Biochemical characterization of lysozyme extracted from Caspian kutum, Rutilus kutum, Kamensky ۱۹۰۱
محل انتشار: مجله علوم زیستی خاورمیانه، دوره: 17، شماره: 3
سال انتشار: 1398
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 193
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شناسه ملی سند علمی:
JR_CJES-17-3_008
تاریخ نمایه سازی: 27 خرداد 1403
چکیده مقاله:
This paper presents the findings of a basic study on biochemical characteristics and activity of lysozyme extracted from a commercially important fish, Caspian kutum, Rutilus kutum, Kamensky ۱۹۰۱. The enzyme was purified by the ammonium sulphate precipitation method and cationic exchange chromatography. Molecular weight of lysozyme was estimated as ۱۵.۸kDa by SDS-PAGE. The optimum pH and temperature were ۶.۰ and ۴۵.۰°C, respectively,while the Km and Vmax values were ۰.۰۰۰۰۷g mL-۱ and ۲۰۰units min-۱, respectively. Thermo-stability of the enzyme was low at the temperatures higher than ۵۰°C. The enzyme activity increased in the presence of NaCl (۱-۵۰mM), KCl (۱-۵۰mM) and CrCl۲ (۱-۵mM), then decreased at the higher concentrations. Furthermore, the enzyme activity significantly decreased in the presence of FeCl۲ and CuCl۲ (۱-۱۰۰mM), but not stable in the presence of MgCl۲. SDS inhibited the activity, but the enzyme exhibited a good degree of resistance to urea. Fluorescence quenching was observed in the presence of FeCl۲ and CuCl۲. Emission intensities in the presence of NaCl, KCl, CrCl۲ and SDS were elevated, while was negligible for the urea. Our results exhibitedthat NaCl and KCl are well-established salts for elevating the enzyme activity.However, the purified lysozyme did not display a moderate stability against others salts. Besides, the purified lysozyme from R. kutum was not heat stable. Therefore, some phenomena such as water hardness and warming can exert negative effects on the innate immunity of the fish. So, the enzyme structure can be made more stable by medium engineering through changing the salt composition of aqueous solution.
کلیدواژه ها:
نویسندگان
Behnaz Tolouei Nia
Department of Biology, Faculty of Science, University of Guilan, Rasht, Iran
Mahmoud Reza Aghamaali
Department of Biology, Faculty of Science, University of Guilan, Rasht, Iran
Ahmad Asoodeh
Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran
Mohsen Mehregan
Department of Physics, Faculty of Science, Payame Noor University, Theran, Iran
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