Antifungal compounds that target fungal membranes: applications in plant disease control
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[1] R. Tweddell,et al. Role of Lipid Composition and Lipid Peroxidation in the Sensitivity of Fungal Plant Pathogens to Aluminum Chloride and Sodium Metabisulfite , 2007, Applied and Environmental Microbiology.
[2] H. Vogel,et al. Tryptophan- and arginine-rich antimicrobial peptides: structures and mechanisms of action. , 2006, Biochimica et biophysica acta.
[3] E. Bardaji,et al. Inhibition of Plant-Pathogenic Bacteria by Short Synthetic Cecropin A-Melittin Hybrid Peptides , 2006, Applied and Environmental Microbiology.
[4] Kyung-Soo Hahm,et al. Interactions between the plasma membrane and the antimicrobial peptide HP (2-20) and its analogues derived from Helicobacter pylori. , 2006, The Biochemical journal.
[5] K. Bogucka,et al. Antibacterial Activity of Synthetic Peptides Against Plant Pathogenic Pectobacterium Species , 2005 .
[6] Á. Trigos,et al. Ergosterol from Phytophthora drechsleri,a unusual metabolite of a member of this genus , 2005, Mycopathologia.
[7] K. Brogden. Antimicrobial peptides: pore formers or metabolic inhibitors in bacteria? , 2005, Nature Reviews Microbiology.
[8] Michael R. Yeaman,et al. Mechanisms of Antimicrobial Peptide Action and Resistance , 2003, Pharmacological Reviews.
[9] R. Tweddell,et al. Effect of Organic and Inorganic Salts on the Development of Helminthosporium solani, the Causal Agent of Potato Silver Scurf. , 2002, Plant disease.
[10] D. Ebbole,et al. Independent and Synergistic Activity of Synthetic Peptides Against Thiabendazole-Resistant Fusarium sambucinum. , 2002, Phytopathology.
[11] E. Earle,et al. Sensitivity of bacterial and fungal plant pathogens to the lytic peptides, MSI-99, magainin II, and cecropin B. , 2002, Molecular plant-microbe interactions : MPMI.
[12] R. Tweddell,et al. Effect of organic and inorganic salts on the growth and development of Fusarium sambucinum, a causal agent of potato dry rot , 2002 .
[13] Z. Punja,et al. Hydrolytic enzymes and antifungal compounds produced by Tilletiopsis species, phyllosphere yeasts that are antagonists of powdery mildew fungi. , 2002, Canadian journal of microbiology.
[14] R. Bélanger,et al. Mechanisms and means of detection of biocontrol activity of Pseudozyma yeasts against plant-pathogenic fungi. , 2002, FEMS yeast research.
[15] M. Zasloff. Antimicrobial peptides of multicellular organisms , 2002, Nature.
[16] R. Bélanger,et al. Specificity and Mode of Action of the Antifungal Fatty Acid cis-9-Heptadecenoic Acid Produced byPseudozyma flocculosa , 2001, Applied and Environmental Microbiology.
[17] R. Hamelin,et al. In vitro toxicity of natural and designed peptides to tree pathogens and pollen , 2000 .
[18] R. Hamelin,et al. Structural changes of spores of tree fungal pathogens after treatment with the designed antimicrobial peptide D2A21 , 2000 .
[19] R. Bélanger,et al. Synthesis and Biological Characterization of (Z)-9-Heptadecenoic and (Z)-6-Methyl-9-Heptadecenoic Acids: Fatty Acids with Antibiotic Activity Produced by Pseudozyma flocculosa , 2000, Journal of Chemical Ecology.
[20] C. Hou,et al. Growth inhibition of plant pathogenic fungi by hydroxy fatty acids , 2000, Journal of Industrial Microbiology and Biotechnology.
[21] L. Marnett. Lipid peroxidation-DNA damage by malondialdehyde. , 1999, Mutation research.
[22] T. C. White,et al. Clinical, Cellular, and Molecular Factors That Contribute to Antifungal Drug Resistance , 1998, Clinical Microbiology Reviews.
[23] D. Andreu,et al. Cecropin A-derived peptides are potent inhibitors of fungal plant pathogens. , 1998, Molecular plant-microbe interactions : MPMI.
[24] Carlos Gonzalez,et al. Synthetic peptide combinatorial libraries: a method for the identification of bioactive peptides against phytopathogenic fungi. , 1997, Molecular plant-microbe interactions : MPMI.
[25] M. Gullino,et al. Effectiveness of antifungal compounds against rose powdery mildew (Sphaerotheca pannosa var. rosae) in glasshouses , 1997 .
[26] R. Hancock,et al. Peptide antibiotics , 1997, The Lancet.
[27] F. Odds,et al. Molecular mechanisms of drug resistance in fungi. , 1994, Trends in microbiology.
[28] B. Halliwell,et al. Lipid peroxidation: its mechanism, measurement, and significance. , 1993, The American journal of clinical nutrition.
[29] Y. Yamaguchi,et al. Structure and synthesis of 11,12,13-trihydroxy-9Z,15Z-octadecadienoic acids from rice plant suffering from rice blast disease. , 1986 .
[30] O. Kodama,et al. Edifenphos, Inhibitor of Phosphatidylcholine Biosynthesis in Pyricularia oryzae , 1980 .
[31] O. Kodama,et al. Kitazin P, Inhibitor of Phosphatidylcholine Biosynthesis in Pyricularia oryzae , 1979 .
[32] J. Weete. Fungal Lipid Biochemistry: Distribution and Metabolism , 1974 .
[33] A. Bryskier. Antimicrobial agents: antibacterials and antifungals. , 2005 .
[34] Y. Uesugi. Fungal choline biosynthesis - a target for controlling rice blast , 2001 .
[35] A. Osbourn. Saponins and plant defence — a soap story , 1996 .
[36] T. Zitter,et al. Effects of bicarbonates and film-forming polymers on cucurbit foliar diseases , 1992 .
[37] R. Horst,et al. Effect of sodium bicarbonate and oils on the control of powdery mildew and black spot of roses , 1992 .
[38] T. Kondo,et al. An antifungal compound, 9,12,13-trihydroxy-(E)-10-octadecenoic acid, from Colocasia antiquorum inoculated with Ceratocystis fimbriata , 1989 .
[39] C. Steel,et al. Electrolyte leakage from plant and fungal tissues and disruption of liposome membranes by α-tomatine , 1988 .
[40] L. Crombie,et al. Pathogenicity of ‘take-all’ fungus to oats: Its relationship to the concentration and detoxification of the four avenacins , 1986 .
[41] Y. Yamaguchi,et al. Structure and synthesis of unsaturaded trihydroxy c18 fatty , 1985 .
[42] Mitsuru Yoshida,et al. Observation of Transmethylation from Methionine into Choline in the Intact Mycelia of Pyricularia oryzae by 13 C NMR under the Influence of Fungicides , 1984 .
[43] K. Bloch,et al. Sterol structure and membrane function. , 1981, Current topics in cellular regulation.
[44] J. G. Roddick. The steroidal glycoalkaloid α-tomatine , 1974 .
[45] J. Weete. Fungal Lipid Biochemistry , 1974, Monographs in Lipid Research.
[46] K. Maruthachalam,et al. Fungal Biology , 1971, Nature.