丁香假单胞菌海藻酸解酶基因algL的分析与表达。两

Lori A. Preston, C. Bender, N. Schiller
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引用次数: 8

摘要

丁香假单胞菌产生海藻酸盐,这是一种外源性多糖,有助于这种植物致病细菌的毒力和附生适应性。紫丁香假单胞菌也产生azgl编码的海藻酸裂解酶,该酶通过β-消除反应裂解海藻酸生物聚合物。紫丁香假单胞菌的algL基因位于藻酸盐生物合成操纵子内1134 bp的区域,与滨海盐单胞菌、铜绿假单胞菌、绿球菌固氮菌和葡萄球菌的algL基因相似。丁香假单胞菌的algL在大肠杆菌中过表达;两种周质形态的AlgL过量产生(40和37kDa)。这两种形式都具有酶活性,并被铜绿假单胞菌的AlgL抗体所识别。对algL两侧区域的分析显示,该区域与先前在其他产藻酸盐细菌的生物合成操纵子中发现的algX和algL基因具有显著的同源性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis and Expression of algL, which Encodes Alginate Lyase in Pseudomonas Syringae Pv. Syringae
Pseudomonas syringae produces alginate, an exopo-lysaccharide that contributes to the virulence and epiphytic fitness of this phytopathogenic bacterium. P. syringae also produces the aZgL-encoded alginate lyase, which cleaves the alginate biopolymer via a β-elimination reaction. The algL gene from P. syringae maps to a 1134 bp region within the alginate biosynthetic operon, and is similar to algL from Halomonas marina, P. aeruginosa, Azotobacter chroococcum, and A. vinelandii. algL from P. syringae was over expressed in Escherichia coli; two periplas-mic forms of AlgL were overproduced (40 and 37kDa). Both forms were enzymatically active and recognized by antibodies raised against AlgL from P. aeruginosa. Analysis of the regions flanking algL revealed significant homology to algX and algl, genes previously identified in the biosynthetic operon of other alginate-producing bacteria.
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