Establishment of the CRISPR-Cpf1 gene editing system in Bacillus licheniformis and multiplexed gene knockout

• Published in: Synthetic and systems biotechnology Vol. 10; no. 1; pp. 39 - 48
• Main Authors: Liu, Suxin, Xiao, Fengxu, Li, Youran, Zhang, Yupeng, Wang, Yanling, Shi, Guiyang
• Format: Journal Article
• Language: English
• Published: China Elsevier B.V 01.01.2025; KeAi Publishing Communications Ltd; KeAi Publishing; KeAi Communications Co., Ltd
• Subjects: Bacillus licheniformis; Cell growth; Cloning; CRISPR; CRISPR-Cpf1; E coli; Editing; Efficiency; Endonuclease; Enzymatic activity; Enzyme activity; Enzymes; Gene editing; Gene regulation; Genes; Genetic engineering; Genetic modification; Genome editing; Homologous recombination; MCherry; Metabolism; Microorganisms; Multiplexing; Original; Plasmids; Protease; Proteins; Reporter gene; Toxicity; China; CRISPR-Cpf1; MCherry; Bacillus licheniformis; Gene editing
• ISSN: 2405-805X; 2405-805X
• DOI: 10.1016/j.synbio.2024.08.002

Bacillus licheniformis is a significant industrial microorganism. Traditional gene editing techniques relying on homologous recombination often exhibit low efficiency due to their reliance on resistance genes. Additionally, the established CRISPR gene editing technology, utilizing Cas9 endonuclease, faces challenges in achieving simultaneous knockout of multiple genes. To address this limitation, the CRISPR-Cpf1 system has been developed, enabling multiplexed gene editing across various microorganisms. Key to the efficient gene editing capability of this system is the rigorous screening of highly effective expression elements to achieve conditional expression of protein Cpf1. In this study, we employed mCherry as a reporter gene and harnessed Pmal for regulating the expression of Cpf1 to establish the CRISPR-Cpf1 gene editing system in Bacillus licheniformis. Our system achieved a 100 % knockout efficiency for the single gene vpr and up to 80 % for simultaneous knockout of the double genes epr and mpr. Furthermore, the culture of a series of protease-deficient strains revealed that the protease encoded by aprE contributed significantly to extracellular enzyme activity (approximately 80 %), whereas proteases encoded by vpr, epr, and mpr genes contributed to a smaller proportion of extracellular enzyme activity. These findings provide support for effective molecular modification and metabolic regulation in industrial organisms.