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pubmed-article:8499446pubmed:abstractTextThe wax ester n-dodecyl palmitate is shown to be synthesized by retinal pigment epithelial membranes. The biosynthesis of this ester is phospholipid dependent and occurs via the transfer of a palmitoyl group from the sn-1 position of lecithin to n-dodecanol. When retinal pigment epithelial membranes are used as the source of enzyme, the apparent Michaelis constant for n-dodecanol in this process is 65.8 microM, and the maximal velocity for n-dodecyl palmitate synthesis is 16.2 nmol/(h.mg of protein). The enzymatic activity is membrane associated and shows a maximum velocity between pH8 and pH9. This transesterification process appears to be similar to the lecithin retinol acyl transferase reaction and is a further example of acyl group transfer reactions from the sn-1 position of phospholipids.lld:pubmed
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pubmed-article:8499446pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:8499446pubmed:articleTitleAcyl group transfer from the sn-1 position of phospholipids in the biosynthesis of n-dodecyl palmitate.lld:pubmed
pubmed-article:8499446pubmed:affiliationDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115.lld:pubmed
pubmed-article:8499446pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8499446pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed