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从大豆丁香假单胞菌中克隆的两个无毒基因的特性及表达

Characterization and expression of two avirulence genes cloned from Pseudomonas syringae pv. glycinea.

作者信息

Tamaki S, Dahlbeck D, Staskawicz B, Keen N T

机构信息

Department of Plant Pathology, University of California, Riverside 92521.

出版信息

J Bacteriol. 1988 Oct;170(10):4846-54. doi: 10.1128/jb.170.10.4846-4854.1988.

Abstract

Two avirulence genes, avrB and avrC, from race 0 of Pseudomonas syringae pv. glycinea, were sequenced and found to encode single protein products of 36 and 39 kilodaltons, respectively. The proteins had neither recognizable signal peptide sequences nor significant stretches of hydrophobic amino acids that might indicate membrane association. Both avrB and avrC had relatively low position 3 and overall G+C contents, which suggests that they may have been recently introduced into P. syringae pv. glycinea. The deduced amino acid sequences of the proteins encoded by avrB and avrC shared 42% identical amino acids. However, when introduced into race 4 of P. syringae pv. glycinea, each gene directed a unique pattern of hypersensitive reactions on several differential soybean cultivars. The avrC protein was overproduced in Escherichia coli cells and deposited as insoluble inclusion bodies in the cell cytoplasm. The avrC protein could be solubilized with urea-octyl glucoside treatment, but neither the solubilized protein nor the intact inclusion bodies elicited a hypersensitive reaction in soybean leaves.

摘要

对来自丁香假单胞菌大豆致病变种0号小种的两个无毒基因avrB和avrC进行了测序,发现它们分别编码36千道尔顿和39千道尔顿的单一蛋白质产物。这些蛋白质既没有可识别的信号肽序列,也没有可能表明与膜相关的显著疏水氨基酸区段。avrB和avrC的第3位碱基和总体G+C含量相对较低,这表明它们可能是最近才被引入到丁香假单胞菌大豆致病变种中的。avrB和avrC编码的蛋白质的推导氨基酸序列有42%的相同氨基酸。然而,当将它们导入丁香假单胞菌大豆致病变种4号小种时,每个基因在几个鉴别大豆品种上引发了独特的过敏反应模式。avrC蛋白在大肠杆菌细胞中过量表达,并以不溶性包涵体的形式沉积在细胞质中。avrC蛋白可用尿素-辛基葡糖苷处理溶解,但溶解后的蛋白和完整的包涵体在大豆叶片中均未引发过敏反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9364/211529/5d911588d065/jbacter00188-0435-a.jpg

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