Corynebacterium glutamicum sigma(E) is involved in responses to cell surface stresses and its activity is controlled by the anti-sigma factor CseE
DC Field | Value | Language |
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dc.contributor.author | Park, Soo-Dong | - |
dc.contributor.author | Youn, Jung-Won | - |
dc.contributor.author | Kim, Young-Joon | - |
dc.contributor.author | Lee, Seok-Myung | - |
dc.contributor.author | Kim, Younhee | - |
dc.contributor.author | Lee, Heung-Shick | - |
dc.date.accessioned | 2021-09-09T10:30:39Z | - |
dc.date.available | 2021-09-09T10:30:39Z | - |
dc.date.created | 2021-06-10 | - |
dc.date.issued | 2008-03 | - |
dc.identifier.issn | 1350-0872 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/123927 | - |
dc.description.abstract | In this study, we demonstrate that a, an alternative a factor of Corynebacterium glutamicum, is involved in cell surface stresses. Cells in which the sigE gene was deleted evidenced increased sensitivity to magnesium deficiency, as well as to SDS, lysozymes, EDTA and heat. We utilized physiological analyses to show that the downstream gene, designated cseE, encodes an anti-sigma factor. The retarded growth of the cseE mutant cells under ordinary growth conditions could be recovered by an additional deletion of sigE encoding a E. Under stress conditions, the phenotype of the cseE-overexpressing cells mimicked that of the sigE mutant. The sigE and cseE genes were transcribed into a single transcript, and gene transcription was stimulated by heat. The SigE and CseE proteins interacted physically in vitro, in the form of glutathione S-transferase (GST) and maltose binding protein (MBP) fusion proteins, respectively. 2D-PAGE analysis of the wild-type and mutant crude extracts showed that the sigE mutant failed to synthesize a 34 kDa polypeptide that was normally induced in wild-type cells grown under heat (or SDS)-stressed conditions. The protein turned out to be expressed from ORF NCgI 1070 and showed similarity to methyltransferases which may confer resistance to antibiotics. Accordingly, the sigE mutant evidenced extreme sensitivity to antibiotics, including nalidixic acid, penicillin and vancomycin. Finally, we present a discussion of the possible role of the sigE and cseE genes in the acclimation of C. glutamicum to cell surface stress conditions. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | SOC GENERAL MICROBIOLOGY | - |
dc.subject | OXYGENATED MYCOLIC ACIDS | - |
dc.subject | MYCOBACTERIUM-TUBERCULOSIS | - |
dc.subject | STREPTOMYCES-COELICOLOR | - |
dc.subject | REGULATORY NETWORK | - |
dc.subject | GENE-EXPRESSION | - |
dc.subject | TRANSCRIPTION | - |
dc.subject | CLONING | - |
dc.subject | GENOME | - |
dc.subject | BIOSYNTHESIS | - |
dc.subject | ATCC-13032 | - |
dc.title | Corynebacterium glutamicum sigma(E) is involved in responses to cell surface stresses and its activity is controlled by the anti-sigma factor CseE | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Lee, Heung-Shick | - |
dc.identifier.doi | 10.1099/mic.0.2007/012690-0 | - |
dc.identifier.scopusid | 2-s2.0-42949151549 | - |
dc.identifier.wosid | 000254451500023 | - |
dc.identifier.bibliographicCitation | MICROBIOLOGY-SGM, v.154, pp.915 - 923 | - |
dc.relation.isPartOf | MICROBIOLOGY-SGM | - |
dc.citation.title | MICROBIOLOGY-SGM | - |
dc.citation.volume | 154 | - |
dc.citation.startPage | 915 | - |
dc.citation.endPage | 923 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Microbiology | - |
dc.relation.journalWebOfScienceCategory | Microbiology | - |
dc.subject.keywordPlus | OXYGENATED MYCOLIC ACIDS | - |
dc.subject.keywordPlus | MYCOBACTERIUM-TUBERCULOSIS | - |
dc.subject.keywordPlus | STREPTOMYCES-COELICOLOR | - |
dc.subject.keywordPlus | REGULATORY NETWORK | - |
dc.subject.keywordPlus | GENE-EXPRESSION | - |
dc.subject.keywordPlus | TRANSCRIPTION | - |
dc.subject.keywordPlus | CLONING | - |
dc.subject.keywordPlus | GENOME | - |
dc.subject.keywordPlus | BIOSYNTHESIS | - |
dc.subject.keywordPlus | ATCC-13032 | - |
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