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棒状链霉菌中参与克拉维酸生物合成的不同基因发生破坏的突变体产生大量全霉素:两条不相关的次级代谢途径可能存在交叉调控。

Mutants of Streptomyces clavuligerus with disruptions in different genes for clavulanic acid biosynthesis produce large amounts of holomycin: possible cross-regulation of two unrelated secondary metabolic pathways.

作者信息

de la Fuente Alvaro, Lorenzana Luis M, Martín Juan F, Liras Paloma

机构信息

Area de Microbiología, Facultad de Ciencias Biológicas y Ambientales, Universidad de León, 24071 León, Spain.

出版信息

J Bacteriol. 2002 Dec;184(23):6559-65. doi: 10.1128/JB.184.23.6559-6565.2002.

Abstract

A Streptomyces clavuligerus ccaR::aph strain, which has a disruption in the regulatory gene ccaR, does not produce cephamycin C or clavulanic acid, but does produce a bioactive compound that was identified as holomycin by high-performance liquid chromatography (HPLC) and infrared and mass spectrometry. S. clavuligerus strains with disruptions in different genes of the clavulanic acid pathway fall into three groups with respect to holomycin biosynthesis. (i) Mutants with mutations in the early steps of the pathway blocked in the gene ceaS (pyc) (encoding carboxyethylarginine synthase), bls (encoding a beta-lactam synthetase), or open reading frame 6 (ORF6; coding for an acetyltransferase of unknown function) are holomycin nonproducers. (ii) Mutants blocked in the regulatory gene ccaR or claR or blocked in the last gene of the pathway encoding clavulanic acid reductase (car) produce holomycin at higher levels than the wild-type strain. (iii) Mutants with disruption in cyp (coding for cytochrome P450), ORF12, and ORF15, genes that appear to be involved in the conversion of clavaminic acid into clavaldehyde or in secretion steps, produce up to 250-fold as much holomycin as the wild-type strain. An assay for holomycin synthetase was developed. This enzyme forms holomycin from holothin by using acetyl coenzyme A as an acetyl group donor. The holomycin synthase activities in the different clavulanic acid mutants correlate well with their production of holomycin.

摘要

棒状链霉菌ccaR::aph菌株的调控基因ccaR发生了破坏,该菌株不产生头孢霉素C或克拉维酸,但确实产生了一种生物活性化合物,通过高效液相色谱(HPLC)、红外光谱和质谱鉴定为全霉素。就全霉素生物合成而言,克拉维酸途径中不同基因发生破坏的棒状链霉菌菌株可分为三组。(i)在途径早期步骤中发生突变且基因ceaS(pyc)(编码羧乙基精氨酸合酶)、bls(编码β-内酰胺合成酶)或开放阅读框6(ORF6;编码功能未知的乙酰转移酶)被阻断的突变体不产生全霉素。(ii)在调控基因ccaR或claR中被阻断或在编码克拉维酸还原酶(car)的途径最后一个基因中被阻断的突变体产生的全霉素水平高于野生型菌株。(iii)cyp(编码细胞色素P450)、ORF12和ORF15基因发生破坏的突变体,这些基因似乎参与了克拉维酸向克拉醛的转化或分泌步骤,其产生的全霉素是野生型菌株的250倍之多。开发了一种全霉素合成酶检测方法。该酶以乙酰辅酶A作为乙酰基供体,由全硫辛形成全霉素。不同克拉维酸突变体中的全霉素合成酶活性与其全霉素产量密切相关。

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