Nakamura N, Murayama K, Kinoshita T
Anal Biochem. 1986 Feb 1;152(2):386-90. doi: 10.1016/0003-2697(86)90424-0.
Uricase was found to be stabilized by protamine from salmon testis. Protamine was then bound to controlled-pore glass beads aminohexyl CPG 500 using glutaraldehyde. Microbial uricase was readily immobilized on the protamine bound to glass beads. The immobilized uricase proved to be stable even at 70 degrees C, whereas free uricase was inactivated at 45 degrees C and showed activity over a broader pH range than free uricase. Automated analysis of uric acid was facilitated using the immobilized uricase. The standard curve for uric acid was linear in the range of 2 to 10 micrograms/sample and passed through the origin. This automated procedure was also applicable to the determination of uric acid in human serum. Protamine bound to glass beads is expected to be useful for the simple immobilization and stabilization of enzymes.
人们发现,鲑鱼精巢中的鱼精蛋白可使尿酸酶稳定。随后,使用戊二醛将鱼精蛋白结合到可控孔径玻璃珠氨基己基CPG 500上。微生物尿酸酶很容易固定在结合到玻璃珠上的鱼精蛋白上。事实证明,固定化尿酸酶即使在70摄氏度时仍很稳定,而游离尿酸酶在45摄氏度时就会失活,并且与游离尿酸酶相比,其在更宽的pH范围内都具有活性。使用固定化尿酸酶有助于实现尿酸的自动化分析。尿酸的标准曲线在2至10微克/样品范围内呈线性,且通过原点。该自动化程序也适用于人血清中尿酸的测定。结合到玻璃珠上的鱼精蛋白有望用于酶的简单固定化和稳定化。