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Team:Groningen/Notebook/Wetwork 18July2012
From 2012.igem.org
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A= RBS+CII - Fwd primer homolgue to P A (pRE, PluxR), Rev primer homologue to RBS+GFP | A= RBS+CII - Fwd primer homolgue to P A (pRE, PluxR), Rev primer homologue to RBS+GFP | ||
| - | + | or | |
| + | |||
| + | A = RBS+luxI - For RBS use BBA_537034 (exclude terminator) | ||
B=RBS+GFP - Fwd primer homologue to (A), Rev primer+ suffix | B=RBS+GFP - Fwd primer homologue to (A), Rev primer+ suffix | ||
Revision as of 09:25, 24 July 2012
Tom
Incubating Bacillus in LB medium for overnight growth. Next day: growth curves in SMM medium.
Nisa
Possible promoter (inducible promoter)
1. Strong pBAD promoter (BBa_K206000)
2. LacZ regulated lambda pl hybrid promoter (BBa_R0011)
Allows for strong promotion that can be:
a) repressed by lacI
b) induced by IPTG in E.coli DH5a over a >600 fold range
Pactivator: pRE (BBa_K116603) or pluxR (BBa_R0062)
actvator: CII or luxI
... and CIII cd for promoter leakiness
For BBa_R0011 (pL hybrid -> inducible promoter)
Forward primer=prefix-Fprimer Reverse primer= Rprimer-Pactivator homology (pRE, pluxR)
For P actvator-Actvator-GFP
A= RBS+CII - Fwd primer homolgue to P A (pRE, PluxR), Rev primer homologue to RBS+GFP
or
A = RBS+luxI - For RBS use BBA_537034 (exclude terminator)
B=RBS+GFP - Fwd primer homologue to (A), Rev primer+ suffix
Emeraldo
PCR AlsT (150F, 205F, 300F, 500F -R) and GFP Fwd and Rev using Phusion polymerase. Result=OK! Now we have fragments of 150bp, 250bp, 300bp ,500bp and 850bp.
Nanodrop concentrations (ng/ul):
150_alsT = 31,6
250_alsT = 20,5
300_alsT = 22
500_alsT = 27,6
GFP = 39
