首页> 外文期刊>Frontiers in Marine Science >Metabolic Remodeling of Membrane Glycerolipids in the Microalga Nannochloropsis oceanica under Nitrogen Deprivation
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Metabolic Remodeling of Membrane Glycerolipids in the Microalga Nannochloropsis oceanica under Nitrogen Deprivation

机译:氮剥夺下微藻Nannochloropsis oceanica中膜甘油脂的代谢重塑

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The lack of lipidome analytical tools has limited our ability to gain new knowledge about lipid metabolism in microalgae, especially for membrane glycerolipids. An electrospray ionization mass spectrometry-based lipidomics method was developed for Nannochloropsis oceanica IMET1, which resolved 41 membrane glycerolipids molecular species belonging to eight classes. Changes in membrane glycerolipids under nitrogen deprivation and high-light (HL) conditions were uncovered. The results showed that the amount of plastidial membrane lipids including monogalactosyldiacylglycerol, phosphatidylglycerol, and the extraplastidic lipids diacylglyceryl-O-4’-(N, N, N,-trimethyl) homoserine and phosphatidylcholine decreased drastically under HL and nitrogen deprivation stresses. Algal cells accumulated considerably more digalactosyldiacylglycerol and sulfoquinovosyldiacylglycerols under stresses. The genes encoding enzymes responsible for biosynthesis, modification and degradation of glycerolipids were identified by mining a time-course global RNA-seq data set. It suggested that reduction in lipid contents under nitrogen deprivation is not attributable to the retarded biosynthesis processes, at least at the gene expression level, as most genes involved in their biosynthesis were unaffected by nitrogen supply, yet several genes were significantly up-regulated. Additionally, a conceptual eicosapentaenoic acid (EPA) biosynthesis network is proposed based on the lipidomic and transcriptomic data, which underlined import of EPA from cytosolic glycerolipids to the plastid for synthesize EPA-containing chloroplast membrane lipids.
机译:缺少脂质组分析工具限制了我们获得有关微藻中脂质代谢的新知识的能力,特别是对于膜甘油脂。开发了一种基于电喷雾电离质谱的脂质组学方法,用于分离拟南芥IMET1,可分离出八类41种膜甘油脂分子。未发现氮缺乏和高光(HL)条件下膜甘油脂的变化。结果表明,在HL和氮剥夺胁迫下,包括单半乳糖基二酰基甘油,磷脂酰甘油和塑性外脂二酰基甘油-O-4’-(N,N,N,-三甲基)高丝氨酸和磷脂酰胆碱在内的质膜脂质的含量急剧下降。在压力下,藻类细胞积聚了更多的二半乳糖基二酰基甘油和磺基喹喔基二酰基甘油。通过挖掘随时间变化的全局RNA-seq数据集,可以确定编码负责甘油的生物合成,修饰和降解的酶的基因。这表明至少在基因表达水平上,氮剥夺下脂质含量的降低并非归因于生物合成过程的延迟,因为大多数参与其生物合成的基因不受氮供应的影响,但几个基因却被显着上调。另外,基于脂质组和转录组数据,提出了概念性二十碳五烯酸(EPA)生物合成网络,该网络强调了EPA从胞质甘油脂到质体的导入,以合成含EPA的叶绿体膜脂质。

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