The Ezpression of Bovine Enterokinase Catalytic Subunit in Methylotropic Yeast Pichia pastoris
The objective of the study was to acquire the bovine enterokinase light chain (EKL) expressed in Pichia pastoris, which would be used in the cleavage and purification of fusion proteins. The fragment of EKL cDNA was obtained by RT-PCR from a sold bovines duodenal mucosa, then cloned into the pUCm-T cloning vector and sequenced. Compared with the sequence deposited in GenBank, the cloned gene sequence is correct. Then the interested gene fragment was inserted into the pPIC9 expression plasmid. The recombinant vector pPIC9-EKL was linearized and introduced into pichia pastoris GS115 with the method of PEG1000.The recombinant EKL was secreted in fermentation supernatant with molecular weight of 36KDa. The yield of EKL was 32.8％ of total supernatant protein. After separation and purification by STI resin affinity chromatography, the production of rEKL was about 10.9ug/mL fermented solution, which had a specific activity of 2.88×107U/mg.
bovine enterokinase light chain(EKL) Pichia pastoris secreting ezpression
ZJ Fang H Huang
Department of Bioengineering,School of Biochemical Engineering Key Laboratory of Systems Bioengineering,Ministry of Education Tianjin University Tianjin 300072,China
国际会议
北京
英文
1-3
2009-06-11（万方平台首次上网日期，不代表论文的发表时间）