| 摘要: |
| 【目的】克隆南方番茄病毒(STV)的外壳蛋白(CP)基因，构建其原核表达载体并进行诱导表达，为制备检测该病毒的高效价血清提供参考。【方法】利用一步法RT-PCR从新疆加工番茄上克隆STV CP基因，将其连接到原核表达载体pET-28a(+)上，获得重组质粒pET-28a-STV CP。将重组质粒转化大肠杆菌BL21后用IPTG进行诱导表达。【结果】成功克隆了STV CP基因，其长度为1 134 bp。构建了原核重组表达质粒pET-28a-STV CP，其在1 mmol/L IPTG诱导下，成功表达出分子质量约47 ku的蛋白。【结论】成功克隆了STV CP基因，并诱导了pET-28a-STV CP重组蛋白的原核表达。 |
| 关键词: 南方番茄病毒 外壳蛋白基因 原核表达 |
| DOI： |
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| 基金项目:国家自然科学基金项目(31260420）；国际科技合作与交流专项(20072072) |
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| Cloning and prokaryotic expression of coat protein gene of Southern tomato virus from processing tomato in Xinjiang |
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ZHANG Qiang,CUI Bai-ming,ZHENG Yin-ying,et al
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| Abstract: |
| 【Objective】This paper aimed to clone the coat protein (CP) gene of Southern tomato virus (STV),and construct and express its prokaryotic expression vector,providing reference for preparation and detection of high titer serum of the virus.【Method】The STV CP gene was cloned by One-Step RT-PCR and connected with pET-28a(+) to obtain pET-28a-STV CP.Then the recombinant plasmid was transformed into E.coli BL21 and induced by IPTG.【Result】The STV CP gene was cloned successfully with the size of 1 134 bp and prokaryotic expression vector pET-28a-STV CP was also constructed.The CP protein with molecular weight of 47 ku was highly expressed after being induced by 1 mmol/L IPTG.【Conclusion】STV CP gene was successfully cloned,and the expression of recombinant protein was induced successfully. |
| Key words: Southern tomato virus coat protein gene prokaryotic expression |
