The biosynthesis of squalene in germinating the seeds of Pisum sativum

Capstack, E.; Baisted, D.J.; Newschwander, W.W.; Blondin, G.; Rosin, N.L.; Nes, W.R.

Biochemistry 1(6): 1178-1183

1962


ISSN/ISBN: 0006-2960
Accession: 025692548

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Abstract
The biosynthesis of squalene has been demonstrated in peas (Pisum sativum) in two different ways. The first of these involved germination of the seeds for a 5-day period in the presence of a large amount of mevalonic acid. The squalene, which was produced in a 40% yield, was identified by several physical and chemical properties. The second way in which squalene was experimentally biosynthesized was through a very short (24 hours) germination in the presence of a small quantity of 2-Cl4-mevalonic acid. The radioactive hydrocarbon was produced in a 38% yield and was identified by conversion to the hexahydrochloride and co-crystallization with a standard sample until constant specific activity was reached. Furthermore, the radioactive squalene was incubated with a rat liver homogenate, and radioactive cholesterol (purified through the dibromide) was produced in a 7% yield. This work represents the first experimentally achieved biosynthesis of squalene in a flowering plant, and it gives credence to the previous assumption that the β-amyrin and β-sitosterol biosynthesized in peas arise by hydroxylative cyclization of this hydrocarbon. Evidence is presented which indicates that isopentenoid biosynthesis is regulated physiologically by the control of mevalonic acid formation.