合成生物学
生物
甲基营养素
嗜热菌
计算生物学
生产过剩
质粒
代谢工程
电穿孔
基因组编辑
基因组
模式生物
重组工程
染色体
遗传学
系统生物学
多路复用
基因
工业生物技术
内切酶
基因组工程
工业微生物学
细菌人工染色体
染色体分离
可进化性
代谢途径
杆菌科
清脆的
基因组学
生物生产
作者
Pan Liu,Qianqian Yuan,Xueting Yang,Qian Wang,Tao Chang,Yaning Bi,Peng Wu,Tong Zhang,Jinxing Yang,Shiting Guo,Chaoyou Xue,Zhaojuan Zheng,Bo Xin,Hongwu Ma,YU WANG
出处
期刊:Cell Reports
[Cell Press]
日期:2025-12-24
卷期号:45 (1): 116788-116788
被引量:4
标识
DOI:10.1016/j.celrep.2025.116788
摘要
Bacillus methanolicus, a unique plasmid-dependent and thermophilic methylotroph, is an ideal chassis for one-carbon (C1) biomanufacturing. Despite its evolutionary uniqueness and industrial promise, the synthetic biology toolkit remains limited in comparison to that of conventional model microorganisms. Here, we present a comprehensive toolkit comprising a high-efficiency electroporation protocol, a CRISPR-Cas9 method enabling robust and multiplex genome editing, diverse neutral loci for gene integration, and a cloud-based genome-scale metabolic model iBM822 for user-friendly biodesign. Leveraging this toolkit, we systematically dissected plasmid-dependent methylotrophy, restriction-modification machinery, and the functional significance of chromosomal methylotrophic genes. To address plasmid loss-induced strain degeneration, we integrated the large endogenous plasmid pBM19 into the chromosome for stable and intact methylotrophic growth. Finally, by integrating metabolic modeling with CRISPR-Cas9 editing, we engineered L-arginine feedback regulation to achieve L-arginine overproduction from methanol. This study establishes a synthetic biology framework for B. methanolicus, promoting mechanistic exploration of methylotrophy and C1 biomanufacturing.
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