Structural insights into the regulation of sialic acid catabolism by the Vibrio vulnificus transcriptional repressor NanR

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dc.contributor.authorJungwon Hwang-
dc.contributor.authorB S Kim-
dc.contributor.authorSong Yee Jang-
dc.contributor.authorJ G Lim-
dc.contributor.authorD J You-
dc.contributor.authorH S Jung-
dc.contributor.authorTae Kwang Oh-
dc.contributor.authorJ O Lee-
dc.contributor.authorS H Choi-
dc.contributor.authorMyung Hee Kim-
dc.date.accessioned2017-04-19T09:41:30Z-
dc.date.available2017-04-19T09:41:30Z-
dc.date.issued2013-
dc.identifier.issn0027-8424-
dc.identifier.uri10.1073/pnas.1302859110ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11429-
dc.description.abstractPathogenic and commensal bacteria that experience limited nutrient availability in their host have evolved sophisticated systems to catabolize the mucin sugar N-acetylneuraminic acid, thereby facilitating their survival and colonization. The correct function of the associated catabolic machinery is particularly crucial for the pathogenesis of enteropathogenic bacteria during infection, although the molecular mechanisms involved with the regulation of the catabolic machinery are unknown. This study reports the complex structure of NanR, a repressor of the N-acetylneuraminate (nan) genes responsible for N-acetylneuraminic acid catabolism, and its regulatory ligand, N-acetylmannosamine 6-phosphate (ManNAc-6P), in the human pathogenic bacterium Vibrio vulnificus. Structural studies combined with electron microscopic, biochemical, and in vivo analysis demonstrated that NanR forms a dimer in which the two monomers create an arched tunnel-like DNA-binding space, which contains positively charged residues that interact with the nan promoter. The interaction between the NanR dimer and DNA is alleviated by the ManNAc-6P-mediated relocation of residues in the ligand-binding domain of NanR, which subsequently relieves the repressive effect of NanR and induces the transcription of the nan genes. Survival studies in which mice were challenged with a ManNAc-6P-binding-defective mutant strain of V. vulnificus demonstrated that this relocation of NanR residues is critical for V. vulnificus pathogenesis. In summary, this study presents a model of the mechanism that regulates sialic acid catabolism via NanR in V. vulnificus.-
dc.publisherNatl Acad Sciences-
dc.titleStructural insights into the regulation of sialic acid catabolism by the Vibrio vulnificus transcriptional repressor NanR-
dc.title.alternativeStructural insights into the regulation of sialic acid catabolism by the Vibrio vulnificus transcriptional repressor NanR-
dc.typeArticle-
dc.citation.titleProceedings of National Academy of Sciences of United States of America-
dc.citation.number30-
dc.citation.endPageE2837-
dc.citation.startPageE2829-
dc.citation.volume110-
dc.contributor.affiliatedAuthorJungwon Hwang-
dc.contributor.affiliatedAuthorSong Yee Jang-
dc.contributor.affiliatedAuthorTae Kwang Oh-
dc.contributor.affiliatedAuthorMyung Hee Kim-
dc.contributor.alternativeName황중원-
dc.contributor.alternativeName김병식-
dc.contributor.alternativeName장송이-
dc.contributor.alternativeName임종규-
dc.contributor.alternativeName유동주-
dc.contributor.alternativeName정현숙-
dc.contributor.alternativeName오태광-
dc.contributor.alternativeName이지오-
dc.contributor.alternativeName최상호-
dc.contributor.alternativeName김명희-
dc.identifier.bibliographicCitationProceedings of National Academy of Sciences of United States of America, vol. 110, no. 30, pp. E2829-E2837-
dc.identifier.doi10.1073/pnas.1302859110-
dc.subject.keywordMucin sugar utilization-
dc.subject.keywordNan gene repressor-
dc.subject.localMucin sugar utilization-
dc.subject.localNan gene repressor-
dc.description.journalClassY-
Appears in Collections:
Division of Biomedical Research > Microbiome Convergence Research Center > 1. Journal Articles
Division of Bio Technology Innovation > Core Research Facility & Analysis Center > 1. Journal Articles
Division of Biomedical Research > Metabolic Regulation Research Center > 1. Journal Articles
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