Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

CcpA-dependent carbon catabolite repression in bacteria.

Jessica B Warner1, Juke S Lolkema

  • 1Molecular Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Haren, The Netherlands.

Microbiology and Molecular Biology Reviews : MMBR
|December 11, 2003
PubMed
Summary

Carbon catabolite repression (CCR) mechanisms differ between bacteria. This review finds CcpA-dependent CCR is widespread beyond gram-positive bacteria, potentially involving nitrogen regulation systems in Proteobacteria.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Models to determine the kinetic mechanisms of ion-coupled transporters.

The Journal of general physiology·2019
Same author

Arginine and Citrulline Catabolic Pathways Encoded by the <i>arc</i> Gene Cluster of Lactobacillus brevis ATCC 367.

Journal of bacteriology·2018
Same author

Convergent evolution of the arginine deiminase pathway: the ArcD and ArcE arginine/ornithine exchangers.

MicrobiologyOpen·2016
Same author

Structure and elevator mechanism of the Na<sup>+</sup>-citrate transporter CitS.

Current opinion in structural biology·2016
Same author

ArcD1 and ArcD2 Arginine/Ornithine Exchangers Encoded in the Arginine Deiminase Pathway Gene Cluster of Lactococcus lactis.

Journal of bacteriology·2015
Same author

The Hill analysis and co-ion-driven transporter kinetics.

The Journal of general physiology·2015

Area of Science:

  • Microbiology
  • Molecular Biology
  • Bacterial Physiology

Background:

  • Carbon catabolite repression (CCR) regulates gene expression based on carbon source availability.
  • Mechanisms of CCR, particularly CcpA-dependent CCR, vary significantly between gram-positive and gram-negative bacteria.
  • In gram-positive bacteria, CcpA-dependent CCR involves HPr kinase-mediated phosphorylation of HPr.

Purpose of the Study:

  • To investigate the distribution of CcpA-dependent CCR across the bacterial kingdom.
  • To identify homologues of HPr kinase and HPr-like proteins.
  • To analyze the functional and evolutionary relationships of these proteins in different bacterial phyla.

Main Methods:

  • Bioinformatic analysis of public databases for HPr kinase and HPr-like protein homologues.

Related Experiment Videos

  • Phylogenetic analysis of identified protein sequences.
  • Genomic context analysis of genes encoding HPr kinase and HPr-like proteins.
  • Main Results:

    • Homologues of HPr kinase are prevalent in Firmicutes and found in Proteobacteria, Fusobacteria, Spirochaetes, and Chlorobi.
    • Proteobacteria, particularly alpha and beta subdivisions, commonly possess HPr kinase and an associated HPr-like protein (XPr).
    • Evidence suggests a potential link between CcpA-dependent CCR and the nitrogen regulation system (Ntr) in Proteobacteria, involving XPr and NPr.

    Conclusions:

    • CcpA-dependent CCR is not exclusive to gram-positive bacteria and is distributed across diverse bacterial phyla.
    • The presence of HPr kinase and XPr in Proteobacteria suggests a conserved regulatory module.
    • A complex regulatory network integrating CCR and Ntr systems may exist in certain Proteobacteria.