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Peptidoglycan precursor synthesis along the sidewall of pole-growing mycobacteria.
García-Heredia, Alam; Pohane, Amol Arunrao; Melzer, Emily S; Carr, Caleb R; Fiolek, Taylor J; Rundell, Sarah R; Lim, Hoong Chuin; Wagner, Jeffrey C; Morita, Yasu S; Swarts, Benjamin M; Siegrist, M Sloan.
Afiliação
  • García-Heredia A; Molecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, United States.
  • Pohane AA; Department of Microbiology, University of Massachusetts, Amherst, United States.
  • Melzer ES; Department of Microbiology, University of Massachusetts, Amherst, United States.
  • Carr CR; Department of Microbiology, University of Massachusetts, Amherst, United States.
  • Fiolek TJ; Department of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, United States.
  • Rundell SR; Department of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, United States.
  • Lim HC; Department of Microbiology and Immunobiology, Harvard Medical School, Boston, United States.
  • Wagner JC; Department of Immunology and Infectious Disease, Harvard T.H. Chan School of Public Health, Boston, United States.
  • Morita YS; Molecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, United States.
  • Swarts BM; Department of Microbiology, University of Massachusetts, Amherst, United States.
  • Siegrist MS; Department of Chemistry and Biochemistry, Central Michigan University, Mount Pleasant, United States.
Elife ; 72018 09 10.
Article em En | MEDLINE | ID: mdl-30198841
ABSTRACT
Rod-shaped mycobacteria expand from their poles, yet d-amino acid probes label cell wall peptidoglycan in this genus at both the poles and sidewall. We sought to clarify the metabolic fates of these probes. Monopeptide incorporation was decreased by antibiotics that block peptidoglycan synthesis or l,d-transpeptidation and in an l,d-transpeptidase mutant. Dipeptides complemented defects in d-alanine synthesis or ligation and were present in lipid-linked peptidoglycan precursors. Characterizing probe uptake pathways allowed us to localize peptidoglycan metabolism with precision monopeptide-marked l,d-transpeptidase remodeling and dipeptide-marked synthesis were coincident with mycomembrane metabolism at the poles, septum and sidewall. Fluorescent pencillin-marked d,d-transpeptidation around the cell perimeter further suggested that the mycobacterial sidewall is a site of cell wall assembly. While polar peptidoglycan synthesis was associated with cell elongation, sidewall synthesis responded to cell wall damage. Peptidoglycan editing along the sidewall may support cell wall robustness in pole-growing mycobacteria.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Peptidoglicano / Parede Celular / Alanina Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Peptidoglicano / Parede Celular / Alanina Idioma: En Ano de publicação: 2018 Tipo de documento: Article