Overexpression of the genes of glycerol catabolism and glycerol facilitator improves glycerol conversion to ethanol in the methylotrophic thermotolerant yeast Ogataea polymorpha.

Abstract

Production of fuel ethanol is one of the possible ways to utilize crude glycerol, substantial amounts of which are produced by biodiesel industry. Earlier, we have described construction of the recombinant strains of methylotrophic thermotolerant yeast Ogataea polymorpha with simultaneous overexpression of the genes PDC1 and ADH1, which produced increased amounts of ethanol from glycerol. In this work, we have further improved these strains by overexpression of genes involved either in oxidative (through dihydroxyacetone) or phosphorylative (through glycerol-3-phosphate) pathway of glycerol catabolism, as well as heterologous gene coding for glycerol transporter FPS1 from Komagataella phaffii (formerly, Pichia pastoris). Obtained recombinant strains produced up to 10.7g/L of ethanol (with ethanol productivity 30mg/g of biomass/hr and yield 132mg/g of consumed glycerol) from pure glycerol and up to 3.55g/L of ethanol (with ethanol productivity 11.6mg/g of biomass/hr and yield 72.3mg/g of consumed glycerol) from crude glycerol as a carbon source, which is approximately 15 times more relative to that of the O.polymorpha wild-type strain and 2.2 more relative to the earlier constructed strain.