Gas chromatography of sugar phosphates and sugar nucleotides
Glucose 6-phosphate, various aldose 1-phosphates, and their corresponding sugar nucleotides have been converted into trimethylsilyl ethers and gas chromatographed. Glucose 6-phosphate separates into α- and β-isomers and can be recovered intact on a preparative scale from the column effluent after sp...
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Veröffentlicht in: | Analytical biochemistry 1969-05, Vol.29 (2), p.284-292 |
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creator | Eisenberg, Frank Bolden, Arthur H. |
description | Glucose 6-phosphate, various aldose 1-phosphates, and their corresponding sugar nucleotides have been converted into trimethylsilyl ethers and gas chromatographed. Glucose 6-phosphate separates into α- and β-isomers and can be recovered intact on a preparative scale from the column effluent after spontaneous hydrolysis of the ether linkages. The aldose 1-phosphates and sugar nucleotides are not recoverable intact from the column but lose phosphoric acid and nucleoside diphosphate, respectively, to yield the TMS ether of the sugar anhydride. Since the anhydride patterns are reproducibly characteristic, mixtures of nucleotides can be easily separated and their sugar components identified. |
doi_str_mv | 10.1016/0003-2697(69)90311-X |
format | Article |
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Glucose 6-phosphate separates into α- and β-isomers and can be recovered intact on a preparative scale from the column effluent after spontaneous hydrolysis of the ether linkages. The aldose 1-phosphates and sugar nucleotides are not recoverable intact from the column but lose phosphoric acid and nucleoside diphosphate, respectively, to yield the TMS ether of the sugar anhydride. Since the anhydride patterns are reproducibly characteristic, mixtures of nucleotides can be easily separated and their sugar components identified.</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1016/0003-2697(69)90311-X</identifier><identifier>PMID: 5792565</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Chromatography, Gas ; Ethers ; Fructose ; Galactose ; Glucose ; Hexosephosphates - analysis ; Temperature ; Uracil Nucleotides - analysis</subject><ispartof>Analytical biochemistry, 1969-05, Vol.29 (2), p.284-292</ispartof><rights>1969</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-2d9891ce35882705440e11806d660b62952ef198293aa85785998962ced020de3</citedby><cites>FETCH-LOGICAL-c357t-2d9891ce35882705440e11806d660b62952ef198293aa85785998962ced020de3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0003-2697(69)90311-X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/5792565$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eisenberg, Frank</creatorcontrib><creatorcontrib>Bolden, Arthur H.</creatorcontrib><title>Gas chromatography of sugar phosphates and sugar nucleotides</title><title>Analytical biochemistry</title><addtitle>Anal Biochem</addtitle><description>Glucose 6-phosphate, various aldose 1-phosphates, and their corresponding sugar nucleotides have been converted into trimethylsilyl ethers and gas chromatographed. Glucose 6-phosphate separates into α- and β-isomers and can be recovered intact on a preparative scale from the column effluent after spontaneous hydrolysis of the ether linkages. The aldose 1-phosphates and sugar nucleotides are not recoverable intact from the column but lose phosphoric acid and nucleoside diphosphate, respectively, to yield the TMS ether of the sugar anhydride. Since the anhydride patterns are reproducibly characteristic, mixtures of nucleotides can be easily separated and their sugar components identified.</description><subject>Chromatography, Gas</subject><subject>Ethers</subject><subject>Fructose</subject><subject>Galactose</subject><subject>Glucose</subject><subject>Hexosephosphates - analysis</subject><subject>Temperature</subject><subject>Uracil Nucleotides - analysis</subject><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1969</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFLw0AQhRdRaq3-A4WcRA_R2U12kwURpGgVCl4Uelu2m0kTSbJxNxH6701t6NHTwMx7b2Y-Qi4p3FGg4h4AopAJmdwIeSshojRcHZEpBSlCiEAek-lBckrOvP8CoDTmYkImPJGMCz4lDwvtA1M4W-vObpxui21g88D3G-2CtrC-LXSHPtBNNjab3lRouzJDf05Ocl15vBjrjHy-PH_MX8Pl--Jt_rQMTcSTLmSZTCU1GPE0ZQnwOAakNAWRCQFrwSRnmFOZMhlpnfIk5XIwCGYwAwYZRjNyvc9tnf3u0XeqLr3BqtIN2t6rNKaJ5BEfhPFeaJz13mGuWlfW2m0VBbWDpnZE1I6IElL9QVOrwXY15vfrGrODaaQ0zB_3cxye_CnRKW9KbIb7SoemU5kt_1_wC70cee8</recordid><startdate>196905</startdate><enddate>196905</enddate><creator>Eisenberg, Frank</creator><creator>Bolden, Arthur H.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>196905</creationdate><title>Gas chromatography of sugar phosphates and sugar nucleotides</title><author>Eisenberg, Frank ; Bolden, Arthur H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-2d9891ce35882705440e11806d660b62952ef198293aa85785998962ced020de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1969</creationdate><topic>Chromatography, Gas</topic><topic>Ethers</topic><topic>Fructose</topic><topic>Galactose</topic><topic>Glucose</topic><topic>Hexosephosphates - analysis</topic><topic>Temperature</topic><topic>Uracil Nucleotides - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eisenberg, Frank</creatorcontrib><creatorcontrib>Bolden, Arthur H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eisenberg, Frank</au><au>Bolden, Arthur H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gas chromatography of sugar phosphates and sugar nucleotides</atitle><jtitle>Analytical biochemistry</jtitle><addtitle>Anal Biochem</addtitle><date>1969-05</date><risdate>1969</risdate><volume>29</volume><issue>2</issue><spage>284</spage><epage>292</epage><pages>284-292</pages><issn>0003-2697</issn><eissn>1096-0309</eissn><abstract>Glucose 6-phosphate, various aldose 1-phosphates, and their corresponding sugar nucleotides have been converted into trimethylsilyl ethers and gas chromatographed. Glucose 6-phosphate separates into α- and β-isomers and can be recovered intact on a preparative scale from the column effluent after spontaneous hydrolysis of the ether linkages. The aldose 1-phosphates and sugar nucleotides are not recoverable intact from the column but lose phosphoric acid and nucleoside diphosphate, respectively, to yield the TMS ether of the sugar anhydride. Since the anhydride patterns are reproducibly characteristic, mixtures of nucleotides can be easily separated and their sugar components identified.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>5792565</pmid><doi>10.1016/0003-2697(69)90311-X</doi><tpages>9</tpages></addata></record> |
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subjects | Chromatography, Gas Ethers Fructose Galactose Glucose Hexosephosphates - analysis Temperature Uracil Nucleotides - analysis |
title | Gas chromatography of sugar phosphates and sugar nucleotides |
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