Expression of Cloned Genes in Pichia pastoris Using the Methanol-Inducible Promoter AOX1
Clara L. Kielkopf, William R. Bauer, Ina L. Urbatsch
Abstract
Clara L. Kielkopf, William R. Bauer, Ina L. Urbatsch
Abstract
Pichia pastoris is a methylotrophic yeast capable of metabolizing methanol as its sole carbon source. Growth in methanol-containing medium results in dramatic induction of genes in the alcohol oxidation pathway including alcohol oxidase (AOX), formaldehyde dehydrogenase (FLD), and dihydroxyacetone synthase (DHAS). These proteins may comprise up to 30% of the biomass. Investigators have exploited these methanol-dependent genes to generate tightly regulated expression vectors. Most Pichia vectors use the strong and tightly regulated AOX1 promoter to drive heterologous protein expression. Obtaining integrated Pichia transformants requires more DNA than transformations into Saccharomyces cerevisiae , where the gene is expressed from episomal plasmids; however, transformants are extremely stable and can be stored for many years.
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Pichia pastoris is a methylotrophic yeast capable of metabolizing methanol as its sole carbon source. Growth in methanol-containing medium results in dramatic induction of genes in the alcohol oxidation pathway including alcohol oxidase (AOX), formaldehyde dehydrogenase (FLD), and dihydroxyacetone synthase (DHAS). These proteins may comprise up to 30% of the biomass. Investigators have exploited these methanol-dependent genes to generate tightly regulated expression vectors. Most Pichia vectors use the strong and tightly regulated AOX1 promoter to drive heterologous protein expression. Obtaining integrated Pichia transformants requires more DNA than transformations into Saccharomyces cerevisiae , where the gene is expressed from episomal plasmids; however, transformants are extremely stable and can be stored for many years.
Key concepts: Pichia pastoris, Gene, Cloning (programming), Methanol, Pichia, Molecular biology, Biology, Chemistry