Gomaa Ahmed E, Zhang Chen, Yang Zhimin, Shang Liguo, Jiang Shijie, Deng Zhiping, Zhan Yuhua, Lu Wei, Lin Min, Yan Yongliang
Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing, 100081, People's Republic of China.
AMB Express. 2017 Dec;7(1):125. doi: 10.1186/s13568-017-0425-y. Epub 2017 Jun 17.
Vector-free allele exchange (VFAE) is a newly developed protocol for genome editing in Pseudomonas species. Although several parameters have been determined to optimize the procedures for obtaining a stable and high-frequency mutation, numerous false-positive clones still appear on the plate, which increases the difficulty of finding the desired mutants. It has also not been established whether this protocol can be used for genome editing in other bacterial species. In the current study, the protocol was modified to dramatically decrease the occurrence of false-positive colonies using Pseudomonas stutzeri A1501 as a model strain. This improvement was reached by increasing the occurrence of circular-DNA cassettes of the correct size. Furthermore, the enhanced protocol was used to construct mutants in both the gram-negative Escherichia coli BL21 and gram-positive Bacillus subtilis 168 strains. The protocol works well in both strains, yielding ideal results with a low percentage of false-positive colonies. In summary, the enhanced VFAE mutagenesis protocol is a potential tool for use in bacterial genome editing.
无载体等位基因交换(VFAE)是一种新开发的用于假单胞菌属物种基因组编辑的方法。尽管已经确定了几个参数来优化获得稳定且高频突变的程序,但平板上仍出现大量假阳性克隆,这增加了找到所需突变体的难度。此外,该方法是否可用于其他细菌物种的基因组编辑尚未确定。在本研究中,以施氏假单胞菌A1501为模型菌株,对该方法进行了改进,以显著减少假阳性菌落的出现。通过增加正确大小的环状DNA盒的出现频率实现了这一改进。此外,改进后的方法用于构建革兰氏阴性大肠杆菌BL21和革兰氏阳性枯草芽孢杆菌168菌株的突变体。该方法在两种菌株中均有效,产生理想结果,假阳性菌落比例较低。总之,改进后的VFAE诱变方法是一种潜在的用于细菌基因组编辑的工具。