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Spatio-Temporal Metabolite and Elemental Profiling of Salt Stressed Barley Seeds During Initial Stages of Germination by MALDI-MSI and µ-XRF Spectrometry

机译:MALDI-MSI和µ-XRF光谱分析盐胁迫大麦种子萌发初期的时空代谢产物和元素分析

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摘要

Seed germination is the essential first step in crop establishment, and can be severely affected by salinity stress which can inhibit essential metabolic processes during the germination process. Salt stress during seed germination can trigger lipid-dependent signalling cascades that activate plant adaptation processes, lead to changes in membrane fluidity to help resist the stress, and cause secondary metabolite responses due to increased oxidative stress. In germinating barley (Hordeum vulgare), knowledge of the changes in spatial distribution of lipids and other small molecules at a cellular level in response to salt stress is limited. In this study, mass spectrometry imaging (MSI), liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QToF-MS), inductively coupled plasma mass spectrometry (ICP-MS), and X-ray fluorescence (XRF) were used to determine the spatial distribution of metabolites, lipids and a range of elements, such as K+ and Na+, in seeds of two barley genotypes with contrasting germination phenology (Australian barley varieties Mundah and Keel). We detected and tentatively identified more than 200 lipid species belonging to seven major lipid classes (fatty acyls, glycerolipids, glycerophospholipids, sphingolipids, prenol lipids, sterol lipids, and polyketides) that differed in their spatial distribution based on genotype (Mundah or Keel), time post-imbibition (0 to 72 h), or treatment (control or salt). We found a tentative flavonoid was discriminant in post-imbibed Mundah embryos under saline conditions, and a delayed flavonoid response in Keel relative to Mundah. We further employed MSI-MS/MS and LC-QToF-MS/MS to explore the identity of the discriminant flavonoid and study the temporal pattern in five additional barley genotypes. ICP-MS was used to quantify the elemental composition of both Mundah and Keel seeds, showing a significant increase in Na+ in salt treated samples. Spatial mapping of elements using µ-XRF localized the elements within the seeds. This study integrates data obtained from three mass spectrometry platforms together with µ-XRF to yield information on the localization of lipids, metabolites and elements improving our understanding of the germination process under salt stress at a molecular level.
机译:种子发芽是作物生长的重要第一步,盐分胁迫会严重影响种子发芽,而盐分胁迫会抑制发芽过程中必需的代谢过程。种子发芽过程中的盐胁迫会触发脂质依赖性信号传导级联反应,从而激活植物适应过程,导致膜流动性发生变化,从而帮助抵抗胁迫,并由于氧化应激增加而引起次级代谢产物反应。在发芽的大麦(大麦)中,对于盐胁迫响应的脂质和其他小分子在细胞水平上的空间分布变化的认识是有限的。在这项研究中,使用了质谱成像(MSI),液相色谱四极杆飞行时间质谱(LC-QToF-MS),电感耦合等离子体质谱(ICP-MS)和X射线荧光(XRF)确定发芽物候相反的两个大麦基因型种子中的代谢物,脂质和一系列元素(如K + 和Na + )的空间分布(澳大利亚大麦品种Mundah和Keel)。我们检测并初步确定了200多种脂类,它们属于7种主要的脂类(脂酰基,甘油脂,甘油磷脂,鞘脂,烯醇脂,固醇脂和聚酮化合物),其空间分布基于基因型(Mundah或Keel)而有所不同,吸收后的时间(0至72小时)或治疗(对照或盐)。我们发现,暂定类黄酮在盐水条件下在吸收后的Mundah胚胎中是有区别的,相对于Mundah,龙骨中的类黄酮反应延迟。我们进一步采用MSI-MS / MS和LC-QToF-MS / MS来探索鉴别类黄酮的身份,并研究另外5种大麦基因型的时间模式。 ICP-MS定量分析了蒙达和龙骨种子的元素组成,表明盐处理样品中Na + 的显着增加。使用µ-XRF对元素进行空间映射可以将元素定位在种子中。这项研究整合了从三个质谱平台获得的数据以及µ-XRF,以产生有关脂质,代谢物和元素定位的信息,从而提高了我们对分子水平在盐胁迫下发芽过程的理解。

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