Godjevargova Tzonka, Dayal Rajeshwar, Turmanova Sevdalina
Department of Biotechnology, University, Prof. Dr. Assen Zlatarov Prof. Yakimov Street 1, Bourgas 8010, Bulgaria.
Macromol Biosci. 2004 Oct 20;4(10):950-6. doi: 10.1002/mabi.200400058.
Gluconic acid was obtained in the permeate side of the bioreactor with glucose oxidase (GOD) immobilized onto anion-exchange membrane (AEM) of low-density polyethylene grafted with 4-vinylpiridine. The electric resistance of the anion-exchange membranes was increased after the enzyme immobilization on the membrane. The gluconic acid productions were relatively low with the GOD immobilized by any method on the AEM. To increase the enzyme reaction efficiency, GOD was immobilized on membrane of AN copolymer (PAN) adjacent to an anion-exchange membrane in bioreactor. Uses of anion-exchange membrane led to selective removal of the gluconic acid from the glucose solution and reduce the gluconic acid inhibition. The amount of gluconic acid obtained in the permeate side of the bioreactor with the GOD immobilized on the PAN membrane adjacent to the AEM under electrodialysis was about 30 times higher than that obtained with enzyme directly bound to the AEM. The optimal substrate concentration in the feed side was found to be about 1 g/l. Further experiments were carried out with the co-immobilized GOD plus Catalase (CAT) on the PAN membrane adjacent to the AEM to improve the efficiency of the immobilize system. The yield of this process was at least 95%. The storage stability of the co-immobilized GOD and CAT was studied (lost 20% of initial activity for 90 d). The results obtained clearly showed the higher potential of the dual membrane bioreactor with GOD plus CAT bound to ultrafiltration polymer membrane adjacent to the AEM. Storage stability of GOD activity in GOD plus CAT immobilized on PAN//AEM membranes and on AEM.
在生物反应器的渗透侧获得了葡萄糖酸,其中葡萄糖氧化酶(GOD)固定在接枝有4-乙烯基吡啶的低密度聚乙烯阴离子交换膜(AEM)上。在膜上固定酶后,阴离子交换膜的电阻增加。通过任何方法将GOD固定在AEM上时,葡萄糖酸的产量相对较低。为了提高酶反应效率,将GOD固定在生物反应器中与阴离子交换膜相邻的AN共聚物(PAN)膜上。使用阴离子交换膜可导致从葡萄糖溶液中选择性去除葡萄糖酸,并减少葡萄糖酸的抑制作用。在电渗析条件下,将GOD固定在与AEM相邻的PAN膜上的生物反应器渗透侧获得的葡萄糖酸量比酶直接结合到AEM上获得的量高约30倍。发现进料侧的最佳底物浓度约为1 g/l。进一步进行了实验,将GOD与过氧化氢酶(CAT)共固定在与AEM相邻 的PAN膜上,以提高固定系统的效率。该过程的产率至少为95%。研究了共固定的GOD和CAT的储存稳定性(90天内初始活性损失20%)。获得的结果清楚地表明了GOD加CAT结合到与AEM相邻的超滤聚合物膜上的双膜生物反应器具有更高的潜力。GOD活性在固定于PAN//AEM膜和AEM上的GOD加CAT中的储存稳定性。