食品科学2023,Vol.44Issue(24):201-210,10.DOI:10.7506/spkx1002-6630-20230321-203
基于双菌耦合发酵策略的烟酰胺单核苷酸合成
A Dual-Bacterial Coupled Fermentation Strategy for Nicotinamide Mononucleotide Synthesis
摘要
Abstract
In this study,a dual-bacterial coupled fermentation system containing nicotinamide nucleoside kinase(NRK)and polyphosphatase(PPK)was constructed,and the application of PPK-based ATP regeneration system in NMN production was achieved.First,engineering strains expressing NRK1 and NRK2 were constructed,and the highly active Escherichia coli BL21(DE3)-pET28a-NRKl was selected,with NMN yield and productivity of 5.17 g/L and 77.4%,respectively.Then,the induced expression conditions of NRK1 were optimized,and a low temperature of 16 ℃,an isopropyl-β-D-thiogalactopyranoside(IPTG)concentration of 0.7 mmol/L,an inoculation amount of 3%and an induction duration of 22 h were found to be optimal the soluble expression of NRK1 protein.The optimal synthesis conditions of NMN by E.coli BL21(DE3)-pET28a-NRK1 were explored.It was found that after 12 h culture at 18 ℃ at an initial cell concentration of 100 g/L and a ratio of ATP to NR of 1∶1.5,the highest yield of NMN of 5.73 g/L was obtained with a productivity of 85.78%.Finally,the optimal conditions that provided maximal NMN production(11.81 g/L)by coupled fermentation with E.coli BL21(DE3)pET28a-PPK and E.coli BL21(DE3)-pET28a-NRKl were determined as 1∶3.5,1∶2 and 16 h for ATP to NR ratio,initial cell concentration and fermentation time,respectively.The high-density dual-bacterial coupled fermentation strategy established in this study opens up a new pathway for high-efficiency,low-cost and large-scale production of NMN.关键词
烟酰胺单核苷酸/烟酰胺核苷激酶/多聚磷酸酶/ATP再生/耦合发酵Key words
nicotinamide mononucleotide/nicotinamide nucleoside kinase/polyphosphate kinase/ATP regeneration/coupled fermentation分类
生物科学引用本文复制引用
孙婷,张洪涛,杨峰,柴文刚,薛皓阳,谭淑引..基于双菌耦合发酵策略的烟酰胺单核苷酸合成[J].食品科学,2023,44(24):201-210,10.基金项目
解放军后勤保障部开放课题(ZZCWS21J2001) (ZZCWS21J2001)