BBSRC/EPSRC Synthetic Biology Research Centre (SBRC), School of Life Sciences, Biodiscovery Institute, University of Nottingham, University Park, Nottingham NG7 2RD, U.K.
ACS Synth Biol. 2023 Feb 17;12(2):544-554. doi: 10.1021/acssynbio.2c00554. Epub 2023 Jan 23.
Methanotrophic bacteria are Gram-negative, aerobic organisms that use methane as their sole source of carbon and energy. In this study, we constructed and exemplified a CRISPR/Cas9 genome editing system and used it to successfully make gene deletions and insertions in the type I methanotroph Bath and the type II methanotroph OBBP. High frequencies of gene deletions and insertions were achieved in combination with homology-directed repair. In OBBP, we also investigated the impact of several parameters on the CRISPR/Cas9 genome editing, where the gene was targeted with various PAM sequences and guide RNA spacer sequences, homology arms of variable length, differences in the duration of mating during conjugation, and exploiting promoters of different strengths to control the expression of cas9 and sgRNA. Although not the first attempt to develop a CRISPR/Cas system in methanotrophs, this work demonstrated for the first time an efficient CRISPR/Cas9 system generating scarless clean gene deletions and insertions in methanotroph genomes.
产甲烷菌是革兰氏阴性、需氧的生物体,它们将甲烷作为唯一的碳源和能源。在本研究中,我们构建并举例说明了一个 CRISPR/Cas9 基因组编辑系统,并成功地在 I 型甲烷营养菌 Bath 和 II 型甲烷营养菌 OBBP 中进行了基因缺失和插入。同源定向修复与高频基因缺失和插入相结合。在 OBBP 中,我们还研究了几个参数对 CRISPR/Cas9 基因组编辑的影响,其中用不同的 PAM 序列和向导 RNA 间隔序列、不同长度的同源臂、在接合过程中交配时间的差异以及利用不同强度的启动子来控制 cas9 和 sgRNA 的表达来靶向 基因。虽然这不是首次尝试在产甲烷菌中开发 CRISPR/Cas 系统,但这项工作首次证明了一种有效的 CRISPR/Cas9 系统,能够在产甲烷菌基因组中产生无痕的清洁基因缺失和插入。