Efficient Large-Scale and Scarless Genome Engineering Enables the Construction and Screening of Bacillus subtilis Biofuel Overproducers

Bacillus subtilis is a versatile microbial cell factory that can produce valuable proteins and value-added chemicals. Long fragment editing techniques are of great importance for accelerating bacterial genome engineering to obtain desirable and genetically stable host strains. Herein, we develop an efficient CRISPR-Cas9 method for large-scale and scarless genome engineering in the Bacillus subtilis genome, which can delete up to 134.3 kb DNA fragments, 3.5 times as long as the previous report, with a positivity rate of 100%. The effects of using a heterologous NHEJ system, linear donor DNA, and various donor DNA length on the engineering efficiencies were also investigated. The CRISPR-Cas9 method was then utilized for Bacillus subtilis genome simplification and construction of a series of individual and cumulative deletion mutants, which are further screened for overproducer of isobutanol, a new generation biofuel. These results suggest that the method is a powerful genome engineering tool for constructing and screening engineered host strains with enhanced capabilities, highlighting the potential for synthetic biology and metabolic engineering.

Automated summary

Bacillus subtilis is a versatile microbial cell factory that can produce valuable proteins and value-added chemicals. Researchers have developed an efficient CRISPR-Cas9 method for large-scale and scarless genome engineering in Bacillus subtilis. They were able to delete DNA fragments up to 134.3 kb, 3.5 times longer than previous reports, with a positivity rate of 100%. The study also investigated the effects of using a heterologous NHEJ system, linear donor DNA, and various donor DNA lengths on the engineering efficiencies.