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首页> 外文期刊>Applied Microbiology and Biotechnology >Cloning and characterization of a novel chitinase gene (chi46) from Chaetomium globosum and identification of its biological activity
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Cloning and characterization of a novel chitinase gene (chi46) from Chaetomium globosum and identification of its biological activity

机译:球壳拟南芥新几丁质酶基因(chi46)的克隆,鉴定及其生物学活性

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摘要

Chitinases play a major role in the defensive strategies of plants against fungal pathogens. In the current study, the gene for a 46-kDa endochitinase (chi46) was cloned from Chaetomium globosum, an important biocontrol fungus. The corresponding complementary deoxyribonucleic acid sequence was 1,350 bp in length, encoding 449 amino acid residues. The temporal expression of chi46, in response to the treatments of cell walls of six pathogens and confrontation against two fungal pathogens, was measured in C. globosum using real-time reverse transcription polymerase chain reaction. The expression of chi46 can be highly induced by exposure to the cell walls of plant pathogens and living pathogens, suggesting a role in plant disease resistance. The chi46 gene was inserted into the pPIC9 vector and transferred into the cells of Pichia pastoris GS115 for heterologous expression. The optimal reaction conditions for chitinase CHI46 activity were: 45 degrees C, pH of 5.0, and 5 mmol l(-1) of Cu2+. The maximum enzyme activity was 1.42 U ml(-1) following exposure to the cell wall chitin of Septoria tritici. The CHI46 enzyme can efficiently degrade cell walls of the phytopathogenic Rhizoctonia solani, Fusarium oxysporum, Sclerotinia sclerotiorum, Valsa sordida, S. tritici, and Phytophthora sojae, demonstrating that it may be involved in the biocontrol mechanism of C. globosum.
机译:几丁质酶在植物抵抗真菌病原体的防御策略中起着重要作用。在当前的研究中,从重要的生物防治真菌球毛龟(Chaetomium globosum)克隆了一个46 kDa内切几丁质内切酶(chi46)的基因。相应的互补脱氧核糖核酸序列长度为1,350 bp,编码449个氨基酸残基。使用实时逆转录聚合酶链反应,在C. globosum中测量了响应46种病原体的细胞壁处理和对抗两种真菌病原体的chi46的瞬时表达。暴露于植物病原体和活病原体的细胞壁可高度诱导chi46的表达,提示其在植物抗病性中的作用。将chi46基因插入pPIC9载体,并转移至巴斯德毕赤酵母GS115细胞中进行异源表达。几丁质酶CHI46活性的最佳反应条件为:45摄氏度,pH值为5.0,和5 mmol l(-1)的Cu2 +。最大的酶活性为1.42 U ml(-1)暴露于小麦的细胞壁几丁质后。 CHI46酶可有效降解植物致病性茄根枯病菌,尖孢镰刀菌,菌核盘菌,缬草,小麦链霉菌和大豆疫霉菌的细胞壁,表明它可能参与了球孢梭菌的生物防治机制。

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