4.3 Article

Repression of the TreR transcriptional regulator in Streptococcus mutans by the global regulator, CcpA

期刊

FEMS MICROBIOLOGY LETTERS
卷 368, 期 3, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/femsle/fnab004

关键词

Streptococcus mutans; regulation; trehalose; CcpA; TreR; repressor

资金

  1. National Institute for Dental Craniofacial Research [R01 DE013683, R01 DE017425]
  2. National Institute for Dental Craniofacial Research Training Program in Oral Sciences [T90 DE021985]

向作者/读者索取更多资源

Streptococcus mutans, the etiologic agent of dental caries in humans, is a dominating force in the oral microbiome due to its highly-evolved survival propensity. This oral pathogen encodes regulatory elements such as CcpA and TreR, which play key roles in controlling sugar metabolism and stress response. Loss of these regulators impairs growth and fitness response, indicating their involvement in carbon catabolism control and stress response induction.
Streptococcus mutans, the etiologic agent of dental caries in humans, is considered a dominating force in the oral microbiome due to its highly-evolved propensity for survival. The oral pathogen encodes an elaborate array of regulatory elements, including the carbon catabolite-responsive regulator, CcpA, a global regulator key in the control of sugar metabolism and in stress tolerance response mechanisms. The recently characterized trehalose utilization operon, integral for the catabolism of the disaccharide trehalose, is controlled by a local regulator, TreR, which has been implicated in a number of cellular functions outside of trehalose catabolism. Electrophoretic mobility shift assays demonstrated that CcpA bound a putative cre site in the treR promoter. Loss of ccpA resulted in elevated expression of treR in cultures of the organism grown in glucose or trehalose, indicating that CcpA not only acts as a repressor of trehalose catabolism genes, but also the local regulator. The loss of both CcpA and TreR in S. mutans resulted in an impaired growth rate and fitness response, supporting the hypothesis that these regulators are involved in carbon catabolism control and in induction of components of the organism's stress response.

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