首页> 外文期刊>Applied Microbiology >Patchwork Assembly of nag-Like Nitroarene Dioxygenase Genes and the 3-Chlorocatechol Degradation Cluster for Evolution of the 2-Chloronitrobenzene Catabolism Pathway in Pseudomonas stutzeri ZWLR2-1
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Patchwork Assembly of nag-Like Nitroarene Dioxygenase Genes and the 3-Chlorocatechol Degradation Cluster for Evolution of the 2-Chloronitrobenzene Catabolism Pathway in Pseudomonas stutzeri ZWLR2-1

机译:st类似的亚硝基芳烃双加氧酶基因和3-氯邻苯二酚降解簇的拼布组装,用于斯氏假单胞菌ZWLR2-1中2-氯硝基苯分解代谢途径的演变。

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Pseudomonas stutzeri ZWLR2-1 utilizes 2-chloronitrobenzene (2CNB) as a sole source of carbon, nitrogen, and energy. To identify genes involved in this pathway, a 16.2-kb DNA fragment containing putative 2CNB dioxygenase genes was cloned and sequenced. Of the products from the 19 open reading frames that resulted from this fragment, CnbAc and CnbAd exhibited striking identities to the respective α and β subunits of the Nag-like ring-hydroxylating dioxygenases involved in the metabolism of nitrotoluene, nitrobenzene, and naphthalene. The encoding genes were also flanked by two copies of insertion sequence IS 6100 . CnbAa and CnbAb are similar to the ferredoxin reductase and ferredoxin for anthranilate 1,2-dioxygenase from Burkholderia cepacia DBO1. Escherichia coli cells expressing cnbAaAbAcAd converted 2CNB to 3-chlorocatechol with concomitant nitrite release. Cell extracts of E. coli /pCNBC exhibited chlorocatechol 1,2-dioxygenase activity. The cnbCDEF gene cluster, homologous to a 3-chlorocatechol degradation cluster in Sphingomonas sp. strain TFD44, probably contains all of the genes necessary for the conversion of 3-chlorocatechol to 3-oxoadipate. The patchwork-like structure of this catabolic cluster suggests that the cnb cluster for 2CNB degradation evolved by recruiting two catabolic clusters encoding a nitroarene dioxygenase and a chlorocatechol degradation pathway. This provides another example to help elucidate the bacterial evolution of catabolic pathways in response to xenobiotic chemicals.
机译:Stutzeri假单胞菌ZWLR2-1使用2-氯硝基苯(2CNB)作为碳,氮和能量的唯一来源。为了鉴定参与该途径的基因,克隆了包含推定的2CNB双加氧酶基因的16.2kb DNA片段并进行了测序。在此片段产生的19个开放阅读框的产物中,CnbAc和CnbAd与参与硝基甲苯,硝基苯和萘代谢的Nag样环羟化双加氧酶的α和β亚基表现出惊人的同一性。编码基因的侧面还插入了两个拷贝的插入序列IS 6100。 CnbAa和CnbAb与来自伯克霍尔德菌洋葱DBO1的邻氨基苯甲酸酯1,2-二加氧酶的铁氧还蛋白还原酶和铁氧还蛋白相似。表达cnbAaAbAcAd的大肠杆菌细胞将2CNB转化为3-氯邻苯二酚,同时释放亚硝酸盐。大肠杆菌/ pCNBC的细胞提取物表现出氯邻苯二酚1,2-二加氧酶活性。 cnbCDEF基因簇,与鞘氨醇单胞菌属的3-氯邻苯二酚降解簇同源。菌株TFD44可能包含将3-氯邻苯二酚转化为3-氧代己二酸酯所必需的所有基因。该分解代谢簇的拼凑状结构表明,用于2CNB降解的cnb簇是通过募集两个编码硝基芳烃双加氧酶和氯邻苯二酚降解途径的分解代谢簇而进化而来的。这提供了另一个例子来帮助阐明分解代谢途径对异源生物化学物质的细菌进化。

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