Difference between revisions of "Part:BBa K778011"
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<partinfo>BBa_K778011 short</partinfo> | <partinfo>BBa_K778011 short</partinfo> | ||
− | + | You can "enhance" and "see" H2 production with this device. | |
hycAp-GFPgenerator-plac-FhlA363generator | hycAp-GFPgenerator-plac-FhlA363generator | ||
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E.coli overexpressing FhlA produce H2 (since hycAp is the promoter of FHL(formate hydrogen lyase)). | E.coli overexpressing FhlA produce H2 (since hycAp is the promoter of FHL(formate hydrogen lyase)). | ||
fhlA-E363G has one point mutation (A to G, glutamic acid to glycine). | fhlA-E363G has one point mutation (A to G, glutamic acid to glycine). | ||
− | Detailed Information :[http://2012.igem.org/Team:UT-Tokyo/Project/H2_E.coli] | + | This mutation increased H2 production under the conditions in the previous research (Viviana et.al.2009). |
+ | However, in our research (team UT-Tokyo 2012[http://2012.igem.org/Team:UT-Tokyo/Project/H2_E.coli]), this mutation did not increase H2 production. | ||
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+ | Detailed Information :[http://2012.igem.org/Team:UT-Tokyo/Project/H2_E.coli/System] | ||
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<partinfo>BBa_K778011 parameters</partinfo> | <partinfo>BBa_K778011 parameters</partinfo> | ||
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+ | [[Image:Safety.png]] |
Latest revision as of 15:36, 27 September 2012
hycAp-GFPgenerator-plac-FhlA363generator
You can "enhance" and "see" H2 production with this device.
hycAp-GFPgenerator-plac-FhlA363generator
GFP is a reportor of H2 production (strictly speaking,reporter of hycAp activation Part:BBa K778000 (hycAp is the promotor of formate hydrogen lyase of genome)).
FhlA is the trnascriptional activator of hycAp Part:BBa K778000 . E.coli overexpressing FhlA produce H2 (since hycAp is the promoter of FHL(formate hydrogen lyase)). fhlA-E363G has one point mutation (A to G, glutamic acid to glycine). This mutation increased H2 production under the conditions in the previous research (Viviana et.al.2009). However, in our research (team UT-Tokyo 2012[http://2012.igem.org/Team:UT-Tokyo/Project/H2_E.coli]), this mutation did not increase H2 production.
Detailed Information :[http://2012.igem.org/Team:UT-Tokyo/Project/H2_E.coli/System]
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 3266
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 2545
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 828