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Enzyme Microb Technol ; 180: 110482, 2024 Jul 20.
Artigo em Inglês | MEDLINE | ID: mdl-39059289

RESUMO

ß-nicotinamide mononucleotide (ß-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 ß-NMN. Using D-ribose and nicotinamide as substrates, the ß-NMN yield reached 97.5 % catalyzed by purified enzymes. Then, after knocking out the genes encoding proteins that consume ß-NMN in E. coli BL21(DE3), the similar ß-NMN yield, 97.2 %, using the crude enzymes could be also obtained. After that, ß-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 ß-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 ß-NMN preparation level with phosphoribosylpyrophosphate as the core reported till now.

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