Department of Biological Medicines & Shanghai Engineering Research Center of Immunotherapeutics, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Department of Natural Medicine, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Appl Biochem Biotechnol. 2022 Jun;194(6):2528-2541. doi: 10.1007/s12010-022-03799-7. Epub 2022 Feb 15.
Phosphate concentration above 10 mM reduces the production of many secondary metabolites; however, the phenomenon is not mechanistically understood yet. Specifically, the problem of phosphorus limitation in antibiotic production remains unresolved. This study investigates the phosphorus inhibition effect on spinosad production and alleviates it by calcium and phosphate supplementation to fermentation media. Furthermore, we examined the mechanism of fatty acids-induced increase in polyketides production. Four phosphates that were supplemented into the fermentation media include NaHPO, NaHPO, KHPO, and KHPO and NaHPO was found to be the most effective phosphate. Under the optimal phosphate condition of supplementing 20 mM NaHPO on the fourth day and 5 g/L CaCO, the maximal spinosad production reached 520 mg/L, showing a 1.65-fold increase over the control treatment. In the NaHPO-CaCO system, the de novo fatty acid biosynthesis was significantly downregulated while spinosad biosynthesis and β-oxidation were upregulated. The coordination of de novo fatty acid biosynthesis and β-oxidation promoted intracellular acetyl-CoA concentration. The results demonstrate that NaHPO-CaCO combined addition is a simple and effective strategy to alleviate phosphorus inhibition effect through the regulation of fatty acid metabolism and accumulation of immediate precursors. This information improves our understanding of phosphates' influence on the large-scale production of polyketides.
磷酸盐浓度高于 10 mM 会降低许多次生代谢产物的产量;然而,其机制尚未得到充分理解。具体来说,抗生素生产中的磷限制问题仍然没有得到解决。本研究调查了磷酸盐对多杀菌素生产的抑制作用,并通过向发酵培养基中添加钙和磷酸盐来缓解这种抑制作用。此外,我们还研究了脂肪酸诱导多酮产量增加的机制。本研究向发酵培养基中添加了四种磷酸盐,包括 NaHPO、NaHPO、KHPO 和 KHPO,结果发现 NaHPO 是最有效的磷酸盐。在第四天补充 20 mM NaHPO 和 5 g/L CaCO 的最佳磷酸盐条件下,多杀菌素的最大产量达到 520 mg/L,比对照处理提高了 1.65 倍。在 NaHPO-CaCO 体系中,从头脂肪酸生物合成显著下调,而多杀菌素生物合成和β-氧化上调。从头脂肪酸生物合成和β-氧化的协调促进了细胞内乙酰辅酶 A 浓度的增加。结果表明,NaHPO-CaCO 联合添加是一种通过调节脂肪酸代谢和积累直接前体来缓解磷抑制作用的简单有效策略。这些信息提高了我们对磷酸盐对大型多酮生产影响的理解。