Cloning of the thermostable phytase gene (phy) from Bacillus sp. DS11 and its overexpression in Escherichia coli

被引:66
|
作者
Kim, YO
Lee, JK
Kim, HK
Yu, JH
Oh, TK
机构
[1] Korea Res Inst Biosci & Biotechnol, Microbial Enzyme RU, Taejon 305600, South Korea
[2] Yonsei Univ, Dept Food & Biotechnol, Seoul 120749, South Korea
关键词
Bacillus; phytase; phytate; overexpression;
D O I
10.1016/S0378-1097(98)00119-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Phytase hydrolyzes phytate to release inorganic phosphate, which would decrease the addition of phosphorus to feedstuffs for monogastric animals and thus reduce environmental pollution. The gene encoding phytase from Bacillus sp. DS11 was cloned in Escherichia coli and its sequence determined. A 560-bp DNA fragment was used as a probe to screen the genomic library. It was obtained through PCR of Bacillus sp. DS11 chromosomal DNA and two oligonucleotide primers based on N-terminal amino acid sequences of the purified protein and the cyanogen bromide-cleaved 21-kDa fragment. The phy cloned was encoded by a 2.2-kb fragment. This gene comprises 1152 nucleotides and encodes a polypeptide of 353 amino acids with a deduced molecular mass of 41 808 Da. Phytase was produced to 20% content of total soluble proteins in E. coli BL21 (DE3) using the pET22b(+) vector with the inducible T7 promoter. This is the first nucleic sequence report on phytase from a bacterial strain. (C) 1998 Federation of European Microbiological Societies. Published by Elsevier Science B.V.
引用
收藏
页码:185 / 191
页数:7
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