Synergy between circular bacteriocin AS-48 and ethambutol against Mycobacterium tuberculosis
Aguilar-Perez, Clara
Gracia, Begona
Rodrigues, Liliana
Vitoria, Asuncion
Cebrian, Ruben
Deboosere, Nathalie
Song, Ok-Ryul
Brodin, Priscille
Maqueda, Mercedes
Ainsa, Jose A.
Mercedes Maqueda
Maqueda Mercedes
ORCID: 0000-0002-5874-9343
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Priscille Brodin
Brodin Priscille
ORCID: 0000-0003-0991-7344
Email: priscille.brodin@inserm.fr
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Oxadiazolone derivatives, new promising multi-target inhibitors against M. tuberculosis
10.1016/j.bioorg.2018.08.025
Proteomics of Mycobacterium infection: Moving towards a Better Understanding of Pathogen-Driven immunomodulation
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Synergy between circular bacteriocin AS-48 and ethambutol against Mycobacterium tuberculosis
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The EU approved antimalarial pyronaridine shows antitubercular activity and synergy with rifampicin, targeting RNA polymerase
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Cyclipostins and Cyclophostin analogs as promising compounds in the fight against tuberculosis
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Cyclodextrin-based nanocarriers containing a synergic drug combination: A potential formulation for pulmonary administration of antitubercular drugs
10.1016/j.ijpharm.2017.05.030
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10.1016/j.mib.2017.11.017
Legionella pneumophila Modulates Mitochondrial Dynamics to Trigger Metabolic Repurposing of Infected Macrophages
10.1016/j.chom.2017.07.020
Mycobacterium tuberculosis Controls Phagosomal Acidification by Targeting CISH-Mediated Signaling
10.1016/j.celrep.2017.08.101
Phenotypic assays for Mycobacterium tuberculosis infection
10.1002/cyto.a.23129
A fast, fully automated cell segmentation algorithm for high-throughput and high-content screening
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Compartmentalized Encapsulation of Two Antibiotics in Porous Nanoparticles: an Efficient Strategy to Treat Intracellular Infections
10.1002/ppsc.201800360
Spatiotemporal Changes of the Phagosomal Proteome in Dendritic Cells in Response to LPS Stimulation
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Mycolactone as Analgesic: Subcutaneous Bioavailability Parameters
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Intrinsic Antibacterial Activity of Nanoparticles Made of β-Cyclodextrins Potentiates Their Effect as Drug Nanocarriers against Tuberculosis
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Mitochondrial Dynamics and Activity in Legionella-Infected Cells
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Heparin-Binding Hemagglutinin Adhesin (HBHA) Is Involved in Intracytosolic Lipid Inclusions Formation in Mycobacteria
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Dehydrojuncusol, a Natural Phenanthrene Compound Extracted from Juncus maritimus, Is a New Inhibitor of Hepatitis C Virus RNA Replication
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A novel codrug made of the combination of ethionamide and its potentiating booster: synthesis, self-assembly into nanoparticles and antimycobacterial evaluation
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Could Mycolactone Inspire New Potent Analgesics? Perspectives and Pitfalls
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Paradoxical Roles of the MAL/Tirap Adaptor in Pathologies.
10.3389/fimmu.2020.569127
Fragment-Based Optimized EthR Inhibitors with in Vivo Ethionamide Boosting Activity.
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Intracellular and in vivo evaluation of imidazo[2,1-b]thiazole-5-carboxamide anti-tuberculosis compounds.
10.1371/journal.pone.0227224
Preclinical assessment of a new live attenuated Mycobacterium tuberculosis Beijing-based vaccine for tuberculosis.
10.1016/j.vaccine.2019.11.085
IRG1 controls immunometabolic host response and restricts intracellular Mycobacterium tuberculosis infection
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Worms' Antimicrobial Peptides.
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Theaflavins, polyphenols of black tea, inhibit entry of hepatitis C virus in cell culture.
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Plant extracts from Cameroonian medicinal plants strongly inhibit hepatitis C virus infection in vitro.
10.3389/fmicb.2015.00488
Discovery of Q203, a potent clinical candidate for the treatment of tuberculosis.
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Discovery of novel N-phenylphenoxyacetamide derivatives as EthR inhibitors and ethionamide boosters by combining high-throughput screening and synthesis.
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Shortening the drug discovery pipeline: small molecule high content screening for lead discovery in neglected disease.
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Automated HTS/HCS for antivirals using visual HIV full replication assays.
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Influence of ESAT-6 secretion system 1 (RD1) of Mycobacterium tuberculosis on the interaction between mycobacteria and the host immune system.
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Pathogenomic analyses of Mycobacterium microti, an ESX-1-deleted member of the Mycobacterium tuberculosis complex causing disease in various hosts
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Aínsa Claver José Antonio
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ORCID: 0000-0003-2076-844X
Selective Targeting of Human and Animal Pathogens of the Helicobacter Genus by Flavodoxin Inhibitors: Efficacy, Synergy, Resistance and Mechanistic Studies
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Design, synthesis and inhibitory activity against Mycobacterium tuberculosis thymidine monophosphate kinase of acyclic nucleoside analogues with a distal imidazoquinolinone
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Transcriptional analysis of and resistance level conferred by the aminoglycoside acetyltransferase gene aac(2')-Id from Mycobacterium smegmatis.
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Aminoglycoside 2'-N-acetyltransferase genes are universally present in mycobacteria: Characterization of the aac(2')-lc gene from Mycobacterium tuberculosis and the aac(2')-ld gene from Mycobacterium smegmatis
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Construction of a family of Mycobacterium/Escherichia coli shuttle vectors derived from pAL5000 and pACYC184: Their use for cloning an antibiotic-resistance gene from Mycobacterium fortuitum
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Spectinamides: a new class of semisynthetic antituberculosis agents that overcome native drug efflux
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Analysis of Mutations in Streptomycin-Resistant Strains Reveals a Simple and Reliable Genetic Marker for Identification of the Mycobacterium tuberculosis Beijing Genotype
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Zanthoxylum capense constituents with antimycobacterial activity against Mycobacterium tuberculosis in vitro and ex vivo within human macrophages
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Role of the Mmr Efflux Pump in Drug Resistance in Mycobacterium tuberculosis
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Mycobacterial Shuttle Vectors Designed for High-Level Protein Expression in Infected Macrophages
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Functional and Genetic Characterization of the Tap Efflux Pump in Mycobacterium bovis BCG
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A Prodrug Approach for Improving Antituberculosis Activity of Potent Mycobacterium tuberculosis Type II Dehydroquinase Inhibitors
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Antimycobacterial evaluation and preliminary phytochemical investigation of selected medicinal plants traditionally used in Mozambique
10.1016/j.jep.2011.04.062
The complex whiJ locus mediates environmentally sensitive repression of development of Streptomyces coelicolor A3(2)
10.1007/s10482-010-9443-3
Role of the Mycobacterium tuberculosis P55 Efflux Pump in Intrinsic Drug Resistance, Oxidative Stress Responses, and Growth
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Contribution of the Rv2333c efflux pump (the Stp protein) from Mycobacterium tuberculosis to intrinsic antibiotic resistance in Mycobacterium bovis BCG
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Novel streptomycin resistance gene from Mycobacterium fortuitum
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Characterization of tetracycline resistance mediated by the efflux pump Tap from Mycobacterium fortuitum
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Role of mycobacterial efflux transporters in drug resistance: an unresolved question.
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Molecular approaches to tuberculosis.
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Characterization of P55, a multidrug efflux pump in Mycobacterium bovis and Mycobacterium tuberculosis
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WhiA, a protein of unknown function conserved among gram-positive bacteria, is essential for sporulation in Streptomyces coelicolor A3(2)
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A response regulator-like protein that functions at an intermediate stage of sporulation in Streptomyces coelicolor A3(2)
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Inhibitors of mycobacterial efflux pumps as potential boosters for anti-tubercular drugs.
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Lipid transport in Mycobacterium tuberculosis and its implications in virulence and drug development
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Measuring efflux and permeability in mycobacteria.
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Antituberculosis drugs: reducing efflux = increasing activity
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Discovery of antimicrobial compounds targeting bacterial type FAD synthetases
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The EU approved antimalarial pyronaridine shows antitubercular activity and synergy with rifampicin, targeting RNA polymerase.
10.1016/j.tube.2018.08.004
Total Synthesis of Ripostatin B and Structure-Activity Relationship Studies on Ripostatin Analogs.
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Ionophore A23187 shows anti-tuberculosis activity and synergy with tebipenem.
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Structure Guided Lead Generation toward Nonchiral M. tuberculosis Thymidylate Kinase Inhibitors.
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Identification of aminopyrimidine-sulfonamides as potent modulators of Wag31-mediated cell elongation in mycobacteria.
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Structure-Activity Relationships of Spectinamide Antituberculosis Agents: A Dissection of Ribosomal Inhibition and Native Efflux Avoidance Contributions.
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How can nanoparticles contribute to antituberculosis therapy?
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Boldine-Derived Alkaloids Inhibit the Activity of DNA Topoisomerase I and Growth of Mycobacterium tuberculosis.
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Synergy between Circular Bacteriocin AS-48 and Ethambutol against Mycobacterium tuberculosis.
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Inhibition of drug efflux in mycobacteria with phenothiazines and other putative efflux inhibitors.
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New active formulations against M. tuberculosis: Bedaquiline encapsulation in lipid nanoparticles and chitosan nanocapsules
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Polypeptidic Micelles Stabilized with Sodium Alginate Enhance the Activity of Encapsulated Bedaquiline
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Co-delivery of free vancomycin and transcription factor decoy-nanostructured lipid carriers can enhance inhibition of methicillin resistant Staphylococcus aureus (MRSA)
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In silico discovery and biological validation of ligands of FAD synthase, a promising new antimicrobial target
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Nanotechnology‐Based Targeted Drug Delivery: An Emerging Tool to Overcome Tuberculosis
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Liliana Rodrigues
Rodrigues Liliana
ORCID: 0000-0002-2094-2666
Measuring efflux and permeability in mycobacteria.
10.1007/978-1-4939-2450-9_13
Role of the Mmr efflux pump in drug resistance in Mycobacterium tuberculosis.
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Inhibitors of mycobacterial efflux pumps as potential boosters for anti-tubercular drugs.
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Contribution of efflux to the emergence of isoniazid and multidrug resistance in Mycobacterium tuberculosis.
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Genetic response of Salmonella enterica serotype Enteritidis to thioridazine rendering the organism resistant to the agent.
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Contribution of efflux activity to isoniazid resistance in the Mycobacterium tuberculosis complex.
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Inhibition of drug efflux in mycobacteria with phenothiazines and other putative efflux inhibitors.
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Ethidium bromide transport across Mycobacterium smegmatis cell-wall: correlation with antibiotic resistance.
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Physiological characterisation of the efflux pump system of antibiotic-susceptible and multidrug-resistant Enterobacter aerogenes.
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Molecular tools for rapid identification and novel effective therapy against MDRTB/XDRTB infections.
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Evaluation of efflux activity of bacteria by a semi-automated fluorometric system.
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Fluorometric determination of ethidium bromide efflux kinetics in Escherichia coli.
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Identification of nontuberculous mycobacteria in clinical samples using molecular methods: a 3-year study.
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The role of efflux pumps in macrolide resistance in Mycobacterium avium complex.
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An AcrAB-mediated multidrug-resistant phenotype is maintained following restoration of wild-type activities by efflux pump genes and their regulators.
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pH Modulation of efflux pump activity of multi-drug resistant Escherichia coli: protection during its passage and eventual colonization of the colon.
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New methods for the identification of efflux mediated MDR bacteria, genetic assessment of regulators and efflux pump constituents, characterization of efflux systems and screening for inhibitors of efflux pumps.
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Demonstration of intrinsic efflux activity of Escherichia coli K-12 AG100 by an automated ethidium bromide method.
10.1016/j.ijantimicag.2007.12.015
Thioridazine and chlorpromazine inhibition of ethidium bromide efflux in Mycobacterium avium and Mycobacterium smegmatis.
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Antibiotic stress, genetic response and altered permeability of E. coli.
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Direct application of the INNO-LiPA Rif.TB line-probe assay for rapid identification of Mycobacterium tuberculosis complex strains and detection of rifampin resistance in 360 smear-positive respiratory specimens from an area of high incidence of multidrug-resistant tuberculosis.
10.1128/jcm.43.9.4880-4884.2005
Antituberculosis drugs: reducing efflux=increasing activity.
10.1016/j.drudis.2017.01.002
Identification of aminopyrimidine-sulfonamides as potent modulators of Wag31-mediated cell elongation in mycobacteria.
10.1111/mmi.13535
Synergy between Circular Bacteriocin AS-48 and Ethambutol against Mycobacterium tuberculosis.
10.1128/aac.00359-18
The EU approved antimalarial pyronaridine shows antitubercular activity and synergy with rifampicin, targeting RNA polymerase.
10.1016/j.tube.2018.08.004
Boldine-Derived Alkaloids Inhibit the Activity of DNA Topoisomerase I and Growth of Mycobacterium tuberculosis.
10.3389/fmicb.2018.01659
Total Synthesis of Ripostatin B and Structure-Activity Relationship Studies on Ripostatin Analogs.
10.1021/acs.joc.8b00193
Mycobacterial Aminoglycoside Acetyltransferases: A Little of Drug Resistance, and a Lot of Other Roles.
10.3389/fmicb.2019.00046
Design, Synthesis, and Efficacy Testing of Nitroethylene- and 7-Nitrobenzoxadiazol-Based Flavodoxin Inhibitors against Helicobacter pylori Drug-Resistant Clinical Strains and in Helicobacter pylori-Infected Mice
10.1021/acs.jmedchem.9b00355
O contributo dos serviços de diagnóstico laboratorial para o acesso universal à saúde nos países da Comunidade de Língua Portuguesa
10.25761/ANAISIHMT.337
RUBEN CEBRIAN
CEBRIAN RUBEN
/ Rubén Cebrián Castillo
ORCID: 0000-0003-1575-1846
Insights into the Functionality of the Putative Residues Involved in Enterocin AS-48 Maturation
10.1128/aem.01154-10
AS-48 bacteriocin: close to perfection
10.1007/s00018-011-0724-4
Characterization of functional, safety, and probiotic properties of Enterococcus faecalis UGRA10, a new AS-48-producer strain
10.1016/j.fm.2011.12.002
Antimicrobial characterization and safety aspects of the bacteriocinogenic Enterococcus hirae F420 isolated from Moroccan raw goat milk
10.1139/w2012-027
Discovering the Bacterial Circular Proteins: Bacteriocins, Cyanobactins, and Pilins
10.1074/jbc.r112.354688
Analysis of the Promoters Involved in Enterocin AS-48 Expression
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The bacteriocin AS-48 requires dimer dissociation followed by hydrophobic interactions with the membrane for antibacterial activity
10.1016/j.jsb.2015.03.006
Enterocin AS-48 as Evidence for the Use of Bacteriocins as New Leishmanicidal Agents
10.1128/aac.02288-16
Optimization of genotypic and biochemical methods to profile P. acnes isolates from a patient population
10.1016/j.mimet.2017.07.008
Assessing in vitro digestibility of food biopreservative AS-48
10.1016/j.foodchem.2017.10.149
Autophagic-related cell death of Trypanosoma brucei induced by bacteriocin AS-48
10.1016/j.ijpddr.2018.03.002
LAB Bacteriocins Controlling the Food Isolated (Drug-Resistant) Staphylococci
10.3389/fmicb.2018.01143
Synergy between Circular Bacteriocin AS-48 and Ethambutol against Mycobacterium tuberculosis
10.1128/aac.00359-18
Control of Propionibacterium acnes by natural antimicrobial substances: Role of the bacteriocin AS-48 and lysozyme
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Evolution of the phenolic compounds profile of olive leaf extract encapsulated by spray-drying during in vitro gastrointestinal digestion
10.1016/j.foodchem.2018.11.127
Insights into Chagas treatment based on the potential of bacteriocin AS-48
10.1016/j.ijpddr.2019.03.003
Preclinical studies of toxicity and safety of the AS-48 bacteriocin
10.1016/j.jare.2019.06.003
Design and Expression of Specific Hybrid Lantibiotics Active Against Pathogenic Clostridium spp.
10.3389/fmicb.2019.02154
Role of maltodextrin and inulin as encapsulating agents on the protection of oleuropein during in vitro gastrointestinal digestion
10.1016/j.foodchem.2019.125976
Synergy of the Bacteriocin AS-48 and Antibiotics against Uropathogenic Enterococci
10.3390/antibiotics9090567
Assessing the effectiveness of AS-48 in experimental mice models of Chagas' disease.
10.1093/jac/dkaa030
High-Throughput Screening for Substrate Specificity-Adapted Mutants of the Nisin Dehydratase NisB.
10.1021/acssynbio.0c00130
Outer-membrane-acting peptides and lipid II-targeting antibiotics cooperatively kill Gram-negative pathogens.
10.1038/s42003-020-01511-1
Antimicrobial Activity of the Circular Bacteriocin AS-48 against Clinical Multidrug-Resistant Staphylococcus aureus
10.3390/antibiotics10080925
Elucidating the mechanism by which synthetic helper peptides sensitize Pseudomonas aeruginosa to multiple antibiotics
10.1371/journal.ppat.1009909