ŞahutoĞlu Arif Sercan, Duman Hatice, Frese Steven Alex, Karav Sercan
Department of Chemistry, Faculty of Arts and Sciences, Çanakkale Onsekiz Mart University, Çanakkale Turkey.
Department of Molecular Biology and Genetics, Faculty of Arts and Sciences, Çanakkale Onsekiz Mart University, Çanakkale Turkey.
Turk J Chem. 2020 Dec 16;44(6):1703-1712. doi: 10.3906/kim-2006-19. eCollection 2020.
EndoBI-1 and EndoBI-2 are two endo- acetylglucosaminidase isoenzymes that cleave diacetylchitobiosyl moieties found in various types of native -glycans. These -glycans are indigestible by human infants and adults due to the lack of responsible glycosyl hydrolases and they act as selective prebiotics for a probiotic microorganism, subsp , in the large intestine. The selectivity and the thermostability of EndoBI-1 and EndoBI-2 suggest that these enzymes may be useful for many scientific and industrial applications. In this study, the growing numbers of homologous sequences in different databases were exploited in a comparative approach to investigate structural properties of EndoBI-1 and EndoBI-2 enzymes. Moreover, the complete and partial homology models of these two enzymes were generated and evaluated. Selected models were used for docking studies of the plus subsite ligand of these enzymes for further understanding on the substrate selectivity of EndoBI enzymes.
EndoBI-1和EndoBI-2是两种内切乙酰氨基葡萄糖苷酶同工酶,可切割各种天然聚糖中存在的二乙酰壳二糖部分。由于缺乏相应的糖基水解酶,这些聚糖对人类婴儿和成年人来说是不可消化的,它们作为一种益生菌微生物——亚种在大肠中的选择性益生元。EndoBI-1和EndoBI-2的选择性和热稳定性表明,这些酶可能在许多科学和工业应用中有用。在本研究中,利用不同数据库中不断增加的同源序列,采用比较方法研究EndoBI-1和EndoBI-2酶的结构特性。此外,还生成并评估了这两种酶的完整和部分同源模型。选择的模型用于这些酶的正亚位点配体的对接研究,以进一步了解EndoBI酶的底物选择性。