Carbon-Nitrogen Metabolic Responses and Adaptive Strategies to Low-Nitrogen Stress in Glycine soja

Authors

  • He WANG Chang Chun Normal University, School of Life Sciences, 130024, Changchun (CN)
  • Rui GUO Chinese Academy of Agricultural Sciences, Institute of Environment and Sustainable Development in Agriculture, Key Laboratory of Dryland Agriculture, 100081, Beijing (CN)
  • Yongjun HU Chang Chun Normal University, School of Life Sciences, 130024, Changchun (CN)
  • Defu HAN Chang Chun Normal University, School of Life Sciences, 130024, Changchun (CN)

DOI:

https://doi.org/10.15835/nbha47411567

Keywords:

carbon-nitrogen mechanism; Glycine soja; low-nitrogen; physiology; stress

Abstract

Nitrogen (N) is an essential mineral nutrient for plant growth and development. Wild soybean (Glycine soja), which has many superior traits, is an important germplasm resource and is also an excellent experimental material for researching the mechanisms of low-N tolerance. In this study, the physiological differences between common wild soybean (W1) and low-N tolerant wild soybean (W2) among growth characteristics, photosynthetic carbon (C) metabolism, N metabolism and C-N metabolic-coupling relationship were investigated, and the mechanism of low-N tolerance of wild soybean was explained at three different levels of low-N stress. Both W1 and W2 showed some resistance to low-level N stress. However, W2 could withstand the damage by increasing the root length and root–shoot ratio under high-level stress conditions. Moreover, when resisting low-N stress, W2 maintained a stable photosynthetic rate and coordinated ion balance to maintain required nutrient levels. W2 also tolerated low N by coordinating the C-N metabolic balance through the accumulation of soluble sugars to provide energy and C skeletons for N metabolism and through enhanced N metabolic enzyme activities and soluble protein accumulation levels to supply the enzyme proteins and photosynthetic pigments for C metabolism. The current results provide a physiological methodology and theoretical basis for protecting wild soybean germplasm resources and improving cultivated soybean.

References

Akay G, Burke DR (2012). Agro-process intensification through synthetic rhizosphere media for nitrogen fixation and yield enhancement in plants. American Journal of Agricultural and Biological Science 7(2):150-172.

Alemán F, Nievescordones M, Martínez V, Rubio F (2011). Root k (+) acquisition in plants the Arabidopsis thaliana model. Plant and Cell Physiology 52(9):1603-1612.

Amiour N, Imbaud S, Cl Mao Ment G, Agier N, Zivy M, Valot B (2012). The use of metabolomics integrated with transcriptomic and proteomic studies for identifying key steps involved in the control of nitrogen metabolism in crops such as maize. Journal of Experimental Botany 63(14):5017.

Chang JF, Dong PF, Wang XL, Liu WL, Chaohai LI, University HA (2017). Effect of nitrogen application on carbon and nitrogen metabolism of different summer maize varieties. Scientia Agricultura Sinica 50(12):2282-2293.

Chen JK, Tan LT, Chun-Ming YU, Zhu AG, Ping C, Wang YZ (2017). Effects of different nitrogen levels on key enzyme activities associated with nitrogen metabolism of feed ramie. Acta Prataculturae Sinica 10:29.

Ciocco CD, Penón E, Coviella C, López S, Diaz-Zorita M, Momo F (2011). Nitrogen fixation by soybean in the pampas: relationship between yield and soil nitrogen balance. Agrochimica 55(6):1-10.

Duanmu HZ, Wang Y, Bai X, Cheng SF, Deyholos MK, Wong GKS, … Zhu YM (2015). Wild soybean roots depend on specific transcription factors and oxidation reduction related genes in response to alkaline stress. Functional and Integrative Genomics 15(6):651-660.

Farag MA, Porzel A, Wessjohann LA (2012). Comparative metabolite profiling and fingerprinting of medicinal licorice roots using a multiplex approach of GC-MS, LC-MS and 1D NMR techniques. Phytochemistry 76:60-72.

Gupta N, Gupta AK, Gaur VS, Kumar A (2012). Relationship of nitrogen use efficiency with the activities of enzymes involved in nitrogen uptake and assimilation of finger millet genotypes grown under different nitrogen inputs. The Scientific World Journal 10:625731.

Hao Q, Shang W, Zhang C, Chen H, Chen L, Yuan S (2016). Identification and comparative analysis of cbs domain-containing proteins in soybean (Glycine max) and the primary function of gmcbs21 in enhanced tolerance to low nitrogen stress. International Journal of Molecular Sciences 17(5):620.

Hashimoto H, Uragami C, Cogdell RJ (2016). Carotenoids and photosynthesis. In: Carotenoids in Nature. Springer, Cham pp111-139.

Holm G (1954). Chlorophyll mutation in barley. Acta Agriculturae Scandinavica 4(1):457-471.

Huang SJ, Chen S, Liang ZH, Zhang CM, Yan M, Chen JG (2015). Knockdown of the partner protein OsNAR2.1 for high-affinity nitrate transport represses lateral root formation in a nitrate-dependent manner. Scientific Reports 5:18192.

Jiao Y, Bai Z, Xu J, Zhao M, Khan Y, Hu Y (2018). Metabolomics and its physiological regulation process reveal the salt-tolerant mechanism in Glycine soja seedling roots. Plant Physiology and Biochemistry 126:187-196.

Ju X (2014). The concept and meanings of nitrogen fertilizer availability ratio-discussing misunderstanding of traditional nitrogen use efficiency. Acta Pedologica Sinica 51(5):921-933.

Ju XT, Xing GX, Chen XP, Zhang SL, Zhang LJ, Liu XJ (2009). Reducing environmental risk by improving N management in intensive Chinese agricultural systems. Proceedings of the National Academy of Sciences 106(9):3041-3046.

Kaiser WM, Huber SC (2001). Post-translational regulation of nitrate reductase: mechanism, physiological relevance and environmental triggers. Journal of Experimental Botany 52(363):1981-1989.

Liu C, Wang Y, Pan K, Zhu T, Li W, Zhang L (2014). Carbon and nitrogen metabolism in leaves and roots of dwarf bamboo (Fargesia denudata Yi) subjected to drought for two consecutive years during sprouting period. Journal of Plant Growth Regulators 33(2):243-255.

Lowry OH, Brough NTR, Fair LA, Randall RJ (1951). Protein measurement with folin phenol reagent. The Journal of Biological Chemistry 193:265-275.

Mauromicale G, Ierna A, Marchese M (2006). Chlorophyll fluorescence and chlorophyll content in field-grown potato as affected by nitrogen supply, genotype, and plant age. Photosynthetica 44(1):76-82.

Li M, Xu J, Wang X, Fu H, Zhao M, Wang H, Shi L (2018). Photosynthetic characteristics and metabolic analyses of two soybean genotypes revealed adaptive strategies to low-nitrogen stress. Journal of Plant Physiology 229:132-141.

Mohammed AR, Tarpley L (2011). Morphological and physiological responses of nine southern US rice cultivars differing in their tolerance to enhanced ultraviolet-b radiation. Environmental and Experimental Botany 69(2):174-184.

Niyokuri OKAN, Rono JJ, Fashaho A, Ogweno JO (2013). Effect of different rates of nitrogen fertilizer on the growth and yield of zucchini (Cucurbita pepo cv. Diamant L.) hybrid F1 in Rwandan high altitude zone. International Journal of Agriculture & Crop Sciences 5(1):54-62.

Nunes-Nesi A, Fernie AR, Stitt M (2010). Metabolic and signalling aspects underpinning the regulation of plant carbon–nitrogen interactions. Molecular Plant 3(6):973-996.

Oosterhuis DM, Zhou Z (2012). Physiological mechanism of nitrogen mediating cotton (Gossypium hirsutum L.) seedlings growth under water-stress conditions. American Journal of Plant Sciences 3(6):721-730.

Osborne SL, Riedell WE (2006). Soybean growth response to low rates of nitrogen applied at planting in the northern great plains. Journal of Plant Nutrition 29(6):985-1002.

Pang LD, Wei-Jun LI, Zhu JZ, University XA (2015). Effects of carbon and nitrogen metabolism and the seed yield of Sudan grass under different topdressing nitrogen fertilizers. Acta Agrestia Sinica 23(1):180-186.

Phang TH, Shao G, Lam HM (2008). Salt tolerance in soybean. Journal of Integrative Plant Biology 50(10):1196-1212.

Prasanna BM, Araus JL, Crossa J, Cairns JE, Palacios N, Das B (2013). High-throughput and precision phenotyping for cereal breeding programs. In: Cereal genomics II, Springer, Dordrecht pp 341-374.

Quain MD, Makgopa ME, Cooper JW, Kunert KJ, Foyer CH (2015). Ectopic phytocystatin expression increases nodule numbers and influences the responses of soybean (Glycine max) to nitrogen deficiency. Phytochemistry 112(1):179-187.

Ren C, Liu J, Gong Q (2014). Functions of autophagy in plant carbon and nitrogen metabolism. Frontiers in Plant Science 5:301.

Robin P (1979). Etude de quelques conditions d’extraction de la nitrate reductase des racines et des feuilles de plantules de maıs. No. 79-463276. CIMMYT.

Shah JM, Asgher Z, Zeng J, Quan X, Ali E, Shamsi IH (2017). Growth and physiological characterization of low nitrogen responses in Tibetan wild barley (Hordeum spontaneum) and cultivated barley (Hordeum vulgare). Journal of Plant Nutrition 40(6):861-868.

Shang Jie, Yin Xiaoyu (2016). Present situation and reduction of chemical fertilizer non-point source pollution in China [J]. Eco-Economy 232(05):196-199.

Shao S, Li M, Yang D, Zhang J, Shi L (2016). The physiological variations of adaptation mechaniam in Glycine soja seedlings under saline and alkaline stresses. Pakistan Journal of Botany 48:2183-2193.

Takehisa H, Sato Y, Antonio BA, Nagamura Y (2013). Global transcriptome profile of rice root in response to essential macronutrient deficiency. Plant Signaling & Behavior 8(6):e24409.

Williamson JM (2011). The role of information and prices in the nitrogen fertilizer management decision: new evidence from the agricultural resource management survey. Journal of Agricultural and Resource Economics 36:552-572.

Xue Z, Zhao S, Gao H, Sun S (2014). The salt resistance of wild soybean (Glycine soja Sieb. et Zucc. ZYD 03262) under NaCl stress is mainly determined by Na+ distribution in the plant. Acta Physiologiae Plantarum 36(1):61-70.

Yu JL, Zhang L, Zhang ZH, Shu JB, Song HX, Guan CY (2015). The relationship of carbon-nitrogen metabolism between nitrogen efficiency and its characteristics of rape. Acta Agriculturae Boreali-Sinica 30(1):219-224.

Yu N, Hui-Hui D, Qing-Ming LI, Qing-Hua MI, Bin H, Xi-Zhen AI (2015). Effects of red and blue light quality on the metabolites and key enzyme activities of carbon-nitrogen metabolism in celery. Plant Physiology Journal 51(1):112-118.

Yu XZ, Zhang FZ (2012). Activities of nitrate reductase and glutamine synthetase in rice seedlings during cyanide metabolism. Journal of Hazardous Materials 225:190-194.

Zhang ZL, Qu W (2004). Experimental guidance of plant physiology. Higher Education Press: Beijing.

Zhao MH, Sun J, Wang JY, Xu H, Tang L, Chen WF (2011). Global genome expression analysis of photosynthesis-related genes under low nitrogen stress in rice flag leaf. Scientia Agricultura Sinica 44(1):1-8.

Zhao X, Wang W, Xie Z, Gao Y, Wang C, Rashid MM (2018). Comparative analysis of metabolite changes in two contrasting rice genotypes in response to low-nitrogen stress. The Crop Journal 6(5):464-474.

Downloads

Published

2019-11-28

How to Cite

WANG, H., GUO, R., HU, Y., & HAN, D. . (2019). Carbon-Nitrogen Metabolic Responses and Adaptive Strategies to Low-Nitrogen Stress in Glycine soja. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 47(4), 1215–1223. https://doi.org/10.15835/nbha47411567

Issue

Section

Research Articles
CITATION
DOI: 10.15835/nbha47411567