中华鲟半胱氨酸蛋白酶抑制剂C基因的原核表达
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中国水产科学研究院珠江水产研究所

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中国水产科学院基金,广东省自然科学基金


Expression of Acipenser sinensis cystatin C in prokaryote
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Key Laboratory of Tropical & Subtrop ical Fish Breeding & Cultivation Certificated by the Ministry of Agriculture . Pearl River Fishery Research I nstitute , Chinese Academy of Fishery Sciences, Guangz hou .. 510380, China

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    摘要:

    为了研究鱼类半胱氨酸蛋白酶抑制剂(cystatm)的功能并探索其在水产品加工和病害防治中的应用潜力,将改造后的中华鲟(Acipenser sinensis)cystatin C cDNA亚克隆到原核表达载体pBV220,构建表达cystatin C的大肠杆菌基因工程菌.该工程菌经温度诱导、SDS-PAGE检测,在约12.4 kD处有一特异蛋白带,该特异蛋白的含量约为菌体总蛋白的25%.重组半胱氨酸蛋白酶抑制剂经洗涤、溶解、透析、复性后纯度为85%,实现了中华鲟cystatin C在大肠杆菌中的高效表达.木瓜蛋白酶活性抑制实验结果表明该重组cystatin C具有明显的酶活抑制作用.

    Abstract:

    In order to explore the functions of f ish cystatin and the potential values in the f ish disease prevention and cure, as well as seafood process industry, polymerase chain reaction ( PCR) technique was used to modify the cDNA of Chinese sturgeon ( Acipenser sinensis ) cystatin mature peptide, The cDNA was subcloned into expression vector pBV220, then a cystat in recombinant expression bacteria was constructed. After temperature inducement and SDS..PAGE analysis, the recombinant expression bacteria produced a special protein about 12. 4 kD in molecular weight. The proportion of recombinant protein in total bacterial protein was about 25%. The purity of the recombinant cystatin, which was washed, dissolved, dialysed and renatured, was about 85%. The inhibitory activity of recombinant cystatin could be measured by inhibiting the protease activity of papain. The inhibitory activity of recombinant cystatin was 48U....g- 1.

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马冬梅.中华鲟半胱氨酸蛋白酶抑制剂C基因的原核表达[J].水产学报,2003,27(3):

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  • 收稿日期:2014-03-18
  • 最后修改日期:2014-03-18
  • 录用日期:2014-03-18
  • 在线发布日期: 2014-03-18
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