利用粗酶级联催化反应高效制备 β-烟酰胺单核苷酸。

IF 3.4 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jiehu Liu , Runtian Huo , Huixian Fu , Shiheng Chen , Xueyi Qiao , Bo Xu , Zhaoyuan Zhang , Jing Wu , Lingqia Su
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引用次数: 0

摘要

β-烟酰胺单核苷酸(β-NMN)是烟酰胺腺嘌呤二核苷酸的一种关键前体,在营养和保健领域颇具吸引力,但其酶法合成成本高昂。本研究构建了一个六酶级联催化系统来生产β-NMN。以 D-核糖和烟酰胺为底物,在纯化酶的催化下,β-NMN 的产率达到 97.5%。然后,在敲除大肠杆菌 BL21(DE3)中编码消耗 β-NMN 蛋白的基因后,使用粗酶也能获得类似的 β-NMN 产率,即 97.2%。随后,在底物浓度增加的条件下进行β-NMN合成,并提出了 "模块化 "粗酶级联催化反应体系,以减少多聚磷酸对核糖磷酸二磷激酶活性的抑制,在10 mM D-核糖条件下,β-NMN产率达到78.4%,是 "一锅式 "反应的1.82倍,代表了目前报道的以磷酸核糖基焦磷酸盐为核心的β-NMN制备的最高水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-efficient preparation of β-nicotinamide mononucleotides by crude enzymes cascade catalytic reaction

β-nicotinamide mononucleotide (β-NMN) is a key precursor of nicotinamide adenine dinucleotide, and becomes attractive in the nutrition and health care fields, but its enzymatic synthesis is expensive. In this study, a six-enzyme cascade catalytic system was constructed to produce β-NMN. Using D-ribose and nicotinamide as substrates, the β-NMN yield reached 97.5 % catalyzed by purified enzymes. Then, after knocking out the genes encoding proteins that consume β-NMN in E. coli BL21(DE3), the similar β-NMN yield, 97.2 %, using the crude enzymes could be also obtained. After that, β-NMN synthesis was performed under increased substrate concentration, and 'modular' crude enzymes cascade catalytic reaction system was proposed to reduce the inhibition of polyphosphate on ribose-phosphate diphosphokinase activity, and the β-NMN yield reached 78.4 % at 10 mM D-ribose, which is 1.82 times of that in 'one-pot' reaction and represents the highest β-NMN preparation level with phosphoribosylpyrophosphate as the core reported till now.

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来源期刊
Enzyme and Microbial Technology
Enzyme and Microbial Technology 生物-生物工程与应用微生物
CiteScore
7.60
自引率
5.90%
发文量
142
审稿时长
38 days
期刊介绍: Enzyme and Microbial Technology is an international, peer-reviewed journal publishing original research and reviews, of biotechnological significance and novelty, on basic and applied aspects of the science and technology of processes involving the use of enzymes, micro-organisms, animal cells and plant cells. We especially encourage submissions on: Biocatalysis and the use of Directed Evolution in Synthetic Biology and Biotechnology Biotechnological Production of New Bioactive Molecules, Biomaterials, Biopharmaceuticals, and Biofuels New Imaging Techniques and Biosensors, especially as applicable to Healthcare and Systems Biology New Biotechnological Approaches in Genomics, Proteomics and Metabolomics Metabolic Engineering, Biomolecular Engineering and Nanobiotechnology Manuscripts which report isolation, purification, immobilization or utilization of organisms or enzymes which are already well-described in the literature are not suitable for publication in EMT, unless their primary purpose is to report significant new findings or approaches which are of broad biotechnological importance. Similarly, manuscripts which report optimization studies on well-established processes are inappropriate. EMT does not accept papers dealing with mathematical modeling unless they report significant, new experimental data.
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