| 刘丽娜,胡福泉,朱军民,赵岩,潘渠,李明,唐家琪.猪链球菌2型溶血素sly基因的表达及其产物的纯化和活性研究[J].中华流行病学杂志,2007,28(12):1198-1202 |
| 猪链球菌2型溶血素sly基因的表达及其产物的纯化和活性研究 |
| Study on expression of Streptococcus suis serotype 2 sly gene, purification and activity of its product |
| 收稿日期:2007-08-30 出版日期:2014-09-12 |
| DOI： |
| 中文关键词: 猪链球菌2型 sly基因 表达 活性研究 |
| 英文关键词: Streptococcus suis serotype 2 sly gene Expression Activity analysis |
| 基金项目:1.国家高技术研究发展计划(863计划)，2.国家自然科学基金 |
| 作者 | 单位 | E-mail | | 刘丽娜 | 第三军医大学基础医学部微生物学教研室, 重庆, 400038 | | | 胡福泉 | 第三军医大学基础医学部微生物学教研室, 重庆, 400038 | | | 朱军民 | 第三军医大学基础医学部微生物学教研室, 重庆, 400038 | | | 赵岩 | 第三军医大学基础医学部微生物学教研室, 重庆, 400038 | | | 潘渠 | 第三军医大学基础医学部微生物学教研室, 重庆, 400038 | | | 李明 | 第三军医大学基础医学部微生物学教研室, 重庆, 400038 | | | 唐家琪 | 南京军区军事医学研究所 | tjq85@botmail.com |
|
| 摘要点击次数: 2451 |
| 全文下载次数: 0 |
| 中文摘要: |
| 目的克隆并表达猪链球菌2型(SS2)溶血素基因(sly),为筛选SS2疫苗保护性抗原奠定基础.方法用PCR方法从SS2临床分离株05ZYH33的基因组DNA中扩增出溶血素基因片段,将目的 基因插入表达载体pET-30b(+)中,构建重组表达载体pET30b-sly.重组载体经限制性内切酶酶切和DNA测序鉴定后,转化大肠埃希菌(E.coli Rosetta).IPTG诱导表达,镍离子亲和层析纯化重组蛋白,鉴定目的蛋白的免疫学活性以及溶血活性.结果PCR扩增的sly基因长度约为1500 bp,经测序分析,插入载体的sly基因序列准确并保持了正确的读框.经IPTG诱导的目的蛋白表达量约占总蛋白的30%,亲和层析纯化后,蛋白纯度达80%以上.Western blot检测证实该蛋白能与感染SS2的人血清发生特异性结合.溶血试验表明重组蛋白溶血素能使猪红细胞发生溶解,溶血价为256.结论 成功构建了表达载体pET30b-sly,该载体可在大肠埃希菌中表达,表达蛋白具有免疫反应原性及溶血活性. |
| 英文摘要: |
| ObjectiveTo clone and express Streptococcus suis serotype 2(S.suis 2) sly gene for constructing an foundation on identification of S.suis 2 protective antigen.MethodsThe sly gene was amplified from S.suis 2 clinical isolate strain 05ZYH33 genome DNA by PCR.The gene fragment was inserted into the expression vector pET-30b(+) to build pET3Ob-sly.When recombinant vector pET30b- sly was identified by restriction enzyme cutting and DNA sequencing as a correct one,subsequently it was transformed to E.coli Rosetta for expression under IPTG induction.The obtained fusion protein was purified by Ni-NTA affinity chromatography.The immunologic and hemolysis activity of the purified protein was proved through Western blot and hemolysis assay respectively.ResultsThe PCR product was around 1500 bp.The gene segment inserted into the recombinant vector was proven to be completely identical with the sly gene sequence in the total genome sequence of S.suis 2.The target protein expressed was up to 30 % of the total somatic protein under IPTG induction.The protein purity reached above 80 % after purification.The protein could be recognized by human serum infected with S.suis 2 and could dissolve swine erythrocytes with the Hemolytic titer as 256.ConclusionThe expression vector pET30b- sly was successfully constructed.The target protein could be over-expressed in E.coli and possessed its biological activity after purification. |
|
查看全文
Html全文
查看/发表评论 下载PDF阅读器 |
|
| 关闭 |
|
|
|
