Identification and Rational Design of Novel Antimicrobial Peptides for Plant Protection

Antimicrobial peptides of multicellular organisms

Zasloff, M. (2002) · Nature · doi:10.1038/415389a · Cited by 8,457 · see citing works

Antimicrobial peptides: pore formers or metabolic inhibitors in bacteria?

Brogden, K. A. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1098 · Cited by 5,829 · see citing works

Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies

Hancock, R. E. W., & Sahl, H. (2006) · Nature Biotechnology · doi:10.1038/nbt1267 · Cited by 4,233 · see citing works

Significance of Inducible Defense-related Proteins in Infected Plants

van Loon, L. C., Rep, M., & Pieterse, C. M. J. (2006) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.44.070505.143425 · Cited by 3,401 · see citing works

Mechanisms of Antimicrobial Peptide Action and Resistance

Yeaman, M. R., & Yount, N. Y. (2003) · Pharmacological Reviews · doi:10.1124/pr.55.1.2 · Cited by 2,998 · see citing works

Peptide Antimicrobial Agents

Jenssen, H., Hamill, P., & Hancock, R. E. W. (2006) · Clinical Microbiology Reviews · doi:10.1128/cmr.00056-05 · Cited by 2,532 · see citing works

In Vivo Protein Transduction: Delivery of a Biologically Active Protein into the Mouse

Schwarze, S. R., Ho, A. L., Vocero-Akbani, A. M., & Dowdy, S. F. (1999) · Science · doi:10.1126/science.285.5433.1569 · Cited by 2,418 · see citing works

Bacteriocins: Developing innate immunity for food

Cotter, P. D., Hill, C., & Ross, R. P. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1273 · Cited by 2,380 · see citing works

A Truncated HIV-1 Tat Protein Basic Domain Rapidly Translocates through the Plasma Membrane and Accumulates in the Cell Nucleus

Vivès, É., Brodin, P. M., & Lebleu, B. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.25.16010 · Cited by 2,377 · see citing works

Magainins, a class of antimicrobial peptides from Xenopus skin: isolation, characterization of two active forms, and partial cDNA sequence of a precursor.

Zasloff, M. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.15.5449 · Cited by 2,305 · see citing works

The third helix of the Antennapedia homeodomain translocates through biological membranes.

Derossi, D., Joliot, A., Chassaing, G., & Prochiantz, A. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)34080-2 · Cited by 2,034 · see citing works

Diversity of antimicrobial peptides and their mechanisms of action

Epand, R. M., & Vogel, H. J. (1999) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(99)00198-4 · Cited by 1,354 · see citing works

Cationic peptides: a new source of antibiotics

Hancock, R. E. W., & Lehrer, R. I. (1998) · Trends in biotechnology · doi:10.1016/s0167-7799(97)01156-6 · Cited by 1,348 · see citing works

The co-evolution of host cationic antimicrobial peptides and microbial resistance

Peschel, A., & Sahl, H. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1441 · Cited by 1,052 · see citing works

Tryptophan- and arginine-rich antimicrobial peptides: Structures and mechanisms of action

Chan, D. I., Prenner, E. J., & Vogel, H. J. (2006) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2006.04.006 · Cited by 1,043 · see citing works

A peptide carrier for the delivery of biologically active proteins into mammalian cells

Morris, M. C., Depollier, J., Méry, J., Heitz, F., & Divita, G. (2001) · Nature Biotechnology · doi:10.1038/nbt1201-1173 · Cited by 1,019 · see citing works

Inactivation of the dlt Operon inStaphylococcus aureus Confers Sensitivity to Defensins, Protegrins, and Other Antimicrobial Peptides

Peschel, A., Otto, M. J., Jack, R. W., Kalbacher, H., Jung, G., & Götz, F. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.13.8405 · Cited by 999 · see citing works

Cationic peptides: effectors in innate immunity and novel antimicrobials

Hancock, R. E. (2001) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(01)00092-5 · Cited by 978 · see citing works

The relationship between peptide structure and antibacterial activity

Powers, J.-P. S., & Hancock, R. E. W. (2003) · Peptides · doi:10.1016/j.peptides.2003.08.023 · Cited by 947 · see citing works

Use of the Cell Wall Precursor Lipid II by a Pore-Forming Peptide Antibiotic

Breukink, E. J., Wiedemann, I., van Kraaij, C., Kuipers, O. P., Sahl, H., & KRUIJFF, B. D. (1999) · Science · doi:10.1126/science.286.5448.2361 · Cited by 815 · see citing works

Mechanism of Interaction of Different Classes of Cationic Antimicrobial Peptides with Planar Bilayers and with the Cytoplasmic Membrane of Escherichia coli

Wu, M., Maier, E., Benz, R., & Hancock, R. E. W. (1999) · Biochemistry · doi:10.1021/bi9826299 · Cited by 737 · see citing works

Lactoferrin—a multifunctional protein with antimicrobial properties

Farnaud, S., & Evans, R. W. (2003) · Molecular Immunology · doi:10.1016/s0161-5890(03)00152-4 · Cited by 731 · see citing works

Antimicrobial Peptides from Plants

Broekaert, W. F., Cammue, B. P. A., Bolle, M. F. C. D., Thevissen, K., Samblanx, G. W. D., Osborn, R. W., & Nielson, K. (1997) · Critical Reviews in Plant Sciences · doi:10.1080/07352689709701952 · Cited by 678 · see citing works

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 · see citing works

Plant defensins

Thomma, B. P. H. J., Cammue, B. P. A., & Thevissen, K. (2002) · Planta · doi:10.1007/s00425-002-0902-6 · Cited by 662 · see citing works

Melittin: a Membrane-active Peptide with Diverse Functions

Raghuraman, H., & Chattopadhyay, A. (2006) · Bioscience Reports · doi:10.1007/s10540-006-9030-z · Cited by 652 · see citing works

Mechanisms of action on Escherichia coli of cecropin P1 and PR-39, two antibacterial peptides from pig intestine

Boman, H. G., Agerberth, B., & Boman, A. (1993) · Infection and Immunity · doi:10.1128/iai.61.7.2978-2984.1993 · Cited by 554 · see citing works

Recognition of Antimicrobial Peptides by a Bacterial Sensor Kinase

Bader, M. W., Sanowar, S., Daley, M. E., Schneider, A. R., Cho, U., Xu, W., Klevit, R. E., Moual, H. L., & Miller, S. I. (2005) · Cell · doi:10.1016/j.cell.2005.05.030 · Cited by 554 · see citing works

Lactoferricin

Gifford, J. L., Hunter, H. N., & Vogel, H. J. (2005) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-005-5373-z · Cited by 529 · see citing works

Plant defense peptides

García‐Olmedo, F., Molina, A., Alamillo, J. M., & Rodríguez‐Palenzuela, P. (1998) · Biopolymers · doi:10.1002/(sici)1097-0282(1998)47:6 · Cited by 521 · see citing works

Transduction peptides: from technology to physiology

Joliot, A., & Prochiantz, A. (2004) · Nature Cell Biology · doi:10.1038/ncb0304-189 · Cited by 495 · see citing works

Fungal pathogen protection in potato by expression of a plant defensin peptide

Gao, A.-G., Hakimi, S. M., Mittanck, C. A., Wu, Y., Woerner, B. M., Stark, D. M., Shah, D. M., Liang, J., & Rommens, C. M. T. (2000) · Nature Biotechnology · doi:10.1038/82436 · Cited by 472 · see citing works

Small cysteine‐rich peptides resembling antimicrobial peptides have been under‐predicted in plants

Silverstein, K. A. T., Moskal, W. A., Wu, H. C., Underwood, B. A., Graham, M. A., Town, C. D., & VandenBosch, K. A. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03136.x · Cited by 470 · see citing works

Apidaecins: antibacterial peptides from honeybees.

Casteels, P., Ampè, C., Jacobs, F. H. H., Vaeck, M., & Tempst, P. (1989) · The EMBO Journal · doi:10.1002/j.1460-2075.1989.tb08368.x · Cited by 469 · see citing works

Mode of Action of the Antimicrobial Peptide Indolicidin

Falla, T. J., Karunaratne, D. N., & Hancock, R. E. W. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.32.19298 · Cited by 467 · see citing works

Mechanism of antimicrobial action of indolicidin

Subbalakshmi, C., & Sitaram, N. (1998) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1998.tb12896.x · Cited by 455 · see citing works

Potent Antibacterial Peptides Generated by Pepsin Digestion of Bovine Lactoferrin

TOMITA, M., Bellamy, W., Takase, M., Yamauchi, K., Wakabayashi, H., & Kawase, K. (1991) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(91)78608-6 · Cited by 445 · see citing works

Proteinases of common pathogenic bacteria degrade and inactivate the antibacterial peptide LL‐37

Schmidtchen, A., Frick, I.-M., Andersson, E., Tapper, H., & Björck, L. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.03146.x · Cited by 440 · see citing works

An automated quantitative assay for fungal growth inhibition

Broekaert, W. F., Terras, F. R. G., Cammue, B. P. A., & Vanderleyden, J. (1990) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1990.tb04174.x · Cited by 438 · see citing works

Cationic antimicrobial peptides activate a two‐component regulatory system, PmrA‐PmrB, that regulates resistance to polymyxin B and cationic antimicrobial peptides in Pseudomonas aeruginosa

McPhee, J. B., Lewenza, S., & Hancock, R. E. W. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03673.x · Cited by 436 · see citing works

Cell-penetrating peptides and antimicrobial peptides: how different are they?

Henriques, S. T., Melo, M. N., & Castanho, M. A. R. B. (2006) · Biochemical Journal · doi:10.1042/bj20061100 · Cited by 410 · see citing works

Permeabilization of Fungal Membranes by Plant Defensins Inhibits Fungal Growth

Thevissen, K., Terras, F. R. G., & Broekaert, W. F. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.12.5451-5458.1999 · Cited by 388 · see citing works

Antimicrobial peptides and plant disease control

Montesinos, E. (2007) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2007.00683.x · Cited by 376 · see citing works

Defensins from Insects and Plants Interact with Fungal Glucosylceramides

Thevissen, K., Warnecke, D. C., François, I., Leipelt, M., Heinz, E., Ott, C., Zähringer, U., Thomma, B. P. H. J., Ferket, K. K. A., & Cammue, B. P. A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m311165200 · Cited by 355 · see citing works

Structural and DNA-binding studies on the bovine antimicrobial peptide, indolicidin: evidence for multiple conformations involved in binding to membranes and DNA

Hsu, C. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki725 · Cited by 337 · see citing works

Translocation of a Channel-Forming Antimicrobial Peptide, Magainin 2, across Lipid Bilayers by Forming a Pore

Matsuzaki, K., Murase, O., Fujii, N., & Miyajima, K. (1995) · Biochemistry · doi:10.1021/bi00019a033 · Cited by 308 · see citing works

A Novel Antimicrobial Peptide fromBufo bufo gargarizans

Park, C. B., Kim, M. S., & Kim, S. C. (1996) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1996.0071 · Cited by 300 · see citing works

Expression of an Antimicrobial Peptide via the Chloroplast Genome to Control Phytopathogenic Bacteria and Fungi

DeGray, G., Rajasekaran, K., Smith, F., Sanford, J., & Daniell, H. (2001) · Plant Physiology · doi:10.1104/pp.010233 · Cited by 299 · see citing works

Antimicrobial Peptides, Isolated from Horseshoe Crab Hemocytes, Tachyplesin II, and Polyphemusins I and II: Chemical Structures and Biological Activity1

Miyata, T., Tokunaga, F., Yoneya, T., Yoshikawa, K., Iwanaga, S., Niwa, M., Takao, T., & Shimonishi, Y. (1989) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a122913 · Cited by 294 · see citing works

A linguistic model for the rational design of antimicrobial peptides

Loose, C. R., Jensen, K. L., Rigoutsos, I., & Stephanopoulos, G. N. (2006) · Nature · doi:10.1038/nature05233 · Cited by 248 · see citing works

Transgenic plants expressing cationic peptide chimeras exhibit broad-spectrum resistance to phytopathogens

Osusky, M., Zhou, G., Osuska, L., Hancock, R. E. W., Kay, W. W., & Misra, S. (2000) · Nature Biotechnology · doi:10.1038/81145 · Cited by 246 · see citing works

Molecular genetic analysis of a locus required for resistance to antimicrobial peptides in Salmonella typhimurium.

Parra-Lopez, C., Baer, M. T., & Groisman, E. A. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb06089.x · Cited by 230 · see citing works

Molecular mechanisms of membrane perturbation by antimicrobial peptides and the use of biophysical studies in the design of novel peptide antibiotics.

Lohner, K., & Blondelle, S. (2005) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/1386207053764576 · Cited by 222 · see citing works

Enhanced tolerance to bacterial pathogens caused by the transgenic expression of barley lipid transfer protein LTP2

Molina, A., & García‐Olmedo, F. (1997) · The Plant Journal · doi:10.1046/j.1365-313x.1997.00669.x · Cited by 216 · see citing works

Polarity in filamentous fungi: moving beyond the yeast paradigm

Harris, S. D., & Momany, M. (2003) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2003.11.007 · Cited by 209 · see citing works

Structure-Based Design of an Indolicidin Peptide Analogue with Increased Protease Stability ,

Rozek, A., Powers, J.-P. S., Friedrich, C. L., & Hancock, R. E. W. (2003) · Biochemistry · doi:10.1021/bi035643g · Cited by 207 · see citing works

Expression of the α‐thionin gene from barley in tobacco confers enhanced resistance to bacterial pathogens

Carmona, M. J., Molina, A., Fernández, J. A., López‐Fando, J. J., & García‐Olmedo, F. (1993) · The Plant Journal · doi:10.1111/j.1365-313x.1993.tb00165.x · Cited by 205 · see citing works

Interactions of antifungal plant defensins with fungal membrane components

Thevissen, K., Ferket, K. K. A., François, I., & Cammue, B. P. A. (2003) · Peptides · doi:10.1016/j.peptides.2003.09.014 · Cited by 187 · see citing works

Cyclization Increases the Antimicrobial Activity and Selectivity of Arginine- and Tryptophan-Containing Hexapeptides

Dathe, M., Nikolenko, H., Klose, J., & Bienert, M. (2004) · Biochemistry · doi:10.1021/bi035948v · Cited by 186 · see citing works

The mammalian ionic environment dictates microbial susceptibility to antimicrobial defense peptides

Dorschner, R. A., López‐García, B., Peschel, A., Kraus, D., Morikawa, K., Nizet, V., & Gallo, R. L. (2006) · The FASEB Journal · doi:10.1096/fj.05-4406com · Cited by 186 · see citing works

Recombinant production of antimicrobial peptides in heterologous microbial systems

Ingham, A. B., & Moore, R. J. (2007) · Biotechnology and Applied Biochemistry · doi:10.1042/ba20060207 · Cited by 176 · see citing works

A library of linear undecapeptides with bactericidal activity against phytopathogenic bacteria

Badosa, E., Ferré, R., Planas, M., Feliu, L., Besalú, E., Cabrefiga, J., Bardajı́, E., & Montesinos, E. (2007) · Peptides · doi:10.1016/j.peptides.2007.09.010 · Cited by 173 · see citing works

MSI-99, a magainin analogue, imparts enhanced disease resistance in transgenic tobacco and banana

Chakrabarti, A. K., Ganapathi, T. R., Mukherjee, P. K., & Bapat, V. A. (2002) · Planta · doi:10.1007/s00425-002-0918-y · Cited by 172 · see citing works

Improvement of outer membrane-permeabilizing and lipopolysaccharide-binding activities of an antimicrobial cationic peptide by C-terminal modification

Piers, K. L., Brown, M. H., & Hancock, R. E. W. (1994) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.38.10.2311 · Cited by 167 · see citing works

Antifungal Pisum sativum Defensin 1 Interacts with Neurospora crassa Cyclin F Related to the Cell Cycle

Lobo, D. S., Pereira, I. B., Madeira, L. F., de Medeiros, L. N., Cabral, L. M., Faria, J., Bellio, M., Campos, R. C., Linden, R., & Kurtenbach, E. (2007) · Biochemistry · doi:10.1021/bi061441j · Cited by 165 · see citing works

Heterologous Expression of Genes Mediating Enhanced Fungal Resistance in Transgenic Wheat

Oldach, K., Becker, D., & Lörz, H. (2001) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2001.14.7.832 · Cited by 165 · see citing works

Expression of a Cecropin B lytic peptide analog in transgenic tobacco confers enhanced resistance to bacterial wilt caused by Pseudomonas solanacearum

Jaynes, J. M., Nagpala, P., Destéfano‐Beltrán, L., Huang, J. H., Kim, J., Denny, T. P., & Çetiner, S. (1993) · Plant Science · doi:10.1016/0168-9452(93)90169-z · Cited by 161 · see citing works

Cecropin A—Derived Peptides Are Potent Inhibitors of Fungal Plant Pathogens

Cavallarin, L., Andreu, D., & Segundo, B. S. (1998) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1998.11.3.218 · Cited by 153 · see citing works

Stress proteins on the yeast cell surface determine resistance to osmotin, a plant antifungal protein

Yun, D., Zhao, Y., Pardo, J. M., Narasimhan, M. L., Damsz, B., Lee, H., Abad, L. R., D’Urzo, M. P., Hasegawa, P. M., & Bressan, R. A. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.13.7082 · Cited by 152 · see citing works

Antimicrobial Peptides from Food Proteins

Pellegrini, A. (2003) · Current Pharmaceutical Design · doi:10.2174/1381612033454865 · Cited by 144 · see citing works

Design of self-processing antimicrobial peptides for plant protection

Powell, W. A., Catranis, C. M., & Maynard, C. A. (2000) · Letters in Applied Microbiology · doi:10.1046/j.1365-2672.2000.00782.x · Cited by 143 · see citing works

Transgenic expression of a gene encoding a synthetic antimicrobial peptide results in inhibition of fungal growth in vitro and in planta

Cary, J. W., Rajasekaran, K., Jaynes, J. M., & Cleveland, T. E. (2000) · Plant Science · doi:10.1016/s0168-9452(00)00189-8 · Cited by 136 · see citing works

Two mitogen-activated protein kinase signalling cascades mediate basal resistance to antifungal plant defensins in Fusarium graminearum

Ramamoorthy, V., Zhao, X., Snyder, A. K., Xu, J., & Shah, D. M. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00887.x · Cited by 136 · see citing works

Membrane Translocation Mechanism of the Antimicrobial Peptide Buforin 2

Kobayashi, S., Chikushi, A., Tougu, S., Imura, Y., Nishida, M., Yano, Y., & Matsuzaki, K. (2004) · Biochemistry · doi:10.1021/bi048206q · Cited by 135 · see citing works

Apidaecin-Type Peptide Antibiotics Function through a Nonporeforming Mechanism Involving Stereospecificity

Casteels, P., & Tempst, P. (1994) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1994.1234 · Cited by 134 · see citing works

Enhanced resistance to the rice blast fungus Magnaporthe grisea conferred by expression of a cecropin A gene in transgenic rice

Coca, M. A., Peñas, G., Gómez‐Ariza, J., Campo, S., Bortolotti, C., Messeguer, J., & Segundo, B. S. (2005) · Planta · doi:10.1007/s00425-005-0069-z · Cited by 134 · see citing works

Inactivation of the sapA to sapF Locus of Erwinia chrysanthemi Reveals Common Features in Plant and Animal Bacterial Pathogenesis

López‐Solanilla, E., García‐Olmedo, F., & Rodríguez‐Palenzuela, P. (1998) · The Plant Cell · doi:10.1105/tpc.10.6.917 · Cited by 129 · see citing works

Transgenic expression of cecropin B, an antibacterial peptide from Bombyx mori, confers enhanced resistance to bacterial leaf blight in rice

Sharma, A. K., Sharma, R., Imamura, M., Yamakawa, M., & Machii, H. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)02106-2 · Cited by 128 · see citing works

The antimicrobial peptides lactoferricin B and magainin 2 cross over the bacterial cytoplasmic membrane and reside in the cytoplasm

Haukland, H. H., Ulvatne, H., Sandvik, K., & Vorland, L. H. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)03100-3 · Cited by 128 · see citing works

Improved activity of a synthetic indolicidin analog

Falla, T. J., & Hancock, R. E. W. (1997) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.41.4.771 · Cited by 127 · see citing works

Lactoferricin B inhibits bacterial macromolecular synthesis in and

Ulvatne, H., Samuelsen, Ø., Haukland, H. H., KRAMER, M., & Vorland, L. H. (2004) · FEMS Microbiology Letters · doi:10.1016/j.femsle.2004.07.001 · Cited by 122 · see citing works

Quantitatively determined uptake of cell-penetrating peptides in non-mammalian cells with an evaluation of degradation and antimicrobial effects

Palm‐Apergi, C., Netzereab, S., & Hällbrink, M. (2006) · Peptides · doi:10.1016/j.peptides.2006.01.006 · Cited by 122 · see citing works

Antibiotic activities of peptides, hydrogen peroxide and peroxynitrite in plant defence

García‐Olmedo, F., Rodríguez‐Palenzuela, P., Molina, A., Alamillo, J. M., López‐Solanilla, E., Berrocal‐Lobo, M., & Poza‐Carrión, C. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)02456-5 · Cited by 115 · see citing works

Naturally Processed Dermcidin-Derived Peptides Do Not Permeabilize Bacterial Membranes and Kill Microorganisms Irrespective of Their Charge

Steffen, H. K., Rieg, S., Wiedemann, I., Kalbacher, H., Deeg, M., Sahl, H., Peschel, A., Götz, F., Garbe, C., & Schittek, B. (2006) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00181-06 · Cited by 114 · see citing works

The Antifungal Protein from Aspergillus giganteus Causes Membrane Permeabilization

Theis, T., Wedde, M., Meyer, V., & Ståhl, U. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.2.588-593.2003 · Cited by 113 · see citing works

Expression of an Engineered Cecropin Gene Cassette in Transgenic Tobacco Plants Confers Disease Resistance to Pseudomonas syringae pv. tabaci

Huang, Y. P., Nordeen, R. O., Di, M., Owens, L. D., & McBeath, J. H. (1997) · Phytopathology · doi:10.1094/phyto.1997.87.5.494 · Cited by 113 · see citing works

Process development and economic evaluation of recombinant human lactoferrin expressed in rice grain

Nandi, S., Yalda, D., Lu, S. M., Nikolov, Z. L., Misaki, R., Fujiyama, K., & Huang, N. (2005) · Transgenic Research · doi:10.1007/s11248-004-8120-6 · Cited by 112 · see citing works

Inhibition of Plant-Pathogenic Bacteria by Short Synthetic Cecropin A-Melittin Hybrid Peptides

Ferré, R., Badosa, E., Feliu, L., Planas, M., Montesinos, E., & Bardajı́, E. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.5.3302-3308.2006 · Cited by 112 · see citing works

Structure and Function of Membrane-Lytic Peptides

Bechinger, B. (2004) · Critical Reviews in Plant Sciences · doi:10.1080/07352680490452825 · Cited by 111 · see citing works

Fungicidal activity of cecropin A

DeLucca, A. J., Bland, J. M., Jacks, T. J., Grimm, C. C., Cleveland, T. E., & Walsh, T. J. (1997) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.41.2.481 · Cited by 109 · see citing works

Enhanced disease resistance conferred by expression of an antimicrobial magainin analog in transgenic tobacco

Li, Q. Q., Lawrence, C. B., Hong-yan, X., Babbitt, R. A., Bass, W. T., Maiti, I. B., & Everett, N. P. (2001) · Planta · doi:10.1007/s004250000480 · Cited by 109 · see citing works

A pathogenesis related protein, AhPR10 from peanut: an insight of its mode of antifungal activity

Chadha, P., & Das, R. H. (2006) · Planta · doi:10.1007/s00425-006-0344-7 · Cited by 109 · see citing works

Disease resistance conferred by the expression of a gene encoding a synthetic peptide in transgenic cotton ( Gossypium hirsutum L.) plants

Rajasekaran, K., Cary, J. W., Jaynes, J. M., & Cleveland, T. E. (2005) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2005.00145.x · Cited by 107 · see citing works

Transgenic Potatoes Expressing a Novel Cationic Peptide are Resistant to Late Blight and Pink Rot

Osusky, M., Osuska, L., Hancock, R. E. W., Kay, W. W., & Misra, S. (2004) · Transgenic Research · doi:10.1023/b:trag.0000026076.72779.60 · Cited by 106 · see citing works

Antimicrobial Peptides

Rao, A. G. (1995) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-8-0006 · Cited by 106 · see citing works

Cloning, structural organization and regulation of expression of the Penicillium chrysogenum paf gene encoding an abundantly secreted protein with antifungal activity

Marx, F., Haas, H., Reindl, M., Stöffler, G., Lottspeich, F., & Redl, B. (1995) · Gene · doi:10.1016/0378-1119(95)00701-6 · Cited by 102 · see citing works

The Antifungal Protein AFP from Aspergillus giganteus Inhibits Chitin Synthesis in Sensitive Fungi

Hagen, S., Marx, F., Ram, A. F. J., & Meyer, V. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.02497-06 · Cited by 102 · see citing works

Purification, characterization, and cell wall localization of an α‐fucosidase that inactivates a xyloglucan oligosaccharin

Augur, C., Benhamou, N., Darvill, A. G., & Albersheim, P. (1993) · The Plant Journal · doi:10.1046/j.1365-313x.1993.t01-24-00999.x · Cited by 102 · see citing works

Identification of Novel Hexapeptides Bioactive against Phytopathogenic Fungi through Screening of a Synthetic Peptide Combinatorial Library

López‐García, B., Pérez‐Payá, E., & Marcos, J. F. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.5.2453-2460.2002 · Cited by 102 · see citing works

Expression of giant silkmoth cecropin B genes in tobacco

Florack, D. E. A., Allefs, S. J. H. M., Bollen, R., Bosch, D., Visser, B., & Stiekema, W. J. (1995) · Transgenic Research · doi:10.1007/bf01969415 · Cited by 101 · see citing works

Studies on the Mode of Action of the Antifungal Hexapeptide PAF26

Muñoz, A., López‐García, B., & Marcos, J. F. (2006) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00650-06 · Cited by 96 · see citing works

Inhibition of Fungal and Bacterial Plant Pathogens by Synthetic Peptides: In Vitro Growth Inhibition, Interaction Between Peptides and Inhibition of Disease Progression

Ali, G. S., & Reddy, A. S. N. (2000) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2000.13.8.847 · Cited by 95 · see citing works

Synthetic Antimicrobial Peptide Design

Powell, W. A. (1995) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-8-0792 · Cited by 95 · see citing works

Biodiversity of apidaecin-type peptide antibiotics. Prospects of manipulating the antibacterial spectrum and combating acquired resistance

Casteels, P., Romagnolo, J., Castle, M., Casteels-Josson, K., Erdjument‐Bromage, H., & Tempst, P. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47165-7 · Cited by 93 · see citing works

Pathogen-induced expression of a cecropin A-melittin antimicrobial peptide gene confers antifungal resistance in transgenic tobacco

Yevtushenko, D. P., Romero, R., Forward, B. S., Hancock, R. E. W., Kay, W. W., & Misra, S. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/eri165 · Cited by 92 · see citing works

Role of chitin synthase genes in Fusarium oxysporum

Martin-Udiroz, M. (2004) · Microbiology · doi:10.1099/mic.0.27236-0 · Cited by 88 · see citing works

Congeners of SMAP29 Kill Ovine Pathogens and Induce Ultrastructural Damage in Bacterial Cells

Kalfa, V. C., Jia, H. P., Kunkle, R. A., McCray, P. B., Tack, B. F., & Brogden, K. A. (2001) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.45.11.3256-3261.2001 · Cited by 86 · see citing works

Bacterial disease resistance of transgenic hybrid poplar expressing the synthetic antimicrobial peptide D4E1

Mentag, R., Luckevich, M. D., Morency, M., & Séguin, A. (2003) · Tree Physiology · doi:10.1093/treephys/23.6.405 · Cited by 83 · see citing works

Activity of the Antifungal Protein from Aspergillus giganteus Against Botrytis cinerea

Moreno, A. B., Martínez‐del‐Pozo, Á., Borja, M., & Segundo, B. S. (2003) · Phytopathology · doi:10.1094/phyto.2003.93.11.1344 · Cited by 82 · see citing works

Peptide-mediated broad-spectrum plant resistance to tospoviruses

Rudolph, C., Schreier, P. H., & Uhrig, J. F. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0730832100 · Cited by 81 · see citing works

Evaluation of Transgenic ‘Chardonnay’ (Vitis vinifera) Containing Magainin Genes for Resistance to Crown Gall and Powdery Mildew

Vidal, J. R., Kikkert, J. R., Malnoy, M., Wallace, P. G., Barnard, J. A., & Reisch, B. I. (2006) · Transgenic Research · doi:10.1007/s11248-005-4423-5 · Cited by 80 · see citing works

Design and mechanism of action of a novel bacteria-selective antimicrobial peptide from the cell-penetrating peptide Pep-1

Zhu, W. L., Lan, H., Park, I., Kim, J. I., Jin, H. Z., Hahm, K., & Shin, S. Y. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.08.094 · Cited by 79 · see citing works

Expression of an Antifungal Peptide in <i>Saccharomyces</i>: A New Approach for Biological Control of the Postharvest Disease Caused by <i>Colletotrichum coccodes</i>

Jones, R. W., & Prusky, D. (2002) · Phytopathology® · doi:10.1094/phyto.2002.92.1.33 · Cited by 79 · see citing works

Sensitivity of Bacterial and Fungal Plant Pathogens to the Lytic Peptides, MSI-99, Magainin II, and Cecropin B

Alan, A. R., & Earle, E. D. (2002) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2002.15.7.701 · Cited by 78 · see citing works

The Medicinal Chemistry of Short Lactoferricin-Based Antibacterial Peptides

Haug, B. E., Strøm, M. B., & Svendsen, J. S. M. (2006) · Current Medicinal Chemistry · doi:10.2174/092986707779313435 · Cited by 78 · see citing works

Mutants of Ralstonia (Pseudomonas) solanacearum sensitive to antimicrobial peptides are altered in their lipopolysaccharide structure and are avirulent in tobacco

Titarenko, E., López‐Solanilla, E., García‐Olmedo, F., & Rodríguez‐Palenzuela, P. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.21.6699-6704.1997 · Cited by 77 · see citing works

Genetic modification of potato against microbial diseases: in vitro and in planta activity of a dermaseptin B1 derivative, MsrA2

Osusky, M., Osuska, L., Kay, W. W., & Misra, S. (2005) · Theoretical and Applied Genetics · doi:10.1007/s00122-005-2056-y · Cited by 76 · see citing works

Identification and Characterization of a Hexapeptide with Activity Against Phytopathogenic Fungi That Cause Postharvest Decay in Fruits

López‐García, B., González-Candelas, L., Pérez‐Payá, E., & Marcos, J. F. (2000) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2000.13.8.837 · Cited by 76 · see citing works

Design of Host Defence Peptides for Antimicrobial and Immunity Enhancing Activities

McPhee, J. B., Scott, M. G., & Hancock, R. E. W. (2005) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/1386207053764558 · Cited by 75 · see citing works

Induced Expression of Sarcotoxin IA Enhanced Host Resistance Against Both Bacterial and Fungal Pathogens in Transgenic Tobacco

Mitsuhara, I., Matsufuru, H., Ohshima, M., Kaku, H., Nakajima, Y., Murai, N., Natori, S., & Ohashi, Y. (2000) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2000.13.8.860 · Cited by 73 · see citing works

Increasing bacterial disease resistance in plants utilizing antibacterial genes from insects

Jaynes, J. M., Xanthopoulos, K. G., Destéfano‐Beltrán, L., & Dodds, J. H. (1987) · BioEssays · doi:10.1002/bies.950060605 · Cited by 72 · see citing works

A Single Amino Acid Substitution in the Antimicrobial Defense Protein Cecropin B Is Associated with Diminished Degradation by Leaf Intercellular Fluid

Owens, L. D., & Heutte, T. M. (1997) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1997.10.4.525 · Cited by 71 · see citing works

Biotechnologically relevant enzymes and proteins

Moreno, A. B., Martínez‐del‐Pozo, Á., & Segundo, B. S. (2006) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-006-0362-1 · Cited by 71 · see citing works

Comparison of the activity of antifungal hexapeptides and the fungicides thiabendazole and imazalil against postharvest fungal pathogens

López‐García, B., Veyrat, A., Pérez-Payá, E., González-Candelas, L., & Marcos, J. F. (2003) · International Journal of Food Microbiology · doi:10.1016/s0168-1605(03)00118-1 · Cited by 70 · see citing works

In vitro inhibition of postharvest pathogens of fruit and control of gray mold of strawberry and green mold of citrus by aureobasidin A

Liu, X., Wang, J., Ping, G., Mao, C., Zhu, Z., & Li, H. (2007) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2007.07.054 · Cited by 69 · see citing works

Amino acid sequence and disulfide bridges of an antifungal protein isolated from Aspergillus giganteus

Nakaya, K., Omata, K., Okahashi, I., Nakamura, Y., Kolkenbrock, H., & ULBRICH, N. (1990) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1990.tb19300.x · Cited by 68 · see citing works

Broad-Spectrum Antimicrobial Activity in vitro of the Synthetic Peptide D4E1

Rajasekaran, K., Stromberg, K. D., Cary, J. W., & Cleveland, T. E. (2001) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf010154d · Cited by 66 · see citing works

Surface-Active Fungicidal d -Peptide Inhibitors of the Plasma Membrane Proton Pump That Block Azole Resistance

Monk, B. C., Niimi, K., Lin, S. X., Knight, A., Kardos, T. B., Cannon, R. D., Parshot, R., King, A., Lun, D. J., & Harding, D. R. K. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.49.1.57-70.2005 · Cited by 66 · see citing works

Improvement of cyclic decapeptides against plant pathogenic bacteria using a combinatorial chemistry approach

Monroc, S., Badosa, E., Besalú, E., Planas, M., Bardajı́, E., Montesinos, E., & Feliu, L. (2006) · Peptides · doi:10.1016/j.peptides.2006.05.001 · Cited by 64 · see citing works

Molecular farming in plants: Oilseeds as vehicles for the production of pharmaceutical proteins

Boothe, J. G., Saponja, J. A., & Parmenter, D. L. (1997) · Drug Development Research · doi:10.1002/(sici)1098-2299(199711/12)42:3/4 · Cited by 63 · see citing works

Expression of the cationic antimicrobial peptide lactoferricin fused with the anionic peptide in Escherichia coli

Kim, H.-K., Chun, D.-S., Kim, J.-S., Yun, C.-H., Lee, J.-H., Hong, S., & Kang, D. (2006) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-005-0266-5 · Cited by 62 · see citing works

De novo designed cyclic cationic peptides as inhibitors of plant pathogenic bacteria

Monroc, S., Badosa, E., Feliu, L., Planas, M., Montesinos, E., & Bardajı́, E. (2006) · Peptides · doi:10.1016/j.peptides.2006.04.019 · Cited by 62 · see citing works

Activity of cecropin SB37 against protoplasts from several plant species and their bacterial pathogens

Nordeen, R. O., Sinden, S. L., Jaynes, J. M., & Owens, L. D. (1992) · Plant Science · doi:10.1016/0168-9452(92)90012-b · Cited by 61 · see citing works

Biological activity of Tat (47–58) peptide on human pathogenic fungi

Jung, H. J., Park, Y., Hahm, K., & Lee, D. G. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.04.059 · Cited by 60 · see citing works

Synthetic peptides derived from the β2−β3 loop of Raphanus sativus antifungal protein 2 that mimic the active site

Schaaper, W. M. M., Posthuma, G. A., Meloen, R. H., Plasman, H. H., Sijtsma, L., van Amerongen, A., Fant, F., BORREMANS, F. A. M., Thevissen, K., & Broekaert, W. F. (2001) · Journal of Peptide Research · doi:10.1034/j.1399-3011.2001.00842.x · Cited by 60 · see citing works

Expression of a magainin-type antimicrobial peptide gene (MSI-99) in tomato enhances resistance to bacterial speck disease

Alan, A. R., Blowers, A. D., & Earle, E. D. (2004) · Plant Cell Reports · doi:10.1007/s00299-003-0702-x · Cited by 59 · see citing works

Activity and mode of action against fungal phytopathogens of bovine lactoferricin-derived peptides

Muñoz, A., & Marcos, J. F. (2006) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2006.03089.x · Cited by 59 · see citing works

Expression of Human Lactoferrin cDNA Confers Resistance to Ralstonia solanacearum in Transgenic Tobacco Plants

Zhang, Z., Coyne, D. P., Vidaver, A. K., & Mitra, A. (1998) · Phytopathology · doi:10.1094/phyto.1998.88.7.730 · Cited by 58 · see citing works

Inhibition of a plant virus infection by analogs of melittin.

Marcos, J. F., Beachy, R. N., Houghten, R. A., Blondelle, S. E., & Pérez‐Payá, E. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.26.12466 · Cited by 57 · see citing works

Peptide Aptamers That Bind to a Geminivirus Replication Protein Interfere with Viral Replication in Plant Cells

López-Ochoa, L., Ramírez-Prado, J. H., & Hanley-Bowdoin, L. K. (2006) · Journal of Virology · doi:10.1128/jvi.02698-05 · Cited by 57 · see citing works

Neuronal uptake of pesticides disrupts chemosensory cells of nematodes

Winter, M. D., McPherson, M. J., & Atkinson, H. J. (2002) · Parasitology · doi:10.1017/s0031182002002482 · Cited by 55 · see citing works

Synthetic Peptide Combinatorial Libraries: A Method for the Identification of Bioactive Peptides Against Phytopathogenic Fungi

Reed, J. D., Edwards, D. L., & Gonzalez, C. F. (1997) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.1997.10.5.537 · Cited by 55 · see citing works

Characterization of antimicrobial peptides against a US strain of the rice pathogen Rhizoctonia solani

Oard, S. V., Rush, M. C., & Oard, J. H. (2004) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2004.02291.x · Cited by 55 · see citing works

Rapid identification of compounds with enhanced antimicrobial activity by using conformationally defined combinatorial libraries

Blondelle, S. E., Takahashi, E., Houghten, R. A., & Pérez‐Payá, E. (1996) · Biochemical Journal · doi:10.1042/bj3130141 · Cited by 54 · see citing works

Fungicidal properties, sterol binding, and proteolytic resistance of the synthetic peptide D4E1

Lucca, A. J. D., Bland, J. M., Grimm, C. C., Jacks, T. J., Cary, J. W., Jaynes, J. M., Cleveland, T. E., & Walsh, T. J. (1998) · Canadian Journal of Microbiology · doi:10.1139/w98-032 · Cited by 54 · see citing works

Antimicrobial properties of derivatives of the cationic tryptophan-rich hexapeptide PAF26

Muñoz, A., López‐García, B., Pérez‐Payá, E., & Marcos, J. F. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.12.173 · Cited by 54 · see citing works

An amphibian antimicrobial peptide variant expressed in Nicotiana tabacum confers resistance to phytopathogens

Ponti, D., Mangoni, M. L., Mignogna, G., Simmaco, M., & Barra, D. (2003) · Biochemical Journal · doi:10.1042/bj20021444 · Cited by 53 · see citing works

The production of synthetic chemodisruptive peptides in planta disrupts the establishment of cyst nematodes

Liu, B., Hibbard, J. K., Urwin, P. E., & Atkinson, H. J. (2005) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2005.00139.x · Cited by 52 · see citing works

Enhanced resistance to bacterial infection byErwinia carotovora subsp.atroseptica in transgenic potato plants expressing the attacin or the cecropin SB-37 genes

Arce‐Johnson, P., Moreno, M., Gutierrez, M., Gebauer, M., Dell’Orto, P., Torres, H., Acuña, I., Oliger, P., Venegas, A., Jordana, X., et al. (1999) · American Journal of Potato Research · doi:10.1007/bf02853582 · Cited by 51 · see citing works

The Antimicrobial Peptide Polyphemusin Localizes to the Cytoplasm of Escherichia coli following Treatment

Powers, J.-P. S., Martin, M. M., Goosney, D. L., & Hancock, R. E. W. (2006) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.50.4.1522-1524.2006 · Cited by 51 · see citing works

Erwinia soft rot resistance of potato cultivars expressing antimicrobial peptide tachyplesin I

Allefs, S. J. H. M., de Jong, E. R., Florack, D. E. A., Hoogendoorn, C., & Stiekema, W. J. (1996) · Molecular Breeding · doi:10.1007/bf00441425 · Cited by 50 · see citing works

Evidence for the breakdown of cecropin B by proteinases in the intercellular fluid of peach leaves

Mills, D., Hammerschlag, F. A., Nordeen, R. O., & Owens, L. D. (1994) · Plant Science · doi:10.1016/0168-9452(94)90186-4 · Cited by 50 · see citing works

Response of transgenic Royal Gala apple (Malus × domestica Borkh.) shoots carrying a modified cecropin MB39 gene, to Erwinia amylovora

Liu, Q., Ingersoll, J. C., Owens, L. D., Salih, S., Meng, R., & Hammerschlag, F. A. (2001) · Plant Cell Reports · doi:10.1007/s002990100333 · Cited by 50 · see citing works

Enhanced resistance to the poplar fungal pathogen, Septoria musiva, in hybrid poplar clones transformed with genes encoding antimicrobial peptides

Liang, H., Catranis, C. M., Maynard, C. A., & Powell, W. A. (2002) · Biotechnology Letters · doi:10.1023/a:1014552503140 · Cited by 48 · see citing works

Quest for antimicrobial genes to engineer disease-resistant crops

van der Biezen, E. A. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)01870-2 · Cited by 46 · see citing works

Partial Resistance to Bacterial Wilt in Transgenic Tomato Plants Expressing Antibacterial Lactoferrin Gene

Lee, T.-J., Coyne, D. P., Clemente, T. E., & Mitra, A. (2002) · Journal of the American Society for Horticultural Science · doi:10.21273/jashs.127.2.158 · Cited by 46 · see citing works

Comparison of pathogen‐induced expression and efficacy of two amphibian antimicrobial peptides, MsrA2 and temporin A, for engineering wide‐spectrum disease resistance in tobacco

Yevtushenko, D. P., & Misra, S. (2007) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2007.00277.x · Cited by 44 · see citing works

Structure and fungicidal activity of a synthetic antimicrobial peptide, P18, and its truncated peptides

Lee, D. G., Hahm, K., & Shin, S. Y. (2004) · Biotechnology Letters · doi:10.1023/b:bile.0000015472.09542.6d · Cited by 41 · see citing works

Effect of an antifungal peptide from oyster enzymatic hydrolysates for control of gray mold (Botrytis cinerea) on harvested strawberries

Liu, Z., Zeng, M., Dong, S., Xu, J., Song, H., & Zhao, Y. (2007) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2007.03.013 · Cited by 41 · see citing works

Role of the PhoP-PhoQ System in the Virulence of Erwinia chrysanthemi Strain 3937: Involvement in Sensitivity to Plant Antimicrobial Peptides, Survival at Acid pH, and Regulation of Pectolytic Enzymes

Llama‐Palacios, A., López‐Solanilla, E., & Rodríguez‐Palenzuela, P. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.6.2157-2162.2005 · Cited by 41 · see citing works

Comparative Study of Antimicrobial Peptides To Control Citrus Postharvest Decay Caused by Penicillium digitatum

Muñoz, A., López‐García, B., & Marcos, J. F. (2007) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf0718143 · Cited by 40 · see citing works

Recombinant expression of indolicidin concatamers in Escherichia coli

Morin, K. M., Arcidiacono, S. M., Beckwitt, R., & Mello, C. M. (2005) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-005-0132-5 · Cited by 37 · see citing works

Formation and Characterization of a Single Trp-Trp Cross-link in Indolicidin That Confers Protease Stability without Altering Antimicrobial Activity

Ősapay, K., Tran, D., Ladokhin, A. S., White, S. H., Henschen, A., & Selsted, M. E. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.16.12017 · Cited by 37 · see citing works

Structural Dissection of a Highly Knotted Peptide Reveals Minimal Motif with Antimicrobial Activity

Vila‐Perelló, M., Sánchez‐Vallet, A., García‐Olmedo, F., Molina, A., & Andreu, D. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m410577200 · Cited by 36 · see citing works

Phage-Displayed Peptides as Developmental Agonists for Phytophthora capsici Zoospores

Bishop‐Hurley, S. L., Mounter, S. A., Laskey, J. G., Morris, R. O., Elder, J., Roop, P., Rouse, C., Schmidt, F. J., & English, J. T. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.7.3315-3320.2002 · Cited by 35 · see citing works

Improving on Natures Defenses: Optimization & High Throughput Screening of Antimicrobial Peptides

Raventós, D., Taboureau, O., Mygind, P. H., Nielsen, J., Sönksen, C. P., & Kristensen, H. H. (2005) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/1386207053764549 · Cited by 35 · see citing works

Banana (Musa sp.)

Pérez, J. B., Remy, S., Swennen, R. L., & Sági, L. (2006) · Humana Press eBooks · doi:10.1385/1-59745-131-2:167 · Cited by 33 · see citing works

Construction of a novel synergistic system for production and recovery of secreted recombinant proteins by the cell surface engineering

Shibasaki, S., Kawabata, A., Ishii, J., Yagi, S., Kadonosono, T., Kato, M., 福田, 展., Kondo, A., & Ueda, M. (2007) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-007-0868-1 · Cited by 33 · see citing works

In vitro activities of antibiotics and antimicrobial peptides against the plant pathogenic bacterium Xylella fastidiosa

Kuzina, L. V., Miller, T. A., & Cooksey, D. A. (2006) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.2006.01898.x · Cited by 32 · see citing works

Neutral glycolipids of the filamentous fungus Neurospora crassa:altered expression in plant defensin-resistant mutants

Park, C., Bennion, B., François, I., Ferket, K. K. A., Cammue, B. P. A., Thevissen, K., & Levery, S. B. (2005) · Journal of Lipid Research · doi:10.1194/jlr.m400457-jlr200 · Cited by 30 · see citing works

Increased pathogen resistance and yield in transgenic plants expressing combinations of the modified antimicrobial peptides based on indolicidin and magainin

Xing, H., Lawrence, C. B., Chambers, O. D., Davies, H. M., Everett, N. P., & Li, Q. Q. (2005) · Planta · doi:10.1007/s00425-005-0143-6 · Cited by 30 · see citing works

Antiviral indolicidin variant peptides: Evaluation for broad-spectrum disease resistance in transgenic Nicotiana tabacum

Bhargava, A., Osusky, M., Hancock, R. E. W., Forward, B. S., Kay, W. W., & Misra, S. (2006) · Plant Science · doi:10.1016/j.plantsci.2006.10.016 · Cited by 29 · see citing works

In vitro toxicity of natural and designed peptides to tree pathogens and pollen

Jacobi, V., Plourde, A., Charest, P. J., & Hamelin, R. C. (2000) · Canadian Journal of Botany · doi:10.1139/cjb-78-4-455 · Cited by 28 · see citing works

Constitutive expression of human lactoferrin and its N-lobe in rice plants to confer disease resistance

Takase, K., Hagiwara, K., Onodera, H., Nishizawa, Y., Ugaki, M., Omura, T., Numata, S., Akutsu, K., Kumura, H., & Shimazaki, K. (2005) · Biochemistry and Cell Biology · doi:10.1139/o05-022 · Cited by 27 · see citing works

Independent and Synergistic Activity of Synthetic Peptides Against Thiabendazole-Resistant Fusarium sambucinum

Gonzalez, C. F., Provin, E. M., Zhu, L., & Ebbole, D. J. (2002) · Phytopathology · doi:10.1094/phyto.2002.92.8.917 · Cited by 27 · see citing works

Antibacterial Activity of Synthetic Peptides Against Plant Pathogenic Pectobacterium Species

Kamysz, W., Królicka, A., Bogucka, K., Ossowski, T., Łukasiak, J., & Łojkowska, E. (2005) · Journal of Phytopathology · doi:10.1111/j.1439-0434.2005.00976.x · Cited by 26 · see citing works

Combinatorially selected defense peptides protect plant roots from pathogen infection

Fang, Z., Laskey, J. G., Huang, S., Bilyeu, K., Morris, R. O., Schmidt, F. J., & English, J. T. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605542103 · Cited by 25 · see citing works

A Minimalist Design Approach to Antimicrobial Agents Based on a Thionin Template

Vila‐Perelló, M., Tognon, S., Sánchez‐Vallet, A., García‐Olmedo, F., Molina, A., & Andreu, D. (2005) · Journal of Medicinal Chemistry · doi:10.1021/jm050882i · Cited by 25 · see citing works

An integrated analysis of the effects of Esculentin 1–21 on Saccharomyces cerevisiae

Gamberi, T., Cavalieri, D., Magherini, F., Mangoni, M. L., Filippo, C. D., Borro, M., Gentile, G., Simmaco, M., & Modesti, A. (2007) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2007.04.006 · Cited by 23 · see citing works

Release of aqueous contents from phospholipid vesicles induced by cecropin A (1–8)‐magainin 2 (1–12) hybrid and its analogues

Kang, J. H., Shin, S. Y., Jang, S. Y., Lee, M. K., & Hahm, K. S. (1998) · Journal of Peptide Research · doi:10.1111/j.1399-3011.1998.tb00651.x · Cited by 22 · see citing works

Transgenic Paulownia Expressing shiva‐1 Gene Has Increased Resistance to Paulownia Witches' Broom Disease

Tao, D. U., Yao, W. A. N. G., Qin‐Xue, H. U., Chen, J., Liu, S., HUANG, W., & Mulan, L. (2005) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2005.00168.x · Cited by 22 · see citing works

Plant defense gene promoter enhances the reliability of shiva-1 gene-induced resistance to soft rot disease in potato

Yi, J.-Y., Seo, H. W., Yang, M., Robb, E. J., Nazar, R. N., & Lee, S. W. (2004) · Planta · doi:10.1007/s00425-004-1346-y · Cited by 22 · see citing works

Magainin 2 effects on the ultrastructure of five plant pathogens

Kristyanne, E. S., Kim, K. S., & Stewart, J. M. (1997) · Mycologia · doi:10.1080/00275514.1997.12026794 · Cited by 22 · see citing works

Expression of an Antimicrobial Peptide via the Chloroplast Genome to Control Phytopathogenic Bacteria and Fungi

DeGray, G. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.127.3.852 · Cited by 22 · see citing works

In silicoanalysis of antifungal peptides

Soltani, S., Keymanesh, K., & Sardari, S. (2007) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2.6.837 · Cited by 17 · see citing works

A tridecapeptide possesses both antimicrobial and protease-inhibitory activities

Li, Q. Q., Lawrence, C. B., Davies, H. M., & Everett, N. P. (2002) · Peptides · doi:10.1016/s0196-9781(01)00572-1 · Cited by 17 · see citing works

Expression of a polyphemusin variant in transgenic tobacco confers resistance against plant pathogenic bacteria, fungi and a virus

Bhargava, A., Osusky, M., Forward, B. S., Hancock, R. E. W., Kay, W. W., & Misra, S. (2007) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-007-9204-9 · Cited by 17 · see citing works

Structural changes of spores of tree fungal pathogens after treatment with the designed antimicrobial peptide D2A21

Rioux, D., Jacobi, V., Simard, M., & Hamelin, R. C. (2000) · Canadian Journal of Botany · doi:10.1139/b00-007 · Cited by 16 · see citing works

Transgenic Paulownia Expressing shiva-1 Gene Has Increased Resistance to Paulownia Witches＇ Broom Disease

Tao, T., Du, YAO, Y., Wang, Qin-Xue, Hu, Jie, J., Chen, C., Sheng, S., Liu, et al. (2005) · Journal of Integrative Plant Biology · Cited by 16 · see citing works

Magainin 2 Effects on the Ultrastructure of Five Plant Pathogens

Kristyanne, E. S., Kim, K. S., & Stewart, J. M. (1997) · Mycologia · doi:10.2307/3761029 · Cited by 16 · see citing works

The Interaction of Endochitinase, A Synthetic Peptide and Resveratrol in Controlling Fungi in vitro

Ali, G. S., Harman, G. E., & Reisch, B. I. (2003) · European Journal of Plant Pathology · doi:10.1023/a:1024797132744 · Cited by 15 · see citing works

Prosystemin-antimicrobial-peptide fusion reduces tomato late blight lesion expansion

Jones, R. W., Ospina-Giraldo, M. D., & Clemente, T. E. (2004) · Molecular Breeding · doi:10.1023/b:molb.0000038001.22029.07 · Cited by 15 · see citing works

Synthetic Combinatorial Libraries as an Alternative Strategy for the Development of Novel Treatments for Infectious Diseases

Blondelle, S. E., Pinilla, C., & Boggiano, C. (2003) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(03)69018-x · Cited by 14 · see citing works

Prospects for Combinatorial Chemistry in the Agrosciences

Lindell, S. D., & Scherkenbeck, J. (2005) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/138620705774575319 · Cited by 14 · see citing works

Modification of a Synthetic Antimicrobial Peptide (ESF1) for Improved Inhibitory Activity

Dykes, G. A., Aimoto, S., & Hastings, J. W. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.8940 · Cited by 13 · see citing works

Application of the “Codon-shuffling” Method

Rao, A., Chopra, S., Ram, G., Gupta, A., & Ranganathan, A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503056200 · Cited by 13 · see citing works

Sinorhizobium melilotigenes involved in tolerance to the antimicrobial peptide protamine

Nogales, J., Muñoz, S., Olivares, J., & Sanjuán, J. (2006) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2006.00445.x · Cited by 11 · see citing works

Identification of Cecropin A Proteolytic Cleavage Sites Resulting from Aspergillus flavus Extracellular Protease(s)

Bland, J. M., & Lucca, A. J. D. (1998) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf980638i · Cited by 8 · see citing works

Design and screening of in vivo expressed antimicrobial peptide library

Choi, K.-C., Kim, H., Park, Y., Park, S.-M., & Kim, J. (2002) · Biotechnology Letters · doi:10.1023/a:1014076426705 · Cited by 5 · see citing works

Structural changes of spores of tree fungal pathogens after treatment with the designed antimicrobial peptide D2A21

Rioux, D., Jacobi, V., Simard, M., et al. (2000) · Canadian Journal of Botany · doi:10.1139/cjb-78-4-462 · Cited by 5 · see citing works

Biofuels from algae: Challenges and potential

Hannon, M., Gimpel, J., Tran, M., Rasala, B., & Mayfield, S. (2010) · Biofuels · doi:10.4155/bfs.10.44 · Cited by 813 · see citing works

GRAS, plant- and animal-derived compounds as alternatives to conventional fungicides for the control of postharvest diseases of fresh horticultural produce

Palou, L., Ali, A., Fallik, E., & Romanazzi, G. (2016) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2016.04.017 · Cited by 286 · see citing works

Antimicrobial peptides and bacteriocins: alternatives to traditional antibiotics

Sang, Y., & Blecha, F. (2008) · Animal Health Research Reviews · doi:10.1017/s1466252308001497 · Cited by 253 · see citing works

Protease Inhibitors from Plants with Antimicrobial Activity

Kim, J. Y., Park, S., Hwang, I., Cheong, H., Nah, J., Hahm, K., & Park, Y. (2009) · International Journal of Molecular Sciences · doi:10.3390/ijms10062860 · Cited by 243 · see citing works

Biotechnological advances for combating Aspergillus flavus and aflatoxin contamination in crops

Bhatnagar‐Mathur, P., Sunkara, S., Bhatnagar-Panwar, M., Waliyar, F., & Sharma, K. K. (2015) · Plant Science · doi:10.1016/j.plantsci.2015.02.009 · Cited by 200 · see citing works

Application of antimicrobial peptides in agriculture and food industry

Keymanesh, K., Soltani, S., & Sardari, S. (2009) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-009-9984-7 · Cited by 162 · see citing works

Trichoderma/pathogen/plant interaction in pre-harvest food security

Silva, R. N., Monteiro, V. N., Steindorff, A. S., Gomes, E. V., Noronha, E. F., & Ulhôa, C. J. (2019) · Fungal Biology · doi:10.1016/j.funbio.2019.06.010 · Cited by 120 · see citing works

Multitasking antimicrobial peptides in plant development and host defense against biotic/abiotic stress

Goyal, R. K., & Mattoo, A. K. (2014) · Plant Science · doi:10.1016/j.plantsci.2014.05.012 · Cited by 112 · see citing works

Biotechnological concepts for improving plant innate immunity

Gust, A. A., Brunner, F., & Nürnberger, T. (2010) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2010.02.004 · Cited by 108 · see citing works

Antimicrobial peptides

Rahnamaeian, M. (2011) · Plant Signaling & Behavior · doi:10.4161/psb.6.9.16319 · Cited by 96 · see citing works

Antimicrobial peptides: to membranes and beyond

Marcos, J. F., & Gandía, M. (2009) · Expert Opinion on Drug Discovery · doi:10.1517/17460440902992888 · Cited by 95 · see citing works

Backbone dynamics of the antifungal Psd1 pea defensin and its correlation with membrane interaction by NMR spectroscopy

de Medeiros, L. N., Angeli, R., Sarzedas, C. G., Barreto‐Bergter, E., Valente, A. P., Kurtenbach, E., & Almeida, F. C. L. (2009) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2009.07.013 · Cited by 94 · see citing works

Review on PLGA Polymer Based Nanoparticles with Antimicrobial Properties and Their Application in Various Medical Conditions or Infections

Shakya, A. K., Al-Sulaibi, M., Naik, R. R., Nsairat, H., Suboh, S., & Abulaila, A. (2023) · Polymers · doi:10.3390/polym15173597 · Cited by 88 · see citing works

Three Antifungal Proteins From Penicillium expansum: Different Patterns of Production and Antifungal Activity

Garrigues, S., Gandía, M., Castillo, L., Coca, M. A., Marx, F., Marcos, J. F., & Manzanares, P. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02370 · Cited by 87 · see citing works

Rational design of a ligand-based antagonist of jasmonate perception

Monte, I., Hámberg, M., Chini, A., Ibanez, S. G., García‐Casado, G., Porzel, A., Pazos, F., Botër, M., & Solano, R. (2014) · Nature Chemical Biology · doi:10.1038/nchembio.1575 · Cited by 84 · see citing works

Insect peptide metchnikowin confers on barley a selective capacity for resistance to fungal ascomycetes pathogens

Rahnamaeian, M., Langen, G., Imani, J., Khalifa, W., Altincicek, B., von WETTSTEIN, D., Kogel, K., & Vilcinskas, A. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp240 · Cited by 79 · see citing works

Antimicrobial random peptide cocktails: a new approach to fight pathogenic bacteria

Amso, Z., & Hayouka, Z. (2019) · Chemical Communications · doi:10.1039/c8cc09961h · Cited by 74 · see citing works

Improving Health-Promoting Effects of Food-Derived Bioactive Peptides through Rational Design and Oral Delivery Strategies

Manzanares, P., Gandía, M., Garrigues, S., & Marcos, J. F. (2019) · Nutrients · doi:10.3390/nu11102545 · Cited by 72 · see citing works

Production of cecropin A antimicrobial peptide in rice seed endosperm

Bundó, M., Montesinos, L., Izquierdo, E., Campo, S., Mieulet, D., Guiderdoni, E., Rossignol, M., Badosa, E., Montesinos, E., San Segundo, B., et al. (2014) · BMC Plant Biology · doi:10.1186/1471-2229-14-102 · Cited by 70 · see citing works

Developing Resistance to Aflatoxin in Maize and Cottonseed

Cary, J. W., Rajasekaran, K., Brown, R. L., Luo, M., Chen, Z.-Y., & Bhatnagar, D. (2011) · Toxins · doi:10.3390/toxins3060678 · Cited by 68 · see citing works

Sporicidal Activity of Synthetic Antifungal Undecapeptides and Control of <i>Penicillium</i> Rot of Apples

Badosa, E., Ferré, R., Francés, J., Bardají, E., Feliu, L., Planas, M., & Montesinos, E. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.00711-09 · Cited by 67 · see citing works

De-Novo Design of Antimicrobial Peptides for Plant Protection

Zeitler, B., Díaz, A. H., Dangel, A., Thellmann, M., Meyer, H., Sattler, M., & Lindermayr, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071687 · Cited by 66 · see citing works

Antimicrobial activity of a new synthetic peptide loaded in polylactic acid or poly(lactic-co-glycolic) acid nanoparticles against Pseudomonas aeruginosa , Escherichia coli O157:H7 and methicillin resistant Staphylococcus aureus (MRSA)

Cruz, J., Flórez, J., Torres, R. G., Urquiza, M., Gutiérrez, J. A., Guzmán, F., & Ortiz, C. C. (2017) · Nanotechnology · doi:10.1088/1361-6528/aa5f63 · Cited by 64 · see citing works

Improvement of the Efficacy of Linear Undecapeptides against Plant-Pathogenic Bacteria by Incorporation of d -Amino Acids

Güell, I., Cabrefiga, J., Badosa, E., Ferré, R., Talleda, M., Bardajı́, E., Planas, M., Feliu, L., & Montesinos, E. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.02759-10 · Cited by 61 · see citing works

Efficient Screening of a Novel Antimicrobial Peptide from Jatropha curcas by Cell Membrane Affinity Chromatography

Xiao, J., Zhang, H., Niu, L., & Wang, X. (2011) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf103876b · Cited by 61 · see citing works

Occurrence and function of fungal antifungal proteins: a case study of the citrus postharvest pathogen Penicillium digitatum

Garrigues, S., Gandía, M., & Marcos, J. F. (2015) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-015-7110-3 · Cited by 61 · see citing works

Antifungal Peptides and Proteins to Control Toxigenic Fungi and Mycotoxin Biosynthesis

Martínez‐Culebras, P. V., Gandía, M., Garrigues, S., Marcos, J. F., & Manzanares, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413261 · Cited by 60 · see citing works

Constitutive expression of transgenes encoding derivatives of the synthetic antimicrobial peptide BP100: impact on rice host plant fitness

Nadal, A., Montero, M., Badosa, E., Messeguer, J., Montesinos, L., Montesinos, E., & Pla, M. (2012) · BMC Plant Biology · doi:10.1186/1471-2229-12-159 · Cited by 58 · see citing works

Derivatives of the Antimicrobial Peptide BP100 for Expression in Plant Systems

Badosa, E., Moiset, G., Montesinos, L., Talleda, M., Bardajı́, E., Feliu, L., Planas, M., & Montesinos, E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0085515 · Cited by 58 · see citing works

Concentration‐dependent mechanisms of cell penetration and killing by the de novo designed antifungal hexapeptide PAF26

Muñoz, A., Marcos, J., & Read, N. (2012) · Molecular Microbiology · doi:10.1111/j.1365-2958.2012.08091.x · Cited by 62 · see citing works

Inactivation effects of plasma-activated water on Fusarium graminearum

Guo, J., Wang, J., Xie, H., Jiang, J., Li, C., Li, W., Li, L., Liu, X., & Lin, F. (2021) · Food Control · doi:10.1016/j.foodcont.2021.108683 · Cited by 57 · see citing works

Transgenic expression of lactoferrin imparts enhanced resistance to head blight of wheat caused by Fusarium graminearum

Han, J., Lakshman, D. K., Galvez, L. C., Mitra, S., Baenziger, P. S., & Mitra, A. (2012) · BMC Plant Biology · doi:10.1186/1471-2229-12-33 · Cited by 57 · see citing works

Site-specific cleavage of bacterial MucD by secreted proteases mediates antibacterial resistance in Arabidopsis

Wang, Y., Garrido‐Oter, R., Wu, J., Winkelmüller, T. M., Agler, M. T., Colby, T., Nobori, T., Kemen, E. M., & Tsuda, K. (2019) · Nature Communications · doi:10.1038/s41467-019-10793-x · Cited by 57 · see citing works

The <i> <scp>P</scp> enicillium digitatum </i> protein <i> <scp>O</scp> </i> ‐mannosyltransferase <scp>P</scp> mt2 is required for cell wall integrity, conidiogenesis, virulence and sensitivity to the antifungal peptide <scp>PAF26</scp>

Harries, E., Gandía, M., Carmona, L., & Marcos, J. F. (2015) · Molecular Plant Pathology · doi:10.1111/mpp.12232 · Cited by 56 · see citing works

Understanding the mechanism of action of cell-penetrating antifungal peptides using the rationally designed hexapeptide PAF26 as a model

Muñoz, A., Gandía, M., Harries, E., Carmona, L., Read, N. D., & Marcos, J. F. (2012) · Fungal Biology Reviews · doi:10.1016/j.fbr.2012.10.003 · Cited by 56 · see citing works

Identification and Design of Antimicrobial Peptides for Therapeutic Applications

Ahmad, A., Ahmad, E., Rabbani, G., Haque, S., Arshad, M., & Khan, R. H. (2012) · Current Protein and Peptide Science · doi:10.2174/138920312800785076 · Cited by 54 · see citing works

Control of sour rot in citrus fruit by three insect antimicrobial peptides

Liu, S., Wang, W., Deng, L., Ming, J., Yao, S., & Zeng, K. (2018) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2018.11.025 · Cited by 54 · see citing works

The Neutrally Charged Diarylurea Compound PQ401 Kills Antibiotic-Resistant and Antibiotic-Tolerant Staphylococcus aureus

Kim, W., Zou, G., Pan, W., Fricke, N., Faizi, H. A., Kim, S. M., Khader, R., Li, S., Lee, K., Escorba, I., et al. (2020) · mBio · doi:10.1128/mbio.01140-20 · Cited by 52 · see citing works

Functional Peptides for Plant Disease Control

Montesinos, E. (2023) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-021722-034312 · Cited by 53 · see citing works

Application of antimicrobial peptides in plant protection: making use of the overlooked merits

Tang, R., Tan, H. M., Dai, Y., Li, L., Huang, Y., Yao, H., Cai, Y., & Yu, G. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1139539 · Cited by 50 · see citing works

The myosin motor domain-containing chitin synthase PdChsVII is required for development, cell wall integrity and virulence in the citrus postharvest pathogen Penicillium digitatum

Gandía, M., Harries, E., & Marcos, J. F. (2014) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2014.04.002 · Cited by 48 · see citing works

The development of antimicrobial peptides as an approach to prevention of antibiotic resistance

Moghaddam, M. M., Aghamollaei, H., Kooshki, H., Barjini, K. A., Mirnejad, R., & Choopani, A. (2015) · Reviews in Medical Microbiology · doi:10.1097/mrm.0000000000000032 · Cited by 48 · see citing works

A perspective on general direction and challenges facing antimicrobial peptides

Zhu, M., Liu, P., & Niu, Z. (2016) · Chinese Chemical Letters · doi:10.1016/j.cclet.2016.10.001 · Cited by 47 · see citing works

Acquired resistance to the rice blast in transgenic rice accumulating the antimicrobial peptide thanatin

Imamura, T., Yasuda, M., Kusano, H., Nakashita, H., Ohno, Y., Kamakura, T., Taguchi, S., & Shimada, H. (2009) · Transgenic Research · doi:10.1007/s11248-009-9320-x · Cited by 46 · see citing works

Screening Antimicrobial Peptides In Vitro for Use in Developing Transgenic Citrus Resistant to Huanglongbing and Citrus Canker

Stover, E. W., Stange, R. R., McCollum, T. G., Jaynes, J. M., Irey, M. S., & Mirkov, E. (2013) · Journal of the American Society for Horticultural Science · doi:10.21273/jashs.138.2.142 · Cited by 46 · see citing works

Integrating Genomics and Metabolomics for the Targeted Discovery of New Cyclopeptides with Antifungal Activity from a Marine-Derived Fungus Beauveria felina

Jiang, M., Chen, S., Lu, X., Guo, H., Chen, S., Yin, X., Li, H., Dai, G., & Liu, L. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c02415 · Cited by 44 · see citing works

Antifungal Activity of Cyclic Tetrapeptide from Bacillus velezensis CE 100 against Plant Pathogen Colletotrichum gloeosporioides

Choub, V., Maung, C. E. H., Won, S., Moon, J., Kim, K. Y., Han, Y. S., Cho, J., & Ahn, Y. S. (2021) · Pathogens · doi:10.3390/pathogens10020209 · Cited by 44 · see citing works

Synthetic Ultrashort Cationic Lipopeptides Induce Systemic Plant Defense Responses against Bacterial and Fungal Pathogens

Brotman, Y., Makovitzki, A., Shai, Y., Chet, I., & Viterbo, A. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.00724-09 · Cited by 43 · see citing works

Expression of a recombinant hybrid antimicrobial peptide magainin II-cecropin B in the mycelium of the medicinal fungus Cordyceps militaris and its validation in mice

Zhang, M., Shan, Y., Gao, H., Wang, B., Liu, X., Dong, Y., Liu, X., Yao, N., Zhou, Y., Li, X., et al. (2018) · Microbial Cell Factories · doi:10.1186/s12934-018-0865-3 · Cited by 42 · see citing works

Antimicrobial Peptides as a Promising Alternative for Plant Disease Protection

López‐García, B., Segundo, B. S., & Coca, M. A. (2012) · ACS symposium series · doi:10.1021/bk-2012-1095.ch013 · Cited by 41 · see citing works

Two Functional Motifs Define the Interaction, Internalization and Toxicity of the Cell-Penetrating Antifungal Peptide PAF26 on Fungal Cells

Muñoz, A., Harries, E., Valenzuela, A. C., Carmona, L., Read, N. D., & Marcos, J. F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054813 · Cited by 41 · see citing works

Biotic stress resistance in agriculture through antimicrobial peptides

Sarika, S., Iquebal, M. A., & Rai, A. K. (2012) · Peptides · doi:10.1016/j.peptides.2012.05.012 · Cited by 41 · see citing works

Random peptide mixtures as new crop protection agents

Topman‐Rakover, S., Tamir‐Ariel, D., Bochnic‐Tamir, H., Bauer, T. S., Shafir, S., Burdman, S., & Hayouka, Z. (2018) · Microbial Biotechnology · doi:10.1111/1751-7915.13258 · Cited by 41 · see citing works

Candidate Gene Networks for Acylsugar Metabolism and Plant Defense in Wild Tomato Solanum pennellii

Mandal, S., Ji, W., & McKnight, T. D. (2019) · The Plant Cell · doi:10.1105/tpc.19.00552 · Cited by 41 · see citing works

Potential of Antifungal Proteins (AFPs) to Control Penicillium Postharvest Fruit Decay

Gandía, M., Kakar, A., Giner‐Llorca, M., Holzknecht, J., Martínez‐Culebras, P. V., Galgóczy, L., Marx, F., Marcos, J. F., & Manzanares, P. (2021) · Journal of Fungi · doi:10.3390/jof7060449 · Cited by 41 · see citing works

Synthetic dual hormone-responsive promoters enable engineering of plants with broad-spectrum resistance

Li, X., Niu, G., Fan, Y., Liu, W., Wu, Q., Chen, Y. X., Wang, J., Xiao, Y., Hou, L., Jin, D., et al. (2023) · Plant Communications · doi:10.1016/j.xplc.2023.100596 · Cited by 40 · see citing works

A structural perspective of plant antimicrobial peptides

Campos, M. L., Lião, L. M., Alves, E. S. F., Migliolo, L., Dias, S. C., & Franco, O. L. (2018) · Biochemical Journal · doi:10.1042/bcj20180213 · Cited by 39 · see citing works

A genomic approach highlights common and diverse effects and determinants of susceptibility on the yeast Saccharomyces cerevisiae exposed to distinct antimicrobial peptides

López‐García, B., Gandía, M., Muñoz, A., Carmona, L., & Marcos, J. F. (2010) · BMC Microbiology · doi:10.1186/1471-2180-10-289 · Cited by 39 · see citing works

Antimicrobial Peptides for Plant Disease Control. From Discovery to Application

Montesinos, E., Badosa, E., Cabrefiga, J., Planas, M., Feliu, L., & Bardajı́, E. (2012) · ACS symposium series · doi:10.1021/bk-2012-1095.ch012 · Cited by 38 · see citing works

New Recombinant Antimicrobial Peptides Confer Resistance to Fungal Pathogens in Tobacco Plants

Khademi, M., Varasteh-Shams, M., Firouzabadi, F. N., & Ismaili, A. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.01236 · Cited by 38 · see citing works

Targeting of anti-microbial proteins to the hyphal surface amplifies protection of crop plants against Phytophthora pathogens

Zhou, Y., Yang, K., Yan, Q., Wang, X., Cheng, M., Si, J., Xue, X., Shen, D., Jing, M., Tyler, B. M., et al. (2021) · Molecular Plant · doi:10.1016/j.molp.2021.05.007 · Cited by 38 · see citing works

Investigating the effects of L- to D-amino acid substitution and deamidation on the activity and membrane interactions of antimicrobial peptide anoplin

Won, A. M., Khan, M., Gustin, S., Akpawu, A., Seebun, D., Avis, T. J., Leung, B. O., Hitchcock, A. P., & Ianoul, A. I. (2010) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2010.11.010 · Cited by 37 · see citing works

Design of a Helical-Stabilized, Cyclic, and Nontoxic Analogue of the Peptide Cm-p5 with Improved Antifungal Activity

Morales-Vicente, F., González-García, M., Pico, E. D., Castillo, E. M., Garay, H., Rosi, P. E., Jimenez, A. M., Delgado, J. A. C., Rivera, D. G., Chinea, G., et al. (2019) · ACS Omega · doi:10.1021/acsomega.9b02201 · Cited by 36 · see citing works

From Design to Screening: A New Antimicrobial Peptide Discovery Pipeline

Guralp, S. A., Murgha, Y. E., Rouillard, J. M., & Gülari, E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059305 · Cited by 35 · see citing works

Antimicrobial genes from Allium sativum and Pinellia ternata revealed by a Bacillus subtilis expression system

Kong, X., Yang, M., Abbas, H. M. K., Wu, J., Li, M., & Dong, W. (2018) · Scientific Reports · doi:10.1038/s41598-018-32852-x · Cited by 35 · see citing works

A novel antimicrobial protein for plant protection consisting of a Xanthomonas oryzae harpin and active domains of cecropin A and melittin

Che, Y., Li, Y., Zou, H., Zou, L., Zhang, B., & Chen, G. (2011) · Microbial Biotechnology · doi:10.1111/j.1751-7915.2011.00281.x · Cited by 35 · see citing works

Distinct profiling of antimicrobial peptide families

Khamis, A. M., Essack, M., Gao, X., & Bajić, V. B. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu738 · Cited by 34 · see citing works

Production of Biologically Active Cecropin A Peptide in Rice Seed Oil Bodies

Montesinos, L., Bundó, M., Izquierdo, E., Campo, S., Badosa, E., Rossignol, M., Montesinos, E., Segundo, B. S., & Coca, M. A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146919 · Cited by 34 · see citing works

Biotechnological Production of the Cell Penetrating Antifungal PAF102 Peptide in Pichia pastoris

Popa, C., Shi, X., Ruiz, T., Ferrer, P., & Coca, M. A. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01472 · Cited by 34 · see citing works

Mapping and Identification of Antifungal Peptides in the Putative Antifungal Protein AfpB from the Filamentous Fungus Penicillium digitatum

Garrigues, S., Gandía, M., Borics, A., Marx, F., Manzanares, P., & Marcos, J. F. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00592 · Cited by 32 · see citing works

Production of the biotechnologically relevant AFP from Aspergillus giganteus in the yeast Pichia pastoris

López‐García, B., Moreno, A. B., Segundo, B. S., Rı́os, V. D. L., Manning, J. M., Gavilanes, J. G., & Martínez‐del‐Pozo, Á. (2009) · Protein Expression and Purification · doi:10.1016/j.pep.2009.11.002 · Cited by 32 · see citing works

New proteins orthologous to cerato-platanin in various Ceratocystis species and the purification and characterization of cerato-populin from Ceratocystis populicola

Comparini, C., Carresi, L., Pagni, E., Sbrana, F., Sebastiani, F., Luchi, N., Santini, A., Capretti, P., Tiribilli, B., Pazzagli, L., et al. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-009-1998-4 · Cited by 36 · see citing works

Production of BP178, a derivative of the synthetic antibacterial peptide BP100, in the rice seed endosperm

Montesinos, L., Bundó, M., Badosa, E., Segundo, B. S., Coca, M. A., & Montesinos, E. (2017) · BMC Plant Biology · doi:10.1186/s12870-017-1011-9 · Cited by 31 · see citing works

Killer Peptide: A Novel Paradigm of Antimicrobial, Antiviral and Immunomodulatory Auto-Delivering Drugs

Magliani, W., Conti, S., Ciociola, T., Giovati, L., Zanello, P. P., Pertinhez, T. A., Spisni, A., & Polonelli, L. (2011) · Future Medicinal Chemistry · doi:10.4155/fmc.11.71 · Cited by 31 · see citing works

Antimicrobial peptide isolated from Bacillus amyloliquefaciens K14 revitalizes its use in combinatorial drug therapy

Regmi, S., Choi, Y., Choi, Y. S., Kim, M. R., & Yoo, J. C. (2016) · Folia Microbiologica · doi:10.1007/s12223-016-0479-2 · Cited by 30 · see citing works

The production of recombinant cationic α‐helical antimicrobial peptides in plant cells induces the formation of protein bodies derived from the endoplasmic reticulum

Nadal, A., Paz, J.-L. L., Martínez, S., Rasche, S., Schillberg, S., Montesinos, E., & Pla, M. (2013) · Plant Biotechnology Journal · doi:10.1111/pbi.12119 · Cited by 30 · see citing works

Differential roles, crosstalk and response to the Antifungal Protein AfpB in the three Mitogen-Activated Protein Kinases (MAPK) pathways of the citrus postharvest pathogen Penicillium digitatum

Gandía, M., Garrigues, S., Hernanz-Koers, M., Manzanares, P., & Marcos, J. F. (2018) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2018.12.006 · Cited by 30 · see citing works

ARACINs, Brassicaceae-Specific Peptides Exhibiting Antifungal Activities against Necrotrophic Pathogens in Arabidopsis

Neukermans, J., Inzé, A., Mathys, J., Coninck, B. D., van de Cotte, B., Cammue, B. P. A., & Breusegem, F. V. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.255505 · Cited by 28 · see citing works

Lysozyme enhances the bactericidal effect of BP100 peptide against Erwinia amylovora, the causal agent of fire blight of rosaceous plants

Cabrefiga, J., & Montesinos, E. (2017) · BMC Microbiology · doi:10.1186/s12866-017-0957-y · Cited by 28 · see citing works

Control of Aspergillus flavus growth and aflatoxin production in transgenic maize kernels expressing a tachyplesin-derived synthetic peptide, AGM182

Rajasekaran, K., Sayler, R. J., Sickler, C. M., Majumdar, R., Jaynes, J. M., & Cary, J. W. (2018) · Plant Science · doi:10.1016/j.plantsci.2018.02.006 · Cited by 28 · see citing works

Constitutive expression of human lactoferrin and its N-lobe in rice plants to confer disease resistance

Takase, K., Hagiwara, K., Onodera, H., Nishizawa, Y., Ugaki, M., Omura, T., Numata, S., Akutsu, K., Kumura, H., & Shimazaki, K. (2005) · Biochemistry and Cell Biology · doi:10.1139/o05-022 · Cited by 27 · see citing works

Peptidotriazoles with antimicrobial activity against bacterial and fungal plant pathogens

Güell, I., Micaló, L., Cano, L., Badosa, E., Ferré, R., Montesinos, E., Bardajı́, E., Feliu, L., & Planas, M. (2011) · Peptides · doi:10.1016/j.peptides.2011.12.003 · Cited by 27 · see citing works

The Myosin Motor Domain-Containing Chitin Synthases Are Involved in Cell Wall Integrity and Sensitivity to Antifungal Proteins in Penicillium digitatum

Gandía, M., Garrigues, S., Bolós, B., Manzanares, P., & Marcos, J. F. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02400 · Cited by 26 · see citing works

Recombinant production of antimicrobial peptides in plants

Firouzabadi, F. N., Torres, M. D. T., & de la Fuente‐Núñez, C. (2023) · Biotechnology Advances · doi:10.1016/j.biotechadv.2023.108296 · Cited by 26 · see citing works

Concatemerization increases the inhibitory activity of short, cell-penetrating, cationic and tryptophan-rich antifungal peptides

López‐García, B., Harries, E., Carmona, L., Campos‐Soriano, L., López, J. J., Manzanares, P., Gandía, M., Coca, M. A., & Marcos, J. F. (2015) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-015-6541-1 · Cited by 25 · see citing works

Membrane-active peptides as anti-infectious agents

Rivas, L., Luque-Ortega, J. R., Fernández‐Reyes, M., & Andreu, D. (2010) · Journal of Applied Biomedicine · doi:10.2478/v10136-009-0019-3 · Cited by 24 · see citing works

Lactoferrin-Derived Resistance against Plant Pathogens in Transgenic Plants

Lakshman, D. K., Natarajan, S. S., Mandal, S., & Mitra, A. (2013) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf400756t · Cited by 25 · see citing works

De Novo Cyclic Pseudopeptides Containing Aza-β3-amino Acids Exhibiting Antimicrobial Activities

Laurencin, M., Mosbah, A., Fleury, Y., & Baudy-Floc’h, M. (2012) · Journal of Medicinal Chemistry · doi:10.1021/jm3009037 · Cited by 25 · see citing works

First report of antifungal activity conferred by non‐conventional peptides

Tian, L., Chen, X., Jia, X., Wang, S., Wang, X., Zhang, J., Zhang, Y., Wu, S., Chen, Y., & Wu, L. (2021) · Plant Biotechnology Journal · doi:10.1111/pbi.13691 · Cited by 24 · see citing works

Transient expression and characterization of the antimicrobial peptide protegrin-1 in Nicotiana tabacum for control of bacterial and fungal mammalian pathogens

Patiño-Rodríguez, O., Ortega-Berlanga, B., Llamas-González, Y. Y., Flores‐Valdez, M. A., Herrera‐Díaz, A., Montes‐de‐Oca‐Luna, R., Korban, S. S., & Alpuche-Solis, A. G. (2013) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-013-0344-9 · Cited by 24 · see citing works

Novel antimicrobial peptides identified from an endoparasitic wasp cDNA library

Shen, X., Yè, G., Cheng, X., Yu, C., Yao, H., & Hu, C. (2009) · Journal of Peptide Science · doi:10.1002/psc.1195 · Cited by 24 · see citing works

Sensitivity of Saccharomyces cerevisiae to the cell-penetrating antifungal peptide PAF26 correlates with endogenous nitric oxide (NO) production

Carmona, L., Gandía, M., López‐García, B., & Marcos, J. F. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.11.050 · Cited by 24 · see citing works

Antimicrobial peptide KSL-W and analogues: Promising agents to control plant diseases

Camó, C., Bonaterra, A., Badosa, E., Baró, A., Montesinos, L., Montesinos, E., Planas, M., & Feliu, L. (2018) · Peptides · doi:10.1016/j.peptides.2018.11.009 · Cited by 24 · see citing works

Effects of the peptide H-OOWW-NH2 and its derived lipopeptide C12-OOWW-NH2 on controlling of citrus postharvest green mold

Li, X., Wang, W., Liu, S., Ruan, C., Yi, L., Deng, L., Yao, S., & Zeng, K. (2019) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2019.110979 · Cited by 23 · see citing works

Fighting pathogenic yeasts with plant defensins and anti-fungal proteins from fungi

Manzanares, P., Giner‐Llorca, M., Marcos, J. F., & Garrigues, S. (2024) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-024-13118-1 · Cited by 24 · see citing works

Identification and Functional Characterization of a Novel Insecticidal Decapeptide from the Myrmicine Ant Manica rubida

Heep, J., Škaljac, M., Grotmann, J., Kessel, T., Seip, M., Schmidtberg, H., & Vilcinskas, A. (2019) · Toxins · doi:10.3390/toxins11100562 · Cited by 24 · see citing works

Ergosterol‐targeting fusion antifungal peptide significantly increases the Verticillium wilt resistance of cotton

Tong, S., Yuan, M., Liu, Y., Li, X., Jin, D., Cheng, X., Lin, D., Ling, H., Yang, D., Wang, Y., et al. (2020) · Plant Biotechnology Journal · doi:10.1111/pbi.13517 · Cited by 22 · see citing works

Novel insights in the production, activity and protective effect of Penicillium expansum antifungal proteins

Gandía, M., Monge, A., Garrigues, S., Orozco, H., Giner‐Llorca, M., Marcos, J. F., & Manzanares, P. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.08.208 · Cited by 21 · see citing works

Production of a Recombinant Dermaseptin Peptide in Nicotiana tabacum Hairy Roots with Enhanced Antimicrobial Activity

Varasteh-Shams, M., Firouzabadi, F. N., Ismaili, A., & Shirzadian-Khorramabad, R. (2019) · Molecular Biotechnology · doi:10.1007/s12033-019-00153-x · Cited by 21 · see citing works

Prospects for synthetic biology in 21st century agriculture

Ye, X., Qin, K., Fernie, A. R., & Zhang, Y. (2024) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2024.12.016 · Cited by 22 · see citing works

Identification and rational design of novel antimicrobial peptides for plant protection, Annu

Muñoz, A., Pérez-payá, E., Investigación, C., Felipe, P., Profile, S., Misra, S., López‐García, B., Profile, S., Protection, P. F. P., Marcos, J. F., et al. (2016)

De-Novo Design of Antimicrobial Peptides for Plant Protection

Zeitler, B., Díaz, A. H., Dangel, A., Thellmann, M., Meyer, H., Sattler, M., & Lindermayr, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071687 · Cited by 66 · see citing works

Design of Antifungal Peptides for Agricultural Applications

Everett, N. P. (1993) · ACS symposium series · doi:10.1021/bk-1994-0551.ch020 · Cited by 17 · see citing works

De Novo Design of Antimicrobial Peptides With a Special Charge Pattern and Their Application in Combating Plant Pathogens

Chen, E. H. L., Weng, C., Li, Y., Wu, M.-C., Yang, C., Lee, K., Chen, R. P. ‐., & Cheng, C. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.753217 · Cited by 18 · see citing works

Harnessing Plant Antimicrobial Peptides for Crop Protection: From Molecular Defence Mechanisms to Peptide Engineering and Field Applications

Nwankwo, C. T., Alhaji, A. I., Abdulsalami, M. S., Haroun, A. A., Egbe, N. E., Oyong, A. I., & Okorie, J. M. (2026) · doi:10.9734/ajbge/2026/v9i2191