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Cloning and Expression of Recombinant Human Thymosin in Yeast Pichia pastoris
作者姓名:曹俊霞  Jin Liji  Duan Yanlong  An Lijia
作者单位:DepartmentofBioengieering,DalianUniverSityofTechnology,Dalian116012,P.R.China
基金项目:theLiaoningProvinceScienceandTechnologyFundProgram(GrantNo .993 0 5 0 0 1)
摘    要:The gene of human thyrnosin alpha 1 (hT(1)was synthesised according to favorite eodons of Pichia pastoris by PCR. N-terminal 28 amino acid residues of 40S ribosomal protein (RP), S24Ethat is N-aeetylserine were replaced by hT( 1 for the constitution of hT(1-RP fusion gene in order to express acetyllated thyrnosin α1. And also, the Asn-Gly bond was designed to faeiliate isolation of the target protein. The fusion gene was cloned into the expression vector, pPIC/gK. The constructs were transformed into HIS4 mutant strain GS115 by eleetroporation. Both SDS-PAGE analysis and Western blot analysis indicated that the fusion protein was expressed successfully.

关 键 词:重组人胸腺激素α1基因  基因克隆  基因表达  酵母  PCR  核糖体蛋白

Cloning and Expression of Recombinant Human Thymosin in Yeast Pichia pastoris
Jin Liji,Duan Yanlong,An Lijia.Cloning and Expression of Recombinant Human Thymosin in Yeast Pichia pastoris[J].High Technology Letters,2003,9(3):60-64.
Authors:Jin Liji  Duan Yanlong  An Lijia
Abstract:The gene of human thymosin alpha 1(hT(1)was synthesised according to favorite codons of Pichia pastoris by PCR. N-terminal 28 amino acid residues of 40S ribosomal protein (RP), S24E that is N-acetylserine were replaced by hT(1 for the constitution of hT(1-RP fusion gene in order to express acetyllated thymosin α1. And also,the Asn-Gly bond was designed to faciliate isolation of the target protein.The fusion gene was cloned into the expression vector, pPIC/9K. The constructs were transformed into HIS4 mutant strain GS115 by electroporation. Both SDS-PAGE analysis and Western blot analysis indicated that the fusion protein was expressed successfully.
Keywords:expression  Pichia pastoris
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