Exogenous trehalose alleviates the inhibitory effects of salt stress in strawberry plants

• Autorzy: Samadi S. , Habibi G. , Vaziri A.
• Języki publikacji: EN

Abstrakty

EN

We investigated the role of trehalose (Tre) root pretreatment (10 and 30 mM) in photosynthesis, phenolic metabolism, antioxidant properties and ion homeostasis of strawberry plants when exposed to 50-mM NaCl for 7 days. Salinity caused an adverse effect on the shoot dry weight, whereas root pretreatment with 30-mM Tre mitigated these inhibitory effects. Under no stress, development of flowers was greatly enhanced by the supply of Tre. Plants exposed to salt stress after root pretreatment with 30-mM Tre maintained their photosynthetic electron transport rate, compared with NaCl-alone-treated plants, contributing to the improvement of photosystem Performance Index (PIabs), and oxygen-evolving complex efficiency of PSII (Fv/Fo). Although NaCl stress resulted in the highest Na accumulation, the application of Tre reduced shoot Na accumulation. In addition, the oxidative burst and lipid peroxidation observed in plants subjected to salinity conditions was greatly mitigated after root pretreatment with 30-mM Tre, as evidenced by lower malondialdehyde and superoxide radical (O₂˙⁻) levels, compared with NaCl-alone-treated plants. To sum up, root pretreatments with 30-mM Tre were more effective than with 10-mM Tre in alleviation of salt stress in strawberry. This positive effect of Tre was possibly attributed to the improvement of carotenoids, flavonoids and anthocyanins compounds in leaves resulting in normal photochemical functioning, the activation of the enzymatic antioxidants and the compartmentalization of Na for better growth under salt stress.

• Wydawca: -
• Czasopismo: Acta Physiologiae Plantarum
• Rocznik: 2019
• Tom: 41
• Numer: 07
• Opis fizyczny: Article 112 [11p.], fig.,ref.

Twórcy

autor

Samadi S.

• Department of Biology, Payame Noor University (PNU), PO Box 19395‑3697, Tehran, Iran

autor

Habibi G.

• Department of Biology, Payame Noor University (PNU), PO Box 19395‑3697, Tehran, Iran

autor

Vaziri A.

• Department of Biology, Payame Noor University (PNU), PO Box 19395‑3697, Tehran, Iran

Bibliografia

• Abdallah MS, Abdelgawad ZA, El-Bassiouny HM (2016) Alleviation of the adverse effects of salinity stress using trehalose in two rice varieties. S Afr J Bot 103:275–282
• Akram NA, Waseem M, Ameen R, Ashraf M (2016) Trehalose pretreatment induces drought tolerance in radish (Raphanus sativus L.) plants: some key physio-biochemical traits. Acta Physiol Plant 38(1):3
• Ashraf M (2009) Biotechnological approach of improving plant salt tolerance using antioxidants as markers. Biotechnol Adv 27:84–93
• Babitha KC, Vemanna RS, Nataraja KN, Udayakumar M (2015) Overexpression of EcbHLH57 transcription factor from Eleusine coracana L. in tobacco confers tolerance to salt, oxidative and drought stress. PLoS One 10:e0137098
• Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water-stress studies. Plant Soil 39(1):205–207
• Blasco B, Leyva R, Romero L, Ruiz JM (2013) Iodine effects on phenolic metabolism in lettuce plants under salt stress. J Agric Food Chem 61:2591–2596
• Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
• Burchard P, Bilger W, Weissenböck G (2000) Contribution of hydroxycinnamates and flavonoids to epidermal shielding of UV-A and UV-B radiation in developing rye primary leaves as assessed by ultraviolet-induced chlorophyll fluorescence measurements. Plant Cell Environ 23:1373–1380
• Carillo P, Feil R, Gibon Y, Satoh-Nagasawa N, Jackson D, Bläsing OE, Stitt M, Lunn JE (2013) A fluorometric assay for trehalose in the picomole range. Plant Methods 9(1):21
• Chang B, Yang L, Cong W, Zu Y, Tang Z (2014) The improved resistance to high salinity induced by trehalose is associated with ionic regulation and osmotic adjustment in Catharanthus roseus. Plant Physiol Biochem 77:140–148
• Fernandez O, Béthencourt L, Quero A, Sangwan RS, Clément C (2010) Trehalose and plant stress responses: friend or foe? Trends Plant Sci 15:409–417
• Flohé L, Günzler WA (1984) Assays of glutathione peroxidase. In: Packer L (ed) Methods in enzymology, vol 105. Academic Press Inc, Orlando, pp 114–121
• Garcia AB, Engler JD, Iyer S, Gerats T, Van Montagu M, Caplan AB (1997) Effects of osmoprotectants upon NaCl stress in rice. Plant Physiol 115:159–169
• Govind SR, Jogaiah S, Abdelrahman M, Shetty HS, Tran LS (2016) Exogenous trehalose treatment enhances the activities of defense-related enzymes and triggers resistance against downy mildew disease of pearl millet. Front Plant Sci 7:1593
• Gururani MA, Venkatesh J, Tran LSP (2015) Regulation of photosynthesis during abiotic stress-induced photoinhibition. Mol Plant 8(9):1304–1320
• Habibi G (2017) Physiological, photochemical and ionic responses of sunflower seedlings to exogenous selenium supply under salt stress. Acta Physiol Plant 39:213
• Habibi G, Ajory N (2015) The effect of drought on photosynthetic plasticity in Marrubium vulgare plants growing at low and high altitudes. J Plant Res 128:987–994
• Habibi G, Hajiboland R (2012) Comparison of photosynthesis and antioxidative protection in Sedum album and Sedum stoloniferum (Crassulaceae) under water stress. Photosynthetica 50:508–518
• Hajiboland R, Norouzi F, Poschenrieder C (2014) Growth, physiological, biochemical and ionic responses of pistachio seedlings to mild and high salinity. Trees 28:1065–1078
• Hasanuzzaman M, Nahar K, Fujita M (2013) Plant response to salt stress and role of exogenous protectants to mitigate salt-induced damages. In: Prasad MNV (ed) Ecophysiology and responses of plants under salt stress. Springer, New York, pp 25–87
• Jiang C, Zu C, Lu D, Zheng Q, Shen J, Wang H, Li D (2017) Effect of exogenous selenium supply on photosynthesis, Na⁺ accumulation and antioxidative capacity of maize (Zea mays L.) under salinity stress. Sci Rep 7:42039
• Kalaji HM, Bosa K, Kościelniak J, Żuk-Gołaszewska K (2011) Effects of salt stress on photosystem II efficiency and CO₂ assimilation of two Syrian barley landraces. Environ Exp Bot 73:64–72
• Kalaji HM, Jajoo A, Oukarroum A, Brestic M, Zivcak M, Samborska IA, Cetner MD, Łukasik I, Goltsev V, Ladle RJ (2016) Chlorophyll a fluorescence as a tool to monitor physiological status of plants under abiotic stress conditions. Acta Physiol Plant 38:102
• Krizek DT, Kramer GF, Upadhyaya A, Mirecki RM (1993) UV-B response of cucumber seedlings grown under metal halide and high pressure sodium/deluxe lamps. Physiol Plant 88:350–358
• Li X, Baio G, Yun W (2013) Heat stress mitigation by exogenous nitric oxide application involves polyamine metabolism and PSII physiological strategies in ginger leaves. Agric Sci China 47:1171–1179
• Li ZG, Luo LJ, Zhu LP (2014) Involvement of trehalose in hydrogen sulfide donor sodium hydrosulfide-induced the acquisition of heat tolerance in maize (Zea mays L.) seedlings. Bot Stud 55:20
• Lichtenthaler HK, Wellburn AR (1983) Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochem Soc Trans 11:591–592
• Lin Y, Zhang J, Gao W, Chen Y, Li H, Lawlor DW, Paul MJ, Pan W (2017) Exogenous trehalose improves growth under limiting nitrogen through upregulation of nitrogen metabolism. BMC Plant Biol 17:247
• Lunn JE, Delorge I, Figueroa CM, Van Dijck P, Stitt M (2014) Trehalose metabolism in plants. Plant J 79:544–567
• Ma C, Wang Z, Kong B, Lin T (2013) Exogenous trehalose differentially modulate antioxidant defense system in wheat callus during water deficit and subsequent recovery. Plant Growth Regul 70:275–285
• Mahmoudi H, Huang J, Gruber MY, Kaddour R, Lachaâl M, Ouerghi Z, Hannoufa A (2010) The impact of genotype and salinity on physiological function, secondary metabolite accumulation, and antioxidative responses in lettuce. J Agric Food Chem 58:5122–5130
• Meda A, Lamien CE, Romito M, Millogo J, Nacoulma OG (2005) Determination of the total phenolic, flavonoid and proline contents in Burkina Fasan honey, as well as their radical scavenging activity. Food Chem 91:571–577
• Mittler R, Vanderauwera S, Gollery M, Van Breusegem F (2004) Reactive oxygen gene network of plants. Trends Plant Sci 9:490–498
• Mostofa MG, Hossain MA, Fujita M, Tran LS (2015) Physiological and biochemical mechanisms associated with trehalose-induced copper-stress tolerance in rice. Sci Rep 5:11433
• Müller J, Staehelin C, Mellor RB, Boller T, Wiemken A (1992) Partial purification and characterization of trehalase from soybean nodules. J Plant Physiol 140:8–13
• Nounjan N, Nghia PT, Theerakulpisut P (2012) Exogenous proline and trehalose promote recovery of rice seedlings from salt-stress and differentially modulate antioxidant enzymes and expression of related genes. J Plant Physiol 169:596–604
• Oh MM, Trick HN, Rajashekar CB (2009) Secondary metabolism and antioxidants are involved in environmental adaptation and stress tolerance in lettuce. J Plant Biol 166:180–191
• Pirlak L, Eşitken A (2004) Salinity effects on growth, proline and ion accumulation in strawberry plants. Acta Agric Scand Sect B 54:189–192
• Saied AS, Keutgen AJ, Noga G (2005) The influence of NaCl salinity on growth, yield and fruit quality of strawberry cvs. ‘Elsanta’and ‘Korona’. Sci Hortic 103:289–303
• Shahbaz M, Abid A, Masood A, Waraich EA (2017) Foliar-applied trehalose modulates growth, mineral nutrition, photosynthetic ability, and oxidative defense system of rice (Oryza sativa L.) under saline stress. J Plant Nutr 40:584–599
• Shinogi T, Suzuki T, Kurihara T, Narusaka Y, Park P (2003) Microscopic detection of reactive oxygen species generation in the compatible and incompatible interactions of Alternaria alternata Japanese pear pathotype and host plants. J Gen Plant Pathol 69:7–16
• Strasser RJ, Tsimilli-Michael M, Srivastava A (2004) Analysis of the chlorophyll a fluorescence transient. In: Papageorgiou G, Govindjee (eds) Advances in photosynthesis and respiration. Chlorophyll a fluorescence: a signature of photosynthesis. Springer, Dordrecht, pp 321–362
• Velikova V, Yordanov I, Edreva A (2000) Oxidative stress and some antioxidant systems in acid rain-treated bean plants: protective role of exogenous polyamines. Plant Sci 151:59–66
• Velioglu YS, Mazza G, Gao L, Oomah BD (1998) Antioxidant activity and total phenolics in selected fruits, vegetables, and grain products. J Agric Food Chem 46:4113–4117
• Wahid A, Ghazanfar A (2006) Possible involvement of some secondary metabolites in salt tolerance of sugarcane. J Plant Physiol 163:723–730
• Xu Z, Rothstein SJ (2018) ROS-induced anthocyanin production provides feedback protection by scavenging ROS and maintaining photosynthetic capacity in Arabidopsis. Plant Signal Behav 58:1
• Xu Z, Mahmood K, Rothstein SJ (2017) ROS induces anthocyanin production via late biosynthetic genes and anthocyanin deficiency confers the hypersensitivity to ROS-generating stresses in Arabidopsis. Plant Cell Physiol 58:1364–1377
• Yang Y, Guo Y (2018) Elucidating the molecular mechanisms mediating plant salt-stress responses. New Phytol 217:523–539
• Yang L, Zhao X, Zhu H, Paul M, Zu Y, Tang Z (2014) Exogenous trehalose largely alleviates ionic unbalance, ROS burst, and PCD occurrence induced by high salinity in Arabidopsis seedlings. Front Plant Sci 5:570
• Zeid IM (2009) Trehalose as osmoprotectant for maize under salinity-induced stress. Res J Agric Biol Sci 5:613–622
• Zhu JK (2003) Regulation of ion homeostasis under salt stress. Curr Opin Plant Biol 6:441–445
• Zucker M (1965) Induction of phenylalanine deaminase by light and its relation to chlorogenic acid synthesis in potato tuber tissue. Plant Physiol 40:779

Identyfikatory

DOI

10.1007/s11738-019-2905-y