Degradation of cellulose by basidiomycetous fungi.

By Petr Baldrian, V. Valášková. FEMS Microbiology Reviews, 2008

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In Plant Science

Citations in the corpus

Fungal Bioconversion of Lignocellulosic Residues; Opportunities & Perspectives (2009, background): “Cellobiose, the end product of CBHs, acts as a competitive inhibitor, which can limit the ability of the enzymes to degrade all of cellulose molecules in a system [36,44,60].”
Production of extracellular enzymes and degradation of biopolymers by saprotrophic microfungi from the upper layers of forest soil (2010, background): “However, the ability to produce the individual components of this cellulolytic system varies among cellulolytic fungi (Baldrian and Valášková 2008; Lynd et al. 2002).”
Fungal community on decomposing leaf litter undergoes rapid successional changes (2012, background): “Among these, cellobiohydrolases (exocellulases), which catalyses the rate-limiting step of cellulose decomposition (Baldrian and Valášková, 2008), and the cbhI gene represent suitable markers for the study of cellulolytic fungi (Edwards et al., 2008; Weber et al., 2011; Baldrian et al., 2012).”
Pollutants Biodegradation by Fungi (2009, background): “For the degradation of cellulose, basidiomycetes utilize a set of hydrolytic enzymes typically composed of endoglucanase, cellobiohydrolase and -glycosidase [225, 226, 227].”
Genome, transcriptome, and secretome analysis of wood decay fungus Postia placenta supports unique mechanisms of lignocellulose conversion (2009, background): “The sequence corresponding to another fungal protein implicated in Fe3 reduction, CDH (6), appears to be absent in P.”
Fueling the future with fungal genomics (2011, background): “In addition, Postia lacks exocellobiohydrolases and cellulose-binding modules, which are previously known from all cellulolytic fungi (Baldrian and Valaskova 2008).”
Lignin degradation: microorganisms, enzymes involved, genomes analysis and evolution (2017, background): “CDH was also isolated from the soil plant pathogen Sclerotium rolfsii and detected in the ECM fungi Pisolithus tinctorius, Suillus variegatus and Cortinarius sp. (Baldrian and Valaskova 2008).”
Active and total microbial communities in forest soil are largely different and highly stratified during decomposition (2011, background): “Because most of the analysed fungi harbour more than one cbhI gene (Baldrian and Valášková, 2008; Edwards et al., 2008), the diversity of cellulolytic fungi in forest topsoil can be estimated only roughly at 50–300.”