Effects of sodium nitroprusside on callus browning of Ficus religiosa: an important medicinal plant

Mohsen Hesami , Masoud Tohidfar , Milad Alizadeh , Mohammad Hosein Daneshvar

Journal of Forestry Research ›› 2018, Vol. 31 ›› Issue (3) : 789 -796.

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Journal of Forestry Research ›› 2018, Vol. 31 ›› Issue (3) : 789 -796. DOI: 10.1007/s11676-018-0860-x
Original Paper

Effects of sodium nitroprusside on callus browning of Ficus religiosa: an important medicinal plant

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Abstract

Tissue browning is a major problem in tissue culturing of woody plants, especially for Ficus religiosa which occurs by the accumulation and oxidation of phenolic compounds. This study aimed to determine the effect of different concentrations of sodium nitroprusside on the appearance of callus browning from leaf explants. The results indicate that callus browning was significantly reduced by supplementation of sodium nitroprusside to the MS medium and supplemented with 2.26 μM of 2,4-dichlorophenoxyacetic acid and 0.22 μM of 6-benzyl amino purine. The accumulation of hydrogen peroxide and phenolic compounds in the callus tissues decreased at the 50 μM concentration of sodium nitroprusside. Although catalase and peroxidase activities decreased at the 50 μM concentration, the activity of superoxide dismutase and polyphenol oxidases, as well as proline content, increased exponentially. Sodium nitroprusside could be useful for the formation of non-embryogenic callus with high levels of metabolic activity for the production and isolation of secondary metabolites.

Keywords

Nitric oxide / Oxidative enzymes / Proline / Reactive oxygen species

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Mohsen Hesami, Masoud Tohidfar, Milad Alizadeh, Mohammad Hosein Daneshvar. Effects of sodium nitroprusside on callus browning of Ficus religiosa: an important medicinal plant. Journal of Forestry Research, 2018, 31(3): 789-796 DOI:10.1007/s11676-018-0860-x

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References

[1]

Arasimowicz M, Floryszak-Wieczorek J. Nitric oxide as a bioactive signalling molecule in plant stress responses. Plant Sci, 2007, 172: 876-887.

[2]

Beauchamp C, Fridovich I. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal Biochem, 1971, 44: 276-287.

[3]

Cakmak I, Horst WJ. Effect of aluminium on lipid peroxidation, superoxide dismutase, catalase, and peroxidase activities in root tips of soybean (Glycine max). Physiol Plant, 1991, 83: 463-468.

[4]

Chugh S, Guha S, Rao IU. Micropropagation of orchids: a review on the potential of different explants. Sci Hortic, 2009, 122: 507-520.

[5]

Corpas FJ, Barroso JB. Lead-induced stress, which triggers the production of nitric oxide (NO) and superoxide anion (O2·−) in Arabidopsis peroxisomes, affects catalase activity. Nitric Oxide, 2017, 68: 103-110.

[6]

de Pinto MC, De Gara L. Changes in the ascorbate metabolism of apoplastic and symplastic spaces are associated with cell differentiation. J Exp Bot, 2004, 55: 2559-2569.

[7]

de Pinto MC, Tommasi F, De Gara L. Changes in the antioxidant systems as part of the signaling pathway responsible for the programmed cell death activated by nitric oxide and reactive oxygen species in tobacco Bright-Yellow 2 cells. Plant Physiol, 2002, 130: 698-708.

[8]

Dehon L, Macheix J, Durand M. Involvement of peroxidases in the formation of the brown coloration of heartwood in Juglans nigra. J Exp Bot, 2002, 53: 303-311.

[9]

Duncan DB. Multiple range and multiple F tests. Biometrics, 1955, 11: 1-42.

[10]

Errabii T, Gandonou CB, Essalmani H, Abrini J, Idaomar M, Senhaji NS. Effects of NaCl and mannitol induced stress on sugarcane (Saccharum sp.) callus cultures. Acta Physiol Plant, 2007, 29: 95.

[11]

Flora SJ. Structural, chemical and biological aspects of antioxidants for strategies against metal and metalloid exposure. Oxid Med Cell Longev, 2009, 2: 191-206.

[12]

Foyer C, Descourvieres P, Kunert K. Protection against oxygen radicals: an important defence mechanism studied in transgenic plants. Plant Cell Environ, 1994, 17: 507-523.

[13]

Gill SS, Tuteja N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem, 2010, 48: 909-930.

[14]

Guo Y, Tian Z, Yan D, Zhang J, Qin P. Effects of nitric oxide on salt stress tolerance in Kosteletzkya virginica. Life Sci J, 2009, 6: 67-75.

[15]

Han X, Yang H, Duan K, Zhang X, Zhao H, You S, Jiang Q. Sodium nitroprusside promotes multiplication and regeneration of Malus hupehensis in vitro plantlets. Plant Cell Tiss Organ Cult, 2009, 96: 29-34.

[16]

Hayat S, Alyemeni MN, Hasan SA. Foliar spray of brassinosteroid enhances yield and quality of Solanum lycopersicum under cadmium stress. Saudi J Biol Sci, 2012, 19: 325-335.

[17]

Hesami M, Daneshvar MH. In vitro adventitious shoot regeneration through direct and indirect organogenesis from seedling-derived hypocotyl segments of Ficus religiosa L.: an important medicinal plant. HortScience, 2018, 53: 55-61.

[18]

Hesami M, Daneshvar MH. Indirect organogenesis through seedling-derived leaf segments of Ficus religiosa—a multipurpose woody medicinal plant. J Crop Sci Biotechnol, 2018, 21: 129-136.

[19]

Hesami M, Daneshvar MH, Lotfi A. In vitro shoot proliferation through cotyledonary node and shoot tip explants of Ficus religiosa L. Plant Tissue Cult Biotechnol, 2017, 27: 85-88.

[20]

Hesami M, Naderi R, Yoosefzadeh-Najafabadi M, Rahmati M. Data-driven modeling in plant tissue culture. J Appl Environ Biol Sci, 2017, 7: 37-44.

[21]

Hesami M, Daneshvar MH, Yoosefzadeh-Najafabadi M. n efficient in vitro shoot regeneration through direct organogenesis from seedling-derived petiole and leaf segments and acclimatization of Ficus religiosa. J For Res, 2018

[22]

Hesami M, Daneshvar MH, Yoosefzadeh-Najafabadi M. Establishment of a protocol for in vitro seed germination and callus formation of Ficus religiosa L., an important medicinal plant. Jundishapur J Nat Pharm Prod, 2018, 13(e62682): 1-8.

[23]

Hesami M, Daneshvar MH, Yoosefzadeh-Najafabadi M, Alizadeh M. Effect of plant growth regulators on indirect shoot organogenesis of Ficus religiosa through seedling derived petiole segments. J Gen Eng Biotechnol, 2018, 16: 175-180.

[24]

Jedinák A, Faragó J, Psenakova I, Maliar T. Approaches to flavonoid production in plant tissue cultures. Biologia, 2004, 59: 697-710.

[25]

Jimenez-Quesada MJ, Carmona R, Lima-Cabello E, Traverso , Castro AJ, Claros MG, de Dios Alché J. Generation of nitric oxide by olive (Olea europaea L.) pollen during in vitro germination and assessment of the S-nitroso-and nitro-proteomes by computational predictive methods. Nitric Oxide, 2017, 68: 23-37.

[26]

Kalra C, Babbar SB. Nitric oxide promotes in vitro organogenesis in Linum usitatissimum L. Plant Cell Tiss Organ Cult, 2010, 103: 353-359.

[27]

Ko W, Su C, Chen C, Chao C. Control of lethal browning of tissue culture plantlets of Cavendish banana cv. Formosana with ascorbic acid. Plant Cell Tissue Organ Cult, 2009, 96: 137-141.

[28]

Kolbert Z, Bartha B, Erdei L. Exogenous auxin-induced NO synthesis is nitrate reductase-associated in Arabidopsis thaliana root primordia. J Plant Physiol, 2008, 165: 967-975.

[29]

Kratsch H, Wise RR. The ultrastructure of chilling stress. Plant, Cell Environ, 2000, 23: 337-350.

[30]

Laspina N, Groppa M, Tomaro M, Benavides M. Nitric oxide protects sunflower leaves against Cd-induced oxidative stress. Plant Sci, 2005, 169: 323-330.

[31]

Leng P, Su S, Wei F, Yu F, Duan Y. Correlation between browning, total phenolic content, polyphenol oxidase and several antioxidation enzymes during pistachio tissue culture. Acta Hortic Sin, 2009, 829: 127-132.

[32]

Ling A, Yap C, Shaib JM, Vilasini P. Induction and morphogenesis of Phalaenopsis callus. J Trop Agric Food Sci, 2007, 35: 147-152.

[33]

Liu F, Chen L. Redox dynamics during embryogenic callus induction of Phalaenopsis spp. J Wuhan Bot Res, 2010, 28: 737-743.

[34]

Maggio A, Miyazaki S, Veronese P, Fujita T, Ibeas JI, Damsz B, Narasimhan ML, Hasegawa PM, Joly RJ, Bressan RA. Does proline accumulation play an active role in stress-induced growth reduction?. Plant J, 2002, 31: 699-712.

[35]

Mayer AM. Polyphenol oxidases in plants and fungi: going places? A review. Phytochemistry, 2006, 67: 2318-2331.

[36]

Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci, 2002, 7: 405-410.

[37]

Mondal T, Aditya S, Banerjee N. In vitro axillary shoot regeneration and direct protocorm-like body induction from axenic shoot tips of Doritis pulcherrima Lindl. Plant Tissue Cult Biotechnol, 2014, 23: 251-261.

[38]

Naz S, Ali A, Iqbal J. Phenolic content in vitro cultures of chick pea (Cicer arietinum L.) during callogenesis and organogenesis. Pak J Bot, 2008, 40: 2525-2539.

[39]

Neill SJ, Desikan R, Hancock JT. Nitric oxide signalling in plants. New Phytol, 2003, 159: 11-35.

[40]

Niazian M, Noori SAS, Galuszka P, Tohidfar M, Mortazavian SMM. Genetic stability of regenerated plants via indirect somatic embryogenesis and indirect shoot regeneration of Carum copticum L. Ind Crops Prod, 2017, 97: 330-337.

[41]

Nickel KS, Cunningham B. Improved peroxidase assay method using leuco 2, 3′, 6-trichloroindophenol and application to comparative measurements of peroxidatic catalysis. Anal Biochem, 1969, 27: 292-299.

[42]

Parani M, Rudrabhatla S, Myers R, Weirich H, Smith B, Leaman DW, Goldman SL. Microarray analysis of nitric oxide responsive transcripts in Arabidopsis. Plant Biotechnol J, 2004, 2: 359-366.

[43]

Park S-Y, Shin KS, Paek KY. Increased ethylene and decreased phenolic compounds stimulate somatic embryo regeneration in leaf thin section cultures of Doritaenopsis hybrid. J Plant Biol, 2006, 49: 358-363.

[44]

Pitzschke A, Djamei A, Bitton F, Hirt H. A major role of the MEKK1–MKK1/2–MPK4 pathway in ROS signalling. Mol Plant, 2009, 2: 120-137.

[45]

Qiao W, Fan LM. Nitric oxide signaling in plant responses to abiotic stresses. Integr Plant Biol, 2008, 50: 1238-1246.

[46]

Ramamoorthy V, Raguchander T, Samiyappan R. Induction of defense-related proteins in tomato roots treated with Pseudomonas fluorescens Pf1 and Fusarium oxysporum f. sp. lycopersici. Plant Soil, 2002, 239: 55-68.

[47]

Rico-Lemus M, Rodríguez-Garay B. SNP as an effective donor of nitric oxide for in vitro plant cell and tissue culture. J Plant Biochem Physiol, 2014, 2: 127-128.

[48]

Salmi MS, Hesami M. Time of collection, cutting ages, auxin types and concentrations influence rooting Ficus religiosa L. stem cuttings. J Appl Environ Biol Sci, 2016, 6: 124-132.

[49]

Sarropoulou V, Maloupa E. Effect of the NO donor “sodium nitroprusside”(SNP), the ethylene inhibitor “cobalt chloride”(CoCl2) and the antioxidant vitamin E “α-tocopherol” on in vitro shoot proliferation of Sideritis raeseri Boiss. & Heldr. subsp. raeseri. Plant Cell Tiss Organ Cult, 2017, 128: 619-629.

[50]

Sarropoulou V, Dimassi-Theriou K, Therios I. Ιn vitro plant regeneration from leaf explants of the cherry rootstocks CAB-6P, Gisela 6, and MxM 14 using sodium nitroprusside. Vitro Cell Dev Biol Plant, 2014, 50: 226-234.

[51]

Sarropoulou V, Dimassi-Theriou K, Therios I. Effect of the ethylene inhibitors silver nitrate, silver sulfate, and cobalt chloride on micropropagation and biochemical parameters in the cherryrootstocks CAB-6P and Gisela 6. Turk J Biol, 2016, 40: 670-683.

[52]

Sharma P, Jha AB, Dubey RS, Pessarakli M. Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. J Bot, 2012, 217037: 1-26.

[53]

Singh D, Singh B, Goel RK. Traditional uses, phytochemistry and pharmacology of Ficus religiosa: a review. J Ethnopharmacol, 2011, 134: 565-583.

[54]

Tripathy BC, Oelmüller R. Reactive oxygen species generation and signaling in plants. Plant Signal Behav, 2012, 7: 1621-1633.

[55]

Tun NN, Holk A, Scherer GF. Rapid increase of NO release in plant cell cultures induced by cytokinin. FEBS Lett, 2001, 509: 174-176.

[56]

Uchida A, Jagendorf AT, Hibino T, Takabe T, Takabe T. Effects of hydrogen peroxide and nitric oxide on both salt and heat stress tolerance in rice. Plant Sci, 2002, 163: 515-523.

[57]

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: 59-66.

[58]

Wahid A, Gelani S, Ashraf M, Foolad MR. Heat tolerance in plants: an overview. Environ Exp Bot, 2007, 61: 199-223.

[59]

Wang X-D, Nolan KE, Irwanto RR, Sheahan MB, Rose RJ. Ontogeny of embryogenic callus in Medicago truncatula: the fate of the pluripotent and totipotent stem cells. Ann Bot, 2011, 107: 599-609.

[60]

Wi SG, Chung BY, Kim J-H, Baek M-H, Yang DH, Lee J-W, Kim J-S. Ultrastructural changes of cell organelles in Arabidopsis stems after gamma irradation. J Plant Biol, 2005, 48: 195-200.

[61]

Xu CJ, Li L, Li H, Zhang M. Preliminary studies on the elements of browning and the changes in cellular texture of leaf explant browning in Phalaenopsis. Acta Hortic Sin, 2005, 32: 1111-1113.

[62]

Xu J, Yin H, Wang W, Mi Q, Liu X. Effects of sodium nitroprusside on callus induction and shoot regeneration in micropropagated Dioscorea opposita. Plant Growth Regul, 2009, 59: 279-285.

[63]

Yingsanga P, Srilaong V, Kanlayanarat S, Noichinda S, McGlasson W. Relationship between browning and related enzymes (PAL, PPO and POD) in rambutan fruit (Nephelium lappaceum Linn.) cvs. Rongrien and See-Chompoo. Postharvest Biol Technol, 2008, 50: 164-168.

[64]

Yoruk R, Marshall MR. Physicochemical properties and function of plant polyphenol oxidase: a review. J Food Biochem, 2003, 27: 361-422.

[65]

Zamani M, Hakimi M, Mosleh Arany A, Kiani B, Rashtian A. The effects of salicylic acid (SA) and sodium nitroprusside (SNP) on physical and growth characteristics of Pinus eldarica. Bull Environ Pharmacol Life Sci, 2014, 3: 31-35.

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