Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Av. da República, 2780-157 Oeiras, Portugal; Instituto de Biologia Experimental e Tecnológica (IBET), Apartado 12, 2781-901 Oeiras, Portugal.
Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Av. da República, 2780-157 Oeiras, Portugal.
J Proteomics. 2014 Feb 26;98:175-88. doi: 10.1016/j.jprot.2013.11.023. Epub 2013 Dec 4.
Cork, the outer bark of Quercus suber, shows a unique compositional structure, a set of remarkable properties, including high recalcitrance. Cork colonisation by Ascomycota remains largely overlooked. Herein, Aspergillus nidulans secretome on cork was analysed (2DE). Proteomic data were further complemented by microscopic (SEM) and spectroscopic (ATR-FTIR) evaluation of the colonised substrate and by targeted analysis of lignin degradation compounds (UPLC-HRMS). Data showed that the fungus formed an intricate network of hyphae around the cork cell walls, which enabled polysaccharides and lignin superficial degradation, but probably not of suberin. The degradation of polysaccharides was suggested by the identification of few polysaccharide degrading enzymes (β-glucosidases and endo-1,5-α-l-arabinosidase). Lignin degradation, which likely evolved throughout a Fenton-like mechanism relying on the activity of alcohol oxidases, was supported by the identification of small aromatic compounds (e.g. cinnamic acid and veratrylaldehyde) and of several putative high molecular weight lignin degradation products. In addition, cork recalcitrance was corroborated by the identification of several protein species which are associated with autolysis. Finally, stringent comparative proteomics revealed that A. nidulans colonisation of cork and wood share a common set of enzymatic mechanisms. However the higher polysaccharide accessibility in cork might explain the increase of β-glucosidase in cork secretome.
Cork degradation by fungi remains largely overlook. Herein we aimed at understanding how A. nidulans colonise cork cell walls and how this relates to wood colonisation. To address this, the protein species consistently present in the secretome were analysed, as well as major alterations occurring in the substrate, including lignin degradation compounds being released. The obtained data demonstrate that this fungus has superficially attacked the cork cell walls apparently by using both enzymatic and Fenton-like reactions. Only a few polysaccharide degrading enzymes could be detected in the secretome which was dominated by protein species associated with autolysis. Lignin degradation was corroborated by the identification of some degradation products, but the suberin barrier in the cell wall remained virtually intact. Comparative proteomics revealed that cork and wood colonisation share a common set of enzymatic mechanisms.
栓皮栎的外皮栓皮栎显示出独特的组成结构和一系列显著的特性,包括高抗降解性。栓皮栎的曲霉属真菌定殖仍然很大程度上被忽视。在此,对栓皮栎上的aspergillus nidulans 分泌蛋白进行了分析(2DE)。通过对定殖基质的微观(SEM)和光谱(ATR-FTIR)评价以及木质素降解化合物的靶向分析(UPLC-HRMS)进一步补充了蛋白质组数据。数据表明,真菌在栓皮栎细胞壁周围形成了一个错综复杂的菌丝网络,这使得多糖和木质素表面降解成为可能,但可能不是对栓皮素的降解。通过鉴定几种多糖降解酶(β-葡萄糖苷酶和内切-1,5-α-l-阿拉伯糖苷酶),推测多糖的降解。木质素的降解可能是通过依赖醇氧化酶活性的芬顿样机制进化而来的,这得到了小芳香族化合物(如肉桂酸和藜芦醛)和几种假定的高分子量木质素降解产物的鉴定的支持。此外,通过鉴定几种与自溶相关的蛋白质物种,证实了栓皮栎的抗降解性。最后,严格的比较蛋白质组学表明,A. nidulans 对栓皮栎和木材的定殖共享一套共同的酶机制。然而,栓皮栎中较高的多糖可及性可能解释了栓皮栎分泌蛋白中β-葡萄糖苷酶的增加。
真菌对栓皮栎的降解仍然很大程度上被忽视。在此,我们旨在了解 A. nidulans 如何定殖栓皮栎细胞壁,以及这与木材定殖有何关系。为了解决这个问题,分析了分泌蛋白中一致存在的蛋白质种类,以及基质中发生的主要变化,包括释放的木质素降解化合物。获得的数据表明,这种真菌表面上通过使用酶和芬顿样反应来攻击栓皮栎细胞壁。在以自溶相关蛋白质物种为主导的分泌蛋白中,只检测到几种多糖降解酶。木质素降解得到了一些降解产物的证实,但细胞壁中的栓皮素屏障几乎保持完整。比较蛋白质组学表明,栓皮栎和木材的定殖共享一套共同的酶机制。