首页> 美国卫生研究院文献>Journal of Bacteriology >Functional Analysis of Genes for Biosynthesis of Pyocyanin and Phenazine-1-Carboxamide from Pseudomonas aeruginosa PAO1
【2h】

Functional Analysis of Genes for Biosynthesis of Pyocyanin and Phenazine-1-Carboxamide from Pseudomonas aeruginosa PAO1

机译:铜绿假单胞菌PAO1中合成花青素和吩嗪-1-羧酰胺基因的功能分析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Two seven-gene phenazine biosynthetic loci were cloned from Pseudomonas aeruginosa PAO1. The operons, designated phzA1B1C1D1E1F1G1 and phzA2B2C2D2E2F2G2, are homologous to previously studied phenazine biosynthetic operons from Pseudomonas fluorescens and Pseudomonas aureofaciens. Functional studies of phenazine-nonproducing strains of fluorescent pseudomonads indicated that each of the biosynthetic operons from P. aeruginosa is sufficient for production of a single compound, phenazine-1-carboxylic acid (PCA). Subsequent conversion of PCA to pyocyanin is mediated in P. aeruginosa by two novel phenazine-modifying genes, phzM and phzS, which encode putative phenazine-specific methyltransferase and flavin-containing monooxygenase, respectively. Expression of phzS alone in Escherichia coli or in enzymes, pyocyanin-nonproducing P. fluorescens resulted in conversion of PCA to 1-hydroxyphenazine. P. aeruginosa with insertionally inactivated phzM or phzS developed pyocyanin-deficient phenotypes. A third phenazine-modifying gene, phzH, which has a homologue in Pseudomonas chlororaphis, also was identified and was shown to control synthesis of phenazine-1-carboxamide from PCA in P. aeruginosa PAO1. Our results suggest that there is a complex pyocyanin biosynthetic pathway in P. aeruginosa consisting of two core loci responsible for synthesis of PCA and three additional genes encoding unique enzymes involved in the conversion of PCA to pyocyanin, 1-hydroxyphenazine, and phenazine-1-carboxamide.
机译:从铜绿假单胞菌PAO1克隆了两个七基因吩嗪生物合成基因座。这些操纵子称为phzA1B1C1D1E1F1G1和phzA2B2C2D2E2F2G2,与先前研究的荧光假单胞菌和金黄色假单胞菌的吩嗪生物合成操纵子同源。对不产生吩嗪的荧光假单胞菌菌株的功能研究表明,来自铜绿假单胞菌的每个生物合成操纵子足以产生单一化合物吩嗪-1-羧酸(PCA)。随后,PCA向绿脓杆菌的转化是由两个新的吩嗪修饰基因phzM和phzS在铜绿假单胞菌中介导的,它们分别编码假定的吩嗪特异性甲基转移酶和含黄素的单加氧酶。 phzS单独在大肠埃希氏菌中或在不产黄素的荧光假单胞菌的酶中表达导致PCA转化为1-羟基吩嗪。插入灭活的phzM或phzS的铜绿假单胞菌发展为缺乏花青素的表型。还鉴定了第三个吩嗪修饰基因phzH,该基因在 Pseudomonas chlororaphis 中具有一个同源物,并被证明可以控制PCA中 P合成吩嗪-1-羧酰胺。铜绿 PAO1。我们的结果表明在 P中存在复杂的绿脓素生物合成途径。铜绿假单胞菌由两个负责PCA合成的核心基因座和三个附加的编码独特的酶的基因组成,这些基因参与PCA转化为花青素,1-羟基吩嗪和吩嗪-1-羧酰胺。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号