil-DT (1-7)
J23106-kil-DT (1-2)

2×Quick Taq	VF	VR	MilliQ	Total
23	1	1	25	50

Gel extraction

GFP generator (Xba1, Pst1) 14.1μg/mL
LacP-torA-GFP-DT (Spe1, Pst1) 42.9μg/mL 1.13(260/280) 1.19(260/230)
LacP-pspA-DT (Xba1, Pst1) 20.0μg/mL 1.01(260/280) 1.30(260/230)

Electrophoresis

J23107-TatABCD-DT (1-8)
J23106-kil-DT (1, 2)
J23100-kil-DT (1-4)

Liquid culture

LacP-torA-GFP-DT
pSB1C3

Colony PCR

We did PCR 10 more cycle to amplify products of PCR on 9/11 of J23107-TatABCD-pspA-DT and J23107-TatABCD-DT.

September 12

Colony PCR

J23107-TatABCD-pspA-DT (9-15) 94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 4min
→26cycles

Check the effect of Amp

We cultured pSB1C3 for overnight.
→See "September 7 -Liquid culture-"
We diluted it with LB, and dispensed it.
We added Amp(50mg/mL) to it until density of Amp was 1/10, 1/30, 1/50 .

Amp	start	5 hours
1/10	0.557	0.077
1/30	0.628	0.166
1/50	0.472	0.055
0	0.594	2.585

Electrophoresis

J23107-TatABCD-pspA-DT

J23101-kil-DT (1-7)

Restrictive Digestion

pspA(pSB3C5) (106μg/mL)	EcoR1	Pst1	BufferH	MilliQ	Total
15	1	1	3	10	30

pspA-DT-3	Xba1	Pst1	BufferM	BSA	MilliQ	Total
15	1	1	3	3	7	30

J23107-TatABCD (102.4μg/mL)	EcoR1	Spe1	BufferM	MilliQ	Total
15	1	1	3	10	30

Electrophoresis

pspA(pSB3C5)(EcoR1, Pst1)
pspA-DT(Xba1, Pst1)
J23107-TatABCD(EcoR1, Spe1)
pSB1C3(EcoR1, Spe1)

Transformation

J23107-TatABCD-pspA-DT(pSB3C5)

DNA	Competent cell	Total
2	20	22

on ice for 30 minites heatshock at 42℃ for 1 hour on ice 2 minites then add SOC medium 200μl preculture at 37℃ for 1 hour incubate CP culture plate

Gel extraction

pspA(pSB3C5)(EcoR1, Pst1) 26.8μg/mL 1.27(260/280) 0.32(260/230)
pspA-DT(Xba1, Pst1) 26.1μg/mL 1.13(260/280) 0.55(260/230)
J23107-TatABCD(EcoR1, Spe1) 1.5μg/mL 1.99(260/280) 0.06(260/230)

Ligation

pSB3C5(EcoR1, Pst1) 26.8μg/mL	pspA-DT(Xba1, Pst1) 26.1μg/mL	J23107-TatABCD(EcoR1, Spe1) 1.5μg/mL	Ligation High Ver.2	Total
1	3	6	5	15

pSB3C5(EcoR1, Pst1) 26.8μg/mL	MilliQ	Ligation High Ver.2	Total
1	9	5	15

LacP(pSB3C5)(Spe1, Pst1) 10μg/mL	GFP-DT(Xba1, Pst1) 7.0μg/mL	Ligation High Ver.2	Total
1	5	3	9

LacP(pSB3C5)(Spe1, Pst1) 10μg/mL	MilliQ	Ligation High Ver.2	Total
1	5	3	9

4℃, overnight

Observation through a confocal microscope

left:E.coli sample stained with Hoechstunder and observed with 352nm wavelength
right:E.coli having Lacp-torA-GFP-DT and observed with 489nm wavelength

September 13

Miniprep

J23107-TatABCD-pspA-DT(pSB3C5)-1 130μg/mL 1.37(260/280) 0.79(260/230)

Restrictive Digestion

J23107-TatABCD-pspA-DT(pSB3C5) (130μg/mL)	Spe1	Pst1	BufferH	MilliQ	Total
10	1	1	3	15	30

Transformation

LacP-GFP generater

LacP
J23107-TatABCD-pspA-DT(pSB3C5)
J23107-TatABCD

Colony PCR

J23107-TatABCD-pspA-DT

→See "September 14 -Colony PCR-"

September 14

Colony PCR

See "September 13 -Colony PCR-"
J23107-TatABCD-pspA-DT

Colony PCR

J23107-TatABCD-pspA-DT (1-6)

2×Quick Taq	VF	VR	MilliQ	Total
23	1	1	25	50

94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 4min
→30cycles

September 15

Liquid culture

J23107-TatABCD-pspA-DT-1
J23107-TatABCD-pspA-DT-2
J23107-TatABCD-pspA-DT-3

Miniprep

J23107-TatABCD-pspA-DT-1 22.9μg/mL
J23107-TatABCD-pspA-DT-2 51.8μg/mL 1.57(260/280) 1.01(260/230)
J23107-TatABCD-pspA-DT-3 28.5μg/mL 1.57(260/280) 0.94(260/230)

Restrictive Digestion

J23107-TatABCD-pspA-DT (51.8μg/mL)	EcoR1	Spe1	BufferM	MilliQ	Total
15	0.5	0.5	3	11	30

LacP-torA-GFP-DT (79.6μg/mL)	EcoR1	Xba1	BufferM	BSA	MilliQ	Total
10	0.5	0.5	3	0.5	15.5	30

LacP-kil-DT (56.0μg/mL)	EcoR1	Xba1	BufferM	BSA	MilliQ	Total
15	0.5	0.5	3	0.5	10.5	30

J23107-TatABCD-pspA-DT (51.8μg/mL)	EcoR1	Pst1	BufferM	MilliQ	Total
15	0.5	0.5	3	11	30

37℃, 2 hours

Electrophoresis

①. 1kb ladder
②. J23107-TatABCD-pspA-DT
③. J23107-TatABCD-pspA-DT(EcoR1, Spe1)
④. J23107-TatABCD-pspA-DT(EcoR1, Pst1)
⑤. LacP-kil-DT
⑥. LacP-kil-DT(EcoR1, Xba1)
⑦. LacP-torA-GFP-DT
⑧. LacP-torA-GFP-DT(EcoR1, Xba1)

Gel extraction

①. 1kb ladder
②. J23107-TatABCD-pspA-DT(EcoR1, Spe1)
③. J23107-TatABCD-pspA-DT(EcoR1, Spe1)
④. J23107-TatABCD-pspA-DT(EcoR1, Pst1)
⑤. J23107-TatABCD-pspA-DT(EcoR1, Pst1)
⑥. 1kb ladder

J23107-TatABCD-pspA-DT(EcoR1, Spe1) 14.2μg/mL 1.28(260/280) 0.54(260/230)
J23107-TatABCD-pspA-DT(EcoR1, Pst1) 7.3μg/mL 1.55(260/280) 0.38(260/230)

Purification

LacP-torA-GFP-DT(EcoR1, Xba1) 7.7μg/mL 1.41(260/280) 0.99(260/230)
LacP-kil-DT(EcoR1, Xba1) →failed

Ligation

LacP-torA-GFP-DT(EcoR1, Xba1)	J23107-TatABCD-pspA-DT(EcoR1, Spe1)	Ligation High Ver.2	Total
4	10	7	21

pSB1C3(EcoR1, Pst1)	J23107-TatABCD-pspA-DT(EcoR1, Pst1)	Ligation High Ver.2	Total
4	10	7	21

at 16℃ for overnight

September 16

Transformation

LacP-torA-GFP-DT-J23107-TatABCD-pspA-DT
J23107-TatABCD-pspA-DT(pSB1C3)

September 17

Colony PCR

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT (1-6)
J23107-TatABCD-pspA-DT(pSB1C3) (1-6)
J23107-kil-DT (6-10)

Restrictive Digestion

LacP-torA-GFP-DT (126μg/mL)	EcoR1	Xba1	BufferM	BSA	MilliQ	Total
10	1	1	3	3	12	30

LacP-torA-GFP-DT (126μg/mL)	Xba1	BufferM	BSA	MilliQ	Total
3	1	3	3	20	30

Electrophoresis

A1-A6. J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT (1-6)
B1-B6. J23107-TatABCD-pspA-DT(pSB1C3) (1-6)

Liquid culture

J23107-TatABCD-pspA-DT(pSB1C3)
J23107-TatABCD-pspA-DT(pSB3C5)
LacP-torA-GFP-DT(pSB3C5)

Electrophoresis

lane1. 1kb ladder
lane2. J23101-kil-DT-6
lane3. J23101-kil-DT-7
lane4. J23101-kil-DT-8
lane5. J23101-kil-DT-10
lane6. LacP-torA-GFP-DT
lane7. LacP-torA-GFP-DT(EcoR1, Xba1)
lane8. LacP-torA-GFP-DT(Xba1)

Miniprep

J23106-kil-DT 11.7μg/mL 1.93(260/280) 1.46(260/230)

September 18

Gel extraction

LacP-torA-GFP-DT(EcoR1, Xba1) 36.9μg/mL 1.37(260/280) 0.82(260/230)

Ligation

J23107-TatABCD-pspA-DT(EcoR1, Spe1) 14.2μg/mL	LacP-torA-GFP-DT(EcoR1, Xba1) 36.9μg/mL	Ligation High Ver.2	Total
8	1.5	9.5	19

LacP-torA-GFP-DT(EcoR1, Xba1) 36.9μg/mL	Ligation High Ver.2	Total
1.5	1.5	3

at 4℃ for 1 hour

Transformation

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT
LacP-torA-GFP-DT(EcoR1, Xba1)

Observation through a confocal microscope

We made sample for observation through a confocal microscope.
We incubated sample with 0mM/0.5mM IPTG for 1.5 hours.
Then, we incubated onto medium without IPTG for 2.5 hours.

IPTG(mM)	medium
0	LB
0.1	LB
0.1	LB with 0.1mM IPTG (positive control)
0	LB with 2 percent glucose
0.1	LB with 2 percent glucose
0	LB with 5 percent glucose
0.1	LB with 5 percent glucose
0	LB with 2 percent glucose (make medium new after incubate for 1.5 hours)
0	LB with 2 percent glucose (make medium new after incubate for 1.5 hours)

Restrictive Digestion

pSB4K5	EcoR1	Pst1	BufferH	MilliQ	Total
10	1	1	3	15	30

pSB4K5	EcoR1	BufferH	MilliQ	Total
3	0.5	1	5.5	30

pSB4K5	Pst1	BufferH	MilliQ	Total
3	0.5	1	5.5	10

LacP-torA-GFP-DT	Xba1	Pst1	BufferM	BSA	MilliQ	Total
10	1	1	3	3	12	30

LacP-torA-GFP-DT	Xba1	BufferM	BSA	MilliQ	Total
2	1	1	1	5	10

LacP-torA-GFP-DT	Pst1	BufferH	MilliQ	Total
2	1	1	6	10

37℃, 2 hours

Gel extraction

LacP-torA-GFP-DT(Xba1, Pst1) 9.7μg/mL 1.34(260/280) 0.62(260/230)
pSB4K5(EcoR1, Pst1) 9.6μg/mL 1.28(260/280) 0.32(260/230)

Miniprep

J23107-TatABCD-psp-DT(pSB1C3) 78μg/mL
J23107-TatABCD-psp-DT(pSB1C3) 48μg/mL
LacP-torA-GFP-DT 29μg/mL
J23101-kil-DT 25μg/mL

Restrictive Digestion

J23101-Kil-DT 25µg/ml	BufferM	Xba1	Pst1	BSA	MilliQ	Total
40	6	1	1	6	6	60

J23101-Kil-DT 25µg/ml	BufferM	Xba1	BSA	MilliQ	Total
3	1	0.5	1	4.5	10

J23101-Kil-DT 25µg/ml	BufferH	Pst1	MilliQ	Total
3	1	0.5	5.5	60

at 37℃ for 2 hours

Electrophoresis

①. pSB4K5
②. pSB4K5(Pst1)
③. pSB4K5(EcoR1)
④. pSB4K5(EcoR1, Pst1)
⑤. LacP-torA-GFP-DT
⑥. LacP-torA-GFP-DT(Xba1)
⑦. LacP-torA-GFP-DT(Pst1)
⑧. LacP-torA-GFP-DT(Xba1, Pst1)

①. 1kb ladder
②. J23101-Kil-DT(Xba1, Pst1)
③. J23101-Kil-DT(Xba1, Pst1)
④. J23101-Kil-DT(Xba1, Pst1)
⑤. J23101-Kil-DT(Xba1, Pst1)
⑥. 1kb ladder

Restrictive Digestion

J23101-Kil-DT	BufferM	Xba1	Pst1	BSA	MilliQ	Total
15	3	1	1	3	7	30

J23101-Kil-DT	BufferM	Xba1	BSA	MilliQ	Total
3	1	0.5	1	4.5	10

J23101-Kil-DT	BufferH	Pst1	MilliQ	Total
3	1	0.5	5.5	10

37℃

September 19

Gel extraction

lane1. 1kb ladder
lane2. pSB4K5(EcoR1, Pst1)
lane3. pSB4K5(EcoR1, Pst1)
lane4. empty
lane5. LacP-torA-GFP-DT(Xba1, Pst1)
lane6. LacP-torA-GFP-DT(Xba1, Pst1)

Ligation

LacP-torA-GFP-DT(Xba1,Pst1) 9.7μg/mL	pSB4K5(EcoR1,Pst1) 9.6μg/mL	J23107-TatABCD-PsPA-DT(EcoR1,Spe1) 14.2μg/mL	Ligation High Ver.2	Total
7	2	7	8	24μL

pSB4K5(EcoR1,Pst1) 9.6μg/mL	Ligation High Ver.2	MilliQ	Total
2	1	21	24μL

incubate at 37℃ for 2h

Electrophoresis

J23101-kil-DT (Xba1,Pst1), (Xba1), (Pst1)
Lane1: 1kb ladder
Lane2: empty
Lane3: plasmid
Lane4: (Xba1)
Lane5: (Pst1)
Lane6: (Xba1, Pst1)

Liquid Culture

We did liquid culture J23106-kil-DT(9/10, Amp)'s 6,7 at LB mediumAmp.

Transformation

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT
pSB4K5 negative control

Liquid culture

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT:1~5

Colony PCR

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT

VF2	VR	Quick tag	MilliQ	Total
1	1	25	23	50

Predenature 94℃ 2min
Denature 94℃ 30sec
Annealing 55℃ 30sec
Extension 68℃ 5min
→30cycles

Restrictive Digestion

LacP-kil-DT(4) 62.5μg/mL	Xba1	Pst1	10xBSA	MilliQ	BufferM	Total
10	1	1	3	12	3	30

LacP-kil-DT(4)	EcoR1	Pst1	MilliQ	BufferH	Total
10	1	1	15	3	30

LacP-kil-DT	Xba1	10xBSA	MilliQ	BufferM	Total
2	0.5	1	5.5	1	10

LacP-kil-DT	EcoR1	MilliQ	BufferH	Total
2	0.5	6.5	1	10

LacP-kil-DT	Pst1	MilliQ	BufferH	Total
2	0.5	6.5	1	10

at 37℃, 2 hours

Electrophoresis

LacP-kil-DT
Lane1: 1kb ladder
Lane2: empty
Lane3: plasmid
Lane4: (EcoR1)
Lane5: (Xba1)
Lane6: (Pst1)
Lane7: (EcoR1, Pst1)
Lane8: (Xba1, Pst1)

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(1-5)
Lane1: ladder
Lane2: 1
Lane3: 2
Lane4: 3
Lane5: 4
Lane6: 5

Ligation

LacP-torA-GFP-DT(Xba1,Pst1) 9.7μg/mL	pSB4K5(EcoR1,Pst1) 9.6μg/mL	J23107-TatABCD-PsPA-DT(EcoR1,Spe1) 14.2μg/mL	Ligation High Ver.2	Total
7	4	7	9	27μL

(Negative control)

pSB4K5(EcoR1,Pst1) 9.6μg/mL	Ligation High Ver.2	MilliQ	Total
4	9	14	27μL

Restrictive Digestion

torA-R9 101.8μg/mL	bufferH	MilliQ	EcoR1	Pst1	Total
10	3	15	1	1	30

torA-R9 101.8μg/mL	bufferH	MilliQ	EcoR1	Pst1	Total
3	1	5.5	0.5	0	10

torA-R9 101.8μg/mL	bufferH	MilliQ	EcoR1	Pst1	Total
3	1	5.5	0	0.5	10

PCR

torA-R9	MilliQ	10xPCR buffer for KOD plus neo	2mM dNTP3	25mM MgSO4	M13	KOD plus neo	Total
0.5	34	5	5	3	1.5	1	50

Predenature 94℃ 2min
Denature 98℃ 10sec
Annealing 60℃ 30sec
Extension 68℃ 20sec
→35cycles

Electrophoresis

torA-R9 plasmid, (EcoR1), (Pst1), (EcoR1,Pst1)
Lane1: 1kb ladder
Lane2: empty
Lane3: plasmid
Lane4: EcoR1
Lane5: Pst1
Lane6: EcoR1,Pst1
Lane7: empty
Lane8: 1kb ladder

Liquid culture

LacP-TatA-GFP-DT (9/4)

PCR purification

torA-R9 68.0μg/mL

September 20

Gel extraction

LacP-kil-DT (EcoR1,Pst1) (Xba1,Pst1)

Restrictive Digestion

torA-R9 68.0μg/mL	bufferM	Spe1	MilliQ	Total
20	3	1	6	30

at 37℃, 2h

Ligation

LacP-kil-DT(Xba1,Pst1) 12.4μg/mL	pSB1C3(EcoR1,Pst1) 34.2μg/mL	J23107-TatABCD-PsPA-DT(EcoR1,Spe1) 14.2μg/mL	Ligation High Ver.2	Total
7	4	7	9	27μL

16℃, 1h

(Negative control)

pSB1C3(EcoR1,Pst1)	Ligation High Ver.2	MilliQ	Total
4	9	14	27μL

Transformation

Using above Ligation and Negative control's product and torA-R9.

Miniprep

J23106-kil-DT 6; 12.0μg/mL, (260/280): 1.78, (260/230): 1.73
J23106-kil-DT 7; 13.6μg/mL, (260/280): 1.85, (260/230): 1.73

Restrictive Digestion

GFP-DT 84.1μg/mL	bufferM	10xBSA	BbaI	MilliQ	Total
15	3	3	1	8	30

at 37℃, 2 hours

Colony PCR

We made J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT's 1~8 samples.

Quick tag	Tat f primer	VR	MilliQ	Total
25	1	1	23	50

Predenature 94℃ 2min
Denature 94℃ 30sec
Annealing 54℃ 30sec
Extension 68℃ 4min
→30cycles

J23701-TatABCD-pspA-DT-LacP-torA-GFP-DT
Lane1: 1kb ladder
Lane2: 1
Lane3: 2
Lane4: 3
Lane5: 4
Lane6: 5
Lane7: 6
Lane8: 7
Lane9: 8
Lane10: 1kb ladder
Lane11: empty
Lane12: empty

→Bands didn't appear so we do PCR for 10 more cycles.

Liquid culture

We did liquid culture J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT's 1~4 samples.

Gel extraction

torA-R9 (EcoR1,Pst1): 31μg/mL, (280/280): 0.80, (280/230): 0.39
pSB1C3(EcoR1,Pst1): 22μg/mL, (280/280):1.33, (280/230):0.6
torA-R9 (Spe1): 56μg/mL, (280/280): 1.11, (280/230): 0.69
GFP-DT(Xba1): 45μg/mL, (280/280): 1.15, (280/230): 0.88

Ligation

torA-R9 (EcoR1,Pst1)	pSB1C3(EcoR1,Pst1)	Ligation High Ver.2	Total
8	2	5	15μL

torA-R9 (Spe1)	pSB1C3(Xba1)	Ligation High Ver.2	Total
3	3	3	9μL

at 16℃, 1hour

Colony PCR

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT (4k5)
numbering 9~15

Transformation

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT (4k5)
J23107-TatABCD-pspA-DT-LacP-torA-kil-DT(pSB1C3)
Negative control (pSB1C3)
Negative control(pSB4K5)
torA-R9(pSB1C3)

Liquid culture

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT: colony PCR(9~15)

2xQuick tag	VF	VR	MilliQ	Total
25	1	1	23	50

Predenature 94℃ 2min
Denature 94℃ 30sec
Annealing 55℃ 30sec
Extension 68℃ 5min
→30cycles

PCR

torA-R9-GFP-DT	MilliQ	KOD plus ver.2 buffer	dNTP3	MgSO4	M13	VR	KOD plus	Total
1	35	5	5	2	1.5	1.5	1	52

Predenature 94℃ 2min
Denature 94℃ 15sec
Annealing 55℃ 30sec
Extension 68℃ 5min
→30cycles

Miniprep

J23701-TatABCD-pspA-DT-LacP-torA-GFP-DT:2,3
2: 10.4μg/mL, (250/280): 1.45, (260/230): 0.95
3: 6.0μg/mL, (250/280): 1.32, (260/230): 0.79
(*)100μL

Electrophoresis

torA-R9-GFP-DT(after PCR)

September 21

Gel extraction

torA-R9-GFP-DT(after PCR): 10.3μg/mL, (260/280): 1.28, (220/230): 0.49

Electrophoresis

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(kan): 9~15

Electrophoresis

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT: 1,2
Lane1: empty
Lane2: empty
Lane3: 2
Lane4: 3
Lane5: 1kb ladder

Restrictive Digestion

LacP-kil-DT(3)	Xba1	Pst1	10xBSA	MilliQ	BufferM	Total
15	1	1	3	7	3	30

LacP-torA-GFP-DP(9/5)	Xba1	Pst1	10xBSA	MilliQ	BufferM	Total
15	1	1	3	7	3	30

LacP-kil-DT	Xba1	10xBSA	MilliQ	BufferM	Total
2	0.5	1	5.5	1	10

LacP-torA-GFP-DP	Xba1	10xBSA	MilliQ	BufferM	Total
2	0.5	1	5.5	1	10

LacP-kil-DT	Pst1	MilliQ	BufferH	Total
2	0.5	6.5	1	10

LacP-torA-GFP-DP	Xba1	Pst1	MilliQ	BufferH	Total
2	0.5	1	6.5	1	10

J23107-TatABCD-pspA-DT	Spe1	Pst1	BufferH	MilliQ	Total
20	1	1	4	14	40

J23107-TatABCD-pspA-DT	Spe1	BufferM	MilliQ	Total
2	0.5	1	6.5	10

J23107-TatABCD-pspA-DT	Pst1	BufferH	MilliQ	Total
2	0.5	1	6.5	10

at 37℃, 2hours

Electrophoresis

lane1. 1kb ladder
lane2. empty
lane3. LacP-kil-DT plasmid
lane4. LacP-kil-DT(Xba1)
lane5. LacP-kil-DT(Pst1)
lane6. LacP-kil-DT(Xba1, Pst1)
lane7. empty
lane8. LacP-torA-GFP-DP plasmid
lane9. LacP-torA-GFP-DP(Xba1)
lane10. LacP-torA-GFP-DP(Pst1)
lane11. LacP-torA-GFP-DP(Xba1, Pst1)
lane12. 1kb ladder

lane1. 1kb ladder
lane2. empty
lane3. J23107-TatABCD-pspA-DT plasmid
lane4. J23107-TatABCD-pspA-DT(Spe1)
lane5. J23107-TatABCD-pspA-DT(Pst1)
lane6. J23107-TatABCD-pspA-DT(Spe1, Pst1)

Colony PCR

torA-R9(pSB1C3) (1-4)

10×Buffer	2mM dNTPs	25mM MgSO4	VF	VR	KOD Plus Neo	MilliQ	Total
5	5	3	1.5	1.5	1	33	50

94℃, 2min
98℃, 10sec
60℃, 30sec
68℃, 30sec
→30cycles

Electrophoresis

lane1. 1kb ladder
lane2. empty
lane3. torA-R9-1
lane4. torA-R9-2
lane5. torA-R9-3
lane6. torA-R9-4
lane7. empty
lane8. empty

September 22

Miniprep

torA-R9(Amp)1: 113.7μg/mL, (260/280): 1.96, (280/230): 2.42
torA-R9(Amp)2: 97.8μg/mL, (260/280): 1.67, (280/230): 1.72
torA-R9(Amp)3: 104.2μg/mL, (260/280): 1.93, (280/230): 2.67
LacP-torA-GFP-DT 6: 37.4μg/mL, (260/280): 2.24, (280/230): 3.27

Electrophoresis

LaneA: J23107-TatABCD (9/6)
LaneB: J23107-TatABCD-pspA-DT pSB3C5 (9/13)
LaneC: J23107-TatABCD-pspA-DT 1C5 (9/15)
LaneD: J23107-TatABCD-pspA-DT (9/15)
LaneE: J23107-TatABCD-pspA-DT(pSB1C3) (9/18)
LaneF: J23107-TatABCD-pspA-DT(pSB3C5) (9/18)
LaneG: J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT:2 (9/20)
LaneH: J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT:3 (9/20)
LaneA~H are (EcoR1,Pst1)

Restrictive Digestion

J23107-TatABCD-pspA-DT-LacPtorA-GFP-DT:2	BufferH	Pst1	MilliQ	Total
15	3	1	12	30

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT:3	BufferH	Pst1	MilliQ	Total
15	3	1	12	30

Restrictive Digestion

LacP-torA-GFP-DT(37.4μg/mL)	BufferH	EcoR1	Pst1	Total
25	3	1	1	30

Electrophoresis

①: J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT:2
②: LacP-torA-GFP-DT(EcoR1,Pst1) (9/22)
③: J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT:3

Gel extraction

LacP-torA-GFP-DT(EcoR1,Pst1) 5.5μg/ml 1.21(260/280) 0.37(260/230)

Purification

LacP-torA-GFP-DT 78.4μg/ml 1.62(260/280) 1.03(260/230)

Restrictive Digestion

J23107-TatABCD-pspA-DT(pSB1C3) 78μg/ml	BufferH	Spe1	Pst1	MilliQ	Total
15	3	1	1	10	30

J23107-TatABCD-pspA-DT(pSB1C3) 78μg/ml	BufferH	Spe1	MilliQ	Total
3	1	0.5	5.5	10

J23107-TatABCD-pspA-DT(pSB1C3) 78μg/ml	BufferH	Pst1	MilliQ	Total
3	1	0.5	5.5	10

LacP-torA-GFP-DT 78.4μg/ml	BufferM	BSA	Xba1	Pst1	MilliQ	Total
15	3	3	1	1	7	30

LacP-torA-GFP-DT 78.4μg/ml	BufferM	BSA	Xba1	MilliQ	Total
3	1	1	0.5	4.5	10

LacP-torA-GFP-DT 78.4μg/ml	BufferH	Pst1	MilliQ	Total
3	1	0.5	5.5	10

at 37℃ for 2 hours

Electrophoresis

Lane1: 1kb ladder
Lane2: empty
Lane3: J23107-TatABCD-pspA-DT(pSB1C3)
Lane4: J23107-TatABCD-pspA-DT(Spe1, Pst1)
Lane5: J23107-TatABCD-pspA-DT(Spe1)
Lane6: J23107-TatABCD-pspA-DT(Pst1) (9/18)
Lane7: empty
Lane8: LacP-torA-GFP-DT
Lane9: LacP-torA-GFP-DT(Xba1, Pst1)
Lane10: LacP-torA-GFP-DT(Xba1)
Lane11: LacP-torA-GFP-DT(Pst1)
Lane12: empty
Lane13: 1kb ladder

September 23

Gel extraction

LacP-torA-GFP-DT(EcoR1, Pst1)

lane1 1kb ladder
lane3 DNA
lane4 DNA
lane5 DNA
→failed

lane1 1kb ladder
lane3 J23107-TatABCD-pspA-DT(pSB1C3)(Spe1, Pst1)
lane5 LacP-torA-GFP-DT(Xba1, Pst1)
→failed

Restrictive Digestion

LacP-torA-GFP-DT (78.4μg/mL)	Xba1	Pst1	BufferM	BSA	MilliQ	Total
15	1	1	3	3	7	30

LacP-torA-GFP-DT (78.4μg/mL)	Xba1	BufferM	BSA	MilliQ	Total
3	0.5	1	1	4.5	10

J23107-TatABCD-pspA-DT(pSB1C3) (78μg/mL)	Spe1	Pst1	BufferH	MilliQ	Total
9	1	1	2	7	20

Ligation

LacP-torA-GFP-DT(EcoR1, Pst1) (5.5μg/mL)	pSB4K5 (9.6μg/mL)	Ligation High Ver.2	Total
8	4	6	18

at 16℃ for 1 hour

Liquid culture

LacP-TatABCD-pspA-DT (2, 3, 5, 6)

Colony PCR

LacP-TatABCD-pspA-DT (1-6)

2×Quick Taq	VF2	VR	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 4min
→30cycles

Electrophoresis

①, LacP-torA-GFP-DT
②, LacP-torA-GFP-DT(Xba1, Pst1)
③, LacP-torA-GFP-DT(Xba1)
④, LacP-torA-GFP-DT(Pst1)
⑤, J23107-TatABCD-pspA-DT(Spe1, Pst1)

Liquid culture

LacP-torA-GFP-DT (4, 7)
LacP-GFP generater (1-3)
T7-6His-GFP-DT (1, 2)

Gel extraction

LacP-torA-GFP-DT (Xba1, Pst1) 6.8μg/mL 1.27(260/280) 0.40(260/230)

Purification

J23107-TatABCD-pspA-DT(Spe1, Pst1) 15.1μg/mL 1.49(260/280) 0.80(260/230)

Ligation

J23107-TatABCD-pspA-DT(Spe1, Pst1) (15.1μg/mL)	LacP-torA-GFP-DT (Xba1, Pst1) (6.8μg/mL)	Ligation High Ver.2	Total
10	4	7	21

J23107-TatABCD-pspA-DT(Spe1, Pst1) (15.1μg/mL)	LacP-kil-DT (Xba1, Pst1) (12.4μg/mL)	Ligation High Ver.2	Total
8	2	5	15

at 16℃ for 1 hour

Transformation

LacP-torA-GFP-DT(pSB4K5)
J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT
J23107-TatABCD-pspA-DT-LacP-kil-DT

DNA	competent cell	Total
2	10	12

preculture at 37℃ for 1 hour culture at 37℃ for 16 hours

Electrophoresis

J23107-TatABCD-pspA-DT(pSB1C3) (1-6)
lane1 1kb ladder
lane2~7 DNA
lane8 1kb ladder

September 24

Miniprep

J23107-TatABCD-pspA-DT-2 139.4μg/ml 1.69(260/280) 1.83(260/230)
J23107-TatABCD-pspA-DT-3 134.7μg/ml 1.61(260/280) 1.69(260/230)
J23107-TatABCD-pspA-DT-5 139.3μg/ml 1.55(260/280) 1.45(260/230)
J23107-TatABCD-pspA-DT-6 138.5μg/ml 1.58(260/280) 1.40(260/230)
LacP-torA-GFP-DT-4
LacP-torA-GFP-DT-7
T7-6His-GFP-DT-1
T7-6His-GFP-DT-2

Colony PCR

LacP-GFP generater (1-3)

2×Quick Taq	VF2	VR	MilliQ	Total
25	1	1	23	50

94℃, 2min

94℃, 30sec
55℃, 30sec
68℃, 1min
→30cycles

①-③, LacP-GFP generater (1-3)

Liquid culture

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT (1-4)
J23107-TatABCD-pspA-DT-LacP-kil-DT (1-3)

Colony PCR

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT (1-4)
J23107-TatABCD-pspA-DT-LacP-kil-DT (1-3)

2×Quick Taq	VF2	VR	MilliQ	Total
25	1	1	23	50

94℃, 2min
94℃, 30sec
55℃, 30sec
68℃, 5min
→30cycles

Electrophoresis

lane1, 1kb ladder
lane2-5, J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (1-4)
lane6-8, J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3) (1-3)

September 25

Liquid culture

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB4K5)-2

Miniprep

J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3)-3: 26.2μg/mL, (260/280): 1.50, (280/230): 0.65
J23107-TatABCD-pspA-DT-LacP-torA-GFP(pSB1C3)-3: 24.8μg/mL, (260/280): 1.56, (280/230): 0.76
LacP-GFP generater-1: 42.0μg/mL, (260/280): 1.58, (280/230): 0.94

Restrictive Digestion

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (26.2ng/µL)	EcoRl	Spel	buffer M	MiliQ	Total
15	1	1	3	10	30

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (26.2ng/µL)	EcoRl	buffer M	MiliQ	Total
2	0.5	1	6.5	10

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (26.2ng/µL)	Spel	buffer M	MiliQ	Total
2	0.5	1	6.5	10

J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3) (24.8ng/µL)	EcoRl	Pstl	buffer H	MiliQ	Total
15	1	1	3	10	30

J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3) (24.8ng/µL)	Pstl	buffer H	MiliQ	Total
2	0.5	1	6.5	10

J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3) (24.8ng/µL)	EcoRl	buffer H	MiliQ	Total
2	0.5	1	6.5	10

at 37℃ for 2 hours

Electrophoresis

lane1, 1kb ladder
lane2, J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3)
lane3, J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (EcoRl, Spel)
lane4, J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (EcoRl)
lane5, J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (Spel)
lane6, J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3)
lane7, J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3) (EcoRl, Pstl)
lane8, J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3) (EcoRl)
lane9, J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3) (Pstl)
lane10, LacP-torA-GFP-DT(EcoR1,Xba1)(9/15)
lane11, LacP-torA-GFP-DT(EcoR1,Xba1)(9/17)
lane12, 1kb ladder

→The bands didn't appear, so we did one more electrophoresis.

lane1, 1kb ladder
lane2, LacP-torA-GFP-DT(EcoR1,Xba1)(9/17)
lane3, J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3)
lane4, J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (EcoRl, Spel)
lane5, J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (EcoRl)
lane6, J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (Spel)

Liquid culture

LacP-torA-GFP-DT(pSB4K5) (1-4)

Restrictive Digestion

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3)	EcoRl	Spel	buffer M	MiliQ	Total
15	1	1	3	10	30

J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3)	EcoRl	Pstl	buffer H	MiliQ	Total
15	1	1	3	10	30

at 37℃ for 1 hour

Electrophoresis

J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) (EcoRl, Spel)
J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3) (EcoRl, Pstl)
→The bands didn't appear.

Observation through a confocal microscope

① J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) ② J23107-TatABCD-pspA-DT-LacP-torA-GFP-DT(pSB1C3) ③ J23107-TatABCD-pspA-DT-LacP-kil-DT(pSB1C3)

→We observed nothing.

October 12

Transformation

conpetent cell(3/15)	J23107-TatABCD-PspA-DT (9/13) (pSB3C5)	J23107-TatABCD-PspA-DT(9/18)(pSB3C5)	LacP-torA-GFP-DT(9/10)	total
20μL	2μL			22μL
20μL		2μL		22μL
20μL			2μL	22μL

preculture in SOC medium for 1 hour at 25 degree

Checking Colony PCR(negative control)

Quick Taq	VF	VR	MilliQ	total
25μL	1μL	1μL	23μL	50μL

94℃ 2min
94℃ 30sec
55℃ 30sec
68℃ 5min
30 cycles

->Electrophoresis

October 15

Restrictive Digestion & Electrophoresis

pSB4C5	Xba1	Pst1	BSA	BufferM	MilliQ	total
10μL	1μL	1μL	3μL	3μL	12μL	30μL

at 37℃ for 1 hour

Transformation
retry of lab work that we did on 10/12

J23107-TatABCD-PspA-DT	LacP-torA-GFP-DT	competent cell	total
2μL		20μL	22μL
	2μL	20μL	22μL

preculture in 100μL of SOC medium

October 16

Colony PCR

4 colonies of J23107-TatABCD-PspA-DT(9/18)

Quick Taq	VF2	VR	MilliQ	total
25μL	1μL	1μL	23μL	50μL

94℃ 2min
94℃ 30sec
55℃ 30sec
68℃ 4min
30 cycles

4 colonies of LacP-torA-GFP-DT(10/15)

Quick Taq	VF2	VR	MilliQ	total
25μL	1μL	1μL	23μL	50μL

94℃ 2min
94℃ 30sec
55℃ 30sec
68℃ 1.5min
30 cycles

October 17

Electrophoresis

fig.1

fig.2

fig.3

fig.4

product of colony PCR on 10/16

fig.1

lane_1 : 1kb ladder
lane_2-5 : J23107-TatABCD-PspA-DT
lane_6-9 : LacP-torA-GFP-DT
lane_10 : 1kb ladder

we retried this because something is wrong with 1 kb ladder

fig.2

lane_1 : 1kb ladder
lane_2 : J23107-TatABCD-PspA-DT(lane_3)

Liquid culture
J23017-TatABCD-PspA-DT(10/15)

Colony PCR

8 colonies of LacP-torA-GFP-DT(10/15)

Quick Taq	VF2	VR	MilliQ	total
25μL	1μL	1μL	23μL	50μL

94℃ 2min
94℃ 30sec
55℃ 30sec
68℃ 1.5min
30 cycles

->Electrophoresis we named 8 colonies [5]~[12] because on 10/16, we did colony PCR using 4 colonies([1]~[4]) of J23107-TatABCD-PspA-DT.

fig.3

lane_1 : 1kb ladder
lane_2 : [5]
lane_3 : [6]
lane_4 : [7]
lane_5 : [8]

fig.4

lane_1 : 1kb ladder
lane_2 : [9]
lane_3 : [10]
lane_4 : [11]
lane_5 : [12]

Liquid culture [5] and [7]

October 18

Miniprep

gene	ng/μL
J23107-TatABCD-PspA-DT (10/17)	134.0
LacP-torA-GFP-DT [5] (10/17)	94.7

October 19

Restrictive Digestion

fig.1

fig.2

fig.3

sample_1

J23107-TatABCD-PspA-DT	EcoR1	Spe1	BufferM	MilliQ	total
15μL	1μL	1μL	3μL	10μL	30μL

sample_2

LacP-torA-GFP-DT	Xba1	Pst1	BSA	BufferM	MilliQ	total
10μL	1μL	1μL	3μL	3μL	12μL	30μL

sample_3

LacP-kil-DT	Xba1	Pst1	BSA	BufferM	MilliQ	total
12μL	1μL	1μL	3μL	3μL	10μL	30μL

Electrophoresis
lane_1 : 1kb ladder
lane_2 : J23107-TatABCD-PspA-DT
lane_3 : LacP-torA-GFP-DT
lane_4 : LacP-kil-DT

Restrictive Digestion

T7	Spe1	Pst1	BufferH	MilliQ	total
10μL	1μL	1μL	2μL	6μL	20μL

at 37℃ for 1 hour

Eledtrophoresis
lane_1 : 1kb ladder
lane_2 : sample 1
lane_3 : blank
lane_4 : sample 2
lane_5 : blank
lane_6 : sample 3
Though this figure did not indicate, there was a 1000 bp band that seems to be product of LacP-Kil-DT

October 22

Gel extraction

fig.1

fig.2

fig.3

fig.4

fig.5

fig.6

LacP-torA-GFP-DT
LacP-kil-DT

Gene	ng/µL	260/280	260/230
LacP-torA-GFP-DT	4,4	2,02	0,22
LacP-kil-DT	3,8	1,54	0,11

Restrictive Digestion

LacP-torA-GFP-DT(pSB3C5, 9/10)	EcoR1	Pst1	Buffer M	MilliQ	Total
10µL	1µL	1µL	2µL	6µL	20µL

At 37℃ for 1 hour

Electrophoresis

fig.1

Lane_1:1kb ladder
Lane_2:empty
Lane_3:T7(S,P)

fig.2

Lane_1:1kb ladder
Lane_2:LacP-torA-GFP-DT(E,P)

Gel Extraction

fig.3, 4

Lane_1:1kb ladder
Lane_2:blank
Lane_3:T7(S,P)

Gene	ng/µL	260/280	260/230
T7(S,P)	5,4	1,82	0,23

fig.5, 6

Lane_1:1kb ladder
Lane_2: LacP-torA-GFP-DT(E,P)
Lane_3:pSB4C5(X,P)

Gene	ng/µL	260/280	260/230
LacP-torA-GFP-DT(E,P)	4,9	1,66	0,28
pSB4C5	23,9	1,88	0,88

Ligation

LacP-torA-GFP-DT(X,P)	T7(S,P)	Ligation high Ver.2	Total
10µL	2µL	5,5µL	17,5µL

LacP-torA-GFP-DT(E,P)	pSB4K5(E,P)	Ligation high Ver.2	Total
10µL	2µL	5,5µL	17,5µL

LacP-torA-GFP-DT(X,P)	pSB4C5(X,P)	Ligation high Ver.2	Total
10µL	2µL	5,5µL	17,5µL

At 4℃ overnight

October 23

Transformation

T7-LacP-kil-DT
LacP-torA-GFP-DT(pSB4K5)
LacP-torA-GFP-DT(pSB4C5)

transformed competent cells were plated on two plates respectively.(plate a and plate b)

Ligation

pSB4C5(X,P)	LacP-GFP-DT(X,P)	Ligation high Ver.2	Total
2µL	10µL	6µL	18µL

At 4℃ overnight

October 24

Colony PCR

T7-LacP-kil-DT(a1~a8)
LacP-torA-GFP-DT(pSB4C5)(a1~a4,b1~b4)
LacP-torA-GFP-DT(pSB4K5)(a1~a4,b1,b2)

Quick Taq	VF2	VR	MilliQ	Total
25µL	1µL	1µL	23µL	50µL

94℃ 2min
94 30sec
55 30sec
68 1min
30cycles

Transformation

LacP-GFP-DT(pSB4C5)

Electrophoresis
Products of colony PCR

fig.1

fig.1

Lane_1 :1kb ladder
Lane_2 :empty
Lane_3 : T7-LacP-kil-DT(a1)
Lane_4 : T7-LacP-kil-DT(a2)
Lane_5 : LacP-torA-GFP-DT(pSB4C5)(a1)
Lane_6 : LacP-torA-GFP-DT(pSB4C5)(a2)
Lane_7 : LacP-torA-GFP-DT(pSB4C5)(b1)
Lane_8 : LacP-torA-GFP-DT(pSB4C5)(b2)
Lane_9 : LacP-torA-GFP-DT(pSB4K5)(a1)
Lane_10 : LacP-torA-GFP-DT(pSB4K5)(a2)
Lane_11 : LacP-torA-GFP-DT(pSB4K5)(b1)
Lane_12 : LacP-torA-GFP-DT(pSB4K5)(b2)

fig.2

fig.2

Lane_1 :1kb ladder
Lane_2 : T7-LacP-kil-DT(a3)
Lane_3 : T7-LacP-kil-DT(a4)
Lane_4 : T7-LacP-kil-DT(a5)
Lane_5 : T7-LacP-kil-DT(a6)
Lane_6 : T7-LacP-kil-DT(a7)
Lane_7 : T7-LacP-kil-DT(a8)
Lane_8 : LacP-torA-GFP-DT(pSB4K5)(a3)
Lane_9 : LacP-torA-GFP-DT(pSB4K5)(a4)
Lane_10 :1kb ladder

Liquid culture

LacP-torA-GFP-DT(pSB4C5)(a1,a2)
T7-LacP-kil-DT(a6)

October 25

Observation through a confocal microscope

LacP-torA-GFP-DT(pSB4C5)

We observed nothing.

September 6

PCR and Electrophoresis assay

①psB1K3 ②lacI ③GFP ④GFP ⑤RFP ⑥RFP ⑦CFP ⑧DT

Quick Taq	primer F	Primer R	DNA(①-⑧)	milliQ	total
12.5	0.5	0.5	1	10.5	25

94℃ 2min, (94℃ 30sec, 50℃ 30sec)x25cycles, 68℃ 50sec

September 7

PCR and Electrophoresis assay of psB1K3

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA(psB1K3)	KOD plus	milliQ	total
2.5	2.5	1.0	0.75	0.75	0.5	0.5	16.5	25

94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min

September 10

PCR and Electrophoresis assay of CFP

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA(CFP)	KOD plus	milliQ	total
2.5	2.5	1.0	0.75	0.75	0.5	0.5	16.5	25

94℃ 2min, (94℃ 15sec, 48℃ 30sec)x30cycles, 68℃ 45sec

PCR and Electrophoresis assay of lacI

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA(lacI)	KOD plus	milliQ	total
2.5	2.5	1.0	0.75	0.75	0.5	0.5	16.5	25

94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 30sec

PCR

①PCR product of psB1K3 ②psB1K3 ③psB1C3 ④psB1C3 ⑤PCR product of CFP

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA(①-⑤)	KOD plus	milliQ	total
2.5	2.5	1.0	0.75	0.75	0.5	0.5	16.5	25

94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min20sec

September 11

PCR and Electrophoresis assay

①DT ②PCR product of DT ③PCR product of CFP ④CFP(2011 plate)

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA(①-④)	KOD plus	milliQ	total
2.5	2.5	1.0	0.75	0.75	0.5	0.5	16.5	25

94℃ 2min, (94℃ 15sec, 48℃ 30sec)x30cycles, 68℃ 1min

PCR and Electrophoresis assay

①DT 92.1ng/µl ②DT 28.0ng/µl ③DT

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA(①-③)	KOD plus	milliQ	total
2.5	2.5	1.0	0.75	0.75	0.5	0.5	16.5	25

94℃ 2min, (94℃ 15sec, 50℃ 30sec)x30cycles, 68℃ 30sec

September 12

Purification of PCR product

psB1K3(9/10④) 55µg/ml lacI(9/10) 90µg/ml GFP(9/6) 42µg/ml RFP(9/6) 71µg/ml DT(9/11) 81µg/ml GFP 37µg/ml RFP 57µg/ml

Golden Gate Assembly

psB1K3	lacI	GFP(2'-3)	RFP(3'-5)	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
1.8	0.1	1.0	0.6	0.1	1.5	0.15	1.0	1.0	8.15	15

psB1K3	lacI	GFP(2'-5)	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
1.8	0.1	1.0	0.1	1.5	0.15	1.0	1.0	8.75	15

psB1K3	lacI	GFP(2'-3)	RFP(3'-5)	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	0.2	1.0	1.0	0.2	1.5	0.15	1.0	1.0	6.95	15

psB1K3	lacI	GFP(2'-3)	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	0.2	1.0	0.2	1.5	0.15	1.0	1.0	7.95	15

Transformation

①lacI-GFP(2'-3)-RFP(3'-5)-DT ②lacI-GFP(2'-5)-DT ③lacI-GFP(2'-3)-RFP(3'-5)-DT ④lacI-GFP(2'-5)-DT

September 13

Transformation

①lacI-GFP(2'-3)-RFP(3'-5)-DT ②lacI-GFP(2'-5)-DT ③lacI-GFP(2'-3)-RFP(3'-5)-DT ④lacI-GFP(2'-5)-DT

September 14

Liquid Culture

①lacI-GFP(2'-3)-RFP(3'-5)-DT ②lacI-GFP(2'-5)-DT ③lacI-GFP(2'-3)-RFP(3'-5)-DT ④lacI-GFP(2'-5)-DT

September 15

Miniprep

①lacI-GFP(2'-3)-RFP(3'-5)-DT ②lacI-GFP(2'-5)-DT ③lacI-GFP(2'-3)-RFP(3'-5)-DT ④lacI-GFP(2'-5)-DT

①4.0 µg/ml ②17 µg/ml ③15 µg/ml ④8.0 µg/ml

Restriction Enzyme Digestion

①lacI-GFP(2'-3)-RFP(3'-5)-DT ②lacI-GFP(2'-5)-DT ③lacI-GFP(2'-3)-RFP(3'-5)-DT ④lacI-GFP(2'-5)-DT

DNA(①-④)	10x NEB Bufer3	BSA	EcoR1	MilliQ	Total
9	2	0.5	0.5	8	20

September 17

Electrophoresis assay

①lacI-GFP(2'-3)-RFP(3'-5)-DT ②lacI-GFP(2'-5)-DT ③lacI-GFP(2'-3)-RFP(3'-5)-DT ④lacI-GFP(2'-5)-DT

September 18

Restriction Enzyme Digestion

③lacI-GFP(2'-3)-RFP(3'-5)-DT ④lacI-GFP(2'-5)-DT

DNA(③,④)	10x H Bufer	BSA	EcoR1	MilliQ	Total
15	3	0.5	0.5	11	30

Colony PCR

①lacI-GFP(2'-3)-RFP(3'-5)-DT ②lacI-GFP(2'-5)-DT ③lacI-GFP(2'-3)-RFP(3'-5)-DT ④lacI-GFP(2'-5)-DT

2x Quick Tag Dye Mix	VF primer	VR primer	MiliQ	Total
25	1	1	23	50

September 19

DpnI Restriction Enzyme Digestion of psB1K3

psB1K3	DpnI	Total
10	0.2	10.2

37℃ 1h incubate

Ligation of psB1K3

psB1K3	Ligation High	MiliQ	TH Kinase	Total
2	5	7	7	15

16.0℃　1.5h

September 20

Transformation of psB1K3

September 21

PCR of psB3C5 and Electrophoresis assay

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA(psB3C5)	KOD plus	milliQ	total
2.5	2.5	1.0	0.75	0.75	0.5	0.5	16.5	25

94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min

PCR and Electrophoresis assay

①psB3C5 ②psB1K3

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA(①,②)	KOD plus	milliQ	total
5.0	5.0	2.0	1.5	1.5	1.0	1.0	33	50

94℃ 2min, (94℃ 15sec, 58℃ 30sec, 68℃ 2min)x30cycles

PCR of DT and Electrophoresis assay

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA(DT)	KOD plus	milliQ	total
5.0	5.0	2.0	1.5	1.5	1.0	1.0	33	50

94℃ 2min, (94℃ 15sec, 50℃ 30sec, 68℃ 30sec)x30cycles

September 22

Colony PCR (Colony plated in September 20)

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA	KOD plus	milliQ	total
5.0	5.0	2.0	1.5	1.5	1.0	1.0	33	50

94℃ 2min, (94℃ 15sec, 58℃ 30sec, 68℃ 2min20sec)x25cycles

PCR of Primers and Electrophoresis assay

①J23106(1'-2) ②J23106(2'-3) ③J23106(3'-4) ④J23106(4'-5) ⑤J23106(3'-5) ⑥J23106(2'-5) ⑦J23106(1'-5) ⑧araC(1'-6) ⑨araC(5'-6)

10x Buffer KOD plus	2mM dNTPs	25mM MgSO4	F primer	R primer	DNA	KOD plus	milliQ	total
2.5	2.5	1.0	0.75	0.75	0.5	0.5	16.5	25

94℃ 2min, (94℃ 15sec, 56℃ 30sec)x30cycles, 68℃ 20sec

①J23106(1'-2) 60µg/ml ②J23106(2'-3) 63µg/ml ③J23106(3'-4) 48µg/ml ④J23106(4'-5) 60µg/ml ⑤J23106(3'-5) 62µg/ml ⑥J23106(2'-5) 40µg/ml ⑦J23106(1'-5) 29µg/ml ⑧araC(1'-6) 60µg/ml ⑨araC(5'-6) 62µg/ml

Ligation

4 promoters

psB3C5	①J23106 (1'-2)	②J23106 (2'-3)	③J23106 (3'-4)	④J23106 (4'-5)	⑨araC (5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	2.0	2.0	2.5	2.0	2.0	3.0	3.0	1.5	0.15	1.0	1.0	7.85	30

3 promoters

psB3C5	①J23106 (1'-2)	②J23106 (2'-3)	⑤J23106 (3'-5)	⑨araC (5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	2.0	2.0	2.5	2.0	3.0	3.0	1.5	0.15	1.0	1.0	9.85	30

2 promoters

psB3C5	①J23106(1'-2)	⑥J23106(2'-5)	⑨araC(5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	2.0	2.5	2.0	3.0	3.0	1.5	0.15	1.0	11.85	30

1 promoter

psB3C5	⑦J23106(1'-5)	⑨araC(5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	2.5	2.0	3.0	3.0	1.5	0.15	1.0	1.0	13.85	30

0 promoter

psB3C5	⑨araC(5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	2.0	3.0	3.0	1.5	0.15	1.0	1.0	16.35	30

September 23

Transformation of product of ligation(9/22)

September 24

Transformation of product of ligation(9/22)

September 25

Liquid Culture

colony1,2,3 of plate2,3

Ligation

4 promoters

psB3C5	① J23106 (1'-2)	② J23106 (2'-3)	③ J23106 (3'-4)	④ J23106 (4'-5)	⑨ araC (5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	0.2	0.3	0.2	0.2	0.2	1.0	0.2	1.5	0.15	1.0	1.0	7.05	15

3 promoters

psB3C5	①J23106 (1'-2)	②J23106 (2'-3)	⑤J23106 (3'-5)	⑨araC (5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	0.2	0.3	0.2	0.2	1.0	0.2	1.5	0.15	1.0	1.0	7.25	15

2 promoters

psB3C5	①J23106 (1'-2)	⑥J23106 (2'-5)	⑨araC (5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	0.2	0.3	0.2	1.0	0.2	1.5	0.15	1.0	1.0	7.45	15

1 promoter

psB3C5	⑦J23106 (1'-5)	⑨araC (5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	0.6	0.2	1.0	0.2	1.5	0.15	1.0	1.0	7.35	15

0 promoter

psB3C5	⑨araC (5'-6)	GFP	DT	10x NEB T4 Buffer	100x BSA	BsaI	NEB T4 ligase	milliQ	total
2.0	0.2	1.0	0.2	1.5	0.15	1.0	1.0	7.95	15

(37℃ 3min, 16℃ 4min)x25cycles,

@@ Line 1: / Line 1: @@
-=Secretion=
+[[Image:Header_Kyoto_not_home.jpg|975px|link=Team:Kyoto]]
-=Florigen=
+{{Kyoto/header}}
-==August 2==
+<html>
-'''Mutation of FT'''   <small>by Sato</small><br>
+<script type="text/javascript">
-FT gene has two BioBrick restriction enzyme sites, EcoR1 and Pst1 which is next to each other.<br>
+$(function() {
-So we tried to delete both at once by using two primers with mutation.<br>
+ showTab("kyoto-tab-NoteFFE");
-{|class="wikitable"
+});
-|+Inverse PCR
+</script>
-!10xBufer!!2mM dNTPs!!primer fwd!!primer rev!!template!!polymerase!!MilliQ!!Total
+</html>
-|-
-|5||5||1.5||1.5||0.5||1||35.5||50
-|}
-°C 2min, (98°C 10sec, 68°C 4min)x4cycles, 4°C Hold
-{|class="wikitable"
+<ul id="kyoto-tabs">
-|+Dpn1 Digestion
+<li><html><a href="" onclick="showTab('kyoto-tab-NoteFFE'); return false;"></html>
-!PCR product!!Dpn1
+[[Image:KyotoTab_FlowerFairyE.png|link=|NoteFFE]]<html></a></html></li>
-|-
+<li><html><a href="" onclick="showTab('kyoto-tab-NoteGGA'); return false;"></html>
-|50||2
+[[Image:KyotoTab_Golden.png|link=|NoteGGA]]<html></a></html></li>
-|}   37°C,1h incubate
+</ul>
+<div id="kyoto-tab-contents">
-{|class="wikitable"
+<div id="kyoto-tab-NoteFFE">
-|+Self-ligation
+{{Kyoto/Notebook/FlowerFairyEcoli}}
-!product!!MilliQ!!Ligase!!T4 Kinase!!Total
+</div>
-|-
+<div id="kyoto-tab-NoteGGA">
-|2||7||5||1||15
+{{Kyoto/Notebook/GoldenGate}}
-|}
+</div>
-°C, 1h incubate
+</div>
+{{Kyoto/footer}}
-{|class="wikitable"
-|+Transformation
-!competent cell!!DNA
-|-
-|20||2
-|}
-Cells were stored on ice for 30min. <br>
-After 42°C 60sec heat shock, cells were stored on ice for 2min.<br>
-Then cells were precultureed at 37°C for 1hr, plated to Kanamycin plate.
-<br>
-<br>
-==August 13==
-Liquid culture of FT  37°C, overnight
-==August 14==
-'''Miniprep of FT'''<small> : by Sato, Takeuchi</small><br>
-The concentrarion was 81.5ng/uL<br>
-'''Restriction digestion and Electrophoresis'''<small> : by Sato</small><br>
-To check wheter mutation was succeed, we did restriction enzyme digestion.
-{|class="wikitable"
-!DNA(FT,80ng/uL)!!10xBuferH!!EcoR1!!Pst1!!MilliQ!!Total
-|-
-|5||2||1||-||12||20
-|-
-|5||2||-||1||12||20
-|}
-°C 2h incubate<br>
-We did electrophoresis of three FT plasmids, non-cutted, EcoR1 cutted, Pst1 cutted.<br>
-However, we couldn't get any bands (data not shown.)<br>
-<br>
-Liquid culture of FT (4mL)
-==August 15==
-'''Miniprep of FT'''<small> : by Sato, Takeuchi, Hyungcheol</small><br>
-We couldn't get enough concentration of plasmids.<br>
-'''Electrophoresis'''<small> : by Sato</small><br>
-We retried electrophoresis of three samples same as yesterday.<br>
-However, we couldn't get any bands as well.
-==August 16==
-'''Transformation'''<small> : by Takeuchi, Ota</small><br>
-{| class="wikitable"
-!Name||Well||Sample||Competent Cells||Total||Plate||Colony
-|-
-|FT||-||1 &micro;L||10||11||LB (Kan+)||&#xD7;
-|-
-|pSB1C3||1-3-A||1||10||11||LB (CP+)||&#x25CB;
-|-
-|I719005||1-15-N||1||10||11||LB (Amp+)||&#x25CB;
-|}
-==August 17==
-'''Transformation'''<small> : by Takeuchi</small><br>
-{| class="wikitable"
-!Name||Well||Sample||Competent Cells||MilliQ||Total||Plate||Colony
-|-
-|FT||-||2||2||18||22||LB (Kan+)||&#xD7;
-|}
-We found that mutation of FT was not successful.
-==August 20==
-We decided to do PCR using FT specific primers before mutation.<br>
-'''PCR of FT''' <small> : by Sato</small><br>
-{|class="wikitable"
-!10xBufer!!dNTPs!!MgSO4!!primer fwd!!primer rev!!template!!polymerase!!MilliQ!!Total
-|-
-|5||5||3||1||1||1(130ng/&micro;L)||1(KOD plus neo)||33||50
-|}
-°C 2min,  (98°C 10sec, 68°C 15sec)x30cycles,  4°C Hold<br>
-After the ethanol precipitation, we diluted in 30&micro;L of MilliQ.<br>
-The concentration was 203ng/&micro;L.
-<br>
-<br>
-'''Electrophoresis'''[[File:Electrophoresis0821.png|400px|thumb|right]]
-{| class="wikitable"
-!Lane!!Name!!length(bp)
-|-
-|1||1kb ladder||-
-|-
-|2||FT||600
-|}
-<br>
-==August 21==
-'''Restriction digestion''' <small> : by Sato</small><br>
-{|class="wikitable"
-!DNA(FT,203ng/&micro;L)!!10xBuferM!!Xba11!!Pst1!!MilliQ!!Total
-|-
-|10||4||1||1||24||40
-|}
-°C, 5h incubate<br>
-After the ethanol precipitation, we diluted in 30&micro;L of MilliQ.<br>
-The concentration was 54,9ng/&micro;L.<br>
-<br>
-'''Ligation''' <small> : by Sato</small><br>
-{| class="wikitable"
-!colspan="2"|Vector||colspan="2"|Insert||Ligation High Ver.2
-|-
-|pSB1C3||1||FT||10||5.5
-|}
-'''Liquid culture'''<br>
-T7 promoter, pSB1C3 (4mL)
-<br>
-<br>
-==August 22==
-'''Miniprep'''<small> : by Sato</small><br>
-{| class="wikitable"
-!T7 promoter||pSB1C3
-|-
-|85.3ng/&micro;L||82.93ng/&micro;L
-|}
-<br>
-=Golden Gate Assembly=
-==August 10==
-Golden Gate Assembly method
-This method helps us to constract some genes quickly and we can design the order of constractions.
-We are trying to construct a gene cycle composed of 6 genes( pSB1A3, lacI, GFP, RFP, GFP, DT). After this experiment is confirmed to work, we will so some experiment to check how the numbers of promorters influences the strength of transcription.
-{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
-!align="center"|[[Team:Kyoto|Home]]
-!align="center"|[[Team:Kyoto/Team|Team]]
-!align="center"|[https://igem.org/Team.cgi?year=2012&team_name=Kyoto Official Team Profile]
-!align="center"|[[Team:Kyoto/Project|Project]]
-!align="center"|[[Team:Kyoto/Parts|Parts Submitted to the Registry]]
-!align="center"|[[Team:Kyoto/Modeling|Modeling]]
-!align="center"|[[Team:Kyoto/Notebook|Notebook]]
-!align="center"|[[Team:Kyoto/Safety|Safety]]
-!align="center"|[[Team:Kyoto/Attributions|Attributions]]
-|}

Team:Kyoto/Notebook

From 2012.igem.org

Latest revision as of 11:27, 9 October 2012

Contents

Caution

August 2

Mutation of FT

August 13

Liquid culture

August 14

Miniprep of FT

Restriction digestion and Electrophoresis

Liquid culture

August 15

Miniprep of FT

Electrophoresis

August 16

Transformation

August 17

Transformation

August 20

PCR of FT

Electrophoresis

August 21

Restriction digestion

Ligation

Liquid culture

August 22

Miniprep

August 23

Ethanol Precipitation

August 24

Restriction enzyme processing

Ligation

August 27

Colony PCR

FT(TOPO) PCR(re)

Liquid culture

August 28

Mutation of FT (re)

Miniprep FT(TOPO)

Tranformation

August 29

Mutaion of FT(re;re)

Inverse PCR

Self-Ligation

August 30

Liquid culture(FT) 4mL x2

August 31

Miniprep(FT)

Restriction enzyme processing (Mutation checking)

PCR(RBS primer)

PCR(re)

PCR(re)

September 2

PCR(re;re)

September 3

Restriction enzyme processing

September 4

September 5

September 6

September 9

September 10

Restriction enzyme processing

September 11

September 12

September 13

September 14

September 15

September 16

September 17

September 18

September 19

Colony PCR(re)

September 20

September 22

September 23

September 24

September 25

October 12