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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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]
Citations
Cites
Molecular basis of bacterial outer membrane permeability
Nikaido, H., & Vaara, M. (1985) · Microbiological Reviews · doi:10.1128/mr.49.1.1-32.1985 · Cited by 2,458
Self-citationZasloff, M. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.15.5449 · Cited by 2,305
Structure and Function of Lipopolysaccharide Binding Protein
Schumann, R. R., Leong, S. R., Flaggs, G., Gray, P. W., Wright, S. D., Mathison, J. C., Tobias, P. S., & Ulevitch, R. J. (1990) · Science · doi:10.1126/science.2402637 · Cited by 1,672
Neu, H. C., & HEPPEL, L. A. (1965) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)97200-5 · Cited by 1,464
Defensins. Natural peptide antibiotics of human neutrophils.
Ganz, T., Selsted, M. E., Szklarek, D., Harwig, S. S. L., Daher, K. A., Bainton, D. F., & Lehrer, R. I. (1985) · Journal of Clinical Investigation · doi:10.1172/jci112120 · Cited by 1,416
Hultmark, D., Steiner, H., Rasmuson, T., & Boman, H. G. (1980) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1980.tb05991.x · Cited by 1,007
Polymyxin and Related Peptide Antibiotics
Storm, D. R., Rosenthal, K. S., & Swanson, P. E. (1977) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.46.070177.003451 · Cited by 759
Lugtenberg, B. J. J., & van Alphen, L. (1983) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/0304-4157(83)90014-x · Cited by 742
Interaction of human defensins with Escherichia coli. Mechanism of bactericidal activity.
Lehrer, R. I., Barton, A. P., Daher, K. A., Harwig, S. S. L., Ganz, T., & Selsted, M. E. (1989) · Journal of Clinical Investigation · doi:10.1172/jci114198 · Cited by 727
All-D amino acid-containing channel-forming antibiotic peptides.
Wade, D. C., Boman, A., Wåhlin, B., Drain, C. M., Andreu, D., Boman, H. G., & Merrifield, R. B. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4761 · Cited by 677
Cited by
Sorted by citations
Items 701–800 of 1,000
Power, E. G. M. (1997) · Progress in medicinal chemistry · doi:10.1016/s0079-6468(08)70107-3 · Cited by 43
Vollbrecht, E., Heckmann, R., Wray, V., Nimtz, M., & Lang, S. (1998) · Applied Microbiology and Biotechnology · doi:10.1007/s002530051330 · Cited by 43
Higher-Order Structure of Polymyxin B: The Functional Significance of Topological Flexibility
Bruch, M. D., Cajal, Y., Koh, J. T., & Jain, M. K. (1999) · Journal of the American Chemical Society · doi:10.1021/ja992376m · Cited by 43
Ko, K. Y., Mendoncam, A. F., Ismail, H. A.-M. A., & Ahn, D. U. (2009) · Poultry Science · doi:10.3382/ps.2008-00218 · Cited by 43
Tîrşoaga, A., Hamidi, A. E., Perry, M. B., Caroff, M., & Novikov, A. (2007) · Journal of Lipid Research · doi:10.1194/jlr.m700193-jlr200 · Cited by 43
Ma, Q., Davidson, P. M., Critzer, F. J., & Zhong, Q. (2016) · LWT · doi:10.1016/j.lwt.2016.04.021 · Cited by 43
Mannis, M. J. (2002) · PubMed Central · Cited by 42
Medium Effects on Minimum Inhibitory Concentrations of Nylon-3 Polymers against E. coli
Choi, H., Chakraborty, S., Liu, R., Gellman, S. H., & Weisshaar, J. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104500 · Cited by 42
Reinés, M., Llobet, E., Llompart, C. M., Moranta, D., Pérez-Gutiérrez, C., & Bengoechea, J. A. (2012) · Journal of Bacteriology · doi:10.1128/jb.00308-12 · Cited by 42
Bhattacharjya, S. (2015) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026615666150703121943 · Cited by 42
Wang, W., Li, M., Lin, H., Wang, J., & Mao, X. (2016) · Archives of Virology · doi:10.1007/s00705-016-2957-x · Cited by 42
Characterization of the novel T4-like Salmonella enterica bacteriophage STP4-a and its endolysin
Li, M., Li, M., Lin, H., Wang, J., Jin, Y., & Han, F. (2015) · Archives of Virology · doi:10.1007/s00705-015-2647-0 · Cited by 42
Sekaran, S. D. (2014) · Journal of Health and Translational Medicine · doi:10.22452/jummec.vol17no1.1 · Cited by 42
What an Escherichia coli Mutant Can Teach Us About the Antibacterial Effect of Chlorophyllin
Krüger, M., Richter, P. R., Strauch, S. M., Nasir, A., Burkovski, A., Antunes, C. A., Meißgeier, T., Schlücker, E., Schwab, S., & Lebert, M. (2019) · Microorganisms · doi:10.3390/microorganisms7020059 · Cited by 42
Mode of action of novel polyamines increasing the permeability of bacterial outer membrane
Yasuda, K., Ohmizo, C., & Katsu, T. (2004) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2004.01.006 · Cited by 42
Ability of cecropin B to penetrate the enterobacterial outer membrane
Vaara, M., & Vaara, T. (1994) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.38.10.2498 · Cited by 42
Self-citationBetts, J. W., Phee, L. M., Woodford, N., & Wareham, D. W. (2014) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-014-2101-3 · Cited by 42
Rapid Screening Method for Detection of Bacteria in Platelet Concentrates
Ribault, S., Harper, K., Grave, L., Lafontaine, C., Nannini, P., Raimondo, A., & Faure, I. B. (2004) · Journal of Clinical Microbiology · doi:10.1128/jcm.42.5.1903-1908.2004 · Cited by 42
Raj, P. A., Marcus, E., & Edgerton, M. (1996) · Biochemistry · doi:10.1021/bi951681r · Cited by 42
Merighi, M., Carroll‐Portillo, A., Septer, A. N., Bhatiya, A., & Gunn, J. S. (2005) · Journal of Bacteriology · doi:10.1128/jb.188.1.141-149.2006 · Cited by 41
Novel polymyxin derivatives are less cytotoxic than polymyxin B to renal proximal tubular cells
Mingeot‐Leclercq, M., Tulkens, P. M., Denamur, S., Vaara, T., & Vaara, M. (2012) · Peptides · doi:10.1016/j.peptides.2012.03.033 · Cited by 41
Self-citationShavrina, M. S., Zimin, A. A., Molochkov, N. V., Chernyshov, S. V., Валериевич, М. А., & Mikoulinskaia, G. V. (2016) · Journal of Applied Microbiology · doi:10.1111/jam.13251 · Cited by 41
Synthetic Immunotherapeutics against Gram-negative Pathogens
Feigman, M. S., Kim, S., Pidgeon, S. E., Yu, Y., Ongwae, G. M., Patel, D. S., Regen, S. L., Im, W., & Pires, M. M. (2018) · Cell chemical biology · doi:10.1016/j.chembiol.2018.05.019 · Cited by 41
Baker, K. R., Jana, B., Hansen, A. M., Nielsen, H. M., Franzyk, H., & Guardabassi, L. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00236 · Cited by 41
Chan, W. Y., Hickey, E. E., Page, S. W., Trott, D. J., & Hill, P. B. (2019) · Journal of Veterinary Pharmacology and Therapeutics · doi:10.1111/jvp.12811 · Cited by 41
Antimicrobial Activity of Phytic Acid: An Emerging Agent in Endodontics
Nassar, R., Nassar, M., Vianna, M. E., Naidoo, N. S., Alqutami, F., Kaklamanos, E. G., Senok, A. C., & Williams, D. W. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.753649 · Cited by 41
Mills, A. A. S., Platt, H. W., & Hurta, R. A. R. (2006) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2006.03.015 · Cited by 43
Chen, L., Kao, P.-H., Fu, Y., Lin, S., & Chang, L. (2011) · Toxicon · doi:10.1016/j.toxicon.2011.04.021 · Cited by 41
Morono, Y., Takano, S., Miyanaga, K., Tanji, Y., Unno, H., & Hori, K. (2004) · Biotechnology Letters · doi:10.1023/b:bile.0000018255.89810.1a · Cited by 41
In Vitro Antibacterial Activity of NB-003 against Propionibacterium acnes
Pannu, J., McCarthy, A. D., Martín, A. V., Hamouda, T., Ciotti, S., Ma, L., Sutcliffe, J. A., & Baker, J. R. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00561-11 · Cited by 41
Oulahal, N., Martial, A., Bonneau, M., & Blum, L. J. (2004) · Biofilms · doi:10.1017/s1479050504001140 · Cited by 41
Obst, S., KASTOWSKY, M., & Bradaczek, H. (1997) · Biophysical Journal · doi:10.1016/s0006-3495(97)78755-1 · Cited by 41
Cholic acid derivatives: novel antimicrobials
Savage, P. B., & Li, C. (2000) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.9.2.263 · Cited by 41
Padhy, I., Dwibedy, S. K., & Mohapatra, S. S. (2024) · Microbiological Research · doi:10.1016/j.micres.2024.127679 · Cited by 41
Types of Microbicidal and Microbistatic Agents
Al-Adham, I. S. I., Haddadin, R. N., & Collier, P. J. (2012) · Wiley-Blackwell eBooks · doi:10.1002/9781118425831.ch2 · Cited by 40
Surfactants present complex joint effects on the toxicities of metal oxide nanoparticles
Wang, D., Lin, Z., Yao, Z., & Yu, H. (2014) · Chemosphere · doi:10.1016/j.chemosphere.2014.03.010 · Cited by 40
Ruiz, A., Williams, S. K., Djeri, N., Hinton, A., & Rodrick, G. E. (2009) · Poultry Science · doi:10.3382/ps.2008-00521 · Cited by 40
Tischer, K., Zeder, M., Klug, R., Pernthaler, J., Schattenhofer, M., Harms, H., & Wendeberg, A. (2012) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2012.01.004 · Cited by 40
Lai, M., Soo, P., Lin, N., Hu, A., Chen, Y.-J., Chen, L., & Chang, K. (2013) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2013.04.022 · Cited by 40
Ahmad, A., Meng, X., Yun, N. J., & Zhang, Z. (2016) · Journal of Nanomaterials · doi:10.1155/2016/1373725 · Cited by 40
Cao, Y., Zhang, B., Zhu, Z., Xin, X., Wu, H., & Chen, B. (2021) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2021.622108 · Cited by 40
Membrane-active bacteriocins to control Salmonella in foods
Chalón, M. C., Acuña, L., Morero, R. D., Minahk, C. J., & Bellomio, A. (2011) · Food Research International · doi:10.1016/j.foodres.2011.08.024 · Cited by 41
Seoane, A., & Lobo, J. M. G. (2000) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.44.4.905-909.2000 · Cited by 40
Enhanced Inhibition of Escherichia coli O157:H7 by Lysozyme and Chelators
Boland, J. S., Davidson, P. M., & Weiss, J. (2003) · Journal of Food Protection · doi:10.4315/0362-028x-66.10.1783 · Cited by 40
Essential Oils and Future Antibiotics: New Weapons against Emerging‘Superbugs’?
Boire, N. A. (2013) · Journal of Ancient Diseases & Preventive Remedies · doi:10.4172/2329-8731.1000105 · Cited by 40
Preservative properties of Calamintha officinalis essential oil with and without EDTA
Nostro, A., Cannatelli, M. A., Morelli, I., Cioni, P. L., Bader, A., Marino, A., & Alonzo, V. (2002) · Letters in Applied Microbiology · doi:10.1046/j.1472-765x.2002.01216.x · Cited by 40
Alturki, A., El-Ziney, M. G., & Abdel-Salam, A. M. (2008) · Journal of Food Agriculture & Environment · Cited by 40
Dupouy, E. A., Lazzeri, D., & Durantini, E. N. (2004) · Photochemical & Photobiological Sciences · doi:10.1039/b407848a · Cited by 40
Kitamura, S., Owensby, A., Wall, D., & Wolan, D. W. (2018) · Cell chemical biology · doi:10.1016/j.chembiol.2017.12.011 · Cited by 39
Hu, Z. Y., Balay, D. R., Hu, Y., McMullen, L. M., & Gänzle, M. G. (2018) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2018.10.003 · Cited by 39
Malanović, N., Marx, L., Blondelle, S. E., Pabst, G., & Semeraro, E. F. (2020) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2020.183275 · Cited by 40
Gür, S. D., Bakhshpour, M., Bereli, N., & Deni̇zli̇, A. (2021) · Journal of Biomaterials Science Polymer Edition · doi:10.1080/09205063.2021.1892472 · Cited by 39
Alegado, R. ʻ., Chin, C., Monack, D. M., & Tan, M. (2011) · Cellular Microbiology · doi:10.1111/j.1462-5822.2011.01645.x · Cited by 39
Al‐Nabulsi, A. A., & Holley, R. A. (2005) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2005.02785.x · Cited by 39
Lipid-Specific Membrane Activity of Human β-Defensin-3
Böhling, A., Hagge, S. O., Roes, S., Podschun, R., Sahly, H., Harder, J., Schröder, J., Grötzinger, J., Seydel, U., & Gutsmann, T. (2006) · Biochemistry · doi:10.1021/bi052026e · Cited by 39
Antimicrobial Photodynamic Efficacy of Side‐chain Functionalized Benzo[a]phenothiazinium Dyes
Verma, S., Sallum, U. W., Athar, H., Rosenblum, L. T., Foley, J. W., & Hasan, T. G. (2008) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2008.00403.x · Cited by 39
Deciphering the Acylation Pattern of Yersinia enterocolitica Lipid A
Reinés, M., Llobet, E., Dahlström, K. M., Pérez-Gutiérrez, C., Llompart, C. M., Torrecabota, N., Salminen, T. A., & Bengoechea, J. A. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002978 · Cited by 39
Kim, H. K., & Harshey, R. M. (2016) · mBio · doi:10.1128/mbio.00822-16 · Cited by 39
Brennan-Krohn, T., & Kirby, J. E. (2019) · Clinics in Laboratory Medicine · doi:10.1016/j.cll.2019.04.002 · Cited by 38
Creative targeting of the Gram‐negative outer membrane in antibiotic discovery
MacNair, C. R., Tsai, C. N., & Brown, E. D. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14280 · Cited by 38
The Role of Galacturonic Acid in Outer Membrane Stability in Klebsiella pneumoniae
Frirdich, E., Bouwman, C., VINOGRADOV, E. V., & Whitfield, C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m504987200 · Cited by 38
Interaction of a cationic polymer with negatively charged proteoliposomes
Kozlova, N. O., Bruskovskaya, I. B., Okuneva, I. B., Melik‐Nubarov, N. S., Yaroslavov, A. A., Kabanov, V. A., & Menger, F. M. (2001) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(01)00381-9 · Cited by 38
Kumar, S., Kundu, S., Pakshirajan, K., & Dasu, V. V. (2008) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-008-8280-6 · Cited by 38
Use of steroids to monitor alterations in the outer membrane of Pseudomonas aeruginosa
Plésiat, P., Aires, J., Godard, C., & Köhler, T. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.22.7004-7010.1997 · Cited by 38
Ko, K. Y., Mendonça, A. F., & Ahn, D. U. (2008) · Poultry Science · doi:10.3382/ps.2007-00521 · Cited by 38
Ohsuka, S., Ohta, M., Masuda, K., Arakawa, Y., Kaneda, T., & Kato, N. (1994) · Microbiology and Immunology · doi:10.1111/j.1348-0421.1994.tb01803.x · Cited by 38
Enhanced inactivation of Salmonella typhimurium and verotoxigenic Escherichia coli by nisin at 6·5°C
Elliason, D. J., & Tatini, S. R. (1999) · Food Microbiology · doi:10.1006/fmic.1998.0226 · Cited by 38
Origin of antibacterial stasis by polymyxin B in Escherichia coli
Liechty, A., Chen, J., & Jain, M. K. (2000) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(99)00178-9 · Cited by 38
Antibacterial activity of essential oils: potential applications in food
Burt, S. A. (2002) · Utrecht University Repository (Utrecht University) · Cited by 38
A hyperpromiscuous antitoxin protein domain for the neutralization of diverse toxin domains
Kurata, T., Saha, C. K., Buttress, J. A., Mets, T., Brodiazhenko, T., Turnbull, K. J., Awoyomi, O. F., Oliveira, S. R. A., Jimmy, S., Ernits, K., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2102212119 · Cited by 38
Discovery of Novel Polymyxin-Like Antibiotics
Velkov, T., & Roberts, K. D. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-16373-0_20 · Cited by 37
Complexation of fisetin with novel cyclosophoroase dimer to improve solubility and bioavailability
Jeong, D., Choi, J. M., Choi, Y., Jeong, K., Cho, E., & Jung, S. (2013) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2013.04.066 · Cited by 37
A General Workflow for Characterization of Nernstian Dyes and Their Effects on Bacterial Physiology
Mancini, L., Terradot, G., Tian, T., Pu, Y., Li, Y., Lo, C., Bai, F., & Piližota, T. (2019) · Biophysical Journal · doi:10.1016/j.bpj.2019.10.030 · Cited by 37
Urbanavičiūtė, I., Liaudanskas, M., Bobinas, Č., Šarkinas, A., Rezgienė, A., & Viškelis, P. (2020) · Foods · doi:10.3390/foods9081132 · Cited by 37
Chan, L. W., Hern, K. E., Ngambenjawong, C., Lee, K., Kwon, E. J., Hung, D. T., & Bhatia, S. N. (2021) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.0c00805 · Cited by 37
Yasuda, K., Ohmizo, C., & Katsu, T. (2003) · Journal of Microbiological Methods · doi:10.1016/s0167-7012(02)00255-5 · Cited by 37
Bengoechea, J. A., Brandenburg, K., Arraiza, M. D., Seydel, U., Skurnik, M., & Moriyón, I. (2003) · Infection and Immunity · doi:10.1128/iai.71.4.2014-2021.2003 · Cited by 37
Choi, J., & Groisman, E. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303420110 · Cited by 37
Korycka‐Machała, M., Ziółkowski, A., Rumijowska-Galewicz, A., Lisowska, K., & Sedlaczek, L. (2001) · Microbiology · doi:10.1099/00221287-147-10-2769 · Cited by 37
Chemical composition and antimicrobial activity of essential oils from Tunisian Mentha pulegium L
Marzouk, B., Ben, M., Fredj, H., Chraief, I., Mastouri, M., Boukef, K., & Marzouk, Z. (2008) · Journal of Food Agriculture & Environment · Cited by 37
Susceptibilities of Bordetella pertussis strains to antimicrobial peptides
Fernandez, R. C., & Weiss, A. A. (1996) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.40.4.1041 · Cited by 37
Wallace, S. J., Nation, R. L., Li, J., & Boyd, B. J. (2013) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.23508 · Cited by 36
McEvoy, J. G., Bilodeau, D. A., Cui, W., & Zhang, Z. (2013) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2013.04.026 · Cited by 36
In vitro antimicrobial activity of Pistacia lentiscus L. edible oil and phenolic extract
Mezni, F., Aouadhi, C., Khouja, M. L., Khaldi, A., & Maaroufi, A. (2014) · Natural Product Research · doi:10.1080/14786419.2014.952232 · Cited by 36
Nisin Production Utilizing Skimmed Milk Aiming to Reduce Process Cost
Jozala, Â. F., de Andrade, M. S., de Arauz, L. J., Pessoa, A., & Penna, T. C. V. (2007) · Humana Press eBooks · doi:10.1007/978-1-60327-181-3_43 · Cited by 36
Kucharska, I., Liang, B., Ursini, N., & Tamm, L. K. (2016) · Biochemistry · doi:10.1021/acs.biochem.6b00630 · Cited by 36
Lei, E., Tao, H., Jiao, S., Yang, A., Zhou, Y., Wang, M., Wen, K., Wang, Y., Chen, Z., Chen, X., et al. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.2c03784 · Cited by 37
Amplification of a novel gene, sanA, abolishes a vancomycin-sensitive defect in Escherichia coli
Rida, S., Caillet, J., & Alix, J. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.1.94-102.1996 · Cited by 36
Wen, Y., Yao, F., Sun, F. Y., Tan, Z., Tian, L., Xie, L., & Song, Q. (2014) · Materials Science and Engineering C · doi:10.1016/j.msec.2014.11.066 · Cited by 37
Sahalan, A. Z., & DIXON, R. A. (2007) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2007.10.005 · Cited by 36
Inhibitory effect of plantaricin peptides (Pln E/F and J/K) against Escherichia coli
Pal, G., & Srivastava, S. (2014) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-014-1708-y · Cited by 37
Impact of Antimicrobial Properties of Some Essential Oils on Cheese Yoghurt Quality
Zaky, W. M., & Kassem, J. M. (2013) · Cited by 36
Wu, S., Yang, Y., Wang, T., Sun, J., Zhang, Y., Ji, J., & Sun, X. (2021) · Food Research International · doi:10.1016/j.foodres.2021.110359 · Cited by 35
Strategic re-engineering of antibiotics
Homer, J. A., Johnson, R. M., Koelln, R. A., Moorhouse, A. D., & Moses, J. E. (2024) · Nature Reviews Bioengineering · doi:10.1038/s44222-024-00250-w · Cited by 35
Strategies on designing multifunctional surfaces to prevent biofilm formation
Lü, Y., Yue, Z., Wang, W., & Cao, Z. (2015) · Frontiers of Chemical Science and Engineering · doi:10.1007/s11705-015-1529-z · Cited by 35
Leite, C. J. B., de Sousa, J. P., Medeiros, J. A. D. C., da Conceição, M. L., Falcão-Silva, V. D. S., & de Souza, E. L. (2016) · Journal of Food Protection · doi:10.4315/0362-028x.jfp-15-245 · Cited by 35
Moradi, M., Kalantary, R. R., Esrafili, A., Jafari, A. J., & Gholami, M. (2017) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2017.10.115 · Cited by 35
Bennour, I., Ramos, M. N., Nuez‐Martínez, M., Xavier, J. A. M., Buades, A. B., Sillanpää, R., Teixidor, F., Choquesillo‐Lazarte, D., Romero, I., Martínez-Medina, M., et al. (2022) · Dalton Transactions · doi:10.1039/d2dt01015a · Cited by 35
Gahane, A. Y., Singh, V. P., Kumar, A., & Thakur, A. K. (2020) · Biomaterials Science · doi:10.1039/c9bm01978b · Cited by 35
Russell, A. D. (2003) · Science Progress · doi:10.3184/003685003783238608 · Cited by 35
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review