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natural-products-in-plant-pest-management

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Fungal Endophytes 227over 50% of the new chemical <strong>products</strong> registered by the US Food and DrugAdm<strong>in</strong>istration (FDA) as anticancer agents, antimigra<strong>in</strong>e agents and antihypertensiveagents from 1981 to 2002 are <strong>natural</strong> <strong>products</strong> or their derivatives(Newman et al., 2003). Exclud<strong>in</strong>g biologics, between 1989 and 1995, 60% ofapproved drugs and pre-new-drug-application (NDA) candidates were of<strong>natural</strong> orig<strong>in</strong>. From 1983 to 1994, over 60% of all approved and pre-NDAstage cancer drugs were of <strong>natural</strong> orig<strong>in</strong>, as were 78% of all newly approvedantibacterial agents (Concepcion et al., 2001). The discovery and developmentof taxol is a modern example of a <strong>natural</strong> product that has made anenormous impact on medic<strong>in</strong>e (Wani et al., 1971; Suffness, 1995; Schulz andChrist<strong>in</strong>e, 2005).Antibiotics from endophytic fungiGenerally, the most commonly isolated endophytic fungi are <strong>in</strong> the group ofFungi Imperfecti or Deuteromycot<strong>in</strong>a. Also, it is quite common to isolateendophytes that produce no fruit<strong>in</strong>g structures whatsoever such as Mycelia-Sterilia.Cryptosporiopsis cf. querc<strong>in</strong>a is the imperfect stage of Pezicula c<strong>in</strong>namomea,a fungus commonly associated with hardwood species <strong>in</strong> Europe. It was isolatedas an endophyte from Tripterigeum wilfordii, a medic<strong>in</strong>al <strong>plant</strong> native toEurasia (Strobel et al., 1999). On Petri plates, C. querc<strong>in</strong>a demonstrates excellentantifungal activity aga<strong>in</strong>st some important human fungal pathogens<strong>in</strong>clud<strong>in</strong>g C. albicans and Trichophyton spp. Cryptocand<strong>in</strong>, a unique peptideantimycotic related to the ech<strong>in</strong>ocand<strong>in</strong>s and the pneumocand<strong>in</strong>s (Walsh,1992), was isolated and characterized from C. querc<strong>in</strong>a (Strobel et al., 1999).This compound conta<strong>in</strong>s a number of peculiar hydroxylated am<strong>in</strong>o acidsand a novel am<strong>in</strong>o acid, 3-hydroxy-4-hydroxymethyl prol<strong>in</strong>e (Fig. 11.2). It isgenerally true that not one but several bioactive and related compounds areproduced by an endophytic microbe. So it is that other antifungal agentsrelated to cryptocand<strong>in</strong> are also produced by C. querc<strong>in</strong>a. Cryptocand<strong>in</strong> isalso active aga<strong>in</strong>st a number of <strong>plant</strong> pathogenic fungi <strong>in</strong>clud<strong>in</strong>g S. sclerotiorumand Botrytis c<strong>in</strong>erea. Cryptocand<strong>in</strong> and its related compounds are currentlybe<strong>in</strong>g considered for use aga<strong>in</strong>st a number of fungi caus<strong>in</strong>g diseases ofthe sk<strong>in</strong> and nails.Cryptoc<strong>in</strong>, a unique tetramic acid, is also produced by C. querc<strong>in</strong>a(Fig. 11.3) (Li et al., 2000). This unusual compound possesses potent activityaga<strong>in</strong>st Pyricularia oryzae, the causal organism of ‘rice blast’, one of the worst<strong>plant</strong> diseases <strong>in</strong> the world, as well as a number of other <strong>plant</strong> pathogenicfungi (Li et al., 2000). The compound was generally <strong>in</strong>effective aga<strong>in</strong>st anarray of human and <strong>plant</strong> pathogenic fungi. Nevertheless, with m<strong>in</strong>imum<strong>in</strong>hibitory concentrations aga<strong>in</strong>st P. oryzae at 0.39 μg/ml, this compound isbe<strong>in</strong>g exam<strong>in</strong>ed as a <strong>natural</strong> chemical control agent for rice blast and is be<strong>in</strong>gused as a model to synthesize other antifungal compounds.Pestelotiopsis microspora is a common ra<strong>in</strong>forest endophyte (Strobel, 2002;Strobel and Daisy, 2003). It turns out that enormous biochemical diversity

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