Biotechnological Approaches to Enhancing Tropical Fruit Quality - Postharvest Biology and Technology of Fruits, Vegetables, and Flowers - page 381

Flavonoids are derived from phenylalanine and acetyl CoA in a highly branched pathway
leading to flavonols, flavanones, isoflavonoids, and anthocyanins (Forkmann and Martens,
2001). It is known that this complex pathway is regulated at the level of transcription
of structural genes (Forkmann and Martens, 2001). In general, genetic manipulation of
intermediate enzymes of the flavonoid pathway may change the final balance of these colored
compounds and eventually the color of a given plant organ. For example, when a chalcone
reductase gene from Medicagosativa was introduced in Petunia , the flavonoid biosynthesis
pathway was redirected since neither chalcone reductase activity nor the product of the
reaction, which was further transformed into a colored compound, is naturally present in
Petunia , and the plant produced yellow flowers (Davies et al., 1998). Similar results have
been obtained using different enzymes in other plants (Holton, 1995; Markham, 1996;
Su and Hsu, 2003). This illustrates the complex equilibrium of the complete pathway and
the difficulty of predictable effects after plant transformation with heterologous genes.
18.4.8 Parthenocarpy
The absence of seeds in fruits is a valuable trait, not only from the consumer standpoint,
but because it may allow control of fruit development even under adverse environmental
conditions for pollination and may be used in fruit crops to standardize and increase fruit size
(Gorguet et al., 2005). Horticultural methods for inducing parthenocarpy include spraying of
growth regulators, induction of genetic mutations, or modification of ploidy level (Bukovac
and Nakagawa, 1967). The parthenocarpy trait is often polygenic and therefore more difficult
to deal with in-breeding programs (Gorguet et al., 2005). Parthenocarpy development,
in some fruits at least, may be triggered by a deregulation of the hormonal balance in
some specific tissues, in particular, between auxins and gibberellins (Fos et al., 2000). An
increased level of these hormones in the ovary can substitute for pollination and trigger fruit
development. This has been convincingly demonstrated by genetic engineering when the
iaaM gene, coding for the enzyme tryptophan monooxygenase, was introduced in tomato,
tobacco, eggplant, strawberry, and raspberry resulting in parthenocarpic fruits (Rotino et
al., 1997; Acciarri et al., 2002; Mezzetti et al., 2004). The iaaM gene converts tryptophan
to indole acetamide, a precursor of indole acetic acid, and was driven by a placental ovule-
specific promoter (DefH9). The expression of chimeric DefH9 -iaaM starts during early
flower development, and the construct mimics the hormonal effects of pollination and
embryo development by increasing the content and/or the activity of auxin in the ovule.
Parthenocarpic fruits can also result by mutation of the pistillata gene (Yao et al., 2001)
or by downregulation of the sepallata gene (Ampomah-Dwamena et al., 2002). Expression
of the Agrobacterium rhizogenes rolB gene in the ovary can also induce parthenocarpy
(Carmi et al., 2003). This is an equivalent approach to that of increasing the content of
auxins in the ovary as rolB codes for a putative auxin receptor, which makes the plant more
sensitive to auxins (Maurel et al., 1994). Finally, high-temperature stress can also result in
a seedless phenotype (Young et al., 2004).
18.4.9 Nutritional value enhancement
Plants are the staple food for the vast majority of the world's population, but it is known
that they may be deficient in essential nutrients. For that reason, there have been attempts