Literature DB >> 3815628

Conversion of radiolabelled ethanolamine plasmalogen into the dimethylethanolamine and choline analogue via transphosphatidylation by phospholipase D from cabbage.

V Achterberg, H Fricke, G Gercken.   

Abstract

Starting from biosynthetically prepared ethanolamine plasmalogen 14C-labelled in the O-alkenyl moiety, choline and dimethylethanolamine plasmalogen were prepared by transphosphatidylation utilizing phospholipase D from cabbage. Investigation of the time course of the reaction showed that transphosphatidylation was simultaneously accompanied by hydrolysis of both the substrate and the desired product, resulting in a maximum of product yield after 1-3 h under the reaction conditions investigated. Optimal reaction conditions gave yields of 40% and 62% (of total radioactivity) respectively for the purified choline and dimethylethanolamine derivatives.

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Year:  1986        PMID: 3815628     DOI: 10.1016/0009-3084(86)90032-0

Source DB:  PubMed          Journal:  Chem Phys Lipids        ISSN: 0009-3084            Impact factor:   3.329


  1 in total

1.  Synthesis of 6-phosphatidyl-L-ascorbic acid by phospholipase D.

Authors:  A Nagao; N Ishida; J Terao
Journal:  Lipids       Date:  1991-05       Impact factor: 1.880

  1 in total

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