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Construction of an ZEN-jjm expressing vector and its expression in Pichia pastoris.

Qianglai Tan, Feng Xu, Peng Li, Cheng BoCai, Jie Luo, Hua Wei

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Abstract

Objective To construct an Pichia pastoris expressing vector pPIC9-ZEN-jjm and screen the strains which could express high-level active proteins.Method ZEN-jjm gene was spliced into pPIC9 after digested with EcoRⅠand NotⅠ,then transformed into Pichia pastoris GS115 by electroporation.The recombinant yeast strains were screened with RDB medium and methanol inducible expression.The ZEN degradation capabilities of expressed supernatant was verified by HPLC test.Result DNA sequencing demonstrated that ZEN-jjm was inserted into pPIC9.SDS-PAGE demonstrated that one yeast strain with high-level expression was obtained,and the molecular weight of the expressed protein was about 29 kDa.The HPLC result showed that the expressed protein could effectively degrade ZEN.Conclusion ZEN-degrading enzyme is highly expressed in Pichia pastoris.

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What this paper is about

Objective To construct an Pichia pastoris expressing vector pPIC9-ZEN-jjm and screen the strains which could express high-level active proteins.Method ZEN-jjm gene was spliced into pPIC9 after digested with EcoRⅠand NotⅠ,then transformed into Pichia pastoris GS115 by electroporation.The recombinant yeast strains were screened with RDB medium and methanol inducible expression.The ZEN degradation capabilities of expressed supernatant was verified by HPLC test.Result DNA sequencing demonstrated that ZEN-jjm was inserted into pPIC9.SDS-PAGE demonstrated that one yeast strain with high-level expression was obtained,and the molecular weight of the expressed protein was about 29 kDa.The HPLC result showed that the expressed protein could effectively degrade ZEN.Conclusion ZEN-degrading enzyme is highly expressed in Pichia pastoris.

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Available abstract

Objective To construct an Pichia pastoris expressing vector pPIC9-ZEN-jjm and screen the strains which could express high-level active proteins.Method ZEN-jjm gene was spliced into pPIC9 after digested with EcoRⅠand NotⅠ,then transformed into Pichia pastoris GS115 by electroporation.The recombinant yeast strains were screened with RDB medium and methanol inducible expression.The ZEN degradation capabilities of expressed supernatant was verified by HPLC test.Result DNA sequencing demonstrated that ZEN-jjm was inserted into pPIC9.SDS-PAGE demonstrated that one yeast strain with high-level expression was obtained,and the molecular weight of the expressed protein was about 29 kDa.The HPLC result showed that the expressed protein could effectively degrade ZEN.Conclusion ZEN-degrading enzyme is highly expressed in Pichia pastoris.

Key concepts: Pichia pastoris, Pichia, Electroporation, Recombinant DNA, Yeast, Biology, Expression vector, Molecular biology

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Construction of an ZEN-jjm expressing vector and its expression in Pichia pastoris. — Research Paper | ScholarLens