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灰葡萄孢I类几丁质合成酶基因Bcchs1的破坏导致细胞壁弱化和毒力降低。

Disruption of Botrytis cinerea class I chitin synthase gene Bcchs1 results in cell wall weakening and reduced virulence.

作者信息

Soulié M-C, Piffeteau A, Choquer M, Boccara M, Vidal-Cros A

机构信息

Laboratoire de Pathologie Végétale, UMR 217 INRA-Paris VI-INAP-G, 16 rue Claude Bernard, 75005 Paris, France.

出版信息

Fungal Genet Biol. 2003 Oct;40(1):38-46. doi: 10.1016/s1087-1845(03)00065-3.

Abstract

To get a better insight into the relationship between cell wall integrity and pathogenicity of the fungus Botrytis cinerea, we have constructed chitin synthase mutants. A 620 bp class I chitin synthase gene fragment (Bcchs1) obtained by PCR amplification was used to disrupt the corresponding gene in the genome. Disruption of Bcchs1 occurred at a frequency of 8%. Nine independent mutants were obtained and the Bcchs1 mutant phenotype compared to that of transformants in which the gene was not disrupted. These disruption mutants were dramatically reduced in their in vitro Mg2+, Mn2+, and Co2+-dependent chitin synthase activity. Chitin content was reduced by 30%, indicating that Bcchs1p contributes substantially to cell wall composition. Enzymatic degradation by a cocktail of glucanases revealed cell wall weakening in the mutant. Bcchs1 was transcribed at a constant level during vegetative exponential growth, suggesting that it was necessary throughout hyphal development. Bcchs1 mutant growth was identical to undisrupted control transformant growth, however, the mutant exhibited reduced pathogenicity on vine leaves. It can be assumed that disruption of Bcchs1 leads to cell wall weakening which might slow down in planta fungal progression.

摘要

为了更深入地了解灰葡萄孢菌细胞壁完整性与致病性之间的关系,我们构建了几丁质合酶突变体。通过PCR扩增获得的一个620 bp的I类几丁质合酶基因片段(Bcchs1)用于破坏基因组中的相应基因。Bcchs1的破坏频率为8%。获得了9个独立的突变体,并将Bcchs1突变体表型与未破坏该基因的转化体的表型进行了比较。这些破坏突变体的体外Mg2+、Mn2+和Co2+依赖性几丁质合酶活性显著降低。几丁质含量降低了30%,表明Bcchs1p对细胞壁组成有很大贡献。葡聚糖酶混合物的酶促降解显示突变体中细胞壁减弱。Bcchs1在营养指数生长期间以恒定水平转录,表明它在整个菌丝发育过程中都是必需的。Bcchs1突变体的生长与未破坏的对照转化体的生长相同,然而,该突变体在葡萄叶片上的致病性降低。可以推测,Bcchs1的破坏导致细胞壁减弱,这可能会减缓真菌在植物体内的进展。

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