Engineered reversal of function in glycolytic yeast promoters
dc.contributor.author | Rajkumar, Arun S. | |
dc.contributor.author | Ă–zdemir, Emre | |
dc.contributor.author | Lis, Alicia V. | |
dc.contributor.author | Schneider, Konstantin | |
dc.contributor.author | Qin, Jiufu | |
dc.contributor.author | Jensen, Michael K. | |
dc.contributor.author | Keasling, Jay D. | |
dc.contributor.funder | Novo Nordisk Fonden | en |
dc.contributor.funder | Horizon 2020 | en |
dc.date.accessioned | 2019-09-17T13:56:38Z | |
dc.date.available | 2019-09-17T13:56:38Z | |
dc.date.issued | 2019-05-03 | |
dc.description.abstract | Promoters are key components of cell factory design, allowing precise expression of genes in a heterologous pathway. Several commonly used promoters in yeast cell factories belong to glycolytic genes, highly expressed in actively growing yeast when glucose is used as a carbon source. However, their expression can be suboptimal when alternate carbon sources are used, or if there is a need to decouple growth from production. Hence, there is a need for alternate promoters for different carbon sources and production schemes. In this work, we demonstrate a reversal of regulatory function in two glycolytic yeast promoters by replacing glycolytic regulatory elements with ones induced by the diauxic shift. We observe a shift in induction from glucose-rich to glucose-poor medium without loss of regulatory activity, and strong ethanol induction. Applications of these promoters were validated for expression of the vanillin biosynthetic pathway, reaching production of vanillin comparable to pathway designs using strong constitutive promoters. | en |
dc.description.status | Peer reviewed | en |
dc.description.version | Published Version | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.citation | Rajkumar, A. S., Ă–zdemir, E., Lis, A. V., Schneider, K., Qin, J., Jensen, M. K. and Keasling, J. D. (2019) 'Engineered Reversal of Function in Glycolytic Yeast Promoters', ACS Synthetic Biology, 8(6), pp. 1462-1468. (6pp.) DOI: 10.1021/acssynbio.9b00027 | en |
dc.identifier.doi | 10.1021/acssynbio.9b00027 | en |
dc.identifier.eissn | 2161-5063 | |
dc.identifier.endpage | 1468 | en |
dc.identifier.issued | 6 | en |
dc.identifier.journaltitle | ACS Synthetic Biology | en |
dc.identifier.startpage | 1462 | en |
dc.identifier.uri | https://hdl.handle.net/10468/8545 | |
dc.identifier.volume | 8 | en |
dc.language.iso | en | en |
dc.publisher | American Chemical Society | en |
dc.relation.project | info:eu-repo/grantAgreement/EC/FP7::SP1::KBBE/613771/EU/Development of 2nd Generation Biorefineries – Production of Dicarboxylic Acids and Bio-based Polymers Derived Thereof/BIOREFINE-2G | en |
dc.relation.uri | https://pubs.acs.org/doi/10.1021/acssynbio.9b00027 | |
dc.rights | ©2019 American Chemical Society. This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes. | en |
dc.rights.uri | https://pubs.acs.org/page/policy/authorchoice_termsofuse.html | en |
dc.subject | Transcriptome | en |
dc.subject | Synthetic promoter | en |
dc.subject | Glycolysis | en |
dc.subject | Gluconeogenesis | en |
dc.subject | Vanillin | en |
dc.title | Engineered reversal of function in glycolytic yeast promoters | en |
dc.type | Article (peer-reviewed) | en |
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