Jiang Yu, Li Xianping, Zhang Wei, Ji Yadong, Yang Kai, Liu Lu, Zhang Minghui, Qiao Weicang, Zhao Junying, Du Mengjing, Fan Xiaofei, Dang Xingfen, Chen Huo, Jiang Tiemin, Chen Lijun
South Asia Branch of National Engineering Center of Dairy for Maternal and Child Health, Guilin University of Technology, Guilin, China.
National Engineering Research Center of Dairy Health for Maternal and Child, Beijing Sanyuan Foods Co., Ltd., Beijing, China.
Front Microbiol. 2024 May 15;15:1402654. doi: 10.3389/fmicb.2024.1402654. eCollection 2024.
Folate supplementation is crucial for the human body, and the chemically synthesized folic acid might have undesirable side effects. The use of molecular breeding methods to modify the genes related to the biosynthesis of folate by probiotics to increase folate production is currently a focus of research.
In this study, the folate-producing strain of B1-28 was isolated from human breast milk, and the difference between B1-28 and gene deletion strain was investigated by phenotyping, probiotic evaluation, metabolism and transcriptome analysis.
The results showed that the folate producted by the was 2-3 folds that of the B1-28. Scanning electron microscope showed that had rougher surface, and the acid-producing capacity ( = 0.0008) and adhesion properties ( = 0.0096) were significantly enhanced than B1-28. Transcriptomic analysis revealed that differentially expressed genes were mainly involved in three pathways, among which the biosynthesis of ribosome and aminoacyl-tRNA occurred in the key metabolic pathways. Metabolomics analysis showed that affected 5 metabolic pathways, involving 89 different metabolites.
In conclusion, the editing of a key gene of in folate biosynthesis pathway provides a feasible pathway to improve folate biosynthesis in breast milk-derived probiotics.
叶酸补充对人体至关重要,化学合成的叶酸可能有不良副作用。利用分子育种方法修饰益生菌中与叶酸生物合成相关的基因以增加叶酸产量是目前的研究热点。
本研究从人母乳中分离出产叶酸菌株B1-28,并通过表型分析、益生菌评估、代谢和转录组分析研究了B1-28与基因缺失菌株之间的差异。
结果表明,[此处原文缺失菌株名称]产生的叶酸是B1-28的2至3倍。扫描电子显微镜显示,[此处原文缺失菌株名称]表面更粗糙,产酸能力([此处原文缺失产酸能力相关数值的比较对象] = 0.0008)和黏附特性([此处原文缺失黏附特性相关数值的比较对象] = 0.0096)比B1-28显著增强。转录组分析表明,差异表达基因主要涉及三条途径,其中核糖体和氨酰基-tRNA的生物合成发生在关键代谢途径中。代谢组学分析表明,[此处原文缺失菌株名称]影响5条代谢途径,涉及89种不同代谢物。
总之,对[此处原文缺失菌株名称]叶酸生物合成途径中的关键基因进行编辑为改善母乳来源益生菌中的叶酸生物合成提供了一条可行途径。