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D9515

Sigma-Aldrich

Driselase™ from Basidiomycetes sp.

greener alternative

powder, Protein ≥10 % by biuret

Synonyme(s) :

cellulase, laminarinase, xylanase

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About This Item

Numéro CAS:
85186-71-6
Numéro CE :
286-055-3
Numéro MDL:
MFCD00130978
Code UNSPSC :
12352204
Nomenclature NACRES :
NA.54

Conjugué

conjugate (Glucosaminoglycan)

Niveau de qualité

200

Forme

powder

Composition

Protein, ≥10% biuret

Caractéristiques du produit alternatif plus écologique

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

sustainability

Greener Alternative Product

Autre catégorie plus écologique

, Enabling

Conditions d'expédition

wet ice

Température de stockage

−20°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 and Enzymes for Alternative Energy Research.

Application

Driselase from Basidiomycetes has been used in a study to assess the digestion by fungal glycanases of arabinoxylans with different feruloylated side-chains. Driselase from Basidiomycetes has also been used in a study to investigate the purification, characterization, and mode of action of a rhamnogalacturonan hydrolase.
The enzyme from Sigma has been used as a control while testing the ability of p-coumaroyl esterase to release p-coumaroyl and feruloyl groups from intact cell walls. It has also been used in the protoplast preparation from mycelia during a study to investigate the pathogenicity of Cochliobolus carbonum on Maize.

Actions biochimiques/physiologiques

Driselase is a cell wall degrading enzyme that contains cellulase, hemicellulase, pectinase etc. Therefore, it is very effective in removing plant cell walls to make protoplasts.

Autres remarques

Crude powder containing laminarinase, xylanase and cellulase.
View more information on enzymes for complex carbohydrate analysis at www.sigma-aldrich.com/enzymeexplorer

Informations légales

Driselase is a trademark of ASKA Animal Health Co. Ltd.

Pictogrammes

Health hazard
GHS08

Mention d'avertissement

Danger

Mentions de danger

H334

Conseils de prudence

P261 - P284 - P501

Classification des risques

Resp. Sens. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

J S Scott-Craig et al.
The Plant cell, 2(12), 1191-1200 (1990-12-01)
A gene (PGN1) encoding extracellular endopolygalacturonase was isolated from the fungal maize pathogen Cochliobolus carbonum race 1. A probe was synthesized by polymerase chain reaction using oligonucleotides based on the endopolygalacturonase amino acid sequence. Genomic and cDNA copies of the
Dan Ye et al.
Scientific reports, 8(1), 12449-12449 (2018-08-22)
Cellulose microfibrils are crucial for many of the remarkable mechanical properties of primary cell walls. Nevertheless, many structural features of cellulose microfibril organization in cell walls are not yet fully described. Microscopy techniques provide direct visualization of cell wall organization
Jiming Li et al.
Environmental microbiology, 22(12), 4985-5004 (2020-05-27)
In Fusarium oxysporum f.sp. lycopersici, all effector genes reported so far - also called SIX genes - are located on a single accessory chromosome which is required for pathogenicity and can also be horizontally transferred to another strain. To narrow
Brian Christopher King et al.
Scientific reports, 6, 25030-25030 (2016-04-30)
Direct assembly of multiple linear DNA fragments via homologous recombination, a phenomenon known as in vivo assembly or transformation associated recombination, is used in biotechnology to assemble DNA constructs ranging in size from a few kilobases to full synthetic microbial
G Wende et al.
Phytochemistry, 45(6), 1123-1129 (1997-07-01)
Alcohol-insoluble residues (AIRs) from Festuca and Zea cell cultures contained 7.4 and 35 nmol esterified ferulate mg-1, respectively. Driselase solubilised 79% of the feruloylated material from both AIRs. Of the feruloyl esters solubilised from Festuca and Zea AIRs, 72 and
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