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Adaptive laboratory evolution of tolerance to dicarboxylic acids in Saccharomyces cerevisiae

Pereira, Rui, 1986 (author)
Chalmers tekniska högskola,Chalmers University of Technology,Novo Nordisk Fonden,Novo Nordisk Foundation
Wei, Yongjun, 1986 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Mohamed, Elsayed (author)
Danmarks Tekniske Universitet,Technical University of Denmark
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Radi, Mohammad (author)
Danmarks Tekniske Universitet,Technical University of Denmark
Malina, Carl, 1992 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Herrgard, M. J. (author)
Danmarks Tekniske Universitet,Technical University of Denmark
Feist, Adam M. (author)
University of California,Danmarks Tekniske Universitet,Technical University of Denmark
Nielsen, Jens B, 1962 (author)
BioInnovation Institute (BII),Chalmers tekniska högskola,Chalmers University of Technology,Danmarks Tekniske Universitet,Technical University of Denmark
Chen, Yun, 1978 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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 (creator_code:org_t)
Elsevier BV, 2019
2019
English.
In: Metabolic Engineering. - : Elsevier BV. - 1096-7176 .- 1096-7184. ; 56, s. 130-141
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Improving the growth phenotypes of microbes in high product concentrations is an essential design objective in the development of robust cell factories. However, the limited knowledge regarding tolerance mechanisms makes rational design of such traits complicated. Here, adaptive laboratory evolution was used to explore the tolerance mechanisms that Saccharomyces cerevisiae can evolve in the presence of inhibiting concentrations of three dicarboxylic acids: glutaric acid, adipic acid and pimelic acid. Whole-genome sequencing of tolerant mutants enabled the discovery of the genetic changes behind tolerance and most mutations could be linked to the up-regulation of multidrug resistance transporters. The amplification of QDR3, in particular, was shown to confer tolerance not only to the three dicarboxylic acids investigated, but also towards muconic acid and glutaconic acid. In addition to increased acid tolerance, QDR3 overexpression also improved the production of muconic acid in the context of a strain engineered for producing this compound.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Andra medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Other Basic Medicine (hsv//eng)
NATURVETENSKAP  -- Biologi -- Mikrobiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Microbiology (hsv//eng)

Keyword

Multidrug resistance transporter
Dicarboxylic acid
Adaptive laboratory evolution

Publication and Content Type

art (subject category)
ref (subject category)

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