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Post harvest diseases fruits and vegetables - Xavier University ...

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FREEDOM PALESTINE FREEDOM PALESTINE FREEDOM PALESTINE<br />

218 <strong>Post</strong><strong>harvest</strong> Diseases of Fruits <strong>and</strong> Vegetables<br />

also been found to retard ripening of several <strong>harvest</strong>ed commodities, such<br />

as tomato <strong>and</strong> peach (Liu et al., 1993; Lu et al., 1991), thus leading<br />

indirectly to reduction in their susceptibility to infection.<br />

Optimum UV-C doses for induced resistance in the various<br />

commodities fall within narrow ranges, specific for each commodity. Also<br />

the maximum protection provided by UV treatments occurs at varying<br />

times after treatment <strong>and</strong> depends on the commodity. Studies with<br />

UV-treated grape<strong>fruits</strong> showed that <strong>fruits</strong> picked at different times<br />

during the growing season responded differently to UV treatments. The<br />

temperature at which the fruit was stored following treatment was<br />

another factor affecting resistance development (Droby et al., 1993a).<br />

Maximum resistance of peaches against Monilinia fructicola <strong>and</strong><br />

tomatoes against Rhizopus stolonifer was observed 48-72 h after UV<br />

treatment, whereas sweet potatoes exhibited maximum protection<br />

against Diplodia tubericola 1-7 days after treatment (Wilson et al.,<br />

1997a).<br />

Ultraviolet Effects<br />

In UV-illuminated apples <strong>and</strong> peaches the induced resistance to decay<br />

has been attributed to the inhibition of ripening <strong>and</strong> the maintenance of<br />

the natural resistance of the young <strong>fruits</strong> to infection (Lu et al., 1991).<br />

Studying the changes found in UV-treated citrus <strong>fruits</strong> indicated that<br />

induced resistance occurs in concomitance with the induced activity of<br />

the enzymes phenylalanine ammonia lyase (PAL) <strong>and</strong> peroxidase<br />

(Chalutz et al., 1992; Droby et al., 1993a). These findings led to the<br />

hypothesis that induced activity of the two enzymes plays a role in the<br />

enhanced resistance to decay that follows UV treatment.<br />

Several investigations indicated the ability of UV illumination to<br />

induce phytoalexin production in various host tissues. UV illumination<br />

(254 nm) of citrus <strong>fruits</strong> was found to induce the phytoalexin scoparon<br />

(Rodov et al., 1995b; Rodov et al., 1992), the production of which is<br />

enhanced both by increasing the UV dose <strong>and</strong> by raising the storage<br />

temperature (Rodov et al., 1992). Its accumulation in kumquat fruit<br />

reached its peak 11 days after illumination, but the amount declined<br />

rapidly, returning to trace levels, typical of non-illuminated fruit, 1<br />

month after treatment. The accumulation of the phytoalexin was<br />

correlated with an increase in the antifungal activity of the flavedo which<br />

led to improved resistance of the fruit to infection by Penicillium<br />

digitatum. Such a defense against infection was achieved when<br />

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