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p-Cymene catabolic pathway in Pseudomonas putida F1: cloning and characterization of DNA encoding conversion of p-cymene to p-cumate.

机译:恶臭假单胞菌F1中的对伞花烃分解代谢途径:编码对伞花木精向对-枯草酸盐转化的DNA的克隆和表征。

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摘要

Pseudomonas putida F1 utilizes p-cymene (p-isopropyltoluene) by an 11-step pathway through p-cumate (p-isopropylbenzoate) to isobutyrate, pyruvate, and acetyl coenzyme A. The cym operon, encoding the conversion of p-cymene to p-cumate, is located just upstream of the cmt operon, which encodes the further catabolism of p-cumate and is located, in turn, upstream of the tod (toluene catabolism) operon in P. putida F1. The sequences of an 11,236-bp DNA segment carrying the cym operon and a 915-bp DNA segment completing the sequence of the 2,673-bp DNA segment separating the cmt and tod operons have been determined and are discussed here. The cym operon contains six genes in the order cymBCAaAbDE. The gene products have been identified both by functional assays and by comparing deduced amino acid sequences to published sequences. Thus, cymAa and cymAb encode the two components of p-cymene monooxygenase, a hydroxylase and a reductase, respectively; cymB encodes p-cumic alcohol dehydrogenase; cymC encodes p-cumic aldehyde dehydrogenase; cymD encodes a putative outer membrane protein related to gene products of other aromatic hydrocarbon catabolic operons, but having an unknown function in p-cymene catabolism; and cymE encodes an acetyl coenzyme A synthetase whose role in this pathway is also unknown. Upstream of the cym operon is a regulatory gene, cymR. By using recombinant bacteria carrying either the operator-promoter region of the cym operon or the cmt operon upstream of genes encoding readily assayed enzymes, in the presence or absence of cymR, it was demonstrated that cymR encodes a repressor which controls expression of both the cym and cmt operons and is inducible by p-cumate but not p-cymene. Short (less than 350 bp) homologous DNA segments that are located upstream of cymR and between the cmt and tod operons may have been involved in recombination events that led to the current arrangement of cym, cmt, and tod genes in P. putida F1.
机译:恶臭假单胞菌(Pseudomonas putida)F1通过对异丙基苯甲酸(p-异丙基苯甲酸酯)的11步途径利用对苯丙氨酸(对异丙基甲苯)生成异丁酸,丙酮酸和乙酰辅酶A。 -cumate位于cmt操纵子的上游,后者编码p-cumate的进一步分解代谢,而又位于恶臭假单胞菌F1中tod(甲苯分解代谢)操纵子的上游。已经确定了携带cym操纵子的11236 bp DNA片段的序列和完成了将cmt和tod操纵子分开的2673 bp DNA片段的序列的915 bp DNA片段的序列,并在此进行了讨论。 cym操纵子包含cymBCAaAbDE顺序的六个基因。基因产物已通过功能测定和通过比较推导的氨基酸序列与公开的序列进行鉴定。因此,cymAa和cymAb分别编码对-异丙基单加氧酶的两个成分,即羟化酶和还原酶。 cymB编码对枯基醇脱氢酶; cymC编码对枯基醛脱氢酶; cymD编码一种假定的外膜蛋白,该蛋白与其他芳香烃分解代谢操纵子的基因产物有关,但在对伞花烃分解代谢中功能未知; cymE编码乙酰辅酶A合成酶,其在该途径中的作用也未知。 cym操纵子的上游是调控基因cymR。通过在存在或不存在cymR的情况下,使用携带cym操纵子操纵子启动子区域或cmt操纵子在编码易分析酶的基因上游的重组细菌,证明cymR编码的阻遏物控制着两个cymR的表达和cmt操纵子,可通过对-异丙基而不是对-异丙基苯来诱导。位于cymR上游且在cmt和tod操纵子之间的短(少于350 bp)同源DNA片段可能参与了重组事件,导致了恶臭假单胞菌F1中cym,cmt和tod基因的当前排列。

著录项

  • 作者

    Eaton, R W;

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  • 年度 1997
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  • 原文格式 PDF
  • 正文语种 en
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