Difference between revisions of "Part:BBa K778005"
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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). | ||
+ | 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] | Detailed Information :[http://2012.igem.org/Team:UT-Tokyo/Project/H2_E.coli] | ||
Revision as of 00:08, 27 September 2012
RBS-fhlA363-d.term
FhlA-E363G generator without promoter (RBS-fhlAE363G-d.term)
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]
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2115
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1394
- 1000COMPATIBLE WITH RFC[1000]