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Composition of tomatoes and tomato products in antioxidants (WG1) page 15<br />

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4. Breeding and biotechnology methods for high lycopene content<br />

The biochemical pathway involved in lycopene production has been largely<br />

elucidated. Until recently, the mevalonate (MVA) (Fig 1) pathway was believed to be the only<br />

route for the provision of the key isoprenoid intermediate, IPP (Britton 1990).<br />

Figure 1. Main stages of carotenoid synthesis in plants<br />

Mevalonate<br />

Isopentenyl diphosphate (IPP)<br />

Geranylgeranydiphosphate (GGDP)<br />

Phytoene synthase Phytoene<br />

Phytoene desaturase Lycopene<br />

Lycopene cyclase β- carotene<br />

Recently a non-MVA pathway has been identified (Schwender et al.1996). This is<br />

localised in the plastid in contrast to the MVA pathway which is localised in the cytoplasm of<br />

the cell. In this pathway, glyceraldehyde 3-phosphate (GAD) and pyruvate are the first<br />

precursors. Pyruvate is first decarboxylated and then condensated on the carbonyl of GAP<br />

yielding 1-deoxy-d-xylulose 5-phosphate and finally IPP. This novel mevalonate-independent<br />

biosynthesis pathway was first demonstrated in bacteria and then was shown to be involved in<br />

the carotenoid synthesis in higher plants.<br />

Then condensation of IPP molecules results in Geranylgeranyl diphosphate (GGDP)<br />

formation. The first C40 carotenoid phytoene is formed from two molecules of GGDP. The<br />

non-coloured phytoene undergoes a series of sequential desaturation reactions to produce<br />

phytofluene, ζ-carotene, neurosporene and finally the coloured lycopene. It was suggested<br />

that during these reactions cis-trans double bond isomerization occured. Finally, cyclization

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