Find en forsker – Københavns Universitet

Videresend til en ven Resize Print Bookmark and Share

Find en forsker

Kenn Gerdes

Kenn Gerdes


Gerdes Research Group

  • Birgitte Haugan Ullerup, PA and Center administrator
  • Solveig Walløe Harpøth, PA and Center administrator (maternity cover)
  • Sidsel Henriksen, Lab Manager
  • Ragnhild Jørgensen Bager, post doc
  • Kristoffer Winther, post doc
  • Mohammad Roghanian, post doc
  • Szabolcs Semsey, post doc
  • Alexander Harms, post doc
  • Yong Zhang, post doc
  • Farshid Jalalvand, post doc
  • Kirtimaan Syal, post doc
  • Georgia Hann, PhD student
  • Kathryn Turnbull, PhD student
  • Emilie Søndberg, PhD student
  • Stine Vang Nielsen, PhD student
  • Meiqin Zhang, Research assistent
  • Simon Gerbild, Master student

We have vacant PhD and Post Doc positions for highly qualified applicants. Please send your CV directly to Kenn Gerdes 

Current Collaborators

  • Ditlev Brodersen, Aarhus University
  • David Clarke, University College Cork, Ireland
  • Christoph Dehio, Biozentrum, Basel, Switzerland
  • Vasili Hauryliuk, Umeå University, Sweden
  • Boris Macek, University of Tübingen, Germany
  • Kim Sneppen, Niels Bohr Institute, University of Copenhagen
  • Namiko Mitarai, Niels Bohr Institute, University of Copenhagen


Introduction to Current Research

The overarching research themes in the Gerdes group are Bacterial Stress Responses and Antibiotic Multidrug Tolerance (Persistence). Research within these fields facilitated the establishment of a research centre funded by the Danish National Research Foundation and the Novo Nordisk Foundation called Centre for Bacterial Stress Responses and Persistence (BASP). This long-term funding enables us to attack difficult but important basic research questions.

Most bacteria live in constantly changing environments and, accordingly, have evolved highly sophisticated regulatory mechanisms that allow them to withstand stressful conditions. In particular, almost all bacteria depend on the ubiquitous regulatory molecules tetra and penta-guanosine phosphate, collectively called (p)ppGpp or Magic Spot, for the survival in the environment and during infections. Thus, the (p)ppGpp-mediated response is required for almost all pathogenic bacteria to be virulent, and thus our basic research will lead to an increased general understanding of bacterial survival and virulence mechanisms.  

Magic Spot was discovered in experiments with the model organism E. coli undergoing amino acid starvation elicits the “stringent response”. In that response, (p)ppGpp reprograms cellular metabolism from rapid to slow growth or dormancy. Here, (p)ppGpp increases dramatically in concentration and profoundly influences gene expression such that the cells manage to adapt to and survive the limited nutrient supply. Importantly, rRNA synthesis is severely curtailed while transcription of amino acid biosynthetic operons is stimulated. Thus, a primary role of (p)ppGpp is to adjust cell growth to the available nutrient resources. However, (p)ppGpp affects many other cellular processes, such as replication, transcription and protein turnover, either directly or indirectly. Stunningly, even though (p)ppGpp has been known for almost 50 years, it is not yet understood how its synthesis is controlled. Magic Spots is synthesized and hydrolysed by the bifunctional Rel enzymes (RelA and SpoT) that are regulated by a number of factors including ribosome-bound tRNA and essential GTPases. However, at the molecular level surprisingly little is known about how Rel enzymes are regulated.As described further below, a long-term goal of our research is to understanding how the enzymatic activities of RelA and SpoT are regulated and how (p)ppGpp contributes to bacterial virulence and persistence (multidrug tolerance).

Current Research Projects

Toxin – Antitoxins

(Mohammad Roghanian and Kathryn Turnbull)

Usually, TA modules code for two components, a toxin that reversibly inhibits cell growth and an antitoxin that counteracts toxin activity; three types of TA loci have been identified. Type I and type III TA loci encode small RNAs that counter the toxins at the translational and posttranslational levels, respectively. Toxins encoded by type II TA loci are inhibited by protein antitoxins via direct protein – protein interaction. Owing to sequence conservation of the toxins, type II TA loci have been divided into families that are broadly conserved in bacteria, or in some cases even in both bacteria and archaea. Thus, members of the relBE, vapBC, and hicAB families are abundant in these two domains of

Both of these gene modules function in persistence but we do not exclude that the genes have other functions as well.

Toxin – Antitoxins of Mycobacterium tuberculosis

(Kristoffer Skovbo Winther)

Some organisms have mystifying high numbers of TA genes. For example, the highly pathogenic and extremely persistent deadly bacterium M. tuberculosis has approximately 80 TA loci. Remarkably, at least 45 of these modules are vapBC genes that encode PIN domain RNA endonucleases. We are now identifying the targets of these difficult-to-analyse toxins, using an array of different approaches. Using a method developed in David Tollervey’s lab, we have now identified the singular molecular targets of a substantial number of these exciting RNases.

(p)ppGpp and Toxin – Antitoxins of Photorhabdus luminescence

(Ragnhild Jørgensen Bager in collaboration with David Clarke, Cork, Ireland)

P. luminescens is a Gram-negative belonging to the family Enterobacteriaceae. Being both a pathogen of a wide range of insects, as well as mutualistic associated with nematodes from the family Heterorhabditis, the bacterium is an excellent model system in which to study the genetics of both mutualism and pathogenicity. Similar to M. tuberculosis, the P. luminescence has a cohort of TA genes. We are now validating some of the TA modules experimentally. We are also investigating the effects of deleting different regulatory genes (relA, spoT, lon, ppk, ppx and TAs) on various phenotypes of this insect pathogen, primarily the effects on its persistence, symbiosis and virulence.

The highly conserved RtcB RNA ligase

(Georgia Hann)

RtcB is a phylogenetically conserved RNA ligase with homologues in all three domains of life. In E. coli, RtcB is expressed from the rtcBA operon that also encodes a 3’-terminal RNA cyclase, RtcA.  The rtcBA operon is transcribed by σ54-associated RNA polymerase and requires the product of the neighbouring gene rtcR, which encodes a transcriptional activator that binds to an upstream activating sequence (UAS).  However, the signal that activates RtcR has not been identified. Moreover, the function of bacterial RtcB ligase is unknown, but a range of RNA ligation activities have been demonstrated.  Recombinant RtcB from E. coli complemented the normally lethal deletion of Trl1 RNA ligase in Yeast and was found to seal both tRNA and mRNA halves after intron removal. We are trying to identify the natural substrate(s) of bacterial RtcB and the signal that activates RtcR.

(p)ppGpp controls cell wall synthesis

(Patricia Dominguez Cuevas)

Observations in the literature indicate that the stringent response controls cell wall synthesis. We are investigating the underlying molecular mechanism.

ID: 44167188