从发酵基质中对一种新型的大肠杆菌菌体TR1进行了表征,完整基因组测序和基于CRISPR/Cas9系统的消毒
Yuqi Dong1, Yunfei Huang1, Huahao Fan1
1College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
Frontiers in microbiology
|August 28, 2023
概括
我们开发了一个CRISPR/Cas9系统,用于对抗像大肠杆菌这样的工业细菌中的菌体污染. 这种防御策略有效降解菌体DNA,保护发酵过程并确保细菌的生产.
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:
- 菌体污染对使用埃舍里希亚大肠杆菌BL21(DE3) 等细菌的工业发酵构成重大威胁.
- 现有的菌体控制方法往往不足以应对快速发展的菌体种群.
研究的目的:
- 开发一种基于CRISPR/Cas9的精确和适应性强的防御系统,以防工业大肠杆菌的菌体污染.
- 描述一个新分离的菌体,TR1,并设计耐药的细菌菌株.
主要方法:
- 从发酵基质中分离和描述一种新型菌体 (TR1).
- 全基因组测序和菌体TR1.1的遗传学分析.
- 构建CRISPR/Cas9工程的Escherichia coli BL21(DE3) 菌株,以获得菌体的耐药性.
主要成果:
- 菌体TR1被确定为克里斯森病毒属中的新物种,表现出高生育率.
- 工程化大肠杆菌菌株 (BL21-C,BL21-T) 在不影响生长的情况下对菌素TR1表现出强大的耐药性.
- 该CRISPR/Cas9系统有效地向并降解了菌体DNA.
结论:
- 可定制的CRISPR/Cas9系统为防止工业发酵中的菌体污染提供了弹性解决方案.
- 这种菌体防御机制在面对菌体-宿主进化军备竞赛的生物技术过程中具有广泛的适用性.
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