Onal Seçil, Telefoncu Azmi
Department of Biochemistry, Faculty of Science, Ege University, Bornova-Izmir, Turkey.
Artif Cells Blood Substit Immobil Biotechnol. 2003 Aug;31(3):339-55. doi: 10.1081/bio-120023163.
alpha-Galactosidase (alpha-D-galactoside galactohydrolase, EC 3.2.1.22) from watermelon was covalently immobilized on chitin. The immobilized alpha-galactosidase exhibited an activity of 0.61 U per g of carrier and an activity yield of 67%. The properties of free and immobilized alpha-galactosidase were also searched and compared. The results showed that, optimum conditions for activity were not affected by immobilization. The optimum pH and temperature for free and immobilized enzyme found as pH 6.0 and 65 degress C, respectively. Compared with the free enzyme, the temperature and pH stabilities of the immobilized enzyme were similar. Both the enzymes were stable between pH 2-10 and below 50 degrees C. The Km values for free and immobilized enzyme were determined using p-nitrophenyl-alpha-D-galactopyranoside (PNPG) and raffinose as substrates. Operational stability of the immobilized enzyme was investigated by using both substrates. The operational half-life (t 1/2) was calculated as 34 h for PNPG and 28 h for raffinose. The immobilized alpha-galactosidase was also utilized in the hydrolysis of raffinose. The immobilization procedure on chitin was cheap and also easy to carry out, and the immobilized enzyme had good properties that the potential for practical application is considerable.
将西瓜中的α-半乳糖苷酶(α-D-半乳糖苷半乳糖水解酶,EC 3.2.1.22)共价固定在几丁质上。固定化的α-半乳糖苷酶每克载体表现出0.61 U的活性,活性产率为67%。还对游离和固定化α-半乳糖苷酶的性质进行了研究和比较。结果表明,固定化不影响酶活性的最佳条件。游离和固定化酶的最佳pH值和温度分别为pH 6.0和65℃。与游离酶相比,固定化酶的温度和pH稳定性相似。两种酶在pH 2-10和低于50℃时都很稳定。以对硝基苯基-α-D-吡喃半乳糖苷(PNPG)和棉子糖为底物测定游离和固定化酶的Km值。使用两种底物研究了固定化酶的操作稳定性。计算得出,以PNPG为底物时操作半衰期(t1/2)为34小时,以棉子糖为底物时为28小时。固定化α-半乳糖苷酶还用于棉子糖的水解。在几丁质上的固定化过程成本低廉且易于实施,固定化酶具有良好的性质,具有相当大的实际应用潜力。