环糊精糖基转移酶变体经历不同的产物抑制模式

Caiming Li , Qi Xu , Zhengbiao Gu , Shuangdi Chen , Jing Wu , Yan Hong , Li Cheng , Zhaofeng Li
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引用次数: 7

摘要

环糊精糖基转移酶(CGTase)可用于环糊精的工业生产。然而,环糊精的产物抑制作用在很大程度上抑制了CGTase的环化活性,严重限制了环糊精的应用。本文研究了三种环化反应的动力学机理,并比较了不同来源的两种cgtase对产物的抑制模式。结果证实,每种环糊精的合成都受到相应环糊精的抑制。同时,产物抑制研究表明α-CGTase呈竞争性抑制,而β-CGTase呈混合型抑制。这说明抑制类型不是由环糊精的种类或环化反应的种类决定的,而是由CGTase的结构决定的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Cyclodextrin glycosyltransferase variants experience different modes of product inhibition

Cyclodextrin glycosyltransferase (CGTase) can be used for the industrial production of cyclodextrins. However, product inhibition by cyclodextrins largely restrains the cyclization activities of CGTase and severely limits the application of cyclodextrins. In this paper, the kinetic mechanisms of the three kinds of cyclization reaction were studied, and the product inhibition modes of two CGTases from different sources were compared. The results confirm that the synthesis of each cyclodextrin is substantially inhibited by the corresponding cyclodextrin. Meanwhile, product inhibition studies indicate competitive inhibition for α-CGTase and a mixed pattern for β-CGTase. This demonstrates that the inhibition type is not decided by the kinds of cyclodextrins or the varieties of cyclization reactions, but by the structure of the CGTase.

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来源期刊
Journal of Molecular Catalysis B-enzymatic
Journal of Molecular Catalysis B-enzymatic 生物-生化与分子生物学
CiteScore
2.58
自引率
0.00%
发文量
0
审稿时长
3.4 months
期刊介绍: Journal of Molecular Catalysis B: Enzymatic is an international forum for researchers and product developers in the applications of whole-cell and cell-free enzymes as catalysts in organic synthesis. Emphasis is on mechanistic and synthetic aspects of the biocatalytic transformation. Papers should report novel and significant advances in one or more of the following topics; Applied and fundamental studies of enzymes used for biocatalysis; Industrial applications of enzymatic processes, e.g. in fine chemical synthesis; Chemo-, regio- and enantioselective transformations; Screening for biocatalysts; Integration of biocatalytic and chemical steps in organic syntheses; Novel biocatalysts, e.g. enzymes from extremophiles and catalytic antibodies; Enzyme immobilization and stabilization, particularly in non-conventional media; Bioprocess engineering aspects, e.g. membrane bioreactors; Improvement of catalytic performance of enzymes, e.g. by protein engineering or chemical modification; Structural studies, including computer simulation, relating to substrate specificity and reaction selectivity; Biomimetic studies related to enzymatic transformations.
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