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- W2391191710 abstract "A pair of primers were designed according to the bmr gene sequence published by NCBI.The whole bmr gene was amplified by PCR from Bacillus subtilis genome DNA,then cloned into pMD18-T and sequenced.The result showed that the nucleotide sequence of this gene was(1 170) bp and have five nucleotides different from published sequence.Then,this bmr gene was cloned into the prokaryotic expressing plasmid vector pET-28a(+) and transformed into the host E.coli strain BL21(DE3) for expression.Induced by 1 mmol/L IPTG at 37℃,the expression product of this bmr gene was identified by SDS-PAGE.The results revealed that Bmr protein had been expressed successfully." @default.
- W2391191710 created "2016-06-24" @default.
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- W2391191710 date "2005-01-01" @default.
- W2391191710 modified "2023-09-25" @default.
- W2391191710 title "Cloning and Prokaryotic Expression of Multidrug Resistance bmr Gene in Bacillus subtilis" @default.
- W2391191710 hasPublicationYear "2005" @default.
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