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    Analysis of cellular damage resulting from exposure of bacteria to graphene oxide and hybrids using Fourier Transform Infrared Spectroscopy

    Liauw, Christopher M, Vaidya, Misha, Slate, Anthony J, Hickey, Niall A, Ryder, Steven, Martínez-Periñán, Emiliano, McBain, Andrew J, Banks, Craig E ORCID logoORCID: https://orcid.org/0000-0002-0756-9764 and Whitehead, Kathryn A (2023) Analysis of cellular damage resulting from exposure of bacteria to graphene oxide and hybrids using Fourier Transform Infrared Spectroscopy. Antibiotics, 12 (4). p. 776. ISSN 2079-6382

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    Abstract

    With the increase in antimicrobial resistance, there is an urgent need to find new antimicrobials. Four particulate antimicrobial compounds, graphite (G), graphene oxide (GO), silver–graphene oxide (Ag-GO) and zinc oxide–graphene oxide (ZnO-GO) were tested against Enterococcus faecium, Escherichia coli, Klebsiella pneumoniae and Staphylococcus aureus. The antimicrobial effects on the cellular ultrastructure were determined using Fourier transform infrared spectroscopy (FTIR), and selected FTIR spectral metrics correlated with cell damage and death arising from exposure to the GO hybrids. Ag-GO caused the most severe damage to the cellular ultrastructure, whilst GO caused intermediate damage. Graphite exposure caused unexpectedly high levels of damage to E. coli, whereas ZnO-GO exposure led to relatively low levels of damage. The Gram-negative bacteria demonstrated a stronger correlation between FTIR metrics, indicated by the perturbation index and the minimal bactericidal concentration (MBC). The blue shift of the combined ester carbonyl and amide I band was stronger for the Gram-negative varieties. FTIR metrics tended to provide a better assessment of cell damage based on correlation with cellular imaging and indicated that damage to the lipopolysaccharide, peptidoglycan and phospholipid bilayers had occurred. Further investigations into the cell damage caused by the GO-based materials will allow the development of this type of carbon-based multimode antimicrobials.

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