Department of Refrigeration and Livestock Products Technology, Faculty of Food Science, Szent István University, Ménesi út 43-45, Building "D", 1118, Budapest, Hungary.
J Fluoresc. 2017 Mar;27(2):433-437. doi: 10.1007/s10895-016-2002-1. Epub 2016 Dec 19.
A method to directly determine enzyme activity in cheese has not been published yet despite the fact that mTG mediated gel strength or hardness modification may be unpredictable and unfavorable during ripening and/or storage. The present study was performed to determine enzyme activity of semi-fat semi-hard Hungarian Trappist cheese. The widely known hydroxamate method was not suitable to even detect enzyme treatment, because of the disturbing effect of milk proteins. However incorporation of a dansylated glutamine dipeptide into milk protein contributed to monitoring the enzyme activity. The fluorescent measurement reflected mTG activity by increasing fluorescence intensity at 532 nm in a 5-min continuously running assay. The presented dipeptide assay allows the determination of enzyme activity after 2 min measurement by the manufacturing stage: cutting and up-heating. This assay can be used to monitor mTG activity during manufacture of low-fat semi-hard cheese type, in case if it was produced according to general recommendation of enzyme preparation providers (enzyme dosage: 0.1%, v/w). According to the preliminary calibration this assay can define mTG activity in the range of 0.05-0.3 U/g.
尽管 mTG 介导的凝胶强度或硬度改性在成熟和/或储存过程中可能是不可预测和不利的,但目前尚未发表直接测定奶酪中酶活性的方法。本研究旨在测定半脂肪半硬匈牙利特拉普斯特奶酪的酶活性。由于牛奶蛋白的干扰作用,即使是众所周知的羟肟酸法也不适合检测酶处理。然而,将丹磺酰基谷氨酰胺二肽掺入牛奶蛋白有助于监测酶活性。荧光测量通过在 5 分钟的连续运行测定中在 532nm 处增加荧光强度来反映 mTG 活性。该二肽测定法可在制造阶段(切割和加热)后通过 2 分钟的测量来确定酶活性:切割和加热。如果按照酶制剂供应商的一般建议(酶用量:0.1%,v/w)生产低脂半硬奶酪类型,则可以使用该测定法来监测 mTG 活性。根据初步校准,该测定法可以在 0.05-0.3U/g 的范围内定义 mTG 活性。