Team:Tokyo-NoKoGen/Notebook/diary

From 2012.igem.org

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“Coli express for long distance communication”<BR><BR>
“Coli express for long distance communication”<BR><BR>
Lux team :<BR>
Lux team :<BR>
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lux operon was cloned from photobacterim phosphorium genome DNA. Most sequence was confirmed by sequence analysis.  
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lux operon was cloned from <I>Photobacterim phosphorium</I> genome DNA. Most sequence was confirmed by sequence analysis.  
<br><br>
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<div align=center><img src="https://static.igem.org/mediawiki/2012/f/f8/Coli3.jpg" height="50%" width="50%"/></div>
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<div align=center><img src="https://static.igem.org/mediawiki/2012/f/f8/Coli3.jpg" height="50%" width="65%"/></div>
<BR><BR>
<BR><BR>
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  lux team and rhodopsin team made small presentation about experiments.<BR><BR>
  lux team and rhodopsin team made small presentation about experiments.<BR><BR>
Rhodopsin team :<BR>
Rhodopsin team :<BR>
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  insertion of PompR(+)-RBS-GFP-DT under blue light sensor biobrick.(BBa~)<BR>
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  insertion of PompR(+)-RBS-GFP-DT under blue light sensor biobrick.(BBa_K769000)<BR>
plasmid extraction of blue light sensor + GFP and sequence analysis.
plasmid extraction of blue light sensor + GFP and sequence analysis.
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<h3>9-15</h3>
<h3>9-15</h3>
Lux team : <BR>
Lux team : <BR>
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lux bio-brick (pSB1C3-PBAD-RBS-lux operon-DT) was constructed! E. coli TOP10 was transformed with this plasmid.<BR>
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lux bio-brick (pSB1C3-PBAD-RBS-lux operon-DT) was constructed! <I>E. coli</I> TOP10 was transformed with this plasmid.<BR>
Evaluation of lux bio-brick. Luminescence was measured using plate reader. We could see luminescence in dark room.<BR>
Evaluation of lux bio-brick. Luminescence was measured using plate reader. We could see luminescence in dark room.<BR>
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Design primers to clone rib operon from E.coli genome DNA<BR>
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Design primers to clone rib operon from <I>E.coli</I> genome DNA<BR>
lux bio-brick that constitutive expression of lux gene was constructed. We expected more luminescence using strong constitutive expression promoter.<BR>
lux bio-brick that constitutive expression of lux gene was constructed. We expected more luminescence using strong constitutive expression promoter.<BR>
<BR>
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Meeting :<BR>
Meeting :<BR>
Our team T-shirt design idea has been completed.<BR>
Our team T-shirt design idea has been completed.<BR>
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<div align=center><img src="https://static.igem.org/mediawiki/2012/0/02/Tshirt.png"></div>
<BR><BR>
<BR><BR>
<h3>16-22</h3>
<h3>16-22</h3>
Lux team :<BR>
Lux team :<BR>
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  rib operon was cloned fromE.coli genome DNA. Most sequence was confirmed by sequence analysis<BR>
+
  rib operon was cloned from <I>E.coli</I> genome DNA. Most sequence was confirmed by sequence analysis<BR>
Evaluation of color change biobrick.<BR><BR>
Evaluation of color change biobrick.<BR><BR>
Meeting :<BR><BR>
Meeting :<BR><BR>
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Poster session team<BR>
Poster session team<BR>
We began to design poster and slide.<BR>
We began to design poster and slide.<BR>
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<div align=center><img src="https://static.igem.org/mediawiki/2012/0/02/Col.png"></div>
<BR><BR>
<BR><BR>
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After preculture, transformants were culture under white light or dark condition.<BR><BR>
After preculture, transformants were culture under white light or dark condition.<BR><BR>
Lux team :<BR>
Lux team :<BR>
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  evaluation of fast luminescence biobrick.<BR><BR>
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  evaluation of fast luminescence biobrick.
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<br>
 +
<div align=center><img src="https://static.igem.org/mediawiki/2012/5/59/Fast.png"></div>
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<BR><BR>

Latest revision as of 03:39, 27 September 2012



Diary

July

8-14

Meeting :
lux team member: Jinhee LEE, Sumiya KAWAI, Miho NARITA, Tomomi YOKOYAMA, Mayumi NAKAMURA
rhodopsin team member: Hiroto OKANO, Genki SAKAI, Hayato TSURUTA, Somin LEE

August

5-11

Meeting :
Small session on gene experiments using iGEM biobrick.

Lux team :
Design primers to clone lux operon from photobacterim phosphorium genome DNA.

19-25

Rhodopsin team :
construction of blue light sensor.
Pconst.(H)-RBS-NpSRII-9a.a.linker_NpHtrII-EnvZ-DT
sequence analysis of constructed blue light sensor biobrick.

Meeting :
lux team and rhodopsin team made small presentation about experiments.

26-9/1

Rhodopsin team :
construction of ⊿EnvZ competent cell

Meeting :
Our project title and team character was desided!
“Coli express for long distance communication”

Lux team :
lux operon was cloned from Photobacterim phosphorium genome DNA. Most sequence was confirmed by sequence analysis.



2-8

Meeting :
lux team and rhodopsin team made small presentation about experiments.

Rhodopsin team :
insertion of PompR(+)-RBS-GFP-DT under blue light sensor biobrick.(BBa_K769000)
plasmid extraction of blue light sensor + GFP and sequence analysis.

9-15

Lux team :
lux bio-brick (pSB1C3-PBAD-RBS-lux operon-DT) was constructed! E. coli TOP10 was transformed with this plasmid.
Evaluation of lux bio-brick. Luminescence was measured using plate reader. We could see luminescence in dark room.
Design primers to clone rib operon from E.coli genome DNA
lux bio-brick that constitutive expression of lux gene was constructed. We expected more luminescence using strong constitutive expression promoter.

Rhodopsin team :
evaluation of blue light sensor.
After preculture, transformants were culture under blue light or dark condition.
But cells were not growth well.

Meeting :
Our team T-shirt design idea has been completed.


16-22

Lux team :
rib operon was cloned from E.coli genome DNA. Most sequence was confirmed by sequence analysis
Evaluation of color change biobrick.

Meeting :

Presentation team
Poster session team
We began to design poster and slide.


23-29

Rhodopsin team :
Reevaluation of blue light sensor.
After preculture, transformants were culture under white light or dark condition.

Lux team :
evaluation of fast luminescence biobrick.