Enhancing the biosynthesis of nicotinamide mononucleotide in Lactococcus lactis by heterologous expression of FtnadE

被引:13
|
作者
Kong, Ling-Hui [1 ]
Liu, Tai-Yu [2 ]
Yao, Qing-Shou [1 ]
Zhang, Xiao-Hua [1 ]
Xu, Wei-Na [1 ]
Qin, Jia-Yang [1 ]
机构
[1] Binzhou Med Univ, Sch Pharm, Yantai 264003, Shandong, Peoples R China
[2] Shanghai BEIONMED Technol Co Ltd, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
nicotinamide mononucleotide; heterologous expression; CRISPR; nCas9; Lactococcus lactis;
D O I
10.1002/jsfa.12253
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
BACKGROUND Nicotinamide mononucleotide (NMN), a key intermediate of nicotinamide adenine dinucleotide, plays an important in anti-aging and disease. Lactococcus lactis, an important probiotic lactic acid bacteria (LAB), has shown great potential for the biosynthesis of NMN, which will significantly affect the probiotic effects of the dairy products. RESULTS We used the CRISPR/nCas9 technique to knockout nadR gene of L. lactis NZ9000 to enhance the accumulation of NMN by 61%. The nadE* gene from Francisella tularensis with codon optimization was heterologous in L. lactis NZ9000 Delta nadR and has a positive effect on NMN production. Combined with optimization of the concentration of substrate nicotinamide, a final intracellular NMN titer was 2289 mu mol L-1 mg(-1) with 10 g L-1 nicotinamide supplement, which was 5.7-fold higher than that of the control. The transcription levels of key genes (pncA, nadD and prs1) involved in NMN biosynthesis were up-regulated by more than two-fold, indicating that the increase of NMN titer was attributed to FtnadE* heterologous expression. CONCLUSION Our study provides a better understanding of the NMN biosynthesis pathway in L. lactis, and can facilitate NMN production in LAB via synthetic biology approaches. (c) 2022 Society of Chemical Industry.
引用
收藏
页码:450 / 456
页数:7
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