Xylanase, CAS No.9025-57-4

CAS: 9025-57-4 Cat. No.: X195724 Numero EC: 232-800-2

GRADE & PURITY EnzymoPure™, ＞100000 U/g

Panoramica

This product has been enhanced for energy efficiency and waste prevention when used in cellulosic ethanol research. 

Xylanase is a hemicellulolytic enzyme. It is synthesized by microorganisms like bacteria, yeast and fungi.

Xylanase from Trichoderma viride has been used as a component of an enzyme mixture for the hydrolysis of hemicellulose-rich solution (autohydrolysate). It has also been used as a cell-wall degrading enzyme to determine the efficiency of p-coumaryl esterase to release p-coumaroyl and feruloyl group

Specifications

Product Name

Xylanase, CAS No.9025-57-4

Sinonimi

benzoquinonium-dibromide | Benzoquinonium | N,N'-((3,6-DIOXO-1,4-CYCLOHEXADIENE-1,4-DIYL)BIS(IMINO-3,1-PROPANEDIYL))BIS(N,N-DIETHYLBENZENEMETHANAMINIUM | E.C. 3.2.1.8 | Q27289827 | benzyl-[3-[[4-[3-[benzyl(diethyl)azaniumyl]propylamino]-3,6-dioxocyclohexa

Grado

EnzymoPure™

Specifiche e purezza

EnzymoPure™, ＞100000 U/g

Meccanismi biochimici e fisiologici

Endohydrolysis of (1->4)-beta-D-xylosidic linkages in xylans.

CAS

9025-57-4

Numero della Commissione Enzimi

3.2.1.8

Tipo di molecola

Enzima

Stoccaggio e spedizione

Concentrazione

＞100000 U/g

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

Definizione dell'unità

At 50°C and pH 4.80, the amount of enzyme required to degrade and release 1μmol of reducing sugar from an oat xylan solution with a concentration of 10mg/ml per minute is an activity unit (IU), and the amount of reducing sugar is xylose equivalent. .

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Phenylmethylamines

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Phenylmethylamines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylmethylamines
• Alternative Parents: P-benzoquinones Benzylamines Aralkylamines Vinylogous amides Tetraalkylammonium salts Enamines Dialkylamines Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzylamine - P-benzoquinone - Phenylmethylamine - Quinone - Aralkylamine - Tetraalkylammonium salt - Vinylogous amide - Quaternary ammonium salt - Ketone - Cyclic ketone - Secondary aliphatic amine - Enamine - Secondary amine - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic salt - Amine - Carbonyl group - Organic cation - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as phenylmethylamines. These are compounds containing a phenylmethtylamine moiety, which consists of a phenyl group substituted by an methanamine.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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