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2019 | 41 | 06 |

Tytuł artykułu

Tolerance of two apple rootstocks to short-term salt stress: focus on chlorophyll degradation, photosynthesis, hormone and leaf ultrastructures

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
To elucidate the salt tolerance of Malus halliana Koehne and Malus robusta Rehd., changes of photosynthetic parameters, hormone content and chlorophyll degradation enzymes of them were compared after treated with different concentration of NaCl. Salt stresses were simulated using 50, 100, 200 mM of NaCl solution, and 1/2 Hoagland nutrient solution was used instead of NaCl solution as control (CK). Except for the indole acetic acid (IAA) content, the changes of Chlorophyll (Chl) content, net photosynthetic rate (PN), stomatal conductance (gs), IAA/ABA ratio, intercellular CO₂ concentration (Ci), transpiration rate, abscisic acid content (ABA), Pheophytinase (PPH) and Pheophorbide a monooxygenase (PaO) in Malus halliana were lower than those in Malus robusta under 100 and 200 mM NaCl condition. The values of Chlase, PPH and Pao in Malus robusta were significantly higher than that in Malus halliana. According to correlation analysis, the Chl was extremely positively correlated with Chla, Chlb, IAA/ABA, PN and gs, significantly negative correlation with Chla/b, ABA and PaO, and negative correlation with Ci, Chlase and PPH. The chloroplast ultrastructure of Malus robusta was greatly damaged resulting in chloroplasts disintegration and that of Malus halliana was maintained to be completed at 100 and 200 mM NaCl. In certain range of salt concentrations, Malus halliana could be better to adjust the levels of Chlorophyll content, Chlase, PPH, PaO and the number of starch grain and osmiophilic granules to relieve the damage of photosynthetic system due to salt stress. In a word, the Malus halliana could be better adapted to high salt concentration than Malus robusta.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

41

Numer

06

Opis fizyczny

Article 87 [14p.], fig.,ref.

Twórcy

autor
  • College of Horticulture, Gansu Agricultural University, Lanzhou 730000, Gansu Province, China
autor
  • College of Horticulture, Gansu Agricultural University, Lanzhou 730000, Gansu Province, China
autor
  • College of Horticulture, Gansu Agricultural University, Lanzhou 730000, Gansu Province, China
autor
  • College of Horticulture, Gansu Agricultural University, Lanzhou 730000, Gansu Province, China
autor
  • College of Horticulture, Gansu Agricultural University, Lanzhou 730000, Gansu Province, China
autor
  • College of Horticulture, Gansu Agricultural University, Lanzhou 730000, Gansu Province, China
autor
  • College of Horticulture, Gansu Agricultural University, Lanzhou 730000, Gansu Province, China

Bibliografia

  • Abdel Latef AAH (2011) Ameliorative effect of calcium chloride on growth antioxidant enzymes, protein patterns and some metabolic activities of canola (Brassica napus L.) under seawater stress. J Plant Nutri 34:1303–1320. https://doi.org/10.1080/01904167.2011.580817
  • Amir-Shapira D, Goldschmidt EE, Altman A (1987) Chlorophyll catabolism in senescing plant tissues: in vivo breakdown intermediates suggest different degradative pathways for Citrus fruit and parsley leaves. Proc Nat Acad Sci USA 84:1901–1905. https://doi.org/10.1073/pnas.84.7.1901
  • Arnon DI (1949) Copper enzymes in isolated chloroplasts polyphenoloxidase in beta vulgaris. Plant Physiol 24(1):1–15
  • Azeem A, Wu Y, Xing D (2017) Photosynthetic response of two okra cultivars under salt stress and re-watering. J Plant Interact 12(1):67–77. https://doi.org/10.1080/17429145.2017.1279356
  • Bao ST (1999) Analysis of soil agrochemical, 3rd edn. China Agricultural Press, Beijing
  • Beritognolo I, Harfouche A, Brilli F (2011) Comparative study of transcriptional and physiological responses to salinity stress in two contrasting Populus alba L. genotypes. Tree Phys 31(12):1335. https://doi.org/10.1093/treephys/tpr083
  • Büchert AM, Civello PM, Martínez GA (2011) Chlorophyllase versus pheophytinase as candidates for chlorophyll dephytilation during senescence of broccoli. J Plant Physiol 168(4):337–343. https://doi.org/10.1016/j.jplph.2010.07.011
  • Cao M, Liu X, Zhang Y (2013) An ABA-mimicking ligand that reduces water loss and promotes drought resistance in plants. Cell Res 23(8):1043. https://doi.org/10.1038/cr.2013.95
  • Chen LT, Ming L, Wang YY (2010) Involvement of Arabidopsis histone deacetylase HDA6 in ABA and salt stress response. J Experi Bot 61(12):3345–3353. https://doi.org/10.1093/jxb/erq154
  • Christ B, Egert A, Süssenbacher I (2015) Water deficit induces chlorophyll degradation via the ‘PAO/phyllobilin’ pathway in leaves of homoio- (Craterostigma pumilum) and poikilochlorophyllous (Xerophyta viscosa) resurrection plants[J]. Plant Cell Environ 37(11):2521–2531. https://doi.org/10.1111/pce.12308
  • Christian Z, Christoph-Martin G, Karl HM (2013) The influence of salt stress on ABA and auxin concentrations in two maize cultivars differing in salt resistance. J Plant Physiol 170(2):220–224. https://doi.org/10.1016/j.jplph.2012.09.012
  • Costa ML, Civello PM, Chaves AR, Martinez GA (2002) Characterization of Mg-dechelatase activity obtained from Fragaria ananassa fruit. Plant Physiol Biochem 40:111–118. https://doi.org/10.1016/S0981-9428(01)01358-4
  • Delmas F, Sankaranarayanan S, Deb S, Widdup E, Bournonville C, Bollier N, Northey JG, McCourt P, Samuel MA (2013) ABI3 controls embryo degreening through Mendel’s I locus. Proc Nat Acad Sci USA 110:E3888–E3894. https://doi.org/10.1073/pnas.1308114110
  • Du X, Du B, Chen X (2014) Overexpression of the MhTGA2 gene from crab apple (Malus hupehensis) confers increased tolerance to salt stress in transgenic apple (Malus domestica). J Agri Sci 152(4):634–641. https://doi.org/10.1017/S0021859613000130
  • Esau K (1977) Anatomy of seed plants. Wiley, New York
  • Fang ZY, Bouwkmp JS, Solomos T (1996) Chlorophyllase activities and chlorophyll degradation during leaf senescence in non-yellowing mutant and wild type of Phaseolus vulgaris L. J of Experi Bota 49:503–510. https://doi.org/10.1093/jexbot/49.320.503
  • Fernandez-Lopez JA, Almela L, Soledad AM (1992) Partial purification and properties of chlorophyllase from chlorotic citrus limon leaves. Phytochemistry 31:447–449. https://doi.org/10.1016/0031-9422(92)90015-I
  • Fidalgo F, Santos A, Santos I (2015) Effects of long-term salt stress on antioxidant defence systems, leaf water relations and chloroplast ultrastructure of potato plants. Ann of Appl Biol 145(2):185–192. https://doi.org/10.1111/j.1744-7348.2004.tb00374.x
  • Forieri I, Hildebrandt U, Rostás M (2016) Salinity stress effects on direct and indirect defence metabolites in maize. Envir Experi Bota 122:68–77. https://doi.org/10.1016/j.envexpbot.2015.09.007
  • Garousi F, Kovács B, Várallyay S (2017) Relative chlorophyll content changes during uptaking of selenite and selenate by maize plants grown in nutrient solution. In: International conference “biothechnology and quality of raw materials and foodstuffs” 44–47. https://doi.org/10.15414/jmbfs.2015.4.special3.44-47
  • Geilfus CM, Zörb C, Mühling KH (2010) Salt stress differentially affects growth-mediating β-expansins in resistant and sensitive maize (Zea mays L.). Plant Physiol Biochemi 48(12):993. https://doi.org/10.1016/j.plaphy.2010.09.011
  • Geilfus CM, Zörb C, Neuhaus C, Hansen T, Lüthen H, Mühling KH (2011) Differential transcript expression of wall-loosening candidates in leaves of maize cultivars differing in salt resistance. J Plant Growth Regul 30:387–395. https://doi.org/10.1007/s00344-011-9201-4
  • Hameed M, Ashraf M, Naz N (2009) Anatomical adaptations to salinity in cogon grass [Imperata cylindrical (L.) Raeuschel] from the Salt Range. Pakinstan. Plant Soil 322:229–238. https://doi.org/10.1007/s11104-009-9911-6
  • Hörtensteiner S (2013) Update on the biochemistry of chlorophyll breakdown. Plant Mol Biol 82:505–517. https://doi.org/10.1007/s11103-012-9940-z
  • Hörtensteiner S, Kräutler B (2011) Chlorophyll breakdown in higher plants. Biochim Biophys Acta 1807:977–988. https://doi.org/10.1007/s000180050
  • James RA, Blake C, Byrt CS, Munns R (2011) Major genes for Na⁺ exclusion, Nax1 and Nax2 (wheat HKT1;4 and HKT1;5), decrease Na⁺ accumulation in bread wheat leaves under saline and waterlogged conditions. J Experi Bot 62:2939–2947. https://doi.org/10.1093/jxb/err003
  • Jananve M (1997) Enzymatic degradation of chlorophyII in Cavendish bananas: in vitro evidence for two independent degradative pathways. Plant Physiol Biochem 35:837–846
  • Karel W (2013) Effects of salinity stress on growth and organic osmolytes accumulation of callus and tissue culture seedlings of two Malus. Acta Agri Boreal Occident Sin 22(2):112–118
  • Kaya C, Ashraf M, Di̇ki̇li̇tas M (2013) Alleviation of salt stress-induced adverse effects on maize plants by exogenous application of indoleacetic acid (IAA) and inorganic nutrients a field trial. Aust J Crop Sci 7(2):249–254
  • Koyro HW (1996) Ultrastructural and physiological changes in root cells of sorghum plants (Sorghum bicolor × S. sudanensis cv. sweet sioux) induced by NaCl. J Experi Bot 48:693–706. https://doi.org/10.1093/jxb/48.3.693
  • Koyro HW (2006) Effect of salinity on growth, photosynthesis, water relations and solute composition of the potential cash crop halophyte Plantago coronopus (L.). Environ Experi Bot 56(136–146):2006. https://doi.org/10.1016/j.envexpbot.2005.02.001
  • Kunieda T, Amano T, Shioi Y (2005) Search for chlorophyll degradation enzyme, Mg-dechelatase, from extracts of Chenopodium album with native and artificial substrates. Plant Sci 169:177–183. https://doi.org/10.1016/j.plantsci.2005.03.010
  • Lee SY, Oh DH, Bressan RA (2010) Intracellular consequences of SOS1 deficiency during salt stress. J Experi Bota 61(4):1205–1213. https://doi.org/10.1093/jxb/erp391
  • Liu J, Shi DC (2010) Photosynthesis, chlorophyll fluorescence, inorganic ion and organic acid accumulations of sunflower in responses to salt and salt-alkaline mixed stress. Photosynthetica 48(1):127–134. https://doi.org/10.1007/s11099-010-0017-4
  • Lu XY, Lai W, Xu XP (2014) Effects of NaCl stress on photosynthetic characteristics in Malus robusta and Malus baccata. J Arid Land Resour Envir 62:765–794
  • Ma L, Wu YX, He TM (2016) Effects of salt stress on anatomical structure of leaves of Malus sieversii and Malus robusta. Agri Sci Technol 17(8):1777–1779
  • Matile P, Hörtensteiner S, Thomas H (1999) Chlorophyll degradation. Ann Revi Plant Physiol 50:67–95. https://doi.org/10.1146/annurev.arplant.57.032905.105212
  • Mosquera MI, Rojas BG, Guerrero IG (1994) Measurement of chlorophyllase activity in olive fruit (Olea europaea). J Biochem 116(2):263–268. https://doi.org/10.1093/oxfordjournals.jbchem.a124517
  • Parida AK, Jha B (2010) Salt tolerance mechanisms in mangroves: a review. Trees 24:199–217. https://doi.org/10.1007/s00468-010-0417-x
  • Pavlović I, Pěnčík A, Novák O (2018) Short-term salt stress in Brassica rapa seedlings causes alterations in auxin metabolism. Plant Physiol Biochem 125:74–84. https://doi.org/10.1016/j.plaphy.2018.01.026
  • Peleg Z, Walia H, Blumwald E (2012) Integrating genomics and genetics to accelerate development of drought and salinity tolerant crops. Plant Biotechnol Agri 18:271–286. https://doi.org/10.1016/b978-0-12-381466-1.00018-3
  • Qu C, Liu C, Gong X (2012) Impairment of maize seedling photosynthesis caused by a combination of potassium deficiency and salt stress. Environ Experi Bot 75(75):134–141. https://doi.org/10.1016/j.envexpbot.2011.08.019
  • Rahnama A, James RA, Poustini K, Munns R (2010) Stomatal conductance as a screen for osmotic stress tolerance in durum wheat growing in saline soil. Function Plant Biol 37:255–263. https://doi.org/10.1071/FP09148
  • Rattan KJ (2017) Comparative analyses of physiological assays and chlorophyll a, variable fluorescence parameters: investigating the importance of phosphorus availability in oligotrophic and eutrophic freshwater systems. Aquat Ecol 12:1–17. https://doi.org/10.1007/s10452-017-9622-7
  • Ren HL, Liu B (1994) The young rootstock of Malus halliana overwintered cultivation and management with orchard saplings. Gansu Agri Sci and Technol 4:21–22
  • Robinson SP, Jones GP (1986) Accumulation of glycinebetaine in chloroplasts provides osmotic adjustment during salt stress. Funct Plant Biol 13(5):659–668. https://doi.org/10.1071/PP9860659
  • Rong Y, Bai TH, Ma FW, Ma FW, Wang XJ, Li YH (2010) Physiological responses and relative tolerance by Chinese apple rootstocks to NaCl stress. Sci Horti 126(2):247–252. https://doi.org/10.1016/j.scienta.2010.07.027
  • Saboora A, Kiarostami K, Behroozbayati F (2006) Salinity (NaCl) tolerance of wheat genotypes at germination and early seedling growth. Pakistan J Biol Sci 9(11):263–268. https://doi.org/10.3923/pjbs.2006.2009.2021
  • Song L J (2010) The characteristics and evaluation on soil quality of grassland in Loess Plateau. PhD thesis, Northwest Agri and Forestry Uni, China
  • Sultana N, Ikeda T, Itoh R (1999) Effect of NaCl salinity on photosynthesis and dry matter accumulation in developing rice grains. Envir Experi Bot 42:211–220. https://doi.org/10.1016/S0098-8472(00)00049-6
  • Tanaka R, Kobayashi K, Masuda T (2011) Tetrapyrrole metabolism in Arabidopsis thaliana. Arabidopsis Book 9:e0145. https://doi.org/10.1199/tab.0145
  • Tang LA, Okazawa E, Kobayashi A (2000) Removal of magnesium by Mg-dechelatase is a major step in the chlorophyll-degrading pathway in Ginkgo biloba in the process of autumnal tints. Z Naturforsch 55:923–926. https://doi.org/10.1074/jbc.m703283200
  • Terletskaya N (2017) Growth and photosynthetic reactions of different species of wheat seedlings under drought and salt stress. Periodicum Biologorum 119(1):37–45. https://doi.org/10.18054/pb.v119i1.4408
  • Verslues PE, Agarwal M, Katiyar-Agarwal S, Zhu J, Zhu JK (2006) Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stress that affect plant water status. Plant J 45:523–539. https://doi.org/10.1111/j.1365-313X.2005.02593.x
  • Vicentini F, Iten F, Matile P (1995) Development of an assay for Mg-dechelatase of oilseed rape cotyledons, using chlorophyllin as the substrate. Physiol Plant 94:57–63. https://doi.org/10.1111/j.1399-3054.1995.tb00784.x
  • Wang R, Hua C, Luo Q (2002) Na⁺ and Cl⁻ accumulation in chloroplasts results in a decrease in net photosynthetic ratein rice leaves under salt stress. Acta Photophysiol Sin 28(5):385–390
  • Wang K, Zhang L, Gao M (2013) Influence of salt stress on growth and antioxidant responses of two Malus species at callus and plantlet stages. Pakistan J Bot 45(2):375–381
  • Wang R, Guo S, Jiang J (2015) Tree-scale spatial variation of soil respiration and its influence factors in apple orchard in loess plateau. Nutri Cycl Agroecosyst 102(2):285–297. https://doi.org/10.1007/s10705-015-9699-0
  • Zhang YM, Ma HL, Calderón-Urrea A (2016) Anatomical changes to protect organelle integrity account for tolerance to alkali and salt stresses in Melilotus officinalis. Plant Soil 406(1–2):1–14. https://doi.org/10.1007/s11104-016-2875-4
  • Zhu GL, Zhang HW, Zhang AQ (1990) Plant physiological experiments, 1st edn. Peking University Press, Beijing
  • Zörb C, Geilfus CM, Mühling KH (2013) The influence of salt stress on ABA and auxin concentrations in two maize cultivars differing in salt resistance. J Plant Physiol 170(2):220–224. https://doi.org/10.1016/j.jplph.2012.09.012
  • Zouhaier B, Abdallah A, Najla T (2015) Scanning and transmission electron microscopy and X-ray analysisof leaf salt glands of Limoniastrum guyonianum Boiss. under NaCl salinity. Micron 78:1–9. https://doi.org/10.1016/j.micron.2015.06.001

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Bibliografia

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