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Improving Lipid Production of Yarrowia lipolytica by the Aldehyde Dehydrogenase-Mediated Furfural Detoxification
Authors:Jiwon Kim  Hyeoncheol Francis Son  Sungmin Hwang  Gyeongtaek Gong  Ja Kyong Ko  Youngsoon Um  Sung Ok Han  Sun-Mi Lee
Affiliation:1.Clean Energy Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792, Korea; (J.K.); (H.F.S.); (S.H.); (G.G.); (J.K.K.); (Y.U.);2.Department of Biotechnology, Korea University, Seoul 02841, Korea;3.Division of Energy and Environment, University of Science and Technology, Daejeon 34113, Korea;4.KU-KIST Green School (Graduate School of Energy and Environment), Korea University, Seoul 02841, Korea
Abstract:Yarrowia lipolytica, the non-conventional yeast capable of high lipogenesis, is a microbial chassis for producing lipid-based biofuels and chemicals from renewable resources such as lignocellulosic biomass. However, the low tolerance of Y. lipolytica against furfural, a major inhibitory furan aldehyde derived from the pretreatment processes of lignocellulosic biomass, has restricted the efficient conversion of lignocellulosic hydrolysates. In this study, the furfural tolerance of Y. lipolytica has been improved by supporting its endogenous detoxification mechanism. Specifically, the endogenous genes encoding the aldehyde dehydrogenase family proteins were overexpressed in Y. lipolytica to support the conversion of furfural to furoic acid. Among them, YALI0E15400p (FALDH2) has shown the highest conversion rate of furfural to furoic acid and resulted in two-fold increased cell growth and lipid production in the presence of 0.4 g/L of furfural. To our knowledge, this is the first report to identify the native furfural detoxification mechanism and increase furfural resistance through rational engineering in Y. lipolytica. Overall, these results will improve the potential of Y. lipolytica to produce lipids and other value-added chemicals from a carbon-neutral feedstock of lignocellulosic biomass.
Keywords:Yarrowia lipolytica  lipids  furfural  tolerance  aldehyde dehydrogenase  YALI0E15400p
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