pubmed-article:8499446 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8499446 | lifeskim:mentions | umls-concept:C0031676 | lld:lifeskim |
pubmed-article:8499446 | lifeskim:mentions | umls-concept:C0733755 | lld:lifeskim |
pubmed-article:8499446 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
pubmed-article:8499446 | lifeskim:mentions | umls-concept:C1705822 | lld:lifeskim |
pubmed-article:8499446 | lifeskim:mentions | umls-concept:C0348011 | lld:lifeskim |
pubmed-article:8499446 | lifeskim:mentions | umls-concept:C0659254 | lld:lifeskim |
pubmed-article:8499446 | lifeskim:mentions | umls-concept:C0596038 | lld:lifeskim |
pubmed-article:8499446 | pubmed:issue | 20 | lld:pubmed |
pubmed-article:8499446 | pubmed:dateCreated | 1993-6-29 | lld:pubmed |
pubmed-article:8499446 | pubmed:abstractText | The 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 |
pubmed-article:8499446 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8499446 | pubmed:language | eng | lld:pubmed |
pubmed-article:8499446 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8499446 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:8499446 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8499446 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8499446 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8499446 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8499446 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8499446 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8499446 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8499446 | pubmed:month | May | lld:pubmed |
pubmed-article:8499446 | pubmed:issn | 0006-2960 | lld:pubmed |
pubmed-article:8499446 | pubmed:author | pubmed-author:RandoR RRR | lld:pubmed |
pubmed-article:8499446 | pubmed:author | pubmed-author:NyoM MMM | lld:pubmed |
pubmed-article:8499446 | pubmed:author | pubmed-author:FuruyoshiSS | lld:pubmed |
pubmed-article:8499446 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8499446 | pubmed:day | 25 | lld:pubmed |
pubmed-article:8499446 | pubmed:volume | 32 | lld:pubmed |
pubmed-article:8499446 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8499446 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8499446 | pubmed:pagination | 5425-30 | lld:pubmed |
pubmed-article:8499446 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:8499446 | pubmed:year | 1993 | lld:pubmed |
pubmed-article:8499446 | pubmed:articleTitle | Acyl group transfer from the sn-1 position of phospholipids in the biosynthesis of n-dodecyl palmitate. | lld:pubmed |
pubmed-article:8499446 | pubmed:affiliation | Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115. | lld:pubmed |
pubmed-article:8499446 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:8499446 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |