Eaton R W
National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Gulf Breeze, Florida 32561, USA.
J Bacteriol. 1997 May;179(10):3171-80. doi: 10.1128/jb.179.10.3171-3180.1997.
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.
恶臭假单胞菌F1通过一条11步的途径利用对异丙基甲苯(对伞花烃),该途径经对异丙基苯甲酸生成异丁酸、丙酮酸和乙酰辅酶A。编码将对伞花烃转化为对异丙基苯甲酸的cym操纵子位于cmt操纵子的上游,cmt操纵子编码对异丙基苯甲酸的进一步分解代谢,而cmt操纵子又位于恶臭假单胞菌F1中tod(甲苯分解代谢)操纵子的上游。已确定并在此讨论了携带cym操纵子的11236 bp DNA片段的序列以及完成分隔cmt和tod操纵子的2673 bp DNA片段序列所需的915 bp DNA片段的序列。cym操纵子按cymBCAaAbDE的顺序包含六个基因。基因产物已通过功能测定以及将推导的氨基酸序列与已发表序列进行比较来鉴定。因此,cymAa和cymAb分别编码对伞花烃单加氧酶的两个组分,即一种羟化酶和一种还原酶;cymB编码对异丙基苯甲醇脱氢酶;cymC编码对异丙基苯甲醛脱氢酶;cymD编码一种推定外膜蛋白,与其他芳烃分解代谢操纵子基因产物相关,但在对伞花烃分解代谢中功能未知;cymE编码一种乙酰辅酶A合成酶,其在该途径中的作用也未知。cym操纵子的上游是一个调控基因cymR。通过使用携带cym操纵子的操纵子 - 启动子区域或编码易于检测酶的基因上游的cmt操纵子的重组细菌,在有或没有cymR的情况下,证明cymR编码一种阻遏物,它控制cym和cmt操纵子的表达,并且可被对异丙基苯甲酸诱导,但不能被对伞花烃诱导。位于cymR上游以及cmt和tod操纵子之间的短(小于350 bp)同源DNA片段可能参与了导致恶臭假单胞菌F1中cym、cmt和tod基因当前排列的重组事件。