Expression of a Codon-Optimized Carica papaya Papain Sequence in the Methylotrophic Yeast Pichia pastoris

Abstract

The cysteine endoprotease papain is one of the most widely used plant proteases for industrial applications. However the traditional isolation of papain from the latex of papaya plants cannot cover the world-wide? demand. To increase papain production for industrial applications, several expression systems were studied in the last years for its recombinant production. While expression in Eschericha coli resulted in accumulation of insoluble protein, expression in baculovirus/ insect system and Saccharomyes cerevisiae resulted in low yields of soluble protein inadequate for large-scale production. Here we describe the heterologous expression of a synthetic codon-optimized propapain sequence in the Pichia pastoris strains X33 (Mut +) and KM71H (Mut s). The recombinant propapain could be expressed as soluble protein and secreted in the culture medium through the α-factor signal peptide. Highest activities were obtained in the Mut s strain when cultivated in complex medium. After purification by Ni-NTA chromatography 463 mg/L recombinant propapain was obtained comparable to the so far highest reported propapain yields in E. coli after protein solublilization and refolding and with a specific activity similar to a commercial papain from papaya latex.

Chromosome Engineering in Tropical Cash Crops

“…In addition, the expression of N1-demethylase genes from the Pseudomonas putida strain CBB5 in E. coli allowed for the recovery of theobromine from caffeine 47 . The synthesis of soluble papain has been achieved in cells of S. cerevisiae and the Pichia pastoris strain KM71H, with yields comparable to those of pure papaya latex in the latter 48 .…”