Characterization and phylogenitic analaysis of ecotine biosynthesis genes from bacillus halodurans
Characterization and phylogenitic analaysis of ecotine biosynthesis genes from bacillus halodurans
dc.contributor.author | Rajan, A. | |
dc.contributor.author | Joseph, C.T. | |
dc.contributor.author | Thampuran, N. | |
dc.contributor.author | James, R. | |
dc.contributor.author | Viswanathan, C. | |
dc.contributor.author | Bansal, K.C. | |
dc.date.accessioned | 2013-12-20T06:00:40Z | |
dc.date.available | 2013-12-20T06:00:40Z | |
dc.date.issued | 2008 | |
dc.description.abstract | Ectoine, a cyclic tetrahydropyrimidine (2- methyl-1,4,5,6-tetrahydropyrimidine-4-carboxylic acid), is a natural compound, which serves as a protective substance in many bacterial cells. In this study, the putative ectABC gene cluster from Bacillus halodurans was heterologously expressed in E. coli and the production of ectoine was con- Wrmed by HPLC analysis. The activity of the enzymes coded by the ectA, B and C genes were found to be higher in induced transgenic cells compared to the uninduced cells. Phylogenetic analysis revealed sequence identities ranging from 36–73% for ectA gene, 55–81% for ectB gene and 55–80% for ectC gene indicating that the enzymes are evolutionarily well conserved. | en_US |
dc.identifier.citation | Archives of Microbiology 2008: 190, 481-487 | en_US |
dc.identifier.uri | http://hdl.handle.net/123456789/1015 | |
dc.language.iso | en | en_US |
dc.publisher | Springer | en_US |
dc.subject | B. halodurans | en_US |
dc.subject | compatible solutes | en_US |
dc.subject | salt stress | en_US |
dc.subject | ectoine genes | en_US |
dc.subject | osmoregulation | en_US |
dc.title | Characterization and phylogenitic analaysis of ecotine biosynthesis genes from bacillus halodurans | en_US |
dc.type | Article | en_US |
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