炭疽杆菌
内切酶
可选择标记
生物
遗传学
基因
核酸内切酶
遗传标记
计算生物学
质粒
细菌
作者
Yanchun Wang,Li-si Yuan,Haoxia Tao,Wei Jiang,Chunjie Liu
标识
DOI:10.1016/j.mimet.2018.05.024
摘要
Several genetic tools have been developed for use in Bacillus anthracis, but there is still a need for a more marker-free gene inactivation protocols. Thus, we report a method to generate unmarked mutations in B. anthracis. This approach was based on the counter-selectable pheS* gene with assistance by the I-SceI homing endonuclease. Using this strategy, the NprR gene, a transcriptional activator of B. anthracis, was deleted at an extremely high efficiency. Our study indicates that mutated pheS is a useful counter-selective marker to design a valuable genetic tool for in-frame and unmarked gene deletions of B. anthracis.
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