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FtsZ phosphorylation pleiotropically affects Z-ladder formation, antibiotic production, and morphogenesis in Streptomyces coelicolor.
Yagüe, Paula; Willemse, Joost; Xiao, Xiansha; Zhang, Le; Manteca, Angel; van Wezel, Gilles P.
Affiliation
  • Yagüe P; Department of Molecular Biotechnology, Institute of Biology Leiden, Leiden University, PO Box 9505, 2300 AB, Leiden, The Netherlands. yaguepaula@uniovi.es.
  • Willemse J; Department of Molecular Biotechnology, Institute of Biology Leiden, Leiden University, PO Box 9505, 2300 AB, Leiden, The Netherlands.
  • Xiao X; Department of Molecular Biotechnology, Institute of Biology Leiden, Leiden University, PO Box 9505, 2300 AB, Leiden, The Netherlands.
  • Zhang L; Department of Molecular Biotechnology, Institute of Biology Leiden, Leiden University, PO Box 9505, 2300 AB, Leiden, The Netherlands.
  • Manteca A; Departamento de Biología Funcional e IUOPA, Área de Microbiología, Facultad de Medicina, Universidad de Oviedo, 33006, Oviedo, Spain.
  • van Wezel GP; Department of Molecular Biotechnology, Institute of Biology Leiden, Leiden University, PO Box 9505, 2300 AB, Leiden, The Netherlands.
Antonie Van Leeuwenhoek ; 116(1): 1-19, 2023 Jan.
Article de En | MEDLINE | ID: mdl-36383329
ABSTRACT
The GTPase FtsZ forms the cell division scaffold in bacteria, which mediates the recruitment of the other components of the divisome. Streptomycetes undergo two different forms of cell division. Septa without detectable peptidoglycan divide the highly compartmentalised young hyphae during early vegetative growth, and cross-walls are formed that dissect the hyphae into long multinucleoid compartments in the substrate mycelium, while ladders of septa are formed in the aerial hyphae that lead to chains of uninucleoid spores. In a previous study, we analysed the phosphoproteome of Streptomyces coelicolor and showed that FtsZ is phosphorylated at Ser 317 and Ser389. Substituting Ser-Ser for either Glu-Glu (mimicking phosphorylation) or Ala-Ala (mimicking non-phosphorylation) hinted at changes in antibiotic production. Here we analyse development, colony morphology, spore resistance, and antibiotic production in FtsZ knockout mutants expressing FtsZ alleles mimicking Ser319 and Ser387 phosphorylation and non-phosphorylation AA (no phosphorylation), AE, EA (mixed), and EE (double phosphorylation). The FtsZ-eGFP AE, EA and EE alleles were not able to form observable FtsZ-eGFP ladders when they were expressed in the S. coelicolor wild-type strain, whereas the AA allele could form apparently normal eGFP Z-ladders. The FtsZ mutant expressing the FtsZ EE or EA or AE alleles is able to sporulate indicating that the mutant alleles are able to form functional Z-rings leading to sporulation when the wild-type FtsZ gene is absent. The four mutants were pleiotropically affected in colony morphogenesis, antibiotic production, substrate mycelium differentiation and sporulation (sporulation timing and spore resistance) which may be an indirect result of the effect in sporulation Z-ladder formation. Each mutant showed a distinctive phenotype in antibiotic production, single colony morphology, and sporulation (sporulation timing and spore resistance) indicating that the different FtsZ phosphomimetic alleles led to different phenotypes. Taken together, our data provide evidence for a pleiotropic effect of FtsZ phosphorylation in colony morphology, antibiotic production, and sporulation.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Streptomyces / Streptomyces coelicolor Langue: En Journal: Antonie Van Leeuwenhoek Année: 2023 Type de document: Article Pays d'affiliation: Pays-Bas

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Streptomyces / Streptomyces coelicolor Langue: En Journal: Antonie Van Leeuwenhoek Année: 2023 Type de document: Article Pays d'affiliation: Pays-Bas
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