- -

Uncovering salt tolerance mechanisms in pepper plants: a physiological and transcriptomic approach.

RiuNet: Repositorio Institucional de la Universidad Politécnica de Valencia

Compartir/Enviar a

Citas

Estadísticas

  • Estadisticas de Uso

Uncovering salt tolerance mechanisms in pepper plants: a physiological and transcriptomic approach.

Mostrar el registro completo del ítem

Lopez-Serrano, L.; Calatayud, Á.; López Galarza, SV.; Serrano Salom, R.; Bueso Rodenas, E. (2021). Uncovering salt tolerance mechanisms in pepper plants: a physiological and transcriptomic approach. BMC Plant Biology. 21(1):1-17. https://doi.org/10.1186/s12870-021-02938-2

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/182306

Ficheros en el ítem

Thumbnail
Nombre: Lopez-SerranoCala ...
Tamaño: 1.111Mb
Formato: PDF
Descripción: Versión editorial
Abrir/Preview

Metadatos del ítem

Título: Uncovering salt tolerance mechanisms in pepper plants: a physiological and transcriptomic approach.
Autor: Lopez-Serrano, Lidia Calatayud, Ángeles López Galarza, Salvador Vicente Serrano Salom, Ramón Bueso Rodenas, Eduardo
Entidad UPV: Universitat Politècnica de València. Departamento de Producción Vegetal - Departament de Producció Vegetal
Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia
Fecha difusión:
Resumen:
[EN] Background Pepper is one of the most cultivated crops worldwide, but is sensitive to salinity. This sensitivity is dependent on varieties and our knowledge about how they can face such stress is limited, mainly according ...[+]
Palabras clave: Abscisic acid , Growth , Ion homeostasis , Photosynthesis , Salt stress , Tolerant accessions , Pepper
Derechos de uso: Reconocimiento (by)
Fuente:
BMC Plant Biology. (issn: 1471-2229 )
DOI: 10.1186/s12870-021-02938-2
Editorial:
Springer (Biomed Central Ltd.)
Versión del editor: https://doi.org/10.1186/s12870-021-02938-2
Código del Proyecto:
info:eu-repo/grantAgreement/MICINN//RTA2017-00030-C02-00/
Agradecimientos:
This work was financed by the INIA (Spain) and the Ministerio de Ciencia, Innovacion y Universidades (RTA2017-00030-C02-00) and the European Regional Development Fund (ERDF). Lidia Lopez-Serrano is a beneficiary of a ...[+]
Tipo: Artículo

References

Tripodi P, Kumar S. The Capsicum Crop: An Introduction. In: Ramchiary N, Kole C, editors. The Capsicum genome. Switzerland: Springer; 2019. p. 1–8. https://doi.org/10.1007/978-3-319-97217-6_1.

Condés Rodríguez LF. Pimiento. In: Maroto Borrego JV, Baixauli Soria C, editors. Cultivos hortícolas al aire libre. Cajamar. Cajamar; 2017. p. 471–507.

Ayers RS, Westcot DW. Water quality for agriculture. Rome: FAO; 1985. [+]
Tripodi P, Kumar S. The Capsicum Crop: An Introduction. In: Ramchiary N, Kole C, editors. The Capsicum genome. Switzerland: Springer; 2019. p. 1–8. https://doi.org/10.1007/978-3-319-97217-6_1.

Condés Rodríguez LF. Pimiento. In: Maroto Borrego JV, Baixauli Soria C, editors. Cultivos hortícolas al aire libre. Cajamar. Cajamar; 2017. p. 471–507.

Ayers RS, Westcot DW. Water quality for agriculture. Rome: FAO; 1985.

Bojórquez-Quintal E, Velarde-Buendía A, Ku-González Á, Carillo-Pech M, Ortega-Camacho D, Echevarría-Machado I, et al. Mechanisms of salt tolerance in habanero pepper plants (Capsicum chinense Jacq.): Proline accumulation, ions dynamics and sodium root-shoot partition and compartmentation. Front Plant Sci. 2014;5:1–14. https://doi.org/10.3389/fpls.2014.00605.

Zaman M, Shahid SA, Heng L. Guideline for salinity assessment, mitigation and adaptation using nuclear and related techniques. Cham: Springer; 2018. https://doi.org/10.1007/978-3-319-96190-3.

De Pascale S, Ruggiero C, Barbieri G, Maggio A. Physiological Responses of Pepper to Salinity and Drought. J Am Soc Hortic Sci. 2003;128:48–54. https://doi.org/10.21273/JASHS.128.1.0048.

Bojórquez-Quintal JE, Echevarría-Machado L, Medina-Lara Á, Martinez-Estevez M. Plants’ challenges in a salinized world: the case of Capsicum. Afri J Biotechnol. 2012;11(72):13614–26. https://doi.org/10.5897/AJB12.2145.

Munns R, Tester M. Mechanisms of salinity tolerance. Annu Rev Plant Biol. 2008;59(1):651–81. https://doi.org/10.1146/annurev.arplant.59.032607.092911.

Isayenkov SV, Maathuis FJM. Plant salinity stress: many unanswered questions remain. Front Plant Sci. 2019;10:1–11. https://doi.org/10.3389/fpls.2019.00080.

Hossain MR, Bassel GW, Pritchard J, Sharma GP, Ford-Lloyd BV. Trait specific expression profiling of salt stress responsive genes in diverse Rice genotypes as determined by modified significance analysis of microarrays. Front Plant Sci. 2016;7:1–17. https://doi.org/10.3389/fpls.2016.00567.

Aktas H, Abak K, Cakmak I. Genotypic variation in the response of pepper to salinity. Sci Hortic (Amsterdam). 2006;110(3):260–6. https://doi.org/10.1016/j.scienta.2006.07.017.

Penella C, Nebauer SG, Lopéz-Galarza S, San Bautista A, Gorbe E, Calatayud A. Evaluation for salt stress tolerance of pepper genotypes to be used as rootstocks. J Food, Agric Environ. 2013;11:1101–7.

Özdemir B, Tanyolaç ZÖ, Ulukapı K, Onus AN. Evaluation of salinity tolerance level of some pepper (Capsicum annuum L.) cultivars. Int J Agric Innov Res. 2016;5:2319–1473.

López-Serrano L, Penella C, San-Bautista A, López-Galarza S, Calatayud A. Physiological changes of pepper accessions in response to salinity and water stress. Spanish J Agric Res. 2017;15(3):1–10. https://doi.org/10.5424/sjar/2017153-11147.

Penella C, Nebauer SG, Quiñones A, San Bautista A, López-Galarza S, Calatayud A. Some rootstocks improve pepper tolerance to mild salinity through ionic regulation. Plant Sci. 2015;230:12–22. https://doi.org/10.1016/j.plantsci.2014.10.007.

López-Serrano L, Canet-Sanchis G, Vuletin Selak G, Penella C, San Bautista A, López-Galarza S, et al. Physiological characterization of a pepper hybrid rootstock designed to cope with salinity stress. Plant Physiol Biochem. 2020;148:207–19. https://doi.org/10.1016/j.plaphy.2020.01.016.

Li T, Xu X, Li Y, Wang H, Li Z, Li Z. Comparative transcriptome analysis reveals differential transcription in heat-susceptible and heat-tolerant pepper (Capsicum annum L.) cultivars under heat stress. J Plant Biol. 2015;58(6):411–24. https://doi.org/10.1007/s12374-015-0423-z.

Wang J, Lv J, Liu Z, Liu Y, Song J, Ma Y, et al. Integration of Transcriptomics and metabolomics for pepper (Capsicum annuum L.) in response to heat stress. Int J Mol Sci. 2019;20(20):5042. https://doi.org/10.3390/ijms20205042.

Rai VP, Rai A, Kumar R, Kumar S, Kumar S, Singh M, et al. Microarray analyses for identifying genes conferring resistance to pepper leaf curl virus in chilli pepper ( Capsicum spp.). Genomics Data. 2016;9:140–2. https://doi.org/10.1016/j.gdata.2016.08.002.

Li J, Yang P, Kang J, Gan Y, Yu J, Calderón-Urrea A, et al. Transcriptome analysis of pepper (Capsicum annuum) revealed a role of 24-Epibrassinolide in response to chilling. Front Plant Sci. 2016;7:1–17. https://doi.org/10.3389/fpls.2016.01281.

Lim CW, Lim S, Baek W, Lee SC. The pepper late embryogenesis abundant protein CaLEA1 acts in regulating abscisic acid signaling, drought and salt stress response. Physiol Plant. 2015;154(4):526–42. https://doi.org/10.1111/ppl.12298.

Wang J-E, Liu K-K, Li D-W, Zhang Y-L, Zhao Q, He Y-M, et al. A novel peroxidase CanPOD gene of pepper is involved in defense responses to Phytophtora capsici infection as well as abiotic stress tolerance. Int J Mol Sci. 2013;14(2):3158–77. https://doi.org/10.3390/ijms14023158.

Bulle M, Yarra R, Abbagani S. Enhanced salinity stress tolerance in transgenic chilli pepper (Capsicum annuum L.) plants overexpressing the wheat antiporter (TaNHX2) gene. Mol Breed. 2016;36. https://doi.org/10.1007/s11032-016-0451-5.

Penella C, Landi M, Guidi L, Nebauer SG, Pellegrini E, Bautista AS, et al. Salt-tolerant rootstock increases yield of pepper under salinity through maintenance of photosynthetic performance and sinks strength. J Plant Physiol. 2016;193:1–11. https://doi.org/10.1016/j.jplph.2016.02.007.

Ryu H, Cho Y-G. Plant hormones in salt stress tolerance. J Plant Biol. 2015;58(3):147–55. https://doi.org/10.1007/s12374-015-0103-z.

Ding H, Lai J, Wu Q, Zhang S, Chen L, Dai Y-S, et al. Jasmonate complements the function of Arabidopsis lipoxygenase3 in salinity stress response. Plant Sci. 2016;244:1–7. https://doi.org/10.1016/j.plantsci.2015.11.009.

Balfagón D, Sengupta S, Gómez-Cadenas A, Fritschi FB, Azad RK, Mittler R, et al. Jasmonic acid is required for plant acclimation to a combination of high light and heat stress. Plant Physiol. 2019;181(4):1668–82. https://doi.org/10.1104/pp.19.00956.

Ghaffari H, Tadayon MR, Nadeem M, Razmjoo J, Cheema M. Foliage applications of jasmonic acid modulate the antioxidant defense under water deficit growth in sugar beet. Spanish J Agric Res. 2020;17(4):1–12. https://doi.org/10.5424/sjar/2019174-15380.

Kitaoka N, Matsubara T, Sato M, Takahashi K, Wakuta S, Kawaide H, et al. Arabidopsis CYP94B3 encodes Jasmonyl-l-isoleucine 12-hydroxylase, a key enzyme in the oxidative catabolism of Jasmonate. Plant Cell Physiol. 2011;52(10):1757–65. https://doi.org/10.1093/pcp/pcr110.

Ahmad P, Azooz MM, Prasad MNV. Ecophysiology and responses of plants under salt stress. Springer New York: Springer; 2013. https://doi.org/10.1007/978-1-4614-4747-4.

Alam MM, Nahar K, Hasanuzzaman M, Fujita M. Exogenous jasmonic acid modulates the physiology, antioxidant defense and glyoxalase systems in imparting drought stress tolerance in different Brassica species. Plant Biotechnol Rep. 2014;8(3):279–93. https://doi.org/10.1007/s11816-014-0321-8.

Fernando VCD, Schroeder DF. Role of ABA in Arabidopsis Salt, Drought, and Desiccation Tolerance. In: Shanker A, Shanker C, editors. Abiotic and Biotic Stress in Plants - Recent Advances and Future Perspectives. IntechOpen. 2016. p. 507–24. https://doi.org/10.5772/61957.

He T, Cramer GR. Abscisic acid concentrations are correlated with leaf area reductions in two salt-stressed rapid-cycling Brassica species. Plant Soil. 1996;179(1):25–33. https://doi.org/10.1007/BF00011639.

Saez A, Apostolova N, Gonzalez-Guzman M, Gonzalez-Garcia MP, Nicolas C, Lorenzo O, et al. Gain-of-function and loss-of-function phenotypes of the protein phosphatase 2C HAB1 reveal its role as a negative regulator of abscisic acid signalling. Plant J. 2004;37(3):354–69. https://doi.org/10.1046/j.1365-313X.2003.01966.x.

Wang Z, Ji H, Yuan B, Wang S, Su C, Yao B, et al. ABA signalling is fine-tuned by antagonistic HAB1 variants. Nat Commun. 2015;6:1–12.

Schweighofer A, Hirt H, Meskiene I. Plant PP2C phosphatases: emerging functions in stress signaling. Trends Plant Sci. 2004;9(5):236–43. https://doi.org/10.1016/j.tplants.2004.03.007.

Wei M, Xu X, Li C. Identification and expression of CAMTA genes in Populus trichocarpa under biotic and abiotic stress. Sci Rep. 2017;7(1):17910. https://doi.org/10.1038/s41598-017-18219-8.

Galon Y, Finkler A, Fromm H. Calcium-regulated transcription in plants. Mol Plant. 2010;3(4):653–69. https://doi.org/10.1093/mp/ssq019.

Xie Z, Nolan T, Jiang H, Tang B, Zhang M, Li Z, et al. The AP2/ERF transcription factor TINY modulates Brassinosteroid-regulated plant growth and drought responses in Arabidopsis. Plant Cell. 2019;31(8):1788–806. https://doi.org/10.1105/tpc.18.00918.

Galon Y, Nave R, Boyce JM, Nachmias D, Knight MR, Fromm H. Calmodulin-binding transcription activator (CAMTA) 3 mediates biotic defense responses in Arabidopsis. FEBS Lett. 2008;582(6):943–8. https://doi.org/10.1016/j.febslet.2008.02.037.

Doherty CJ, Van Buskirk HA, Myers SJ, Thomashow MF. Roles for Arabidopsis CAMTA transcription factors in cold-regulated gene expression and freezing tolerance. Plant Cell. 2009;21(3):972–84. https://doi.org/10.1105/tpc.108.063958.

Shkolnik D, Finkler A, Pasmanik-Chor M, Fromm H. Calmodulin-binding transcription activator 6: a key regulator of Na+ homeostasis during germination. Plant Physiol. 2019;180(2):1101–18. https://doi.org/10.1104/pp.19.00119.

Kusvuran S, Yasar F, Ellialtioglu S, Abak K. Utilizing some of screening Methots in order to determine of tolerance of salt stress in the melon (Cucumis melo L.). Res J Agric Biol Sci. 2007;3:40–5.

Tiwari JK, Munshi AD, Kumar R, Pandey RN, Arora A, Bhat JS, et al. Effect of salt stress on cucumber: Na+−K+ ratio, osmolyte concentration, phenols and chlorophyll content. Acta Physiol Plant. 2010;32(1):103–14. https://doi.org/10.1007/s11738-009-0385-1.

Ferreira JFS, Liu X, Suarez DL. Fruit yield and survival of five commercial strawberry cultivars under field cultivation and salinity stress. Sci Hortic (Amsterdam). 2019;243:401–10. https://doi.org/10.1016/j.scienta.2018.07.016.

Bartha C, Fodorpataki L, Del Carmen M-BM, Popescu O, Carvajal M. Sodium accumulation contributes to salt stress tolerance in lettuce cultivars. J Appl Bot Food Qual. 2015;88:42–8.

Liu Y, Li H, Shi Y, Song Y, Wang T, Li Y. A maize early responsive to dehydration gene, ZmERD4, provides enhanced drought and salt tolerance in Arabidopsis. Plant Mol Biol Report. 2009;27(4):542–8. https://doi.org/10.1007/s11105-009-0119-y.

Acosta-Motos J, Ortuño M, Bernal-Vicente A, Diaz-Vivancos P, Sanchez-Blanco M, Hernandez J. Plant responses to salt stress: adaptive mechanisms. Agronomy. 2017;7(1):1–38. https://doi.org/10.3390/agronomy7010018.

Sun Y, Kong X, Li C, Liu Y, Ding Z. Potassium retention under salt stress is associated with natural variation in salinity tolerance among Arabidopsis accessions. PLoS One. 2015;10(5):e0124032. https://doi.org/10.1371/journal.pone.0124032.

Qi F, Zhang F. Cell cycle regulation in the plant response to stress. Front Plant Sci. 2020;10:1765. https://doi.org/10.3389/fpls.2019.01765.

Schuppler U, He P-H, John PCL, Munns R. Effect of water stress on cell division and Cdc2-like cell cycle kinase activity in wheat leaves. Plant Physiol. 1998;117(2):667–78. https://doi.org/10.1104/pp.117.2.667.

Marowa P, Ding A, Kong Y. Expansins: roles in plant growth and potential applications in crop improvement. Plant Cell Rep. 2016;35(5):949–65. https://doi.org/10.1007/s00299-016-1948-4.

Chen L, Zou W, Fei C, Wu G, Li X, Lin H, et al. α-Expansin EXPA4 positively regulates abiotic stress tolerance but negatively regulates pathogen resistance in Nicotiana tabacum. Plant Cell Physiol. 2018;59:2317–30. https://doi.org/10.1093/pcp/pcy155.

Geilfus C-M, Zörb C, Mühling KH. Salt stress differentially affects growth-mediating β-expansins in resistant and sensitive maize (Zea mays L.). Plant Physiol Biochem. 2010;48(12):993–8. https://doi.org/10.1016/j.plaphy.2010.09.011.

Thalmann M, Santelia D. Starch as a determinant of plant fitness under abiotic stress. New Phytol. 2017;214(3):943–51. https://doi.org/10.1111/nph.14491.

Riffat A, Sajid M, Ahmad A. Alleviation of Adverse Effects of Salt Stress on Growth og Maize (Zea mays L.) by Sulfur Supplementation. Pak J Bot. 2020;52:763–73. https://doi.org/10.30848/PJB2020-3(38.

Chaves MM, Flexas J, Pinheiro C. Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot. 2009;103(4):551–60. https://doi.org/10.1093/aob/mcn125.

Zanella M, Borghi GL, Pirone C, Thalmann M, Pazmino D, Costa A, et al. β-Amylase 1 (BAM1) degrades transitory starch to sustain proline biosynthesis during drought stress. J Exp Bot. 2016;67(6):1819–26. https://doi.org/10.1093/jxb/erv572.

Valerio C, Costa A, Marri L, Issakidis-Bourguet E, Pupillo P, Trost P, et al. Thioredoxin-regulated β-amylase (BAM1) triggers diurnal starch degradation in guard cells, and in mesophyll cells under osmotic stress. J Exp Bot. 2011;62(2):545–55. https://doi.org/10.1093/jxb/erq288.

Munns R. Genes and salt tolerance: bringing them together. New Phytol. 2005;167(3):645–63. https://doi.org/10.1111/j.1469-8137.2005.01487.x.

Hasegawa PM, Bressan RA, Zhu JK, Bohnert HJ. Plant cellular and molecular responses to high salinity. Annu Rev Plant Biol. 2000;51(1):463–99. https://doi.org/10.1146/annurev.arplant.51.1.463.

Chartzoulakis K, Psarras G, Vemmos S, Loupassaki M, Bertaki M. Response of two olive cultivars to salt stress and potassium supplement. J Plant Nutr. 2006;29(11):2063–78. https://doi.org/10.1080/01904160600932682.

Wu H, Zhang X, Giraldo JP, Shabala S. It is not all about sodium: revealing tissue specificity and signalling roles of potassium in plant responses to salt stress. Plant Soil. 2018;431(1-2):1–17. https://doi.org/10.1007/s11104-018-3770-y.

Spalding EP, Hirsch RE, Lewis DR, Qi Z, Sussman MR, Lewis BD. Potassium uptake supporting plant growth in the absence of AKT1 channel activity. J Gen Physiol. 1999;113(6):909–18. https://doi.org/10.1085/jgp.113.6.909.

Zhang F, Li L, Jiao Z, Chen Y, Liu H, Chen X, et al. Characterization of the calcineurin B-like (CBL) gene family in maize and functional analysis of ZmCBL9 under abscisic acid and abiotic stress treatments. Plant Sci. 2016;253:118–29. https://doi.org/10.1016/j.plantsci.2016.09.011.

Xu J, Li H-D, Chen L-Q, Wang Y, Liu L-L, He L, et al. A protein kinase, interacting with two Calcineurin B-like proteins, regulates K+ transporter AKT1 in Arabidopsis. Cell. 2006;125(7):1347–60. https://doi.org/10.1016/j.cell.2006.06.011.

Bhaskara GB, Nguyen TT, Verslues PE. Unique drought resistance functions of the highly ABA-induced clade a protein phosphatase 2Cs. Plant Physiol. 2012;160(1):379–95. https://doi.org/10.1104/pp.112.202408.

Lee SC, Lan W-Z, Kim B-G, Li L, Cheong YH, Pandey GK, et al. A protein phosphorylation/dephosphorylation network regulates a plant potassium channel. Proc Natl Acad Sci. 2007;104(40):15959–64. https://doi.org/10.1073/pnas.0707912104.

Apse MP, Aharon GS, Snedden WA, Blumwald E. Salt Tolerance Conferred by Overexpression of a Vacuolar Na+/H+ Antiport in Arabidopsis. Science. 1999;285:1256–8. https://doi.org/10.1126/science.285.5431.1256.

Navarro JM, Garrido C, Martínez V, Carvajal M. Water relations and xylem transport of nutrients in pepper plants grown under two different salts stress regimes. Plant Growth Regul. 2003;41(3):237–45. https://doi.org/10.1023/B:GROW.0000007515.72795.c5.

Munns R, Husain S, Rivelli AR, James RA, Condon AG, Lindsay MP, et al. Avenues for increasing salt tolerance of crops, and the role of physiologically based selection traits. Plant Soil. 2002;247(1):93–105. https://doi.org/10.1023/A:1021119414799.

Chakauya E, Coxon KM, Whitney HM, Ashurst JL, Abell C, Smith AG. Pantothenate biosynthesis in higher plants: advances and challenges. Physiol Plant. 2006;126(3):319–29. https://doi.org/10.1111/j.1399-3054.2006.00683.x.

Huang L, Pyc M, Alseekh S, McCarty DR, de Crécy-Lagard V, Gregory JF, et al. A plastidial pantoate transporter with a potential role in pantothenate synthesis. Biochem J. 2018;475(4):813–25. https://doi.org/10.1042/BCJ20170883.

Abo-Ogiala A, Carsjens C, Diekmann H, Fayyaz P, Herrfurth C, Feussner I, et al. Temperature-induced lipocalin (TIL) is translocated under salt stress and protects chloroplasts from ion toxicity. J Plant Physiol. 2014;171(3-4):250–9. https://doi.org/10.1016/j.jplph.2013.08.003.

Küfner I, Koch W. Stress regulated members of the plant organic cation transporter family are localized to the vacuolar membrane. BMC Res Notes. 2008;1(1):43. https://doi.org/10.1186/1756-0500-1-43.

Jacques F, Rippa S, Perrin Y. Physiology of L-carnitine in plants in light of the knowledge in animals and microorganisms. Plant Sci. 2018;274:432–40. https://doi.org/10.1016/j.plantsci.2018.06.020.

Stepien P, Johnson GN. Contrasting responses of photosynthesis to salt stress in the Glycophyte Arabidopsis and the halophyte Thellungiella: role of the plastid terminal oxidase as an alternative Electron sink. Plant Physiol. 2009;149(2):1154–65. https://doi.org/10.1104/pp.108.132407.

Yang Y, Sulpice R, Himmelbach A, Meinhard M, Christmann A, Grill E. Fibrillin expression is regulated by abscisic acid response regulators and is involved in abscisic acid-mediated photoprotection. Proc Natl Acad Sci. 2006;103(15):6061–6. https://doi.org/10.1073/pnas.0501720103.

You J, Chan Z. ROS regulation during abiotic stress responses in crop plants. Front Plant Sci. 2015;6:1–15. https://doi.org/10.3389/fpls.2015.01092.

Pérez-Labrada F, López-Vargas ER, Ortega-Ortiz H, Cadenas-Pliego G, Benavides-Mendoza A, Juárez-Maldonado A. Responses of tomato plants under saline stress to foliar application of copper nanoparticles. Plants. 2019;8(6):151. https://doi.org/10.3390/plants8060151.

Banu MNA, Hoque MA, Watanabe-Sugimoto M, Matsuoka K, Nakamura Y, Shimoishi Y, et al. Proline and glycinebetaine induce antioxidant defense gene expression and suppress cell death in cultured tobacco cells under salt stress. J Plant Physiol. 2009;166(2):146–56. https://doi.org/10.1016/j.jplph.2008.03.002.

Saleethong P, Sanitchon J, Kong-ngern K, Theerakulp P. Pretreatment with Spermidine reverses inhibitory effects of salt stress in two Rice (Oryza sativa L.) cultivars differing in salinity tolerance. Asian J Plant Sci. 2011;10(4):245–54. https://doi.org/10.3923/ajps.2011.245.254.

Khoshbakht D, Asghari MR, Haghighi M. Effects of foliar applications of nitric oxide and spermidine on chlorophyll fluorescence, photosynthesis and antioxidant enzyme activities of citrus seedlings under salinity stress. Photosynthetica. 2018;56(4):1313–25. https://doi.org/10.1007/s11099-018-0839-z.

Roychoudhury A, Basu S, Sengupta DN. Amelioration of salinity stress by exogenously applied spermidine or spermine in three varieties of indica rice differing in their level of salt tolerance. J Plant Physiol. 2011;168(4):317–28. https://doi.org/10.1016/j.jplph.2010.07.009.

Szymańska KP, Polkowska-Kowalczyk L, Lichocka M, Maszkowska J, Dobrowolska G. SNF1-Related Protein Kinases SnRK2.4 and SnRK2.10 Modulate ROS Homeostasis in Plant Response to Salt Stress. Int J Mol Sci. 2019;20:143. https://doi.org/10.3390/ijms20010143.

McCready RM, Guggolz J, Silviera V, Owens HS. Determination of starch and amylose in vegetables application to peas. Anal Chem. 1950;22(9):1156–8.  https://doi.org/10.1021/ac60045a016.

Koç E, İşlek C, Üstün AS. Effect of cold on protein, Proline, phenolic compounds and chlorophyll content of two pepper (Capsicum annuum L.) varieties. GU J Sci. 2010;23:1–6 http://gujs.gazi.edu.tr/article/view/1060000016.

Sergiev I, Alexieva V, Karanov E. Effect of spermine, atrazine and combination between them on some endogenous protective systems and stress markers in plants. Compt Rend Acad Bulg Sci. 1997;51:121–4.

Velikova V, Yordanov I, Edreva A. Oxidative stress and some antioxidant systems in acid rain-treated bean plants protective role of exogenous polyamines. Plant Sci. 2000;151(1):59–66. https://doi.org/10.1016/S0168-9452(99)00197-1.

Bates LS, Waldren RP, Teare ID. Rapid determination of free proline for water-stress studies. 39:205–7. https://doi.org/10.1007/BF00018060.

Medina I, Carbonell J, Pulido L, Madeira SC, Goetz S, Conesa A, et al. Babelomics: an integrative platform for the analysis of transcriptomics, proteomics and genomic data with advanced functional profiling. Nucleic Acids Res. 2010;38(suppl_2):W210–3. https://doi.org/10.1093/nar/gkq388.

Huang DW, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2009;4(1):44–57. https://doi.org/10.1038/nprot.2008.211.

Bin WS, Wei LK, Ping DW, Li Z, Wei G, Bing LJ, et al. Evaluation of appropriate reference genes for gene expression studies in pepper by quantitative real-time PCR. Mol Breed. 2012;30(3):1393–400. https://doi.org/10.1007/s11032-012-9726-7.

Wan H, Yuan W, Ruan M, Ye Q, Wang R, Li Z, et al. Identification of reference genes for reverse transcription quantitative real-time PCR normalization in pepper (Capsicum annuum L.). Biochem Biophys Res Commun. 2011;416(1-2):24–30. https://doi.org/10.1016/j.bbrc.2011.10.105.

[-]

recommendations

 

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro completo del ítem