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Repurposing a chemosensory macromolecular machine.
Ortega, Davi R; Yang, Wen; Subramanian, Poorna; Mann, Petra; Kjær, Andreas; Chen, Songye; Watts, Kylie J; Pirbadian, Sahand; Collins, David A; Kooger, Romain; Kalyuzhnaya, Marina G; Ringgaard, Simon; Briegel, Ariane; Jensen, Grant J.
Afiliação
  • Ortega DR; Division of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Blvd, Pasadena, CA, C1125, USA.
  • Yang W; Institute of Biology, Leiden University, 2333 BE, Leiden, The Netherlands.
  • Subramanian P; Division of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Blvd, Pasadena, CA, C1125, USA.
  • Mann P; Department of Ecophysiology, Max Planck Institute for Terrestrial Microbiology, D-35043, Marburg, Germany.
  • Kjær A; Division of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Blvd, Pasadena, CA, C1125, USA.
  • Chen S; Rex Richards Building, South Parks Road, Oxford, OX1 3QU, UK.
  • Watts KJ; Division of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Blvd, Pasadena, CA, C1125, USA.
  • Pirbadian S; Division of Microbiology and Molecular Genetics, School of Medicine, Loma Linda University, Loma Linda, CA, 92350, USA.
  • Collins DA; Department of Physics and Astronomy, University of Southern California, Los Angeles, CA, 90089, USA.
  • Kooger R; Department of Biology, Viral Information Institute, San Diego State University, San Diego, CA, 92182, USA.
  • Kalyuzhnaya MG; Institute of Molecular Biology and Biophysics, Eidgenössische Technische Hochschule Zürich, CH-8093, Zürich, Switzerland.
  • Ringgaard S; Department of Biology, Viral Information Institute, San Diego State University, San Diego, CA, 92182, USA.
  • Briegel A; Department of Ecophysiology, Max Planck Institute for Terrestrial Microbiology, D-35043, Marburg, Germany.
  • Jensen GJ; Institute of Biology, Leiden University, 2333 BE, Leiden, The Netherlands. a.briegel@biology.leidenuniv.nl.
Nat Commun ; 11(1): 2041, 2020 04 27.
Article em En | MEDLINE | ID: mdl-32341341
How complex, multi-component macromolecular machines evolved remains poorly understood. Here we reveal the evolutionary origins of the chemosensory machinery that controls flagellar motility in Escherichia coli. We first identify ancestral forms still present in Vibrio cholerae, Pseudomonas aeruginosa, Shewanella oneidensis and Methylomicrobium alcaliphilum, characterizing their structures by electron cryotomography and finding evidence that they function in a stress response pathway. Using bioinformatics, we trace the evolution of the system through γ-Proteobacteria, pinpointing key evolutionary events that led to the machine now seen in E. coli. Our results suggest that two ancient chemosensory systems with different inputs and outputs (F6 and F7) existed contemporaneously, with one (F7) ultimately taking over the inputs and outputs of the other (F6), which was subsequently lost.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pseudomonas aeruginosa / Vibrio cholerae / Methylococcaceae / Shewanella / Substâncias Macromoleculares Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pseudomonas aeruginosa / Vibrio cholerae / Methylococcaceae / Shewanella / Substâncias Macromoleculares Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article