The stereochemistry of phytoene biosynthesis
- 18 January 1966
- journal article
- Published by The Royal Society in Proceedings of the Royal Society of London. B. Biological Sciences
- Vol. 163 (993) , 515-518
- https://doi.org/10.1098/rspb.1966.0005
Abstract
Experiments with carrot root preparations have demonstrated that all the eliminations of hydrogen at C-4 of mevalonic acid during its conversion into phytoene have the same stereospecificity; the 4-R hydrogen is retained and the 4S hydrogen is eliminated. The same stereospecific elimination is also involved in squalene formation in carrot slices.Keywords
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