Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12934-018-1014-8
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dc.titleAn oleaginous yeast platform for renewable 1-butanol synthesis based on a heterologous CoA-dependent pathway and an endogenous pathway 06 Biological Sciences 0604 Genetics
dc.contributor.authorYu, A
dc.contributor.authorZhao, Y
dc.contributor.authorPang, Y
dc.contributor.authorHu, Z
dc.contributor.authorZhang, C
dc.contributor.authorXiao, D
dc.contributor.authorChang, M.W
dc.contributor.authorLeong, S.S.J
dc.date.accessioned2020-10-27T10:05:41Z
dc.date.available2020-10-27T10:05:41Z
dc.date.issued2018
dc.identifier.citationYu, 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
dc.identifier.issn14752859
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181174
dc.description.abstractBackground: 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).
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectbutanol
dc.subjectcoenzyme A
dc.subjectglyceraldehyde 3 phosphate dehydrogenase
dc.subjectmalate dehydrogenase
dc.subjectbutanol
dc.subjectcoenzyme A
dc.subjectArticle
dc.subjectbiosynthesis
dc.subjectconcentration (parameters)
dc.subjectcontrolled study
dc.subjectETR1 gene
dc.subjectEutE gene
dc.subjectfungal gene
dc.subjectgene function
dc.subjectgene identification
dc.subjectgene overexpression
dc.subjectmetabolic engineering
dc.subjectnonhuman
dc.subjectregulatory mechanism
dc.subjectYarrowia lipolytica
dc.subjectgene expression
dc.subjectmetabolism
dc.subjectplasmid
dc.subjectYarrowia
dc.subject1-Butanol
dc.subjectCoenzyme A
dc.subjectGene Expression
dc.subjectMetabolic Engineering
dc.subjectPlasmids
dc.subjectYarrowia
dc.typeArticle
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1186/s12934-018-1014-8
dc.description.sourcetitleMicrobial Cell Factories
dc.description.volume17
dc.description.issue1
dc.description.page166
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