The mechanism of alkyldihydroxyacetone-P synthase. Formation of [3H]H2O from acyl[1-R-3H]dihydroxyacetone-P by purified alkyldihydroxyacetone-P synthase in the absence of acylhydrolase activity.

This publication has 28 references indexed in Scilit:

• Absolute configuration of tritiated O-alkyl glycerol synthesized enzymically from [1,3-³H₂, 1,3-¹⁴C₂]dihydroxyacetone phosphate
  Biochemistry, 1977
• A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
  Analytical Biochemistry, 1976
• Hydrogen exchange in the synthesis of glyceryl ether and in the formation of dihydroxyacetone in Tetrahymena pyriformis
  Biochemistry, 1973
• Synthesis of Acyl Dihydroxyacetone Phosphates and Related Derivatives
  Journal of Pharmaceutical Sciences, 1972
• Mechanism of O-alkyl lipid synthesis
  Biochemistry, 1972
• Specificities of alkaline and acid phosphatases in the dephosphorylation of phospholipids
  Biochemistry, 1970
• Acyl dihydroxyacetone phosphate: Precursor of alkyl ethers
  Biochemical and Biophysical Research Communications, 1970
• Haloacetol phosphates. Potential active-site reagents for aldolase, triose phosphate isomerase, and glycerophosphate dehydrogenase. I. Preparation and properties
  Biochemistry, 1970
• PERIODATE–PERMANGANATE OXIDATIONS: V. OXIDATION OF LIPIDS IN MEDIA CONTAINING ORGANIC SOLVENTS
  Canadian Journal of Chemistry, 1956
• Syntheses of Derivatives of Dihydroxyacetone and of Glycerides^1,2
  Journal of the American Chemical Society, 1952