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假单胞菌属CF600菌株完整苯酚/3,4-二甲基苯酚分解代谢途径的核苷酸序列及功能分析

Nucleotide sequence and functional analysis of the complete phenol/3,4-dimethylphenol catabolic pathway of Pseudomonas sp. strain CF600.

作者信息

Shingler V, Powlowski J, Marklund U

机构信息

Unit for Applied Cell and Molecular Biology, University of Umeå, Sweden.

出版信息

J Bacteriol. 1992 Feb;174(3):711-24. doi: 10.1128/jb.174.3.711-724.1992.

Abstract

The meta-cleavage pathway for catechol is one of the major routes for the microbial degradation of aromatic compounds. Pseudomonas sp. strain CF600 grows efficiently on phenol, cresols, and 3,4-dimethylphenol via a plasmid-encoded multicomponent phenol hydroxylase and a subsequent meta-cleavage pathway. The genes for the entire pathway were previously found to be clustered, and the nucleotide sequences of dmpKLMNOPBC and D, which encode the first four biochemical steps of the pathway, were determined. By using a combination of deletion mapping, nucleotide sequence determinations, and polypeptide analysis, we identified the remaining six genes of the pathway. The fifteen genes, encoded in the order dmpKLMNOPQBCDEFGHI, lie in a single operon structure with intergenic spacing that varies between 0 to 70 nucleotides. Homologies found between the newly determined gene sequences and known genes are reported. Enzyme activity assays of deletion derivatives of the operon expressed in Escherichia coli were used to correlate dmpE, G, H, and I with known meta-cleavage enzymes. Although the function of the dmpQ gene product remains unknown, dmpF was found to encode acetaldehyde dehydrogenase (acylating) activity (acetaldehyde:NAD+ oxidoreductase [coenzyme A acylating]; E.C.1.2.1.10). The role of this previously unknown meta-cleavage pathway enzyme is discussed.

摘要

儿茶酚的间位裂解途径是微生物降解芳香族化合物的主要途径之一。假单胞菌属CF600菌株通过质粒编码的多组分苯酚羟化酶和随后的间位裂解途径,能有效地利用苯酚、甲酚和3,4-二甲基苯酚生长。此前发现整个途径的基因是成簇的,并测定了编码该途径前四个生化步骤的dmpKLMNOPBC和D的核苷酸序列。通过缺失定位、核苷酸序列测定和多肽分析相结合的方法,我们鉴定出了该途径其余的六个基因。这15个基因按dmpKLMNOPQBCDEFGHI的顺序编码,位于一个单一的操纵子结构中,基因间间隔在0到70个核苷酸之间变化。报告了新测定的基因序列与已知基因之间的同源性。利用在大肠杆菌中表达的操纵子缺失衍生物进行酶活性测定,将dmpE、G、H和I与已知的间位裂解酶相关联。虽然dmpQ基因产物的功能仍然未知,但发现dmpF编码乙醛脱氢酶(酰化)活性(乙醛:NAD+氧化还原酶[辅酶A酰化];E.C.1.2.1.10)。讨论了这种以前未知的间位裂解途径酶的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5708/206147/390499eff32c/jbacter00069-0075-a.jpg

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