在Saccharopolyspora erythraea中使用CRISPR/Cas9介导的促进器工程
Yue Zhang1,2, Hui Qi3,4,5, Meng Wang6,7
1Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China. zhangy@tib.cas.cn.
Methods in molecular biology (Clifton, N.J.)
|July 27, 2024
概括
这项研究介绍了一种CRISPR/Cas9协议,用于Saccharopolyspora erythraea的现场促进器工程. 这种方法可以在不添加额外的DNA序列的情况下在actinomycetes中精确编辑基因.
科学领域:
- 微生物学 微生物学
- 分子生物学分子生物学
- 生物技术是生物技术.
背景情况:
- 在现场促进器工程修改基因表达没有外来DNA.
- 克里斯普尔/Cas9技术促进了有效的,无痕迹的基因组编辑.
研究的目的:
- 描述CRISPR/Cas9介导促进器工程的常规协议.
- 为了在Saccharopolyspora erythraea中实现精确的基因修饰NRRL 23338.8.
主要方法:
- 利用CRISPR/Cas9系统进行针对性基因组编辑.
- 开发了一种S. erythraea.在现场促进器工程中的协议.
主要成果:
- 建立了一种可靠的无痕基因编辑方法.
- 证明了CRISPR/Cas9对促进体修饰的有效性.
结论:
- 该协议提供了一种有效的方法,用于S. erythraea.ea中的促进体工程.
- 这种方法可以适应在其他类型菌体中更广泛的CRISPR/Cas9介导基因编辑.
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