Abstract
Isotopic labelling experiments have been carried out in Dautura stramonium root cultures with the Following isotopically labelled precursors; [H-2(3)]-, [2-C-13, H-2(3)], [1-C-13, O-18(2)]-acetates, 2H(2)O, [H-2(3)-methyl]-methionine, [2-C-13]-phenyllacetate, [3-H-3]-tropine and [2'-C-13, 3-H-2]-littorine. The study explored the incorporation of isotope into the tropane ring system of littorine 1 and hyoscyamine 2 and revealed that deuterium from acetate is incorporated only into C-6 and C-7, and not into C-2 and C-4 as previously reported. Oxygen-18 was not retained at a detectable level into the C(3)-O bond from [1-C-13, O-18(2)]-acetate. The intramolecular nature of the rearrangement of littorine 1 to hyoscyamine 2 is revealed again by a labelling study using [2'-C-13, 3-H-2]-littorine, [2-C-13]-phenyllactate and [3-H-2]-tropine. (C) 2000 Elsevier Science Ltd. All rights reserved.
Original language | English |
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Volume | 53 |
Publication status | Published - Apr 2000 |
Keywords
- Datura stramonium
- biosynthesis
- tropane alkaloids
- hyoscyamine
- littorine
- TROPIC ACID
- HYOSCYAMUS-ALBUS
- ROOT CULTURES
- OXYGEN-ATOMS
- REARRANGEMENT
- INTERMEDIATE
- ORIGIN