Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kim, Tae-Su | - |
dc.contributor.author | Yoo, Ji-Hyun | - |
dc.contributor.author | Kim, Sang-Yong | - |
dc.contributor.author | Pan, Cheol-Ho | - |
dc.contributor.author | Kalia, Vipin C. | - |
dc.contributor.author | Kang, Yun Chan | - |
dc.contributor.author | Lee, Jung-Kul | - |
dc.date.accessioned | 2024-01-20T08:03:28Z | - |
dc.date.available | 2024-01-20T08:03:28Z | - |
dc.date.created | 2021-08-31 | - |
dc.date.issued | 2015-01 | - |
dc.identifier.issn | 1359-5113 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/125973 | - |
dc.description.abstract | A mutant of Agrobacterium tumefaciens (S02-13) producing high levels of coenzyme Q(10) (CoQ(10)), was selected by high-throughput screening after repeated NTG mutagenesis. Mutant S02-13 was resistant to sodium azide and menadione and showed an eight-fold increase in CoQ(10) production, as compared to that of the parent strain. The amount of CoQ(10) produced by this mutant reached 350 mg l(-1) in pH-stat fed-batch culture. Mutant S02-13 differed from wild-type in morphology, biochemical properties, and proteome profiles. Scanning electron microscopy results revealed a remarkable change in morphology: the wild-type strain had a rod shape, whereas the mutant S02-13 was coccoid. In contrast to wild-type, the mutant S02-13 strain showed a negative reaction to tryptophan deaminase and N-2 reduction, and a positive reaction to nitrate production in API kit assays. The spots representing proteins that were increased in the proteome expression of the mutant S02-13 strain were identified as glyceraldehyde-3-phosphate dehydrogenase (GAPDH), glucosaminitol dehydrogenase (GlcNOH), and superoxide dismutase (SOD). In particular, the enzyme activities of GAPDH and G1cNOH increased eight-fold and three-fold, respectively, in the mutant, as compared to the wild-type. (C) 2014 Elsevier Ltd. All rights reserved. | - |
dc.language | English | - |
dc.publisher | ELSEVIER SCI LTD | - |
dc.subject | CYTOCHROME-C-OXIDASE | - |
dc.subject | COCCOID FORMS | - |
dc.subject | UBIQUINONE | - |
dc.subject | MORPHOLOGY | - |
dc.subject | OXIDATION | - |
dc.subject | PROTEIN | - |
dc.subject | OXIDOREDUCTASE | - |
dc.subject | DEHYDROGENASE | - |
dc.subject | PEROXIDATION | - |
dc.subject | ALCOHOL | - |
dc.title | Screening and characterization of an Agrobacterium tumefaciens mutant strain producing high level of coenzyme Q(10) | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.procbio.2014.10.024 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | PROCESS BIOCHEMISTRY, v.50, no.1, pp.33 - 39 | - |
dc.citation.title | PROCESS BIOCHEMISTRY | - |
dc.citation.volume | 50 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 33 | - |
dc.citation.endPage | 39 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000349500800006 | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Biotechnology & Applied Microbiology | - |
dc.relation.journalWebOfScienceCategory | Engineering, Chemical | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Biotechnology & Applied Microbiology | - |
dc.relation.journalResearchArea | Engineering | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | CYTOCHROME-C-OXIDASE | - |
dc.subject.keywordPlus | COCCOID FORMS | - |
dc.subject.keywordPlus | UBIQUINONE | - |
dc.subject.keywordPlus | MORPHOLOGY | - |
dc.subject.keywordPlus | OXIDATION | - |
dc.subject.keywordPlus | PROTEIN | - |
dc.subject.keywordPlus | OXIDOREDUCTASE | - |
dc.subject.keywordPlus | DEHYDROGENASE | - |
dc.subject.keywordPlus | PEROXIDATION | - |
dc.subject.keywordPlus | ALCOHOL | - |
dc.subject.keywordAuthor | Coenzyme Q(10) | - |
dc.subject.keywordAuthor | Mutagenesis | - |
dc.subject.keywordAuthor | Production | - |
dc.subject.keywordAuthor | 2-Dimensional electrophoresis | - |
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