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Alteration of Zeta potential and membrane permeability in bacteria: a study with cationic agents.

作者信息

Halder Suman, Yadav Kirendra Kumar, Sarkar Ratul, Mukherjee Sudipta, Saha Pritam, Haldar Saubhik, Karmakar Sanmoy, Sen Tuhinadri

机构信息

Division of Pharmacology, Department of Pharmaceutical Technology, Jadavpur University, Kolkata, 700032 West Bengal India.

Department of Chemistry, Jadavpur University, Kolkata, 700032 India.

出版信息

Springerplus. 2015 Nov 4;4:672. doi: 10.1186/s40064-015-1476-7. eCollection 2015.


DOI:10.1186/s40064-015-1476-7
PMID:26558175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4633473/
Abstract

In the present study, we have tried to establish the correlation between changes in Zeta potential with that of cell surface permeability using bacteria (Escherichia coli and Staphylococcus aureus). An effort has been made to establish Zeta potential as a possible marker for the assessment of membrane damage, with a scope for predicting alteration of cell viability. Cationic agents like, cetyl trimethyl ammonium bromide and polymyxin B were used for inducing alteration of Zeta potential, and the changes occurring in the membrane permeability were studied. In addition, assessment of poly-dispersity index (PDI), cell viability along with confocal microscopic analysis were performed. Based on our results, it can be suggested that alteration of Zeta potential may be correlated to the enhancement of membrane permeability and PDI, and it was observed that beyond a critical point, it leads to cell death (both Gram-positive and Gram-negative bacteria). The present findings can not only be used for studying membrane active molecules but also for understanding the surface potential versus permeability relationship.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5471/4633473/b546f1161455/40064_2015_1476_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5471/4633473/6545f4ba5bbe/40064_2015_1476_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5471/4633473/eea2053ac589/40064_2015_1476_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5471/4633473/8a053aa29102/40064_2015_1476_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5471/4633473/b546f1161455/40064_2015_1476_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5471/4633473/6545f4ba5bbe/40064_2015_1476_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5471/4633473/eea2053ac589/40064_2015_1476_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5471/4633473/8a053aa29102/40064_2015_1476_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5471/4633473/b546f1161455/40064_2015_1476_Fig4_HTML.jpg

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本文引用的文献

[1]
The effects of interfacial potential on antimicrobial propensity of ZnO nanoparticle.

Sci Rep. 2015-4-15

[2]
Antimicrobial properties of Kalanchoe blossfeldiana: a focus on drug resistance with particular reference to quorum sensing-mediated bacterial biofilm formation.

J Pharm Pharmacol. 2015-7

[3]
Antimicrobial protein rBPI21-induced surface changes on Gram-negative and Gram-positive bacteria.

Nanomedicine. 2013-11-18

[4]
The antimicrobial activity of Sub3 is dependent on membrane binding and cell-penetrating ability.

Chembiochem. 2013-8-26

[5]
Membrane selectivity and biophysical studies of the antimicrobial peptide GL13K.

Biochim Biophys Acta. 2013-9

[6]
Biophysical characterization of polymyxin B interaction with LPS aggregates and membrane model systems.

Biopolymers. 2012

[7]
Electrical properties of the red blood cell membrane and immunohematological investigation.

Rev Bras Hematol Hemoter. 2011

[8]
Overview on the recent study of antimicrobial peptides: origins, functions, relative mechanisms and application.

Peptides. 2012-7-16

[9]
Modifications in erythrocyte membrane zeta potential by Plasmodium falciparum infection.

Exp Parasitol. 2012-3-21

[10]
The expanding scope of antimicrobial peptide structures and their modes of action.

Trends Biotechnol. 2011-6-15

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