Articles

METABOLIC ENGINEERING OF FLAVONOID BIOSYNTHESIS IN APPLE (MALUS DOMESTICA BORKH.)

Article number
814_86
Pages
511 – 516
Language
English
Abstract
Flavonoids are a large family of polyphenolic compounds with manifold functions in plants including pathogen defence.
Present in a wide range of vegetables and fruits, flavonoids form an integral part of the human diet and confer multiple health benefits.
Modifying flavonoid biosynthesis in fruit crops, such as apple, offers the opportunity to increase plant resistance against pathogens and the health benefit potential of the fruit.
Both overexpression and RNAi-based suppression strategies were used to modify flavonoid biosynthesis in apple.
Introducing the maize Lc transcription factor gene, responsible for controlling the expression of structural genes of the flavonoid biosynthetic pathway in maize, into Malus domestica Borkh. cv. ‘Holsteiner Cox’ resulted in increased mRNA levels for most of the structural genes of the flavonoid pathway. Lc transgenic plants accumulated higher levels of the anthocyanin idaein, the flavan-3-ols epicatechin, catechin, and some distinct dimeric proanthocyanidins.
In a second approach, the consequences of RNAi silencing of the genes for anthocyanidin synthase (ANS) and UDP-galactose:flavonoid 3-O-galactosyltransferase (FGT) gene to induce a shift towards flavan-3-ols were examined.
Preliminary results obtained from transgenic plants of the cv. ‘Holsteiner Cox’ and of the red-leaved type TNR 31-35 (a descendent from Malus sieversii var. sieversii f. niedzwetzkyana (Dieck)) revealed that suppression of ANS or FGT resulted in increased amounts of flavan-3-ols and flavonols.
In the red leaved type TNR 31-35, anthocyanin accumulation decreased after ANS silencing.

Publication
Authors
I. Szankowski, H. Li, H. Flachowsky, M. Höfer, M.-V. Hanke, T. Fischer, G. Forkmann, D. Treutter, W. Schwab, T. Hoffmann
Keywords
anthocyanidin synthase, Lc transcription factor, RNAi, transgenic apple, UDP-galactose:flavonoid 3-O-galactosyltransferase
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