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Environmental Abiotic Stress and Secondary Metabolites Production in Medicinal Plants: A Review

Year 2022, Volume: 28 Issue: 3, 351 - 362, 05.09.2022
https://doi.org/10.15832/ankutbd.999117

Abstract

Medicinal plants that produce various secondary metabolites are quite useful to us owing to their anti-microbial properties, presence of huge amounts of anti-oxidants, cytotoxic nature, and various other medically significant properties. Medicinal plants, therefore, serve as raw materials for modern pharmaceutical medicines and several herbal medical supplements. Expansion and advancement of growing medicinal plants on large scale has flourished over the last few years. However, prolonged environmental changes have made medicinal plants susceptible to numerous abiotic stresses. On being exposed to abiotic stresses chiefly light (quality and quantity), extreme temperature conditions, water stress (drought or flooding), nutrients available, presence of heavy metals and salt content in the soil, medicinal plants undergo several changes physiologically and their chemical composition also gets altered. To combat the effects of abiotic stress, several mechanisms at morphological, anatomical, biochemical, and molecular levels are adapted by plants, which also include a change in the production of the secondary metabolites. However, plants cannot cope with extreme events of stress and eventually die. Several strategies stress such as the use of endophytes, chemical treatment, and biotechnological methods have therefore been introduced to help the plants tolerate the period of extreme stress. Moreover, nano bionics is also being developed as new technology to help plants survive stressful conditions.

Supporting Institution

NA

Project Number

NA

References

  • Abd El-Azim W M & Ahmed S T H (2009). Effect of salinity and cutting date on growth and chemical constituents of Achillea fragratissima Forssk, under Ras Sudr conditions. Research Journal of Agriculture and Biological Sciences 5(6): 1121–1129
  • Ali R M, Elfeky S S & Abbas H (2008). Response of salt stressed Ricinus communis L. to exogenous application of glycerol and/or aspartic acid. Journal of Biological Sciences 8(1): 171–175
  • Anasori P & Asghari G (2008). Effects of light and differentiation on gingerol and zingiberene production in callus culture of Zingiber officinale Rosc. Research in Pharmaceutical Sciences 3: 59–63
  • Arbona V & Gómez-Cadenas A (2015). Metabolomics of disease resistance in crops. Current Issues in Molecular Biology 19:13–29
  • Azhar N, Hussain B, Ashraf Y M & Abbasim K Y (2011). Water stress mediated changes in growth, physiology and secondary metabolites of desi ajwain (Trachyspermum ammi). Pakistan Journal of Botany 43(9): 15–19
  • Bhat M A, Ahmad S, Aslam J, Mujib A & Mahmooduzzfar (2008). Salinity stress enhances production of solasodine in Solanum nigrum L. Chemical and Pharmaceutical Bulletin 56(1): 17-21
  • Bourgou S, Kchouk M E, Bellila A & Marzouk B (2010). Effect of salinity on phenolic composition and biological activity of Nigella sativa. Acta Horticulturae 853: 57–60
  • Casal J J & Yanovsky M J (2005). Regulation of gene expression by light. The International Journal of Developmental Biology 49: 501–511
  • Chan L K, Koay S S, Boey P L & Bhatt A (2010). Effects of abiotic stress on biomass and anthocyanin production in cell cultures of Melastoma malabathricum. Biological Research 43: 27–135 PMID: 21157639.
  • Chen Y, Guo Q, Liu L, Liao L & Zhu Z (2011) Influence of fertilization and drought stress on the growth and production of secondary metabolites in Prunella vulgaris L. Journal of Medicinal Plants Research 5: 1749–1755
  • Cheng L, Han M, Yang L M, Yang L, Sun Z & Zhang T (2018). Changes in the physiological characteristics and baicalin biosynthesis metabolism of Scutellaria baicalensis Georgi under drought stress. Industrial Crops & Products 122: 473–482
  • Cheynier V, Comte G, Davies KM, Lattanzio V & Martens S (2013). Plant phenolics: recent advances on their biosynthesis, genetics, and ecophysiology. Plant Physiology and Biochemistry 72: 1–20
  • Cik J K, Klejdus, B, Hedbavny J & Backor M (2009). Salicylic acid alleviates NaCl-induced changes in the metabolism of Matricaria chamomilla plants. Ecotoxicology 18(5): 544–554
  • Espinoza A, San Martín A, López-Climent M, Ruiz-Lara S, Gómez-Cadenas A & Casaretto J A (2013). Engineered drought-induced biosynthesis of α-tocopherol alleviates stress-induced leaf damage in tobacco. Journal of Plant Physiology 170: 1285–1294
  • Estell R E, Fredrickson E L & James D K (2016). Effect of light intensity and wavelength on concentration of plant secondary metabolites in the leaves of Flourensia cernua. Biochemical Systematics and Ecology 65: 108–114
  • Fahad, Balouch A, Agheem M H, Memon S A, Baloch A R, Tunio A, Abdullah, Pato A H, Jagirani M S & Panah P (2020). Efficient mitigation of cadmium and lead toxicity in coriander plant utilizing magnetite (Fe3O4) nanofertilizer as growth regulator and antimicrobial agent. International Journal of Environmental Analytical Chemistry 1-12
  • Ghavam M (2019). Effect of silver nanoparticles on tolerance to drought stress in Thymus daenensis Celak and Thymus vulgaris L. in germination and early growth stages. Environmental Stresses in Crop Sciences 12: 555–566
  • Goławska S, Sprawka I, Łukasik I & Goławski A (2014). Are naringenin and quercetin useful chemicals in pest-management strategies? Journal of Pest Science 87(1):173-180
  • Gurib-Fakim A (2006). Medicinal plants: traditions of yesterday and drugs of tomorrow. Molecular Aspects of Medicine 27(1): 1–93
  • Haghighi Z, Modarresi M & Mollayi S (2012). Enhancement of compatible solute and secondary metabolites production in Plantago ovata Forsk. by salinity stress. Journal of Medicinal Plants Research 6(18): 3495–3500
  • Hasanuzzaman M, Hossain M A, da Silva J A T & Fujita M (2012). Plant responses and tolerance to abiotic oxidative stress: antioxidant defenses is a key factor. In: Bandi V, Shanker AK, Shanker C, Mandapaka M (eds) Crop stress and its management: perspectives and strategies, Springer, Berlin, pp. 261–316
  • Hoffmann D (2003). Medical Herbalism: The Science and Practice of Herbal Medicine. Healing Arts Press One Park Street, Rochester, Vermont
  • Irani S & Todd C D (2018). Exogenous allantoin increases Arabidopsis seedlings tolerance to NaCl stress and regulates expression of oxidative stress response genes. Journal of Plant Physiology 221: 43-50
  • Jaleel C A, Manivannan P, Sankar B, Kishorekumar A, Gopi R & Somasundaram R (2007). Induction of drought stress tolerance by ketoconazole in Catharanthus roseus is mediated by enhanced antioxidant potentials and secondary metabolite accumulation. Colloids and Surfaces B: Biointerfaces 60: 201–206
  • Jamil M, Lee D B, Jung K Y, Lee S C & Rha E S (2006). Effect of salt (NaCl) stress on germination and early seedling growth of four vegetables species. Journal of Central European Agriculture 7(2): 273–282
  • Jin Z, Wang Z, Ma Q, Sun L, Zhang L, Liu Z, Liu D, Hao X & Pei Y (2017). Hydrogen sulfide mediates ion fluxes inducing stomatal closure in response to drought stress in Arabidopsis thaliana. Plant Soil 419: 141-152
  • Jochum G M, Mudge K W & Thomas R B (2007). Elevated temperatures increase leaf senescence and root secondary metabolite concentration in the understory herb Panax quinquefolius (Araliaceae). American Journal of Botany 94: 819–826
  • Karamian R, Ghasemlou F & Amiri H (2020). Physiological evaluation of drought stress tolerance and recovery in Verbascum sinuatum plants treated with methyl jasmonate, salicylic acid and titanium dioxide nanoparticles. Plant Biosystems 154: 277–287
  • Katerova Z, Todorova D & Sergiev I (2017). Plant Secondary Metabolites and Some Plant Growth Regulators Elicited by UV Irradiation, Light And/or Shade. Medicinal Plants and Environmental Challenges 97–121
  • Khan A L, Hamayun M, Hussain J, Kang S M & Lee I J (2012). The newly isolated endophytic fungus Paraconiothyrium sp. LK1 produces ascotoxin. Molecules 17: 1103–1112
  • Khan M N, Mobin M, Abbas Z K & ALMutairi K A (2016). Impact of varying elevations on growth and activities of antioxidant enzymes of some medicinal plants of Saudi Arabia. Acta Ecologica Sinica 36:141–148 doi:10.1016/j.chnaes.2015.12.009
  • Ksouri R, Megdiche W, Debez A, Falleh H, Grignon C & Abdelly C (2007). Salinity effects on polyphenol content and antioxidant activities in leaves of the halophyte Cakile maritima. Plant Physiology and Biochemistry 45: 244–249
  • Liang Y, Zheng P, Li S, Li KZ & Xu HN (2018b). Nitrate reductase-dependent NO production is involved in H2S-induced nitrate stress tolerance in tomato via activation of antioxidant enzymes. Scientia Horticulturae 229: 207-214
  • Liu H, Wang X, Wang D, Zou Z & Liang Z (2011). Effect of drought stress on growth and accumulation of active constituents in Salvia miltiorrhiza Bunge. Industrial Crops and Products 33: 84–88
  • Loreto F & Schnitzler JP (2010). Abiotic stress and induced BVOCs. Trends in Plant Science 15(3): 154–166
  • Ma CH, Chu JZ, Shi XF, Liu CQ & Yao XQ (2016). Effects of enhanced UV-B radiation on the nutritional and active ingredient contents during the floral development of medicinal chrysanthemum. Journal of Photochemistry and Photobiology B: Biology 158: 228–234
  • Mohammadi H, Esmailpour M & Gheranpaye A (2016). Effects of TiO2 nanoparticles and water-deficit stress on morpho-physiological characteristics of dragonhead (Dracocephalum moldavica L.) plants. Acta agriculturae Slovenicais 107:385–396
  • Moradbeygi H, Jamei R, Heidari R & Darvishzadeh R (2020). Investigating the enzymatic and non-enzymatic antioxidant defense by applying iron oxide nanoparticles in Dracocephalum moldavica L. plant under salinity stress. Scientia Horticulturae 272: 109537
  • Naghiloo S, Movafeghi A, Delazar A, Nazemiyeh H, Asnaashari S & Dadpour MR (2012a). Ontogenetic variation of total phenolics and antioxidant activity in roots: leaves and flowers of Astragalus compactus Lam. (Fabaceae). Bioimpacts 2(2):105–109
  • Paramo LA. Feregrino-Perez AA, Guevara R, Mendoza S & Esquivel K (2020). Nanoparticles in agroindustry: Applications, toxicity, challenges, and trends. Nanomaterials 10: 1654
  • Pateraki I & Kanellis AK (2010). Stress and developmental responses of terpenoid biosynthetic genes in Cistus creticus subsp. creticus. Plant Cell Reports 29:629–641
  • Pell EJ, Schlagnhaufer CD, Arteca RN (1997). Ozone induced oxidative stress: mechanism of action and reaction. Physiologia Plantarum 100: 264–273
  • Pradhan J, Sahoo SK, Laloltra S & Sarma RS (2017). Positive impact of abiotic stress on medicinal and aromatic plants. International Journal of Plant Science 12(2): 309–313
  • Queslati S, Karray-Bouraoui N, Attia H, Rabhi M, Ksouri R & Lachaal M (2010). Physiological and antioxidant responses of Mentha pulegium (Pennyroyal) to salt stress. Acta Physiologiae Plantarum 32(2): 289–296
  • Radasci P, Inotai K, Sarosi S, Czovek P, Bernath J & Nemeth E (2010). Effect of water supply on the physiological characterstics and production of basil (Ocimum basilicum L). European Journal of Horticultural Science 75:193–197
  • Rathore S, Singh N & Singh SK (2014). Influence of NaCl on biochemical parameters of two cultivars of Stevia rebaudiana regenerated in vitro. Journal of Stress Physiology and Biochemistry 10(2): 287–296
  • Reguera M, Z Peleg & E Blumwald (2012). Targeting metabolic pathways for genetic engineering abiotic stress-tolerance in crops. Biochimica et Biophysica Acta 1819: 186-194
  • Sampaio BL, Edrada-ebel R, Batista F & Costa D (2016). Effect of the environment on the secondary metabolic profile of Tithonia diversifolia : a model for environmental metabolomics of plants. Scientific Reports 6: 1–11. doi:10.1038/srep29265
  • Sanchita A & Sharma (2018). Gene Expression Analysis in Medicinal Plants under Abiotic Stress Conditions. Plant Metabolites and Regulation under Environmental Stress pp. 407-414
  • Savvides A, Ali S, Tester M & Fotopoulos V (2016). Chemical priming of plants against multiple abiotic stresses: Mission possible? Trends in Plant Science 21: 329-340
  • Schenke D, Böttcher C, & Scheel D (2011). Crosstalk between abiotic ultraviolet-B stress and biotic (flg22) stress signalling in Arabidopsis prevents flavonol accumulation in favor of pathogen defence compound production. Plant Cell and Environment 34:1849–1864
  • Sharkey TD & Yeh S (2001). Isoprene emission from plants. Annual Review of Plant Biology 52: 407-436. DOI: 10.1146/annurev.arplant.52.1.407
  • Shi H, Jiang C, Ye T, Tan D-X, Reiter RJ, Zhang H, Liu R & Chan Z (2014). Comparative physiological, metabolomic, and transcriptomic analyses reveal mechanisms of improved abiotic stress resistance in bermudagrass [Cynodon dactylon (L). Pers.] by exogenous melatonin. Journal of Experimental Botany 66: 681-694
  • Soufi S, Rezgui S & Bettaeib T (2015). Early effects of chilling stress on the morphological and physiological statut of pretreated Stevia rebaudiana Bert. seedlings. Journal of New Sciences, Agriculture and Biotechnology 14(5): 467–472
  • Taiz L &Zeiger E (2006). Plant physiology. Sinauer Associates Inc., Sunderland, Massachusetts, USA.
  • Vashisth D, Kumar R, Rastogi S, Patel VK, Kalra A, Gupta MM, Gupta AK & Shasany AK (2018). Transcriptome changes induced by abiotic stresses in Artemisia annua. Scientific Reports 8: 3423. https://doi.org/10.1038/s41598-018-21598-1.
  • Verma N & Shukla S (2015). Impact of various factors responsible for fluctuation in plant secondary metabolites. Journal of Applied Research on Medicinal and Aromatic Plants 2:105–113. doi:10.1016/j.jarmap.2015.09.002
  • Volkova L, Tausz M, Bennett LT & Dreyer E (2009). Interactive effects of high irradiance and moderate heat on photosynthesis, pigments, and tocopherol in the tree-fern Dicksonia antarctica. Functional Plant Biology 36:1046
  • Yang L, Wu L, Chang W, Li Z, Miao M, Li Y, Yang J, Liu Z & Tan J (2018). Overexpression of the maize E3 ubiquitin ligase gene ZmAIRP4 enhances drought stress tolerance in Arabidopsis. Plant Physiology and Biochemistry 123: 34-42
  • Zhang LX, Guo QS, Chang QS, Zhu ZB, Liu L & Chen YH (2015). Chloroplast ultrastructure, photosynthesis and accumulation of secondary metabolites in Glechoma longituba in response to irradiance. Photosynthetica 53(1): 144–153
  • Zhao BT, Kim TI, Kim YH, Kang JS, Min BS, Son JK, et al. (2018). A comparative study of Mentha arvensis L. and Mentha haplocalyx Briq. by HPLC. Natural Product Research 32(2):239-242
  • Zhou R, Su WH, Zhang GF, Zhang YN & Guo XR (2016). Relationship between flavonoids and photoprotection in shade-developed Erigeron breviscapus transferred to sunlight. Photosynthetica 54(2): 201–209
Year 2022, Volume: 28 Issue: 3, 351 - 362, 05.09.2022
https://doi.org/10.15832/ankutbd.999117

Abstract

Project Number

NA

References

  • Abd El-Azim W M & Ahmed S T H (2009). Effect of salinity and cutting date on growth and chemical constituents of Achillea fragratissima Forssk, under Ras Sudr conditions. Research Journal of Agriculture and Biological Sciences 5(6): 1121–1129
  • Ali R M, Elfeky S S & Abbas H (2008). Response of salt stressed Ricinus communis L. to exogenous application of glycerol and/or aspartic acid. Journal of Biological Sciences 8(1): 171–175
  • Anasori P & Asghari G (2008). Effects of light and differentiation on gingerol and zingiberene production in callus culture of Zingiber officinale Rosc. Research in Pharmaceutical Sciences 3: 59–63
  • Arbona V & Gómez-Cadenas A (2015). Metabolomics of disease resistance in crops. Current Issues in Molecular Biology 19:13–29
  • Azhar N, Hussain B, Ashraf Y M & Abbasim K Y (2011). Water stress mediated changes in growth, physiology and secondary metabolites of desi ajwain (Trachyspermum ammi). Pakistan Journal of Botany 43(9): 15–19
  • Bhat M A, Ahmad S, Aslam J, Mujib A & Mahmooduzzfar (2008). Salinity stress enhances production of solasodine in Solanum nigrum L. Chemical and Pharmaceutical Bulletin 56(1): 17-21
  • Bourgou S, Kchouk M E, Bellila A & Marzouk B (2010). Effect of salinity on phenolic composition and biological activity of Nigella sativa. Acta Horticulturae 853: 57–60
  • Casal J J & Yanovsky M J (2005). Regulation of gene expression by light. The International Journal of Developmental Biology 49: 501–511
  • Chan L K, Koay S S, Boey P L & Bhatt A (2010). Effects of abiotic stress on biomass and anthocyanin production in cell cultures of Melastoma malabathricum. Biological Research 43: 27–135 PMID: 21157639.
  • Chen Y, Guo Q, Liu L, Liao L & Zhu Z (2011) Influence of fertilization and drought stress on the growth and production of secondary metabolites in Prunella vulgaris L. Journal of Medicinal Plants Research 5: 1749–1755
  • Cheng L, Han M, Yang L M, Yang L, Sun Z & Zhang T (2018). Changes in the physiological characteristics and baicalin biosynthesis metabolism of Scutellaria baicalensis Georgi under drought stress. Industrial Crops & Products 122: 473–482
  • Cheynier V, Comte G, Davies KM, Lattanzio V & Martens S (2013). Plant phenolics: recent advances on their biosynthesis, genetics, and ecophysiology. Plant Physiology and Biochemistry 72: 1–20
  • Cik J K, Klejdus, B, Hedbavny J & Backor M (2009). Salicylic acid alleviates NaCl-induced changes in the metabolism of Matricaria chamomilla plants. Ecotoxicology 18(5): 544–554
  • Espinoza A, San Martín A, López-Climent M, Ruiz-Lara S, Gómez-Cadenas A & Casaretto J A (2013). Engineered drought-induced biosynthesis of α-tocopherol alleviates stress-induced leaf damage in tobacco. Journal of Plant Physiology 170: 1285–1294
  • Estell R E, Fredrickson E L & James D K (2016). Effect of light intensity and wavelength on concentration of plant secondary metabolites in the leaves of Flourensia cernua. Biochemical Systematics and Ecology 65: 108–114
  • Fahad, Balouch A, Agheem M H, Memon S A, Baloch A R, Tunio A, Abdullah, Pato A H, Jagirani M S & Panah P (2020). Efficient mitigation of cadmium and lead toxicity in coriander plant utilizing magnetite (Fe3O4) nanofertilizer as growth regulator and antimicrobial agent. International Journal of Environmental Analytical Chemistry 1-12
  • Ghavam M (2019). Effect of silver nanoparticles on tolerance to drought stress in Thymus daenensis Celak and Thymus vulgaris L. in germination and early growth stages. Environmental Stresses in Crop Sciences 12: 555–566
  • Goławska S, Sprawka I, Łukasik I & Goławski A (2014). Are naringenin and quercetin useful chemicals in pest-management strategies? Journal of Pest Science 87(1):173-180
  • Gurib-Fakim A (2006). Medicinal plants: traditions of yesterday and drugs of tomorrow. Molecular Aspects of Medicine 27(1): 1–93
  • Haghighi Z, Modarresi M & Mollayi S (2012). Enhancement of compatible solute and secondary metabolites production in Plantago ovata Forsk. by salinity stress. Journal of Medicinal Plants Research 6(18): 3495–3500
  • Hasanuzzaman M, Hossain M A, da Silva J A T & Fujita M (2012). Plant responses and tolerance to abiotic oxidative stress: antioxidant defenses is a key factor. In: Bandi V, Shanker AK, Shanker C, Mandapaka M (eds) Crop stress and its management: perspectives and strategies, Springer, Berlin, pp. 261–316
  • Hoffmann D (2003). Medical Herbalism: The Science and Practice of Herbal Medicine. Healing Arts Press One Park Street, Rochester, Vermont
  • Irani S & Todd C D (2018). Exogenous allantoin increases Arabidopsis seedlings tolerance to NaCl stress and regulates expression of oxidative stress response genes. Journal of Plant Physiology 221: 43-50
  • Jaleel C A, Manivannan P, Sankar B, Kishorekumar A, Gopi R & Somasundaram R (2007). Induction of drought stress tolerance by ketoconazole in Catharanthus roseus is mediated by enhanced antioxidant potentials and secondary metabolite accumulation. Colloids and Surfaces B: Biointerfaces 60: 201–206
  • Jamil M, Lee D B, Jung K Y, Lee S C & Rha E S (2006). Effect of salt (NaCl) stress on germination and early seedling growth of four vegetables species. Journal of Central European Agriculture 7(2): 273–282
  • Jin Z, Wang Z, Ma Q, Sun L, Zhang L, Liu Z, Liu D, Hao X & Pei Y (2017). Hydrogen sulfide mediates ion fluxes inducing stomatal closure in response to drought stress in Arabidopsis thaliana. Plant Soil 419: 141-152
  • Jochum G M, Mudge K W & Thomas R B (2007). Elevated temperatures increase leaf senescence and root secondary metabolite concentration in the understory herb Panax quinquefolius (Araliaceae). American Journal of Botany 94: 819–826
  • Karamian R, Ghasemlou F & Amiri H (2020). Physiological evaluation of drought stress tolerance and recovery in Verbascum sinuatum plants treated with methyl jasmonate, salicylic acid and titanium dioxide nanoparticles. Plant Biosystems 154: 277–287
  • Katerova Z, Todorova D & Sergiev I (2017). Plant Secondary Metabolites and Some Plant Growth Regulators Elicited by UV Irradiation, Light And/or Shade. Medicinal Plants and Environmental Challenges 97–121
  • Khan A L, Hamayun M, Hussain J, Kang S M & Lee I J (2012). The newly isolated endophytic fungus Paraconiothyrium sp. LK1 produces ascotoxin. Molecules 17: 1103–1112
  • Khan M N, Mobin M, Abbas Z K & ALMutairi K A (2016). Impact of varying elevations on growth and activities of antioxidant enzymes of some medicinal plants of Saudi Arabia. Acta Ecologica Sinica 36:141–148 doi:10.1016/j.chnaes.2015.12.009
  • Ksouri R, Megdiche W, Debez A, Falleh H, Grignon C & Abdelly C (2007). Salinity effects on polyphenol content and antioxidant activities in leaves of the halophyte Cakile maritima. Plant Physiology and Biochemistry 45: 244–249
  • Liang Y, Zheng P, Li S, Li KZ & Xu HN (2018b). Nitrate reductase-dependent NO production is involved in H2S-induced nitrate stress tolerance in tomato via activation of antioxidant enzymes. Scientia Horticulturae 229: 207-214
  • Liu H, Wang X, Wang D, Zou Z & Liang Z (2011). Effect of drought stress on growth and accumulation of active constituents in Salvia miltiorrhiza Bunge. Industrial Crops and Products 33: 84–88
  • Loreto F & Schnitzler JP (2010). Abiotic stress and induced BVOCs. Trends in Plant Science 15(3): 154–166
  • Ma CH, Chu JZ, Shi XF, Liu CQ & Yao XQ (2016). Effects of enhanced UV-B radiation on the nutritional and active ingredient contents during the floral development of medicinal chrysanthemum. Journal of Photochemistry and Photobiology B: Biology 158: 228–234
  • Mohammadi H, Esmailpour M & Gheranpaye A (2016). Effects of TiO2 nanoparticles and water-deficit stress on morpho-physiological characteristics of dragonhead (Dracocephalum moldavica L.) plants. Acta agriculturae Slovenicais 107:385–396
  • Moradbeygi H, Jamei R, Heidari R & Darvishzadeh R (2020). Investigating the enzymatic and non-enzymatic antioxidant defense by applying iron oxide nanoparticles in Dracocephalum moldavica L. plant under salinity stress. Scientia Horticulturae 272: 109537
  • Naghiloo S, Movafeghi A, Delazar A, Nazemiyeh H, Asnaashari S & Dadpour MR (2012a). Ontogenetic variation of total phenolics and antioxidant activity in roots: leaves and flowers of Astragalus compactus Lam. (Fabaceae). Bioimpacts 2(2):105–109
  • Paramo LA. Feregrino-Perez AA, Guevara R, Mendoza S & Esquivel K (2020). Nanoparticles in agroindustry: Applications, toxicity, challenges, and trends. Nanomaterials 10: 1654
  • Pateraki I & Kanellis AK (2010). Stress and developmental responses of terpenoid biosynthetic genes in Cistus creticus subsp. creticus. Plant Cell Reports 29:629–641
  • Pell EJ, Schlagnhaufer CD, Arteca RN (1997). Ozone induced oxidative stress: mechanism of action and reaction. Physiologia Plantarum 100: 264–273
  • Pradhan J, Sahoo SK, Laloltra S & Sarma RS (2017). Positive impact of abiotic stress on medicinal and aromatic plants. International Journal of Plant Science 12(2): 309–313
  • Queslati S, Karray-Bouraoui N, Attia H, Rabhi M, Ksouri R & Lachaal M (2010). Physiological and antioxidant responses of Mentha pulegium (Pennyroyal) to salt stress. Acta Physiologiae Plantarum 32(2): 289–296
  • Radasci P, Inotai K, Sarosi S, Czovek P, Bernath J & Nemeth E (2010). Effect of water supply on the physiological characterstics and production of basil (Ocimum basilicum L). European Journal of Horticultural Science 75:193–197
  • Rathore S, Singh N & Singh SK (2014). Influence of NaCl on biochemical parameters of two cultivars of Stevia rebaudiana regenerated in vitro. Journal of Stress Physiology and Biochemistry 10(2): 287–296
  • Reguera M, Z Peleg & E Blumwald (2012). Targeting metabolic pathways for genetic engineering abiotic stress-tolerance in crops. Biochimica et Biophysica Acta 1819: 186-194
  • Sampaio BL, Edrada-ebel R, Batista F & Costa D (2016). Effect of the environment on the secondary metabolic profile of Tithonia diversifolia : a model for environmental metabolomics of plants. Scientific Reports 6: 1–11. doi:10.1038/srep29265
  • Sanchita A & Sharma (2018). Gene Expression Analysis in Medicinal Plants under Abiotic Stress Conditions. Plant Metabolites and Regulation under Environmental Stress pp. 407-414
  • Savvides A, Ali S, Tester M & Fotopoulos V (2016). Chemical priming of plants against multiple abiotic stresses: Mission possible? Trends in Plant Science 21: 329-340
  • Schenke D, Böttcher C, & Scheel D (2011). Crosstalk between abiotic ultraviolet-B stress and biotic (flg22) stress signalling in Arabidopsis prevents flavonol accumulation in favor of pathogen defence compound production. Plant Cell and Environment 34:1849–1864
  • Sharkey TD & Yeh S (2001). Isoprene emission from plants. Annual Review of Plant Biology 52: 407-436. DOI: 10.1146/annurev.arplant.52.1.407
  • Shi H, Jiang C, Ye T, Tan D-X, Reiter RJ, Zhang H, Liu R & Chan Z (2014). Comparative physiological, metabolomic, and transcriptomic analyses reveal mechanisms of improved abiotic stress resistance in bermudagrass [Cynodon dactylon (L). Pers.] by exogenous melatonin. Journal of Experimental Botany 66: 681-694
  • Soufi S, Rezgui S & Bettaeib T (2015). Early effects of chilling stress on the morphological and physiological statut of pretreated Stevia rebaudiana Bert. seedlings. Journal of New Sciences, Agriculture and Biotechnology 14(5): 467–472
  • Taiz L &Zeiger E (2006). Plant physiology. Sinauer Associates Inc., Sunderland, Massachusetts, USA.
  • Vashisth D, Kumar R, Rastogi S, Patel VK, Kalra A, Gupta MM, Gupta AK & Shasany AK (2018). Transcriptome changes induced by abiotic stresses in Artemisia annua. Scientific Reports 8: 3423. https://doi.org/10.1038/s41598-018-21598-1.
  • Verma N & Shukla S (2015). Impact of various factors responsible for fluctuation in plant secondary metabolites. Journal of Applied Research on Medicinal and Aromatic Plants 2:105–113. doi:10.1016/j.jarmap.2015.09.002
  • Volkova L, Tausz M, Bennett LT & Dreyer E (2009). Interactive effects of high irradiance and moderate heat on photosynthesis, pigments, and tocopherol in the tree-fern Dicksonia antarctica. Functional Plant Biology 36:1046
  • Yang L, Wu L, Chang W, Li Z, Miao M, Li Y, Yang J, Liu Z & Tan J (2018). Overexpression of the maize E3 ubiquitin ligase gene ZmAIRP4 enhances drought stress tolerance in Arabidopsis. Plant Physiology and Biochemistry 123: 34-42
  • Zhang LX, Guo QS, Chang QS, Zhu ZB, Liu L & Chen YH (2015). Chloroplast ultrastructure, photosynthesis and accumulation of secondary metabolites in Glechoma longituba in response to irradiance. Photosynthetica 53(1): 144–153
  • Zhao BT, Kim TI, Kim YH, Kang JS, Min BS, Son JK, et al. (2018). A comparative study of Mentha arvensis L. and Mentha haplocalyx Briq. by HPLC. Natural Product Research 32(2):239-242
  • Zhou R, Su WH, Zhang GF, Zhang YN & Guo XR (2016). Relationship between flavonoids and photoprotection in shade-developed Erigeron breviscapus transferred to sunlight. Photosynthetica 54(2): 201–209
There are 62 citations in total.

Details

Primary Language English
Journal Section Makaleler
Authors

Arjita Punetha This is me 0000-0002-1784-1856

Dipender Kumar 0000-0001-8120-7158

Priyanka Suryavanshi 0000-0002-9676-5475

Rc Padalıa This is me 0000-0001-6637-1144

Venkatesha K.t. This is me 0000-0002-6375-7225

Project Number NA
Publication Date September 5, 2022
Submission Date September 24, 2021
Acceptance Date May 11, 2022
Published in Issue Year 2022 Volume: 28 Issue: 3

Cite

APA Punetha, A., Kumar, D., Suryavanshi, P., Padalıa, R., et al. (2022). Environmental Abiotic Stress and Secondary Metabolites Production in Medicinal Plants: A Review. Journal of Agricultural Sciences, 28(3), 351-362. https://doi.org/10.15832/ankutbd.999117

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