Production of pinostilbene compounds by the expression of resveratrol O-methyltransferase genes in Escherichia coli

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dc.contributor.authorYu Jeong Jeong-
dc.contributor.authorChul-Han An-
dc.contributor.authorSu Gyeong Woo-
dc.contributor.authorHyung Jae Jeong-
dc.contributor.authorYoung-Min Kim-
dc.contributor.authorSu-Jin Park-
dc.contributor.authorByung Dae Yoon-
dc.contributor.authorCha Young Kim-
dc.date.accessioned2017-04-19T09:47:56Z-
dc.date.available2017-04-19T09:47:56Z-
dc.date.issued2014-
dc.identifier.issn0141-0229-
dc.identifier.uri10.1016/j.enzmictec.2013.09.005ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11721-
dc.description.abstractResveratrol (3,4',5 trans-trihydroxystilbene) is a polyphenolic phytoalexin that belongs to a family of naturally occurring stilbenes. It has been reported that the health-promoting activities of certain methylated resveratrol derivatives are more effective than those of unmodified resveratrol. In this study, we isolated two candidate genes with resveratrol O-methyltransferase (ROMT) activity from grape (Vitis riparia) and sorghum (Sorghum bicolor). To assess their ROMT activities in vivo, we synthesized VrROMT and SbROMT3 following codon-optimization and expressed the VrROMTsyn and SbROMT3syn genes using a dual expression vector system. Furthermore, we attempted to produce pterostilbene from resveratrol as a substrate by the expression of two putative ROMT proteins in Escherichia coli. Unexpectedly, expression of the SbROMT3syn gene in E. coli led to the production of mono-methylated stilbene (3,4'-dihydroxy-5-methoxy trans-stilbene, pinostilbene) from resveratrol compounds. However, a very small amount of di-methylated stilbene (3,5-dimethoxy-4'-hydroxy trans-stilbene, pterostilbene) was also detected. Consistently, we found that in vitro methylation assays of resveratrol by recombinant SbROMT3syn produced pinostilbene as the major product besides a very small amount of pterostilbene. By contrast, very small amounts of methylated resveratrol derivatives were detected in E. coli expressing the VrROMTsyn protein. This suggests that the SbROMT3syn is more useful in the production of pinostilbene compounds than pterostilbene from resveratrol in E. coli.-
dc.publisherElsevier-
dc.titleProduction of pinostilbene compounds by the expression of resveratrol O-methyltransferase genes in Escherichia coli-
dc.title.alternativeProduction of pinostilbene compounds by the expression of resveratrol O-methyltransferase genes in Escherichia coli-
dc.typeArticle-
dc.citation.titleEnzyme and Microbial Technology-
dc.citation.number1-
dc.citation.endPage14-
dc.citation.startPage8-
dc.citation.volume54-
dc.contributor.affiliatedAuthorYu Jeong Jeong-
dc.contributor.affiliatedAuthorChul-Han An-
dc.contributor.affiliatedAuthorSu Gyeong Woo-
dc.contributor.affiliatedAuthorHyung Jae Jeong-
dc.contributor.affiliatedAuthorYoung-Min Kim-
dc.contributor.affiliatedAuthorSu-Jin Park-
dc.contributor.affiliatedAuthorByung Dae Yoon-
dc.contributor.affiliatedAuthorCha Young Kim-
dc.contributor.alternativeName정유정-
dc.contributor.alternativeName안철한-
dc.contributor.alternativeName우수경-
dc.contributor.alternativeName정형재-
dc.contributor.alternativeName김영민-
dc.contributor.alternativeName박수진-
dc.contributor.alternativeName윤병대-
dc.contributor.alternativeName김차영-
dc.identifier.bibliographicCitationEnzyme and Microbial Technology, vol. 54, no. 1, pp. 8-14-
dc.identifier.doi10.1016/j.enzmictec.2013.09.005-
dc.subject.keywordMetabolic engineering-
dc.subject.keywordPinostilbene-
dc.subject.keywordPterostilbene-
dc.subject.keywordResveratrol-
dc.subject.keywordResveratrol O-Methyltransferase-
dc.subject.localMetabolic Engineering-
dc.subject.localMetabolic engineering-
dc.subject.localmetabolic engineering-
dc.subject.localPinostilbene-
dc.subject.localPterostilbene-
dc.subject.localResveratrol-
dc.subject.localresveratrol-
dc.subject.localResveratrol O-Methyltransferase-
dc.subject.localResveratrol O-methyltransferase-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Biological Resource Center > 1. Journal Articles
Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
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