Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/58056
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dc.contributor.authorYardimci, Berna Kavakcioglu-
dc.date.accessioned2024-10-20T16:20:49Z-
dc.date.available2024-10-20T16:20:49Z-
dc.date.issued2024-
dc.identifier.issn1517-8382-
dc.identifier.issn1678-4405-
dc.identifier.urihttps://doi.org/10.1007/s42770-024-01525-5-
dc.identifier.urihttps://hdl.handle.net/11499/58056-
dc.description.abstractVery high gravity (VHG) fermentation is an industrial-scale process utilizing a sugar concentration above 250 g/L to attain a significant ethanol concentration, with the advantages of decreased labor, production costs, water usage, bacterial contamination, and energy consumption. Saccharomyces cerevisiae is one of the most extensively employed organisms in ethanol fermentation through VHG technology. Conversely, high glucose exposure leads to numerous stress factors that negatively impact the ethanol production efficiency of this organism. Here, the impact of various phytochemicals added to the VHG medium on viability, glucose consumption, ethanol production efficiency, total antioxidant-oxidant status (TAS and TOS), and the response of the enzymatic antioxidant system of yeast were investigated. 2.0 mM naringenin and caffeic acid increased ethanol production by 2.453 +/- 0.198 and 1.261 +/- 0.138-fold, respectively. The glucose consumption rate exhibited a direct relationship with ethanol production in the naringenin-supplemented group. The highest TAS was determined as 0.734 +/- 0.044 mmol Trolox Eq./L in the same group. Furthermore, both phytochemical compounds exhibited robust positive correlations with TAS (rnaringenin = 0.9986; rcaffeic acid = 0.9553) and TOS levels (rnaringenin = -0.9824; rcaffeic acid = -0.9791). While naringenin caused statistically significant increases in glutathione reductase (GR) and thioredoxin reductase (TrxR) activities, caffeic acid significantly increased TrxR and superoxide dismutase (SOD). Both phytochemicals seem to impact the ethanol production ability by regulating the redox status of the cells. We believe that the incorporation of particularly cost-effective antioxidants into the fermentation medium may serve as an alternative way to enhance the efficiency of bioethanol production using VHG technology.en_US
dc.description.sponsorshipScientific Research Projects Unit of Pamukkale University [2023FEBE006]en_US
dc.description.sponsorshipThis study was supported by the Scientific Research Projects Unit of Pamukkale University (PAUBAP 2023FEBE006).en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofBrazilian Journal of Microbiologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectVery high gravity fermentationen_US
dc.subjectYeasten_US
dc.subjectEthanol productionen_US
dc.subjectPhytochemicalsen_US
dc.subjectOxidative stressen_US
dc.subjectSaccharomyces-Cerevisiaeen_US
dc.subjectGlutathioneen_US
dc.subjectGlucoseen_US
dc.subjectPolyphenolsen_US
dc.subjectQuercetinen_US
dc.subjectRosen_US
dc.subjectSupplementationen_US
dc.subjectOptimizationen_US
dc.subjectAntioxidantsen_US
dc.subjectMetabolismen_US
dc.titleNaringenin and caffeic acid increase ethanol production in yeast cells by reducing very high gravity fermentation-related oxidative stressen_US
dc.typeArticleen_US
dc.typeArticle; Early Accessen_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.1007/s42770-024-01525-5-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid57206722539-
dc.identifier.pmid39320639en_US
dc.identifier.scopus2-s2.0-85205067921en_US
dc.identifier.wosWOS:001320148900002en_US
dc.institutionauthor-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.openairetypeArticle; Early Access-
item.cerifentitytypePublications-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.dept17.01. Chemistry-
Appears in Collections:Fen Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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