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dc.contributor.authorThiyagarajan, S-
dc.contributor.authorArumugam, M-
dc.contributor.authorSenthil, N-
dc.contributor.authorVellaikumar, S-
dc.contributor.authorKathiresan, S-
dc.date.accessioned2018-07-26T05:27:01Z-
dc.date.available2018-07-26T05:27:01Z-
dc.date.issued2018-03-
dc.identifier.citationBiotechnology Letters, 40(3):577-584en_US
dc.identifier.urihttp://10.10.100.66:8080/xmlui/handle/123456789/3209-
dc.description.abstractObjectives 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.isoenen_US
dc.publisherSpringeren_US
dc.subjectD6-Desaturaseen_US
dc.subjectEscherichia colien_US
dc.subjectc-Linolenic aciden_US
dc.subjectPolyunsaturated fatty acidsen_US
dc.subjectStearidonic aciden_US
dc.subjectSubstrate specificityen_US
dc.titleFunctional characterization and substrate specificity analysis of D6-desaturase from marine microalga Isochrysis sp.en_US
dc.typeArticleen_US
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