Literature DB >> 7603971

Identification, characterization, and partial purification of glucoamylase from Aspergillus niger (syn A. ficuum) NRRL 3135.

A S Vandersall1, R G Cameron, C J Nairn, G Yelenosky, R J Wodzinski.   

Abstract

The crude extracellular extract of Aspergillus niger (syn A. ficuum) NRRL 3135 contains glucoamylase (exo-1,4-alpha-D-glucanohydrolase, EC 3.2.1.2). The enzyme, a glycoprotein, was purified 7-fold by ion-exchange chromatography, chromatofocusing, and conconavalin A affinity chromatography. The molecular weight of the enzyme was estimated to be 90 kDa by SDS-PAGE and gel permeation chromatography. The pI of the enzyme was 3.4. The temperature optimum of the enzyme was 60 degrees C and the pH optimum was 5.0. The Vmax values for soluble starch, maltose, maltotriose, maltotretraose, maltopentaose, and isomaltose were 55.2, 11.7, 32.3, 47.8, 59.2, 12.5 nKat glucose/sec, respectively and the Km values for the same substrates were 0.09%, 0.67 mM, 0.76 mM, 0.76 mM, 0.68 mM, and 122.01 mM, respectively.

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Year:  1995        PMID: 7603971     DOI: 10.1080/10826069508010106

Source DB:  PubMed          Journal:  Prep Biochem        ISSN: 0032-7484


  1 in total

1.  Physiochemical properties and kinetics of glucoamylase produced from deoxy-d-glucose resistant mutant of Aspergillus niger for soluble starch hydrolysis.

Authors:  Muhammad Riaz; Muhammad Hamid Rashid; Lindsay Sawyer; Saeed Akhtar; Muhammad Rizwan Javed; Habibullah Nadeem; Martin Wear
Journal:  Food Chem       Date:  2012-01-01       Impact factor: 7.514

  1 in total

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