High-level expression of Proteinase K from Tritirachium album Limber in Pichia pastoris using multi-copy expression strains

• Published in: Protein expression and purification 2016-06, Vol.122, p.38-44
• Main Authors: Yang, Hu, Zhai, Chao, Yu, Xianhong, Li, Zhezhe, Tang, Wei, Liu, Yunyun, Ma, Xiaojian, Zhong, Xing, Li, Guolong, Wu, Di, Ma, Lixin
• Format: Article
• Language: English
• Subjects: Ascomycota - enzymology; Ascomycota - genetics; Ascomycota - metabolism; Cloning, Molecular - methods; Endopeptidase K - genetics; Endopeptidase K - isolation & purification; Endopeptidase K - metabolism; Fermentation; Gene Dosage; Multi-copy expression; Open Reading Frames; Pichia - genetics; Pichia pastoris; Plasmids - genetics; Proteinase K; Recombinant Proteins - genetics; Recombinant Proteins - isolation & purification; Recombinant Proteins - metabolism; Recombination, Genetic
• ISSN: 1046-5928; 1096-0279
• DOI: 10.1016/j.pep.2016.02.006

Proteinase K is widely used in scientific research and industries. This report was aimed to achieve high-level expression of proteinase K using Pichia pastoris GS115 as the host strain. The coding sequence of a variant of proteinase K that has higher activity than the wild type protein was chosen and optimized based on the codon usage preference of P. pastoris. The novel open reading frame was synthesized and a series of multi-copy expression vectors were constructed based on the pHBM905BDM plasmid, allowing for the tandem integration of multiple copies of the target gene into the genome of P. pastoris with a single recombination. These strains were used to study the correlation between the gene copy number and the expression level of proteinase K. The results of quantitative polymerase chain reaction (qPCR) indicated that the tandem expression cassettes were integrated into the host genome stably. Meanwhile, the results of qPCR and enzyme activity assays indicated that the mRNA and protein expression levels of the target gene increased as the gene copy number increased. Moreover, the effect of gene dosage on the expression level of the recombinant protein was more obvious using high-density fermentation. The maximum expression level and enzyme activity of proteinase K, which were obtained from the recombinant yeast strain bearing 5 copies of the target gene after an 84-h induction, were approximately 8.069 mg/mL and 108,295 U/mL, respectively. The recombinant proteinase was purified and characterized. The optimum pH and temperature for the activity of this protease were approximately pH 11 and 55 °C, respectively. •Proteinase K was expressed in Pichia pastoris for the first time.•The gene of proteinase K was modified based on the codon usage bias of P. pastoris.•Multi-copy expression strategy could increase the yield of the recombinant proteinase K.•Compared with shaker flasks, the enzyme activity increased under high-density fermentation.