Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12934-018-1014-8
Title: An oleaginous yeast platform for renewable 1-butanol synthesis based on a heterologous CoA-dependent pathway and an endogenous pathway 06 Biological Sciences 0604 Genetics
Authors: Yu, A
Zhao, Y
Pang, Y
Hu, Z
Zhang, C
Xiao, D
Chang, M.W 
Leong, S.S.J 
Keywords: butanol
coenzyme A
glyceraldehyde 3 phosphate dehydrogenase
malate dehydrogenase
butanol
coenzyme A
Article
biosynthesis
concentration (parameters)
controlled study
ETR1 gene
EutE gene
fungal gene
gene function
gene identification
gene overexpression
metabolic engineering
nonhuman
regulatory mechanism
Yarrowia lipolytica
gene expression
metabolism
plasmid
Yarrowia
1-Butanol
Coenzyme A
Gene Expression
Metabolic Engineering
Plasmids
Yarrowia
Issue Date: 2018
Citation: Yu, A, Zhao, Y, Pang, Y, Hu, Z, Zhang, C, Xiao, D, Chang, M.W, Leong, S.S.J (2018). An oleaginous yeast platform for renewable 1-butanol synthesis based on a heterologous CoA-dependent pathway and an endogenous pathway 06 Biological Sciences 0604 Genetics. Microbial Cell Factories 17 (1) : 166. ScholarBank@NUS Repository. https://doi.org/10.1186/s12934-018-1014-8
Rights: Attribution 4.0 International
Abstract: Background: Microbial biofuel production provides a promising sustainable alternative to fossil fuels. 1-Butanol is recognized as an advanced biofuel and is gaining attention as an ideal green replacement for gasoline. In this proof-of-principle study, the oleaginous yeast Yarrowia lipolytica was first engineered with a heterologous CoA-dependent pathway and an endogenous pathway, respectively. Results: The co-overexpression of two heterologous genes ETR1 and EutE resulted in the production of 1-butanol at a concentration of 65 μg/L. Through the overexpression of multiple 1-butanol pathway genes, the titer was increased to 92 μg/L. Cofactor engineering through endogenous overexpression of a glyceraldehyde-3-phosphate dehydrogenase and a malate dehydrogenase further led to titer improvements to 121 μg/L and 110 μg/L, respectively. In addition, the presence of an endogenous 1-butanol production pathway and a gene involved in the regulation of 1-butanol production was successfully identified in Y. lipolytica. The highest titer of 123.0 mg/L was obtained through this endogenous route by combining a pathway gene overexpression strategy. Conclusions: This study represents the first report on 1-butanol biosynthesis in Y. lipolytica. The results obtained in this work lay the foundation for future engineering of the pathways to optimize 1-butanol production in Y. lipolytica. © 2018 The Author(s).
Source Title: Microbial Cell Factories
URI: https://scholarbank.nus.edu.sg/handle/10635/181174
ISSN: 14752859
DOI: 10.1186/s12934-018-1014-8
Rights: Attribution 4.0 International
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