Anaerobic gut fungi are the primary colonizers of plant material in the rumen microbiome, but are poorly studied
due to a lack of characterized isolates. While most genera of gut fungi form extensive rhizoidal networks, which likely
participate in mechanical disruption of plant cell walls, fungi within the Caecomyces genus do not possess these
rhizoids. Here, we describe a novel fungal isolate, Caecomyces churrovis, which forms spherical sporangia with a limited
rhizoidal network yet secretes a diverse set of carbohydrate active enzymes (CAZymes) for plant cell wall hydrolysis.
Despite lacking an extensive rhizoidal system, C. churrovis is capable of growth on fibrous substrates like switchgrass,
reed canary grass, and corn stover, although faster growth is observed on soluble sugars. Gut fungi have been shown
to use enzyme complexes (fungal cellulosomes) in which CAZymes bind to non-catalytic scaffoldins to improve biomass
degradation efficiency. However, transcriptomic analysis and enzyme activity assays reveal that C. churrovis relies
more on free enzymes compared to other gut fungal isolates. Only 15% of CAZyme transcripts contain non-catalytic
dockerin domains in C. churrovis, compared to 30% in rhizoid-forming fungi. Furthermore, C. churrovis is enriched in
GH43 enzymes that provide complementary hemicellulose degrading activities, suggesting that a wider variety of
these activities are required to degrade plant biomass in the absence of an extensive fungal rhizoid network. Overall,
molecular characterization of a non-rhizoid-forming anaerobic fungus fills a gap in understanding the roles of CAZyme
abundance and associated degradation mechanisms during lignocellulose breakdown within the rumen microbiome.
Revised: May 29, 2019 |
Published: December 20, 2017
Citation
Henske J.K., S.P. Gilmore, D. Knop, F.J. Cunningham, J.A. Sexton, C.R. Smallwood, and V. Shutthanandan, et al. 2017.Transcriptomic characterization of Caecomyces churrovis: a novel, non-rhizoid-forming lignocellulolytic anaerobic fungus.Biotechnology for Biofuels 10.PNNL-SA-134108.doi:10.1186/s13068-017-0997-4