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- W2393346217 abstract "A 837 bp gene fragment was amplified by Polymerase Chain Reaction(PCR) from Bacillus sublitis (notto strain) genomic DNA, which was prepared with CTAB method.Then it was ligated into pMD18-Tvector and transformed into E.coli DH5α.The PCR amplification,restriction enzyme analysis and sequencing demonstrated that the nottokinase gene fragment has been cloned.The IPTG induced efficiently expression of nattokinase(NK protein) gene in E.coli BL21(DE3)plysS.The SDS-PAGE and bandscan analysis indicated that fusion NK protein is about 33.4 kD,which agrees with its theoretical calculation and accounts for up to 29.4% of the total bacterial protein." @default.
- W2393346217 created "2016-06-24" @default.
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- W2393346217 date "2005-01-01" @default.
- W2393346217 modified "2023-09-25" @default.
- W2393346217 title "Cloning and Expression of Nattokinase Gene in E.coli BL21(DE3)plysS" @default.
- W2393346217 hasPublicationYear "2005" @default.
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