Le Havre Normandie University (ULHN), FR CNRS 3730 SCALE, UMR-INERIS 02 Environmental Stresses and Biomonitoring of Aquatic Ecosystems (SEBIO), 25 rue Philippe Le Bon, 76600 Le Havre, France.
Le Havre Normandie University (ULHN), FR CNRS 3730 SCALE, UMR-INERIS 02 Environmental Stresses and Biomonitoring of Aquatic Ecosystems (SEBIO), 25 rue Philippe Le Bon, 76600 Le Havre, France.
Comp Biochem Physiol A Mol Integr Physiol. 2021 Jun;256:110932. doi: 10.1016/j.cbpa.2021.110932. Epub 2021 Mar 4.
Chitinolytic enzymes fulfil a key role in the moulting process of crustaceans, in degrading the endocuticle during apolysis. Measuring the enzyme activity is an interesting manner to monitor the moult process at sub-individual level, complementary to the classical observation of the integument morphogenesis, ecdysis success, or moult cycle duration. The present study aimed to optimise the methodology of using N-acetyl-β-D-glucosaminidase (NAGase) activity to monitor moulting in the marine prawn Palaemon serratus, and to compare NAGase activity levels along the moult cycle of both male and female specimens. First, to optimise protocols for five different organs, different reaction medium compositions were tested, considering the type buffer, concentration of the substrate, and the load in enzymatic extract. Second, levels of NAGase activity were closely monitored during eight moulting stages in male prawns. Variations in NAGase activity were observed during the moult cycle, with an increase in activity in the late premoult phase of approximately 2.4-fold the level of the intermoult phase. This response profile was observed for each tested organ. The levels of NAGase activity of male and female specimens were compared during three stages of the premoult phase. The patterns observed for both sexes were similar for all the tested organs.
几丁质酶在甲壳动物的蜕皮过程中起着关键作用,在蜕皮时降解内角质层。测量酶活性是一种有趣的方法,可以在亚个体水平上监测蜕皮过程,补充经典的观察表皮形态发生、蜕皮成功或蜕皮周期持续时间。本研究旨在优化使用 N-乙酰-β-D-氨基葡萄糖苷酶(NAGase)活性监测海洋对虾 Palaemon serratus 蜕皮的方法,并比较雌雄个体在蜕皮周期中 NAGase 活性水平。首先,为了优化五种不同器官的方案,测试了不同的反应介质组成,考虑了缓冲液的类型、底物的浓度和酶提取物的负载。其次,在雄性对虾的八个蜕皮阶段中密切监测 NAGase 活性水平。在蜕皮周期中观察到 NAGase 活性的变化,在晚期预蜕皮阶段的活性增加约 2.4 倍,而在间蜕皮阶段的活性增加。这种反应模式在每个测试的器官中都观察到。在预蜕皮阶段的三个阶段比较了雌雄标本的 NAGase 活性水平。对于所有测试的器官,两性观察到的模式相似。