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一株产纤溶酶菌株的分离鉴定及其纤溶组分分析
引用本文:袁慎亮,邢德明,窦少华,王晓辉,张庆芳,迟乃玉.一株产纤溶酶菌株的分离鉴定及其纤溶组分分析[J].微生物学通报,2014,41(9):1843-1849.
作者姓名:袁慎亮  邢德明  窦少华  王晓辉  张庆芳  迟乃玉
作者单位:1.大连大学 生命科学与技术学院 辽宁省海洋微生物工程技术研究中心 辽宁 大连 116622;1.大连大学 生命科学与技术学院 辽宁省海洋微生物工程技术研究中心 辽宁 大连 116622; 2.沈阳农业大学 食品学院 辽宁 沈阳 110866;1.大连大学 生命科学与技术学院 辽宁省海洋微生物工程技术研究中心 辽宁 大连 116622;1.大连大学 生命科学与技术学院 辽宁省海洋微生物工程技术研究中心 辽宁 大连 116622;1.大连大学 生命科学与技术学院 辽宁省海洋微生物工程技术研究中心 辽宁 大连 116622;1.大连大学 生命科学与技术学院 辽宁省海洋微生物工程技术研究中心 辽宁 大连 116622
基金项目:国家863计划项目(No. 2007AA021306)
摘    要:【目的】筛选性能良好的产纤溶酶菌株,对菌株进行多项分类鉴定,分析其纤溶酶系的组成特征及纤溶能力。【方法】通过酪蛋白培养基初筛,琼脂-纤维蛋白双层平板复筛,从海泥、土壤等环境中筛选纤维蛋白降解菌,以尿激酶为标准测定纤溶酶活性。通过形态学、生理生化特征研究,结合16S rDNA基因序列分析菌株种类及系统分类地位。通过SDS-PAGE和纤维蛋白酶谱法分析胞外纤溶酶系的组成特征。【结果】筛选到一株能降解纤维蛋白的细菌CNY16,鉴定其为沙福芽孢杆菌(Bacillus safensis)。该酶为胞外酶,SDS-PAGE和纤维蛋白酶谱结果表明该纤溶酶系有至少两种分子量大小不同的纤溶酶,分别约33 kD和23 kD。能有效溶解血块中纤维蛋白,并且对红细胞无降解作用。【结论】细菌CNY16是一株新的纤溶酶产生菌,纤溶酶活性及稳定性较好,具有潜在开发价值。为获取新型纤溶酶提供了一种新的菌源。

关 键 词:纤溶酶,沙福芽孢杆菌,鉴定,纤维蛋白酶谱

Isolation and identification of a fibrinolytic enzyme producing bacterium and its analysis of the fibrinolytic components
YUAN Shen-Liang,XING De-Ming,DOU Shao-Hu,WANG Xiao-Hui,ZHANG Qing-Fang and CHI Nai-Yu.Isolation and identification of a fibrinolytic enzyme producing bacterium and its analysis of the fibrinolytic components[J].Microbiology,2014,41(9):1843-1849.
Authors:YUAN Shen-Liang  XING De-Ming  DOU Shao-Hu  WANG Xiao-Hui  ZHANG Qing-Fang and CHI Nai-Yu
Institution:1. Liaoning Marine Microbial Engineering and Technology Center, College of Life Science and Technology, Dalian University, Dalian, Liaoning 116622, China;1. Liaoning Marine Microbial Engineering and Technology Center, College of Life Science and Technology, Dalian University, Dalian, Liaoning 116622, China; 2. College of Food Science, Shenyang Agricultural University, Shenyang, Liaoning 110866, China;1. Liaoning Marine Microbial Engineering and Technology Center, College of Life Science and Technology, Dalian University, Dalian, Liaoning 116622, China;1. Liaoning Marine Microbial Engineering and Technology Center, College of Life Science and Technology, Dalian University, Dalian, Liaoning 116622, China;1. Liaoning Marine Microbial Engineering and Technology Center, College of Life Science and Technology, Dalian University, Dalian, Liaoning 116622, China;1. Liaoning Marine Microbial Engineering and Technology Center, College of Life Science and Technology, Dalian University, Dalian, Liaoning 116622, China
Abstract:Objective] To isolate and identify a fibrinolytic enzyme producing bacterium, and to analyze the component and characteristic of fibrinolytic enzyme. Methods] Plasmin-producing bacterium was isolated by casein medium and AGAR-fibrin double-layer tablets from sea mud, soil, etc. Then its enzyme activity was measured by urokinase standard curve. The morphological, biochemical and physiological characteristics and 16S rDNA gene were analyzed to identify the taxonomic position of strain CNY16. The composition of the extracellular plasmin system was analyzed by SDS-PAGE and fiber protease zymogram. Results] A strain named CNY16 with fibrinolytic activity was isolated and identified as Bacillus safensis. The results of SDS-PAGE and fiber protease zymogram showed that the extracellular fibrinolytic enzyme system contained at least two fibrinolytic enzymes with molecular masses of approximately 33 kD and 23 kD, respectively. The plasmin effectively dissolved fibrin clots, but did not hydrolyze blood cells. Conclusion] CNY16 was a novel plasmin-producing bacterium, the fibrinolytic enzyme produced by strain CNY16 hold the valuable property in high activity and good stability. The strain might provide a new source for novel fibrinolytic enzymes.
Keywords:Fibrinolytic enzyme  Bacillus safensis  Identification  Fiber protease zymogra
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