†INRA, UR342 Technologie et Analyses Laitières, F-39800 Poligny, France.
∥ACTALIA, F-25620 Mamirolle, France.
J Agric Food Chem. 2015 May 20;63(19):4799-804. doi: 10.1021/acs.jafc.5b00990. Epub 2015 May 6.
Chymosin is the major enzyme of natural rennet, traditionally used in cheese making for its high milk-clotting activity. For technical reasons, an accurate characterization of rennet should include its total clotting activity and also its enzymatic composition. Monoclonal antibodies specific to chymosin were obtained from mice immunized with purified bovine chymosin, and an inhibition enzyme-linked immunosorbent assay (ELISA) was developed for the quantification of chymosin in solution. No cross-reactivity was observed with other milk-clotting enzymes commonly used in cheese making. The limit of detection and limit of quantification were 125 and 400 ng/mL, respectively. The values of precision within and among runs were 7.23 and 7.39%, respectively, and satisfying recovery, from 92 to 119%, was found for spiked samples. The inhibition ELISA was successfully applied to commercial rennets, and the results were consistent with those obtained using the standard chromatographic method (IDF 110: A, 1987).
凝乳酶是天然凝乳酶的主要酶,因其具有较高的牛奶凝结活性而在奶酪制作中传统使用。出于技术原因,对凝乳酶的准确描述应包括其总凝结活性和酶组成。从小鼠免疫纯化的牛凝乳酶中获得了特异性针对凝乳酶的单克隆抗体,并开发了抑制酶联免疫吸附测定法(ELISA)来定量溶液中的凝乳酶。该方法与奶酪制作中常用的其他牛奶凝结酶没有交叉反应。检测限和定量限分别为 125 和 400 ng/mL。批内和批间精密度分别为 7.23%和 7.39%,并且添加的样品回收率令人满意,为 92%至 119%。抑制 ELISA 成功地应用于商业凝乳酶,并且与使用标准色谱法(IDF 110:A,1987)获得的结果一致。