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Postharvest Biology and Technology of Fruits, Vegetables, and Flowers

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THE BREAKDOWN OF CELL WALL COMPONENTS 167<br />

Level<br />

Arabinose<br />

loss<br />

Galactose<br />

loss<br />

Pectin<br />

solubilization<br />

Pectin<br />

depolymerization<br />

Absent<br />

Apricot<br />

Plum<br />

Watermelon<br />

Cucumber<br />

Plum<br />

Apple<br />

Watermelon<br />

Apricot<br />

Plum<br />

Watermelon<br />

Some<br />

Pepper<br />

Tomato<br />

Apricot<br />

Blueberry<br />

Apple<br />

Pepper<br />

Tomato<br />

Intermediate<br />

Avocado<br />

Peach<br />

Kiwifruit<br />

Apple<br />

Melon<br />

Peach<br />

Banana<br />

Plum<br />

Strawberry<br />

Tomato<br />

Avocado<br />

Peach<br />

Kiwifruit<br />

Extensive<br />

Pear<br />

Blueberry<br />

Muskmelon<br />

Pepper<br />

Tomato<br />

Avocado<br />

Blackberry<br />

Kiwifruit<br />

Pear<br />

Blueberry<br />

Fig. 8.1 Classification <strong>of</strong> fruits based on extent <strong>of</strong> cell wall polysaccharide modifications during ripening.<br />

Shown are ripening-associated losses <strong>of</strong> arabinose <strong>and</strong> galactose <strong>and</strong> solubilization <strong>and</strong> depolymerization <strong>of</strong><br />

pectic component from cell walls <strong>of</strong> fruits <strong>of</strong> various species. Levels represent: Extensive >70%, intermediate<br />

25–70%, some ≤25%, <strong>and</strong> absent undetectable. (Redrawn from Brummell, 2006.)<br />

changes. Substantial differences in proportion <strong>of</strong> pectin solubilization exist between species;<br />

greatest solubilization occurring in ripening avocado followed by kiwifruit <strong>and</strong> blackberry,<br />

whereas solubilization was very low or absent in apples <strong>and</strong> watermelon (Brummell, 2006).<br />

The increased pectin solubilization is correlated with a swelling <strong>of</strong> cell wall (Redgwell<br />

et al., 1997a). In persimmon, avocado, blackberry, strawberry, <strong>and</strong> plum fruit that ripens to<br />

a s<strong>of</strong>t melting texture, wall swelling was pronounced, particularly in vitro. In vivo swelling<br />

was marked only in avocado <strong>and</strong> blackberry. Fruit that ripened to a crisp, fracturable texture<br />

such as apple, pear, <strong>and</strong> watermelon did not show either in vivo or in vitro swelling <strong>of</strong> the<br />

cell wall. There is a correlation between swelling <strong>and</strong> the degree <strong>of</strong> pectin solubilization,<br />

suggesting that wall swelling occurred as a result <strong>of</strong> changes to the viscoelastic properties<br />

<strong>of</strong> the cell wall during pectin solubilization. The pectin that is solubilized during ripening<br />

generally has a low Gal (Redgwell et al., 1997b) <strong>and</strong> Ara content (Brummell et al.,<br />

2004a). This indicates that either solubilization <strong>and</strong> Gal/Ara loss largely affects different<br />

pectic molecules (Redgwell et al., 1997b) or loss <strong>of</strong> almost complete side chain results in<br />

polyuronide solubilization. Swelling was associated with movement <strong>of</strong> water into voids left<br />

in the cellulose–hemicellulose network by the solubilized pectin (Redgwell et al., 1997a).<br />

These processes combined with the loss <strong>of</strong> pectic side chains increase wall porosity that<br />

may allow increased access <strong>of</strong> degradative enzymes to their substrates later in ripening<br />

(Brummell, 2006). The walls <strong>of</strong> fleshy fruits become much more open, <strong>and</strong> hydrophilic environment<br />

exists as ripening progresses. The increased accessibility <strong>of</strong> hydrolytic enzymes<br />

to their substrate further promotes polymer dismantling.

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