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苯酚降解假单胞菌属菌株EST1001中质粒编码的儿茶酚1,2-双加氧酶表达基因pheB的序列。

Sequence of the plasmid-encoded catechol 1,2-dioxygenase-expressing gene, pheB, of phenol-degrading Pseudomonas sp. strain EST1001.

作者信息

Kivisaar M, Kasak L, Nurk A

机构信息

Laboratory of Plasmid Biology, Estonian Biocenter, Tartu, U.S.S.R.

出版信息

Gene. 1991 Feb 1;98(1):15-20. doi: 10.1016/0378-1119(91)90098-v.

Abstract

Phenol monooxygenase (PMO) and catechol 1,2-dioxygenase (C12O), the two first enzymes of the phenol-degradation pathways, are encoded by a 3.4-kb DNA fragment cloned from Pseudomonas sp. EST1001 plasmid DNA. We have previously shown that activation of the cloned genes in Pseudomonas putida PaW85 is controlled by insertion of the 17-kb transposon, Tn4652, from the host chromosome into the plasmid carrying these genes [Kivisaar et al. Plasmid 24 (1990) 25-36]. Transcription of the DNA encoding PMO (pheA) and C12O (pheB) is activated by a promoter located on a 0.2-kb SacI-ClaI fragment from Tn4652. We have determined the nucleotide sequence of pheB. The 906-bp gene encodes a protein product with a deduced Mr of 33,362. The relationship between the pheB gene and other C12O-encoding genes has been shown: comparison of the pheB sequence with sequences of catA of Alcaligenes calcoaceticus, tfdC of A. eutrophus and clcA of P. putida demonstrated that there are conserved residues in all the four protein products of these genes.

摘要

苯酚单加氧酶(PMO)和邻苯二酚1,2-双加氧酶(C12O)是苯酚降解途径中的前两种酶,由从假单胞菌属EST1001质粒DNA克隆的一个3.4 kb DNA片段编码。我们之前已经表明,恶臭假单胞菌PaW85中克隆基因的激活是由宿主染色体上的17 kb转座子Tn4652插入携带这些基因的质粒所控制的[基维萨尔等人。质粒24(1990)25 - 36]。编码PMO(pheA)和C12O(pheB)的DNA转录由位于Tn4652的一个0.2 kb SacI-ClaI片段上的启动子激活。我们已经确定了pheB的核苷酸序列。这个906 bp的基因编码一个推导分子量为33362的蛋白质产物。已经表明了pheB基因与其他编码C12O的基因之间的关系:将pheB序列与产碱杆菌的catA、真养产碱菌的tfdC和恶臭假单胞菌的clcA的序列进行比较,结果表明这些基因的所有四个蛋白质产物中都存在保守残基。

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