Abstract

During seed imbibition, lipids are engaged in membrane reorganization while facing free radical-mediated oxidative injury. In the present work, we explored changes in lipid components at different timepoints of imbibition (0.5, 2, 4, 6, and 8 h) in the legume Medicago truncatula, by combining biochemical approaches with targeted lipidomics and untargeted metabolomics. ROS and RNS (reactive oxygen and nitrogen species) accumulation was observed throughout the tested timepoints whereas lipid peroxidation increased at 4 h of imbibition. The seed response to oxidative damage was evidenced by a significant increase in tocopherols starting from 0.5 h of imbibition as well as by the reduction in total thiol content occurring at 2 h of imbibition. Since under physiological conditions, the proper functions of the cell membranes are strongly dependent on the qualitative and quantitative balance of fatty acid residues in phospholipids, the investigation was expanded to the fatty acid cohort of M. truncatula seeds. Total saturated fatty acids (SFAs), monounsaturated fatty acids (MUFAs), polyunsaturated fatty acids (PUFAs), omega(ω)-3 and omega(ω)-6 fatty acids showed fluctuations during seed imbibition. The most remarkable finding was the profile of the ω-3 PUFA docosopentaenoic acid (DPA, 7 cis, 10 cis, 13 cis, 16 cis, and 19 cis-22:5) that showed a peak (up to 1.0% of the total fatty acid content) at 0.5 and 8 h of imbibition, concomitant with the peaks observed in tocopherol levels. It is possible that the observed changes in DPA alter the physical properties of membranes, as reported in animal cells, triggering signaling pathways relevant for the cell defense against oxidative injury. Furthermore, the content and balance between tocopherols and PUFAs is regarded as a determinant of storage stability. No enhancement in trans-fatty acids occurred throughout imbibition, suggesting for a proper antioxidant response carried by the seed. Fatty acids profiles were integrated with data from untargeted metabolomics showing changes in lipid sub-pathways, among which fatty acid amide, lyso-phospholipids, and phospholipid metabolism. The emerging lipid profiles and dynamics are discussed in view of the overall imbibition damage generated during M. truncatula seed imbibition.

Highlights

  • Seed germination is a crucial event in the plant life cycle and, depending on seed quality, this step can severely constrain crop yield with a negative impact on the food chain

  • We explored changes in lipid metabolism concomitant with early seed imbibition in the model legume Medicago truncatula by combining approaches that highlight lipid oxidative damage profiles, as well as the antioxidant response, with targeted fatty acid lipidomics and untargeted metabolomics

  • M. truncatula seeds were collected at selected timepoints during imbibition and ROS levels were measured in dry seeds (DS) and rehydrated seeds (0.5, 2, 4, 6, and 8 h of imbibition) using the dichlorofluorescein diacetate (DCF-differentially accumulated (DA)) fluorescent dye (Figure 1B)

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Summary

Introduction

Seed germination is a crucial event in the plant life cycle and, depending on seed quality, this step can severely constrain crop yield with a negative impact on the food chain. The progressive depletion of oxygen generates conditions that almost achieve anaerobiosis and fermentation is triggered as the main source of cellular ATP, supporting the reduction of electron transferring compounds, e.g. NAD and NADP, and inevitably leading to ROS (reactive oxygen species) accumulation (Ma et al, 2016). At this stage, mitochondria, peroxisomes and the plasma membrane NADPH oxidases are the main sources of ROS, together with lipid catabolism and lipid β-oxidation in the glyoxysomes (Rajjou et al, 2012). NO turnover, by means of RNS (reactive nitrogen species) scavenging mechanisms, contributes to maintain a redox balance within the seed (Wulff et al, 2009)

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Conclusion

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