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The genus Cinnamomum

The genus Cinnamomum

The genus Cinnamomum

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90 U.M. Senanayake and R.O.B. Wijesekera<br />

Figure 3.2 GLC chart of commercial cinnamon bark oil on SCOT column.<br />

Following the development of solid injection techniques, Senanayake et al. (1975),<br />

Wijesekera et al. (1975) and Wijesekera (1978) employed this methodology for the study<br />

of volatile constituents of morphologically distinct parts of the cinnamon tree, employing<br />

as little as 15 mg of plant material. Use of this technique has revealed that during<br />

the normal steam distillation, cinnamon volatiles do not undergo any significant chemical<br />

changes, that leaf veins contain more cinnamic aldehyde (30%) than the rest of the<br />

leaf, and many other useful biosynthetic features.<br />

Location of Cinnamon Volatiles in C. verum<br />

C. verum is interesting in that it yields three types of oils from the leaf, stem bark<br />

and root bark. <strong>The</strong> major constituent in the leaf oil is eugenol, in the stem bark oil it is<br />

cinnamic aldehyde while camphor is the major constituent in the root bark oil. Solid<br />

injection techniques have revealed that the young and old leaves are deficient in volatiles;<br />

only mature leaves (about four leaves below the apical bud) have the general volatile<br />

pattern of the distilled oil. It is also found that the leaf petiole and veins contained more<br />

cinnamic aldehyde than in the leaf lamina. This is in agreement with the view (Neish,<br />

1960) that cinnamic aldehyde will eventually be converted to lignin in the xylem vessels<br />

found in cinnamon stem, petiole and vein.<br />

Cinnamic aldehyde and eugenol are components of the shikimic acid pathway<br />

leading to lignin formation. Cinnamic aldehyde is directly formed by the reduction of<br />

cinnamic acid, the latter being formed from phenylalanine (PA). It was shown that<br />

cinnamic aldehyde gets further reduced to cinnamyl alcohol, which is a precursor of<br />

lignin. Eugenol, due to the absence of a hydroxy group in the allyl side-chain, cannot<br />

readily contribute to the lignin formation. However, Siegel (1955) and Higuchi (1957)<br />

have shown that eugenol is capable of polymerising to lignin-like substances.<br />

Since lignification occurs in the xylem tissues, it has to be established whether synthesis<br />

of cinnamic aldehyde and eugenol occurs in the xylem tissues or whether they are

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