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dc.contributor.authorNoppon Lertwattanasakulen_US
dc.contributor.authorSuprayogien_US
dc.contributor.authorMasayuki Murataen_US
dc.contributor.authorNadchanok Rodrussameeen_US
dc.contributor.authorSavitree Limtongen_US
dc.contributor.authorTomoyuki Kosakaen_US
dc.contributor.authorMamoru Yamadaen_US
dc.date.accessioned2018-09-04T09:22:47Z-
dc.date.available2018-09-04T09:22:47Z-
dc.date.issued2013-04-01en_US
dc.identifier.issn15729699en_US
dc.identifier.issn00036072en_US
dc.identifier.other2-s2.0-84876681117en_US
dc.identifier.other10.1007/s10482-012-9874-0en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84876681117&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52259-
dc.description.abstractBy random integrative mutagenesis with a kanMX4 cassette in Kluyveromyces marxianus DMKU 3-1042, we obtained three mutants of COX15, ATP25 and CYC3 encoding a cytochrome oxidase assembly factor (singleton), a transcription factor required for assembly of the Atp9p subunit of mitochondrial ATP synthase and cytochrome c heme lyase, respectively, as mutants lacking growth capability on xylose and/or arabinose. They exhibited incapability of growth on non-fermentable carbon sources, such as acetate or glycerol, and thermosensitiveness. Their biomass formation in glucose medium was reduced, but ethanol yields were increased with a high ethanol level in the medium, compared to those of the parental strain. Experiments with respiratory inhibitors showed that cox15 and cyc3, but not atp25, were able to grow in glucose medium containing antimycin A and that the atp25 mutant was KCN-resistant. Activities of NADH and ubiquinol oxidases in membrane fractions of each mutant became a half of that of the parent and negligible, respectively, and their remaining NADH oxidase activities were found to be resistant to KCN. Absolute absorption spectral analysis revealed that the peak corresponding to a + a3was very small in atp25 and negligible in cox15 and cyc3. These findings suggest that the K. marxianus strain possesses an alternative KCN-resistant oxidase that is located between primary dehydrogenases and the ubiquinone pool and that the respiratory activity is essential for utilization of pentoses. © 2013 Springer Science+Business Media Dordrecht.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.titleEssentiality of respiratory activity for pentose utilization in thermotolerant yeast Kluyveromyces marxianus DMKU 3-1042en_US
dc.typeJournalen_US
article.title.sourcetitleAntonie van Leeuwenhoek, International Journal of General and Molecular Microbiologyen_US
article.volume103en_US
article.stream.affiliationsYamaguchi Universityen_US
article.stream.affiliationsKasetsart Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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