Bacillus subtilis is a well-characterized model bacterium frequently used for a number of biotechnology and synthetic biology applications. Novel strategies combining the advantages of B. subtilis with the DNA assembly and editing tools of Escherichia coli are crucial for B. subtilis engineering efforts. We combined Gibson Assembly and λ red recombineering in E. coli with RecA-mediated homologous recombination in B. subtilis for bacterial artificial chromosome-mediated DNA integration into the well-characterized amyE target locus of the B. subtilis chromosome. The engineered integrative bacterial artificial chromosome iBAC(cav) can accept any DNA fragment for integration into B. subtilis chromosome and allows rapid selection of transformant...
Recombinogenic engineering or recombineering is a powerful new method to engineer DNA without the ne...
The majority of the good DNA editing techniques have been developed in Escherichia coli; however, Ba...
Recombinogenic engineering or recombineering is a powerful new method to engineer DNA without the ne...
$\textbf{Background}$ $\textit{Escherichia coli}$ K-12 is a frequently used host for a number of sy...
Abstract Background Promoter-specific expression of foreign DNA in transgenic organisms often relies...
Bacillus subtilis DNA was cloned by ligating restriction endonuclease-generated fragments to plasmid...
The ability to efficiently and reliably transfer genetic circuits between the key synthetic biology ...
Bacillus subtilis plays an important role in fundamental and applied research, and it has been widel...
Genome engineering without leaving foreign DNA be-hind requires an efficient counter-selectable mark...
The ability to efficiently and reliably transfer genetic circuits between the key synthetic biology ...
Bacillus subtilis has been a model for gram-positive bacteria and it has long been exploited for ind...
Bacillus subtilis has been a model for gram-positive bacteria and it has long been exploited for ind...
We have constructed shuttle vectors for integration of genes via double homologous recombination int...
Most bacteria can only be transformed with circular plasmids, so robust DNA integration methods for ...
Using plasmid pHV60, which contains a chloramphenicol resistance (Cmr) gene that is expressed in Bac...
Recombinogenic engineering or recombineering is a powerful new method to engineer DNA without the ne...
The majority of the good DNA editing techniques have been developed in Escherichia coli; however, Ba...
Recombinogenic engineering or recombineering is a powerful new method to engineer DNA without the ne...
$\textbf{Background}$ $\textit{Escherichia coli}$ K-12 is a frequently used host for a number of sy...
Abstract Background Promoter-specific expression of foreign DNA in transgenic organisms often relies...
Bacillus subtilis DNA was cloned by ligating restriction endonuclease-generated fragments to plasmid...
The ability to efficiently and reliably transfer genetic circuits between the key synthetic biology ...
Bacillus subtilis plays an important role in fundamental and applied research, and it has been widel...
Genome engineering without leaving foreign DNA be-hind requires an efficient counter-selectable mark...
The ability to efficiently and reliably transfer genetic circuits between the key synthetic biology ...
Bacillus subtilis has been a model for gram-positive bacteria and it has long been exploited for ind...
Bacillus subtilis has been a model for gram-positive bacteria and it has long been exploited for ind...
We have constructed shuttle vectors for integration of genes via double homologous recombination int...
Most bacteria can only be transformed with circular plasmids, so robust DNA integration methods for ...
Using plasmid pHV60, which contains a chloramphenicol resistance (Cmr) gene that is expressed in Bac...
Recombinogenic engineering or recombineering is a powerful new method to engineer DNA without the ne...
The majority of the good DNA editing techniques have been developed in Escherichia coli; however, Ba...
Recombinogenic engineering or recombineering is a powerful new method to engineer DNA without the ne...