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Purification, Characterization, and Sequencing of a Novel Type of Antimicrobial Peptides,<i>Fa</i>-AMP1 and<i>Fa</i>-AMP2, from Seeds of Buckwheat (<i>Fagopyrum esculentum</i>Moench.)
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Citations
22
References
2003
Year
Bioorganic ChemistryPeptide EngineeringGlycobiologyAntimicrobial PeptidesNovel Antimicrobial PeptidesPeptide SciencePeptide TherapeuticsBioanalysisBasic PeptidesAntimicrobial ResistanceAntimicrobial Drug DiscoveryNovel TypeBiochemistryAntimicrobial CompoundNatural SciencesPeptide LibraryPeptide TherapeuticPeptide SynthesisProtein EngineeringMicrobiologyMedicine
Novel antimicrobial peptides (AMP), designated Fa-AMP1 and Fa-AMP2, were purified from the seeds of buckwheat (Fagopyrum esculentum Moench.) by gel filtration on Sephadex G75, ion-exchange HPLC on SP COSMOGEL, and reverse-phase HPLC. They were basic peptides having isoelectric points of over 10. Fa-AMP1 and Fa-AMP2 had molecular masses of 3,879 Da and 3,906 Da on MALDI-TOF MS analysis, and their extinction coefficients in 1% aqueous solutions at 280 nm were 42.8 and 38.9, respectively. Half of all amino acid residues of Fa-AMP1 and Fa-AMP2 were cysteine and glycine, and they had continuous sequences of cysteine and glycine. The concentrations of peptides required for 50% inhibition (IC50) of the growth of plant pathogenic fungi, and Gram-positive and -negative bacteria were 11 to 36 microg/ml. The structural and antimicrobial characteristics of Fa-AMPs indicated that they are a novel type of antimicrobial peptides belonging to a plant defensin family.
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