Abstract
The gene coding for isochorismate synthase (EC 5.4.99.6) was amplified by the polymerase chain reaction from Escherichia coli. cloned into a binary vector and mobilised into Agrobacterium rhizogenes LBA9402 which was used to transform Rubia peregrina. Transgenic roots containing bacterial isochorismate synthase cDNA expressed twice as much isochorismate synthase activity (4.88 pkat/mg protein) as the control roots (2.45 pkat/mg protein) after 10 days in culture, and accumulated ca. 20% higher levels of total anthraquinones after 30 days in culture. Whilst the amount of total alizarin (free and bound) in the transgenic roots was 30% higher than in control roots, the level of free alizarin was ca. 85% higher.
Original language | English |
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Pages (from-to) | 54-57 |
Number of pages | 4 |
Journal | Plant Cell Reports |
Volume | 16 |
Issue number | 1-2 |
Early online date | Nov 1996 |
DOIs | |
Publication status | E-pub ahead of print - Nov 1996 |
Keywords
- alizarin production
- isochorismate synthase
- Rubia peregrina
- transgenic roots