ABSTRACT
In order to facilitate Golden Gate DNA assembly, we have constructed a collection of Bacillus subtilis replicative plasmids representing five origins of replication derived from plasmids pUB110, pE194, pWV01, pBS72, and pTH1030. The first three of these plasmids use rolling circle replication and the latter two use theta replication. All of the plasmids carry the same multiple cloning site surrounded by transcriptional terminators. The plasmids are about three kilobases in size, allowing them to be easily amplified by inverse PCR using a common set of primers to generate cloning-ready amplicons. This plasmid PCR amplification approach also facilitates a workflow that eliminates Escherichia coli as a shuttle intermediate. All of the plasmids lack a site for at least three of the type IIS restriction enzymes BbsI, BsaI, Esp3I, PaqCI, or SapI, making them compatible with Golden Gate DNA assembly. We have demonstrated the utility of the plasmids by performing Golden Gate assembly of gusA and bgaB-reporter gene fragments and in expressing plasmid-borne red fluorescent protein under the control of RNA polymerase from bacteriophage K1E.
