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Postharvest Biology and Technology of Fruits, Vegetables, and Flowers

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

Table 12.1<br />

The major classes <strong>of</strong> phenolic compounds present in fruits<br />

Number <strong>of</strong> Carbon<br />

carbons skeleton Class <strong>and</strong> subclass Example<br />

6 C 6 Simple phenols Catechol<br />

7 C 6 C 1 Hydroxybenzoates (phenolic<br />

acids)<br />

Gallic acid, protocatechuic acid, syringic<br />

acid, gentisic acid, p-hydroxybenzoic acid<br />

9 C 6 C 3 Hydroxycinnamates<br />

Caffeic, p-coumaric, ferulic, is<strong>of</strong>erulic<br />

(phenolic acids)<br />

Coumarins<br />

Scopoletin, aesculetin, umbelliferone,<br />

limmettin, herniarin<br />

10 C 6 C 4 Naphthoquinones Juglone<br />

13 C 6 C 1 C 6 Xanthones Mangiferin, mangostin, gartanins<br />

14 C 6 C 2 C 6 Stilbenes Resveratrol<br />

15 C 6 C 3 C 6 Flavonoids<br />

Flavanone<br />

Naringenin, hesperetin, neohesperidin,<br />

eriodictyol, citromitin, pinostrobin<br />

Flavone<br />

Luteolin, apigenin, tangeretin, nobiletin,<br />

sinensetin<br />

Flavonol<br />

Quercetin, kaempferol, myricetin<br />

Flavan-3-ol<br />

Catechin, epicatechin, gallocatechins,<br />

epigallocatechin, epicatechin gallate<br />

Anthocyanins<br />

Cyanidin, delphinidin, malvidin, peonidin,<br />

petunidin, pelargonidin<br />

Dihydrochalcones<br />

Phloretin, phloridzin<br />

18 (C 6 C 3 )2 Lignans Secoisolariciresinol, matairesinol<br />

30 (C 6 C 3 C 6 )2 Biflavonoids Ament<strong>of</strong>lavone<br />

n (C 6 C 3 )n Lignins Guaiacyl lignins<br />

n (C 6 C 1 )n: Hydrolysable tannins<br />

Gallotannins, ellagitannins, castalagin,<br />

Glu<br />

corilagin, chebulagic acid<br />

n (C 6 C 3 C 6 )n Condensed tannins<br />

(flavolans)<br />

Procyanidins (catechin polymers)<br />

Adapted from Harborne (1980).<br />

12.3 Distribution <strong>of</strong> phenolic acids in fruits<br />

In literature, both hydroxybezoates <strong>and</strong> hydroxycinnamates <strong>and</strong> their derivatives are referred<br />

collectively as phenolic acids. Phenolic acids are found predominantly <strong>and</strong> widely<br />

in almost all fruits (Herrmann, 1989) (Table 12.2). The most commonly found hydroxycinnamic<br />

acids are p-coumaric, caffeic, ferulic, <strong>and</strong> sinapic acids, while p-hydroxybenzoic,<br />

protocatechuic, vanillic, <strong>and</strong> syringic acids are the common hydroxybenzoic acids in fruits.<br />

These derivatives differ in their structure only by the degree <strong>of</strong> the hydroxylations <strong>and</strong><br />

methoxylations <strong>of</strong> their aromatic rings. In fruits, phenolic acids are commonly found as<br />

conjugated forms with quinic acid. It seems that chlorogenic acid, which is derived from<br />

caffeic <strong>and</strong> quinic acids, is the most common hydroxybenzoic acid derivative in berry,<br />

pome, <strong>and</strong> stone fruits (Mattila et al., 2006). The general term “chlorogenic acid” includes<br />

three positional is<strong>of</strong>orms. These is<strong>of</strong>orms differ from one another based on which hydroxyl<br />

group <strong>of</strong> quinic acid is used to combine the two precursor molecules, quinic acid <strong>and</strong><br />

caffeic acid. The following common (<strong>and</strong> chemical) names have been given to these is<strong>of</strong>orms:<br />

chlorogenic acid (5-caffeoylquinic acid), cryptochlorogenic acid (4-caffeoylquinic<br />

acid), <strong>and</strong> neochlorogenic acid (3-caffeoylquinic acid). The presence <strong>of</strong> chlorogenic acid

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