Chemically Induced Cell Wall Stapling in Bacteria. Issue 2 (18th February 2021)
- Record Type:
- Journal Article
- Title:
- Chemically Induced Cell Wall Stapling in Bacteria. Issue 2 (18th February 2021)
- Main Title:
- Chemically Induced Cell Wall Stapling in Bacteria
- Authors:
- Rivera, Sylvia L.
Espaillat, Akbar
Aditham, Arjun K.
Shieh, Peyton
Muriel-Mundo, Chris
Kim, Justin
Cava, Felipe
Siegrist, M. Sloan - Abstract:
- Summary: Transpeptidation reinforces the structure of cell-wall peptidoglycan, an extracellular heteropolymer that protects bacteria from osmotic lysis. The clinical success of transpeptidase-inhibiting β-lactam antibiotics illustrates the essentiality of these cross-linkages for cell-wall integrity, but the presence of multiple, seemingly redundant transpeptidases in many species makes it challenging to determine cross-link function. Here, we present a technique to link peptide strands by chemical rather than enzymatic reaction. We employ biocompatible click chemistry to induce triazole formation between azido- and alkynyl-d -alanine residues that are metabolically installed in the peptidoglycan of Gram-positive or Gram-negative bacteria. Synthetic triazole cross-links can be visualized using azidocoumarin-d -alanine, an amino acid derivative that undergoes fluorescent enhancement upon reaction with terminal alkynes. Cell-wall stapling protects Escherichia coli from treatment with the broad-spectrum β-lactams ampicillin and carbenicillin. Chemical control of cell-wall structure in live bacteria can provide functional insights that are orthogonal to those obtained by genetics. Graphical Abstract: Highlights: The bacterial cell wall is crosslinked by d -amino acid-containing peptides β-Lactam antibiotics interfere with cell-wall crosslinking We developed a d -amino acid-based method for introducing synthetic crosslinks The crosslinks protect Escherichia coli fromSummary: Transpeptidation reinforces the structure of cell-wall peptidoglycan, an extracellular heteropolymer that protects bacteria from osmotic lysis. The clinical success of transpeptidase-inhibiting β-lactam antibiotics illustrates the essentiality of these cross-linkages for cell-wall integrity, but the presence of multiple, seemingly redundant transpeptidases in many species makes it challenging to determine cross-link function. Here, we present a technique to link peptide strands by chemical rather than enzymatic reaction. We employ biocompatible click chemistry to induce triazole formation between azido- and alkynyl-d -alanine residues that are metabolically installed in the peptidoglycan of Gram-positive or Gram-negative bacteria. Synthetic triazole cross-links can be visualized using azidocoumarin-d -alanine, an amino acid derivative that undergoes fluorescent enhancement upon reaction with terminal alkynes. Cell-wall stapling protects Escherichia coli from treatment with the broad-spectrum β-lactams ampicillin and carbenicillin. Chemical control of cell-wall structure in live bacteria can provide functional insights that are orthogonal to those obtained by genetics. Graphical Abstract: Highlights: The bacterial cell wall is crosslinked by d -amino acid-containing peptides β-Lactam antibiotics interfere with cell-wall crosslinking We developed a d -amino acid-based method for introducing synthetic crosslinks The crosslinks protect Escherichia coli from broad-spectrum β-lactam antibiotics Abstract : We developed a chemical method for introducing synthetic cross-links into the cell walls of live Gram-positive and Gram-negative bacteria. The cross-links protect Escherichia coli from broad-spectrum β-lactam antibiotics. Chemically induced cross-linking complements genetics as an independent way to investigate the physiological roles of cell-wall connectivity. … (more)
- Is Part Of:
- Cell chemical biology. Volume 28:Issue 2(2021)
- Journal:
- Cell chemical biology
- Issue:
- Volume 28:Issue 2(2021)
- Issue Display:
- Volume 28, Issue 2 (2021)
- Year:
- 2021
- Volume:
- 28
- Issue:
- 2
- Issue Sort Value:
- 2021-0028-0002-0000
- Page Start:
- 213
- Page End:
- 220.e4
- Publication Date:
- 2021-02-18
- Subjects:
- peptidoglycan -- cell wall -- bacteria -- cross-linking -- d-amino acid -- metabolic labeling -- click chemistry -- antibiotic -- transpeptidase
Biochemistry -- Periodicals
572.05 - Journal URLs:
- http://www.cell.com/cell-chemical-biology/home ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.chembiol.2020.11.006 ↗
- Languages:
- English
- ISSNs:
- 2451-9456
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.733000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 15790.xml