Difference between revisions of "Part:BBa K1316007"
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This construct is, then, designed to be able to detect and quantify the presence of compunds such as 2,4,6-TNT, 2,4-DNT and 1,3-DNB. The presence of the N-genes aims to enhance this response. | This construct is, then, designed to be able to detect and quantify the presence of compunds such as 2,4,6-TNT, 2,4-DNT and 1,3-DNB. The presence of the N-genes aims to enhance this response. | ||
− | Adding these genes did unfortunately show no clear improvement on the response of the ''yqjF'' promoter in front of 2,4-DNT. | + | |
+ | <h3>Characterisation</h3> | ||
+ | |||
+ | Adding these genes did unfortunately show no clear improvement on the response of the ''yqjF'' promoter in front of 2,4-DNT (Data not shown). | ||
Revision as of 14:08, 15 October 2014
yqjF promoter coupled to mKate2 reporter gene and Rhamnose promoter coupled to N-genes
Promoter of the yqjF gene, which is activated by the presence of several nitrogen-based compounds such as 2,4,6-TNT, 2,4-DNT and 1,3-DNB. mKate2 is a far-red fluorescent protein used with reporting purposes. mKate2 codon usage is optimised for high expression in mammalian cells (humanised). It is, nevertheless, suitable for propagation in E. coli. nfsA, nfsB and nemA (refered here as N-genes) are the genes for NfsA, NfsB and NEM reductases, which presumably play a role in 2,4-DNT and 2,4,6-TNT metabolism. These genes are regulated by the inducible Rhamnose promoter This construct is, then, designed to be able to detect and quantify the presence of compunds such as 2,4,6-TNT, 2,4-DNT and 1,3-DNB. The presence of the N-genes aims to enhance this response.
Characterisation
Adding these genes did unfortunately show no clear improvement on the response of the yqjF promoter in front of 2,4-DNT (Data not shown).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 128
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 733
Illegal BsaI.rc site found at 922