Difference between revisions of "Part:BBa K515100"
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===Functional Parameters=== | ===Functional Parameters=== | ||
− | <partinfo>BBa_K515100 parameters</partinfo> | + | <partinfo><b>BBa_K515100 parameters</b></partinfo> |
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<h2>References</h2> | <h2>References</h2> | ||
[1]Palm, CJ et al., 1989. Cotranscription of genes encoding indoleacetic acid production in Pseudomonas syringae subsp. savastanoi. <i>Journal of Bacteriology</i>, 171(2), pp.1002-1009.</p> | [1]Palm, CJ et al., 1989. Cotranscription of genes encoding indoleacetic acid production in Pseudomonas syringae subsp. savastanoi. <i>Journal of Bacteriology</i>, 171(2), pp.1002-1009.</p> |
Revision as of 14:46, 12 September 2011
IAA biosynthetic genes under control of the Pveg2 promoter
The IAM pathway is a two step pathway which generates indole-3-acetic acid (auxin) from the precursor tryptophan. IAA tryptophan monooxygenase (IaaM) BBa_K515000, catalyzes the oxidative carboxylation of L-tryptophan to indole-3-acetamide which is hydrolyzed to indole-3-acetic acid and ammonia by indoleacetamide hydrolase (IaaH) BBa_K515001 . There are several different pathways that produce indole-3-acetic acid. IaaM and IaaH originate from P.savastanoi and have been expressed in E. coli previously, and shown to secrete auxin into cell supernatant, however without sufficient characterisation. [1]
CompatabilityChassis: This device has been tested in E. coli strain DH5α as a construct assembled with the pSB1C3 backbone vector.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 547
Illegal BamHI site found at 1492 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 254
Illegal NgoMIV site found at 2835 - 1000COMPATIBLE WITH RFC[1000]
References
[1]Palm, CJ et al., 1989. Cotranscription of genes encoding indoleacetic acid production in Pseudomonas syringae subsp. savastanoi. Journal of Bacteriology, 171(2), pp.1002-1009.</p>