Effect of sodium nitroprusside on micropropagation and biochemical parameters of CAB-6P and Gisela 6 cherry rootstocks

The effects of sodium nitroprusside (SNP) on micropropagation of CAB-6P and Gisela 6 cherry rootstocks were investigated. Shoot multiplication of CAB-6P was reduced by adding 4.4 $\mu$M 6-benzylaminopurine (BA) and SNP. Gisela 6 microcuttings treated with BA + 30 $\mu$M SNP gave the highest average shoot number (4.15) and multiplication percentage (100%). In CAB-6P, $\alpha$-naphthaleneacetic acid (NAA) + 30 $\mu$M SNP led to the maximum root number (13.79) and fresh weight (0.336 g); average root length (82 mm) and rooting percentage (95.45%) were greatest after adding 40 and 10 $\mu$M SNP + NAA, respectively. In Gisela 6, NAA + 40 $\mu$M SNP resulted in the highest root number (9.75) and fresh weight (0.238 g), while NAA + 30 $\mu$M SNP enabled maximum root length (30.77 mm). Rooting percentage was greatest (84.62%) when Gisela 6 microcuttings were treated only with NAA. Application of SNP alone in CAB-6P reduced leaf chlorophyll, carbohydrate, and pr?line levels. In contrast, 30?50 $\mu$M SNP increased leaf chlorophyll levels of Gisela 6. SNP augmented leaf carbohydrate and proline content, but it diminished root carbohydrate content. In BA + SNP or NAA + SNP treatments, changes in biochemical constituents were dependent on SNP concentrations and genotypes.

Effect of sodium nitroprusside on micropropagation and biochemical parameters of CAB-6P and Gisela 6 cherry rootstocks

The effects of sodium nitroprusside (SNP) on micropropagation of CAB-6P and Gisela 6 cherry rootstocks were investigated. Shoot multiplication of CAB-6P was reduced by adding 4.4 $\mu$M 6-benzylaminopurine (BA) and SNP. Gisela 6 microcuttings treated with BA + 30 $\mu$M SNP gave the highest average shoot number (4.15) and multiplication percentage (100%). In CAB-6P, $\alpha$-naphthaleneacetic acid (NAA) + 30 $\mu$M SNP led to the maximum root number (13.79) and fresh weight (0.336 g); average root length (82 mm) and rooting percentage (95.45%) were greatest after adding 40 and 10 $\mu$M SNP + NAA, respectively. In Gisela 6, NAA + 40 $\mu$M SNP resulted in the highest root number (9.75) and fresh weight (0.238 g), while NAA + 30 $\mu$M SNP enabled maximum root length (30.77 mm). Rooting percentage was greatest (84.62%) when Gisela 6 microcuttings were treated only with NAA. Application of SNP alone in CAB-6P reduced leaf chlorophyll, carbohydrate, and pr?line levels. In contrast, 30?50 $\mu$M SNP increased leaf chlorophyll levels of Gisela 6. SNP augmented leaf carbohydrate and proline content, but it diminished root carbohydrate content. In BA + SNP or NAA + SNP treatments, changes in biochemical constituents were dependent on SNP concentrations and genotypes.

___

  • Aka-Kacar Y, Akpinar C, Agar A, Yalcin-Mendi Y, Serce S, Ortas I (2010). The effect of mycorrhiza in nutrient uptake and biomass of cherry rootstocks during acclimatization. Rom Biotechnol Lett 15: 5246–5252.
  • Arasimowicz M, Wieczorek JF (2007). Nitric oxide as a bioactive signaling molecule in plant stress responses. Plant Sci 172: 876–887.
  • Beligni MV, Lamattina L (2000). Nitric oxide stimulates seed germination and de-etiolation and inhibits hypocotyl elongation, three light inducible responses in plants. Planta 210: 215–221.
  • Bethke PC, Libourel IGL, Aoyama N, Chung YY, Still DW, Jones RL (2007). The Arabidopsis aleurone layer responds to nitric oxide, gibberellin, and abscisic acid and is sufficient and necessary for seed dormancy. Plant Physiol 143: 1173–1188.
  • Brault M, Maldiney R (1999). Mechanisms of cytokinin action. Plant Physiol Biochem 37: 403–412.
  • Cag S, Palavan-Ünsal N, Büyüktuncer D (2003). Comparison of the effects of meta-topolin and other cytokinins on chlorophyll and protein contents and peroxidase activity in cucumber cotyledons. Israel J Plant Sci 51: 261–265.
  • Correa-Aragunde N, Graziano M, Chevalier C, Lamattina L (2006). Nitric oxide modulates the expression of cell cycle regulatory genes during lateral root formation in tomato. J Exp Bot 57: 581–588.
  • Correa-Aragunde N, Graziano M, Lamattina L (2004). Nitric oxide plays a central role in determining lateral root development in tomato. Planta 218: 900–905.
  • Gagneja D, Kaur N, Setia N (2011). Exogenous application of sodium nitroprusside (nitric oxide donor) improves yield potential and seed quality of Brassica napus L. Indian J Plant Physiol 16: 162–166.
  • Gouvêa CMCP, Souza JF, Magalhas ACN, Martins IS (1997). NO releasing substances that induce growth elongation in maize root segments. Plant Growth Regul 21: 183–187.
  • Guo Y, Tian Z, Yan D, Zhang J, Qin P (2009). Effects of nitric oxide on salt stress tolerance in Kosteletzkya virginica. Life Sci J 6: 67–75.
  • Han SS (1997). Preventing post-production leaf yellowing in Easter lily. J Am Soc Hort Sci 122: 868–872.
  • Han XJ, Yang HQ, Duan KX, Zhang XR, Zhao HZ, You SZ, Jiang QQ (2009). Sodium nitroprusside promotes multiplication and regeneration of Malus hupehensis in vitro plantlets. Plant Cell Tiss Org Cult 96: 29–34.
  • Hao GP, Du XH, Shi RJ (2007). Exogenous nitric oxide accelerates soluble sugar, proline and secondary metabolite synthesis in Ginkgo biloba under drought stress. Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Xue Bao 33: 499–506 (article in Chinese with English abstract).
  • Hasanuzzaman M, Nahar K, Alam MM, Fujita M (2012). Exogenous nitric oxide alleviates high temperature induced oxidative stress in wheat (Triticum aestivum L.) seedlings by modulating the antioxidant defence and glyoxalase system. Aust J Crop Sci 6: 1314–1323.
  • HsuanHsuan W, MingChiang T, FureChyi C (2009). Effects of supplemental chemicals and light quality on adventitious root induction of in vitro grown Phalaenopsis and Doritaenopsis shoots. J Taiwan Soc Hort Sci 55: 127–135.
  • Huang AX, She XP, Huang C, Song TS (2007). The dynamic distribution of NO and NADPH–diaphorase activity during IBA-induced adventitious root formation. Physiol Plant 130: 240–249.
  • Huang AX, She XP (2003). Effect of SNP on rooting of hypocotyls cutting from mung bean seedling. Acta Bot Boreali-Occident Sin 23: 2196–2199.
  • Jhanji S, Setia RC, Kaur N, Kaur P, Setia N (2012). Role of nitric oxide in cadmium-induced stress on growth, photosynthetic components and yield of Brassica napus L. J Environ Biol 33:
  • Kalra C, Babbar SB (2012). Stimulatory and period-specific effect of nitric oxide on in vitro caulogenesis in Albizzia lebbeck (L.) Benth. Acta Physiol Plant 34: 387–392.
  • Kalra C, Babbar SB (2010). Nitric oxide promotes in vitro organogenesis in Linum usitatissimum L. Plant Cell Tiss Org Cult 103: 353–359.
  • Khan MA, Gul B, Weber DJ (2000). Germination responses of Salicornia rubra to temperature and salinity. J Arid Environ 45: 207–214.
  • Kolberz Z, Bartha B, Erdei L (2008). Exogenous auxin-induced NO synthesis is nitrate reductase-associated in Arabidopsis thaliana root primordial. J Plant Physiol 165: 967–975.
  • Lamattina L, Garcia-Mata C, Graziano M, Pagnussat G (2003). Nitric oxide: the versatility of an extensive signal molecule. Annu Rev Plant Biol 54: 109–136.
  • Laspina NV, Groppa MD, Tomaro ML, Benavides MP (2005). Nitric oxide protects sunflower leaves against Cd-induced oxidative stress. Plant Sci 169: 323–330.
  • Lei Y, Yin C, Ren J, Li C (2007). Effect of osmotic stress and sodium nitroprusside pretreatment on proline metabolism of wheat seedlings. Biol Plant 51: 386–390.
  • Leon J, Lozano-Juste J (2011). Nitric oxide regulates DELLA content and PIF expression to promote photomorphogenesis in Arabidopsis. Plant Physiol 156: 1410–1423.
  • Leterrier M, Valderrama R, Chaki M, Airaki M, Palma JM, Barroso JB, Corpas FJ (2012). Function of nitric oxide under environmental stress conditions. In: Khan NA, Nazar R, Iqbal N, Anjum NA, editors. Phytohormones and Abiotic Stress Tolerance in Plants. Berlin, Germany: Springer, pp. 99–113.
  • Liao WB, Huang GB, Yu JH, Zhang ML (2012). Nitric oxide and hydrogen peroxide alleviate drought stress in marigold explants and promote its adventitious root development. Plant Physiol Biochem 58: 6–15.
  • Liu Y, He J, Jiang L, Wu H, Xiao Y, Liu Y, Li G, Du Y, Liu C, Wan J (2011a). Nitric oxide production is associated with response to brown planthopper infestation in rice. J Plant Physiol 168: 739–745.
  • Liu X, Wang L, Liu L, Guo Y, Ren H (2011b). Alleviating effect of exogenous nitric oxide in cucumber seedlings against chilling stress. Afr J Biotechnol 10: 4380–4386.
  • Millar AH, Day DA (1996). Nitric oxide inhibits the cytochrome oxidase but not the alternative oxidase of plant mitochondria. FEBS Lett 398: 155–158.
  • Murashige T, Skoog F (1962). A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15: 473–497.
  • Nacheva L, Gercheva P (2009). Micropropagation of Gisela 5 (cherry dwarf rootstock): the effect of type and the concentration of the carbohydrates in the nutrient medium. Proceedings of the 1st Balkan Symposium on Fruit Growing. Acta Hort 825.
  • Nejadalimoradi H, Nasibi F, Kalantari KM, Zanganeh R (2014). Effect of seed priming with L-arginine and sodium nitroprusside on some physiological parameters and antioxidant enzymes of sunflower plants exposed to salt stress. Agric Commun 2: 23–30.
  • Pagnussat GC, Lanteri ML, Lamattina L (2003). Nitric oxide and cyclic GMP are messengers in the indole acetic acid-induced adventitious rooting process. Plant Physiol 132: 1241–1248.
  • Pahwa S, Setia RC, Setia N (2009). Effect of exogenous nitric oxide on chlorophyll content and Hill reaction activity in leaves of Brassica napus L. Environ Ecol 27: 278–280.
  • Plummer DT (1987). An Introduction to Practical Biochemistry. 3rd ed. London, UK: McGraw-Hill, pp. 179–180.
  • Qian HF, Chen W, Li JJ, Wang J, Zhou Z, Liu WP, Fu ZG (2009). The effect of exogenous nitric oxide on alleviating herbicide damage in Chlorella vulgaris. Aquat Toxicol 92: 250–257.
  • Qiao W, Fan LM (2008). Nitric oxide signaling in plant responses to abiotic stresses. J Integr Plant Biol 50: 1238–1246.
  • Sarropoulou V, Dimassi-Theriou K, Therios I (2014). Ιn vitro plant regeneration from leaf explants of the cherry rootstocks CAB- 6P, Gisela 6 and M×M 14 using sodium nitroprusside. In Vitro Cellular Develop Biol-Plant 50: 226–234.
  • Shallan MA, Hassan HMM, Namich AAM, Ibrahim AA (2012). Effect of sodium nitroprusside, putrescine and glycine betaine on alleviation of drought stress in cotton plant. American- Eurasian J Agric & Environ Sci 12: 1252–1265.
  • Sung CH, Hong JK (2010). Sodium nitroprusside mediates seedling development and attenuation of oxidative stresses in Chinese cabbage. Plant Biotechnol Rep 4: 243–251.
  • Tewari RK, Kim SY, Hahn EJ, Paek KY (2008). Involvement of nitric oxide-induced NADPH oxidase in adventitious root growth and antioxidant defence in Panax ginseng. Plant Biotechnol Rep 2: 113–122.
  • Thorpe TA (1993). In vitro organogenesis and somatic embryogenesis: physiological and biochemical aspects. In: Roubelakis- Angelakis T, Tran Thanh Van K, editors. Morphogenesis in Plants. New York, NY, USA: Plenum Press, pp. 19–38.
  • Tian X, Lei Y (2006). Nitric oxide treatment alleviates drought stress in wheat seedlings. Biol Plant 50: 775–778.
  • Tian XR, Lei YB (2007). Physiological responses of wheat seedlings to drought and UV-B radiation. Effect of exogenous sodium nitroprusside application. Russ J Plant Physiol 54: 676–682.
  • Troll W, Lindsley J (1955). A photometric method for determination of proline. J Biol Chem 215: 655–660.
  • Tun NN, Holk A, Scherer FE (2001). Rapid increase of NO release in plant cell cultures induced by cytokinin. FEBS Lett 509: 174–176.
  • Wang H, Zhang S, Zhang W, Wei C, Wang P (2010). Effects of nitric oxide on the growth and antioxidant response of submerged plants Hydrilla verticillata (L.f.) Royle. Afr J Biotechnol 9:
  • Wintermans JFGM, De Mots A (1965). Spectrophotometric characteristics of chlorophylls a and b and their pheophytins in ethanol. Biochim Biophys Acta 109: 448–453.
  • Xu J, Yin H, Wang W, Mi Q, Liu X (2009). Effects of sodium nitroprusside on callus induction and shoot regeneration in micropropagated Dioscorea opposita. Plant Growth Regul 59: 279–285.
  • Yang Y,Yongzhong Y,Xiaoyun Z,Zhiliang Y,Fan S,Huiling Z (2005). Effects of external hormone on chlorophyll content of Dioscorea zingiberensis leaves. Henan Sci 23: 44–46.
  • Yaronskaya E, Vershilovskaya I, Poers Y, Alawady AE, Averina N, Grimm B (2006). Cytokinin effects on tetrapyrrole biosynthesis and photosynthetic activity in barley seedlings. Planta 224: 700–709.
  • Yoshiba Y, Kiyosue T, Nakashima K (1997). Regulation of levels of proline as an osmolyte in plants under water stress. Plant Cell Physiol 38: 1095–1102.
  • Zhang L, Wang Y, Zhao L, Shi S, Zhang L (2006). Involvement of nitric oxide in light-mediated greening of barley seedlings. J Plant Physiol 163: 818–826.
  • Zhang LP, Mehta SK, Liu ZP, Yang ZM (2008). Copper-induced proline synthesis is associated with nitric oxide generation in Chlamydomonas reinhardtii. Plant Cell Physiol 49: 411–419.
Turkish Journal of Biology-Cover
  • ISSN: 1300-0152
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Expression, purification, and characterization of recombinant human paraoxonase 1 (rhPON1) in Pichia pastoris

YAĞMUR ÜNVER, ESABİ BAŞARAN KURBANOĞLU, ORHAN ERDOĞAN

The biochemical and histoanatomical response of some woody species to anthropic impact in Suceava County, Romania

ELENA CIORNEA, IRINA BOZ, ELENA IONEL, SABINA IOANA COJOCARU, GABRIELA DUMITRU

Storage temperature of boar semen and its relationship to changes in sperm plasma membrane integrity, mitochondrial membrane potential, and oxidoreductive capability

DARIUSZ GACZARZEWICZ, JAN UDALA, MALGORZATA PIASECKA, BARBARA BLASZCZYK, TOMASZ STANKIEWICZ

Biological synthesis of silver nanoparticles and evaluation of antibacterial and antifungal properties of silver and copper nanoparticles

AZAM JAFARI, LATIFEH POURAKBAR, KHALIL FARHADI, Lida MOHAMMAD GHOLIZAD, YOBERT GOOSTA

Genetic integrity assessment of cryopreserved tomato (Lycopersicon esculentum Mill.) genotypes

ANA COSTE, DANA SUTEU, IOAN BACILA, CONSTANTIN DELIU, SERGIU VALIMAREANU, ADELA HALMAGYI

S. cerevisiae $\beta$-glucan reduced viability of mouse hepatoma cells in vitro

ARTUR JAVMEN, AUSRA NEMEIKAITE-CENIENE, SAULIUS GRIGISKIS, IRENA JONAUSKIENE, MARK RUDENKOV, DARIUS KACIANAUSKAS, MYKOLAS MAURICAS

Use of in vitro propagation of `Obla?inska? sour cherry in rootstock breeding

DUSICA DORIC, VLADISLAV OGNJANOV, GORAN BARAC, MIRJANA LJUBOJEVIC, ANKICA PRANJIC, KRUNOSLAV DUGALIC, SEZAİ ERCİŞLİ

cDNA cloning, molecular characterization, and expression analyses of two novel porcine ARRDC genes ARRDC1 and ARRDC5

Pei WANG, Hailong HUO, Shuyan WANG, Yongwang MIAO, Hongjiang WEI, Yongyun ZHANG, Qiaoling ZHANG, Fuquan LI, Rui WANG, Weizhen LI, Yue ZHAO, Heng XIAO, Lixian LIU, Jinlong HUO

cDNA cloning, molecular characterization, and expression analyses of two novel porcine ARRDC genes-ARRDC1 and ARRDC

Hailong HUO, Pei WANG, Shuyan WANG, Yongwang MIAO, Hongjiang WEI, Yongyun ZHANG, Qiaoling ZHANG, Fuquan LI, Lixian LIU, Rui WANG, Weizhen LI, Yue ZHAO, Jinlong HUO, Heng XIAO

Designing a bacterial biosensor for detection of mercury in water solutions

AMIR ROOINTAN, NOOSHIN SHABAB, JAMSHID KARIMI, ALIREZA RAHMANI, MOHAMMAD YOUSEF ALIKHANI, MASSOUD SAIDIJAM