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G0395

Sigma-Aldrich

β-Glucosidase from almonds

greener alternative

lyophilized powder, ≥2 units/mg solid

Synonyma:

β-D-Glucoside glucohydrolase

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About This Item

Číslo CAS:
9001-22-3
Číslo enzymu podle klasifikace EK:
3.2.1.21 (BRENDA, IUBMB)
EC Number:
232-589-7
MDL number:
MFCD00130628
UNSPSC Code:
12352204
NACRES:
NA.54

form

lyophilized powder

Quality Level

300

specific activity

≥2 units/mg solid

mol wt

135 kDa

greener alternative product characteristics

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

sustainability

Greener Alternative Product

impurities

salt, essentially free

greener alternative category

Enabling,

storage temp.

2-8°C

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Související kategorie

General description

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.

Biochem/physiol Actions

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.

Quality

Crude

Unit Definition

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

inhibitor

Č. produktu
Popis
Stanovení ceny

D9305

1-Deoxynojirimycin hydrochloride

C5424

Conduritol B epoxide

C3784

Castanospermine, ≥94% (GC), BioUltra, from Castanospermum australe seeds

substrate

Č. produktu
Popis
Stanovení ceny

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H334

Hazard Classifications

Resp. Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Vyberte jednu z posledních verzí:

Osvědčení o analýze (COA)

Lot/Batch Number
0000389750
0000342938
0000342937
0000389750
0000308051

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Navštívit knihovnu dokumentů

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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