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阿维链霉菌宿主体系中通过区域选择性顺序羟化和 O-甲基化反应生产新型 O-甲基异黄酮。

Production of a novel O-methyl-isoflavone by regioselective sequential hydroxylation and O-methylation reactions in Streptomyces avermitilis host system.

机构信息

School of Chemical and Biological Engineering, Institute of Bioengineering, Seoul National University, Seoul, South Korea.

出版信息

Biotechnol Bioeng. 2013 Oct;110(10):2591-9. doi: 10.1002/bit.24931. Epub 2013 Apr 26.

Abstract

Distinct isoflavone O-methyltransferases (IOMTs) from Streptomyces species were isolated and expressed using S. avermitilis host system. Previously reported isoflavone 7-O-methyltransferases (I7OMTs, E.C. 2.1.1.150) and two putative O-methyltransferases (OMTs) from Saccharopolyspora erythraea were selected by comparative sequence grouping and expressed in S. avermitilisΔSaOMT2 under the control of constitutive ermE promoter. During whole-cell biotransformation of 4',7-dihydroxyisoflavone (daidzein) by constructed recombinant strains, production of O-methylated daidzein was investigated. S. avermitilisΔSaOMT2::SeOMT3 (SeOMT3) produced 7-methoxy-4'-hydroxyisoflavone (7-OMD) with 4.5% of low conversion yield due to competitive oxidation reactions. However, SeOMT3 could produce a novel 4',7-dihydroxy-3'-methoxyisoflavone (3'-OMD) (<1%) resulted from subsequent 3'-O-methylation of 3',4',7-trihydroxyisoflavone (3'-OHD) which was a hydroxylated product catalyzed by oxygenases. Although external addition of SAM did not change the conversion yield of O-methylation reaction, co-expression of SAM synthetase gene (metK) with SeOMT3 greatly induced the regiospecific O-methylation reaction at 3'-hydroxyl group with final conversion of 12.1% using 0.1 mM of daidzein.

摘要

从链霉菌属中分离并表达了具有独特结构的异黄酮 O-甲基转移酶(IOMTs)。先前报道的异黄酮 7-O-甲基转移酶(I7OMTs,E.C. 2.1.1.150)和来自红色糖多孢菌的两个假定的 O-甲基转移酶(OMTs)通过比较序列分组选择,并在阿维链霉菌ΔSaOMT2 中在组成型 ermE 启动子的控制下表达。在构建的重组菌株对 4',7-二羟基异黄酮(大豆苷元)的全细胞生物转化过程中,研究了 O-甲基化大豆苷元的产生情况。阿维链霉菌ΔSaOMT2::SeOMT3(SeOMT3)由于竞争氧化反应,仅以 4.5%的低转化率生成 7-甲氧基-4'-羟基异黄酮(7-OMD)。然而,SeOMT3 可以产生一种新型的 4',7-二羟基-3'-甲氧基异黄酮(3'-OMD)(<1%),这是由于 3',4',7-三羟基异黄酮(3'-OHD)的后续 3'-O-甲基化反应生成的,而 3'-OHD 是由加氧酶催化的羟化产物。尽管外部添加 SAM 不会改变 O-甲基化反应的转化率,但与 SeOMT3 共表达 SAM 合成酶基因(metK)可极大地诱导 3'-羟基的区域特异性 O-甲基化反应,最终转化率为 12.1%,使用 0.1mM 的大豆苷元。

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