Your browser doesn't support javascript.
loading
Gene expression and characterisation of three pullulanases from Bacillus cereus GXBC-3 / 生物工程学报
Chinese Journal of Biotechnology ; (12): 466-475, 2012.
Article in Chinese | WPRIM | ID: wpr-342470
ABSTRACT
Exploring excellent new pullulanase genes, and enriching pullulanase theory are of great importance to realize the industrialization of pullulanase. Three genes, pulA, pulB and pulC, encoding pullulanases, were cloned from Bacillus cereus GXBC-3 by bioinformatics analyzing the open reading frame in Bacillus cereus, annotated as putative I and II pullulanases in the GenBank database. Characteristics of these recombinant enzymes were inducible intracellular expressed in Escherichia coli, the results showed PulA was typical II pullulanase. Recombinant PulA could hydrolyze alpha-1,4- and alpha-1,6-glycosidic bonds. Its specific activity was 32.89 U/mg with an optimum temperature of 40 degrees C and optimum pH 6.5 using pullulan as substrate. And for soluble starch substrate, its specific activity was 25.71 U/mg with an optimum temperature of 50 degrees C and optimum pH 7.0. PulB and PulC were I pullulanases and only hydrolyzed alpha-1,6-glycosidic bond. The specific activities, optimum temperature and optimum pH of PulB and PulC for pullulan substrate were 228.54 U/mg, 45 degrees C, 7.0 and 229.65 U/mg, 45 degrees C, 6.5, respectively.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Bacillus cereus / Recombinant Proteins / Cloning, Molecular / Escherichia coli / Genetics / Glucans / Glycoside Hydrolases / Metabolism Language: Chinese Journal: Chinese Journal of Biotechnology Year: 2012 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: WPRIM (Western Pacific) Main subject: Bacillus cereus / Recombinant Proteins / Cloning, Molecular / Escherichia coli / Genetics / Glucans / Glycoside Hydrolases / Metabolism Language: Chinese Journal: Chinese Journal of Biotechnology Year: 2012 Type: Article