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荧光假单胞菌中吡咯菌素生物合成基因编码的功能。

Functions encoded by pyrrolnitrin biosynthetic genes from Pseudomonas fluorescens.

作者信息

Kirner S, Hammer P E, Hill D S, Altmann A, Fischer I, Weislo L J, Lanahan M, van Pée K H, Ligon J M

机构信息

Institut für Mikrobiologie, Universität Hohenheim, Stuttgart, Germany.

出版信息

J Bacteriol. 1998 Apr;180(7):1939-43. doi: 10.1128/JB.180.7.1939-1943.1998.

Abstract

Pyrrolnitrin is a secondary metabolite derived from tryptophan and has strong antifungal activity. Recently we described four genes, prnABCD, from Pseudomonas fluorescens that encode the biosynthesis of pyrrolnitrin. In the work presented here, we describe the function of each prn gene product. The four genes encode proteins identical in size and serology to proteins present in wild-type Pseudomonas fluorescens, but absent from a mutant from which the entire prn gene region had been deleted. The prnA gene product catalyzes the chlorination of L-tryptophan to form 7-chloro-L-tryptophan. The prnB gene product catalyzes a ring rearrangement and decarboxylation to convert 7-chloro-L-tryptophan to monodechloroaminopyrrolnitrin. The prnC gene product chlorinates monodechloroaminopyrrolnitrin at the 3 position to form aminopyrrolnitrin. The prnD gene product catalyzes the oxidation of the amino group of aminopyrrolnitrin to a nitro group to form pyrrolnitrin. The organization of the prn genes in the operon is identical to the order of the reactions in the biosynthetic pathway.

摘要

硝吡咯菌素是一种源自色氨酸的次生代谢产物,具有很强的抗真菌活性。最近我们描述了来自荧光假单胞菌的四个基因prnABCD,它们编码硝吡咯菌素的生物合成。在本文所述的工作中,我们描述了每个prn基因产物的功能。这四个基因编码的蛋白质在大小和血清学上与野生型荧光假单胞菌中存在的蛋白质相同,但在一个缺失了整个prn基因区域的突变体中不存在。prnA基因产物催化L-色氨酸的氯化反应,形成7-氯-L-色氨酸。prnB基因产物催化环重排和脱羧反应,将7-氯-L-色氨酸转化为单脱氯氨基硝吡咯菌素。prnC基因产物在3位对单脱氯氨基硝吡咯菌素进行氯化反应,形成氨基硝吡咯菌素。prnD基因产物催化氨基硝吡咯菌素的氨基氧化为硝基,形成硝吡咯菌素。操纵子中prn基因的组织方式与生物合成途径中反应的顺序相同。

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