Potential of Gas Chromatography−Orthogonal Acceleration Time-of-Flight Mass Spectrometry (GC-oaTOFMS) in Flavor Research
Gas chromatography−orthogonal acceleration time-of-flight mass spectrometry (GC-oaTOFMS) is an emerging technique offering a straightforward access to a resolving power up to 7000. This paper deals with the use of GC-oaTOFMS to identify the flavor components of a complex seafood flavor extract and t...
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Veröffentlicht in: | Journal of agricultural and food chemistry 2003-04, Vol.51 (9), p.2708-2713 |
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creator | Fay, Laurent B. Newton, Anthony Simian, Hervé Robert, Fabien Douce, David Hancock, Peter Green, Martin Blank, Imre |
description | Gas chromatography−orthogonal acceleration time-of-flight mass spectrometry (GC-oaTOFMS) is an emerging technique offering a straightforward access to a resolving power up to 7000. This paper deals with the use of GC-oaTOFMS to identify the flavor components of a complex seafood flavor extract and to quantify furanones formed in model Maillard reactions. A seafood extract was selected as a representative example for complex food flavors and was previously analyzed using GC−quadrupole MS, leaving several molecules unidentified. GC-oaTOFMS analysis was focused on these unknowns to evaluate its potential in flavor research, particularly for determining exact masses. N-Methyldithiodimethylamine, 6-methyl-5-hepten-2-one, and tetrahydro-2,4-dimethyl-4H-pyrrolo[2,1-d]-1,3,5-dithiazine were successfully identified on the basis of the precise mass determination of their molecular ions and their major fragments. A second set of experiments was performed to test the capabilities of the GC-oaTOFMS for quantification. Calibration curves were found to be linear over a dynamic range of 103 for the quantification of furanones. The quantitative data obtained using GC-oaTOFMS confirmed earlier results that the formation of 4-hydroxy-2,5-dimethyl-3(2H)-furanone was favored in the xylose/glycine model reaction and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in the xylose/alanine model reaction. It was concluded that GC-oaTOFMS may become a powerful analytical tool for the flavor chemist for both identification and quantification purposes, the latter in particular when combined with stable isotope dilution assay. Keywords: GC-oaTOFMS; flavor; furanones |
doi_str_mv | 10.1021/jf0261203 |
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This paper deals with the use of GC-oaTOFMS to identify the flavor components of a complex seafood flavor extract and to quantify furanones formed in model Maillard reactions. A seafood extract was selected as a representative example for complex food flavors and was previously analyzed using GC−quadrupole MS, leaving several molecules unidentified. GC-oaTOFMS analysis was focused on these unknowns to evaluate its potential in flavor research, particularly for determining exact masses. N-Methyldithiodimethylamine, 6-methyl-5-hepten-2-one, and tetrahydro-2,4-dimethyl-4H-pyrrolo[2,1-d]-1,3,5-dithiazine were successfully identified on the basis of the precise mass determination of their molecular ions and their major fragments. A second set of experiments was performed to test the capabilities of the GC-oaTOFMS for quantification. Calibration curves were found to be linear over a dynamic range of 103 for the quantification of furanones. The quantitative data obtained using GC-oaTOFMS confirmed earlier results that the formation of 4-hydroxy-2,5-dimethyl-3(2H)-furanone was favored in the xylose/glycine model reaction and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in the xylose/alanine model reaction. It was concluded that GC-oaTOFMS may become a powerful analytical tool for the flavor chemist for both identification and quantification purposes, the latter in particular when combined with stable isotope dilution assay. Keywords: GC-oaTOFMS; flavor; furanones</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf0261203</identifier><identifier>PMID: 12696961</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>alanine ; Animals ; Biological and medical sciences ; Calibration ; Chromatography, Gas - methods ; flavor ; Food industries ; Fundamental and applied biological sciences. Psychology ; Furans - analysis ; General aspects ; ions ; isotope dilution technique ; Maillard Reaction ; mass spectrometry ; Mass Spectrometry - methods ; Methods of analysis, processing and quality control, regulation, standards ; Seafood - analysis ; seafoods ; stable isotopes ; Taste ; xylose</subject><ispartof>Journal of agricultural and food chemistry, 2003-04, Vol.51 (9), p.2708-2713</ispartof><rights>Copyright © 2003 American Chemical Society</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a372t-af0d0f4da60d5049961121d0bedddc0cfa514f930c0356367c812e8cf01649973</citedby><cites>FETCH-LOGICAL-a372t-af0d0f4da60d5049961121d0bedddc0cfa514f930c0356367c812e8cf01649973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jf0261203$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf0261203$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14714980$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12696961$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fay, Laurent B.</creatorcontrib><creatorcontrib>Newton, Anthony</creatorcontrib><creatorcontrib>Simian, Hervé</creatorcontrib><creatorcontrib>Robert, Fabien</creatorcontrib><creatorcontrib>Douce, David</creatorcontrib><creatorcontrib>Hancock, Peter</creatorcontrib><creatorcontrib>Green, Martin</creatorcontrib><creatorcontrib>Blank, Imre</creatorcontrib><title>Potential of Gas Chromatography−Orthogonal Acceleration Time-of-Flight Mass Spectrometry (GC-oaTOFMS) in Flavor Research</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Gas chromatography−orthogonal acceleration time-of-flight mass spectrometry (GC-oaTOFMS) is an emerging technique offering a straightforward access to a resolving power up to 7000. This paper deals with the use of GC-oaTOFMS to identify the flavor components of a complex seafood flavor extract and to quantify furanones formed in model Maillard reactions. A seafood extract was selected as a representative example for complex food flavors and was previously analyzed using GC−quadrupole MS, leaving several molecules unidentified. GC-oaTOFMS analysis was focused on these unknowns to evaluate its potential in flavor research, particularly for determining exact masses. N-Methyldithiodimethylamine, 6-methyl-5-hepten-2-one, and tetrahydro-2,4-dimethyl-4H-pyrrolo[2,1-d]-1,3,5-dithiazine were successfully identified on the basis of the precise mass determination of their molecular ions and their major fragments. A second set of experiments was performed to test the capabilities of the GC-oaTOFMS for quantification. Calibration curves were found to be linear over a dynamic range of 103 for the quantification of furanones. The quantitative data obtained using GC-oaTOFMS confirmed earlier results that the formation of 4-hydroxy-2,5-dimethyl-3(2H)-furanone was favored in the xylose/glycine model reaction and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in the xylose/alanine model reaction. It was concluded that GC-oaTOFMS may become a powerful analytical tool for the flavor chemist for both identification and quantification purposes, the latter in particular when combined with stable isotope dilution assay. Keywords: GC-oaTOFMS; flavor; furanones</description><subject>alanine</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Calibration</subject><subject>Chromatography, Gas - methods</subject><subject>flavor</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Furans - analysis</subject><subject>General aspects</subject><subject>ions</subject><subject>isotope dilution technique</subject><subject>Maillard Reaction</subject><subject>mass spectrometry</subject><subject>Mass Spectrometry - methods</subject><subject>Methods of analysis, processing and quality control, regulation, standards</subject><subject>Seafood - analysis</subject><subject>seafoods</subject><subject>stable isotopes</subject><subject>Taste</subject><subject>xylose</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0c1uEzEQB3ALgWgoHHgB8KUSPWw7sx_e3WO1JQGpVSqSnq2p185u2Kwj20WEJ-DMI_IkuErUXJAPPszPM_bfjL1HuEBI8XJtIBWYQvaCTbBIISkQq5dsArGYVIXAE_bG-zUAVEUJr9kJpqKOCyfs150Negw9DdwaPiPPm87ZDQW7crTtdn9__5m70NmVHSO5UkoP2lHo7ciX_UYn1iTToV91gd-S93yx1SrE8zq4Hf80axJLy_n0dnHO-5FPB_phHf-mvSanurfslaHB63eH_ZTdTz8vmy_JzXz2tbm6SSgr05CQgRZM3pKAtoC8jtfGFFt40G3bKlCGCsxNnYGCrBCZKFWFqa6UARRRl9kpO9_3Vc5677SRW9dvyO0kgnzKTz7nF-2Hvd0-Pmx0e5SHwCI4OwDyigbjaFS9P7q8xLyuILpk73of9M_nOrnvUpRZWcjl3UJeiwYLhGv5NPjj3huyklYu9rxfpIA5AGJZ1eI4mZSXa_vo4of4_zzhHxcVm_c</recordid><startdate>20030423</startdate><enddate>20030423</enddate><creator>Fay, Laurent B.</creator><creator>Newton, Anthony</creator><creator>Simian, Hervé</creator><creator>Robert, Fabien</creator><creator>Douce, David</creator><creator>Hancock, Peter</creator><creator>Green, Martin</creator><creator>Blank, Imre</creator><general>American Chemical Society</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20030423</creationdate><title>Potential of Gas Chromatography−Orthogonal Acceleration Time-of-Flight Mass Spectrometry (GC-oaTOFMS) in Flavor Research</title><author>Fay, Laurent B. ; Newton, Anthony ; Simian, Hervé ; Robert, Fabien ; Douce, David ; Hancock, Peter ; Green, Martin ; Blank, Imre</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a372t-af0d0f4da60d5049961121d0bedddc0cfa514f930c0356367c812e8cf01649973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>alanine</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Calibration</topic><topic>Chromatography, Gas - methods</topic><topic>flavor</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Furans - analysis</topic><topic>General aspects</topic><topic>ions</topic><topic>isotope dilution technique</topic><topic>Maillard Reaction</topic><topic>mass spectrometry</topic><topic>Mass Spectrometry - methods</topic><topic>Methods of analysis, processing and quality control, regulation, standards</topic><topic>Seafood - analysis</topic><topic>seafoods</topic><topic>stable isotopes</topic><topic>Taste</topic><topic>xylose</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fay, Laurent B.</creatorcontrib><creatorcontrib>Newton, Anthony</creatorcontrib><creatorcontrib>Simian, Hervé</creatorcontrib><creatorcontrib>Robert, Fabien</creatorcontrib><creatorcontrib>Douce, David</creatorcontrib><creatorcontrib>Hancock, Peter</creatorcontrib><creatorcontrib>Green, Martin</creatorcontrib><creatorcontrib>Blank, Imre</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fay, Laurent B.</au><au>Newton, Anthony</au><au>Simian, Hervé</au><au>Robert, Fabien</au><au>Douce, David</au><au>Hancock, Peter</au><au>Green, Martin</au><au>Blank, Imre</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potential of Gas Chromatography−Orthogonal Acceleration Time-of-Flight Mass Spectrometry (GC-oaTOFMS) in Flavor Research</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2003-04-23</date><risdate>2003</risdate><volume>51</volume><issue>9</issue><spage>2708</spage><epage>2713</epage><pages>2708-2713</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Gas chromatography−orthogonal acceleration time-of-flight mass spectrometry (GC-oaTOFMS) is an emerging technique offering a straightforward access to a resolving power up to 7000. This paper deals with the use of GC-oaTOFMS to identify the flavor components of a complex seafood flavor extract and to quantify furanones formed in model Maillard reactions. A seafood extract was selected as a representative example for complex food flavors and was previously analyzed using GC−quadrupole MS, leaving several molecules unidentified. GC-oaTOFMS analysis was focused on these unknowns to evaluate its potential in flavor research, particularly for determining exact masses. N-Methyldithiodimethylamine, 6-methyl-5-hepten-2-one, and tetrahydro-2,4-dimethyl-4H-pyrrolo[2,1-d]-1,3,5-dithiazine were successfully identified on the basis of the precise mass determination of their molecular ions and their major fragments. A second set of experiments was performed to test the capabilities of the GC-oaTOFMS for quantification. Calibration curves were found to be linear over a dynamic range of 103 for the quantification of furanones. The quantitative data obtained using GC-oaTOFMS confirmed earlier results that the formation of 4-hydroxy-2,5-dimethyl-3(2H)-furanone was favored in the xylose/glycine model reaction and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in the xylose/alanine model reaction. It was concluded that GC-oaTOFMS may become a powerful analytical tool for the flavor chemist for both identification and quantification purposes, the latter in particular when combined with stable isotope dilution assay. Keywords: GC-oaTOFMS; flavor; furanones</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>12696961</pmid><doi>10.1021/jf0261203</doi><tpages>6</tpages></addata></record> |
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subjects | alanine Animals Biological and medical sciences Calibration Chromatography, Gas - methods flavor Food industries Fundamental and applied biological sciences. Psychology Furans - analysis General aspects ions isotope dilution technique Maillard Reaction mass spectrometry Mass Spectrometry - methods Methods of analysis, processing and quality control, regulation, standards Seafood - analysis seafoods stable isotopes Taste xylose |
title | Potential of Gas Chromatography−Orthogonal Acceleration Time-of-Flight Mass Spectrometry (GC-oaTOFMS) in Flavor Research |
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