Purification and Characterization of Exo-β- d -Glucosaminidase from a Cellulolytic Fungus, Trichoderma reesei PC-3-7
0303 health sciences
03 medical and health sciences
DOI:
10.1128/aem.64.3.890-895.1998
Publication Date:
2019-12-19T19:32:02Z
AUTHORS (6)
ABSTRACT
ABSTRACT
Chitosan-degrading activities induced by glucosamine (GlcN) or
N
-acetylglucosamine (GlcNAc) were found in a culture filtrate of
Trichoderma reesei
PC-3-7. One of the chitosan-degrading enzymes was purified to homogeneity by precipitation with ammonium sulfate followed by anion-exchange and hydrophobic-interaction chromatographies. The enzyme was monomeric, and its molecular mass was 93 kDa. The optimum pH and temperature of the enzyme were 4.0 and 50°C, respectively. The activity was stable in the pH range 6.0 to 9.0 and at a temperature below 50°C. Reaction product analysis from the viscosimetric assay and thin-layer chromatography and
1
H nuclear magnetic resonance spectroscopy clearly indicated that the enzyme was an exo-type chitosanase, exo-β-
d
-glucosaminidase, that releases GlcN from the nonreducing end of the chitosan chain.
1
H nuclear magnetic resonance spectroscopy also showed that the exo-β-
d
-glucosaminidase produced a β-form of GlcN, demonstrating that the enzyme is a retaining glycanase. Time-dependent liberation of the reducing sugar from partially acetylated chitosan with exo-β-
d
-glucosaminidase and the partially purified exo-β-
d
-
N
-acetylglucosaminidase from
T. reesei
PC-3-7 suggested that the exo-β-
d
-glucosaminidase cleaves the glycosidic link of either GlcN-β(1→4)-GlcN or GlcN-β(1→4)-GlcNAc.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (33)
CITATIONS (60)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....