Awde Sahar, Marty-Gasset Nathalie, Prahkarnkaeo Kriengkrai, Rémignon Hervé
UMR1388 GENEPHYSE, INRA , F-31326 Castanet-Tolosan, France.
UMR1388 GENEPHYSE, Université de Toulouse INP-ENSAT , F-31326 Castanet-Tolosan, France.
J Agric Food Chem. 2014 Apr 9;62(14):3262-3268. doi: 10.1021/jf4051057. Epub 2014 Mar 28.
We investigated liver protease activities to better understand the mechanisms responsible for losses during the cooking of Mule ducks' fatty livers. Fatty livers of similar masses (520 g) were randomly selected among a large flock of overfed male Mule ducks and divided into two groups on the basis of their cooking loss rate, L+ (high cooking losses, 36%) and L- (low cooking losses, 21%). In addition to dry matter and total lipid contents, main hepatic protease (matrix metalloproteinase 2, cathepsins, and calpains) activities were measured by zymography. The results show that L+ samples present higher total relative proteolytic activity (6.15 ± 1.07 vs 4.46 ± 0.52 for L+ and L- samples, respectively) and total lipid content (61.0 ± 3.03% vs 53.7 ± 3.22% for L+ and L- samples, respectively) than L- samples. The results imply that proteases could be involved in the fragilization of the hepatocyte structure, resulting thus in higher cooking losses in L+ samples.
我们研究了肝脏蛋白酶活性,以更好地了解骡鸭肥肝烹饪过程中损失的机制。在一大群过度喂养的雄性骡鸭中随机挑选了质量相似(520克)的肥肝,并根据其烹饪损失率分为两组,L+组(高烹饪损失,36%)和L-组(低烹饪损失,21%)。除了测定干物质和总脂质含量外,还通过酶谱法测量了主要肝脏蛋白酶(基质金属蛋白酶2、组织蛋白酶和钙蛋白酶)的活性。结果表明,L+组样品的总相对蛋白水解活性(L+组和L-组样品分别为6.15±1.07和4.46±0.52)和总脂质含量(L+组和L-组样品分别为61.0±3.03%和53.7±3.22%)均高于L-组样品。结果表明,蛋白酶可能参与了肝细胞结构的脆弱化,从而导致L+组样品的烹饪损失更高。