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D9515

Sigma-Aldrich

Driselase™ from Basidiomycetes sp.

greener alternative

powder, Protein ≥10 % by biuret

Synonym(s):

cellulase, laminarinase, xylanase

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About This Item

CAS Number:
85186-71-6
EC Number:
286-055-3
MDL number:
MFCD00130978
UNSPSC Code:
12352204
NACRES:
NA.54

conjugate

conjugate (Glucosaminoglycan)

Quality Level

200

form

powder

composition

Protein, ≥10% biuret

greener alternative product characteristics

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

sustainability

Greener Alternative Product

greener alternative category

, Enabling

shipped in

wet ice

storage temp.

−20°C

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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 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.

Biochem/physiol Actions

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.

Other Notes

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

Legal Information

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

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H334

Hazard Classifications

Resp. Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Q Chen et al.
Plant physiology, 94(4), 1820-1829 (1990-12-01)
Treating carrot (Daucus carota L.) suspension culture cells with a mixture of cell wall degrading enzymes, Driselase, resulted in an increase in the percentage of [(3)H]phosphatidylinositol bisphosphate. Analysis of the lipid kinase activities in the isolated plasma membranes after whole
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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