Cloning of a Family 11 Xylanase Gene from Bacillus amyloliquefaciens CH51 Isolated from Cheonggukjang

被引:13
作者
Baek, C. U. [1 ]
Lee, S. G. [1 ]
Chung, Y. R. [1 ]
Cho, I. [2 ]
Kim, J. H. [1 ]
机构
[1] Gyeongsang Natl Univ, Div Appl Life Sci Bk21, Grad Sch, Life Sci Res Inst, Jinju, South Korea
[2] SK Energy, Energy R&D Ctr, Taejon, South Korea
关键词
Family; 11; xylanase; Bacillus amyloliquefaciens; Overexpression; Purification; FIBRINOLYTIC ENZYME; EXPRESSION; DEFICIENT; PROTEINS; SYSTEM;
D O I
10.1007/s12088-012-0260-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Bacillus amyloliquefaciens CH51, an isolate from cheonggukjang, Korean fermented soyfood, secretes several enzymes into culture medium. A gene encoding 19 kDa xylanase was cloned by PCR. Sequencing showed that the gene encoded a glycohydrolase family 11 xylanase and named xynA. xynAHis, xynA with additional codons for his-tag, was overexpressed in Escherichia coli BL21(DE3) using pET-26b(+). XynAHis was purified using HisTrap affinity column. K-m and V-max of XynAHis were 0.363 mg/ml and 701.1 mu mol/min/mg, respectively with birchwood xylan as a substrate. The optimum pH and temperature were pH 4 and 25 A degrees C, respectively. When xynA was introduced into Bacillus subtilis WB600, active XynA was secreted into culture medium.
引用
收藏
页码:695 / 700
页数:6
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