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海栖热袍菌极端耐热木聚糖酶B的提纯

Purification of an Extrem-thermostable Xylanase B From Thermotoga maritima

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【作者】 江正强; 李里特; 林清; Mohammad Mainul Ahsan;

【Author】 Jiang Zhengqiang 1 Li Lite 1 Kyoshi Hayashi 2 Mohammad Mainul Ahsan 2 (1 College of Food Science and Engineering, CAU 2 Enzyme Applications Laboratory of National Food Research Institute in Japan)

【机构】 中国农业大学食品学院; 日本食品综合研究所酵素利用研究室; 日本食品综合研究所酵素利用研究室;

【摘要】 克隆并在大肠杆菌中表达的海栖热袍菌的 xyn B基因 ,其表达产物木聚糖酶 B的 C 末端带有 6×His标签 ,研究了这种基因重组酶的提纯方法。通过对粗酶提取液的热变性处理 ,Ni NTA亲和柱层析和离子柱层析 ,最终得到了电泳纯的木聚糖酶 B,提纯倍数 4 4.4 ,得率 11。SDS PAGE法测定木聚糖酶 B的相对分子质量为 4 2 ku,与理论推算值 4 2 333u相吻合

【Abstract】 The xyn B gene of Thermotoga maritima MSB8 was cloned and expressed in E.coli , the C terminal His tag was introduced, and purification methods of the recombinant enzyme were studied. The xylanase B was purified to homogeneity by heat treatment, affinity chromatography and ion exchange chromatography. The purified enzyme showed as a single protein band on SDS PAGE with a molecular weight of 42 ku, this is in good agreement with the molecular mass of enzyme deduced from the DNA sequence, 42 333 u.

【基金】 联合国大学基金资助项目
  • 【文献出处】 中国农业大学学报 ,Journal of China Agricultural University , 编辑部邮箱 ,2001年06期
  • 【分类号】O629
  • 【被引频次】20
  • 【下载频次】215
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