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dc.contributor.authorKeerthiraju, E
dc.contributor.authorDu, C
dc.contributor.authorTucker, G
dc.contributor.authorGreetham, D
dc.coverage.spatialSwitzerland
dc.date.accessioned2023-05-19T10:08:14Z
dc.date.available2023-05-19T10:08:14Z
dc.date.issued2019-11-18
dc.identifierARTN 575
dc.identifiermicroorganisms7110575
dc.identifier.citationMicroorganisms, 2019, 7 (11), pp. E575 -en_US
dc.identifier.issn2076-2607
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5794
dc.identifier.eissn2076-2607
dc.identifier.eissn2076-2607
dc.identifier.doi10.3390/microorganisms7110575
dc.description.abstractIndustrial production of bioethanol from lignocellulosic materials (LCM's) is reliant on a microorganism being tolerant to the stresses inherent to fermentation. Previous work has highlighted the importance of a cytochrome oxidase chaperone gene (COX20) in improving yeast tolerance to acetic acid, a common inhibitory compound produced during pre-treatment of LCM's. The presence of acetic acid has been shown to induce oxidative stress and programmed cell death, so the role of COX20 in oxidative stress was determined. Analysis using flow cytometry revealed that COX20 expression was associated with reduced levels of reactive oxygen species (ROS) in hydrogen peroxide and metal-induced stress, and there was a reduction in apoptotic and necrotic cells when compared with a strain without COX20. Results on the functionality of COX20 have revealed that overexpression of COX20 induced respiratory growth in Δimp1 and Δcox18, two genes whose presence is essential for yeast respiratory growth. COX20 also has a role in protecting the yeast cell against programmed cell death.
dc.formatElectronic
dc.format.extentE575 -
dc.languageeng
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.relation.ispartofMicroorganisms
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectCOX20
dc.subjectoxidative stress
dc.subjectprogrammed cell death
dc.subjectrespiratory growth
dc.subjectyeast
dc.titleA Role for COX20 in Tolerance to Oxidative Stress and Programmed Cell Death in Saccharomyces cerevisiae.en_US
dc.typeJournal Article
dcterms.dateAccepted2019-11-15
dc.date.updated2023-05-19T09:50:52Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.3390/microorganisms7110575en_US
rioxxterms.licenseref.startdate2019-11-18
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/31752220
pubs.issue11
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Structural Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Structural Biology/Structural Biology of Cell Signalling
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.3390/microorganisms7110575
pubs.volume7
icr.provenanceDeposited by Mr Keerthiraju Ethiraju Ravichandran on 2023-05-19. Deposit type is initial. No. of files: 1. Files: A Role for iCOX20i in Tolerance to Oxidative Stress and Programmed Cell Death in iSaccharomyces cerevisiaei.pdf


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