Difference between revisions of "Part:BBa J153001"
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P''trc1O'', or the ''trc'' promoter, is a hybrid of the ''Escherichia coli trp'' promoter and the ''lacUV5'' promoter (Brosius etal 1985) [http://www.ncbi.nlm.nih.gov/pubmed/2579077]. | P''trc1O'', or the ''trc'' promoter, is a hybrid of the ''Escherichia coli trp'' promoter and the ''lacUV5'' promoter (Brosius etal 1985) [http://www.ncbi.nlm.nih.gov/pubmed/2579077]. | ||
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It was characterized with a GFP reporter construct ([[Part:BBa_I13504]]) carried on the broad-host-range shuttle vector pPMQAK1 ([[Part:BBa_J153000]]) to be stronger than both the ''lacZYA'' operon promoter ([[Part:BBa_R0010]]) (ca 35% stronger) and a cI-based TetR-repressible promoter ([[Part:BBa_R0040]]) (ca 320 % stronger) in ''E. coli'' DH5alpha. Characterization in the cyanobacterium ''Synechocystis'' sp. PCC 6803 revealed strong fluorescence from the P''trc1O''-driven construct but no detectable signal from the “Plac” construct and only a weak signal from the “PtetR” construct. Repression of P''trc1O'' by LacI in ''Synechocystis'' was very modest (Huang etal 2010) [http://www.ncbi.nlm.nih.gov/pubmed/20236988]. | It was characterized with a GFP reporter construct ([[Part:BBa_I13504]]) carried on the broad-host-range shuttle vector pPMQAK1 ([[Part:BBa_J153000]]) to be stronger than both the ''lacZYA'' operon promoter ([[Part:BBa_R0010]]) (ca 35% stronger) and a cI-based TetR-repressible promoter ([[Part:BBa_R0040]]) (ca 320 % stronger) in ''E. coli'' DH5alpha. Characterization in the cyanobacterium ''Synechocystis'' sp. PCC 6803 revealed strong fluorescence from the P''trc1O''-driven construct but no detectable signal from the “Plac” construct and only a weak signal from the “PtetR” construct. Repression of P''trc1O'' by LacI in ''Synechocystis'' was very modest (Huang etal 2010) [http://www.ncbi.nlm.nih.gov/pubmed/20236988]. | ||
The P''trc2O'' promoter (Part:BBa_J153002) is of similar strength as P''trc1O'' but significantly more repressed by LacI in ''Synechocystis''. However, there are problems inducing this promoter to its full strength, limiting its usability. | The P''trc2O'' promoter (Part:BBa_J153002) is of similar strength as P''trc1O'' but significantly more repressed by LacI in ''Synechocystis''. However, there are problems inducing this promoter to its full strength, limiting its usability. | ||
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+ | <span class='h3bb'>Sequence and Features</span> | ||
+ | <partinfo>BBa_J153001 SequenceAndFeatures</partinfo> | ||
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+ | <!-- Uncomment this to enable Functional Parameter display | ||
+ | ===Functional Parameters=== | ||
+ | <partinfo>BBa_J153001 parameters</partinfo> | ||
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Revision as of 12:14, 3 February 2012
Ptrc1O
Ptrc1O, or the trc promoter, is a hybrid of the Escherichia coli trp promoter and the lacUV5 promoter (Brosius etal 1985) [http://www.ncbi.nlm.nih.gov/pubmed/2579077].
It contains the lac O1 operator (proximal to the core promoter) that allows for LacI repression and subsequent induction by IPTG.
Usage and Biology
It was characterized with a GFP reporter construct (Part:BBa_I13504) carried on the broad-host-range shuttle vector pPMQAK1 (Part:BBa_J153000) to be stronger than both the lacZYA operon promoter (Part:BBa_R0010) (ca 35% stronger) and a cI-based TetR-repressible promoter (Part:BBa_R0040) (ca 320 % stronger) in E. coli DH5alpha. Characterization in the cyanobacterium Synechocystis sp. PCC 6803 revealed strong fluorescence from the Ptrc1O-driven construct but no detectable signal from the “Plac” construct and only a weak signal from the “PtetR” construct. Repression of Ptrc1O by LacI in Synechocystis was very modest (Huang etal 2010) [http://www.ncbi.nlm.nih.gov/pubmed/20236988].
The Ptrc2O promoter (Part:BBa_J153002) is of similar strength as Ptrc1O but significantly more repressed by LacI in Synechocystis. However, there are problems inducing this promoter to its full strength, limiting its usability.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]