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Serine-based surfactants as effective antimicrobial agents against multiresistant bacteria

Title
Serine-based surfactants as effective antimicrobial agents against multiresistant bacteria
Type
Article in International Scientific Journal
Year
2022
Authors
Sandra G. Silva
(Author)
FCUP
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Pinheiro, M
(Author)
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Pereira, R
(Author)
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Dias, AR
(Author)
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Ferraz, R
(Author)
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Prudencio, C
(Author)
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Eaton, PJ
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Salette Reis
(Author)
FFUP
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Journal
Vol. 1864
ISSN: 0005-2736
Publisher: Elsevier
Other information
Authenticus ID: P-00W-MGY
Abstract (EN): The antimicrobial activity of two serine derived gemini cationic surfactants, amide (12Ser)2CON12 and ester (12Ser)2COO12, was tested using sensitive, E. coli ATCC 25922 and S. aureus ATCC 6538, and resistant, E. coli CTX M2, E. coli TEM CTX M9 and S. aureus ATCC 6538 and S. aureus MRSA ATCC 43300 Gram-positive and Gram-negative bacteria strains. Very low MIC values (5 mu M) were found for the two resistant strains E.coli TEM CTX M9 and S. aureus MRSA ATCC 43300, in the case of the amide derivative, and for S. aureus MRSA ATCC 43300, in the case of the ester derivative. The interaction of the serine amphiphiles with lipid-model membranes (DPPG and DPPC) was investigated using Langmuir monolayers. A more pronounced effect on the DPPG than on the DPPC monolayer was observed. The effect induced by the surfactants on bacteria membrane was explored by Atomic Force Microscopy. A clear disruption of the bacteria membrane was observed for E. coli TEM CTX M9 upon treatment with (12ser)2CON12, whereas for the S. aureus MRSA few observable changes in cell morphology were found after treatment with either of the two surfactants. The cytotoxicity of the two compounds was assessed by hemolysis assay on human red blood cells (RBC). The compounds were shown to be non-cytotoxic up to 10 mu M. Overall, the results reveal a promising potential, in particular of the amide derivative, as antimicrobial agent for two strains of antibiotic resistant bacteria.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 10
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