The DOI matches its Crossref record; 230 of the 230 references it cites were found in a registry or an index.
Agents that increase the permeability of the outer membrane
Open accessAbstract
The outer membrane of gram-negative bacteria provides the cell with an effective permeability barrier against external noxious agents, including antibiotics, but is itself a target for antibacterial agents such as polycations and chelators. Both groups of agents weaken the molecular interactions of the lipopolysaccharide constituent of the outer membrane. Various polycations are able, at least under certain conditions, to bind to the anionic sites of lipopolysaccharide. Many of these disorganize and cross the outer membrane and render it permeable to drugs which permeate the intact membrane very poorly. These polycations include polymyxins and their derivatives, protamine, polymers of basic amino acids, compound 48/80, insect cecropins, reptilian magainins, various cationic leukocyte peptides (defensins, bactenecins, bactericidal/permeability-increasing protein, and others), aminoglycosides, and many more. However, the cationic character is not the sole determinant required for the permeabilizing activity, and therefore some of the agents are much more effective permeabilizers than others. They are useful tools in studies in which the poor permeability of the outer membrane poses problems. Some of them undoubtedly have a role as natural antibiotic substances, and they or their derivatives might have some potential as pharmaceutical agents in antibacterial therapy as well. Also, chelators (such as EDTA, nitrilotriacetic acid, and sodium hexametaphosphate), which disintegrate the outer membrane by removing Mg2+ and Ca2+, are effective and valuable permeabilizers.
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“However, thymol and carvacrol do not directly act as OM permeabilising agents (unlike EDTA or polyethylenimine, which disintegrate the OM at sub-lethal concentrations) [9,14].”
From Effect of essential oils on pathogenic bacteria (2013) · cites this paper as [9]
In the citing paper
“The presence of an outer membrane in Gram-negative bacteria acts as a powerful barrier, restricting the diffusion of compounds through its lipopolysaccharide layer [56].”
From Comparison of Techniques and Solvents on the Antimicrobial and Antioxidant Potential of Extracts from Acacia dealbata and Olea europaea (2020) · cites this paper as [56]
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Items 201–230 of 230
Increases in permeability of Escherichia coli outer membrane induced by polycations
Katsu, T., Yoshimura, S., & Fujita, Y. (1984) · FEBS Letters · doi:10.1016/0014-5793(84)80067-8 · Cited by 17
Uratani, Y. (1982) · Journal of Bacteriology · doi:10.1128/jb.149.2.523-528.1982 · Cited by 16
Mingeot‐Leclercq, M., Piret, J., Tulkens, P. M., & Brasseur, R. (1990) · Biochemical Pharmacology · doi:10.1016/0006-2952(90)90548-y · Cited by 16
ITO-KAGAWA, M., & KOYAMA, Y. (1984) · The Journal of Antibiotics · doi:10.7164/antibiotics.37.926 · Cited by 16
Shafer, W. M., Engle, S. A., Martin, L. E., & Spitznagel, J. K. (1988) · Infection and Immunity · doi:10.1128/iai.56.1.51-53.1988 · Cited by 15
Protein–lipopolysaccharide interactions. 1. The reaction of lysozyme with Pseudomonas aeruginosa LPS
Day, D. F., Marceau-Day, M. L., & Ingram, J. (1978) · Canadian Journal of Microbiology · doi:10.1139/m78-035 · Cited by 15
Viljanen, P., Käyhty, H. M., Vaara, M., & Vaara, T. (1986) · Canadian Journal of Microbiology · doi:10.1139/m86-013 · Cited by 15
Self-citationDication and trication which can increase the permeability of Escherichia coli outer membrane
Katsu, T., Shibata, M., & Fujita, Y. (1985) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(85)90138-5 · Cited by 14
Relationship between structure and histamine releasing action of polymyxin B and its analogues
Voitenko, V. G., Bayramashvili, D. I., Zebrev, A. I., & Zinchenko, A. A. (1990) · Inflammation Research · doi:10.1007/bf01969025 · Cited by 13
Polymyxin B nonapeptide sensitizesEscherichia colito valinomycin and A23187 ionophores
Alatossava, T., Vaara, M., & Baschong, W. (1984) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1984.tb00736.x · Cited by 13
Self-citationTecoma, E. S., & Wu, D. (1980) · Journal of Bacteriology · doi:10.1128/jb.142.3.931-938.1980 · Cited by 12
Effect of ionic strength on polymyxin resistance ofpmrAmutants ofSalmonella
Vaara, M. (1981) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1981.tb06989.x · Cited by 12
Self-citationVaara, M. (1990) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1990.tb13828.x · Cited by 12
Self-citationReversible binding of Salmonella typhimurium lipopolysaccharides by immobilized protamine
Helander, I. M., & Vaara, M. (1987) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1987.tb10735.x · Cited by 12
Self-citationAntibiotic Uptake Pathways across the Outer Membrane of Pseudomonas aeruginosa
Moore, R. A., Woodruff, W. A., & Hancock, R. E. W. (2015) · Antibiotics and chemotherapy/Antibiotica et chemotherapia · doi:10.1159/000414344 · Cited by 11
Membrane permeability of Pseudomonas aeruginosa to 4-quinolones
Kubesch, P., Wehsling, M., & Tümmler, B. (1987) · Zentralblatt für Bakteriologie Mikrobiologie und Hygiene Series A Medical Microbiology Infectious Diseases Virology Parasitology · doi:10.1016/s0176-6724(87)80166-9 · Cited by 10
Vaara, M. (1988) · Journal of Chromatography A · doi:10.1016/s0021-9673(01)83889-9 · Cited by 10
Self-citationVaara, M., & Viljanen, P. (1983) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1983.tb00552.x · Cited by 9
Self-citationEffects of polymyxin B nonapeptide on Aeromonas salmonicida
McCashion, R. N., & Lynch, W. H. (1987) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.31.9.1414 · Cited by 9
MacDonald, E. (1988) · Pharmacology & Toxicology · doi:10.1111/j.1600-0773.1988.tb00938.x · Cited by 8
Gentamicin-lipopolysaccharide interactions inPseudomonas aeruginosa
Day, D. F. (1980) · Current Microbiology · doi:10.1007/bf02602831 · Cited by 8
Hossack, D. J. N., Bird, M. C., & Fowler, G. G. (1984) · Elsevier eBooks · doi:10.1016/b978-0-408-11155-3.50040-0 · Cited by 8
Antimicrobial Action of Compound 48/80 against Protozoa, Bacteria, and Fungi
Lenney, J. F., Siddiqui, W. A., Schnell, J. V., Furusawa, E., & Read, G. W. (1977) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.2600660524 · Cited by 7
Antimicrobial action of compound 48/80—II. Mechanism of action
Hall, J. B., Hino, G. N., Inouye, L., Nada, A., Lau, C. K. H., & Read, G. W. (1983) · Biochemical Pharmacology · doi:10.1016/0006-2952(83)90522-1 · Cited by 6
Seltmann, G., & Wolter, E. (1987) · Journal of Basic Microbiology · doi:10.1002/jobm.3620270305 · Cited by 5
Effects of cations on the outer membrane permeability of Escherichia coli.
Homma, T., & Nakae, T. (1982) · PubMed · Cited by 5
Influence of far-ultraviolet radiation on the permeability of the outer membrane of Escherichia coli
Mody, R. S., Krishnamurthy, S., & Dave, P. (1989) · Canadian Journal of Microbiology · doi:10.1139/m89-170 · Cited by 4
Vaara, M. (1990) · PubMed · Cited by 2
Self-citationTraub, W. H., Kohl, K.-H., Spohr, M., & Bauer, D. (2009) · Chemotherapy · doi:10.1159/000238571 · Cited by 1
Homma, T., & Nakae, T. (1982) · Tokai journal of experimental and clinical medicine · Cited by 1
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Essential oils: Their antibacterial properties and potential applications in foods—A review
Burt, S. (2004) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2004.03.022 · Cited by 10,488
Antiseptics and Disinfectants: Activity, Action, and Resistance
McDonnell, G. E., & Russell, A. D. (1999) · Clinical Microbiology Reviews · doi:10.1128/cmr.12.1.147 · Cited by 4,795
Molecular Basis of Bacterial Outer Membrane Permeability Revisited
Nikaido, H. (2003) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.67.4.593-656.2003 · Cited by 4,316
Effect of essential oils on pathogenic bacteria
Nazzaro, F., Fratianni, F., De Martino, L., Coppola, R., & De Feo, V. (2013) · Pharmaceuticals · doi:10.3390/ph6121451 · Cited by 2,186
Outer membrane permeability and antibiotic resistance
Delcour, A. H. (2008) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2008.11.005 · Cited by 1,756
Metadata
- Authors
- Vaara, M.
- Affiliations
- University of Helsinki (FI)
- Corresponding author
- Vaara, M
- ORCID
- Vaara, M
- Venue
- Microbiological Reviews
- Publisher
- American Society for Microbiology
- Published
- 1992-09
- Volume
- 56
- Issue
- 3
- Pages
- 395-411
- ISSN
- 0146-0749 (ISSN-L)
- PMC
- PMC372877
- OpenAlex
- W1895129045
- Cited by
- 1,879
- References
- 229
- Citations by year
- 2026: 33 · 2025: 73 · 2024: 48 · 2023: 70 · 2022: 89 · 2021: 104 · 2020: 75 · 2019: 99 · 2018: 75 · 2017: 91 · 2016: 91 · 2015: 72 · 2014: 77 · 2013: 79 · 2012: 77
- FWCI
- 16.64
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Locations
- Microbiological Reviews (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Immunology and Microbiology › Microbiology › Antimicrobial Peptides and Activities
- Life Sciences › Immunology and Microbiology › Applied Microbiology and Biotechnology › Antimicrobial agents and applications
- Keywords
- outer membrane permeabilization, Gram-negative bacterial outer membrane, lipopolysaccharide, cationic polymers, cationic antimicrobial peptides, polymyxins, magainin, cecropin, defensins, bactenecin, bactericidal/permeability-increasing protein, aminoglycosides, chelating agents, EDTA, antibiotic resistance, antibacterial agents
- MeSH terms
- Amino Acid Sequence, Anti-Bacterial Agents, Bacterial Outer Membrane Proteins, Cell Membrane Permeability, Drug Resistance, Microbial, Gram-Negative Bacteria, Lipopolysaccharides, Molecular Sequence Data
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