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A construction strategy for a baculovirus-silkworm multigene expression system and its application for coexpression of type I and type II interferons.


ABSTRACT: The Bombyx mori nucleopolyhedrovirus (BmNPV) baculovirus expression system (BES) is a eukaryotic expression system. It possesses great capability for post-translation modification in expression of foreign proteins. With the counterselection cassette rpsL-neo and phage ?-Red recombinase, the defective-rescue BmNPV BES reBmBac can be employed for efficient heterologous multigene coexpression at different gene sites in one baculovirus genome. In the present study, a recombinant baculovirus, reBm-C??, carrying two types of chicken interferon (IFN) genes (chIFN-? and chIFN-?) was constructed using the reBmBac system. The chIFN-? and chIFN-? genes were inserted into the same baculovirus genome at the polyhedron and p10 gene sites, respectively. The recombinant baculovirus was capable of coexpressing both chIFN-? and chIFN-?. The expression levels of the two types of IFN in the coexpression product were exponentially high, at approximately 1.7 and 2.5 times higher, respectively, than those in the corresponding single-expression products. The increase in expression level corresponds to replacement of the nonessential p10 gene in the reBm-C?? recombinant baculovirus. This coexpression of recombinant chicken IFNs showed superior antiviral activity.

SUBMITTER: Liu X 

PROVIDER: S-EPMC7066456 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature

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A construction strategy for a baculovirus-silkworm multigene expression system and its application for coexpression of type I and type II interferons.

Liu Xingjian X   Yang Xin X   Mehboob Arslan A   Hu Xiaoyuan X   Yi Yongzhu Y   Li Yinü Y   Zhang Zhifang Z  

MicrobiologyOpen 20191219 3


The Bombyx mori nucleopolyhedrovirus (BmNPV) baculovirus expression system (BES) is a eukaryotic expression system. It possesses great capability for post-translation modification in expression of foreign proteins. With the counterselection cassette rpsL-neo and phage λ-Red recombinase, the defective-rescue BmNPV BES reBmBac can be employed for efficient heterologous multigene coexpression at different gene sites in one baculovirus genome. In the present study, a recombinant baculovirus, reBm-Cα  ...[more]

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