Pan Xueshan, Li Tonggang, Wang Baobei, Qi Shuhua, Yang Dandan, Huang Zheng, Gao Renfei, Li Jingyan, Ling Xueping, Lu Yinghua
Department of Biochemistry and Molecular Biology, School of Laboratory Medicine, Bengbu Medical College, Bengbu, People's Republic of China.
Department of Hygiene, School of Public Health, Bengbu Medical College, Bengbu, People's Republic of China.
Bioresour Bioprocess. 2023 Apr 26;10(1):29. doi: 10.1186/s40643-023-00650-7.
Astaxanthin is an important ketocarotenoid widely used in industries. However, its application is limited because of its low yield. Sodium citrate (Na-citrate), one of the major carbon sources for microorganisms, can promote cell growth and product accumulation. The basidiomycetous red yeast Xanthophyllomyces dendrorhous was thus used to study the effect of Na-citrate on cell growth and astaxanthin synthesis. The highest biomass and astaxanthin yield (6.0 g/L and 22.5 mg/L) were obtained in shake-flask when 3 g/L Na-citrate was added at 24 h and were 1.8 and 2.0 times higher than those of the control group, respectively. Furthermore, metabolomics and real-time reverse transcription PCR (qRT-PCR) analysis were conducted to study the metabolic pathways of X. dendrorhous in response to Na-citrate. The qRT-PCR assay revealed that Na-citrate facilitated glucose consumption, promoted the metabolic flux from glycolysis, and regulated the tricarboxylic acid (TCA) cycle, providing more energy and substrates for the synthesis of astaxanthin. The gene analysis revealed that adding Na-citrate significantly upregulated the expression of six key genes (ICL, HMGS, crtE, crtYB, crtI, and crtS) involved in pathways related to astaxanthin biosynthesis. These results suggest that exogenous Na-citrate treatment is a potentially valuable strategy to stimulate astaxanthin production in X. dendrorhous.
虾青素是一种重要的酮类胡萝卜素,广泛应用于工业领域。然而,由于其产量较低,其应用受到限制。柠檬酸钠(Na-柠檬酸盐)是微生物的主要碳源之一,可促进细胞生长和产物积累。因此,利用担子菌红酵母Xanthophyllomyces dendrorhous研究了柠檬酸钠对细胞生长和虾青素合成的影响。在摇瓶中,当在24小时添加3 g/L柠檬酸钠时,获得了最高生物量和虾青素产量(分别为6.0 g/L和22.5 mg/L),分别比对照组高1.8倍和2.0倍。此外,进行了代谢组学和实时逆转录PCR(qRT-PCR)分析,以研究X. dendrorhous响应柠檬酸钠的代谢途径。qRT-PCR分析表明,柠檬酸钠促进了葡萄糖消耗,促进了糖酵解的代谢通量,并调节了三羧酸(TCA)循环,为虾青素的合成提供了更多能量和底物。基因分析表明,添加柠檬酸钠显著上调了与虾青素生物合成相关途径中六个关键基因(ICL、HMGS、crtE、crtYB、crtI和crtS)的表达。这些结果表明,外源柠檬酸钠处理是刺激X. dendrorhous中虾青素产生的一种潜在有价值的策略。