Difference between revisions of "Part:BBa K1520000:Design"
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===Source=== | ===Source=== | ||
| − | It is synthetic.The gene was discovered in Sphingopyxis sp. C-1,and the sequence of it can be obtained from genebank. | + | It is synthetic.The gene was discovered in Sphingopyxis sp. C-1,and the sequence of it can be obtained from genebank >gi|349500571|dbj|AB591070.1|. |
===References=== | ===References=== | ||
| + | Bourne D G, Riddles P, Jones G J, et al. Characterisation of a gene cluster involved in bacterial degradation of the cyanobacterial toxin microcystin LR[J]. Environmental toxicology, 2001, 16(6): 523-534. | ||
Latest revision as of 17:52, 5 October 2014
MlrD.The protein is involved in microcystin degradation.
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1042
Design Notes
mrlD is a gene involved in degradation of microsystin. The MlrD protein belongs to a protein family which is predicted to carry small peptides across the bacterial cell wall and it is therefore possible that this protein facilitates the transport of microcystin. The taking in process would facility another protein,MrlA,which is an enzyme of microcystin to clean up microcystin successfully.
Source
It is synthetic.The gene was discovered in Sphingopyxis sp. C-1,and the sequence of it can be obtained from genebank >gi|349500571|dbj|AB591070.1|.
References
Bourne D G, Riddles P, Jones G J, et al. Characterisation of a gene cluster involved in bacterial degradation of the cyanobacterial toxin microcystin LR[J]. Environmental toxicology, 2001, 16(6): 523-534.