期刊
FERMENTATION-BASEL
卷 8, 期 12, 页码 -出版社
MDPI
DOI: 10.3390/fermentation8120681
关键词
Pichia pastoris; S-adenosyl-methionine; sodium citrate; untargeted metabolomics; metabolic flux analysis
资金
- National Natural Science Foundation of China
- National Key Research and Development Program of China
- [32071461]
- [2019YFA0904300]
This study investigated the cellular metabolic mechanism of feeding sodium citrate to enhance SAM production in P. pastoris using metabolomics and metabolic flux analysis. The results showed that sodium citrate had a facilitative effect on SAM production and upregulated the levels of certain metabolites and metabolic pathways involved in methanol metabolism and the TCA cycle. The study proposed that the upregulation of dihydroxyacetone level and the enhancement of citrate synthase activity by acetyl coenzyme A contributed to SAM production. These findings provide new insights into increasing the industrial production of SAM in P. pastoris.
S-adenosyl-methionine (SAM) is crucial for organisms to maintain some physiological functions. However, the inconsistency between high L-methionine feeding rate and yield during SAM production at an industrial scale and its metabolic mechanism have not been elucidated. Here, the cellular metabolic mechanism of feeding sodium citrate to the Pichia pastoris (P. pastoris) G12'/AOX-acs2 strain to enhance SAM production was investigated using untargeted metabolomics and metabolic flux analysis. The results indicated that the addition of sodium citrate has a facilitative effect on SAM production. In addition, 25 metabolites, such as citrate, cis-aconitate, and L-glutamine, were significantly up-regulated, and 16 metabolites, such as glutathione, were significantly down-regulated. Furthermore, these significantly differential metabolites were mainly distributed in 13 metabolic pathways, such as the tricarboxylic acid (TCA) cycle. In addition, the metabolic fluxes of the glycolysis pathway, pentose phosphate pathway, TCA cycle, and glyoxylate pathway were increased by 20.45-29.32%, respectively, under the condition of feeding sodium citrate compared with the control. Finally, it was speculated that the upregulation of dihydroxyacetone level might increase the activity of alcohol oxidase AOX1 to promote methanol metabolism by combining metabolomics and fluxomics. Meanwhile, acetyl coenzyme A might enhance the activity of citrate synthase through allosteric activation to promote the flux of the TCA cycle and increase the level of intracellular oxidative phosphorylation, thus contributing to SAM production. These new insights into the L-methionine utilization for SAM biosynthesis by systematic biology in P. pastoris provides a novel vision for increasing its industrial production.
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