首页> 外文期刊>FEMS Microbiology Letters >Real-time RT-PCR expression analysis of chitinase and endoglucanase genes in the three-way interaction between the biocontrol strain Clonostachys rosea IK726, Botrytis cinerea and strawberry
【24h】

Real-time RT-PCR expression analysis of chitinase and endoglucanase genes in the three-way interaction between the biocontrol strain Clonostachys rosea IK726, Botrytis cinerea and strawberry

机译:胰蛋白酶菌株Clonostachys Rosea IK726,Botrytis Cinerea和草莓中的三载酶和内葡聚糖酶基因的实时RT-PCR表达分析。

获取原文
获取原文并翻译 | 示例
           

摘要

Clonostachys rosea is a well-known biocontrol agent against Botrytis cinerea, the causal agent of gray mold in strawberry. The activity of cell wall-degrading enzymes might play a significant role for successful biocontrol by C. rosea. The expression pattern of four chitinases, and two endoglucanase genes from C. rosea strain IK726 was analyzed using real-time RT-PCR in vitro and in strawberry leaves during interaction with B. cinerea. Specific primers were designed for beta-tubulin genes from C. rosea and B. cinerea, respectively, and a gene encoding a DNA-binding protein (DBP) from strawberry, allowing in situ activity assessment of each fungus in vitro and during their interaction on strawberry leaves. Growth of B. cinerea was inhibited in all pathogen-antagonist interactions while the activity of IK726 was slightly increased. In all in vitro interactions, four of the six genes were upregulated while no change in expression of two endochitinases was measured. In strawberry leaves, the chitinase genes were upregulated 2-12-fold, except one of the endochitinases, whereas no change in expression of the two endoglucanases was measured. The results suggest that three out of four chitinase genes of IK726 are involved in biocontrol on leaves. This is the first example of monitoring of expression of chitinolytic genes in interactions between biocontrol agents and pathogens in plant material.
机译:Clonostachys Rosea是一种众所周知的嗜哪种嗜蒜素,草莓中灰霉病的因果剂。细胞壁降解酶的活性可能对C. Rosea成功的生物控制起重要作用。使用实时RT-PCR在与B.Carea的相互作用期间,使用实时RT-PCR分析四花序酶的表达模式和来自C.Rosea菌株IK726的两种内切葡聚糖酶基因。针对来自C.Rosea和B.Cinealea的β-微管蛋白基因设计了特异性引物,以及编码来自草莓的DNA结合蛋白(DBP)的基因,允许在体外和互动期间对每个真菌进行原位活动评估草莓叶。在所有病原体拮抗剂相互作用中抑制了B. cinerea的生长,而IK726的活性略微增加。在所有体外相互作用中,测量六个基因中的四个基因中的四个,同时测量两种中间成分酶的表达的变化。在草莓叶中,除了一个内奇素酶之外,几丁质酶基因被上调2-12倍,而测量两种内切葡聚糖酶的表达的变化。结果表明,IK726的四个几丁质酶基因中的三种含有叶片的生物防治。这是一种监测植物材料中生物防治剂和病原体之间的相互作用中依甲酰基溶解基因的表达的第一例。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号