Mohamadzadeh Mohamadsadegh, Ghiasi Mohsen, Aghamollaei Hossein
Department of Chemical and Petroleum Engineering, Sharif University of Technology, Tehran, Iran.
Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
Arch Microbiol. 2024 Feb 22;206(3):116. doi: 10.1007/s00203-024-03847-2.
Bacillus subtilis can potentially serve as an efficient expression host for biotechnology due to its ability to secrete extracellular proteins and enzymes directly into the culture medium. One of the important challenges in the biotechnology industry is to optimize the transformation conditions of B. subtilis bacteria. This study aims to provide a new method to optimize the transformation conditions and improve the transformation efficiency of B. subtilis WB600. To increase the transformation efficiency in B. subtilis, two methods of adding CM11 antibacterial peptides to the bacterial medium along with electroporation and optimizing the variables including the growth medium composition, time to adding CM11 peptide, electroporation voltage, recovery medium, and cell recovery time are used. The results of this study showed that the addition of antimicrobial peptides (AMPs) with a concentration of 2 μg/ml increases the transformation efficiency by 4 times compared to the absence of AMP in the bacterial medium. Additionally, the findings from our study indicated that the most optimal rate of transformation for B. subtilis was observed at a voltage of 7.5 kV/cm, with a recovery period of 12 h. With the optimized method, the transformation efficiency came up to 1.69 × 10 CFU/µg DNA. This improvement in transformation efficiency will be attributed to the research of expression of exogenous genes in B. subtilis, gene library construction for transformation of wild-type B. subtilis strains.
枯草芽孢杆菌因其能够将细胞外蛋白质和酶直接分泌到培养基中,有潜力成为生物技术领域高效的表达宿主。生物技术产业面临的重要挑战之一是优化枯草芽孢杆菌的转化条件。本研究旨在提供一种优化转化条件、提高枯草芽孢杆菌WB600转化效率的新方法。为提高枯草芽孢杆菌的转化效率,采用了两种方法:在细菌培养基中添加CM11抗菌肽并结合电穿孔,以及优化包括生长培养基组成、添加CM11肽的时间、电穿孔电压、复苏培养基和细胞复苏时间等变量。本研究结果表明,与细菌培养基中不添加抗菌肽相比,添加浓度为2 μg/ml的抗菌肽可使转化效率提高4倍。此外,我们的研究结果表明,枯草芽孢杆菌在电压为7.5 kV/cm、复苏期为12 h时观察到最佳转化效率。采用优化方法后,转化效率达到1.69×10 CFU/μg DNA。转化效率的提高将有助于枯草芽孢杆菌中外源基因表达的研究、野生型枯草芽孢杆菌菌株转化的基因文库构建。