
AbstractThe rhamnose utilization pathway in Pichia pastoris has not been clarified although this strain can grow well on rhamnose as a sole carbon source. In this study, four genes, PAS_chr4_0338, PAS_chr4_0339, PAS_chr4_0340 and PAS_chr4_0341, were, for the first time, predicted to be involved in rhamnose metabolism along with the previously identified gene PAS_chr1_4-0075. Moreover, expression of these genes, especially PAS_chr4_0341 and PAS_chr1_4-0075 designated as LRA4 and LRA3, was confirmed to significantly increase and clearly decrease in the presences of rhamnose and glucose, respectively. LRA4 encoding a putative L-2-keto-3-deoxyrhamnonate aldolase, was further confirmed via gene disruption and gene complementation to participate in rhamnose metabolism. Using β-galactosidase and green fluorescent protein as reporters, the promoters of LRA4 and LRA3 performed well in driving efficient production of heterologous proteins. By using food grade rhamnose instead of the toxic compound methanol as the inducer, the two promoters would be excellent candidates for driving the production of food-grade and therapeutically important recombinant proteins.
Gene Expression Profiling, Genes, Fungal, Genetic Complementation Test, Green Fluorescent Proteins, beta-Galactosidase, Rhamnose, Article, Pichia, Artificial Gene Fusion, Gene Knockout Techniques, Glucose, Genes, Reporter, Technology, Pharmaceutical, Promoter Regions, Genetic, Metabolic Networks and Pathways, Biotechnology
Gene Expression Profiling, Genes, Fungal, Genetic Complementation Test, Green Fluorescent Proteins, beta-Galactosidase, Rhamnose, Article, Pichia, Artificial Gene Fusion, Gene Knockout Techniques, Glucose, Genes, Reporter, Technology, Pharmaceutical, Promoter Regions, Genetic, Metabolic Networks and Pathways, Biotechnology
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