| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2090037 | Journal of Microbiological Methods | 2013 | 8 Pages |
•We use mini Zeocin resistance gene as positive-selectable marker.•Strictly controlled xyl promoter from the Bacillus subtilis replaced non-strictly controlled IPTG-inducible Pspac or xyl promoter from Bacillus megaterium.•The frequency of spontaneous mazF-resistant mutants was lower, and the frequency of generating desired clones was nearly 100%.•The entire procedure for marker-free genetic manipulation using the mini-mazF-cassette can be finished in about 3 days.
There are some drawbacks for MazF-cassette constructed in previous reports for marker-free genetic manipulation in Bacillus subtilis, including cloning-dependent methodology and non-strictly controlled expression system. In our study, the modifications on mazF-cassette are carried out, such as using mini Zeocin resistance gene as positive-selectable marker and strictly controlled xyl promoter from the B. subtilis to replace non-strictly controlled IPTG-inducible Pspac or xyl promoter from Bacillus megaterium. Then the mini-mazF-cassette was successfully applied to knock-out the amyE gene, to delete a 90-kb gene cluster, and to knock-in a green fluorescent protein expression cassette employing a cloning-independent methodology, without introducing undesirable redundant sequences at the modified locus in the B. subtilis 1A751. Besides, the mini-mazF-cassette could be used repeatedly to delete multiple genes or gene clusters with only a 2- to 2.5-kb PCR-fused fragment, which largely reduced the frequency of nucleic acid mutations generated by PCR compared to previous reports. We further demonstrated that the frequency of spontaneous mazF-resistant mutants was lower, and the frequency of generating desired clones was nearly 100%. The entire procedure for marker-free genetic manipulation using the mini-mazF-cassette can be finished in about 3 days. This modified cassette has remarkable improvement compared to existing approaches and is applicable for available manipulating Bacillus species chromosomes.
