Gene cloning and characterization of a xylanase from a newly isolated Bacillus subtilis strain R5

被引:33
|
作者
Jalal, Amir [1 ]
Rashid, Naeem [1 ]
Rasool, Nouman [1 ]
Akhtar, Muhammad [1 ,2 ]
机构
[1] Univ Punjab, Sch Biol Sci, Lahore 54590, Pakistan
[2] Univ Southampton, Sch Biol Sci, Southampton SO16 7PX, Hants, England
关键词
Bacillus subtilis R5; 16S rRNA; Extracellular enzymes; Xylanase; Cloning; Kinetic parameters; PURIFICATION; BIOTECHNOLOGY; PERFORMANCE; DEGRADATION; EXPRESSION; ALIGNMENT; SEQUENCE; WHEAT;
D O I
10.1016/j.jbiosc.2008.12.005
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
A novel mesophilic strain, R5, was isolated from Osaka, Japan. The growth temperature of the strain ranged from 10 to 40 degrees C with optimal growth at 30 degrees C. Cells of strain R5 were highly motile small rods. The full-length 16S rRNA sequence was 99% homologous to that of Bacillus subtilis strain 168. The optimum pH and NaCl concentration for growth of the strain were 7.0 and 3%, respectively. Based on the biochemical characteristics and 16S rRNA sequences R5 was identified as a strain of B. subtilis. The strain R5 produced protease, cellulase, amylase, lipase/esterase, xylanase and a biosurfactant extracellularly. The gene encoding xylanase was cloned and expressed in Escherichia coli. The gene encoded a protein consisting of 213 amino acids with a relative molecular mass of 23 kDa. The gene product was purified and examined for enzymatic characteristics. The recombinant enzyme exhibited highest activity at temperatures ranging from 40 to 50 degrees C and at pH 6.0. The enzyme activity was enhanced in the presence of metal cations. The V-max and K-m values of the recombinant enzyme towards xylan from beechwood were 5550 nkat/mg and 4.5 mg/mL, respectively. (C) 2008, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:360 / 365
页数:6
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