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C型产气荚膜梭菌α毒素基因核苷酸序列的测定与分析 被引量:1

Detection and Analysis of Nucleotide Sequence of Alpha-toxin Gene of Clostridium perfringens Type C
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摘要 [目的]研究C型产气荚膜梭菌α毒素基因核苷酸序列的遗传变异特点。[方法]设计产气荚膜梭菌α毒素基因特异性引物进行PCR扩增,扩增产物纯化后测定核苷酸序列并与NCBI登录的参考序列通过DNAStar软件进行同源比对。[结果]序列分析表明,所测菌株α毒素基因核苷酸组成中腺苷酸含量较高,胞苷酸含量较低。所测菌株与13、C57-1、CER 89L43、S01、S08、T01以及T16菌株的核苷酸序列同源性分别为98.7%、98.7%、98.6%、98.8%、98.7%、97.0%、98.6%,推导的氨基酸序列同源性分别为98.6%、98.6%、98.9%、98.9%、98.9%、98.6%、98.6%。[结论]所测C型产气荚膜梭菌α毒素基因核苷酸序列及推导的氨基酸序列与参考序列同源性均较高。 [Objective]The aim was to study the genetic variation characteristic of nucleotide sequence of alpha-toxin gene within Clostridium perfringens type C.[Method]The special primers of alpha-toxin gene within Clostridium perfringens were designed for PCR amplification.Nucleotide sequence was detected after purification of the PCR products and was compared with the NCBI reference sequences by the DNAStar software.[Result]Sequence analysis indicated that adenosine was higher and cytidine was lower in the tested strain.The rate of nucleotide sequence homology between the tested strain and strain 13,C57-1,CER 89L43,S01,S08,T01,T16 was 98.7%,98.7%,98.6%,98.8%,98.7%,97.0%,98.6% and homology of the deduced a mino acid sequence was 98.6%,98.6%,98.9%,98.9%,98.9%,98.6%,98.6% respectively.[Conclusion]Nucleotide sequence of alpha-toxin gene within Clostridium perfringens type C and the deduced a mino acid sequence both had high homology with the reference sequences.
出处 《安徽农业科学》 CAS 北大核心 2011年第32期19681-19683,共3页 Journal of Anhui Agricultural Sciences
基金 青海大学高层次人才引进项目(2008-QGC-9)
关键词 C型产气荚膜梭菌 Α毒素 同源性 Clostridium perfringens type C Alpha-toxin Homology
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  • 1王景林,杨利敏,吴东林,康琳.重组CPTα的亲和纯化及其单克隆抗体的制备[J].军事医学科学院院刊,2004,28(4):308-310. 被引量:1
  • 2赵立峰,任家琰.产气荚膜梭菌α毒素的研究进展[J].经济动物学报,2004,8(4):243-246. 被引量:2
  • 3许崇波,许崇利,赵志军.A型产气荚膜梭菌α毒素基因表达及其免疫保护作用的初步研究[J].微生物学报,2006,46(4):624-628. 被引量:17
  • 4张红英,杨霞,陈丽颖,王亚宾,金钺,郑杰,卢中华.抗A型产气荚膜梭菌单克隆抗体的研制和鉴定[J].中国畜牧兽医,2006,33(9):62-64. 被引量:5
  • 5URBINA P.Unexpected wide substrate specificity of C.perfringensα-toxinphospholipase C[J].Biochimica et Biophysica Acta,2011,1808:2618-2627.
  • 6URBINA P.Effects of bilayer composition and physical properties on thephospholipase C and sphingomyelinase activities of Clostridium perfringensα-toxin[J].Biochimica et Biophysica Acta,2011,1808:279-286.
  • 7MORRIS W E.Effects of Clostridium perfringens alpha and epsilon toxinsin the bovine gut[J].Anaerobe,2012,18:143-147.
  • 8ODA M.New insight from basic research of Clostridium perfringens alpha-toxin[J].Nihon Rinsho,2012,70(8):1313-1317.
  • 9SAITO H.Identification and sequence determination of recombinant Clos-tridium perfringens alpha-toxin by use of electrospray ionization massspectrometry[J].Rinsho Biseibutshu Jinsoku Shindan Kenkyukai Shi,2009,20(1/2):9-20.
  • 10NAGAHAMA M,ODA M,KOBAYASHI K,et al.A recombinant carboxy-terminal domain of alpha-toxin protects mice against Clostridium perfrin-gens[J].Microbiol Immunol,2013,57(5):340-345.

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