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白腐真菌的腐生木材腐朽能力及植物细胞壁降解酶系统:分泌组、代谢组和基因组研究

Saprotrophic Wood Decay Ability and Plant Cell Wall Degrading Enzyme System of the White Rot Fungus : Secretome, Metabolome and Genome Investigations.

作者信息

Shabaev Alexander V, Savinova Olga S, Moiseenko Konstantin V, Glazunova Olga A, Fedorova Tatyana V

机构信息

A.N. Bach Institute of Biochemistry, Research Center of Biotechnology, Russian Academy of Sciences, Moscow 119071, Russia.

出版信息

J Fungi (Basel). 2024 Dec 31;11(1):21. doi: 10.3390/jof11010021.

DOI:10.3390/jof11010021
PMID:39852439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11766592/
Abstract

The basidiomycete strain LE-BIN1700 (Agaricales, ) is able to grow on agar media supplemented with individual components of lignocellulose such as lignin, cellulose, xylan, xyloglucan, arabinoxylan, starch and pectin, and also to effectively destroy and digest birch, alder and pine sawdust. produces a unique repertoire of proteins for the saccharification of the plant biomass, including predominantly oxidative enzymes such as laccases (family AA1_1 CAZymes), GMC oxidoreductases (family AA3_2 CAZymes), FAD-oligosaccharide oxidase (family AA7 CAZymes) and lytic polysaccharide monooxygenases (family LPMO X325), as well as accompanying acetyl esterases and loosenine-like expansins. Metabolomic analysis revealed that, specifically, monosaccharides and carboxylic acids were the key low molecular metabolites in the culture liquids in the experimental conditions. The proportion of monosaccharides and polyols in the total pool of identified compounds increased on the sawdust-containing media. Multiple copies of the family AA1_1, AA3_2, AA7 and LPMOs CAZyme genes, as well as eight genes encoding proteins of the YvrE superfamily (COG3386), which includes sugar lactone lactonases, were predicted in the genome. According to metabolic pathway analysis, the litter saprotroph can catabolize D-gluconic and D-galacturonic acids, and possibly other aldonic acids, which seems to confer certain ecological advantages.

摘要

担子菌菌株LE - BIN1700(伞菌目,)能够在添加了木质纤维素单个成分(如木质素、纤维素、木聚糖、木葡聚糖、阿拉伯木聚糖、淀粉和果胶)的琼脂培养基上生长,并且还能有效分解和消化桦木、桤木和松木锯末。该菌株产生了一系列独特的用于植物生物质糖化的蛋白质,主要包括氧化酶,如漆酶(AA1_1家族碳水化合物活性酶)、GMC氧化还原酶(AA3_2家族碳水化合物活性酶)、FAD - 寡糖氧化酶(AA7家族碳水化合物活性酶)和裂解多糖单加氧酶(LPMO X325家族),以及伴随的乙酰酯酶和类疏松蛋白。代谢组学分析表明,在实验条件下,单糖和羧酸是培养液中关键的低分子代谢产物。在含锯末的培养基上,已鉴定化合物总库中,单糖和多元醇的比例增加。在该菌株基因组中预测到多个拷贝的AA1_1、AA3_2、AA7家族碳水化合物活性酶基因以及八个编码YvrE超家族(COG3386)蛋白质的基因,该超家族包括糖内酯内酯酶。根据代谢途径分析,该凋落物腐生菌能够分解代谢D - 葡萄糖酸和D - 半乳糖醛酸,以及可能的其他醛糖酸,这似乎赋予了其一定的生态优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/085815ca033d/jof-11-00021-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/9379483709f1/jof-11-00021-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/bb6ea1999e10/jof-11-00021-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/3538053b6710/jof-11-00021-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/2f77e94f4ce0/jof-11-00021-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/6efe364dea88/jof-11-00021-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/6cc6678c73bf/jof-11-00021-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/085815ca033d/jof-11-00021-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/9379483709f1/jof-11-00021-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/f3c76f6a4cd6/jof-11-00021-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/bb6ea1999e10/jof-11-00021-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/3538053b6710/jof-11-00021-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/2f77e94f4ce0/jof-11-00021-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/6efe364dea88/jof-11-00021-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/6cc6678c73bf/jof-11-00021-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be99/11766592/085815ca033d/jof-11-00021-g008.jpg

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