首页> 外文期刊>Glycobiology. >Analysis of subgroup C of fungal chitinases containing chitin-binding and LysM modules in the mycoparasite Trichoderma atroviride.
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Analysis of subgroup C of fungal chitinases containing chitin-binding and LysM modules in the mycoparasite Trichoderma atroviride.

机译:分析霉菌木霉阿魏病毒中含有几丁质结合和LysM模块的真菌几丁质酶C亚组。

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摘要

Fungi have a plethora of chitinases, which can be phylogenetically divided into three subgroups (A, B and C). Subgroup C (sgC) chitinases are especially interesting due to their multiple carbohydrate-binding modules, but they have not been investigated in detail yet. In this study, we analyzed sgC chitinases in the mycoparasites Trichoderma atroviride and Trichoderma virens. The expression of sgC chitinase genes in T. atroviride was induced during mycoparasitism of the fungal prey Botrytis cinerea, but not Rhizoctonia solani and correspondingly only by fungal cell walls of the former. Interestingly, only few sgC chitinase genes were inducible by chitin, suggesting that non-chitinous cell wall components can act as inducers. In contrast, the transcriptional profile of the most abundantly expressed sgC chitinase gene tac6 indicated a role of the protein in hyphal network formation. This shows that sgC chitinases have diverse functions and are not only involved in the mycoparasitic attack. However, sequence analysis and 3D modelling revealed that TAC6 and also its ortholog in T. virens have potentially detrimental deletions in the substrate-binding site and are thus probably not catalytically active enzymes. Genomic analysis showed that the genes neighboring sgC chitinases often encode proteins that are solely composed of multiple LysM modules, which were induced by similar stimuli as their neighboring sgC chitinase genes. This study provides first insights into fungal sgC chitinases and their associated LysM proteins.
机译:真菌具有过多的几丁质酶,可以在系统发育上分为三个亚组(A,B和C)。 C组(sgC)几丁质酶因其具有多个碳水化合物结合模块而特别受关注,但尚未对其进行详细研究。在这项研究中,我们分析了真菌寄生虫木霉木霉和维氏木霉中的sgC几丁质酶。 sgC几丁质酶基因在阿特罗韦德菌中被诱导为真菌捕食性灰葡萄孢的霉菌寄生,但不是由Rhizoctonia solani诱导,相应地仅由前者的真菌细胞壁诱导。有趣的是,几丁质几丁质只能诱导sgC几丁质酶基因,这表明非几丁质细胞壁成分可以起诱导作用。相反,表达最丰富的sgC几丁质酶基因tac6的转录谱表明该蛋白在菌丝网络形成中的作用。这表明sgC几丁质酶具有多种功能,不仅参与了真菌寄生虫攻击。但是,序列分析和3D建模显示,TAC6及其在定向杆状病毒中的直系同源物在底物结合位点具有潜在的有害缺失,因此可能不是催化活性酶。基因组分析表明,邻近sgC几丁质酶的基因通常编码仅由多个LysM模块组成的蛋白质,这些蛋白是由与其邻近sgC几丁质酶基因相似的刺激物诱导的。这项研究提供了真菌sgC几丁质酶及其相关LysM蛋白的初步见解。

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