Camptotheca SLAS
Authors/Creators
- 1. Department of Chemistry, University of Illinois at Urbana-Champaign, 1201 W. Gregory Dr., 162 Edward R. Madigan Laboratory (ERML), Urbana, IL, 61801, USA
Description
For initial analyses, the Camptotheca CYP 72A564, CYP72A565, CYP72A730 and Catharanthus CYP 72A1v3 were expressed in the WAT11 and WAT21 yeast strains, which have been engineered to constitutively express ATR1 or ATR2, respectively (Urban et al., 1997). HPLC analyses of in vitro assays conducted with yeast microsomes followed by LC-MS analyses indicated that, not unexpectedly, both Camptotheca CYP 72A564 and CYP72A565 expressed in the WAT11 and WAT21 yeast strains converted loganic acid into secologanic acid (Fig. 3, S 1, S 4, S 5). In addition, both of these Camptotheca enzymes also converted loganin into secologanin (detected as its sodium salt). Catharanthus CYP 72A1v3 expressed in the WAT11 and WAT21 strains converted only loganin into secologanin and secoxyloganin (Fig. S1, S 2, S 3). In contrast, the more divergent Camptotheca CYP 72A730 expressed in the WAT11 and WAT21 strains failed to metabolize either loganic acid or loganin (Fig. 3, S 1, S 6).
Notes
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Linked records
Additional details
Identifiers
Biodiversity
- Scientific name authorship
- SLAS
- Kingdom
- Plantae
- Phylum
- Tracheophyta
- Order
- Cornales
- Family
- Nyssaceae
- Genus
- Camptotheca
- Taxon rank
- genus
References
- Urban, P., Mignotte, C., Kazmaier, M., Delorme, F., Pompon, D., 1997. Cloning, yeast expression, and characterization of the coupling of two distantly related Arabidopsis thaliana NADPH-cytochrome P 450 reductases with P 450 CYP 73 A 5. J. Biol. Chem. 272 https: // doi. org / 10.1074 / jbc. 272.31.19176, 19176 - 19186.