Suppr超能文献

缺乏 ∆5 去饱和酶活性会损害红鲷鱼和日本牙鲆鱼细胞中 EPA 和 DHA 的合成。

Lack of ∆5 Desaturase Activity Impairs EPA and DHA Synthesis in Fish Cells from Red Sea Bream and Japanese Flounder.

机构信息

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.

出版信息

Mar Biotechnol (NY). 2021 Jun;23(3):472-481. doi: 10.1007/s10126-021-10040-9. Epub 2021 Jun 26.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验