Repository logo
  • Español
  • English
  • Log In
    New user? Click here to register. Have you forgotten your password?
Repository logo
    Communities & Collections
    All of RepHip
  • Ayuda
  • Español
  • English
  • Log In
    New user? Click here to register. Have you forgotten your password?
  1. Home
  2. Browse by Author

Browsing by Author "Thompson, John: provide phosphorylated sugars"

Now showing 1 - 1 of 1
Results Per Page
Sort Options
  • Loading...
    Thumbnail Image
    ItemOpen Access
    Enterococcus faecalis MalR acts as a repressor of the maltose operons and additionally mediates their catabolite repression via direct interaction with seryl-phosphorylated-HPr
    (Wiley, 2019-11-22) Grand, Maxime; Blancato, Víctor Sebastián; Espariz, Martín; Deutscher, Josef; Pikis, Andreas; Hartke, Axel; Magni, Christian; Sauvageot, Nicolas; https://orcid.org/0000-0003-3945-2859; https://orcid.org/0000-0002-4090-515X; https://orcid.org/0000-0002-2537-0062; https://orcid.org/0000-0002-5179-9700; https://orcid.org/0000-0002-7595-4330; Brückner, Reinhold: provide plasmid pRB473; Thompson, John: provide phosphorylated sugars
    Enterococci are gram-positive pathogens and lead to cause hospital-acquired infections worldwide. Central carbon metabolism was shown as highly induced in Enterococcus faecalis during infection context. Metabolism of α-polysaccharides was previously described as an important factor for host colonisation and biofilm formation. A better characterisation of the adaptation of this bacterium to carbohydrate availabilities may lead to a better understanding of the link between carbohydrate metabolism and the infection process of E. faecalis. Here we show that MalR, a LacI/GalR transcriptional regulator, is the main factor in the regulation of the two divergent operons involved in maltose metabolism in this bacterium. The malR gene is transcribed from the malP promoter, but also from an internal promoter inside the gene located upstream of malR. In the absence of maltose, MalR acts as a repressor and in the presence of glucose, it exerts efficient CcpA-independent carbon catabolite repression. The central PTS protein P-Ser-HPr interacts directly with MalR and enhances its DNA binding capacity, which allows E. faecalis to adapt its metabolism to environmental conditions.

RepHipUNR ©2007-2024

Universidad Nacional de Rosario

  • Cookie settings
  • Privacy policy
  • End User Agreement

We collect and process your personal information for the following purposes: Authentication, Preferences, Acknowledgement and Statistics.
To learn more, please read our
privacy policy.

Customize