Cited by 70Biofuel production and bioconversionEnzyme Production and CharacterizationInsect and Arachnid Ecology and Behavior

Metagenomic analysis of novel lignocellulose-degrading enzymes from higher termite guts inhabiting microbes

Nimchua, Thidarat·2012·Journal of Microbiology and Biotechnology

Abstract

A metagenomic fosmid library was constructed from genomic DNA isolated from the microbial community residing in hindguts of a wood-feeding higher termite (Microcerotermes sp.) collected in Thailand. The library was screened for clones expressing lignocellulolytic activities. Fourteen independent active clones (2 cellulases and 12 xylanases) were obtained by functional screening at pH 10.0. Analysis of shotgun-cloning and pyrosequencing data revealed six ORFs, which shared less than 59% identity and 73% similarity of their amino acid sequences with known cellulases and xylanases. Conserved domain analysis of these ORFs revealed a cellulase belonging to the glycoside hydrolase family 5, whereas the other five xylanases showed significant identity to diverse families including families 8, 10, and 11. Interestingly, one fosmid clone was isolated carrying three contiguous xylanase genes that may comprise a xylanosome operon. The enzymes with the highest activities at alkaline pH from the initial activity screening were characterized biochemically. These enzymes showed a broad range of enzyme activities from pH 5.0 to 10.0, with pH optimal of 8.0 retaining more than 70% of their respective activities at pH 9.0. The optimal temperatures of these enzymes ranged from 50 degrees C to 55 degrees C. This study provides evidence for the diversity and function of lignocellulose-degrading enzymes in the termite gut microbial community, which could be of potential use for industrial processes such as pulp biobleaching and denim biostoning.

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Crossref · 10.4014/jmb.1108.08037

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  • Sequencing techniques revealed a large variety of cellulose and hemicellulose hydrolysis related genes, enhancing understanding of cellulase richness.

    “By employing sequencing techniques, it become evident that there are a large variety of cellulose, hemicellulose hydrolysis related genes, which further enhances people's understanding of the richness of cellulase [83,84].”

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References 23 · Cited by 70

Authors
Nimchua, T.
Affiliations
Thailand Science Park (TH)
Corresponding author
Nimchua, Thidarat
Venue
Journal of Microbiology and Biotechnology
Published
2012-04-28
Volume
22
Issue
4
Pages
462-469
ISSN
  • 1017-7825 (ISSN-L)
  • 1738-8872
OpenAlex
W2064323223
Cited by
70
References
23
Citations by year
2025: 2 · 2024: 2 · 2023: 2 · 2022: 5 · 2021: 7 · 2020: 4 · 2019: 6 · 2018: 6 · 2017: 3 · 2016: 7 · 2015: 7 · 2014: 5 · 2013: 13 · 2012: 1
FWCI
4.74
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Microbiology and Biotechnology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Engineering › Biomedical Engineering › Biofuel production and bioconversion
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Enzyme Production and Characterization
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Insect and Arachnid Ecology and Behavior
Keywords
lignocellulose-degrading enzymes, termite gut microbiota, Microcerotermes, cellulase, xylanase, glycoside hydrolase family 5, alkaline pH activity, enzyme characterization, wood-feeding termites
MeSH terms
Amino Acid Sequence, Animals, Bacteria, Bacterial Proteins, Enzyme Stability, Hydrogen-Ion Concentration, Lignin, Molecular Sequence Data, Phylogeny, Xylosidases, Sequence Alignment, Isoptera, Gastrointestinal Tract, Cellulases, Metagenomics

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