Bacterial cell wall material properties determine E. coli resistance to sonolysis.
Bacteria
Cell envelope
Escherichia coli
Sonication
Viability
Journal
Ultrasonics sonochemistry
ISSN: 1873-2828
Titre abrégé: Ultrason Sonochem
Pays: Netherlands
ID NLM: 9433356
Informations de publication
Date de publication:
Feb 2022
Feb 2022
Historique:
received:
21
10
2021
revised:
23
12
2021
accepted:
13
01
2022
pubmed:
26
1
2022
medline:
9
3
2022
entrez:
25
1
2022
Statut:
ppublish
Résumé
The applications of bacterial sonolysis in industrial settings are plagued by the lack of the knowledge of the exact mechanism of action of sonication on bacterial cells, variable effectiveness of cavitation on bacteria, and inconsistent data of its efficiency. In this study we have systematically changed material properties of E. coli cells to probe the effect of different cell wall layers on bacterial resistance to ultrasonic irradiation (20 kHz, output power 6,73 W, horn type, 3 mm probe tip diameter, 1 ml sample volume). We have determined the rates of sonolysis decay for bacteria with compromised major capsular polymers, disrupted outer membrane, compromised peptidoglycan layer, spheroplasts, giant spheroplasts, and in bacteria with different cell physiology. The non-growing bacteria were 5-fold more resistant to sonolysis than growing bacteria. The most important bacterial cell wall structure that determined the outcome during sonication was peptidoglycan. If peptidoglycan was remodelled, weakened, or absent the cavitation was very efficient. Cells with removed peptidoglycan had sonolysis resistance equal to lipid vesicles and were extremely sensitive to sonolysis. The results suggest that bacterial physiological state as well as cell wall architecture are major determinants that influence the outcome of bacterial sonolysis.
Identifiants
pubmed: 35077964
pii: S1350-4177(22)00012-8
doi: 10.1016/j.ultsonch.2022.105919
pmc: PMC8789596
pii:
doi:
Substances chimiques
Escherichia coli Proteins
0
Peptidoglycan
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
105919Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier B.V. All rights reserved.