Proteome analysis of Thermococcus onnurineus NA1 reveals the expression of hydrogen gene cluster under carboxydotrophic growth SCIE SCOPUS

DC Field Value Language
dc.contributor.author Yun, Sung-Ho -
dc.contributor.author Kwon, Sang Oh -
dc.contributor.author Park, Gun Wook -
dc.contributor.author Kim, Jin Young -
dc.contributor.author Kang, Sung Gyun -
dc.contributor.author Lee, Jung-Hyun -
dc.contributor.author Chung, Young-Ho -
dc.contributor.author Kim, Soohyun -
dc.contributor.author Choi, Jong-Soon -
dc.contributor.author Kim, Seung Il -
dc.date.accessioned 2020-04-20T07:43:23Z -
dc.date.available 2020-04-20T07:43:23Z -
dc.date.created 2020-01-28 -
dc.date.issued 2011-09-06 -
dc.identifier.issn 1874-3919 -
dc.identifier.uri https://sciwatch.kiost.ac.kr/handle/2020.kiost/3812 -
dc.description.abstract Thermococcus onnurineus NA1 is a typical sulfur-reducing hyperthermophilic archaeon. Genome sequence analysis has shown that T. onnurineus NA1 retains the metabolic pathways necessary not only for organotrophic, but also for carboxydotrophic, growth. T. onnurineus NA1 carboxydotrophic growth may result in hydrogen production, as this archaeon produces hydrogen during oxidizing formate. In this study, we profiled the proteome of T. onnurineus NA1 cultured under carboxydotrophic conditions using CO as an electron donor by the SDS-PAGE/LC-MS/MS method. A total of 1395 proteins were identified by two independent proteomic analyses, which corresponds to similar to 71% of the total predicted open reading frames. To our knowledge, this level of identification coverage exceeds those of other global proteome profiling studies in Archaea. Furthermore, the biological functions of the identified proteins were predicted and cognate enzymes were mapped to the appropriate metabolic pathways. More than 90% of the genes belonging to hydrogenase gene clusters such as Mbx, Sulf-I, Mbh, Hyg4-I, Hyg4-II, and Hyf4-III were expressed during CO culture. This means that hydrogenases induced under carboxydotrophic conditions surpass those induced under an organotrophic condition (yeast extract-peptone-sulfur). Our data suggest that hydrogen production is caused by the expression and functional assembly of T. onnurineus NA1 hydrogenase genes during culture in the presence of CO. (C) 2011 Elsevier B.V. All rights reserved. -
dc.description.uri 1 -
dc.language English -
dc.publisher ELSEVIER SCIENCE BV -
dc.subject SEA HYDROTHERMAL VENT -
dc.subject COMPLETE GENOME SEQUENCE -
dc.subject HYPERTHERMOPHILIC ARCHAEON -
dc.subject PEPTIDE IDENTIFICATION -
dc.subject PYROCOCCUS-FURIOSUS -
dc.subject SHOTGUN PROTEOMICS -
dc.subject KODAKARAENSIS KOD1 -
dc.subject H-2 PRODUCTION -
dc.subject SP-NOV. -
dc.subject RUBRERYTHRIN -
dc.title Proteome analysis of Thermococcus onnurineus NA1 reveals the expression of hydrogen gene cluster under carboxydotrophic growth -
dc.type Article -
dc.citation.endPage 1933 -
dc.citation.startPage 1926 -
dc.citation.title JOURNAL OF PROTEOMICS -
dc.citation.volume 74 -
dc.citation.number 10 -
dc.contributor.alternativeName 강성균 -
dc.contributor.alternativeName 이정현 -
dc.identifier.bibliographicCitation JOURNAL OF PROTEOMICS, v.74, no.10, pp.1926 - 1933 -
dc.identifier.doi 10.1016/j.jprot.2011.05.010 -
dc.identifier.scopusid 2-s2.0-80052025184 -
dc.identifier.wosid 000295302800010 -
dc.type.docType Article -
dc.description.journalClass 1 -
dc.subject.keywordPlus SEA HYDROTHERMAL VENT -
dc.subject.keywordPlus COMPLETE GENOME SEQUENCE -
dc.subject.keywordPlus HYPERTHERMOPHILIC ARCHAEON -
dc.subject.keywordPlus PEPTIDE IDENTIFICATION -
dc.subject.keywordPlus PYROCOCCUS-FURIOSUS -
dc.subject.keywordPlus SHOTGUN PROTEOMICS -
dc.subject.keywordPlus KODAKARAENSIS KOD1 -
dc.subject.keywordPlus H-2 PRODUCTION -
dc.subject.keywordPlus SP-NOV. -
dc.subject.keywordPlus RUBRERYTHRIN -
dc.subject.keywordAuthor SDS-PAGE/LC-MS/MS -
dc.subject.keywordAuthor Thermococcus onnurineus NA1 -
dc.subject.keywordAuthor Carboxydotrophic growth -
dc.relation.journalWebOfScienceCategory Biochemical Research Methods -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Biochemistry & Molecular Biology -
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