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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2014, Vol. 34 Issue (10): 49-54    DOI: 10.13523/j.cb.20141008
研究报告     
纳豆激酶基因在大肠杆菌中的表达及活性分析
韩慧明1, 李咏梅2
1. 北华大学基础医学院 吉林 132013;
2. 北华大学口腔医学院 吉林 132013
Secretory Expression of Nattokinase from Bacillus natto in Escherichia coli
HAN Hui-ming1, LI Yong-mei2
1. Basic Medical College, Beihua University, Jilin 132013, China;
2. School of Stomatology, Beihua University, Jilin 132013, China
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摘要:

目的:构建纳豆激酶基因的表达载体,鉴定其在大肠杆菌中的表达及表达产物的生物活性鉴定.方法:以纳豆芽胞杆菌基因组为模板,PCR技术克隆出纳豆激酶基因的成熟肽序列,分别克隆进具有信号肽的pMAL-p2x及无信号肽pMAL-c2x质粒中,经酶切和测序鉴定其正确性,分别将重组质粒转化至大肠杆菌中表达.结果:成功构建的两组重组质粒在IPTG诱导下,均能分别在37℃及16℃条件下表达出可溶性的融合蛋白,SDS-PAGE胶检测证实重组质粒在大肠杆菌中可表达出相对分子量约76kDa的纳豆激酶蛋白.纤维蛋白平板实验证明两种融合蛋白均有活性,且有信号肽的融合蛋白的酶活较无信号肽的融合蛋白高.结果:成功构建了两组重组纳豆激酶基因的表达质粒,且该两组重组基因在大肠杆菌中可溶性表达并具有生物活性,因此为下一步研究表达产物纳豆激酶的功能、应用和生产奠定了基础.

关键词: 纳豆激酶基因表达大肠杆菌纤溶活性    
Abstract:

Nattokinase has been reported as an oral health product for the prevention of atherosclerosis. A novel strategy to express a nattokinase from Bacillus natto in a live delivery vehicle E. coli BL21(DE3) was developed. The mature peptide-coding fragment of NK gene was amplified from B. natto total DNA by polymerase chain reaction (PCR). The sequence analysis indicated that the fragment of NK gene consisted of 825 bp, which encoded 275 amino acid residues. The sequence of NK gene has 99% homology with those of the reported ones. The expression plasmids NK-pep-pMAL-p2X and NK-pep-pMAL-c2X are constructed by inserting NK gene into vector pMAL-p2X and pMAL-c2X, and then fusionally expressed with maltose-binding protein (MBP) in Escherichia coli BL21(DE3). SDS-PAGE analysis revealed that the NK protein were secretion expressed after induction with IPTG for 4 hours under 16℃ or 37℃.The characteristic of this recombinant nattokinase is comparable to the native nattokinase. Secretory expression of nattokinase in E. coli would facilitate the development of this enzyme into a therapeutic product for the control and prevention of thrombosis diseases.

Key words: Nattokinase    Gene expression    E. coli    Fibrinolytic
收稿日期: 2014-08-12 出版日期: 2014-10-25
ZTFLH:  Q786  
基金资助:

吉林省卫生厅计划项目(20122097)资助项目

通讯作者: 李咏梅     E-mail: lymjyx@126.com
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引用本文:

韩慧明, 李咏梅. 纳豆激酶基因在大肠杆菌中的表达及活性分析[J]. 中国生物工程杂志, 2014, 34(10): 49-54.

HAN Hui-ming, LI Yong-mei. Secretory Expression of Nattokinase from Bacillus natto in Escherichia coli. China Biotechnology, 2014, 34(10): 49-54.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/10.13523/j.cb.20141008        https://manu60.magtech.com.cn/biotech/CN/Y2014/V34/I10/49


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