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M. 费舍尔对木材的降解:利用代谢组学网络探索真菌适应性

Wood Degradation by M. Fischer: Exploring Fungal Adaptation Using Metabolomic Networking.

作者信息

Schilling Marion, Levasseur Marceau, Barbier Muriel, Oliveira-Correia Lydie, Henry Céline, Touboul David, Farine Sibylle, Bertsch Christophe, Gelhaye Eric

机构信息

INRAE, IAM, Université de Lorraine, 54000 Nancy, France.

CNRS, Institut de Chimie des Substances Naturelles (ICSN), UPR2301, Université Paris-Saclay, Avenue de la Terrasse, 91198 Gif-sur-Yvette, France.

出版信息

J Fungi (Basel). 2023 Apr 30;9(5):536. doi: 10.3390/jof9050536.

Abstract

M. Fischer (Fmed) is a white-rot wood-decaying fungus associated with one of the most important and challenging diseases in vineyards: Esca. To relieve microbial degradation, woody plants, including , use structural and chemical weapons. Lignin is the most recalcitrant of the wood cell wall structural compounds and contributes to wood durability. Extractives are constitutive or de novo synthesized specialized metabolites that are not covalently bound to wood cell walls and are often associated with antimicrobial properties. Fmed is able to mineralize lignin and detoxify toxic wood extractives, thanks to enzymes such as laccases and peroxidases. Grapevine wood's chemical composition could be involved in Fmed's adaptation to its substrate. This study aimed at deciphering if Fmed uses specific mechanisms to degrade grapevine wood structure and extractives. Three different wood species, grapevine, beech, and oak. were exposed to fungal degradation by two Fmed strains. The well-studied white-rot fungus (Tver) was used as a comparison model. A simultaneous degradation pattern was shown for Fmed in the three degraded wood species. Wood mass loss after 7 months for the two fungal species was the highest with low-density oak wood. For the latter wood species, radical differences in initial wood density were observed. No differences between grapevine or beech wood degradation rates were observed after degradation by Fmed or by Tver. Contrary to the Tver secretome, one manganese peroxidase isoform (MnP2l, jgi protein ID 145801) was the most abundant in the Fmed secretome on grapevine wood only. Non-targeted metabolomic analysis was conducted on wood and mycelium samples, using metabolomic networking and public databases (GNPS, MS-DIAL) for metabolite annotations. Chemical differences between non-degraded and degraded woods, and between mycelia grown on different wood species, are discussed. This study highlights Fmed physiological, proteomic and metabolomic traits during wood degradation and thus contributes to a better understanding of its wood degradation mechanisms.

摘要

费氏密环菌(M. Fischer,Fmed)是一种白腐木腐真菌,与葡萄园最重要且最具挑战性的病害之一——葡萄枝干病害(Esca)有关。为了抵御微生物降解,包括葡萄树在内的木本植物会动用结构和化学武器。木质素是木细胞壁结构化合物中最难降解的成分,有助于木材耐久性。提取物是组成型或从头合成的特殊代谢产物,它们并非共价结合在木细胞壁上,且往往具有抗菌特性。由于漆酶和过氧化物酶等酶的作用,Fmed能够使木质素矿化并使有毒的木材提取物解毒。葡萄树木的化学成分可能参与了Fmed对其底物的适应过程。本研究旨在弄清楚Fmed是否利用特定机制来降解葡萄树木结构和提取物。三种不同的木材种类,即葡萄树、山毛榉和橡木,被两种Fmed菌株用于真菌降解实验。被广泛研究的白腐真菌(Tver)用作比较模型。Fmed在三种被降解的木材种类中呈现出同步降解模式。两种真菌在7个月后导致的木材质量损失,在低密度橡木中最高。对于后一种木材种类,观察到初始木材密度存在显著差异。在被Fmed或Tver降解后,未观察到葡萄树或山毛榉木材降解速率之间的差异。与Tver分泌组不同,一种锰过氧化物酶同工型(MnP2l,jgi蛋白ID 145801)仅在Fmed对葡萄树木的分泌组中最为丰富。使用代谢组网络和公共数据库(GNPS、MS-DIAL)对木材和菌丝体样本进行了非靶向代谢组分析以注释代谢物。讨论了未降解和已降解木材之间以及在不同木材种类上生长的菌丝体之间的化学差异。本研究突出了Fmed在木材降解过程中的生理、蛋白质组和代谢组特征,从而有助于更好地理解其木材降解机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b568/10218912/46dc2b66bd10/jof-09-00536-g001.jpg

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