Stereochemical specificity of the biosynthesis of the alkyl ether bond in alkyl ether lipids.
Open Access
- 1 June 1979
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 254 (11) , 4760-4763
- https://doi.org/10.1016/s0021-9258(17)30078-9
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Absolute configuration of tritiated O-alkyl glycerol synthesized enzymically from [1,3-3H2, 1,3-14C2]dihydroxyacetone phosphateBiochemistry, 1977
- Hydrogen exchange in the synthesis of glyceryl ether and in the formation of dihydroxyacetone in Tetrahymena pyriformisBiochemistry, 1973
- Mechanism of O-alkyl lipid synthesisBiochemistry, 1972
- Acyl dihydroxyacetone phosphate: Precursor of alkyl ethersBiochemical and Biophysical Research Communications, 1970
- Biosynthesis of alkyl-ether containing lipid from dihydroxyacetone phosphateBiochemical and Biophysical Research Communications, 1969
- Biosynthesis of phosphatidic acid from dihydroxyacetone phosphateBiochemical and Biophysical Research Communications, 1968
- Studies in stereochemistry. XXXVII. Open-chain models for 1,3-asymmetric induction in stereospecific addition polymerizationJournal of the American Chemical Society, 1968
- Mitochondrial triose phosphate isomeraseBiochimica et Biophysica Acta, 1960
- The Absolute Configuration of Dihydroxyacetone Phosphate Tritiated by Aldolase Reaction1Journal of the American Chemical Society, 1958
- Mechanism of Action of Aldolase and Phosphotriose IsomeraseScience, 1956