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• W2074737103 abstract "We have developed a method to improve the transformation efficiency in genome-sequenced bacteria, using 'Plasmid Artificial Modification' (PAM), using the host's own restriction system. In this method, a shuttle vector was pre-methylated in Escherichia coli cells, which carry all the putative genes encoding the DNA modification enzymes of the target microorganism, before electroporation was performed. In the case of Bifidobacterium adolescentis ATCC15703 and pKKT427 (3.9 kb E. coli-Bifidobacterium shuttle vector), introducing two Type II DNA methyltransferase genes lead to an enhancement in the transformation efficiency by five orders of magnitude. This concept was also applicable to a Type I restriction system. In the case of Lactococcus lactis IO-1, by using PAM with a putative Type I methyltransferase system, hsdMS1, the transformation efficiency was improved by a factor of seven over that without PAM." @default.
• W2074737103 created "2016-06-24" @default.
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• W2074737103 date "2008-11-12" @default.
• W2074737103 modified "2023-10-18" @default.
• W2074737103 title "Improvement of bacterial transformation efficiency using plasmid artificial modification" @default.
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• W2074737103 doi "https://doi.org/10.1093/nar/gkn884" @default.
• W2074737103 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2615632" @default.
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