Selenium and potassium supplementation improve nitrogen metabolism, antioxidant activity, and osmolyte production, reducing the growth and photosynthetic inhibition caused by polyethylene glycol (PEG) in wheat

Authors

  • Ayshah Aysh ALRASHIDI University of Hail, Faculty of Science, Department of Biology, Hail, 81411 (SA)

DOI:

https://doi.org/10.15835/nbha52413936

Keywords:

antioxidant system, nitrogen metabolism, osmoregulation, PEG, selenium, wheat

Abstract

Drought stress has a significant impact on all crops, affecting both their growth and development. In this study, wheat plants were subjected to drought stress induced by 15% of PEG along with or without supplementation of selenium and potassium supplements. Plants subjected to PEG alone showed a decrease in a number of plants morphophysiological and biochemical parameters such as a decline in plant height, dry mass, carotenoids, total chlorophyll, stomatal conductance, net photosynthesis, and intercellular CO2 levels. Nevertheless, adding selenium and potassium supplements effectively mitigated these decreases. PEG's drought also led to the overproduction of harmful ROS-inducing substances, H2O2 and O2. Certain factors led to a significant instance of lipid peroxidation, which the addition of selenium and potassium effectively reduced and leaded to protection of plants from oxidative stress damage. The combination of selenium and potassium also significantly reduced the protease and lipoxygenase activities. This effect was even more noticeable when dealing with synergic Se+K applications. The levels of enzymatic (CAT, SOD, APX, and GR) and non-enzymatic (AsA, GSH, and tocopherol) antioxidants went up a lot after treatment with PEG. Moreover, the inclusion of selenium and potassium supplements further amplified the increase. Adding selenium and potassium supplements improved the activity of nitrate reductase (NR), an enzyme that breaks down nitrogen. The combination treatment has shown remarkable efficacy in reducing the adverse effects caused by PEG. Furthermore, the research revealed that the inclusion of selenium and potassium supplements led to heightened quantities of phenols and flavonoids. As a result of the drought, there was a limited absorption of mineral ions, such as nitrogen, phosphorus, potassium, and calcium. However, the addition of selenium and potassium supplements significantly mitigated this decline.

References

Abid M, Ali S, Qi LK, Zahoor R, Tian Z, Jiang D, Snider JL, Dai T (2018). Physiological and biochemical changes during drought and recovery periods at tillering and jointing stages in wheat (Triticum aestivum L.). Scientific Reports 8:4615. https://doi.org/10.1038/s41598-018-21441-7

Aebi H (1984). Catalase in vitro. Methods in Enzymology 105:121-126. https://doi.org/10.1016/s0076-6879(84)05016-3

Ahanger MA, Agarwal RM, Tomar NS, Shrivastava M (2015). Potassium induces positive changes in nitrogen metabolism and antioxidant system of oat (Avena sativa L cultivar Kent). Journal of Plant Interactions 10(1):211-223. https://doi.org/10.1080/17429145.2015.1056260

Ahanger MA, Agarwal RM. (2017a). Potassium up-regulates antioxidant metabolism and alleviates growth inhibition under water and osmotic stress in wheat (Triticum aestivum L). Protoplasma 254(4):1471-1486. https://doi.org/10.1007/s00709-016-1037-0

Ahanger MA, Agarwal RM (2017b). Salinity stress induced alterations in antioxidant metabolism and nitrogen assimilation in wheat (Triticum aestivum L) as influenced by potassium supplementation. Plant Physiology and Biochemistry 115:449-460. https://doi.org/10.1016/j.plaphy.2017.04.017

Ahanger MA, Gul F, Ahmad P, Akram NA (2018). Environmental stresses and metabolomics - deciphering the role of stress responsive metabolites. In: Plant Metabolites and Regulation under Environmental Stress, pp 53-62. https://doi.org/10.1016/b978-0-12-812689-9.00003-0

Ahanger MA, Qi M, Huang Z, Xu X, Begum N, Qin C, Zhang C, Ahmad N, Mustafa NS, Ashraf M, Zhang L (2021). Improving growth and photosynthetic performance of drought stressed tomato by application of nano-organic fertilizer involves up-regulation of nitrogen, antioxidant and osmolyte metabolism. Ecotoxicology and Environmental Safety 216. https://doi.org/10.1016/j.ecoenv.2021.112195

Ahanger MA, Qin C, Begum N, Maodong Q, Dong XX, El-Esawi M, El-Sheikh MA, Alatar AA, Zhang L (2019a). Nitrogen availability prevents oxidative effects of salinity on wheat growth and photosynthesis by up-regulating the antioxidants and osmolytes metabolism, and secondary metabolite accumulation. BMC Plant Biology 19:479 https://doi.org/10.1186/s12870-019-2085-3

Ahanger MA, Qin C, Maodong Q, Dong XX, Ahmad P, Abd_Allah EF, Zhang L (2019b). Spermine application alleviates salinity induced growth and photosynthetic inhibition in Solanum lycopersicum by modulating osmolyte and secondary metabolite accumulation and differentially regulating antioxidant metabolism. Plant Physiology and Biochemistry 144:1-13. https://doi.org/10.1016/j.plaphy.2019.09.021

Ahanger MA, Tittal M, Mir RA, Agarwal RM (2017b). Alleviation of water and osmotic stress-induced changes in nitrogen metabolizing enzymes in Triticum aestivum L. cultivars by potassium. Protoplasma 254(5):1953-1963. https://doi.org/10.1007/s00709-017-1086-z

Ahanger MA, Tomar NS, Tittal M, Argal S, Agarwal RM. (2017a). Plant growth under water/ salt stress: ROS production; antioxidants and significance of added potassium under such conditions. Physiology and Molecular Biology of Plants 23(4):731-744. https://doi.org/10.1007/s12298-017-0462-7

Ahanger MA, Tyagi SR, Wani MR, Ahmad P (2014). Drought tolerance: roles of organic osmolytes, growth regulators and mineral nutrients. In: Ahmad P, Wani MR (Eds). Physiological mechanisms and adaptation strategies in plants under changing environment. Springer Science + Business media, inc. pp 25-56. https://doi.org/10.1007/978-1-4614-8591-9_2

Ahluwalia O, Singh PC, Bhatia R (2021). A review on drought stress in plants: Implications, mitigation and the role of plant growth promoting rhizobacteria. Resources, Environment and Sustainability 5:100032. https://doi.org/10.1016/j.resenv.2021.100032

Ahmad P, Ahanger MA, Alam P, Alyemeni MN (2018). Modification of osmolytes and antioxidant enzymes by 24-epibrassinolide in chickpea seedlings under mercury (Hg) toxicity. Journal of Plant Growth Regulation 37(1):309-322. https://doi.org/10.1007/s00344-017-9730-6

Ahmad P, Ashraf M, Hakeem KR, Azooz MM, Rasool S, Chandna R, Akram NA (2014). Potassium starvation-induced oxidative stress and antioxidant defense responses in Brassica juncea. Journal of Plant Interactions 9(1):1-9. https://doi.org/10.1080/17429145.2012.747629

Alyemeni MN, Ahanger MA, Wijaya L, Alam P, Bhardwaj R, Ahmad P (2018). Selenium mitigates cadmium-induced oxidative stress in tomato (Solanum lycopersicum L.) plants by modulating chlorophyll fluorescence, osmolyte accumulation, and antioxidant system. Protoplasma 255(2):459-469. https://doi.org/10.1007/s00709-017-1162-4

Annunziata MG, Ciarmiello LF, Woodrow P, Aversana ED, Carillo P (2019). Spatial and temporal profile of glycine betaine accumulation in plants under abiotic stresses. Frontiers in Plant Science. https://doi.org/10.3389/fpls.2019.00230

Arnon DI (1949). Copper enzymes in isolated chloroplast polyphenol oxidase in Beta vulgaris. Plant Physiology 24:1-15. https://doi.org/10.1104/pp.24.1.1

Backer H, Frank O, de Angells B, Feingold S (1980). Plasma tocopherol in man at various times after ingesting free or ocetylaned tocopherol. Nutrition Reports International 21:531-536.

Bahar AA, Faried HN, Razzaq K, Ullah S, Akhtar G, Amin M, … Dessoky ES (2021). Potassium-induced drought tolerance of potato by improving morpho-physiological and biochemical attributes. Agronomy 11:2573. https://doi.org/10.3390/agronomy11122573

Bates LS, Waldren RP, Teare ID (1973). Rapid determination of free proline for water-stress studies. Plant and Soil 39:205-207. https://doi.org/10.1007/bf00018060

Batra NG, Sharma V, Kumari N (2014). Drought-induced changes in chlorophyll fluorescence, photosynthetic pigments, and thylakoid membrane proteins of Vigna radiata. Journal of Plant Interaction 9(1):712-721. https://doi.org/10.1080/17429145.2014.905801

Bayer WF, Fridovich JL (1987). Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Analytical Biochemistry 161:559-566. https://doi.org/10.1016/0003-2697(87)90489-1

Begum N, Ahanger MA, Zhang L (2020). AMF inoculation and phosphorus supplementation alleviates drought induced growth and photosynthetic decline in Nicotiana tabacum by up-regulating antioxidant metabolism and osmolyte accumulation. Environmental and Experimental Botany. https://doi.org/10.1016/j.envexpbot.2020.104088.

Begum N, Akhtar K, Ahanger MA, Iqbal M, Wang P, Mustafa NS, Zhang L (2021). Arbuscular mycorrhizal fungi improve growth, essential oil, secondary metabolism, and yield of tobacco (Nicotiana tabacum L.) under drought stress conditions. Environmental Science and Pollution Research 28(33):45276-45295. https://doi.org/10.1007/s11356-021-13755-3

Bistgani ZE, Hashemi M, Dacosta M, Craker L, Maggi F, Morshedloo MR (2019). Effect of salinity stress on the physiological characteristics, phenolic compounds and antioxidant activity of Thymus vulgaris L. and Thymus daenensis Celak. Industrial Crops and Products 135:311-320. https://doi.org/10.1016/j.indcrop.2019.04.055

Chen THH, Murata N (2011). Glycine betaine protects plants against abiotic stress: mechanisms and biotechnological applications. Plant Cell Environment 34(1):1-20. https://doi.org/10.1111/j.1365-3040.2010.02232.x

Chinnusamy V, Schumaker K, Zhu JK (2004). Molecular genetic perspectives on cross-talk and specificity in abiotic stress signalling in plants. Journal of Experimental Botany 55:1-12. https://doi.org/10.1093/jxb/erh005

Dalal VK, Tripathy BC (2012). Modulation of chlorophyll biosynthesis by water stress in rice seedlings during chloroplast biogenesis. Plant, Cell and Environment 35:1685-1703. https://doi.org/10.1111/j.1365-3040.2012.02520.x

Dellero Y (2020). Manipulating amino acid metabolism to improve crop nitrogen use efficiency for a sustainable agriculture. Frontiers in Plant Science. https://doi.org/10.3389/fpls.2020.602548

Demidchik V, Straltsova V, Medvedev SS, Pozhvanov GA, Sokolik A, Yurin V (2014). Stress-induced electrolyte leakage: the role of K?-permeable channels and involvement in programmed cell death and metabolic adjustment. Journal of Experimental Botany 65:1259-1270. https://doi.org/10.1093/jxb/eru004

Djanaguiraman M, Prasad PVV, Seppaenen M (2010). Selenium protects sorghum leaves from oxidative damage under high temperature stress by enhancing antioxidant defense system. Plant Physiology and Biochemistry 48:999-1007. https://doi.org/10.1016/j.plaphy.2010.09.009

Doderer A, Kokkelink I, van der Veen S, Valk B, Schram A, Douma A (1992). Purification and characterization of two lipoxygenase isoenzymes from germinating barley. Biochimica et Biophysica Acta 112:97-104 https://doi.org/10.1016/0167-4838(92)90429-h

Elkelish EE, Soliman MH, Alhaithloul HA, El-Esawi MA (2019). Selenium protects wheat seedlings against salt stress-mediated oxidative damage by up-regulating antioxidants and osmolytes metabolism. Plant Physiology and Biochemistry 137:144–153 https://doi.org/10.1016/j.plaphy.2019.02.004

Ellman GL (1959). Tissue sulphydryl groups. Archives of Biochemistry and Biophysics 82:70‐77. https://doi.org/10.1016/0003-9861(59)90090-6

Fatma M, Masood A, Per TS, Khan NA (2016). Nitric oxide alleviates salt stress inhibited photosynthetic performance by interacting with sulfur assimilation in mustard. Frontiers in Plant Science 7:521. https://doi.org/10.3389/fpls.2016.00521

Fini A, Brunetti C, Ferdinando MD, Ferrini F, Tattini M (2011). Stress-induced flavonoid biosynthesis and the antioxidant machinery of plants. Plant Signaling & Behavior 6(5):709-711. https://doi.org/10.4161/psb.6.5.15069

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 Biology 24(2):227-239. https://doi.org/10.1111/plb.13363

Ghouri F, Ali Z, Naeem M, Ul-Allah S, Babar M, Baloch FS, Chattah WS, Shahid MQ (2021). Effects of silicon and selenium in alleviation of drought stress in rice. Silicon 14:5453-5461. https://doi.org/10.1007/s12633-021-01277-z

Gigolashvili T, Kopriva S (2014). Transporters in plant sulphur metabolism. Frontiers in Plant Science 5:422. https://doi.org/10.3389/fpls.2014.00442

Giri J (2011). Glycine betaine and abiotic stress tolerance in plants. Plant Signaling & Behavior 6(11):1746-1751. https://doi.org/10.4161/psb.6.11.17801

Green NM, Neurath H (1954). Proteolytic enzymes. In: Neurath H, Vailey K (Eds). The Proteins. vol II, Part B. Academic Press, New York, pp 1057-1198. https://doi.org/10.1016/b978-0-12-395721-4.50011-1

Grieve CM, Grattan SR (1983). Rapid assay for determination of water-soluble quaternary ammonium compounds. Plant and Soil 70:303. https://doi.org/10.1007/bf02374789

Gupta M, Gupta S (2017). An overview of selenium uptake, metabolism, and toxicity in plants. Frontiers in Plant Science 7:2074. https://doi.org/10.3389/fpls.2016.02074

Harbone JB (1997). Ekologia Biochemiczna. Wydawnictwa Naukowe PWN, Warszawa. https://doi.org/10.21852/sem.2009.26.48

Hasanuzzaman M, Bhuyan MHMB, Nahar K, Hossain MS, Al-Mahmud J, Hossen MS, Masud AAC, Moumita, Fujita M (2018). Potassium: a vital regulator of plant responses and tolerance to abiotic stresses. Agronomy 31. https://doi.org/10.3390/agronomy8030031

Hasanuzzaman M, Nahar K, Fujita M (2014). Role of tocopherol (Vitamin E) in plants: abiotic stress tolerance and beyond. In: emerging technologies and management of crop stress tolerance. Volume 2: A Sustainable Approach 267-289. https://doi.org/10.1016/b978-0-12-800875-1.00012-0

Hasanuzzaman M, Nahar K, Anee TI, Fujita M (2017). Glutathione in plants: biosynthesis and physiological role in environmental stress tolerance. Physiology and Molecular Biology of Plants 23(2):249-268. https://doi.org/10.1007/s12298-017-0422-2

Hashem A, Abd_Allah EF, Alqarawi AA, Al-Huqail AA, Wirth S, Egamberdieva D (2016). The interaction between arbuscular mycorrhizal fungi and endophytic bacteria enhances plant growth of Acacia gerrardii under salt stress. Frontiers in Microbiology 7:1089. https://doi.org/10.3389/fmicb.2016.01089

Hawrylak-Nowak, B, Matraszek R, Szymanska M (2010). Selenium modifies the effect of short-term chilling stress on cucumber plants. Biological Trace Element Research 138:307-315. https://doi.org/10.1007/s12011-010-8613-5

Hayat S, Hayat Q, Alyemeni MN, Wani AS, Pichtel J, Ahmad A (2012). Role of proline under changing environments: a review. Plant Signaling & Behavior 7(11):1456-66. https://doi.org/10.4161/psb.21949

Hayzer DJ, Leisinger TH (1980). The gene enzyme relationships of proline biosynthesis in Escherichia coli. Journal of General Microbiology 118:287-293. https://doi.org/10.1099/00221287-118-2-287

Heath RL, Packer L (1968). Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics 125:189-198. https://doi.org/10.1016/j.abb.2022.109248

Huang AHC, Cavalieri AJ (1979). Proline oxidase and water stress induced proline accumulation in spinach leaves. Plant Physiol 63:531-535. https://doi.org/10.1104/pp.63.3.531

Hussain HA, Hussain S, Khaliq A, Ashraf U, Anjum SA, Men S, Wang L (2018). Chilling and drought stresses in crop plants: implications, cross talk, and potential management opportunities. Frontiers in Plant Science. https://doi.org/10.3389/fpls.2018.00393

Iqbal N, Umar S, Khan NA (2015). Nitrogen availability regulates proline and ethylene production and alleviates salinity stress in mustard (Brassica juncea). Journal of Plant Physiology 178:84-91. https://doi.org/10.1016/j.jplph.2015.02.006

Jan R, Kim N, Lee SH, Khan MA, Asaf S, Lubna, Park JR, Asif S, Lee IJ, Kim KM (2021). Enhanced flavonoid accumulation reduces combined salt and heat stress through regulation of transcriptional and hormonal mechanisms. Frontiers in Plant Science 21. https://doi.org/10.3389/fpls.2021.796956

Jatav KS, Agarwal RM, Tomar NS, Tyagi SR (2014). Nitrogen metabolism, growth and yield responses of wheat (Triticum aestivum L) to restricted water supply and varying potassium treatments. Journal of Indian Botanical Society 93:177-189.

Jaworski EG (1971). Nitrate reductase assay in intact plant tissue. Biochemical and Biophysical Research Communications 43:1274-1279. https://doi.org/10.1016/s0006-291x(71)80010-4

Jozwiak W, Politycka B (2019). Effect of selenium on alleviating oxidative stress caused by a water deficit in cucumber roots. Plants 8:217. https://doi.org/10.3390/plants8070217

Khan AA, Wang T, Nisa ZU, Alnusairi GSH, Shi F (2022). Insights into cadmium-induced morphophysiological disorders in Althea rosea Cavan and its phytoremediation through the exogeneous citric acid. Agronomy 12(11):2776. https://doi.org/10.3390/agronomy12112776

Khan MIR, Nazir F, Asgher M, Per TS, Khan NA (2015). Selenium and sulfur influence ethylene formation and alleviate cadmium-induced oxidative stress by improving proline and glutathione production in wheat. Journal of Plant Physiology 173:9-18. https://doi.org/10.1016/j.jplph.2014.09.011

Khan AA, Wang T, Hussain T, Amna Ali, Shi F, Latef AAHA, Ali OM, Hayat K Mehmood S (2021). Halotolerant-Koccuria rhizophila (14asp)-Induced Amendment of salt stress in pea plants by limiting Na+ uptake and elevating production of antioxidants. Agronomy 11:1907. https://doi.org/10.3390/agronomy11101907

Khosravi S, ValizadehKaji B, Abbasifar A (2022). Foliar application of selenium affects nitrate accumulation and morpho-physiochemical responses of garden cress plants. International Journal of Horticultural Science and Technology 9(3):329-338. https://doi.org/10.22059/ijhst.2021.325036.472

Li B, Fan R, Sun G, Sun T, Fan Y, Bai S, Guo S, Huang S, Liu J, Zhang H, Wang P, Zhu X, Song CP (2021). Flavonoids improve drought tolerance of maize seedlings by regulating the homeostasis of reactive oxygen species. Plant and Soil 461:389-405. https://doi.org/10.1007/s11104-020-04814-8

Meena M, Divyanshu K, Kumar S, Swapnil P, Zehra A, Shukla V, Yadav M, Upadhyay RS (2019). Regulation of L-proline biosynthesis, signal transduction, transport, accumulation and its vital role in plants during variable environmental conditions. Heliyon 5(12):e02952 https://doi.org/10.1016/j.heliyon.2019.e02952

Mukherjee SP, Choudhuri MA (1983). Implications of water stress-induced changes in the levels of endogenous ascorbic acid and hydrogen peroxide in Vigna seedlings. Physiologia Plantarum 58:166-170. https://doi.org/10.1111/j.1399-3054.1983.tb04162.x

Munné-Bosch S (2005). The role of α-tocopherol in plant stress tolerance. Journal of Plant Physiology 162(7):743-748. https://doi.org/10.1016/j.jplph.2005.04.022

Nakano Y, Asada K (1981). Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant and Cell Physiology 22:867-880. https://doi.org/10.1093/oxfordjournals.pcp.a076232

Nawaz F, Naeem M, Ashraf MY, Tahir MN, Zulfiqar B, Salahuddin M, Shabbir RN, Aslam M (2016). Selenium supplementation affects physiological and biochemical processes to improve fodder yield and quality of maize (Zea mays L.) under water deficit conditions. Frontiers in Plant Science 7:1438. https://doi.org/10.3389/fpls.2016.01438

Olsen SR, Cole CV, Watandbe F, Dean LA (1954). Estimation of available phosphorus in soil by extraction with sodium bi-carbonate. USDA Circular No. 939, US Government Printing Office, Washington DC.

Qin C, Ahanger MA, Lin B, Huang Z, Zhou J, Ahmed N, Ai S, Mustafa NSA, Ashraf M, Zhang L (2021). Comparative transcriptomic analysis reveals the regulatory effects of acetylcholine on salt tolerance of Nicotiana benthamiana. Phytochemistry 181:112582. https://doi.org/10.1016/j.phytochem.2020.112582

Rosa M, Prado C, Podazza G, Interdonato R, González JA, Hilal M, Prado FE (2009). Soluble sugars—metabolism, sensing and abiotic stress. a complex network in the life of plants. Plant Signal Behav 4(5):388-393. https://doi.org/10.4161/psb.4.5.8294

Samec D, Karalija E, Šola I, Bok VV, Salopek-Sondi B (2021). The role of polyphenols in abiotic stress response: the influence of molecular structure. Plants (Basel) 10(1):118. https://doi.org/10.3390/plants10010118

Sami F, Yusuf M, Faizan M, Faraz A Hayat S (2016). Role of sugars under abiotic stress. Plant Physiology and Biochemistry 109:54-61. https://doi.org/10.1016/j.plaphy.2016.09.005

Sardans J, Peñuelas J (2021). Potassium control of plant functions: ecological and agricultural implications. Plants 10:419. https://doi.org/10.3390/plants10020419

Schields R, Burnett W (1960). Determination of protein-bound carbohydrate in serum by a modified anthrone method. Analytical Chemistry 32:885-886. https://doi.org/10.1021/ac60163a053

Schuppler U, He PH, John PCL, Munns R (1998). Effect of water stress on cell division and Cdc2-Like cell cycle kinase activity in wheat leaves. Plant Physiology 117(2):667-678. https://doi.org/10.1104/pp.117.2.667

Seleiman MF, Al-Suhaibani N, Ali N, Akmal M, Alotaibi M, Refay Y, … Battaglia ML (2021). Drought stress impacts on plants and different approaches to alleviate its adverse effects. Plants (Basel) 10(2):259. https://doi.org/10.3390/plants10020259

Setter TL, Flannigan BA (2001). Water deficit inhibits cell division and expression of transcripts involved in cell proliferation and endoreduplication in maize endosperm. Journal of Experimental Botany 52(360):1401-1408. https://doi.org/10.1093/jexbot/52.360.1401

Sharma A, Thakur S, Kumar V, Kanwar MK, Kesavan AK, Thukral AK, Bhardwaj R, Alam P, Ahmad P (2016). Pre-sowing seed treatment with 24-epibrassinolide ameliorates pesticide stress in Brassica juncea L. through the modulation of stress markers. Frontiers in Plant Science 7:1569. https://doi.org/10.3389/fpls.2016.01569

Sharma A, Yuan H, Kumar V, Ramakrishnan M, Kohli SK, Kaur R, Thukral AK, Bhardwaj R, Zheng B (2019a). Castasterone attenuates insecticide induced phytotoxicity in mustard. Ecotoxicology and Environmental Safety 179:50-61. https://doi.org/10.1016/j.ecoenv.2019.03.120

Sharma A, Shahzad B, Rehman A, Bhardwaj R, Landi M, Zheng B (2019b). Response of phenylpropanoid pathway and the role of polyphenols in plants under abiotic stress. Molecules 24(13):2452. https://doi.org/10.3390/molecules24132452

Shinmachi F, Buchner P, Stroud JL, Parmar S, Zhao FJ, McGrath SP, Hawkesford MJ (2010). Influence of sulfur deficiency on the expression of specific sulfate transporters and the distribution of sulfur, selenium, and molybdenum in wheat. Plant Physiology 153:327-336. https://doi.org/10.1104/pp.110.153759

Shrestha K, Pant S, Huang Y (2021). Genome-wide identification and classification of Lipoxygenase gene family and their roles in sorghum-aphid interaction. Plant Molecular Biology 105:527-541. https://doi.org/10.1007/s11103-020-01107-7

Shrivastava M, Ahanger MA, Agarwal RM (2016). Improved growth of Trigonella foenum-graecum L. with potassium supplementation involves physiological and biochemical implications. Journal of Functional and Environmental Botany 6(2):84-101 https://doi.org/10.5958/2231-1750.2016.00014.7

Singleton VL, Rossi Jr JA (1965). Colorimetry of total phenolics with phosphor-molybdic-phosphotungstic acid reagents. American Journal of Enology and Viticulture 16:144-153. https://doi.org/10.5344/ajev.1965.16.3.144

Sivakumar P, Sharmila P, Jain V, Saradhi PP (2002). Sugars have potential to curtail oxygenase activity of Rubisco. Biochemical and Biophysical Research Communications 298(2):247-250. https://doi.org/10.1016/s0006-291x(02)02437-3

Sivakumar P, Sharmila P, Saradhi PP (2000). Proline alleviates salt stress-induced enhancement in ribulose-1, 5-bisphosphate oxygenase activity. Biochemical and Biophysical Research Communications 279:512-515. https://doi.org/10.1006/bbrc.2000.4005

Soliman M, Alhaithloul HA, Hakeem KR, Alharbi BM, El-Esawi M, Elkelish A (2019). Exogenous nitric oxide mitigates nickel-induced oxidative damage in eggplant by up-regulating antioxidants, osmolyte metabolism, and glyoxalase systems. Plants 8(562); https://doi.org/10.3390/plants8120562

Soliman M, Elkelish A, Souad T, Alhaithloul H, Farooq M (2020). Brassinosteroid seed priming with nitrogen supplementation improves salt tolerance in soybean. Physiology and Molecular Biology of Plants 26(3):501-511. https://doi.org/10.1007/s12298-020-00765-7

Song W, Xue R, Song Y, Bi Y, Liang Z, Meng L, Dong C, Wang C, Liu G, Dong J, Zhang Y (2018). Differential response of first-order lateral root elongation to low potassium involves nitric oxide in two tobacco cultivars. Journal of Plant Growth Regulation 37:14-127

Sutuliene R, Rageliene, L, Samuoliene G, Brazaityte A, Urbutis M, Miliauskiene J (2022). The response of antioxidant system of drought-stressed green pea (Pisum sativum L.) affected by watering and foliar spray with silica nanoparticles. Horticulturae 8(35): https://doi.org/10.3390/horticulturae8010035

Velikova V, Yordanov I, Edreva A (2000). Oxidative stress and some antioxidant systems in acid rain-treated bean plants. Plant Science 151:59-66. https://doi.org/10.1016/s0168-9452(99)00197-1

White PJ, Broadley MR (2009). Biofortification of crops with seven mineral elements often lacking in human diets-iron zinc, copper, calcium, magnesium, selenium and iodine. New Phytologist 182:49-84. https://doi.org/10.1111/j.1469-8137.2008.02738.x

Xu C, He CG, Wang YJ, Bi YF, Jiang H (2020b). Effect of drought and heat stresses on photosynthesis, pigments, and xanthophyll cycle in alfalfa (Medicago sativa L.). Photosynthetica 58(5):1226-1236. https://doi.org/10.32615/ps.2020.073

Xu X, Du X, Wang F, Sha J, Chen Q, Tian G, Zhu Z, Ge S, Jiang Y (2020a). Effects of potassium levels on plant growth, accumulation and distribution of carbon, and nitrate metabolism in apple dwarf rootstock seedlings. Frontiers in Plant Science 11:904. https://doi.org/10.3389/fpls.2020.00904

Yang H, Wu F, Cheng J (2011). Reduced chilling injury in cucumber by nitric oxide and the antioxidant response. Food Chemistry 127:1237-1242. https://doi.org/10.1016/j.foodchem.2011.02.011

Yao X, Chu J, Wang G (2009). Effects of selenium on wheat seedlings under drought stress. Biological Trace Element Research 130:283-290. https://doi.org/10.1007/s12011-009-8328-7

Zhang Q, Zhao Y, Zhang J, Li X, Ma F, Duan M, Zhang B, Li H (2021). The responses of the lipoxygenase gene family to salt and drought stress in foxtail millet (Setaria italica). Life 11:1169. https://doi.org/10.3390/life11111169

Zhishen J, Mengcheng T, Jianming W (1999). The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals. Food Chemistry 64:555-559. https://doi.org/10.1016/S0308-8146(98)00102-2

Zorb C, Senbayram M, Peiter E (2014). Potassium in agriculture – Status and perspectives. Journal of Plant Physiology 171:656-669. https://doi.org/10.1016/j.jplph.2013.08.008

Zucker M (1965). Induction of phenylalanine deaminase by light and its relation to chlorogenic acid synthesis in potato tuber tissue. Plant Physiology 40:779-784. https://doi.org/10.1104/pp.40.5.779

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2024-11-25

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ALRASHIDI, A. A. (2024). Selenium and potassium supplementation improve nitrogen metabolism, antioxidant activity, and osmolyte production, reducing the growth and photosynthetic inhibition caused by polyethylene glycol (PEG) in wheat. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 52(4), 13936. https://doi.org/10.15835/nbha52413936

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DOI: 10.15835/nbha52413936