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首页> 外文期刊>Archives of Microbiology >Ergot alkaloid biosynthesis in Aspergillus fumigatus: conversion of chanoclavine-I to chanoclavine-I aldehyde catalyzed by a short-chain alcohol dehydrogenase FgaDH
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Ergot alkaloid biosynthesis in Aspergillus fumigatus: conversion of chanoclavine-I to chanoclavine-I aldehyde catalyzed by a short-chain alcohol dehydrogenase FgaDH

机译:烟曲霉中麦角生物碱的生物合成:短链醇脱氢酶FgaDH催化Chanoclavine-I向Chanoclavine-I醛的转化

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Ergot alkaloids are toxins and important pharmaceuticals which are produced biotechnologically on an industrial scale. A putative gene fgaDH has been identified in the biosynthetic gene cluster of fumigaclavine C, an ergot alkaloid of the clavine-type. The deduced gene product FgaDH comprises 261 amino acids with a molecular mass of about 27.8 kDa and contains the conserved motifs of classical short-chain dehydrogenases/reductases (SDRs), but shares no worth mentioning sequence similarity with SDRs and other known proteins. The coding region of fgaDH consisting of two exons was amplified by PCR from a cDNA library of Aspergillus fumigatus, cloned into pQE60 and overexpressed in E. coli. The soluble tetrameric His6-FgaDH was purified to apparent homogeneity and characterized biochemically. It has been shown that FgaDH catalyzes the oxidation of chanoclavine-I in the presence of NAD+ resulting in the formation of chanoclavine-I aldehyde, which was unequivocally identified by NMR and MS analyzes. Therefore, FgaDH functions as a chanoclavine-I dehydrogenase and represents a new group of short-chain dehydrogenases. K M values for chanoclavine-I and NAD+ were determined at 0.27 and 1.1 mM, respectively. The turnover number was 0.38 s−1. Keywords Aspergillus fumigatus - Biochemical characterization - Chanoclavine-I aldehyde - Ergot alkaloid biosynthesis - Gene expression - Short-chain alcohol dehydrogenase - Chanoclavine-I oxidase Communicated by Erko Stackebrandt.
机译:麦角生物碱是毒素和重要的药物,它们是通过生物技术以工业规模生产的。已经在烟熏型麦角生物碱烟熏麦角碱C的生物合成基因簇中鉴定出推定基因fgaDH。推导的基因产物FgaDH包含261个氨基酸,分子量约为27.8 kDa,并包含经典短链脱氢酶/还原酶(SDR)的保守基序,但与SDR和其他已知蛋白质的序列相似性不值得一提。通过PCR从烟曲霉的cDNA文库中扩增由两个外显子组成的fgaDH的编码区,将其克隆到pQE60中并在大肠杆菌中过表达。将可溶性四聚体His 6 -FgaDH纯化至表观均一并进行生化表征。研究表明,在NAD + 存在下,FgaDH可以催化chanoclavine-I的氧化,导致chanoclavine-I醛的形成,这一点可以通过NMR和MS分析明确地确定。因此,FgaDH的功能是Chaclaclavine-I脱氢酶,代表了一组新的短链脱氢酶。薄层锁骨链-I和NAD + 的K M 值分别确定为0.27和1.1 mM。周转数为0.38 s -1 。关键字烟曲霉-生化特性-Chanoclavine-I醛-麦角生物碱生物合成-基因表达-短链醇脱氢酶-Chanoclavine-I氧化酶Erko Stackebrandt进行了通讯。

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