Plant and Cell Physiology Advance Access originally published online on October 4, 2007
Plant and Cell Physiology 2007 48(11):1652-1657; doi:10.1093/pcp/pcm125
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Short Communication |
2-Hydroxyisoflavanone Dehydratase is a Critical Determinant of Isoflavone Productivity in Hairy Root Cultures of Lotus japonicus
1Department of Applied Biological Sciences, Nihon University, Fujisawa, Kanagawa, 252-8510 Japan
2Kazusa DNA Research Institute, Kisarazu, Chiba, 292-0818 Japan and
3Graduate School of Pharmaceutical Sciences, Chiba University, Chiba, 263-8522 Japan
*Corresponding author: E-mail, taoki{at}brs.nihon-u.ac.jp; Fax, +81-466-84-3353.
| Abstract |
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Hairy root cultures of a model legume, Lotus japonicus, were established to characterize two heterologous cDNAs encoding enzymes involved in isoflavone biosynthesis, i.e. licorice 2-hydroxyisoflavanone synthase (IFS) and soybean 2-hydroxyisoflavanone dehydratase (HID) catalyzing sequential reactions to yield isoflavones. While the control and the IFS overexpressor did not accumulate detectable isoflavones, the HID overexpressors did accumulate daidzein and genistein, showing that HID is a critical determinant of isoflavone productivity. Production of coumestrol in all the genotypes and isoliquiritigenin/liquiritigenin in IFS + HID-overexpressing lines was also noted. These results provide insight into the regulatory mechanism that controls isoflavonoid biosynthesis.
Keywords: Biosynthesis - Hairy root - 2-Hydroxyisoflavanone synthase - 2-Hydroxyisoflavanone dehydratase - Isoflavone - Lotus japonicus
Abbreviations: GSH, reduced glutathione; GUS, β-glucuronidase; IFS, 2-hydroxyisoflavanone synthatase; HI4'OMT, 2-hydroxyisoflavanone 4'-O-methyltransferase; HID, 2-hydroxyisoflavanone dehydratase; LC-FTICR/MS, liquid chromatography-Fourier transform cyclotron resonance/mass spectrometry; RT–PCR, reverse transcription–PCR.
(Received July 18, 2007; Accepted September 28, 2007)
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