酶法体外高效制备信号分子(pp)pGpp
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作者单位:

作物遗传改良全国重点实验室/湖北洪山实验室/华中农业大学生命科学技术学院,武汉 430070

作者简介:

陈传玉,E-mail:chenchuanyuhazu@163.com

通讯作者:

张德林:zdl@mail.hzau.edu.cn

中图分类号:

Q503

基金项目:

国家自然科学基金面上项目(31770878)


Efficient preparation of signal molecule (pp)pGpp in vitro by enzymatic method
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Affiliation:

National Key Laboratory of Crop Genetic Improvement/Hubei Hongshan Laboratory/ College of Life Science and Technology,Huazhong Agricultural University,Wuhan 430070,China

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    摘要:

    针对目前信使分子(pp)pGpp提取和合成成本高、时间长、技术难的问题,以现有的体外酶合成(pp)pGpp的方法为基础,建立和优化了新的体外合成技术。结果显示,通过(pp)pGpp合成酶RelA、GppA和YvcI在25 mmol/L Tris-HCl(pH 9.0)、15 mmol/L MgCl2、100 mmol/L NaCl条件下于37 ℃反应30 min,经阴离子交换进一步纯化,即可获得高纯度(pp)pGpp分子。此方法与传统的细菌或植物体内直接提取、现有的体外酶法制备流程相比,具有操作简单、快速、成本低、环境友好等优势,能够满足下游生化分析和结构生物学实验需求,为微生物信号通路及开发新的抗菌药物研究提供物质基础。

    Abstract:

    In view of the problems of high cost,long time and technical difficulty in the extraction and synthesis of messenger molecule (pp)pGpp,a new in vitro synthesis technology was established and optimized based on the existing in vitro enzymatic synthesis of (pp)pGpp.This method achieves the goals of high efficiency,convenience,safety and environmental protection,and low cost.The results showed that high purity (pp)pGpp can be obtained by reacting (pp)pGpp synthases:RelA,GppA and YvcI in 25 mmol/L Tris-HCl pH 9.0,15 mmol/L MgCl2,100 mmol/L NaCl at 37 °C for 30 minutes,and further purified by anion exchange (pp)pGpp molecule.Compared with the traditional direct extraction from bacteria or plants and the existing in vitro enzymatic preparation process,this method has the advantages of simple operation,rapidity,low cost,and environmental friendliness,and can meet the needs of downstream biochemical analysis and structural biology experiments.More importantly,it provides a material basis for microbial signaling pathways and the development of new antibacterial drugs.

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陈传玉,谭樊杰,殷平,张德林.酶法体外高效制备信号分子(pp)pGpp[J].华中农业大学学报,2022,41(4):271-278

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  • 收稿日期:2022-05-08
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  • 在线发布日期: 2022-10-12
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