Purification of α-Amylase from Bacillus sp. GHA1 and its partial characterization

被引:0
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作者
A. Ahmadi
S. Ghobadi
K. Khajeh
B. Nomanpour
A. Badoei Dalfard
机构
[1] Razi University,Department of Biology, Faculty of Science
[2] Tarbiat Modarres University,Department of Biochemistry, Faculty of Science
[3] Tehran University of Medical Sciences,Department of Microbiology, School of Medicine
关键词
α-Amylase; sp. GHA1; pH profile; Broad range of pH; Industrial applications;
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摘要
Bacillus sp. GHA1 was isolated from water samples and screened for the production of α-amylase. Maximum production of amylase by this strain occurs at 42 °C, pH 6.5 and 72 h after cultivation in production medium. The enzyme was purified through successive applications of ammonium sulfate precipitation, ion exchange and hydrophobic interaction chromatography, resulting in a single band with an apparent molecular weight of 66 kDa, as judged by SDS-PAGE. Calcium analysis of the purified enzyme revealed that it contained three metal ions per molecule. The new extracellular α-amylase is active in a wide range of pH with its maximum activity at pH values 5.5–8.0. The optimum temperature for enzyme activity is 57 °C and the presence of calcium has relatively low influence on its activity and thermostability. The Bacillus sp. GHA1 α-amylase with these properties may be suitable for use in detergent and food industries.
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页码:432 / 440
页数:8
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