<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(11)</volume><submitter>Gao C</submitter><pubmed_abstract>Among the diverse alkaliphilic Bacillus strains, only a little have been reported to be genetically transformed. In this study, an efficient protoplast transformation procedure was developed for recalcitrant alkaliphilic Bacillus sp. N16-5. The procedure involved polyethylene glycol-induced DNA uptake by the protoplasts and subsequent protoplast regeneration with a developed hard agar regeneration medium. An in vivo methylation strategy was introduced to methylate the exogenous plasmid DNA for improving the transformation efficiency. The transformation efficiency reached to 1.1×10(5) transformants per µg plasmid DNA with methylated plasmid pHCMC04 and the developed hard agar regeneration medium. This procedure might also be applicable to the genetic transformation of other Bacillus strains.</pubmed_abstract><journal>PloS one</journal><pagination>e28148</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3223237</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Protoplast transformation of recalcitrant alkaliphilic Bacillus sp. with methylated plasmid DNA and a developed hard agar regeneration medium.</pubmed_title><pmcid>PMC3223237</pmcid><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Gao C</pubmed_authors><pubmed_authors>Xue Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Protoplast transformation of recalcitrant alkaliphilic Bacillus sp. with methylated plasmid DNA and a developed hard agar regeneration medium.</name><description>Among the diverse alkaliphilic Bacillus strains, only a little have been reported to be genetically transformed. In this study, an efficient protoplast transformation procedure was developed for recalcitrant alkaliphilic Bacillus sp. N16-5. The procedure involved polyethylene glycol-induced DNA uptake by the protoplasts and subsequent protoplast regeneration with a developed hard agar regeneration medium. An in vivo methylation strategy was introduced to methylate the exogenous plasmid DNA for improving the transformation efficiency. The transformation efficiency reached to 1.1×10(5) transformants per µg plasmid DNA with methylated plasmid pHCMC04 and the developed hard agar regeneration medium. This procedure might also be applicable to the genetic transformation of other Bacillus strains.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011</publication><modification>2024-10-18T21:27:23.921Z</modification><creation>2019-03-26T23:18:15Z</creation></dates><accession>S-EPMC3223237</accession><cross_references><pubmed>22132233</pubmed><doi>10.1371/journal.pone.0028148</doi></cross_references></HashMap>