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中国长白山乌苏里蝮蛇降纤酶基因克隆和结构分析

Gene Cloning and Sequence Analysis of Defibrasefrom Gloydius ussuriensis Snake

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【作者】 孙德军闫琪杨春伟杨同书颜伟群侯立中

【Author】 SUN De jun 1,YAN Qi 2,YANG Chun wei 1,YANG Tong shu 1, YAN Wei qun 1,HOU Li zhong 1(1.Institute of Frontier Medical Science,Jilin University, Changchun 130021,China;2. Changchun College of Traditional Chinese Medicine)

【机构】 吉林大学再生医学科学研究所生物化学教研室长春中医学院吉林大学再生医学科学研究所生物化学教研室 吉林长春130021吉林长春130021吉林长春130021

【摘要】 目的 :克隆乌苏里蝮蛇 ( Gloydius ussuriensis)降纤酶 ( Difibrase)基因 ,为用基因工程方法生产降纤酶打下基础。方法 :从乌苏里蝮蛇毒腺制备总 RNA,经 RT- PCR扩增、克隆和顺序测定。结果 :降纤酶 c DNA开框读码序列全长 70 2个核苷酸 ,编码 2 34个氨基酸 ,推测其活性中心为His41、Asp86和 Ser180 ,含有 6对二硫键。结论 :确定乌苏里蝮蛇降纤酶 c DNA顺序 ,推导出其氨基酸顺序和活性中心结构。

【Abstract】 Objective:To clone gene sequence of defibrase from venom gland of Gloidius ussuriensis and gett gene product of defibrase in the future. Methods:Total RNAs were extracted from the venom gland of the Gloydins Ussurisis snake.The thrombin like enzyme gene was amplified by RT PCR, cloned, and its nucleotide sequences had been determined.Results:The enzyme called defibrase cDNA encodes 702 nucleotides, namely 234 amino acids. Based on the homology, the catalytic residues and disulfide bridges of defibrase were deduced as followings: catalytic residues, His 41 ,Asp 86 , Ser 180 and six disulfide bridges. Conclusion:cDNA sequence of defibrase was proved, amino acid sequence and structure of active center were deduced.

【关键词】 乌苏里蝮蛇降纤酶克隆序列分析
【Key words】 Gloidius ussurisisDefibraseCloneSequence analysis
【基金】 国家自然科学基金资助项目 (39870 375 )
  • 【文献出处】 吉林大学学报(医学版) ,Journal of Norman Bethune University of Medical Science , 编辑部邮箱 ,2003年02期
  • 【分类号】R346
  • 【被引频次】7
  • 【下载频次】124
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