Urease-null soybean (eu3-a) under salt and copper stress: nitrogen metabolism, antioxidant defense, and arginine pathway genes.

Bibliographic Details
Title: Urease-null soybean (eu3-a) under salt and copper stress: nitrogen metabolism, antioxidant defense, and arginine pathway genes.
Authors: de Souza SCR; Department of Plant Biology, Institute of Biology, University of Campinas, PO Box 6109, Campinas, SP, 13083-970, Brazil. sarahsouza@ufscar.br.; Department of Botany, Federal University of São Carlos, PO Box 676, São Carlos, SP, 13565-905, Brazil. sarahsouza@ufscar.br., Silveira NM; Department of Biodiversity, Institute of Biosciences, São Paulo State University (UNESP), PO Box 1515, Rio Claro, SP, 13506-900, Brazil., Tofanello VR; Department of Plant Biology, Institute of Biology, University of Campinas, PO Box 6109, Campinas, SP, 13083-970, Brazil., Polacco JC; Department of Biochemistry, Interdisciplinary Plant Group, University of Missouri, 117 Schweitzer Hall, Columbia, MO, 65211, USA., Mazzafera P; Department of Plant Biology, Institute of Biology, University of Campinas, PO Box 6109, Campinas, SP, 13083-970, Brazil.
Source: Planta [Planta] 2026 Apr 16; Vol. 263 (5). Date of Electronic Publication: 2026 Apr 16.
Publication Type: Journal Article
Language: English
Journal Info: Publisher: Springer-Verlag [etc.] Country of Publication: Germany NLM ID: 1250576 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-2048 (Electronic) Linking ISSN: 00320935 NLM ISO Abbreviation: Planta Subsets: MEDLINE
Imprint Name(s): Original Publication: Berlin, New York, Springer-Verlag [etc.]
MeSH Terms: Glycine max*/genetics , Glycine max*/physiology , Glycine max*/drug effects , Glycine max*/enzymology , Glycine max*/metabolism , Nitrogen*/metabolism , Copper*/toxicity , Urease*/genetics , Urease*/metabolism , Antioxidants*/metabolism , Arginine*/metabolism, Photosynthesis/drug effects ; Sodium Chloride/pharmacology ; Gene Expression Regulation, Plant/drug effects ; Plant Leaves/physiology ; Salt Stress ; Stress, Physiological
Abstract: Main Conclusion: The eu3-a mutant exhibited greater tolerance to salt stress but increased sensitivity to copper stress, with distinct impacts on nitrogen metabolism, photosynthesis, and antioxidant responses. The eu3-a soybean mutant is urease-null, lacking all urease activity responsible for catalyzing the hydrolysis of urea into ammonia and carbon dioxide. In this study, the urease-null eu3-a soybean mutant was used to assess the saline and copper stresses on nitrogen metabolism. Seeds of eu3-a/eu3-a and the corresponding dominant homozygous Eu3 precursor line were collectively referred to as near-isogenic lines (NILs). Experiments were conducted under hydroponic conditions using plants at the reproductive stage (R1-R2) and subjected to either salinity stress (NaCl: 0, 50, and 100 mM) or copper stress (CuCl2: 0, 10, and 50 µM) over a 5-day treatment period. The following parameters were assessed in leaf tissue: photosynthetic performance, antioxidant enzyme activity, levels of nitrogenous compounds, and the expression of genes encoding key enzymes in the arginine-derived metabolic network. Overall, salinity imposed more severe physiological disruptions than copper in both lines, as evidenced by an approximately 88% reduction in photosynthetic performance under 100 mM of salt. Both stresses impaired nitrogen metabolism, increasing ammonia levels and reducing nitrate concentration. Interestingly, eu3-a plants demonstrated enhanced tolerance to salt stress relative to Eu3 plants, but this trend was not observed under copper stress. Future work should address nitrogen-related enzymatic activities associated with urease metabolism and elucidate the non-enzymatic antioxidant mechanisms contributing to stress tolerance in eu3-a soybean plants under salt and copper stress.
(© 2026. The Author(s).)
Competing Interests: Declarations. Conflict of interest: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
References: Alexieva V, Sergiev I, Mapelli S, Karanov E (2001) The effect of drought and ultraviolet radiation on growth and stress markers in pea and wheat. Plant Cell Environ 24(12):1337–1344. https://doi.org/10.1046/j.1365-3040.2001.00778.x. (PMID: 10.1046/j.1365-3040.2001.00778.x)
Alfano M, Cavazza C (2020) Structure, function, and biosynthesis of nickel-dependent enzymes. Protein Sci 29:1071–1089. https://doi.org/10.1002/pro.3836. (PMID: 10.1002/pro.3836320223537184782)
Bieleski RL, Turner NA (1966) Separation and estimation of amino acids in crude plant extracts by thin-layer electrophoresis and chromatography. Anal Biochem 17(2):278–293. https://doi.org/10.1016/0003-2697(66)90206-5. (PMID: 10.1016/0003-2697(66)90206-55971422)
Bu Y, Kou J, Sun B, Takano T, Liu S (2015) Adverse effect of urease on salt stress during seed germination in Arabidopsis thaliana. FEBS Lett 589(12):1308–1313. https://doi.org/10.1016/j.febslet.2015.04.016. (PMID: 10.1016/j.febslet.2015.04.01625907538)
Cakmak I, Horst WJ (1991) Effect of aluminium on lipid peroxidation, superoxide dismutase, catalase, and peroxidase activities in root tips of soybean (Glycine max). Physiol Plant 83:463–468. https://doi.org/10.1111/j.1399-3054.1991.tb00121.x. (PMID: 10.1111/j.1399-3054.1991.tb00121.x)
Cataldo DA, Haroon M, Schrader LE, Youngs VL (1975) Rapid colorimetric determination of nitrate in plant tissues by nitration of salicylic acid. Commun Soil Sci Plant Anal 6:71–80. https://doi.org/10.1080/00103627509366547. (PMID: 10.1080/00103627509366547)
Chaves MM, Flexas J, Pinheiro C (2009) Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot 103(4):551–560. https://doi.org/10.1093/aob/mcn125. (PMID: 10.1093/aob/mcn12518662937)
Chen J, Shafi M, Li S, Wang Y, Wu J, Ye Z, Peng D, Yan W, Liu D (2015) Copper-induced oxidative stress, antioxidant responses and phytoremediation potential of Moso bamboo (Phyllostachys pubescens). Sci Rep 5:13554. https://doi.org/10.1038/srep13554. (PMID: 10.1038/srep13554263375514559668)
Chen G, Li J, Han H, Du R, Wang X (2022) Physiological and molecular mechanisms of plant responses to copper stress. Int J Mol Sci 23(21):12950. https://doi.org/10.3390/ijms232112950. (PMID: 10.3390/ijms232112950363617449656524)
Cheng Y, Cheng X, Wei K, Wang Y (2024) Comparative transcriptome analysis of salt-tolerant and salt-sensitive soybean cultivars under salt stress. Int J Mol Sci 25:9818. https://doi.org/10.3390/ijms25189818. (PMID: 10.3390/ijms251898183933730611432363)
Engelhardt MM, Lima FFD, Martins GC, Vasques ICF, Silva AO, Oliveira JR, Reis RHCL, Guilherme LRG, Melo Marques JJGS (2020) Copper phytotoxicity in agricultural crops cultivated in tropical soils. Semina Cienc Agrar 41(Suppl 2):2883–2896. https://doi.org/10.5433/1679-0359.2020v41n6supl2p2883. (PMID: 10.5433/1679-0359.2020v41n6supl2p2883)
Farhangi-Abriz S, Torabian S (2018) Biochar improved nodulation and nitrogen metabolism of soybean under salt stress. Symbiosis 74:215–223. https://doi.org/10.1007/s13199-017-0509-0. (PMID: 10.1007/s13199-017-0509-0)
Farrugia MA, Macomber L, Hausinger RP (2013) Biosynthesis of the urease metallocenter. J Biol Chem 288(19):13178–13185. https://doi.org/10.1139/o80-181. (PMID: 10.1139/o80-181235396183650357)
Felker P (1977) Microdetermination of nitrogen in seed protein extracts. Anal Chem 49:123–126. https://doi.org/10.1021/ac50015a053. (PMID: 10.1021/ac50015a053)
Freyermuth SK, Bacanamwo M, Polacco JC (2000) The soybean Eu3 gene encodes an Ni-binding protein necessary for urease activity. Plant J 21(1):53–60. https://doi.org/10.1046/j.1365-313x.2000.00655.x. (PMID: 10.1046/j.1365-313x.2000.00655.x10652150)
García-Caparrós P, De Filippis L, Gul A, Hasanuzzaman M, Ozturk M, Altay V, Lao MT (2021) Oxidative stress and antioxidant metabolism under adverse environmental conditions: a review. Bot Rev 87:421–466. https://doi.org/10.1007/s12229-020-09231-1. (PMID: 10.1007/s12229-020-09231-1)
Ghosh UK, Islam MN, Siddiqui MN, Cao X, Khan MAR (2022) Proline, a multifaceted signalling molecule in plant responses to abiotic stress: understanding the physiological mechanisms. Plant Biol 24(2):227–239. https://doi.org/10.1111/plb.13363. (PMID: 10.1111/plb.1336334796604)
Giannopolitis CN, Ries SK (1977) Superoxide dismutases: I. Occurrence in higher plants. Plant Physiol 59:309–314. https://doi.org/10.1104/pp.59.2.309. (PMID: 10.1104/pp.59.2.30916659839542387)
Güleryüz G, Erdemir ÜS, Arslan H, Akpinar A, Çiçek A, Güçer Ş (2015) Variation in trace element mobility and nitrogen metabolism of Verbascum olympicum Boiss. under copper stress. Chem Ecol 31(6):494–509. https://doi.org/10.1080/02757540.2015.1043285. (PMID: 10.1080/02757540.2015.1043285)
Han S, Wang Y (2021) Synthesis, characterization and crystal structures of Schiff base copper complexes with urease inhibitory activity. Acta Chim Slov 68(4):829–845. https://doi.org/10.17344/acsi.2021.6965. (PMID: 10.17344/acsi.2021.6965)
Hanci F (2019) The effect of L-tryptophan and melatonin on seed germination of some cool season vegetable species under salinity stress. Duzce Univ J Sci Technol 7(3):1879–1891. https://doi.org/10.24925/turjaf.v8i4.960-964.3224. (PMID: 10.24925/turjaf.v8i4.960-964.3224)
Hanci F, Tuncer G (2020) How do foliar application of melatonin and L-tryptophan affect lettuce growth parameters under salt stress? Turk J Agric Food Sci Technol 8(4):960–964. https://doi.org/10.24925/turjaf.v8i4.960-964.3224. (PMID: 10.24925/turjaf.v8i4.960-964.3224)
Havir EA, McHale NA (1987) Biochemical and developmental characterization of multiple forms of catalase in tobacco leaves. Plant Physiol 84(2):450–455. https://doi.org/10.1104/pp.84.2.450. (PMID: 10.1104/pp.84.2.450166654611056601)
Hippler FW, Mattos-Jr D, Boaretto RM, Williams LE (2018) Copper excess reduces nitrate uptake by Arabidopsis roots with specific effects on gene expression. J Plant Physiol 228:158–165. https://doi.org/10.1016/j.jplph.2018.06.005. (PMID: 10.1016/j.jplph.2018.06.005299331386090090)
Huang L, Li Z, Liu Q, Pu G, Zhang Y, Li J (2019) Research on the adaptive mechanism of photosynthetic apparatus under salt stress: new directions to increase crop yield in saline soils. Ann Appl Biol 175(1):1–17. https://doi.org/10.1111/aab.12510. (PMID: 10.1111/aab.12510)
Hussain S, Khaliq A, Noor MA, Tanveer M, Hussain HA, Hussain S, Shah T, Mehmood T (2020) Metal toxicity and nitrogen metabolism in plants: an overview. In: Datta R, Meena R, Pathan S, Ceccherini M (eds) Carbon and nitrogen cycling in soil. Springer Nature Singapore, Singapore, pp 221–248. (PMID: 10.1007/978-981-13-7264-3_7)
Jian B, Liu B, Bi Y, Hou W, Wu C, Han T (2008) Validation of internal control for gene expression study in soybean by quantitative real-time PCR. BMC Mol Biol 9:59. https://doi.org/10.1186/1471-2199-9-59. (PMID: 10.1186/1471-2199-9-59185732152443375)
Kabata-Pendias A, Pendias H (2001) Trace elements in soils and plants, 3rd edn. CRC Press, New York.
Kawade K, Tabeta H, Ferjani A, Hirai M (2023) The roles of functional amino acids in plant growth and development. Plant Cell Physiol 64(12):1482–1493. https://doi.org/10.1093/pcp/pcad071. (PMID: 10.1093/pcp/pcad07137489637)
Kawakami EM, Oosterhuis DM, Snider JL (2013) Nitrogen assimilation and growth of cotton seedlings under NaCl salinity and in response to urea application with NBPT and DCD. J Agron Crop Sci 199(2):106–117. https://doi.org/10.1111/jac.12002. (PMID: 10.1111/jac.12002)
Khan N, Ali S, Zandi P, Mehmood A, Ullah S, Ikram M et al (2020) Role of sugars, amino acids and organic acids in improving plant abiotic stress tolerance. Pak J Bot 52(2):355–363. https://doi.org/10.30848/PJB2020-2(24). (PMID: 10.30848/PJB2020-2(24))
Kokebie D, Enyew A, Masresha G, Fentie T, Mulat E (2024) Morphological, physiological, and biochemical responses of three soybean (Glycine max L.) varieties under salinity stress conditions. Front Plant Sci 15:1440445. https://doi.org/10.3389/fpls.2024.1440445. (PMID: 10.3389/fpls.2024.14404453935493411443463)
Laira MD, Andrade SA, Silveira NM, Machado EC, Ribeiro RV, Zambrosi FC (2023) High post-flowering phosphorus status promotes the tolerance of soybean to terminal heat stress. Environ Exp Bot 215:105501. https://doi.org/10.1016/j.envexpbot.2023.105501. (PMID: 10.1016/j.envexpbot.2023.105501)
Li W, Keller AA (2023) Assessing the impacts of Cu and Mo engineered nanomaterials on crop plant growth using a targeted proteomics approach. ACS Agric Sci Technol 4(1):103–117. https://doi.org/10.1021/acsagscitech.3c00431. (PMID: 10.1021/acsagscitech.3c004313823957310792604)
Li J, Liu J, Zhu T, Zhao C, Li L, Chen M (2019) The role of melatonin in salt stress responses. Int J Mol Sci 20(7):1735. https://doi.org/10.3390/ijms20071735. (PMID: 10.3390/ijms20071735309656076479358)
Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods 25(4):402–408. https://doi.org/10.1006/meth.2001.1262. (PMID: 10.1006/meth.2001.126211846609)
Malik A, Yadav P, Singh S (2022) Role of polyamines in heavy metal stressed plants. Plant Physiol Rep 27:680–694. https://doi.org/10.1007/s40502-022-00657-w. (PMID: 10.1007/s40502-022-00657-w)
Mazzei L, Musiani F, Ciurli S (2020) The structure-based reaction mechanism of urease, a nickel-dependent enzyme: tale of a long debate. J Biol Inorg Chem 25(6):829–845. https://doi.org/10.1007/s00775-020-01808-w. (PMID: 10.1007/s00775-020-01808-w328090877433671)
Miao F, Wang Y, Haq NU, Lyu MJA, Zhu XG (2024) Rewiring of primary metabolism for ammonium recycling under short-term low CO2 treatment – its implication for C4 evolution. Front Plant Sci 15:1322261. https://doi.org/10.3389/fpls.2024.1322261. (PMID: 10.3389/fpls.2024.13222613914861611324553)
Miller G, Suzuki N, Ciftci-Yilmaz S, Mittler R (2010) Reactive oxygen species homeostasis and signalling during drought and salinity stresses. Plant Cell Environ 33(4):453–467. https://doi.org/10.1111/j.1365-3040.2009.02041.x. (PMID: 10.1111/j.1365-3040.2009.02041.x19712065)
Mokochinski JB, Soares DX, Bruns RE, Mazzafera P, Sawaya ACHF (2013) Optimization of extraction conditions of free amino acids in plants by factorial design. In: Congr Bras Espectrom Massas, Campinas, Brazil. https://doi.org/10.2298/HEMIND150531053S.
Mostofa MG, Seraj ZI, Fujita M (2014) Exogenous sodium nitroprusside and glutathione alleviate copper toxicity by reducing copper uptake and oxidative damage in rice (Oryza sativa L.) seedlings. Protoplasma 251(6):1373–1386. https://doi.org/10.1007/s00709-014-0639-7. (PMID: 10.1007/s00709-014-0639-724752795)
Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22(5):867–880. https://doi.org/10.1093/oxfordjournals.pcp.a076232. (PMID: 10.1093/oxfordjournals.pcp.a076232)
Pál M, Tajti J, Szalai G, Peeva V, Végh B, Janda T (2018) Interaction of polyamines, abscisic acid and proline under osmotic stress in the leaves of wheat plants. Sci Rep 8:12839. https://doi.org/10.1038/s41598-018-31297-6. (PMID: 10.1038/s41598-018-31297-6301506586110863)
Pál M, Szalai G, Gondor OK, Janda T (2021) Unfinished story of polyamines: role of conjugation, transport and light-related regulation in plant polyamine metabolism. Plant Sci 308:110923. https://doi.org/10.1016/j.plantsci.2021.110923. (PMID: 10.1016/j.plantsci.2021.11092334034871)
Paschalidis K, Tsaniklidis G, Wang B-Q, Delis C, Trantas E, Loulakakis K, Makky M, Sarris PF, Ververidis F, Liu J-H (2019) The interplay among polyamines and nitrogen in plant stress responses. Plants 8:315. https://doi.org/10.3390/plants8090315. (PMID: 10.3390/plants8090315314803426784213)
Polacco JC, Holland MA (1993) Roles of urease in plant cells. Int Rev Cytol 145:65–103. https://doi.org/10.1016/S0074-7696(08)60425-8. (PMID: 10.1016/S0074-7696(08)60425-8)
Polacco JC, Winkler RG (1984) Soybean leaf urease: a seed enzyme? Plant Physiol 74:800–803. https://doi.org/10.1104/pp.74.4.800. (PMID: 10.1104/pp.74.4.800166635131066771)
Polacco JC, Thomas AL, Bledsoe PJ (1982) A soybean seed urease null produces urease in cell culture. Plant Physiol 69:1233–1240. https://doi.org/10.1104/pp.69.5.1233. (PMID: 10.1104/pp.69.5.123316662376426390)
Polacco JC, Hyten DL, Medeiros-Silva M, Sleper DA, Bilyeu KD (2011) Mutational analysis of the major soybean UreF paralogue involved in urease activation. J Exp Bot 62(10):3599–3608. https://doi.org/10.1093/jxb/err054. (PMID: 10.1093/jxb/err054214302943130180)
Polacco JC, Mazzafera P, Tezotto T (2013) Opinion: nickel and urease in plants: still many knowledge gaps. Plant Sci 199:79–90. https://doi.org/10.1016/j.plantsci.2012.10.010. (PMID: 10.1016/j.plantsci.2012.10.01023265321)
Puiatti M, Sodek L (1999) Waterlogging affects nitrogen transport in the xylem of soybean. Plant Physiol Biochem 37(10):767–773. https://doi.org/10.1016/S0981-9428(00)86690-5. (PMID: 10.1016/S0981-9428(00)86690-5)
Rosa-Téllez S, Alcántara-Enguídanos A, Martínez-Seidel F, Casatejada-Anchel R, Saeheng S, Bailes CL, Ros R (2024) The serine–glycine–one-carbon metabolic network orchestrates changes in nitrogen and sulfur metabolism and shapes plant development. Plant Cell 36(2):404–426. https://doi.org/10.1093/plcell/koad256. (PMID: 10.1093/plcell/koad2563780409610827325)
Schwalbert R, Silva LOS, Schwalbert RA, Tarouco CP, Fernandes GS, Marques ACR, Costa CC, Hammerschmitt RK, Brunetto G, Nicoloso FT (2019) Physiological responses of soybean (Glycine max (L.) Merrill) cultivars to copper excess. An Acad Bras Cienc 91:e20190121. https://doi.org/10.1590/0001-3795201920190121. (PMID: 10.1590/0001-379520192019012131800705)
Shabbir Z, Sardar A, Shabbir A, Abbas G, Shamshad S, Khalid S, Natasha MG, Dumat C, Shahid M (2020) Copper uptake, essentiality, toxicity, detoxification and risk assessment in soil–plant environment. Chemosphere 259:127436. https://doi.org/10.1016/j.chemosphere.2020.127436. (PMID: 10.1016/j.chemosphere.2020.12743632599387)
Shao J, Huang K, Batool M, Idrees F, Afzal R, Haroon M, Noushahi HA, Wu W, Hu Q, Lu X, Huang G, Aamer M, Hassan MU, El Sabagh A (2022) Versatile roles of polyamines in improving abiotic stress tolerance of plants. Front Plant Sci 13:1003155. https://doi.org/10.3389/fpls.2022.1003155. (PMID: 10.3389/fpls.2022.1003155363111099606767)
Sharma P, Jha AB, Dubey RS, Pessarakli M (2012) Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. J Bot 2012:217037. https://doi.org/10.1155/2012/217037. (PMID: 10.1155/2012/217037)
Sharma N, Jaiswal DK, Kumari S, Dash GK, Panda S, Anandan A, Raghuram N (2023) Genome-wide urea response in rice genotypes contrasting for nitrogen use efficiency. Int J Mol Sci 24(7):6080. https://doi.org/10.3390/ijms24076080. (PMID: 10.3390/ijms240760803704705210093866)
Siddappa S, Marathe GK (2020) What we know about plant arginases? Plant Physiol Biochem 156:600–610. https://doi.org/10.1016/j.plaphy.2020.10.002. (PMID: 10.1016/j.plaphy.2020.10.00233069114)
Singh M, Singh VP, Prasad SM (2016) Responses of photosynthesis, nitrogen and proline metabolism to salinity stress in Solanum lycopersicum under different levels of nitrogen supplementation. Plant Physiol Biochem 109:72–83. https://doi.org/10.1016/j.plaphy.2016.08.021. (PMID: 10.1016/j.plaphy.2016.08.02127639963)
Snieg B, Nowak J (2005) Urease activity and ATP content in soil and plant related to copper concentration. Pol J Ecol 53(1):115–123.
Souza SCR, Mazzafera P, Sodek L (2016) Flooding of the root system in soybean: biochemical and molecular aspects of nitrogen metabolism in the nodule during stress and recovery. Amino Acids 48(5):1285–1295. https://doi.org/10.1007/s00726-016-2179-2. (PMID: 10.1007/s00726-016-2179-226825550)
Souza SC, Souza LA, Schiavinato MA, Oliveira Silva FM, Andrade SAL (2020a) Zinc toxicity in seedlings of three Fabaceae trees associated with arbuscular mycorrhizal fungi. Ecotoxicol Environ Saf 195:110450. https://doi.org/10.1016/j.ecoenv.2020.110450. (PMID: 10.1016/j.ecoenv.2020.11045032197181)
Souza SCR, Sodek L, Polacco JC, Mazzafera P (2020b) Urease deficiency alters nitrogen metabolism and gene expression in urease-null soybean without affecting growth or productivity under nitrate supply. Acta Physiol Plant 42:84. https://doi.org/10.1007/s11738-020-3020-9. (PMID: 10.1007/s11738-020-3020-9)
Tezotto T, Souza SCR, Mihail J, Favarin JL, Mazzafera P, Bilyeu K, Polacco JC (2016) Deletion of the single UreG urease activation gene in soybean NIL lines: characterization and pleiotropic effects. Theor Exp Plant Physiol 28(3):307–320. https://doi.org/10.1007/s40626-016-0052-z. (PMID: 10.1007/s40626-016-0052-z)
Hoagland DR, Arnon DI (1938) The water culture method for growing plants without soil. Calif Agric Exp Stn Circ 347:33–39.
Thounaojam TC, Panda P, Mazumdar P, Kumar D, Sharma GD, Sahoo L, Sanjib P (2012) Excess copper induced oxidative stress and response of antioxidants in rice. Plant Physiol Biochem 53:33–39. https://doi.org/10.1016/j.plaphy.2012.01.006. (PMID: 10.1016/j.plaphy.2012.01.00622306354)
Urra M, Buezo J, Royo B, Cornejo A, López-Gómez P, Cerdán D, Esteban R, Martínez-Merino V, Gogorcena Y, Tavladoraki P, Moran JF (2022) The importance of the urea cycle and its relationships to polyamine metabolism during ammonium stress in Medicago truncatula. J Exp Bot 73(16):5581–5595. https://doi.org/10.1093/jxb/erac235. (PMID: 10.1093/jxb/erac235356088369467648)
Wang Y, Chen X, Chen J (2024) Advances of the mechanism for copper tolerance in plants. Plant Sci 350:112299. https://doi.org/10.1016/j.plantsci.2024.112299. (PMID: 10.1016/j.plantsci.2024.11229939455032)
Witte CP (2011) Urea metabolism in plants. Plant Sci 180(3):431–438. https://doi.org/10.1016/j.plantsci.2010.11.010. (PMID: 10.1016/j.plantsci.2010.11.01021421389)
Xie LB, Sun LN, Zhang ZW, Chen YE, Yuan M, Yuan S (2025) Phenotype assessment and putative mechanisms of ammonium toxicity to plants. Int J Mol Sci 26(6):2606. https://doi.org/10.3390/ijms26062606. (PMID: 10.3390/ijms260626064014124611941816)
Xiong ZT, Liu C, Geng B (2006) Phytotoxic effects of copper on nitrogen metabolism and plant growth in Brassica pekinensis Rupr. Ecotoxicol Environ Saf 64(3):273–280. https://doi.org/10.1016/j.ecoenv.2006.02.003. (PMID: 10.1016/j.ecoenv.2006.02.00316616956)
Zhou Y, Bai L, Song CP (2015) Ammonium homeostasis and signaling in plant cells. Sci Bull 60(8):741–747. https://doi.org/10.1007/s11434-015-0759-2. (PMID: 10.1007/s11434-015-0759-2)
Grant Information: 150069/2017-0 Conselho Nacional de Desenvolvimento Científico e Tecnológico; 2023/13662-3 Fundação de Amparo à Pesquisa do Estado de São Paulo; Grant 14/09730-4 Fundação de Amparo à Pesquisa do Estado de São Paulo
Contributed Indexing: Keywords: Arginase; Nitrate; Polyamines; Proline; Tryptophan; Urea
Substance Nomenclature: N762921K75 (Nitrogen)
789U1901C5 (Copper)
EC 3.5.1.5 (Urease)
0 (Antioxidants)
94ZLA3W45F (Arginine)
451W47IQ8X (Sodium Chloride)
Entry Date(s): Date Created: 20260416 Date Completed: 20260715 Latest Revision: 20260715
Update Code: 20260715
PubMed Central ID: PMC13086885
DOI: 10.1007/s00425-026-05001-2
PMID: 41989567
Database: MEDLINE
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