Team:Tokyo-NoKoGen/Notebook/diary
From 2012.igem.org
(Difference between revisions)
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- | 8-14< | + | <h3>8-14</h3> |
Meeting :<BR> | Meeting :<BR> | ||
lux team member: Jinhee LEE, Sumiya KAWAI, Miho NARITA, Tomomi YOKOYAMA, Mayumi NAKAMURA <BR> | lux team member: Jinhee LEE, Sumiya KAWAI, Miho NARITA, Tomomi YOKOYAMA, Mayumi NAKAMURA <BR> | ||
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- | August< | + | <h2>August</h2> |
- | 5-11< | + | <h3>5-11</h3> |
Meeting : <BR> | Meeting : <BR> | ||
Small session on gene experiments using iGEM biobrick.<BR><BR> | Small session on gene experiments using iGEM biobrick.<BR><BR> | ||
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Rhodopsin team :<BR> | Rhodopsin team :<BR> | ||
construction of blue light sensor.<BR> | construction of blue light sensor.<BR> | ||
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- | 26-9/1< | + | <h3>26-9/1</h3> |
Rhodopsin team :<BR> | Rhodopsin team :<BR> | ||
construction of ⊿EnvZ competent cell<BR><BR> | construction of ⊿EnvZ competent cell<BR><BR> | ||
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Meeting :<BR> | Meeting :<BR> | ||
lux team and rhodopsin team made small presentation about experiments.<BR><BR> | lux team and rhodopsin team made small presentation about experiments.<BR><BR> | ||
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Lux team : <BR> | Lux team : <BR> | ||
lux bio-brick (pSB1C3-PBAD-RBS-lux operon-DT) was constructed! E. coli TOP10 was transformed with this plasmid.<BR> | 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 team :<BR> | Lux team :<BR> | ||
rib operon was cloned fromE.coli genome DNA. Most sequence was confirmed by sequence analysis<BR> | rib operon was cloned fromE.coli genome DNA. Most sequence was confirmed by sequence analysis<BR> | ||
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Rhodopsin team : <BR> | Rhodopsin team : <BR> | ||
Reevaluation of blue light sensor.<BR> | Reevaluation of blue light sensor.<BR> |
Revision as of 01:51, 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~)
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 fromE.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.