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Appl Microbiol Biotechnol ; 79(5): 769-74, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18443780

ABSTRACT

A set of filamentous fungi (42 strains) was screened for alpha-N-acetylgalactosaminidase activity, and a series of inducers and different cultivation conditions were tested. Enzyme production by the best producer Aspergillus niger CCIM K2 was optimized and scaled up. alpha-N-Acetylgalactosaminidase was purified to apparent homogeneity by cation exchange chromatography, gel filtration, and chromatofocusing, and basic biochemical data of the enzyme were determined: The native molecular weight was estimated by gel filtration to be approximately 440 kDa, the molecular weight of the subunit was determined to be 76 kDa and the pI = 4.8. The K (M) was 0.73 mmol/l for o-nitrophenyl 2-acetamido-2-deoxy-alpha-D-galactopyranoside (o-NP-alpha-GalNAc), and optimum enzyme activity was achieved at pH 1.8 and 55 degrees C. This alpha-N-acetylgalactosaminidase is a retaining-type glycosidase, and it was N-deglycosylated without any loss of activity.


Subject(s)
Aspergillus niger/enzymology , Fungal Proteins/chemistry , Fungal Proteins/isolation & purification , alpha-N-Acetylgalactosaminidase/chemistry , alpha-N-Acetylgalactosaminidase/isolation & purification , Aspergillus niger/metabolism , Enzyme Activation , Enzyme Stability , Fungal Proteins/metabolism , Kinetics , Molecular Weight , alpha-N-Acetylgalactosaminidase/metabolism
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