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Plant Physiology 66:649-655 (1980)
© 1980 American Society of Plant Biologists

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Articles

Biosynthesis of C20 and C22 Fatty Acids by Developing Seeds of Limnanthes alba

CHAIN ELONGATION AND {Delta}5 DESATURATION1

Michael R. Pollard2 and Paul K. Stumpf

Department of Biochemistry and Biophysics, University of California, Davis, California 95616

The storage triacylglycerols of meadowfoam (Limnanthes alba) seeds are composed essentially of C20 and C22 fatty acids, which contain an unusual {Delta}5 double bond. When [1-14C]acetate was incubated with developing seed slices, 14C-labeled fatty acids were synthesized with a distribution similar to the endogenous fatty acid profile. The major labeled product was cis-5-eicosenoate, with smaller amounts of palmitate, stearate, oleate, cis-5-octadecenoate, eicosanoate, cis-11-eicosenoate, docosanoate, cis-5-docosenoate, cis-13-docosenoate, and cis-5,cis-13-docosadienoate. The label from [14C]acetate and [14C]malonate was used preferentially for the elongation of endogenous oleate to produce cis-[14C]11-eicosenoate, cis-13-[14C]docosenoate, and cis-5,cis-13-[14C]docosadienoate and for the elongation of endogenous palmitate to produce the remaining C20 and C22 acyl species. The {Delta}5 desaturation of the preformed acyl chain and chain elongation of oleate and palmitate were demonstrated in vivo by incubation of the appropriate 1-14C-labeled free fatty acids. Using [1-14C]acyl-CoA thioesters as substrates, these enzyme activities were also demonstrated in vitro with a cell-free homogenate.


2 Present address: Department of Biochemistry, Medical Sciences Institute, The University, Dundee, DD1 4HN, Scotland, United Kingdom

1 This work was supported by Grant PCM 76 01495 from the National Science Foundation administered by P. K. S.




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