| Enzymatic phosphatidylation of thiamin, pantothenic acid, and their derivatives. | |
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MedLine Citation:
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PMID: 18635914 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Phospholipase D from Streptomyces sp. was found to catalyze the transfer reaction of the dipalmitoylphosphatidyl residue from 1,2-dipalmitoyl-3-sn-phosphatidylcholine to thiamin, pantothenic acid, and their derivatives in a biphasic system. The following phosphatidylated compounds were synthesized: 1,2-dipalmitoyl-3-sn-phosphatidylthiamin, 1,2-dipalmitoyl-3-sn-phosphatidylthiamin propyl disulfide, 1,2-dipalmitoyl-3-sn-phosphatidylthiamin tetrahydrofurfuryl disulfide, 1,2-dipalmitoyl-3-sn-phosphatidylpantothenic acid, and 1,2-dipalmitoyl-3-sn-phosphatidyl-pantothenyl ethyl ether. |
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Authors:
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Naomi Hidaka; Masaaki Takami; Yukio Suzuki |
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Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: Journal of nutritional science and vitaminology Volume: 54 ISSN: 0301-4800 ISO Abbreviation: J. Nutr. Sci. Vitaminol. Publication Date: 2008 Jun |
Date Detail:
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Created Date: 2008-07-18 Completed Date: 2008-12-16 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 0402640 Medline TA: J Nutr Sci Vitaminol (Tokyo) Country: Japan |
Other Details:
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Languages: eng Pagination: 255-61 Citation Subset: IM |
Affiliation:
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Research Institute for Bioresources, Okayama University, Kurashiki, Japan. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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1,2-Dipalmitoylphosphatidylcholine
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chemical synthesis Catalysis Chromatography, Thin Layer Molecular Structure Pantothenic Acid / chemical synthesis*, chemistry Phosphatidylcholines / chemical synthesis Phospholipase D / chemistry* Thiamine / chemical synthesis*, chemistry Time Factors |
| Chemical | |
Reg. No./Substance:
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0/Phosphatidylcholines; 2644-64-6/1,2-Dipalmitoylphosphatidylcholine; 59-43-8/Thiamine; 79-83-4/Pantothenic Acid; EC 3.1.4.4/Phospholipase D |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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