Formation de l'acide pipécolique chez Triglochin maritima
- 1 June 1976
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Botany
- Vol. 54 (11) , 1221-1227
- https://doi.org/10.1139/b76-132
Abstract
Radioactive D-lysine supplied to Triglochin maritima L. shoots can be utilized without configuration inversion. The pipecolic acid is the most radioactive compound. It would be synthetized via the α-ceto-ε-aminocaproïc acid.In the plant, L-lysine can be partly converted into D-lysine; however, the data obtained in the presence of L-[3H1-lysine suggest the possibility of a direct transformation of the L-isomer into pipecolic acid via the adipic semialdehyde.In all cases, the labelled pipecolic acid is the L-enantiomer that is more radioactive in presence of sodium chloride.This publication has 0 references indexed in Scilit: