dc.contributor.author |
Thiyagarajan, S |
|
dc.contributor.author |
Arumugam, M |
|
dc.contributor.author |
Senthil, N |
|
dc.contributor.author |
Vellaikumar, S |
|
dc.contributor.author |
Kathiresan, S |
|
dc.date.accessioned |
2018-07-26T05:27:01Z |
|
dc.date.available |
2018-07-26T05:27:01Z |
|
dc.date.issued |
2018-03 |
|
dc.identifier.citation |
Biotechnology Letters, 40(3):577-584 |
en_US |
dc.identifier.uri |
http://10.10.100.66:8080/xmlui/handle/123456789/3209 |
|
dc.description.abstract |
Objectives To express a D6-desaturase gene and produce gamma-linolenic acid (GLA) and stearidonic acid (SDA) in prokaryotic expression system (Escherichia coli), and analyze its substrate specificity in the omega-3 fatty acid biosynthetic pathway. Results Full-length ORF (1448 bp) of D6Des-Iso was isolated from Isochrysis sp. and characterized using multiple sequence alignment, phylogenetic analysis, transmembrane domain, and protein tertiary structure. D6Des-Iso is a front-end desaturase consisting of three conserved histidine domains and a cytochrome b5 domain. D6Des-Iso was cloned and expressed in E. coli with the production of GLA and
SDA. Recombinant E. coli utilized 27 and 8% of exogenously supplied alpha-linolenic acid (ALA) and linoleic acid (LA) to produce 6.3% of SDA and 2.3% of GLA, respectively, suggesting that isolated D6Des-Iso is specific to the omega-3 pathway. Conclusion For the first time production of GLA and SDA in a prokaryotic system was achieved. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Springer |
en_US |
dc.subject |
D6-Desaturase |
en_US |
dc.subject |
Escherichia coli |
en_US |
dc.subject |
c-Linolenic acid |
en_US |
dc.subject |
Polyunsaturated fatty acids |
en_US |
dc.subject |
Stearidonic acid |
en_US |
dc.subject |
Substrate specificity |
en_US |
dc.title |
Functional characterization and substrate specificity analysis of D6-desaturase from marine microalga Isochrysis sp. |
en_US |
dc.type |
Article |
en_US |