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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 71<br />

However, because of the marked antifungal activity of tomatine <strong>and</strong><br />

other saponins, these preformed compounds are behoved to be involved<br />

in host resistance towards saponin-sensitive fungi. Tomatine presumably<br />

owes its toxic properties to its ability to bind to 3p-hydroxy sterols in<br />

fungal membranes (Steel <strong>and</strong> Drysdale, 1988). Most tomato pathogens,<br />

on the other h<strong>and</strong>, can specifically degrade tomatine <strong>and</strong> detoxify its<br />

effect through the activity of tomatinase (Osbourn et al., 1994).<br />

In a recent study, S<strong>and</strong>rock <strong>and</strong> VanEtten (1998) examined 23 strains<br />

of fungi for their sensitivity to a-tomatine <strong>and</strong> to its two breakdown<br />

products, P2-tomatine <strong>and</strong> tomatidine. The two saprophytes <strong>and</strong> the five<br />

non-pathogens of tomato included in this study were found to be<br />

sensitive to a-tomatine, while all the other fungi tested, except for two<br />

tomato pathogens, were determined to be tolerant to a-tomatine. All the<br />

tomato pathogens tested except Phytophthora infestans <strong>and</strong> Pythium<br />

aphanidermatum were able to degrade a-tomatine. These included<br />

Alternaria alternata, the common post<strong>harvest</strong> pathogen of tomato fruit.<br />

A strong correlation was found between tolerance to a-tomatine, ability<br />

to degrade this compound, <strong>and</strong> pathogenicity to tomato. However,<br />

P2-tomatine <strong>and</strong> tomatidine, which were less toxic to most pathogens<br />

because of their inability to complex with membrane-bound SP-hydroxy<br />

sterols (Steel <strong>and</strong> Drysdale, 1988), were inhibitory to some of the<br />

non-pathogens of tomato, suggesting that tomato pathogens may have<br />

multiple tolerance mechanisms to a-tomatine (S<strong>and</strong>rock <strong>and</strong> VanEtten,<br />

1998).<br />

Tannins in young banana <strong>fruits</strong> (Green <strong>and</strong> Morales, 1967) <strong>and</strong><br />

benzylisothiocyanate in unripe papaya <strong>fruits</strong> (Patil et al., 1973) are<br />

additional examples of in-fruit toxic compounds. Since the concentration<br />

of these compounds decreases with fruit ripening, it has been considered<br />

that they have a role in resistance to decay in young <strong>fruits</strong>.<br />

Antifungal substances isolated from unripe avocado fruit peel include<br />

monoene <strong>and</strong> diene compounds, of which diene is the more important<br />

(Prusky <strong>and</strong> Keen, 1993). Resistance of unripe avocado <strong>fruits</strong> to<br />

post<strong>harvest</strong> pathogens has been suggested to be closely related to the<br />

presence in the peel of the antifungal diene compound (l-acetoxy-2<br />

hydroxy-4-oxo-heneicosa 12,15) (Prusky <strong>and</strong> Keen, 1993). This compound<br />

inhibits spore germination <strong>and</strong> mycelial growth of Colletotrichum<br />

gloeosporioideSy at concentrations lower than those present in the peel<br />

(see Fig. 3). The concentration of diene diminishes considerably as the<br />

fruit ripens <strong>and</strong>, in parallel, the dormant fungus in the peel starts its<br />

development (Prusky et al., 1982) (see Fig. 4). The decrease in the<br />

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