Lazuana Tisha, Astuty Hendri, Sari Ika Puspa
Master Program in Biomedical Sciences, Faculty of Medicine Universitas Indonesia, Indonesia.
Department of Parasitology, Faculty of Medicine Universitas Indonesia, Indonesia.
J Parasitol Res. 2019 Mar 28;2019:8915314. doi: 10.1155/2019/8915314. eCollection 2019.
The goal of this study is to know the potential of cellulase in the degradation of cyst wall .
Sample of . obtained from isolate collection of Department of Parasitology FKUI of which two samples come from patient and one sample is from environment. All three samples were cultured using non-nutrient agar (NNA) media and identified by PCR and sequencing. The concentration of cellulase concentration used was 50 U, 100 U, 150 U, 200 U, 250 U, and 300 U with the incubation time used being 2 hours, 4 hours, 6 hours, 8 hours, and 24 hours. Furthermore, treatment results with the most optimum concentration and incubation time were observed by using SEM to see changes in the surface of the walls of the cyst. A cysticidal test was performed to determine the effectiveness cysticidal action of disinfectant solution, cellulase, and the combination of disinfectant solution and cellulase in killing . cyst assessed by their viability value.
The most optimal cellulase concentration in killing cysts was 300 U with an incubation time of 24 hours. Percentage of viability of . which was exposed to a disinfectant solution for 24 hours was 95%, cellulase alone for 24 hours 75%, and the combination of cellulase and disinfectant solution for 24 hours 25%.
Cellulase is capable of degrading . cyst wall. Optimal cellulase concentration in degrading . cyst wall is 300 U with an optimal incubation time being 24 hours. The addition of cellulase to the disinfectant solution has the potential to increase the effectiveness of the disinfectant solution because cellulase is capable of degrading the cyst wall allowing the disinfectant solution to enter and kill cysts.
本研究的目的是了解纤维素酶在降解囊肿壁方面的潜力。
从印度尼西亚大学医学院寄生虫学系的分离株收集中获取样本,其中两个样本来自患者,一个样本来自环境。所有三个样本均使用无营养琼脂(NNA)培养基培养,并通过聚合酶链反应(PCR)和测序进行鉴定。所使用的纤维素酶浓度分别为50 U、100 U、150 U、200 U、250 U和300 U,孵育时间分别为2小时、4小时、6小时、8小时和24小时。此外,通过扫描电子显微镜(SEM)观察最适宜浓度和孵育时间的处理结果,以查看囊肿壁表面的变化。进行杀囊肿试验,以确定消毒剂溶液、纤维素酶以及消毒剂溶液与纤维素酶组合在杀死囊肿方面的杀囊肿作用效果,通过其活力值进行评估。
杀灭囊肿的最适宜纤维素酶浓度为300 U,孵育时间为24小时。暴露于消毒剂溶液24小时的囊肿活力百分比为95%,单独使用纤维素酶24小时为75%,纤维素酶与消毒剂溶液组合24小时为25%。
纤维素酶能够降解囊肿壁。降解囊肿壁的最适宜纤维素酶浓度为300 U,最适宜孵育时间为24小时。在消毒剂溶液中添加纤维素酶有可能提高消毒剂溶液的效力,因为纤维素酶能够降解囊肿壁,使消毒剂溶液能够进入并杀死囊肿。