中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Theoretical study on the deglycosylation mechanism of rice BGlu1 beta-glucosidase

文献类型:期刊论文

作者Wang, Jinhu1; Hou, Qianqian1; Sheng, Xiang1; Gao, Jun1; Liu, Yongjun1,2; Liu, Chengbu1
刊名international journal of quantum chemistry
出版日期2013-04-15
卷号113期号:8页码:1071-1075
关键词QM MM deglycosylation -glucosidases laminaribiose reaction mechanism
ISSN号0020-7608
通讯作者wang, jh (reprint author), shandong univ, sch chem & chem engn, minist educ, key lab colloid & interface chem, jinan 250100, shandong, peoples r china.
中文摘要it is proposed that the catalysis of gh1 enzymes follows a double-displacement mechanism involving a glycosylation and a deglycosylation steps. in this article, the deglycosylation step was studied using quantum mechanical/molecular mechanical (qm/mm) approach. the calculation results reveal that the nucleophilic water (wat1) attacks to the anomeric c1, and the deglycosylation step experiences a barrier of 21.4 kcal/mol from the glycosyl-enzyme intermediate to the hydrolysis product, in which an oxocarbenium cation-like transition state (ts) is formed. at the ts, the covalent glycosyl-enzyme bond is almost broken (distance of 2.45 angstrom), and the new covalent bond between the attacking oxygen of the water molecule and c1 is basically established (length of 2.14 angstrom). in addition, a short hydrogen bridge is observed between the nucleophilic e386 and the c2oh of sugar ring (distance of 1.94 angstrom) at the ts, which facilitates the ring changing from a chair form to half-chair form, and stabilizes the oxocarbenium cation-like ts. (c) 2013 wiley periodicals, inc.
英文摘要it is proposed that the catalysis of gh1 enzymes follows a double-displacement mechanism involving a glycosylation and a deglycosylation steps. in this article, the deglycosylation step was studied using quantum mechanical/molecular mechanical (qm/mm) approach. the calculation results reveal that the nucleophilic water (wat1) attacks to the anomeric c1, and the deglycosylation step experiences a barrier of 21.4 kcal/mol from the glycosyl-enzyme intermediate to the hydrolysis product, in which an oxocarbenium cation-like transition state (ts) is formed. at the ts, the covalent glycosyl-enzyme bond is almost broken (distance of 2.45 angstrom), and the new covalent bond between the attacking oxygen of the water molecule and c1 is basically established (length of 2.14 angstrom). in addition, a short hydrogen bridge is observed between the nucleophilic e386 and the c2oh of sugar ring (distance of 1.94 angstrom) at the ts, which facilitates the ring changing from a chair form to half-chair form, and stabilizes the oxocarbenium cation-like ts. (c) 2013 wiley periodicals, inc.
WOS标题词science & technology ; physical sciences
类目[WOS]chemistry, physical ; mathematics, interdisciplinary applications ; physics, atomic, molecular & chemical
研究领域[WOS]chemistry ; mathematics ; physics
关键词[WOS]crystal-structure ; molecular-dynamics ; substrate-specificity ; aglycone specificity ; catalytic mechanism ; zeolite structure ; qm/mm ; glycosidase ; insights ; maize
收录类别SCI
语种英语
WOS记录号WOS:000315957500003
公开日期2014-05-09
源URL[http://ir.nwipb.ac.cn/handle/363003/3949]  
专题西北高原生物研究所_中国科学院西北高原生物研究所
作者单位1.Shandong Univ, Sch Chem & Chem Engn, Minist Educ, Key Lab Colloid & Interface Chem, Jinan 250100, Shandong, Peoples R China
2.Chinese Acad Sci, Northwest Inst Plateau Biol, Xining 810001, Qinghai, Peoples R China
推荐引用方式
GB/T 7714
Wang, Jinhu,Hou, Qianqian,Sheng, Xiang,et al. Theoretical study on the deglycosylation mechanism of rice BGlu1 beta-glucosidase[J]. international journal of quantum chemistry,2013,113(8):1071-1075.
APA Wang, Jinhu,Hou, Qianqian,Sheng, Xiang,Gao, Jun,Liu, Yongjun,&Liu, Chengbu.(2013).Theoretical study on the deglycosylation mechanism of rice BGlu1 beta-glucosidase.international journal of quantum chemistry,113(8),1071-1075.
MLA Wang, Jinhu,et al."Theoretical study on the deglycosylation mechanism of rice BGlu1 beta-glucosidase".international journal of quantum chemistry 113.8(2013):1071-1075.

入库方式: OAI收割

来源:西北高原生物研究所

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