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. 2020 Aug 21:2020:2148032.
doi: 10.1155/2020/2148032. eCollection 2020.

Response of Soybean Root to Phosphorus Deficiency under Sucrose Feeding: Insight from Morphological and Metabolome Characterizations

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Response of Soybean Root to Phosphorus Deficiency under Sucrose Feeding: Insight from Morphological and Metabolome Characterizations

Ahui Yang et al. Biomed Res Int. .

Abstract

Phosphorus (P) is one the least available essential plant macronutrients in soils that is a major constraint on plant growth. Soybean (Glycine max L.) production is often limited due to low P availability. The better management of P deficiency requires improvement of soybean's P use efficiency. Sugars are implicated in P starvation responses, and a complete understanding of the role of sucrose together with P in coordinating P starvation responses is missing in soybean. This study explored global metabolomic changes in previously screened low-P-tolerant (Liaodou, L13) and low-P-sensitive (Tiefeng 3, T3) soybean genotypes by liquid chromatography coupled mass spectrometry. We also studied the root morphological response to sucrose application (1%) in P-starved soybean genotypes against normal P supply. Root morphology in L13 genotype has significantly improved P starvation responses as compared to the T3 genotype. Exogenous sucrose application greatly affected root length, root volume, and root surface area in L13 genotype while low-P-sensitive genotype, i.e., T3, only responded by increasing number of lateral roots. Root : shoot ratio increased after sucrose treatment regardless of P conditions, in both genotypes. T3 showed a relatively higher number of differentially accumulated metabolites between P-starved and normal P conditions as compared to L13 genotype. Common metabolites accumulated under the influence of sucrose were 5-O-methylembelin, D-glucuronic acid, and N-acetyl-L-phenylalanine. We have discussed the possible roles of the pathways associated with these metabolites. The differentially accumulated metabolites between both genotypes under the influence of sucrose are also discussed. These results are important to further explore the role of sucrose in the observed pathways. Especially, our results are relevant to formulate strategies for improving P efficiency of soybean genotypes with different P efficiencies.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
(a) Root physiological responses, (b) root : shoot ratio, and (c) root sucrose content of L13 and T3 soybean genotypes grown under P starvation (-P) and normal P (+P) levels fed with (+S) or without (-S) exogenous sucrose application. The error bars represent standard deviation, and the different letters on the bars show significantly different values.
Figure 2
Figure 2
(a) Principle component analysis and KEGG pathway analysis of (b) L13 and (c) T3 soybean roots grown in P-starved conditions (-P) fed with (+S) or without sucrose (-S). ∗, ∗∗, and ∗∗∗ represent KEGG pathways significantly enriched at p < 0.05, 0.01, and 0.001, respectively.
Figure 3
Figure 3
Effect of exogenous sucrose application (+S/-S) on ascorbate and aldarate metabolism in L13 and T3 soybean genotypes' roots under P starvation conditions (-P).

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References

    1. Crafts-Brandner S. J. Phosphorus nutrition influence on starch and sucrose accumulation, and activities of ADP-glucose pyrophosphorylase and sucrose-phosphate synthase during the grain filling period in soybean. Plant Physiology. 1992;98(3):1133–1138. doi: 10.1104/pp.98.3.1133. - DOI - PMC - PubMed
    1. Zhang Z., Liao H., Lucas W. J. Molecular mechanisms underlying phosphate sensing, signaling, and adaptation in plants. Journal of Integrative Plant Biology. 2014;56(3):192–220. doi: 10.1111/jipb.12163. - DOI - PubMed
    1. Rubio V., Linhares F., Solano R., et al. A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae. Genes & Development. 2001;15(16):2122–2133. doi: 10.1101/gad.204401. - DOI - PMC - PubMed
    1. Hammond J. P., Broadley M. R., White P. J. Genetic responses to phosphorus deficiency. Annals of Botany. 2004;94(3):323–332. doi: 10.1093/aob/mch156. - DOI - PMC - PubMed
    1. Miura K., Rus A., Sharkhuu A., et al. The Arabidopsis SUMO E3 ligase SIZ1 controls phosphate deficiency responses. Proceedings of the National Academy of Sciences. 2005;102(21):7760–7765. doi: 10.1073/pnas.0500778102. - DOI - PMC - PubMed

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