Biotechnology and Bioengineering · 2020 · 40 citations · 33 references
Life SciencesBiotechnologyMicrobiologyBiochemical EngineeringBioreactor DesignMetabolic EngineeringIndustrial FermentationMicrobial FermentationMicrobial GrowthMicrobial Metabolic EngineeringMicrobial Metabolite ProductionStrain ImprovementBioreactor CultivationCarbon Source LimitationIndustrial Yeast TechnologyProtein ProductionRecombinant Enzyme ProductionSubstrate Utilization EngineeringYeast Strain EngineeringYeast-based Protein Production
Abstract The methanol utilization (Mut) phenotype in the yeast Pichia pastoris (syn. Komagataella spp.) is defined by the deletion of the genes AOX1 and AOX2 . The Mut − phenotype cannot grow on methanol as a single carbon source. We assessed the Mut − phenotype for secreted recombinant protein production. The methanol inducible AOX1 promoter (P AOX1 ) was active in the Mut − phenotype and showed adequate eGFP fluorescence levels and protein yields (Y P/X ) in small‐scale screenings. Different bioreactor cultivation scenarios with methanol excess concentrations were tested using P AOX1 HSA and P AOX1 vHH expression constructs. Scenario B comprising a glucose‐methanol phase and a 72‐hr‐long methanol only phase was the best performing, producing 531 mg/L HSA and 1631 mg/L vHH. 61% of the HSA was produced in the methanol only phase where no biomass growth was observed, representing a special case of growth independent production. By using the Mut − phenotype, the oxygen demand, heat output, and specific methanol uptake ( q methanol ) in the methanol phase were reduced by more than 80% compared with the Mut S phenotype. The highlighted improved process parameters coupled with growth independent protein production are overlooked benefits of the Mut − strain for current and future applications in the field of recombinant protein production.
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