Abstract
The nuclear capsid protein gene (vp39) ofBombyx mori nuclear polyhedrosis virus (BmNPV) was amplified successfully by PCR technique and inserted into pGEM 3zf(+). The 5′ and 3′ terminal area of the amplified vp39 gene were sequenced with silver-staining dideoxy method. Bmvp39 gene was sub-cloned into the expression vector pRSET-A, and transformed intoE. coli BL21. This gene was highly expressed by IPTG induction. SDS-PAGE analysis showed that the expressed protein is about 38 kd, and the expressed amount reached maxium in 4 h with IPTG induction.
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Supported by the National Natural science Foundation of China and the Doctoral Foundation of Edn carto Committee
Liu Deli: born in 1954, Doctoral Candidate from Huazhong Normal University To whom correspondence should be addressed: (027-7882712-2938)
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Deli, L., Xiaojie, S., Yipeng, Q. et al. Cloning and expression of the vp39 gene ofBombyx mori nuclear polyhedrosis virus inE. coli . Wuhan Univ. J. Nat. Sci. 3, 108–112 (1998). https://doi.org/10.1007/BF02827528
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DOI: https://doi.org/10.1007/BF02827528