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Molecular and biotechnological aspects of xylanases
Open accessAbstract
Hemicellulolytic microorganisms play a significant role in nature by recycling hemicellulose, one of the main components of plant polysaccharides. Xylanases (EC 3.2.1.8) catalyze the hydrolysis of xylan, the major constituent of hemicellulose. The use of these enzymes could greatly improve the overall economics of processing lignocellulosic materials for the generation of liquid fuels and chemicals. Recently cellulase-free xylanases have received great attention in the development of environmentally friendly technologies in the paper and pulp industry. In microorganisms that produce xylanases low molecular mass fragments of xylan and their positional isomers play a key role in regulating its biosynthesis. Xylanase and cellulase production appear to be regulated separately, although the pleiotropy of mutations, which causes the elimination of both genes, suggests some linkage in the synthesis of the two enzymes. Xylanases are found in a cornucopia of organisms and the genes encoding them have been cloned in homologous and heterologous hosts with the objectives of overproducing the enzyme and altering its properties to suit commercial applications. Sequence analyses of xylanases have revealed distinct catalytic and cellulose binding domains, with a separate non-catalytic domain that has been reported to confer enhanced thermostability in some xylanases. Analyses of three-dimensional structures and the properties of mutants have revealed the involvement of specific tyrosine and tryptophan residues in the substrate binding site and of glutamate and aspartate residues in the catalytic mechanism. Many lines of evidence suggest that xylanases operate via a double displacement mechanism in which the anomeric configuration is retained, although some of the enzymes catalyze single displacement reactions with inversion of configuration. Based on a dendrogram obtained from amino acid sequence similarities the evolutionary relationship between xylanases is assessed. In addition the properties of xylanases from extremophilic organisms have been evaluated in terms of biotechnological applications.
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Cites
New families in the classification of glycosyl hydrolases based on amino acid sequence similarities
Henrissat, B., & Bairoch, A. (1993) · Biochemical Journal · doi:10.1042/bj2930781 · Cited by 1,974
Cited by
Biodegradation and biological treatments of cellulose, hemicellulose and lignin: an overview
Pérez, J., Muñoz-Dorado, J., de la Rubia, T., & Martínez, J. (2002) · International Microbiology · doi:10.1007/s10123-002-0062-3 · Cited by 1,717
Microbial xylanases and their industrial applications: a review
Beg, Q. K., Kapoor, M., Mahajan, L., & Hoondal, G. S. (2001) · Applied Microbiology and Biotechnology · doi:10.1007/s002530100704 · Cited by 1,371
Bacteriophage-encoded depolymerases: their diversity and biotechnological applications
Pires, D. P., Oliveira, H., Melo, L. D. R., Sillankorva, S., & Azeredo, J. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-015-7247-0 · Cited by 517
Bioconversion of lignocellulose in solid substrate fermentation
Tengerdy, R. P., & Szakacs, G. (2003) · Biochemical Engineering Journal · doi:10.1016/s1369-703x(02)00129-8 · Cited by 243
Raj, A., Kumar, S., & Singh, S. K. (2013) · Enzyme Research · doi:10.1155/2013/429305 · Cited by 44
Metadata
- Authors
- Kulkarni, N.
- Venue
- FEMS Microbiology Reviews
- Publisher
- Wiley
- Published
- 1999-07
- Volume
- 23
- Issue
- 4
- Pages
- 411-456
- ISSN
- 0168-6445 (ISSN-L)
- OpenAlex
- W2115571077
- Cited by
- 930
- References
- 1
- FWCI
- 17.05
- Type
- journal article
- Language
- en
- Open access
- bronze
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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