Abstract

Our previous work described a clear loss of Escherichia coli (E. coli) membrane integrity after incubation with glycine or its N-methylated derivatives N-methylglycine (sarcosine) and N,N-dimethylglycine (DMG), but not N,N,N-trimethylglycine (betaine), under alkaline stress conditions. The current study offers a thorough viability analysis, based on a combination of real-time physiological techniques, of E. coli exposed to glycine and its N-methylated derivatives at alkaline pH. Flow cytometry was applied to assess various physiological parameters such as membrane permeability, esterase activity, respiratory activity and membrane potential. ATP and inorganic phosphate concentrations were also determined. Membrane damage was confirmed through the measurement of nucleic acid leakage. Results further showed no loss of esterase or respiratory activity, while an instant and significant decrease in the ATP concentration occurred upon exposure to either glycine, sarcosine or DMG, but not betaine. There was a clear membrane hyperpolarization as well as a significant increase in cellular inorganic phosphate concentration. Based on these results, we suggest that the inability to sustain an adequate level of ATP combined with a decrease in membrane functionality leads to the loss of bacterial viability when exposed to the proton scavengers glycine, sarcosine and DMG at alkaline pH.

Highlights

  • We recently described a decrease in the viability of stationary phase enterotoxigenic Escherichia coli (E. coli, ETEC) associated with membrane damage and reduced growth capacity caused by glycine and its N-methylated derivatives N-methylglycine, N,N-dimethylglycine (DMG) under alkaline stress conditions [1]

  • minimal inhibitory concentrations (MIC) determination Concentrations ranging from 25 mM up to 200 mM of each test compound were investigated for their antibacterial potential against ETEC at a pH ranging from 6.5 to 10.0

  • Bacterial viability can be assessed at different levels: growth capacity, structural integrity and physiological integrity

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Summary

Introduction

We recently described a decrease in the viability of stationary phase enterotoxigenic Escherichia coli (E. coli, ETEC) associated with membrane damage and reduced growth capacity caused by glycine and its N-methylated derivatives N-methylglycine (sarcosine), N,N-dimethylglycine (DMG) under alkaline stress conditions [1]. Direct membrane interactions of peptides and amino acid-based surfactants causing antibacterial effects are usually related to a net positive charge of these compounds, enhancing their interaction with anionic lipids and other bacterial targets [2]. Alkaline stress affects bacterial homeostasis mechanisms [6], enhancing ETEC susceptibility to a disturbance of their functional integrity by glycine, sarcosine and DMG. Interference at various levels of the compensation mechanisms may eventually lead to a loss of bacterial viability

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