Department of Bioscience and Biotechnology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, 744 Moto-oka, Nishi-ku, Fukuoka, 819-0395, Japan.
Faculty of Pharma-Science, Teikyo University, Kaga 2-11-1, Itabashi-ku, Tokyo, 173-8605, Japan.
Mar Biotechnol (NY). 2021 Jun;23(3):472-481. doi: 10.1007/s10126-021-10040-9. Epub 2021 Jun 26.
Long-chain (≥ C) polyunsaturated fatty acids (LC-PUFA), such as eicosapentaenoic acid (20:5n-3, EPA) and docosahexaenoic acid (22:6n-3, DHA), are necessary for human health and are obtained from marine fish-derived oils. Marine fish are LC-PUFA-rich animals; however, many of them require LC-PUFA for growth. Therefore, it is suggested that they do not have sufficient ability to biosynthesize LC-PUFA. To evaluate in vivo LC-PUFA synthetic activity in fish cells, fish-derived cell lines from red sea bream (Pagrus major, PMS and PMF), Japanese flounder (Paralichthys olivaceus, HINAE), and zebrafish (Danio rerio, BRF41) were incubated with n-3 fatty acids labeled by radioisotopes or stable isotopes, and then, n-3 PUFA were analyzed by thin-layer chromatography or liquid chromatography-mass spectrometry. Labeled EPA and DHA were biosynthesized from labeled α-linolenic acid (18:3n-3) in BRF41, whereas they were not detected in PMS, PMF, or HINAE cells. We next cloned the fatty acid desaturase 2 (Fads2) cDNAs from PMF cells and zebrafish, expressed in budding yeasts, and then analyzed the substrate specificities of enzymes. As a result, we found that Fads2 from PMF cells was a ∆6/∆8 desaturase. Collectively, our study indicates that cell lines from red sea bream and Japanese flounder were not able to synthesize EPA or DHA by themselves, possibly due to the lack of ∆5 desaturase activity. Furthermore, this study provides a sensitive and reproducible non-radioactive method for evaluating LC-PUFA synthesis in fish cells using a stable isotope and liquid chromatography-mass spectrometry.
长链(≥C)多不饱和脂肪酸(LC-PUFA),如二十碳五烯酸(20:5n-3,EPA)和二十二碳六烯酸(22:6n-3,DHA),对人体健康是必需的,可从海洋鱼类衍生油中获得。海洋鱼类是 LC-PUFA 丰富的动物;然而,它们中的许多鱼类需要 LC-PUFA 才能生长。因此,有人建议它们没有足够的能力生物合成 LC-PUFA。为了评估鱼类细胞中 LC-PUFA 的合成活性,用放射性同位素或稳定同位素标记来自真鲷(Pagrus major,PMS 和 PMF)、牙鲆(Paralichthys olivaceus,HINAE)和斑马鱼(Danio rerio,BRF41)的鱼类细胞系进行孵育,然后通过薄层层析或液相色谱-质谱分析 n-3 多不饱和脂肪酸。BRF41 中标记的 α-亚麻酸(18:3n-3)可生物合成标记的 EPA 和 DHA,而 PMS、PMF 或 HINAE 细胞中则未检测到。接下来,我们从 PMF 细胞和斑马鱼中克隆脂肪酸去饱和酶 2(Fads2)cDNA,在出芽酵母中表达,并分析酶的底物特异性。结果表明,PMF 细胞的 Fads2 是一种 ∆6/∆8 去饱和酶。总之,我们的研究表明,真鲷和牙鲆的细胞系本身不能合成 EPA 或 DHA,可能是由于缺乏 ∆5 去饱和酶活性。此外,本研究提供了一种使用稳定同位素和液相色谱-质谱法评估鱼类细胞中 LC-PUFA 合成的敏感且可重复的非放射性方法。