Purification and characterization of the low molecular weight xylanase from Bacillus cereus L-1
文献类型: 外文期刊
第一作者: Zhang, Ge
作者: Zhang, Ge;Li, Zhihao;Chen, Guoqiang;Deng, Shuaijun;Zhang, Haibo;Li, Zhihao;Zhang, Liang;Cai, Wen;Wu, Lijun;Li, Hongtao;Liu, Haobao
作者机构:
关键词: Bacillus cereus; Enzyme property; Low molecular weight; Production; Purification; Xylanase
期刊名称:BRAZILIAN JOURNAL OF MICROBIOLOGY ( 影响因子:2.2; 五年影响因子:2.8 )
ISSN: 1517-8382
年卷期: 2023 年
页码:
收录情况: SCI
摘要: Xylanase is widely used in various industries such as food processing, paper, textiles, and leather tanning. In this study, Bacillus cereus L-1 strain was isolated and identified as capable of producing low molecular weight xylanase through 16 s rRNA sequencing. Maximum xylanase yield of 15.51 +/- 2.08 U/mL was achieved under optimal fermentation conditions (5% inoculum, 20 g/L xylan, pH 6.0, for 24 h). After purification via ammonium sulfate precipitation and High-S ion exchange chromatography, electrophoretic purity xylanase was obtained with a 28-fold purification and specific activity of 244.97 U/mg. Xylanase had an optimal pH of 6.5 and temperature of 60 degrees C and displayed thermostability at 30 degrees C and 40 degrees C with 48.56% and 45.97% remaining activity after 180 min, respectively. The xylanase retained more than 82.97% of its activity after incubation for 24 h at pH 5.0 and was sensitive to metal ions, especially Mg2+ and Li+. Purified xylanase showed a molecular weight of 23 kDa on SDS-PAGE, and partial peptide sequencing revealed homology to the endo-1,4-beta-xylanase with a molecular weight of 23.3 kDa through LC/MS-MS (liquid chromatography-tandem mass spectrometry). This study suggests that the purified xylanase is easier to purify and enriches low molecular weight xylanases from bacteria source.
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