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A plant-inducible gene of Xanthomonas campestris pv. campestris encodes an exocellular component required for growth in the host and hypersensitivity on nonhosts.

机译:Xanthomonas campestris pv的植物诱导基因。樟脑编码在宿主中生长和对非宿主超敏反应所需的胞外成分。

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摘要

Using Tn4431, a transposon that allows transcriptional fusions to a promoterless luciferase (lux) operon, we have isolated a nonpathogenic mutant of Xanthomonas campestris pv. campestris, i.e., JS111, that does not incite any of the black rot symptoms on all tested cruciferous host plants (J. J. Shaw, L. G. Settles, and C. I. Kado, Mol. Plant Microbe Interact. 1:39-45, 1988). In the study reported here, we determined that in contrast to the wild-type strain, JS111 is unable to induce a hypersensitive necrotic response on nonhost plants such as datura, tomato, and cucumber, suggesting that JS111 is a nonpathogenic, nonhypersensitive Hrp mutant. JS111 displayed culture growth rates, exopolysaccharide production, and protease, pectate lysase, cellulase, amylase, and phosphatase activities comparable to those of the wild-type strain. However, the growth of JS111 in host leaves was markedly attenuated. Coinoculation of JS111 with the wild-type strain in cauliflower or radish leaves rescued the growth deficiency of the mutant to normal levels. The locus mutated in JS111 was cloned and named hrpXc, and transcriptional and genetic complementation analyses of the hrpXc locus were conducted. The regulation of hrpXc expression was also investigated in vitro and in planta, using fusions to a lux or chloramphenicol acetyltransferase reporter gene. The hrpXc gene was found to be strongly induced in radish leaves. This is the first report and analysis of a hrp locus from a Xanthomonas species.
机译:使用Tn4431,一种转座子,可将其转录融合到无启动子的荧光素酶(lux)操纵子上,我们分离出了一种非致病性的油菜黄单胞菌突变体。 campestris,即JS111,不会在所有测试的十字花科寄主植物上引起任何黑腐病症状(J. J. Shaw,L.G. Settles,and C.I. Kado,Mol。Plant Microbe Interact。1:39-45,1988)。在此报告的研究中,我们确定与野生型菌株相反,JS111无法在曼陀罗,番茄和黄瓜等非寄主植物上诱导超敏性坏死反应,这表明JS111是非致病性,非超敏敏Hrp突变体。 JS111显示的培养物生长速率,胞外多糖的产生以及与野生型菌株相当的蛋白酶,果胶酸裂解酶,纤维素酶,淀粉酶和磷酸酶活性。然而,JS111在寄主叶片中的生长明显减弱。用野生型菌株在花椰菜或萝卜叶中共同接种JS111可以使突变体的生长缺陷恢复到正常水平。克隆了在JS111中突变的基因座并命名为hrpXc,并对hrpXc基因座进行了转录和遗传互补分析。还使用与lux或氯霉素乙酰基转移酶报告基因的融合体在体外和植物中研究了hrpXc表达的调节。发现hrpXc基因在萝卜叶中强烈诱导。这是对来自Xanthomonas物种的hrp基因座的首次报道和分析。

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    Kamoun, S; Kado, C I;

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  • 年度 1990
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