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114 L.A. ShcherbakovaTable 5.1. Cont<strong>in</strong>ued.Targeted<strong>plant</strong> pathogens Group of effective AMPM ReferenceSphaerotheca sp. Pseudopeptides Ste<strong>in</strong>, 2005Unc<strong>in</strong>ula nector Pseudopeptides Ste<strong>in</strong>, 2005Ventura <strong>in</strong>aequalis Cyclopeptides Burr et al., 1996Phytophthora <strong>in</strong>festans Cyclopeptides De Bruijn et al., 2007Pythium <strong>in</strong>termedium Cyclopeptides De Souza et al., 2003Pythium ultimum Cyclopeptides Nielsen et al., 2002BacteriaErw<strong>in</strong>ia amylovora Pseudopeptides Brady et al., 1999J<strong>in</strong> et al., 2003Erw<strong>in</strong>ia caratovora Cyclopeptides Selim, 2005Clavibacter michiganesis Peptaibols Xiao-Yan et al., 2006Pseudomonas syr<strong>in</strong>gae Cyclopeptides Bais et al., 2004Rhodococcus fascians Cyclopeptides Bassarello et al., 2004Antimicrobial peptides from <strong>plant</strong>sA broad family compris<strong>in</strong>g antimicrobial peptides produced by <strong>plant</strong>s iscalled defens<strong>in</strong>s. One of their functions <strong>in</strong> <strong>plant</strong>s is the <strong>in</strong>volvement <strong>in</strong> defencemechanisms aga<strong>in</strong>st pathogens, <strong>pest</strong>s and abiotic stresses (Terras et al., 1995;Lay and Anderson, 2005). These are basic peptides structurally and functionallyrelated to the defens<strong>in</strong>s of mammalia and <strong>in</strong>sects. Molecular masses of<strong>plant</strong> defens<strong>in</strong>s that are characterized at present range from 5 to 7 kDa. Theirprimary structure is formed with 45–55 am<strong>in</strong>o acid residues. Two structuralcharacteristics of the defens<strong>in</strong>s, the presence of a pattern of conserved cyste<strong>in</strong>eresidues and a doma<strong>in</strong> with extremely variable am<strong>in</strong>o acid sequence, aretypical components for mature peptide molecules of <strong>plant</strong> defens<strong>in</strong>s. Withrare exceptions, defens<strong>in</strong>s found <strong>in</strong> <strong>plant</strong>s have a similar globular spatialstructure that is stabilized by a structural motif formed us<strong>in</strong>g disulfide bondsbetween eight cyste<strong>in</strong>e residues. Possibly, defens<strong>in</strong>s can aggregate <strong>in</strong> vivo<strong>in</strong>to dimers or oligomers (Terras et al., 1992). A certa<strong>in</strong> correlation is observedbetween the primary structure and antimicrobial activity of some <strong>plant</strong>defens<strong>in</strong>s. In general, the <strong>in</strong>corporation of basic am<strong>in</strong>o acids (viz. arg<strong>in</strong><strong>in</strong>e)that add positive charge to a peptide molecule resulted <strong>in</strong> a considerable<strong>in</strong>crease <strong>in</strong> the antimicrobial activity (Terras et al., 1992; De Samblanx et al.,1997; Landon et al., 2000).In the overwhelm<strong>in</strong>g majority of cases, <strong>plant</strong> defens<strong>in</strong>s possess <strong>in</strong>hibitoryactivity aga<strong>in</strong>st fungi; however, the growth of Gram-negative bacteria isalso arrested after exposure to these peptides (Terras et al., 1993; Segura et al,1998; Wong et al, 2006). An analysis of publications by Carvalho and Gomes(2009) showed many damag<strong>in</strong>g <strong>plant</strong> pathogens of economically importantcrops can be <strong>in</strong>hibited <strong>in</strong> vitro with <strong>plant</strong> defens<strong>in</strong>s. Various fungal species(Alternaria brassicola, Alternaria solani, Botrytis c<strong>in</strong>erea, Cladosporium colocasiae,

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