"beta-Glucosidase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An exocellulase with specificity for a variety of beta-D-glycoside substrates. It catalyzes the hydrolysis of terminal non-reducing residues in beta-D-glucosides with release of GLUCOSE.
| Descriptor ID |
D001617
|
| MeSH Number(s) |
D08.811.277.450.420.200.100
|
| Concept/Terms |
beta-Glucosidase- beta-Glucosidase
- beta Glucosidase
- Gentiobiase
- Cellobiases
- Amygdalase
- Cellobiase
|
Below are MeSH descriptors whose meaning is more general than "beta-Glucosidase".
Below are MeSH descriptors whose meaning is more specific than "beta-Glucosidase".
This graph shows the total number of publications written about "beta-Glucosidase" by people in this website by year, and whether "beta-Glucosidase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 0 | 1 |
| 2002 | 0 | 1 | 1 |
| 2005 | 1 | 0 | 1 |
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Below are the most recent publications written about "beta-Glucosidase" by people in Profiles.
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Biochemical and structural characterization of a thermostable ?-glucosidase from Halothermothrix orenii for galacto-oligosaccharide synthesis. Appl Microbiol Biotechnol. 2015 Feb; 99(4):1731-44.
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Co-refolding of two peptide fragments derived from Agrobacterium tumefaciens beta-glucosidase with catalytic activity. FEBS Lett. 2005 Jun 06; 579(14):3075-80.
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Absorption and metabolism of flavonoids in the caco-2 cell culture model and a perused rat intestinal model. Drug Metab Dispos. 2002 Apr; 30(4):370-7.
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Characterization of a bifunctional cellulase and its structural gene. The cell gene of Bacillus sp. D04 has exo- and endoglucanase activity. J Biol Chem. 1995 Oct 27; 270(43):26012-9.
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Transformed SV3T3 cells have a reduced lysosomal compartment and lower levels of enzyme activity than 3T3 cells. Exp Cell Res. 1990 Jul; 189(1):93-9.
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[Laboratory diagnosis of lysosomal storage disease (glycoproteinosis Pompe's disease and Gaucher disease)]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1985 Dec; 7(6):475-7.