Javascript verkar inte påslaget? - Vissa delar av Lunds universitets webbplats fungerar inte optimalt utan javascript, kontrollera din webbläsares inställningar.
Du är här

The MreB-like protein Mbl of S. coelicolor A3(2) depends on MreB for proper localization and contributes to spore wall synthesis.

  • Andrea Heichlinger
  • Moritz Ammelburg
  • Eva-Maria Kleinschnitz
  • Annette Latus
  • Iris Maldener
  • Klas Flärdh
  • Wolfgang Wohlleben
  • Günther Muth
Publiceringsår: 2011
Språk: Engelska
Sidor: 1533-1542
Publikation/Tidskrift/Serie: Journal of Bacteriology
Volym: 193
Nummer: 7
Dokumenttyp: Artikel i tidskrift
Förlag: American Society for Microbiology


Most bacteria with a rod-shape morphology contain an actin-like cytoskeleton consisting of MreB polymers which form helical spirals underneath the cytoplasmic membrane to direct peptidoglycan synthesis for elongation of the cell wall. In contrast MreB of Streptomyces coelicolor is not required for vegetative growth, but has a role in sporulation. Beside MreB, S. coelicolor encodes two further MreB-like proteins, Mbl and SCO6166, whose function is unknown. Whereas MreB and Mbl are highly similar, SCO6166 is shorter, lacking the subdomains IB and IIB of actin-like proteins. Here we showed that MreB and Mbl are not functionally redundant but cooperate in spore wall synthesis. Expression analysis by semi-quantitative RT-PCR revealed distinct expression patterns. mreB and mbl are predominantly induced during morphological differentiation. In contrast sco6166 is strongly expressed during vegetative growth but switched off during sporulation. All genes could be deleted without affecting viability. Even a ΔmreB/mbl double mutant was viable. Δsco6166 had a wildtype phenotype. ΔmreB, Δmbl and ΔmreB/mbl produced swollen prematurely germinating spores that were sensitive to various kinds of stress, suggesting a defect in spore wall integrity. During aerial mycelium formation an Mbl-mCherry fusion protein colocalized with an MreB-eGFP fusion protein at the sporulation septa. Whereas MreB-eGFP localized properly in the Δmbl mutant, Mbl-mCherry localization depended on the presence of a functional MreB protein. Our results revealed that MreB and Mbl cooperate in synthesis of the thickened spore wall, while SCO6166 has a non-essential function during vegetative growth.


  • Microbiology
  • cytoskeleton
  • cell wall synthesis
  • peptidoglycan
  • actin-like
  • sporulation


  • ISSN: 0021-9193

Box 117, 221 00 LUND
Telefon 046-222 00 00 (växel)
Telefax 046-222 47 20
lu [at] lu [dot] se

Fakturaadress: Box 188, 221 00 LUND
Organisationsnummer: 202100-3211
Om webbplatsen