首页> 美国卫生研究院文献>Journal of Bacteriology >Nucleotide sequence and functional analysis of the meta-cleavage pathway involved in biphenyl and polychlorinated biphenyl degradation in Pseudomonas sp. strain KKS102.
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Nucleotide sequence and functional analysis of the meta-cleavage pathway involved in biphenyl and polychlorinated biphenyl degradation in Pseudomonas sp. strain KKS102.

机译:假单胞菌属物种中联苯和多氯联苯降解涉及的核苷酸裂解序列的核苷酸序列和功能分析。菌株KKS102。

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摘要

Pseudomonas sp. strain KKS102 is able to degrade biphenyl and polychlorinated biphenyls via the meta-cleavage pathway. We sequenced the upstream region of the bphA1A2A3BCD (open reading frame 1 [ORF1]) A4 and found four ORFs in this region. As the deduced amino acid sequences of the first, second, and third ORFs are homologous to the meta-cleavage enzymes from Pseudomonas sp. strain CF600 (V. Shingler, J. Powlowski, and U. Marklund, J. Bacteriol. 174:711-724, 1992), these ORFs have been named bphE, bphG, and bphF, respectively. The fourth ORF (ORF4) showed homology with ORF3 from Pseudomonas pseudoalcaligenes KF707 (K. Taira, J. Hirose, S. Hayashida, and K. Furukawa, J. Biol. Chem. 267:4844-4853, 1992), whose function is unknown. The functions of meta-cleavage enzymes (BphE, BphG, and BphF) were analyzed by using crude extracts of Escherichia coli which expressed the encoding genes. The results showed that bphE, bphG, and bphF encode 2-hydroxypenta-2,4-dienoate hydratase, acetaldehyde dehydrogenase (acylating), and 4-hydroxy-2-oxovalerate aldolase, respectively. The biphenyl and polychlorinated biphenyl degradation pathway of KKS102 is encoded by 12 genes in the order bphEGF (ORF4)A1A2A3BCD (ORF1)A4. The functions of ORF1 and ORF4 are unknown. The features of this bph gene cluster are discussed.
机译:假单胞菌菌株KKS102能够通过间位裂解途径降解联苯和多氯联苯。我们对bphA1A2A3BCD(开放阅读框1 [ORF1])A4的上游区域进行了测序,并在该区域中发现了四个ORF。由于推导的第一,第二和第三ORF的氨基酸序列与来自假单胞菌属物种的元切割酶同源。菌株CF600(V.Shingler,J.Powlowski,和U.Marklund,J.Bacteriol.174:711-724,1992),这些ORF分别被命名为bphE,bphG和bphF。第四ORF(ORF4)与假单胞假单胞菌KF707的ORF3具有同源性(K.Taira,J.Hirose,S.Hayashida和K.Furukawa,J.Biol.Chem.267:4844-4853,1992)。未知。使用表达编码基因的大肠杆菌粗提物分析了元切割酶(BphE,BphG和BphF)的功能。结果表明,bphE,bphG和bphF分别编码2-羟基戊-2,4-二烯酸水合酶,乙醛脱氢酶(酰化)和4-羟基-2-氧戊醛酸醛缩酶。 KKS102的联苯和多氯联苯降解途径由bphEGF(ORF4)A1A2A3BCD(ORF1)A4顺序的12个基因编码。 ORF1和ORF4的功能未知。讨论了此bph基因簇的特征。

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