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Postharvest Biology and Technology of Fruits, Vegetables, and Flowers

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184 POSTHARVEST BIOLOGY & TECHNOLOGY OF FRUITS, VEGETABLES, & FLOWERS<br />

(Amanatidou et al., 2000), <strong>and</strong> strawberries (Wszelaki <strong>and</strong> Mitcham, 2000). Deng et al.<br />

(2005) observed that decrease in firmness <strong>of</strong> grapes under different oxygen storage was<br />

accompanied by a dramatic decrease in hemicellulose <strong>and</strong> moderate decrease in cellulose<br />

<strong>and</strong> total pectins, which indicates that the s<strong>of</strong>tening in grapes is due to increased depolymerization<br />

<strong>and</strong> degradation <strong>of</strong> cell wall polysaccharides. At higher oxygen storage, grapes<br />

maintained firmness, which coincided with higher retention <strong>of</strong> cell wall polysaccharides.<br />

The lower levels <strong>of</strong> water-soluble pectins in high-oxygen atmosphere were correlated with<br />

delayed s<strong>of</strong>tening, <strong>and</strong> the activities <strong>of</strong> PG, PE, β-GAL increased to lower extent than air<br />

storage, which indicates that higher oxygen might have inhibited relative enzyme activities,<br />

reducing the degradation <strong>and</strong> depolymerization <strong>of</strong> pectin substances.<br />

Cellulase activity in grapes increased slightly over time, <strong>and</strong> its activity was slightly<br />

lower in high oxygen compare to air (Deng et al., 2005). In controlled atmosphere (CA)-<br />

stored apples, ripening-related s<strong>of</strong>tening was inhibited after an initial loss <strong>of</strong> firmness.<br />

However, s<strong>of</strong>tening resumed after transfer <strong>of</strong> apples to normal atmosphere storage at 8 ◦ C<br />

(Ingham et al., 1998).<br />

The retardation <strong>of</strong> carambola fruit s<strong>of</strong>tening by MAP <strong>and</strong>/or LT, which correlates closely<br />

with delayed solubilization <strong>and</strong> depolymerization <strong>of</strong> the chelator-soluble polyuronides, may<br />

partly be attributed to suppression <strong>of</strong> the increase in activity <strong>of</strong> the major wall hydrolases.<br />

Suppression <strong>of</strong> the enzyme activities in fruit under MAP also appears to contribute to<br />

increased tolerance <strong>of</strong> the carambolas to CI incidence (Ali et al., 2004).<br />

Delayed (2 days at 20 ◦ C before storage) <strong>and</strong> controlled atmosphere (fruits stored at<br />

10% CO 2 ,3%O 2 ) storage <strong>of</strong> nectarines fruits prevented wooliness during ripening <strong>of</strong> fruits<br />

after 4- to 6-week storage at 0 ◦ C compared to fruits stored immediately in 0 ◦ C, 95% RH air<br />

(Zhou et al., 2000). At the time <strong>of</strong> removal, the delayed stored fruits exhibited similar levels<br />

<strong>of</strong> PG <strong>and</strong> PE transcripts but higher PG <strong>and</strong> lower PE activities compared to control fruits.<br />

CA-repressed transcript levels <strong>of</strong> both PG <strong>and</strong> PE <strong>and</strong> activity <strong>of</strong> PG, but the PG activity<br />

recovered during the 7-day ripening period. Whereas the endoglucanase activity declined<br />

during ripening in all fruits, control fruits retained more activity than DS or CA fruits. On<br />

the basis <strong>of</strong> these results, Zhou et al. (2000) have suggested that the ratio between PG/PE<br />

at the time <strong>of</strong> removal <strong>of</strong> the delayed stored fruits or during ripening <strong>of</strong> CA stored fruits<br />

plays a significant role in the development <strong>of</strong> fruit wooliness.<br />

A hydrophobic coating formulated with maltodextrins, carboxymethylcellulose, propyleneglycol,<br />

<strong>and</strong> a mixture <strong>of</strong> sorbitan esters was applied to preclimacteric “Manila” mangoes.<br />

The fruit treated with the coating suffered less mesocarp s<strong>of</strong>tening along with concomitant<br />

reductions <strong>of</strong> PG <strong>and</strong> cellulase (Cx) activities than did control fruit. After the initial storage<br />

period, activity <strong>of</strong> PG increased steadily during further ripening <strong>of</strong> coated fruit (Diazsobac<br />

et al., 1997).<br />

Coating citrus with low-molecular-weight chitosan (LMWC, Mw = 15 kDa) improved<br />

firmness <strong>and</strong> exhibited greater antifungal resistance than 2-(4-thiazolyl)benzimidazole<br />

(TBZ), <strong>and</strong> its quality was maintained for longer (Chien et al., 2007).<br />

8.12.6 Pathogen attack<br />

In apple <strong>and</strong> tomato fruits, Penicillium expansum infection caused reduction in the molecular<br />

mass <strong>of</strong> hemicelluloses, particularly in the xyloglucan. Xyloglucan endotransglucosylase/hydrolase<br />

(XTH)-specific activity decreased drastically during the infection process

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