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

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FREEDOM PALESTINE FREEDOM PALESTINE FREEDOM PALESTINE<br />

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

the fruit can provide pectic compounds that induce the formation of<br />

pectolytic enzymes <strong>and</strong> their activity, <strong>and</strong> the plant tissue becomes more<br />

susceptible to the pectolytic enzymes secreted by the pathogen. Recent<br />

studies with papapya cell walls suggested that, in addition to pectin<br />

hydroljdsis, the modification of another cell-wall compound - the<br />

hemicellulose - is also involved in fruit softening (PauU et al., 1999).<br />

Another factor that changes during the ripening process is the ability<br />

of the tissues to produce toxic compounds, which inhibit the pathogen<br />

growth; this diminishes as the tissues ripen. These compounds include:<br />

tomatine, which can be found in high concentrations in the green tomato<br />

skin (Verhoeff <strong>and</strong> Liem, 1975); tannins in young bananas (Green <strong>and</strong><br />

Morales, 1967; van Buren, 1970); monoene <strong>and</strong> diene compounds in<br />

young avocado skin; resorcinols in the skin of mangoes in their early<br />

developmental stages (Prusky <strong>and</strong> Keen, 1993); <strong>and</strong> various toxic<br />

compounds found in the oil gl<strong>and</strong>s of young citrus fruit rind (Rodov et al.,<br />

1995b). Polyphenols <strong>and</strong> tannins, highly concentrated in the younger<br />

<strong>fruits</strong>, have been described both as germination <strong>and</strong> growth inhibitors of<br />

microorganisms, <strong>and</strong> as suppressors of enzymatic activity.<br />

Regarding the nutrient availability changes during the advanced<br />

development or ripening of the fruit, a direct relationship was found<br />

between the sugar contents in nectarines <strong>and</strong> plums <strong>and</strong> the late-season<br />

susceptibility of these <strong>fruits</strong> to B. cinerea infection (Fourie <strong>and</strong> Holz,<br />

1998). During their early developmental stages, the young unwounded<br />

<strong>fruits</strong> are resistant to the pathogen. It is not until the early phase of<br />

rapid cell enlargement of the nectarine <strong>and</strong> the last phase of rapid cell<br />

enlargement of the plum that the fruit becomes susceptible to infection,<br />

<strong>and</strong> disease development occurs (Fourie <strong>and</strong> Holz, 1995).<br />

Studying the sugar content in exudates of immature plum <strong>and</strong><br />

nectarine <strong>fruits</strong>, Fourie <strong>and</strong> Holz (1998) found that fructose, glucose <strong>and</strong><br />

sorbitol were the only sugars present, whereas sucrose was first detected<br />

during fruit maturation, which occurs approximately two weeks before<br />

<strong>harvest</strong>. The sugars were exuded at low concentrations by immature<br />

<strong>fruits</strong> but their concentrations increased as the fruit ripened. In<br />

nectarines there was a pronounced increase in the sugar concentrations,<br />

especially that of sucrose, near the picking-ripe stage. Fungal growth was<br />

found to increase when the reducing sugars or sucrose were added to<br />

culture media in excess of 0.27 or 0.14 mM <strong>and</strong> when sorbitol was<br />

supplied in excess of 0.66 mM. With the progress in fruit maturity during<br />

the last two weeks before <strong>harvest</strong>, total sugars in plum exudates<br />

approached these values, whereas in nectarine exudates they far<br />

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