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从细菌体囊蛋白中设计的可以作为合成转录抑制剂起作用
Pankaj V Sharma1, Sriyans Jain2, Ranjan Sen2
1Laboratory of Transcription, Center for DNA Fingerprinting and Diagnostics, Hyderabad, India; Graduate Studies, Manipal Academy of Higher Education, Manipal, Karnataka, India.
The Journal of biological chemistry
|October 21, 2023
概括
从细菌体Psu蛋白中获得的合成可以通过与核酸结合来抑制细菌基因转录. 这些新型的转录抑制剂通过降低基因表达的调节和影响大肠杆菌中的细胞分裂,显示出作为抗菌剂的潜力.
科学领域:
- 分子生物学分子生物学
- 抗菌研究 抗菌研究
- 细菌生物学的生物学
背景情况:
- 菌体Psu蛋白抑制了细菌转录终止因子Rho.
- 以前设计的Psu C-终端作为Rho抑制剂用于新型抗菌剂.
- 这些体表现出正面电荷,并在大肠杆菌中降低基因表达.
研究的目的:
- 为了研究由Psu衍生的的基因抑制机制.
- 确定这些的核酸结合特性和特异性.
- 评估这些合成转录抑制剂的体外和体内效应.
主要方法:
- 在体外转录试验中使用T7A1和Plac促进体.
- 在体内对大肠杆菌的基因表达分析.
- 电泳运动转移测定 (EMSA) 和异热定位热量计 (ITC) 用于研究核酸结合.
主要成果:
- 33有效地抑制转录,通过阻止RNA聚合酶进入促进体.
- 活体内的表达降低了总RNA水平和来自特定促进者的转录 (Plac,Posm).
- 33与单链DNA (ssDNA),双链DNA (dsDNA) 和具有微分子亲和力的RNA结合,更喜欢ssDNA和RNA;结合具有耐盐性和序列非特异性.
结论:
- 通过与核酸相互作用,PSU衍生作为合成转录抑制剂起作用.
- 这些具有类似于非特异性ssDNA结合蛋白和细菌核相关蛋白的特性.
- 观察到的细胞延长和细胞分裂受损表明它们有可能作为新型抗菌剂.
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