|
Plant Physiol, October 2000, Vol. 124, pp. 781-794
Production of the Isoflavones Genistein and Daidzein in
Non-Legume Dicot and Monocot Tissues
Oliver
Yu,
Woosuk
Jung,
June
Shi,
Robert A.
Croes,
Gary M.
Fader,
Brian
McGonigle, and
Joan T.
Odell*
Nutrition and Health, The DuPont Company, Experimental Station,
P.O. Box 80402, Wilmington, Delaware 19880-0402
Metabolic engineering for production of isoflavones in non-legume
plants may provide the health benefits of these phytoestrogens from
consumption of more widely used grains. In legumes, isoflavones function in both the symbiotic relationship with rhizobial bacteria and
the plant defense response. Expression of a soybean isoflavone synthase
(IFS) gene in Arabidopsis plants was previously shown to result in the
synthesis and accumulation of the isoflavone genistein in leaf and stem
tissue (Jung et al., 2000). Here we further investigate the ability of
the heterologous IFS enzyme to interact with the endogenous
phenylpropanoid pathway, which provides the substrate for IFS, and
produces genistein in several plant tissue systems. In tobacco
(Nicotiana tabacum) floral tissue that synthesizes
anthocyanins, genistein production was increased relative to leaves.
Induction of the flavonoid/anthocyanin branch of the phenylpropanoid
pathway through UV-B treatment also enhanced genistein production in
Arabidopsis. In a monocot cell system, introduced expression of a
transcription factor regulating genes of the anthocyanin pathway was
effective in conferring the ability to produce genistein in the
presence of the IFS gene. Introduction of a third gene, chalcone
reductase, provided the ability to synthesize an additional substrate
of IFS resulting in production of the isoflavone daidzein in this
system. The genistein produced in tobacco, Arabidopsis, and maize
(Zea mays) cells was present in conjugated forms,
indicating that endogenous enzymes were capable of recognizing
genistein as a substrate. This study provides insight into requirements
for metabolic engineering for isoflavone production in non-legume dicot
and monocot tissues.
*
Corresponding author; e-mail Joan.T.Odell{at}usa.dupont.com;
fax 302-695-4509.
© 2000 American Society of Plant Physiologists
This article has been cited by other articles:

|
 |

|
 |
 
M. Newell-McGloughlin
Nutritionally Improved Agricultural Crops
Plant Physiology,
July 1, 2008;
147(3):
939 - 953.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Shimamura, T. Akashi, N. Sakurai, H. Suzuki, K. Saito, D. Shibata, S.-i. Ayabe, and T. Aoki
2-Hydroxyisoflavanone Dehydratase is a Critical Determinant of Isoflavone Productivity in Hairy Root Cultures of Lotus japonicus
Plant Cell Physiol.,
November 1, 2007;
48(11):
1652 - 1657.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Zhang, S. Subramanian, Y. Zhang, and O. Yu
Flavone Synthases from Medicago truncatula Are Flavanone-2-Hydroxylases and Are Important for Nodulation
Plant Physiology,
June 1, 2007;
144(2):
741 - 751.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
N Wuyts, G Lognay, R Swennen, and D De Waele
Nematode infection and reproduction in transgenic and mutant Arabidopsis and tobacco with an altered phenylpropanoid metabolism
J. Exp. Bot.,
August 1, 2006;
57(11):
2825 - 2835.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
V. Sreevidya, C Srinivasa Rao, S. Sullia, J. K. Ladha, and P. M. Reddy
Metabolic engineering of rice with soybean isoflavone synthase for promoting nodulation gene expression in rhizobia
J. Exp. Bot.,
June 1, 2006;
57(9):
1957 - 1969.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. van der Rest, S. Danoun, A.-M. Boudet, and S. F. Rochange
Down-regulation of cinnamoyl-CoA reductase in tomato (Solanum lycopersicum L.) induces dramatic changes in soluble phenolic pools
J. Exp. Bot.,
March 1, 2006;
57(6):
1399 - 1411.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. E. Deavours and R. A. Dixon
Metabolic Engineering of Isoflavonoid Biosynthesis in Alfalfa
Plant Physiology,
August 1, 2005;
138(4):
2245 - 2259.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Subramanian, M. Y. Graham, O. Yu, and T. L. Graham
RNA Interference of Soybean Isoflavone Synthase Genes Leads to Silencing in Tissues Distal to the Transformation Site and to Enhanced Susceptibility to Phytophthora sojae
Plant Physiology,
April 1, 2005;
137(4):
1345 - 1353.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
L. Ralston, S. Subramanian, M. Matsuno, and O. Yu
Partial Reconstruction of Flavonoid and Isoflavonoid Biosynthesis in Yeast Using Soybean Type I and Type II Chalcone Isomerases
Plant Physiology,
April 1, 2005;
137(4):
1375 - 1388.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. D. Barabote, O. L. Johnson, E. Zetina, S. K. San Francisco, J. A. Fralick, and M. J. D. San Francisco
Erwinia chrysanthemi tolC Is Involved in Resistance to Antimicrobial Plant Chemicals and Is Essential for Phytopathogenesis
J. Bacteriol.,
October 1, 2003;
185(19):
5772 - 5778.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. A. Dixon and L. W. Sumner
Legume Natural Products: Understanding and Manipulating Complex Pathways for Human and Animal Health
Plant Physiology,
March 1, 2003;
131(3):
878 - 885.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
N. Shimada, T. Aoki, S. Sato, Y. Nakamura, S. Tabata, and S.-i. Ayabe
A Cluster of Genes Encodes the Two Types of Chalcone Isomerase Involved in the Biosynthesis of General Flavonoids and Legume-Specific 5-Deoxy(iso)flavonoids in Lotus japonicus
Plant Physiology,
March 1, 2003;
131(3):
941 - 951.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C.-J. Liu, J. W. Blount, C. L. Steele, and R. A. Dixon
Bottlenecks for metabolic engineering of isoflavone glycoconjugates in Arabidopsis
PNAS,
October 29, 2002;
99(22):
14578 - 14583.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Winkel-Shirley
It Takes a Garden. How Work on Diverse Plant Species Has Contributed to an Understanding of Flavonoid Metabolism
Plant Physiology,
December 1, 2001;
127(4):
1399 - 1404.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
X. Dong, E. L. Braun, and E. Grotewold
Functional Conservation of Plant Secondary Metabolic Enzymes Revealed by Complementation of Arabidopsis Flavonoid Mutants with Maize Genes
Plant Physiology,
September 1, 2001;
127(1):
46 - 57.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Winkel-Shirley
Flavonoid Biosynthesis. A Colorful Model for Genetics, Biochemistry, Cell Biology, and Biotechnology
Plant Physiology,
June 1, 2001;
126(2):
485 - 493.
[Full Text]
[PDF]
|
 |
|
|
|