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对编码联苯/多氯联苯降解途径的假单胞菌基因座的遗传分析。

Genetic analysis of a Pseudomonas locus encoding a pathway for biphenyl/polychlorinated biphenyl degradation.

作者信息

Hofer B, Eltis L D, Dowling D N, Timmis K N

机构信息

Department of Microbiology, Gesellschaft für Biotechnologische Forschung, Braunschweig, Germany.

出版信息

Gene. 1993 Aug 16;130(1):47-55. doi: 10.1016/0378-1119(93)90345-4.

Abstract

The cistronic organization of the bph locus, encoding a biphenyl/polychlorinated biphenyl (PCB) degradation pathway in Pseudomonas sp. LB400, has been elucidated. Seven structural genes, encoding biphenyl dioxygenase (bphA1A2A3A4), biphenyl-2,3-dihydrodiol-2,3-dehydrogenase (bphB), biphenyl-2,3-diol-1,2-dioxygenase (bphC) and 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoate hydrolase (bphD), have been located. The complete sequences of bphB, bphC and bphD are reported. Taken together with the data of Erickson and Mondello [J. Bacteriol. 174 (1992) 2903-2912], Pseudomonas sp. LB400 is now the first strain for which the sequences of all genes encoding the catabolism from biphenyls to benzoates have been determined. Comparisons of the deduced amino acid (aa) sequences of BphB, BphC and BphD with those of related proteins led to predictions about catalytically important aa residues. Six Bph have been detected and identified. Five of them could be obtained as the most abundant proteins when their genes were expressed in Escherichia coli.

摘要

已阐明了假单胞菌属LB400中编码联苯/多氯联苯(PCB)降解途径的bph基因座的顺反子组织。已定位了七个结构基因,它们分别编码联苯双加氧酶(bphA1A2A3A4)、联苯-2,3-二氢二醇-2,3-脱氢酶(bphB)、联苯-2,3-二醇-1,2-双加氧酶(bphC)和2-羟基-6-氧代-6-苯基己-2,4-二烯酸水解酶(bphD)。报道了bphB、bphC和bphD的完整序列。结合埃里克森和蒙代洛的数据[《细菌学杂志》174(1992)2903 - 2912],假单胞菌属LB400现在是第一个已确定从联苯到苯甲酸的所有分解代谢编码基因序列的菌株。将推导的BphB、BphC和BphD氨基酸(aa)序列与相关蛋白质的序列进行比较,得出了关于催化重要氨基酸残基的预测。已检测并鉴定出六种Bph。当它们的基因在大肠杆菌中表达时,其中五种可以作为最丰富的蛋白质获得。

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