Abstract

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.

Highlights

  • Barley is a model organism for investigating the cereal germination process (Gorzolka et al, 2016) which commences with the uptake of water by the quiescent dry seed and finishes with the emergence of the radicle through the seed coat

  • MALDI-Mass Spectrometry Imaging (MSI) analysis was performed for seeds grown under control and saline conditions and harvested at six different time points, namely 0, 8, 16, 24, 48, and 72 h post imbibition (Figure S1)

  • Sublimation of sectioned tissue with dihydroxy benzoic acid (DHB) matrix was used for MALDI-MSI positive mode ionization to image the spatial distribution of a wide range of lipids (m/z 150–2,800) in the seed sections

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Summary

Introduction

Barley is a model organism for investigating the cereal germination process (Gorzolka et al, 2016) which commences with the uptake of water by the quiescent dry seed and finishes with the emergence of the radicle through the seed coat. High intracellular concentrations of both Na+ and Cl− can inhibit the metabolism of dividing and expanding cells (Neumann, 1997), restrict mobilization, and hinder seedling emergence (Marques et al, 2013; Alencar et al, 2015). These conditions result in retarded (Zhang et al, 2010) or delayed (Ashraf et al, 2003) germination. The molecular changes in barley seed during germination that may play a role in tolerance or sensitivity are important in determining a plant’s overall response to salinity

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