Umeå universitets logga

umu.sePublikationer
Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Heterologous expression of 1,4-benzoquinone reductases from white-rot fungi in Saccharomyces cerevisiae confers protection against p-benzoquinone toxicity
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.ORCID-id: 0000-0003-3866-0111
2026 (Engelska)Ingår i: Microbial Cell Factories, E-ISSN 1475-2859, Vol. 25, nr 1, artikel-id 102Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Background: Ethanolic fermentation by Saccharomyces cerevisiae is a key part of biochemical conversion of lignocellulosic feedstocks. Although abundant, lignocellulose typically requires pretreatment for efficient bioconversion. During pretreatment, inhibitory compounds are formed. p-Benzoquinone (p-BQ) is a lignin-derived inhibitor that is highly toxic to S. cerevisiae. White-rot fungi, efficient degraders of lignin, produce 1,4-benzoquinone reductases (QRDs), which have been suggested to play a role in defense against oxidative stress caused by quinones formed during lignin biodegradation. The hypothesis that QRDs from white-rot fungi can be used to engineer S. cerevisiae with improved resistance against quinone toxicity was explored in experiments with QRD-encoding genes, with and without an N-terminal putative leader sequence, the function of which has not yet been deciphered.

Results: Constitutive recombinant expression of QRDs from the white-rot fungi Trametes versicolor and Phanerochaete chrysosporium in S. cerevisiae resulted in increased tolerance against p-BQ toxicity compared to an empty vector control containing insert-less plasmid, with QRD-expressing constructs requiring 34 to 42% less time to reach half-time of maximum growth in p-BQ conditions adverse for the growth of the empty vector control (10 mg L− 1). All QRD constructs were able to overcome p-BQ toxicity in concentrations that would otherwise be strongly inhibitory (20 mg L− 1). Full-length constructs of both T. versicolor and P. chrysosporium QRD typically exhibited 1.5 times higher specific activity than leaderless counterparts and were better detoxifiers. An inverse correlation between QRD enzymatic activity and the time necessary to reach half-time of maximum growth (R2 = 0.954) was observed during strongly inhibitory conditions. Transformants expressing QRD exhibited maintained glycerol and ethanol yields with increasing p-BQ concentrations, up to 0.44 g g− 1 ethanol at 10 mg L− 1p-BQ, whereas the empty vector control exhibited increased glycerol yield and decreased ethanol yield, amounting to 0.15 g g− 1 ethanol at 10 mg L− 1p-BQ.

Conclusions: Heterologous expression of QRDs from white-rot fungi in S. cerevisiae confers protection against p-BQ toxicity. This investigation supports a role of QRD in the protection against toxic quinones and proposes a biodetoxification strategy against lignin-derived inhibitory p-BQ which can occur simultaneously with fermentation of sugars into ethanol in S. cerevisiae.

Ort, förlag, år, upplaga, sidor
BioMed Central (BMC), 2026. Vol. 25, nr 1, artikel-id 102
Nyckelord [en]
1, 4-Benzoquinone reductase, Bioethanol, Inhibitor, Lignin, p-Benzoquinone, Phanerochaete chrysosporium, Saccharomyces cerevisiae, Trametes versicolor
Nationell ämneskategori
Biokemi Molekylärbiologi
Identifikatorer
URN: urn:nbn:se:umu:diva-252568DOI: 10.1186/s12934-026-03001-1ISI: 001742950500001PubMedID: 41952145Scopus ID: 2-s2.0-105035849473OAI: oai:DiVA.org:umu-252568DiVA, id: diva2:2057215
Forskningsfinansiär
Vetenskapsrådet, 2020–05318Bio4EnergyTillgänglig från: 2026-05-04 Skapad: 2026-05-04 Senast uppdaterad: 2026-05-04Bibliografiskt granskad

Open Access i DiVA

fulltext(2552 kB)9 nedladdningar
Filinformation
Filnamn FULLTEXT01.pdfFilstorlek 2552 kBChecksumma SHA-512
957a355f55a7091048d2e1573cd61e566268c2503337db60d72e4ed1db9248c382832ebdb112e7c57af95742c01b893023a5b88f0352447f53abde678ec3db3c
Typ fulltextMimetyp application/pdf

Övriga länkar

Förlagets fulltextPubMedScopus

Person

Bello-Villarino, MateoJönsson, Leif J.

Sök vidare i DiVA

Av författaren/redaktören
Bello-Villarino, MateoJönsson, Leif J.
Av organisationen
Kemiska institutionen
I samma tidskrift
Microbial Cell Factories
BiokemiMolekylärbiologi

Sök vidare utanför DiVA

GoogleGoogle Scholar
Antalet nedladdningar är summan av nedladdningar för alla fulltexter. Det kan inkludera t.ex tidigare versioner som nu inte längre är tillgängliga.

doi
pubmed
urn-nbn

Altmetricpoäng

doi
pubmed
urn-nbn
Totalt: 81 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf