Publication:

Comparative Analysis of Secretome Profiles of Manganese(II)-Oxidizing Ascomycete Fungi

Loading...
Thumbnail Image

Open/View Files

Date

2016

Journal Title

Journal ISSN

Volume Title

Publisher

Public Library of Science
The Harvard community has made this article openly available. Please share how this access benefits you.

Research Projects

Organizational Units

Journal Issue

Citation

Zeiner, C. A., S. O. Purvine, E. M. Zink, L. Paša-Tolić, D. L. Chaput, S. Haridas, S. Wu, et al. 2016. “Comparative Analysis of Secretome Profiles of Manganese(II)-Oxidizing Ascomycete Fungi.” PLoS ONE 11 (7): e0157844. doi:10.1371/journal.pone.0157844. http://dx.doi.org/10.1371/journal.pone.0157844.

Abstract

Fungal secretomes contain a wide range of hydrolytic and oxidative enzymes, including cellulases, hemicellulases, pectinases, and lignin-degrading accessory enzymes, that synergistically drive litter decomposition in the environment. While secretome studies of model organisms such as Phanerochaete chrysosporium and Aspergillus species have greatly expanded our knowledge of these enzymes, few have extended secretome characterization to environmental isolates or conducted side-by-side comparisons of diverse species. Thus, the mechanisms of carbon degradation by many ubiquitous soil fungi remain poorly understood. Here we use a combination of LC-MS/MS, genomic, and bioinformatic analyses to characterize and compare the protein composition of the secretomes of four recently isolated, cosmopolitan, Mn(II)-oxidizing Ascomycetes (Alternaria alternata SRC1lrK2f, Stagonospora sp. SRC1lsM3a, Pyrenochaeta sp. DS3sAY3a, and Paraconiothyrium sporulosum AP3s5-JAC2a). We demonstrate that the organisms produce a rich yet functionally similar suite of extracellular enzymes, with species-specific differences in secretome composition arising from unique amino acid sequences rather than overall protein function. Furthermore, we identify not only a wide range of carbohydrate-active enzymes that can directly oxidize recalcitrant carbon, but also an impressive suite of redox-active accessory enzymes that suggests a role for Fenton-based hydroxyl radical formation in indirect, non-specific lignocellulose attack. Our findings highlight the diverse oxidative capacity of these environmental isolates and enhance our understanding of the role of filamentous Ascomycetes in carbon turnover in the environment.

Description

Research Data

Keywords

Biology and Life Sciences, Organisms, Fungi, Genetics, Fungal Genetics, Fungal Genomics, Mycology, Genomics, Biochemistry, Enzymology, Enzymes, Proteases, Proteins, Ascomycetes, Database and Informatics Methods, Biological Databases, Genomic Databases, Computational Biology, Genome Analysis, Plant Science, Plant Pathology, Plant Pathogens, Plant Fungal Pathogens, Basidiomycetes

Terms of Use

This article is made available under the terms and conditions applicable to Other Posted Material (LAA), as set forth at Terms of Service

Endorsement

Review

Supplemented By

Related Stories