Nagaraj Yashaswini Nagavara, Blomqvist Johanna, Sampels Sabine, Pickova Jana, Sandgren Mats, Gajdoš Peter, Čertík Milan, Passoth Volkmar
Department of Molecular Science, Swedish University of Agricultural Sciences, Uppsala BioCentre, P.O. Box 7051, 750 07, Uppsala, Sweden.
Institute of Biotechnology, Faculty of Chemical and Food Technology, Slovak University of Technology, Radlinského 9, 812 37, Bratislava, Slovakia.
Biotechnol Biofuels Bioprod. 2025 Mar 21;18(1):35. doi: 10.1186/s13068-025-02632-7.
Oil from oleaginous yeasts has the potential to replace non-sustainable vegetable oil as raw material to produce food, feed, biofuels, or biochemicals. Co-produced compounds like carotenoids may be helpful to obtain economically viable bioprocesses. Identifying appropriate extraction methods is a bottleneck both for establishing oleaginous yeasts as cell factories for both oil and carotenoids production and for analysis of intracellular compounds like lipids and carotenoids. We conducted extractions using supercritical carbon dioxide (SC-CO) and conventional solvent methods to extract and analyze lipids and carotenoids from R. toruloides CBS 14 cells grown on wheat straw hydrolysate. The lipid extracts were analyzed using gas chromatography (GC), and the carotenoids were identified and quantified using ultra-high-performance liquid chromatography (UHPLC).
Four main carotenoids in the extracts from both extraction methods were identified including β-carotene, γ-carotene, torularhodin, and torulene. Interestingly, torularhodin was the major carotenoid extracted using SC-CO extraction, followed by torulene. This was different from the conventional acetone extraction method, where β-carotene was the main carotenoid. After the conventional extraction, torularhodin and torulene underwent degradation due to the saponification step, which was necessary to remove lipids before UHPLC analysis. The total carotenoid concentration obtained from SC-CO extraction was 332.09 ± 27.32 μg/g dry weight compared to 19.9 ± 2.74 μg/g dry weight in acetone extraction. A small amount of carotenoids was observed to be lost into the lipid extract, but this loss was not as substantial as that seen with acetone extraction. Additionally, the total lipid content in samples extracted using SC-CO was significantly lower than that obtained using the conventional Folch method. GC analysis revealed that oleic acid was the major fatty acid in both lipid extracts, followed by palmitic acid and linoleic acid. Notably, the proportion of unsaturated fatty acids was higher in the extracts from the SC-CO method compared to the conventional method.
These findings indicate that the SC-CO extraction method outperformed conventional methods by preserving the integrity of unsaturated lipids and retaining an abundance of carotenoids, resulting in high-quality extracts.
产油酵母中的油脂有潜力替代不可持续的植物油,作为生产食品、饲料、生物燃料或生化制品的原料。类胡萝卜素等共生产物可能有助于实现经济上可行的生物工艺。确定合适的提取方法,对于将产油酵母确立为生产油脂和类胡萝卜素的细胞工厂以及分析细胞内化合物(如脂质和类胡萝卜素)而言,都是一个瓶颈。我们采用超临界二氧化碳(SC-CO)和传统溶剂法进行提取,以从小麦秸秆水解物中生长的圆红冬孢酵母CBS 14细胞中提取并分析脂质和类胡萝卜素。脂质提取物采用气相色谱(GC)分析,类胡萝卜素则使用超高效液相色谱(UHPLC)进行鉴定和定量。
两种提取方法的提取物中均鉴定出四种主要类胡萝卜素,包括β-胡萝卜素、γ-胡萝卜素、深红酵母红素和圆酵母素。有趣的是,深红酵母红素是采用SC-CO提取法提取的主要类胡萝卜素,其次是圆酵母素。这与传统的丙酮提取法不同,在传统方法中β-胡萝卜素是主要类胡萝卜素。传统提取后,深红酵母红素和圆酵母素由于皂化步骤而发生降解,皂化步骤是UHPLC分析前去除脂质所必需的。SC-CO提取法获得的总类胡萝卜素浓度为332.09±27.32μg/g干重,而丙酮提取法为19.9±2.74μg/g干重。观察到少量类胡萝卜素损失到脂质提取物中,但这种损失不如丙酮提取法那么大。此外,采用SC-CO提取的样品中的总脂质含量显著低于采用传统Folch法获得的含量。GC分析表明,油酸是两种脂质提取物中的主要脂肪酸,其次是棕榈酸和亚油酸。值得注意的是,与传统方法相比,SC-CO法提取物中不饱和脂肪酸的比例更高。
这些发现表明,SC-CO提取法在保持不饱和脂质完整性和保留大量类胡萝卜素方面优于传统方法,从而得到高质量的提取物。