Changes in Ecophysiology, Osmolytes, and Secondary Metabolites of the Medicinal Plants of Mentha piperita and Catharanthus roseus Subjected to Drought and Heat Stress
Tóm tắt
Từ khóa
Tài liệu tham khảo
Jakada, B.H., Aslam, M., Fakher, B., Greaves, J.G., Li, Z., Li, W., Lai, L., Ayoade, O.A., Cheng, Y., and Cao, S. (2019). Identification of SWI2/SNF2-Related 1 Chromatin Remodeling Complex (SWR1-C) Subunits in Pineapple and the Role of Pineapple SWR1 COMPLEX 6 (AcSWC6) in Biotic and Abiotic Stress Response. Biomolecules, 9.
Li, X., Guo, C., Ahmad, S., Wang, Q., Yu, J., Liu, C., and Guo, Y. (2019). Systematic Analysis of MYB Family Genes in Potato and Their Multiple Roles in Development and Stress Responses. Biomolecules, 9.
El-Esawi, M.A., Al-Ghamdi, A.A., Ali, H.M., and Ahmad, M. (2019). Overexpression of AtWRKY30 Transcription Factor Enhances Heat and Drought Stress Tolerance in Wheat (Triticum aestivum L.). Genes, 10.
El-Esawi, M.A., and Alayafi, A.A. (2019). Overexpression of StDREB2 Transcription Factor Enhances Drought Stress Tolerance in Cotton (Gossypium barbadense L.). Genes, 10.
El-Esawi, M.A., and Alayafi, A.A. (2019). Overexpression of Rice Rab7 Gene Improves Drought and Heat Tolerance and Increases Grain Yield in Rice (Oryza sativa L.). Genes, 10.
Alaraidh, 2018, Bacillus firmus (SW5) augments salt tolerance in soybean (Glycine max L.) by modulating root system architecture, antioxidant defense systems and stress-responsive genes expression, Plant. Physiol. Biochem., 132, 375, 10.1016/j.plaphy.2018.09.026
Ali, 2019, Azospirillum lipoferum FK1 confers improved salt tolerance in chickpea (Cicer arietinum L.) by modulating osmolytes, antioxidant machinery and stress-related genes expression, Environ. Exp. Bot., 159, 55, 10.1016/j.envexpbot.2018.12.001
Elkelish, 2019, Calcium availability regulates antioxidant system, physio-biochemical activities and alleviates salinity stress mediated oxidative damage in soybean seedlings, J. Appl. Bot. Food Qual., 92, 258
Elkeilsh, 2019, Exogenous application of β-sitosterol mediated growth and yield improvement in water-stressed wheat (Triticum aestivum) involves up-regulated antioxidant system, J. Plant. Res., 132, 881, 10.1007/s10265-019-01143-5
Ahmad, 2018, Modification of Osmolytes and Antioxidant Enzymes by 24-Epibrassinolide in Chickpea Seedlings under Mercury (Hg) Toxicity, J. Plant Growth Regul., 37, 309, 10.1007/s00344-017-9730-6
Bennett, 1994, Secondary metabolites in plant defence mechanisms, New Phytol., 127, 617, 10.1111/j.1469-8137.1994.tb02968.x
Yang, L., Wen, K.S., Ruan, X., Zhao, Y.X., Wei, F., and Wang, Q. (2018). Response of Plant Secondary Metabolites to Environmental Factors. Molecules, 23.
Zandalinas, 2018, Plant adaptations to the combination of drought and high temperatures, Physiol. Plant., 162, 2, 10.1111/ppl.12540
Alhaithloul, H.A.S. (2019). Impact of Combined Heat and Drought Stress on the Potential Growth Responses of the Desert Grass Artemisia sieberi alba: Relation to Biochemical and Molecular Adaptation. Plants, 8.
Elansary, 2018, Bioactivities of traditional medicinal plants in Alexandria, Evid. Based. Complement. Altern. Med., 2018, 1463579, 10.1155/2018/1463579
El-Esawi, M.A., Elkelish, A., Elansary, H.O., Ali, H.M., Elshikh, M., Witczak, J., and Ahmad, M. (2018, January 09). Genetic Transformation and Hairy Root Induction Enhance the Antioxidant Potential of Lactuca serriola L.. Available online: https://www.hindawi.com/journals/omcl/2017/5604746/.
Elkelish, 2019, Selenium protects wheat seedlings against salt stress-mediated oxidative damage by up-regulating antioxidants and osmolytes metabolism, Plant Physiol. Biochem., 137, 144, 10.1016/j.plaphy.2019.02.004
Abdou, 2015, Protective Effects of Diallyl Sulfide and Curcumin Separately against Thallium-Induced Toxicity in Rats, Cell J., 17, 379
2015, Synergistic protective effects of ceftriaxone and ascorbic acid against subacute deltamethrin-induced nephrotoxicity in rats, Ren. Fail., 37, 297, 10.3109/0886022X.2014.983017
Zakhary, 2018, Aging, Metabolic, and Degenerative Disorders: Biomedical Value of Antioxidants, Oxidative Med. Cell. Longev., 2018, 2098123
Yeung, A.W.K., Tzvetkov, N.T., El-Tawil, O.S., Bungǎu, S.G., Abdel-Daim, M.M., and Atanasov, A.G. (2019, June 16). Antioxidants: Scientific Literature Landscape Analysis. Available online: https://www.hindawi.com/journals/omcl/2019/8278454/.
Elkelish, 2019, Pretreatment with Trichoderma harzianum alleviates waterlogging-induced growth alterations in tomato seedlings by modulating physiological, biochemical, and molecular mechanisms, Environ. Exp. Bot., 171, 103946, 10.1016/j.envexpbot.2019.103946
Nair, 2001, Final report on the safety assessment of Mentha Piperita (Peppermint) Oil, Mentha Piperita (Peppermint) Leaf Extract, Mentha Piperita (Peppermint) Leaf, and Mentha Piperita (Peppermint) Leaf Water, Int. J. Toxicol., 20, 61, 10.1080/10915810152902592
Diouf, 2015, Association of an inherited genetic variant with vincristine-related peripheral neuropathy in children with acute lymphoblastic leukemia, JAMA, 313, 815, 10.1001/jama.2015.0894
Bradford, 1976, A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding, Anal. Biochem., 72, 248, 10.1016/0003-2697(76)90527-3
Troll, 1955, A photometric method for the determination of proline, J. Biol Chem, 215, 655, 10.1016/S0021-9258(18)65988-5
Grieve, 1983, Rapid assay for determination of water soluble quaternary ammonium compounds, Plant. Soil, 70, 303, 10.1007/BF02374789
Irigoyen, 1992, Water stress induced changes in concentrations of proline and total soluble sugars in nodulated alfalfa (Medicago sativd) plants, Physiol. Plant., 84, 55, 10.1111/j.1399-3054.1992.tb08764.x
Slinkard, 1977, Total Phenol Analysis: Automation and Comparison with Manual Methods, Am. J. Enol Vitic., 28, 49, 10.5344/ajev.1977.28.1.49
1985, Phenolic constituents in the leaves of northern willows: Methods for the analysis of certain phenolics, J. Agric. Food Chem., 33, 213, 10.1021/jf00062a013
Jia, 1999, The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals, Food Chem., 64, 555, 10.1016/S0308-8146(98)00102-2
Obadoni, 2002, Phytochemical studies and comparative efficacy of the crude extracts of some haemostatic plants in Edo and Delta States of Nigeria, Glob. J. Pure Appl. Sci., 8, 203
Ferguson, N.M. (1956). A Textbook of Pharmacognosy, Macmillan Company.
Amadi, B.A., Agomuo, E.N., and Ibegbulem, C.O. (2004). Proximate analysis. Research Methods in Biochemistry, Supreme Publishers.
Ezeonu, 2014, Determination of Physical and Phytochemical Constituents of some Tropical Timbers Indigenous to nigerdelta area of nigeria, Eur. Sci. J., 10, 247
Harborne, A.J. (1998). Phytochemical Methods a Guide to Modern Techniques of Plant Analysis, Springer.
Wichers, 2000, Characterization of the total free radical scavenger capacity of vegetable oils and oil fractions using 2,2-diphenyl-1-picrylhydrazyl radical, J. Agric. Food Chem., 48, 648, 10.1021/jf9908188
Romijn, 1988, Application of the MTT assay to human prostate cancer cell lines in vitro: Establishment of test conditions and assessment of hormone-stimulated growth and drug-induced cytostatic and cytotoxic effects, Prostate, 12, 99, 10.1002/pros.2990120112
Cerrudo, D., González Pérez, L., Mendoza Lugo, J.A., and Trachsel, S. (2017). Stay-Green and Associated Vegetative Indices to Breed Maize Adapted to Heat and Combined Heat-Drought Stresses. Remote Sens., 9.
Perera, R.S., Cullen, B.R., and Eckard, R.J. (2019). Growth and Physiological Responses of Temperate Pasture Species to Consecutive Heat and Drought Stresses. Plants, 8.
Ahanger, 2017, Salinity stress induced alterations in antioxidant metabolism and nitrogen assimilation in wheat (Triticum aestivum L) as influenced by potassium supplementation, Plant. Physiol. Biochem., 115, 449, 10.1016/j.plaphy.2017.04.017
Saleh, 2007, Role of Heat Shock and Salicylic Acid in Antioxidant Homeostasis in Mungbean (Vigna radiata L.) Plant Subjected to Heat Stress, Am. J. Plant. Physiol., 2, 344, 10.3923/ajpp.2007.344.355
Sita, 2018, Impact of heat stress during seed filling on seed quality and seed yield in lentil (Lens culinaris Medikus) genotypes, J. Sci. Food Agric., 98, 5134, 10.1002/jsfa.9054
Sehgal, 2019, Influence of drought and heat stress, applied independently or in combination during seed development, on qualitative and quantitative aspects of seeds of lentil (Lens culinaris Medikus) genotypes, differing in drought sensitivity, Plant Cell Environ., 42, 198, 10.1111/pce.13328
Sehgal, 2017, Effects of Drought, Heat and Their Interaction on the Growth, Yield and Photosynthetic Function of Lentil (Lens culinaris Medikus) Genotypes Varying in Heat and Drought Sensitivity, Front. Plant. Sci., 8, 1776, 10.3389/fpls.2017.01776
Ladher, 1998, Signalling interactions during facial development, Mech. Dev., 75, 3, 10.1016/S0925-4773(98)00082-3
Rymen, 2007, Cold nights impair leaf growth and cell cycle progression in maize through transcriptional changes of cell cycle genes, Plant. Physiol., 143, 1429, 10.1104/pp.106.093948
Slama, 2015, Diversity, distribution and roles of osmoprotective compounds accumulated in halophytes under abiotic stress, Ann. Bot., 115, 433, 10.1093/aob/mcu239
Pade, 2014, Salt Acclimation of Cyanobacteria and Their Application in Biotechnology, Life, 5, 25, 10.3390/life5010025
Sharma, A., Shahzad, B., Kumar, V., Kohli, S.K., Sidhu, G.P.S., Bali, A.S., Handa, N., Kapoor, D., Bhardwaj, R., and Zheng, B. (2019). Phytohormones Regulate Accumulation of Osmolytes under Abiotic Stress. Biomolecules, 9.
Hare, 1998, Dissecting the roles of osmolyte accumulation during stress, Plant Cell Environ., 21, 535, 10.1046/j.1365-3040.1998.00309.x
Parry, 2013, Rubisco activity and regulation as targets for crop improvement, J. Exp. Bot, 64, 717, 10.1093/jxb/ers336
Akhtar, M.S. (2019). Salt Stress, Microbes, and Plant. Interactions: Mechanisms and Molecular Approaches, Springer.
Kishor, 2005, Regulation of proline biosynthesis, degradation, uptake and transport in higher plants: Its implications in plant growth and abiotic stress tolerance, Curr. Sci., 88, 424
Spaans, 2015, NADPH-generating systems in bacteria and archaea, Front. Microbiol., 6, 742, 10.3389/fmicb.2015.00742
Mohammadkhani, 2008, Drought-induced Accumulation of Soluble Sugars and Proline in Two Maize Varieties, World Appl. Sci. J., 6, 448
Iqbal, 2015, Nitrogen availability regulates proline and ethylene production and alleviates salinity stress in mustard (Brassica juncea), J. Plant. Physiol., 178, 84, 10.1016/j.jplph.2015.02.006
Harsh, 2016, Effect of short-term heat stress on total sugars, proline and some antioxidant enzymes in moth bean (Vigna aconitifolia), Ann. Agric. Sci., 61, 57, 10.1016/j.aoas.2016.02.001
Kaushal, 2012, The urban watershed continuum: Evolving spatial and temporal dimensions, Urban Ecosyst., 15, 409, 10.1007/s11252-012-0226-7
Giri, 2011, Glycinebetaine and abiotic stress tolerance in plants, Plant. Signal. Behav., 6, 1746, 10.4161/psb.6.11.17801
El-Esawi, M.A., Al-Ghamdi, A.A., Ali, H.M., Alayafi, A.A., Witczak, J., and Ahmad, M. (2018). Analysis of genetic variation and enhancement of salt tolerance in French pea. Int. J. Mol. Sci., 19.
El-Esawi, M.A., Alaraidh, I.A., Alsahli, A.A., Ali, H.M., Alayafi, A.A., Witczak, J., and Ahmad, M. (2018). Genetic Variation and Alleviation of Salinity Stress in Barley (Hordeum vulgare L.). Molecules, 23.
Kang, 2018, Light Signaling, Root Development, and Plasticity, Plant Physiol., 176, 1049, 10.1104/pp.17.01079
Ahanger, 2017, Plant growth under water/salt stress: ROS production; antioxidants and significance of added potassium under such conditions, Physiol. Mol. Biol. Plants, 23, 731, 10.1007/s12298-017-0462-7
Keunen, 2013, Plant sugars are crucial players in the oxidative challenge during abiotic stress: Extending the traditional concept: Sugars and abiotic stress, Plant Cell Environ., 36, 1242, 10.1111/pce.12061
Abbas, 2017, Volatile terpenoids: Multiple functions, biosynthesis, modulation and manipulation by genetic engineering, Planta, 246, 803, 10.1007/s00425-017-2749-x
Ahmad, 2019, Radiation-mediated molecular weight reduction and structural modification in carrageenan potentiates improved photosynthesis and secondary metabolism in peppermint (Mentha piperita L.), Int. J. Biol. Macromol., 124, 1069, 10.1016/j.ijbiomac.2018.12.022
Gharibi, 2019, Exploiting the Cellular Redox-Control System for Activatable Photodynamic Therapy, ChemBioChem, 20, 345, 10.1002/cbic.201800585
Sarker, U., and Oba, S. (2018). Drought stress enhances nutritional and bioactive compounds, phenolic acids and antioxidant capacity of Amaranthus leafy vegetable. BMC Plant Biol., 18.
Akula, 2011, Influence of abiotic stress signals on secondary metabolites in plants, Plant Signal. Behav., 6, 1720, 10.4161/psb.6.11.17613
Khan, M.I.R., Reddy, P.S., Ferrante, A., and Khan, N.A. (2019). Chapter 10—Bioactive Molecules as Regulatory Signals in Plant Responses to Abiotic Stresses. Plant Signaling Molecules, Woodhead Publishing.
Liu, 2017, Effects of PEG-induced drought stress on regulation of indole alkaloid biosynthesis in Catharanthus roseus, J. Plant. Interact., 12, 87, 10.1080/17429145.2017.1293852
Selmar, 2015, New insights explain that drought stress enhances the quality of spice and medicinal plants: Potential applications, Agron. Sustain. Dev., 35, 121, 10.1007/s13593-014-0260-3
Nantongo, J.S., Odoi, J.B., Abigaba, G., and Gwali, S. (2018). Variability of phenolic and alkaloid content in different plant parts of Carissa edulis Vahl and Zanthoxylum chalybeum Engl. BMC Res. Notes, 11.
Schrader, J., and Bohlmann, J. (2015). Biosynthesis and Biological Functions of Terpenoids in Plants. Biotechnology of Isoprenoids, Advances in Biochemical Engineering/Biotechnology; Springer International Publishing.
Karlic, 2015, Inhibition of the mevalonate pathway affects epigenetic regulation in cancer cells, Cancer Genet., 208, 241, 10.1016/j.cancergen.2015.03.008
Ibrahim, 2010, Elevation of night-time temperature increases terpenoid emissions from Betula pendula and Populus tremula, J. Exp. Bot., 61, 1583, 10.1093/jxb/erq034
Valledor, 2018, Metabolome Integrated Analysis of High-Temperature Response in Pinus radiata, Front. Plant. Sci., 9, 485, 10.3389/fpls.2018.00485
Amarowicz, 2014, Changes in the composition of phenolic compounds and antioxidant properties of grapevine roots and leaves (Vitis vinifera L.) under continuous of long-term drought stress, Acta Physiol. Plant, 36, 1491, 10.1007/s11738-014-1526-8
Zainol, 2003, Antioxidative activity and total phenolic compounds of leaf, root and petiole of four accessions of Centella asiatica (L.) Urban, Food Chem., 81, 575, 10.1016/S0308-8146(02)00498-3
2004, Polifenole jako naturalne antyoksydanty w zywnosci, Przegląd Piek. I Cukier., 6, 12
Singh, 2015, Antibacterial and antioxidant activities of Mentha piperita L., Arab. J. Chem., 8, 322, 10.1016/j.arabjc.2011.01.019
Jirovetz, 2009, Antimicrobial Activities of Essential Oils of Mint and Peppermint as Well as Some of Their Main Compounds, J. Essent. Oil Res., 21, 363, 10.1080/10412905.2009.9700193
Aparna, L.M., Aparna, S., Sarada, I., and Ram, D. (2017). Assessment of Sputum Quality and Its Importance in the Rapid Diagnosis of Pulmonary Tuberculosis. Arch. Clin. Microbiol., 8.
Bupesh, 2007, Antibacterial activity of Mentha piperita L. (peppermint) from leaf extracts—A medicinal plant, Acta Agric. Slov., 89, 73
Samarth, 2006, Protective effects of Mentha piperita Linn on benzo[a]pyrene-induced lung carcinogenicity and mutagenicity in Swiss albino mice, Mutagenesis, 21, 61, 10.1093/mutage/gei075
2017, Comparison of phenolic acids and flavonoids contents in various cultivars and parts of common lavender (Lavandula angustifolia) derived from Poland, Nat. Prod. Res., 31, 2575, 10.1080/14786419.2017.1320792
Spiridon, 2011, Antioxidant capacity and total phenolic contents of oregano (Origanum vulgare), lavender (Lavandula angustifolia) and lemon balm (Melissa officinalis) from Romania, Nat. Prod. Res., 25, 1657, 10.1080/14786419.2010.521502
Alexa, 2018, Phytochemical Screening and Biological Activity of Mentha × piperita L. and Lavandula angustifolia Mill. Extracts, Anal. Cell. Pathol., 2018, 1, 10.1155/2018/2678924
Surendra, 2016, Bioconversion of organic wastes into biodiesel and animal feed via insect farming, Renew. Energy, 98, 197, 10.1016/j.renene.2016.03.022
Arora, R., Malhotra, P., Mathur, A., and Mathur, A. (2010). Anticancer Alkaloids of Catharanthus roseus: Transition from Traditional to Modern Medicine. Herbal Medicine: A Cancer Chemopreventive and Therapeutic Perspective, Jaypee Brothers Medical Publishers (P) Ltd.
Naz, 2015, Evaluation of antimicrobial activity of extracts of in vivo and in vitro grown Vinca rosea L. (Catharanthus roseus) against pathogens, Pak. J. Pharm. Sci., 28, 849
Fa, O., Et, O., Io, O., and Ef, O. (2019). Antimicrobial activity and phytochemical screening of leaf extracts of catharantus roseus against aspergillus niger. Int. J. Pure Appl. Zool., 7.
Raza, 2009, Antibacterial activity of different extracts from the Catharanthus roseus, Clin. Exp. Med. J., 3, 81, 10.1556/CEMED.3.2009.1.7