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dc.contributor.authorWu, Chien-Chenen_US
dc.contributor.authorLin, Ching-Tingen_US
dc.contributor.authorCheng, Wei-Yunen_US
dc.contributor.authorHuang, Ching-Jouen_US
dc.contributor.authorWang, Zhe-Chongen_US
dc.contributor.authorPeng, Hwei-Lingen_US
dc.date.accessioned2014-12-08T15:22:43Z-
dc.date.available2014-12-08T15:22:43Z-
dc.date.issued2012-04-01en_US
dc.identifier.issn1350-0872en_US
dc.identifier.urihttp://hdl.handle.net/11536/16051-
dc.description.abstractType 3 fimbriae play a crucial role in Klebsiella pneumoniae biofilm formation, but the mechanism of the regulation of the type 3 fimbrial operon is largely unknown. In K. pneumoniae CG43, three regulatory genes, mrkH, mrkI and mrkJ, are located downstream of the type 3 fimbrial genes mrkABCDF. The production of the major pilin MrkA is abolished by the deletion of mrkH or mrkI but slightly increased by the deletion of mrkJ. Additionally, quantitative RT-PCR and a promoter reporter assay of mrkHI verified that the transcription of mrkHI was activated by MrkI, suggesting autoactivation of mrkHI transcription. In addition, sequence analysis of the mrkH promoter region revealed a putative ferric uptake regulator (Fur) box. Deletion of fur decreased the transcription of mrkH, mrkI and mrkA. The expression of type 3 fimbriae and bacterial biofilm formation were also reduced by the deletion of fur. Moreover, a recombinant Fur was found to be able to bind both promoters, with higher affinity for P-mrkH than P-mrkA, implying that Fur controls type 3 fimbriae expression via MrkHI. We also proved that iron availability can influence type 3 fimbriae activity.en_US
dc.language.isoen_USen_US
dc.titleFur-dependent MrkHI regulation of type 3 fimbriae in Klebsiella pneumoniae CG43en_US
dc.typeArticleen_US
dc.identifier.journalMICROBIOLOGY-SGMen_US
dc.citation.volume158en_US
dc.citation.issueen_US
dc.citation.epage1045en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department分子醫學與生物工程研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitute of Molecular Medicine and Bioengineeringen_US
dc.identifier.wosnumberWOS:000303633200019-
dc.citation.woscount8-
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