Measuring citrate synthase activity as an enzymatic approach to the differentiation of chilled and frozen/thawed meat
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F19%3A43919184" target="_blank" >RIV/60461373:22330/19:43919184 - isvavai.cz</a>
Výsledek na webu
<a href="https://reader.elsevier.com/reader/sd/pii/S0309174018308933?token=A5C18024985E100A9E670E0CC933486279D1AAC3567EA56F66B13B3154DC23E35D63E4EC86EA8A75C46DB2414D980721" target="_blank" >https://reader.elsevier.com/reader/sd/pii/S0309174018308933?token=A5C18024985E100A9E670E0CC933486279D1AAC3567EA56F66B13B3154DC23E35D63E4EC86EA8A75C46DB2414D980721</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.meatsci.2019.05.027" target="_blank" >10.1016/j.meatsci.2019.05.027</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Measuring citrate synthase activity as an enzymatic approach to the differentiation of chilled and frozen/thawed meat
Popis výsledku v původním jazyce
Citrate synthase belongs between mitochondrial enzymes which are released from the meat tissue after cell membrane damage caused by ice crystal formation. The presence of this enzyme can indicate a previous freezing process. In this study, we determined citrate synthase activity for chilled and frozen/thawed meats (chicken, pork, beef, and salmon). As an additional factor, we examined a potential connection between microbial spoilage and increased enzyme activity. UV spectrophotometry was used for the evaluation of the citrate synthase activity. The effect of microbial spoilage on the enzyme activity was established through microbial analysis, which was carried out for two weeks for chilled and five months for frozen/thawed meats. The citrate synthase activity in the frozen/thawed samples was significantly higher than in the chilled samples. Dependence of microbial contamination and the increased activity of the citrate synthase was not observed. Our results suggest that there could be designed specific limits of citrate synthase activity for the resolution of chilled and frozen/thawed meats. © 2019 Elsevier Ltd
Název v anglickém jazyce
Measuring citrate synthase activity as an enzymatic approach to the differentiation of chilled and frozen/thawed meat
Popis výsledku anglicky
Citrate synthase belongs between mitochondrial enzymes which are released from the meat tissue after cell membrane damage caused by ice crystal formation. The presence of this enzyme can indicate a previous freezing process. In this study, we determined citrate synthase activity for chilled and frozen/thawed meats (chicken, pork, beef, and salmon). As an additional factor, we examined a potential connection between microbial spoilage and increased enzyme activity. UV spectrophotometry was used for the evaluation of the citrate synthase activity. The effect of microbial spoilage on the enzyme activity was established through microbial analysis, which was carried out for two weeks for chilled and five months for frozen/thawed meats. The citrate synthase activity in the frozen/thawed samples was significantly higher than in the chilled samples. Dependence of microbial contamination and the increased activity of the citrate synthase was not observed. Our results suggest that there could be designed specific limits of citrate synthase activity for the resolution of chilled and frozen/thawed meats. © 2019 Elsevier Ltd
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
21101 - Food and beverages
Návaznosti výsledku
Projekt
—
Návaznosti
S - Specificky vyzkum na vysokych skolach
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Meat Science
ISSN
0309-1740
e-ISSN
—
Svazek periodika
158
Číslo periodika v rámci svazku
prosinec
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
5
Strana od-do
—
Kód UT WoS článku
000488322800014
EID výsledku v databázi Scopus
2-s2.0-85070709906