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恶臭假单胞菌TW3中编码4-硝基苯甲酸分解代谢酶的pnb基因的克隆与特性分析

Cloning and characterization of the pnb genes, encoding enzymes for 4-nitrobenzoate catabolism in Pseudomonas putida TW3.

作者信息

Hughes M A, Williams P A

机构信息

School of Biological Sciences, University of Wales Bangor, Bangor, Gwynedd LL57 2UW, Wales, United Kingdom.

出版信息

J Bacteriol. 2001 Feb;183(4):1225-32. doi: 10.1128/JB.183.4.1225-1232.2001.

Abstract

Pseudomonas putida strain TW3 is able to metabolize 4-nitrotoluene via 4-nitrobenzoate (4NBen) and 3, 4-dihydroxybenzoic acid (protocatechuate [PCA]) to central metabolites. We have cloned, sequenced, and characterized a 6-kbp fragment of TW3 DNA which contains five genes, two of which encode the enzymes involved in the catabolism of 4NBen to PCA. In order, they encode a 4NBen reductase (PnbA) which is responsible for catalyzing the direct reduction of 4NBen to 4-hydroxylaminobenzoate with the oxidation of 2 mol of NADH per mol of 4NBen, a reductase-like enzyme (Orf1) which appears to have no function in the pathway, a regulator protein (PnbR) of the LysR family, a 4-hydroxylaminobenzoate lyase (PnbB) which catalyzes the conversion of 4-hydroxylaminobenzoate to PCA and ammonium, and a second lyase-like enzyme (Orf2) which is closely associated with pnbB but appears to have no function in the pathway. The central pnbR gene is transcribed in the opposite direction to the other four genes. These genes complete the characterization of the whole pathway of 4-nitrotoluene catabolism to the ring cleavage substrate PCA in P. putida strain TW3.

摘要

恶臭假单胞菌TW3菌株能够通过4-硝基苯甲酸(4NBen)和3,4-二羟基苯甲酸(原儿茶酸[PCA])将4-硝基甲苯代谢为中心代谢物。我们克隆、测序并鉴定了TW3菌株DNA的一个6kbp片段,该片段包含五个基因,其中两个基因编码参与将4NBen分解代谢为PCA的酶。按顺序,它们编码一种4NBen还原酶(PnbA),负责催化4NBen直接还原为4-羟基氨基苯甲酸,每摩尔4NBen氧化2摩尔NADH;一种类似还原酶的酶(Orf1),在该途径中似乎没有功能;一种LysR家族的调节蛋白(PnbR);一种4-羟基氨基苯甲酸裂解酶(PnbB),催化4-羟基氨基苯甲酸转化为PCA和铵;以及另一种与pnbB紧密相关但在该途径中似乎没有功能的类似裂解酶的酶(Orf2)。中心基因pnbR的转录方向与其他四个基因相反。这些基因完成了恶臭假单胞菌TW3菌株中4-硝基甲苯分解代谢为环裂解底物PCA的整个途径的表征。

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