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pubmed-article:15469740pubmed:dateCreated2004-10-7lld:pubmed
pubmed-article:15469740pubmed:abstractTextGlucose-1-phosphate uridylyltransferase from E. coli K12 was used to convert uridine-5'-triphosphate and glucose-1-phosphate to UDP-D-glucose. The conversion was efficient and completed within 5 minutes under the employed conditions. In addition, thymidine-5'-monophosphate kinase and acetate kinase were proven to be non-specific, converting udridine-5'-monophosphate to uridine-5'-triphosphate with 55% conversion after 6 h, which was much slower than the production of TTP under the same conditions (complete conversion within one hour). Since these two reactions could proceed under the same conditions, a one-pot synthesis of UDP-D-glucose with ATP regeneration was designed from easily available starting materials, and conversion up to 40% by HPLC peak integration was achieved given a reaction time of 4 h.lld:pubmed
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pubmed-article:15469740pubmed:authorpubmed-author:SohngJae...lld:pubmed
pubmed-article:15469740pubmed:authorpubmed-author:LeeHei ChanHClld:pubmed
pubmed-article:15469740pubmed:authorpubmed-author:LiouKwangkyou...lld:pubmed
pubmed-article:15469740pubmed:authorpubmed-author:LeeSeung-DonS...lld:pubmed
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pubmed-article:15469740pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15469740pubmed:year2004lld:pubmed
pubmed-article:15469740pubmed:articleTitleOne-pot enzymatic synthesis of UDP-D-glucose from UMP and glucose-1-phosphate using an ATP regeneration system.lld:pubmed
pubmed-article:15469740pubmed:affiliationInstitute of Biomolecule Reconstruction, Sun Moon University, Chungnam 336-708, Korea.lld:pubmed
pubmed-article:15469740pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15469740pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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