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Carbohydrate esterase family 16 contains fungal hemicellulose acetyl esterases (HAEs) with varying specificity
- Source :
- New Biotechnology, 70, 28. Elsevier, New Biotechnology, 70, 28-38. Elsevier B.V.
- Publication Year :
- 2022
-
Abstract
- Acetyl esterases are an important component of the enzymatic machinery fungi use to degrade plant biomass and are classified in several Carbohydrate Esterase families of the CAZy classification system. Carbohydrate Esterase family 16 (CE16) is one of the more recently discovered CAZy families, but only a small number of its enzyme members have been characterized so far, revealing activity on xylan-derived oligosaccharides, as well as activity related to galactoglucomannan. The number of CE16 genes differs significantly in the genomes of filamentous fungi. In this study, four CE16 members were identified in the genome of Aspergillus niger NRRL3 and it was shown that they belong to three of the four phylogenetic Clades of CE16. Significant differences in expression profiles of the genes and substrate specificity of the enzymes were revealed, demonstrating the diversity within this family of enzymes. Detailed characterization of one of these four A. niger enzymes (HaeA) demonstrated activity on oligosaccharides obtained from acetylated glucuronoxylan, galactoglucomannan and xyloglucan, thus establishing this enzyme as a general hemicellulose acetyl esterase. Their broad substrate specificity makes these enzymes highly interesting for biotechnological applications in which deacetylation of polysaccharides is required.
- Subjects :
- 11832 Microbiology and virology
CE16
Acetyl esterase
DEACETYLATION
Substrate specificity
Esterases
Oligosaccharides
ASPERGILLUS-NIGER
Bioengineering
General Medicine
DEGRADATION
Glucomannan
TRANSCRIPTIONAL ACTIVATOR
TRICHODERMA-REESEI
Xylan
Polysaccharides
GALACTURONIC ACID
CARBON CATABOLITE REPRESSION
Aspergillus niger
Xyloglucan
Molecular Biology
Phylogeny
GENE-EXPRESSION
Biotechnology
Subjects
Details
- Language :
- English
- ISSN :
- 18716784
- Database :
- OpenAIRE
- Journal :
- New Biotechnology, 70, 28. Elsevier, New Biotechnology, 70, 28-38. Elsevier B.V.
- Accession number :
- edsair.doi.dedup.....4efd6d410c1c686301aa63e6135d11ce