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G0395

Sigma-Aldrich

β-Glucosidase from almonds

greener alternative

lyophilized powder, ≥2 units/mg solid

Synonyme(s) :

β-D-Glucoside glucohydrolase

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About This Item

Numéro CAS:
9001-22-3
Numéro de classification (Commission des enzymes):
3.2.1.21 (BRENDA, IUBMB)
Numéro CE :
232-589-7
Numéro MDL:
MFCD00130628
Code UNSPSC :
12352204
Nomenclature NACRES :
NA.54

Forme

lyophilized powder

Niveau de qualité

300

Activité spécifique

≥2 units/mg solid

Poids mol.

135 kDa

Caractéristiques du produit alternatif plus écologique

Waste Prevention
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Impuretés

salt, essentially free

Autre catégorie plus écologique

Enabling,

Température de stockage

2-8°C

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Catégories apparentées

Description générale

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency and waste prevention when used in cellulosic ethanol research. For more information see the article in biofiles.

Application

β-glucosidase is also used in the synthesis of glucosides and fucosides with various potential applications in pharmaceutical, cosmetic and detergent industries, hydrolytic removal of aglycone moiety from flavonoid and isoflavonoid glycosides, flavor enhancement of fruit juices and wine, and biosynthesis of oligosaccharides.

Actions biochimiques/physiologiques

β−glucosidase is involved in the hydrolysis of β−glycosidic bonds connecting carbohydrate residues in β−D-glycosides. It converts cellobiose and cellooligosaccharides produced by the endo and exoglucanases to glucose.
βglucosidase is involved in the hydrolysis of β-glycosidic bonds connecting carbohydrate residues in β-D-glycosides. They convert cellobiose and cellooligosaccharides produced by the endo and exoglucanases to glucose.

Qualité

Crude

Définition de l'unité

One unit will liberate 1.0 μmole of glucose from salicin per min at pH 5.0 at 37 °C.

Inhibiteur

Réf. du produit
Description
Tarif

Substrat

Réf. du produit
Description
Tarif

Pictogrammes

Health hazard
GHS08

Mention d'avertissement

Danger

Mentions de danger

H334

Conseils de prudence

P261 - P342 + P311

Classification des risques

Resp. Sens. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

Response surface optimization of enzymatic hydrolysis of Cistus ladanifer and Cytisus striatus for bio-ethanol production
S. Ferreira et al.
Biochemical Engineering Journal, 45 , 192-200 (2009)
Max F Cowan et al.
Phytochemistry, 184, 112645-112645 (2021-01-23)
Domestication has narrowed the genetic diversity found in crop wild relatives, potentially reducing plasticity to cope with a changing climate. The tissues of domesticated sorghum (Sorghum bicolor), especially in younger plants, are cyanogenic and potentially toxic. Species of wild sorghum
Craig M Dana et al.
Biotechnology and bioengineering, 111(4), 842-847 (2014-01-01)
The commercialization of lignocellulosic biofuels relies in part on the ability to engineer cellulase enzymes to have properties compatible with practical processing conditions. The cellulase Cel7A has been a common engineering target because it is present in very high concentrations
B Garner et al.
The Journal of biological chemistry, 274(30), 20847-20854 (1999-07-20)
A novel fluorophore was isolated from human lenses using high performance liquid chromatography (HPLC). The new fluorophore was well separated from 3-hydroxykynurenine glucoside (3-OHKG) and its deaminated isoform, 4-(2-amino-3-hydroxyphenyl)-4-oxobutanoic acid O-glucoside, which are known UV filter compounds. The new compound
Sibylle Bauer et al.
The Plant cell, 33(3), 714-734 (2021-05-07)
Glucosylation modulates the biological activity of small molecules and frequently leads to their inactivation. The Arabidopsis thaliana glucosyltransferase UGT76B1 is involved in conjugating the stress hormone salicylic acid (SA) as well as isoleucic acid (ILA). Here, we show that UGT76B1
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