Methods of integrating target genes into the B. subtilis genome

Comparing methods of genetic manipulation in Bacillus subtilis for expression of recombinant enzyme: Replicative or integrative (CRISPR-Cas9) plasmid? - ScienceDirect

Construction and Analysis of Two Genome-Scale Deletion Libraries for Bacillus subtilis - ScienceDirect

PDF) Bacillus subtilis Spore Surface Display Technology: A Review of Its Development and Applications

Barriers to simultaneous multilocus integration in Bacillus subtilis tumble down: development of a straightforward screening method for the colorimetric detection of one-step multiple gene insertion using the CRISPR-Cas9 system

A facile and robust T7-promoter-based high-expression of heterologous proteins in Bacillus subtilis, Bioresources and Bioprocessing

Simple and rapid direct cloning and heterologous expression of natural product biosynthetic gene cluster in Bacillus subtilis via Red/ET recombineering

DNA uptake during transformation in B. subtilis. The uptake machinery

Generation of Bacillus subtilis displaying alpha-toxin HlaH35LH48L fused with CotB and CotG, and studying the immune response in mice

Guoyan ZHANG, Master, Jiangsu University, Zhenjiang, Department of Food and Biological Engineering

A dual mode of regulation of flgM by ScoC in Bacillus subtilis

Expression of various target proteins using B. subtilis spore surface

CRISPR-Cas9 editing with an erm gRNA. Plasmid pJOE8999 (7.8 kb; [11])

Multiple integration of the gene ganA into the Bacillus subtilis chromosome for enhanced β-galactosidase production using the CRISPR/Cas9 system, AMB Express