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dc.contributor.authorLin, Hsiao-Hsienen_US
dc.contributor.authorHsu, Chi-Chengen_US
dc.contributor.authorYang, Chi-Dungen_US
dc.contributor.authorJu, Yih-Weien_US
dc.contributor.authorChen, Yi-Peien_US
dc.contributor.authorTseng, Ching-Pingen_US
dc.date.accessioned2014-12-08T15:26:36Z-
dc.date.available2014-12-08T15:26:36Z-
dc.date.issued2011-10-01en_US
dc.identifier.issn0021-9193en_US
dc.identifier.urihttp://dx.doi.org/10.1128/JB.05359-11en_US
dc.identifier.urihttp://hdl.handle.net/11536/18894-
dc.description.abstractGlucose is a carbon source that is capable of modulating the level of cyclic AMP (cAMP)-regulated genes. In the present study, we found that the stability of ompA mRNA was reduced in Escherichia coli when glucose (40 mM) was present in Luria-Bertani (LB) medium. This effect was associated with a low level of cAMP induced by the glucose. The results were confirmed with an adenylyl cyclase mutant with low levels of cAMP that are not modulated by glucose. Northern blot and Western blot analyses revealed that the host factor I (Hfq) (both mRNA and protein) levels were downregulated in the presence of cAMP. Furthermore, we showed that a complex of cAMP receptor protein (CRP) and cAMP binds to a specific P3(hfq) promoter region of hfq and regulates hfq expression. The regulation of the hfq gene was confirmed in vivo using an hfq-deficient mutant transformed with an exogenous hfq gene containing the promoter. These results demonstrated that expression of hfq was repressed by the CRP-cAMP complex. The presence of glucose resulted in increased Hfq protein levels, which decreased ompA mRNA stability. An additional experiment showed that cAMP also increased the stability of fur mRNA. Taken together, these results suggested that the repression of Hfq by cAMP may contribute to the stability of other mRNA in E. coli.en_US
dc.language.isoen_USen_US
dc.titleNegative Effect of Glucose on ompA mRNA Stability: a Potential Role of Cyclic AMP in the Repression of hfq in Escherichia colien_US
dc.typeArticleen_US
dc.identifier.doi10.1128/JB.05359-11en_US
dc.identifier.journalJOURNAL OF BACTERIOLOGYen_US
dc.citation.volume193en_US
dc.citation.issue20en_US
dc.citation.spage5833en_US
dc.citation.epage5840en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000295256100026-
dc.citation.woscount8-
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