Genomic and transcriptomic characterization of carbohydrate-active enzymes in the anaerobic fungus <i>Neocallimastix cameroonii</i> var. <i>constans</i>

Anaerobic gut fungi effectively degrade lignocellulose in the guts of large herbivores, but there remain a limited number of isolated, publicly available, and sequenced strains that impede our understanding of the role of anaerobic fungi within microbial communities. We isolated and characterized a new fungal isolate, Neocallimastix cameroonii var. constans, providing a transcriptomic and genomic understanding of its ability to degrade diverse carbohydrates. This anaerobic fungal strain was stably cultivated for multiple years in vitro among members of an initial enrichment microbial community derived from goat feces, and it demonstrated the ability to pair with other microbial members, namely, archaeal methanogens to produce methane from lignocellulose. Genomic analysis revealed a higher number of predicted carbohydrate-active enzymes encoded in the N. cameroonii var. constans genome compared to most other sequenced anaerobic fungi. The carbohydrate-active enzyme profile for this isolate contained 660 glycoside hydrolases, 160 carbohydrate esterases, 194 glycosyltransferases, and 85 polysaccharide lyases. Differential gene expression analysis showed the upregulation of thousands of genes (including predicted carbohydrate-active enzymes) when N. cameroonii var. constans was grown on lignocellulose (reed canary grass) compared to less complex substrates, such as cellulose (filter paper), cellobiose, and glucose. AlphaFold was used to predict functions of transcriptionally active yet poorly annotated genes, revealing feruloyl esterases that likely play an important role in lignocellulose degradation by anaerobic fungi. The combination of this strain's genomic and transcriptomic characterization, omics-informed structural prediction, and robustness in microbial co-culture make it a well-suited platform to conduct future investigations into bioprocessing and enzyme discovery.

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Publication Details

Journal
G3 Genes Genomes Genetics
Published
2025-06-16
DOI
https://doi.org/10.1093/g3journal/jkaf137
Citations
4
Primary Topic
Biofuel production and bioconversion
Type
article
Field-Weighted Citation Impact
2.70

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article

Genomic and transcriptomic characterization of carbohydrate-active enzymes in the anaerobic fungus Neocallimastix cameroonii var. constans

Igor V. Grigoriev, Stephen J. Mondo, Elaina M. Blair, Kerrie Barry et al.
4 citations
G3 Genes Genomes Genetics
Biofuel production and bioconversion
2.70
article

Genomic and transcriptomic characterization of carbohydrate-active enzymes in the anaerobic fungus Neocallimastix cameroonii var. constans

Igor V. Grigoriev, Stephen J. Mondo, Elaina M. Blair, Kerrie Barry, Jayson Talag, Radwa A. Hanafy, José Gerardo González‐González, Anna Lipzen, Michelle O’Malley, Xuefeng Peng, Tejas Navaratna, Mansi Chovatia, R. Ragunathan, Kurt LaButti, Colleen B. Ahern, Mei Wang, Jennifer L. Brown
article en
4 citations

Abstract

Anaerobic gut fungi effectively degrade lignocellulose in the guts of large herbivores, but there remain a limited number of isolated, publicly available, and sequenced strains that impede our understanding of the role of anaerobic fungi within microbial communities. We isolated and characterized a new fungal isolate, Neocallimastix cameroonii var. constans, providing a transcriptomic and genomic understanding of its ability to degrade diverse carbohydrates. This anaerobic fungal strain was stably cultivated for multiple years in vitro among members of an initial enrichment microbial community derived from goat feces, and it demonstrated the ability to pair with other microbial members, namely, archaeal methanogens to produce methane from lignocellulose. Genomic analysis revealed a higher number of predicted carbohydrate-active enzymes encoded in the N. cameroonii var. constans genome compared to most other sequenced anaerobic fungi. The carbohydrate-active enzyme profile for this isolate contained 660 glycoside hydrolases, 160 carbohydrate esterases, 194 glycosyltransferases, and 85 polysaccharide lyases. Differential gene expression analysis showed the upregulation of thousands of genes (including predicted carbohydrate-active enzymes) when N. cameroonii var. constans was grown on lignocellulose (reed canary grass) compared to less complex substrates, such as cellulose (filter paper), cellobiose, and glucose. AlphaFold was used to predict functions of transcriptionally active yet poorly annotated genes, revealing feruloyl esterases that likely play an important role in lignocellulose degradation by anaerobic fungi. The combination of this strain's genomic and transcriptomic characterization, omics-informed structural prediction, and robustness in microbial co-culture make it a well-suited platform to conduct future investigations into bioprocessing and enzyme discovery.

G3 Genes Genomes GeneticsVol. 15(8)
University of Arizona (US), Lawrence Berkeley National Laboratory (US), University of California, Santa Barbara (US), Joint Genome Institute (US), Joint BioEnergy Institute (US), University of Delaware (US), University of California, Berkeley (US)
National Science Foundation, U.S. Department of Energy, Joint Genome Institute, China Scholarship Council, Office of Science, University of California, Santa Barbara, Materials Research Science and Engineering Center, Harvard University, Division of Materials Research, Biological and Environmental Research, California NanoSystems Institute, Institute for Collaborative Biotechnologies
Life in Land
Openalex Percentile: Top 10%
Biofuel production and bioconversion
2.70
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