Allium discoloration: color compounds formed during greening of processed garlic
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60076658%3A12220%2F17%3A43896177" target="_blank" >RIV/60076658:12220/17:43896177 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1021/acs.jafc.7b04609" target="_blank" >http://dx.doi.org/10.1021/acs.jafc.7b04609</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.jafc.7b04609" target="_blank" >10.1021/acs.jafc.7b04609</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Allium discoloration: color compounds formed during greening of processed garlic
Popis výsledku v původním jazyce
Structures and formation pathways of compounds responsible for blue-green discoloration of processed garlic were studied in model systems. A procedure was developed for isolation of the color compounds and their tentative identification by HPLC-DAD-MS/MS. It was found that the pigment is a mixture of numerous pyrrole-based purple/blue and yellow species. Experiments with isotope-labeled precursors revealed that two molecules of an amino acid are involved in the formation of each color compound. In the purple/blue species (?max 565?600 nm), both amino acid molecules are incorporated into two 3,4-dimethylpyrrole-derived rings linked together by a propenylidine bridge. On the other hand, the yellow compounds (?max 420?450 nm) contain only one N-substituted 3,4-dimethylpyrrole ring to which the second amino acid is bound via a propenylidine side chain.
Název v anglickém jazyce
Allium discoloration: color compounds formed during greening of processed garlic
Popis výsledku anglicky
Structures and formation pathways of compounds responsible for blue-green discoloration of processed garlic were studied in model systems. A procedure was developed for isolation of the color compounds and their tentative identification by HPLC-DAD-MS/MS. It was found that the pigment is a mixture of numerous pyrrole-based purple/blue and yellow species. Experiments with isotope-labeled precursors revealed that two molecules of an amino acid are involved in the formation of each color compound. In the purple/blue species (?max 565?600 nm), both amino acid molecules are incorporated into two 3,4-dimethylpyrrole-derived rings linked together by a propenylidine bridge. On the other hand, the yellow compounds (?max 420?450 nm) contain only one N-substituted 3,4-dimethylpyrrole ring to which the second amino acid is bound via a propenylidine side chain.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
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OECD FORD obor
21101 - Food and beverages
Návaznosti výsledku
Projekt
—
Návaznosti
S - Specificky vyzkum na vysokych skolach
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Agricultural and Food Chemistry
ISSN
0021-8561
e-ISSN
—
Svazek periodika
65
Číslo periodika v rámci svazku
48
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
6
Strana od-do
10615-10620
Kód UT WoS článku
000417670500027
EID výsledku v databázi Scopus
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