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Pyrazine Formation from Amino Acids and Reducing Sugars, a Pathway Other than Strecker Degradation
Because the reaction of acyloins with ammonia generates pyrazines and acyloins are not involved with Strecker degradation, this study uses acetoin (a simple acyloin, from sugar degradation) to react with amino acids to determine whether ammonia is released, leading to the formation of tetramethylpyr...
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Published in: | Journal of agricultural and food chemistry 1998-04, Vol.46 (4), p.1515-1517 |
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container_title | Journal of agricultural and food chemistry |
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creator | Shu, Chi-Kuen |
description | Because the reaction of acyloins with ammonia generates pyrazines and acyloins are not involved with Strecker degradation, this study uses acetoin (a simple acyloin, from sugar degradation) to react with amino acids to determine whether ammonia is released, leading to the formation of tetramethylpyrazine. The results show that all reactions between α-amino acids and acetoin generate not only tetramethylpyrazine but also the corresponding Strecker aldehydes. However, the reactions between β-, γ-, or ε-amino acid and acetoin generate only tetramethylpyrazine. Quantitative analysis shows that among such reactions, both α- and β-amino acids generate significantly higher amounts of tetramethylpyrazine than γ- and ε-amino acids. On the basis of these data, it is proposed mechanistically that α-amino acids decarbonylate to generate the reactive intermediates, 1-hydroxyamines, deamination of which leads to the formation of the Strecker aldehydes. This study demonstrates that pyrazines and Strecker aldehydes are also formed from α-amino acids and reducing sugar via deamination in addition to their formation via the well-known Strecker degradation. Keywords: Strecker degradation; pyrazine formation; deamination; decarbonylation; acyloin; α-amino acid; β-amino acid; γ-amino acid; ε-amino acid; Strecker aldehyde |
doi_str_mv | 10.1021/jf970999i |
format | article |
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The results show that all reactions between α-amino acids and acetoin generate not only tetramethylpyrazine but also the corresponding Strecker aldehydes. However, the reactions between β-, γ-, or ε-amino acid and acetoin generate only tetramethylpyrazine. Quantitative analysis shows that among such reactions, both α- and β-amino acids generate significantly higher amounts of tetramethylpyrazine than γ- and ε-amino acids. On the basis of these data, it is proposed mechanistically that α-amino acids decarbonylate to generate the reactive intermediates, 1-hydroxyamines, deamination of which leads to the formation of the Strecker aldehydes. This study demonstrates that pyrazines and Strecker aldehydes are also formed from α-amino acids and reducing sugar via deamination in addition to their formation via the well-known Strecker degradation. Keywords: Strecker degradation; pyrazine formation; deamination; decarbonylation; acyloin; α-amino acid; β-amino acid; γ-amino acid; ε-amino acid; Strecker aldehyde</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf970999i</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>ACETOIN ; ACYLOINS ; ALDEHYDES ; ALPHA-AMINOBUTYRIC ACID ; AMINO ACIDS ; BETA-AMINOBUTYRIC ACID ; Biological and medical sciences ; CHEMICAL REACTIONS ; DEAMINATION ; EPSILON-AMINOHEXANOIC ACID ; FLAVOUR COMPOUNDS ; Food industries ; Fundamental and applied biological sciences. Psychology ; GABA ; GAMMA-AMINOBUTYRIC ACID ; General aspects ; Miscellaneous ; NONPROTEIN AMINO ACIDS ; PYRAZINES ; QUANTITATIVE ANALYSIS ; REACTION PRODUCTS ; REDUCING SUGARS ; STRECKER ALDEHYDE</subject><ispartof>Journal of agricultural and food chemistry, 1998-04, Vol.46 (4), p.1515-1517</ispartof><rights>Copyright © 1998 American Chemical Society</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a412t-478bb3cadaf90ec41c948aee783089cfa6545e9974a8e4bc331b5f01e1eff47c3</citedby><cites>FETCH-LOGICAL-a412t-478bb3cadaf90ec41c948aee783089cfa6545e9974a8e4bc331b5f01e1eff47c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2228046$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Shu, Chi-Kuen</creatorcontrib><title>Pyrazine Formation from Amino Acids and Reducing Sugars, a Pathway Other than Strecker Degradation</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Because the reaction of acyloins with ammonia generates pyrazines and acyloins are not involved with Strecker degradation, this study uses acetoin (a simple acyloin, from sugar degradation) to react with amino acids to determine whether ammonia is released, leading to the formation of tetramethylpyrazine. The results show that all reactions between α-amino acids and acetoin generate not only tetramethylpyrazine but also the corresponding Strecker aldehydes. However, the reactions between β-, γ-, or ε-amino acid and acetoin generate only tetramethylpyrazine. Quantitative analysis shows that among such reactions, both α- and β-amino acids generate significantly higher amounts of tetramethylpyrazine than γ- and ε-amino acids. On the basis of these data, it is proposed mechanistically that α-amino acids decarbonylate to generate the reactive intermediates, 1-hydroxyamines, deamination of which leads to the formation of the Strecker aldehydes. This study demonstrates that pyrazines and Strecker aldehydes are also formed from α-amino acids and reducing sugar via deamination in addition to their formation via the well-known Strecker degradation. Keywords: Strecker degradation; pyrazine formation; deamination; decarbonylation; acyloin; α-amino acid; β-amino acid; γ-amino acid; ε-amino acid; Strecker aldehyde</description><subject>ACETOIN</subject><subject>ACYLOINS</subject><subject>ALDEHYDES</subject><subject>ALPHA-AMINOBUTYRIC ACID</subject><subject>AMINO ACIDS</subject><subject>BETA-AMINOBUTYRIC ACID</subject><subject>Biological and medical sciences</subject><subject>CHEMICAL REACTIONS</subject><subject>DEAMINATION</subject><subject>EPSILON-AMINOHEXANOIC ACID</subject><subject>FLAVOUR COMPOUNDS</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GABA</subject><subject>GAMMA-AMINOBUTYRIC ACID</subject><subject>General aspects</subject><subject>Miscellaneous</subject><subject>NONPROTEIN AMINO ACIDS</subject><subject>PYRAZINES</subject><subject>QUANTITATIVE ANALYSIS</subject><subject>REACTION PRODUCTS</subject><subject>REDUCING SUGARS</subject><subject>STRECKER ALDEHYDE</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNptkE9LAzEQxYMoWP8c_ABCDnoQXE12kyY5ltZaQbHY9hxm06RNtbuSbNH66Y2u9ORpGN7vPWYeQmeU3FCS09uVU4Iopfwe6lCek4xTKvdRhyQxk7xLD9FRjCtCiOSCdFA53gb48pXFwzqsofF1hV2o17i39lWNe8bPI4Zqjl_sfGN8tcCTzQJCvMaAx9AsP2CLn5ulDbhZQoUnTbDmNW0Duwgw_807QQcO3qI9_ZvHaDa8m_ZH2ePz_UO_95gBo3mTMSHLsjDJ5BSxhlGjmARrhSyIVMZBlzNulRIMpGWlKQpackeopdY5JkxxjK7aXBPqGIN1-j34NYStpkT_lKN35ST2omXfIRp4cwEq4-POkOe5JKybsKzFfGzs506G8Kq7ohBcT8cTPZLDaf8pH2iS-POWd1BrWIQUOZvQdHP6gEuR9MtWBxP1qt6EKhXyz3nfkR-Itg</recordid><startdate>19980401</startdate><enddate>19980401</enddate><creator>Shu, Chi-Kuen</creator><general>American Chemical Society</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19980401</creationdate><title>Pyrazine Formation from Amino Acids and Reducing Sugars, a Pathway Other than Strecker Degradation</title><author>Shu, Chi-Kuen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a412t-478bb3cadaf90ec41c948aee783089cfa6545e9974a8e4bc331b5f01e1eff47c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>ACETOIN</topic><topic>ACYLOINS</topic><topic>ALDEHYDES</topic><topic>ALPHA-AMINOBUTYRIC ACID</topic><topic>AMINO ACIDS</topic><topic>BETA-AMINOBUTYRIC ACID</topic><topic>Biological and medical sciences</topic><topic>CHEMICAL REACTIONS</topic><topic>DEAMINATION</topic><topic>EPSILON-AMINOHEXANOIC ACID</topic><topic>FLAVOUR COMPOUNDS</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GABA</topic><topic>GAMMA-AMINOBUTYRIC ACID</topic><topic>General aspects</topic><topic>Miscellaneous</topic><topic>NONPROTEIN AMINO ACIDS</topic><topic>PYRAZINES</topic><topic>QUANTITATIVE ANALYSIS</topic><topic>REACTION PRODUCTS</topic><topic>REDUCING SUGARS</topic><topic>STRECKER ALDEHYDE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shu, Chi-Kuen</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</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>Shu, Chi-Kuen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyrazine Formation from Amino Acids and Reducing Sugars, a Pathway Other than Strecker Degradation</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>1998-04-01</date><risdate>1998</risdate><volume>46</volume><issue>4</issue><spage>1515</spage><epage>1517</epage><pages>1515-1517</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Because the reaction of acyloins with ammonia generates pyrazines and acyloins are not involved with Strecker degradation, this study uses acetoin (a simple acyloin, from sugar degradation) to react with amino acids to determine whether ammonia is released, leading to the formation of tetramethylpyrazine. The results show that all reactions between α-amino acids and acetoin generate not only tetramethylpyrazine but also the corresponding Strecker aldehydes. However, the reactions between β-, γ-, or ε-amino acid and acetoin generate only tetramethylpyrazine. Quantitative analysis shows that among such reactions, both α- and β-amino acids generate significantly higher amounts of tetramethylpyrazine than γ- and ε-amino acids. On the basis of these data, it is proposed mechanistically that α-amino acids decarbonylate to generate the reactive intermediates, 1-hydroxyamines, deamination of which leads to the formation of the Strecker aldehydes. This study demonstrates that pyrazines and Strecker aldehydes are also formed from α-amino acids and reducing sugar via deamination in addition to their formation via the well-known Strecker degradation. Keywords: Strecker degradation; pyrazine formation; deamination; decarbonylation; acyloin; α-amino acid; β-amino acid; γ-amino acid; ε-amino acid; Strecker aldehyde</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/jf970999i</doi><tpages>3</tpages></addata></record> |
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ispartof | Journal of agricultural and food chemistry, 1998-04, Vol.46 (4), p.1515-1517 |
issn | 0021-8561 1520-5118 |
language | eng |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | ACETOIN ACYLOINS ALDEHYDES ALPHA-AMINOBUTYRIC ACID AMINO ACIDS BETA-AMINOBUTYRIC ACID Biological and medical sciences CHEMICAL REACTIONS DEAMINATION EPSILON-AMINOHEXANOIC ACID FLAVOUR COMPOUNDS Food industries Fundamental and applied biological sciences. Psychology GABA GAMMA-AMINOBUTYRIC ACID General aspects Miscellaneous NONPROTEIN AMINO ACIDS PYRAZINES QUANTITATIVE ANALYSIS REACTION PRODUCTS REDUCING SUGARS STRECKER ALDEHYDE |
title | Pyrazine Formation from Amino Acids and Reducing Sugars, a Pathway Other than Strecker Degradation |
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