Abstract
AbstractInPichia pastoris(Komagataella phaffii), formate is a recognized alternative inducer to methanol for expression systems based on the AOX1 promoter (pAOX1). By disrupting the formate dehydrogenase encodingFDH1gene, we converted such a system into a self-induced one, as adding any inducer in the culture medium is no longer requested for pAOX1 induction. In cells, formate is generated from serine through the THF-C1 metabolism, and it cannot be converted into carbon dioxide in anfdh1Δ strain. Under non-repressive culture conditions, such as on sorbitol, the intracellular formate generated from the THF-C1 metabolism is sufficient to induce pAOX1 and initiate protein synthesis. This was evidenced for two model proteins, namely intracellular eGFP and secreted CalB lipase fromC. antarctica. Similar protein productivities were obtained for anfdh1Δ strain on sorbitol and a non-disrupted strain on sorbitol-methanol. Considering aP. pastoris fdh1Δstrain as a workhorse for recombinant protein synthesis paves the way for the further development of methanol-free processes inP. pastoris.
Publisher
Cold Spring Harbor Laboratory