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

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FREEDOM PALESTINE FREEDOM PALESTINE FREEDOM PALESTINE<br />

Host Protection <strong>and</strong> Defense Mechanisms 67<br />

for cell death <strong>and</strong> the liberation of nutrients, which then become<br />

available to the pathogen. Liberation of nutrients results in a stimulation<br />

of pathogen growth <strong>and</strong> accelerated disease development. This may<br />

explain the great importance attributed to compounds that are capable of<br />

suppressing or preventing enzymatic activity.<br />

Trials with various pathogens have emphasized the point that sugars<br />

in the culture medium, which serve as available nutrients for the<br />

pathogen <strong>and</strong> stimulate its growth, may inhibit pectolytic <strong>and</strong> cellulolytic<br />

enzyme production <strong>and</strong> activity (Spalding et al., 1973; Biehn <strong>and</strong><br />

Dimond, 1973; Bahkali, 1995). It was found that the presence of glucose<br />

in the culture medium, either as a sole source of carbon or in addition to<br />

malic or citric acid, inhibited pectin lyase activity of Penicillium<br />

expansum, while resulting in enhanced fungal growth (Spalding <strong>and</strong><br />

Abdul-Baki, 1973)<br />

Polyphenols <strong>and</strong> tannins have been described by Byrde et al. (1973) as<br />

inhibitors of polygalacturonase (PG) activity of Sclerotinia fructicola<br />

(Monilinia fructicola) in apples <strong>and</strong> other pathogen/host combinations,<br />

although they have no effect on the pathogen itself. Decay development<br />

in many <strong>fruits</strong> <strong>and</strong> <strong>vegetables</strong> may be the result of the delicate balance<br />

between active production of enzymes <strong>and</strong> their inhibition by<br />

polyphenols, mainly in their oxidized condition, as a result of<br />

polyphenol-oxidase activity (Dennis, 1987).<br />

Another class of inhibitors of cell wall-degrading enzymes comprises<br />

the PG-inhibitory proteins present in both infected <strong>and</strong> uninfected plant<br />

tissue (Albersheim <strong>and</strong> Anderson, 1971; Abu-Goukh et al., 1983). A<br />

PG-inhibiting protein from a given plant source may act on pectic<br />

enzymes produced by different fungal species, both pathogenic <strong>and</strong><br />

non-pathogenic, or on various PG isozymes from the same fungus.<br />

Research carried out with pepper <strong>fruits</strong> has shown that cell wall proteins<br />

of the host inhibited pectolytic enzyme production by Glomerella<br />

cinigulata, whereas the pectolytic activity of Botrytis cinerea was much<br />

less affected by these proteins (Brown, A.E. <strong>and</strong> Adikaram, 1983). The<br />

fact that B, cinerea can rot an immature pepper fruit whereas G.<br />

cingulata can attack only the ripened fruit, suggested that protein<br />

inhibitors might play a role in the quiescent infections of pepper <strong>fruits</strong> by<br />

Glomerella,<br />

Purified pear inhibitory proteins were found to inhibit various fungal<br />

PGs, including that of B, cinerea, but did not affect endogenous PG<br />

activity in pear <strong>fruits</strong> (Abu-Goukh <strong>and</strong> Labavitch, 1983). In a later study,<br />

Stotz et al. (1993) reported on the molecular characterization of the<br />

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