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NO·–releasing substances that induce growth elongation in maize root segments

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Abstract

Root segments of maize were incubated in different solutions containing substances that non-enzymatically release nitric oxide, such as sodium nitrite (SN), sodium nitroprusside (SNP), nitrosoglutathione (NGLU) and nitrosocysteine (NCYS). We found that all of these substances induced root tip expansion in a dose-dependent manner. The decreasing order of potency for root-induced elongation was: 10 -7 M SN, pH 4.5; 10 -11 M NCYS, 10 -10 M SNP, 10 -9 M NGLU and 10 -7 M SN, pH 7.0. Nitric oxide scavenger such as methylene blue prevented the elongation induced by NO·–releasing substances, but had no effect on indole-3-acetic acid (IAA)-induced cell expansion. Our results suggest that nitric oxide is the putative elongation inducer and that IAA and NO·–releasing substances conceivably share common steps in the signal transduction pathway, since both elicited the same plant response. Vanadate, a plasmamembrane ATPase inhibitor, significantly reversed IAA-induced elongation when supplied at 10 μM concentration. IAA-induced elongation was strongly enhanced by 10 nM BAY K 8644, an agonist of voltage dependent Ca2+ channels. Promotion of root elongation in the absence of IAA occurred only at higher concentrations of BAY K. Vanadate and BAY K had no influence on the NCYS-induced elongation suggesting that the common steps in the signalling of IAA and NCYS are not at the level of the plasmamembrane.

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References

  • Archer S (1993) Measurement of nitric oxide in biological models. FASEB J 7: 349–360

    Google Scholar 

  • Bean BP (1989) Classes of calcium channels in vertebrate cells. Ann Rev Physiol 51: 367–384

    Google Scholar 

  • Bleiss W and Ehwald R (1993) Transient changes in length and growth of wheat coleoptile segments following treatments with osmotica and auxin. Physiol Plant 88: 541–548

    Google Scholar 

  • Bothe H, Korkdgen H, Lehmacher T and Hundshagen B (1992) Differential effects of Azospirillum auxin and combined nitrogen on the growth of the roots of wheat. Simbiosis 13: 167–179

    Google Scholar 

  • Brummell DA and Hall JL (1987) Rapid cellular responses to auxin and the regulation of growth. Plant Cell Environm 10: 523–543

    Google Scholar 

  • Crossin KL (1991) Nitric oxide (NO): a versatile second messenger in brain. TIBS 16: 81–82

    Google Scholar 

  • Didonet AD and Magalhães AC (1993) The role of auxin-like compounds in plant growth promoting rhyzobacteria: the wheat-Azospirillum association. R Bras Fisiol Veg 5: 179–183

    Google Scholar 

  • Feelisch m and Noack EA (1987) Correlation between nitric oxide formation during degradation of organic nitrates and activation of guanylate cyclase. Eur J Pharmacol 139: 19–30

    Google Scholar 

  • Gruetter CA, Barry BK, Mcnamara DB, Gruetter DY, Kadowitz J and Ignarro LJ (1979) Relaxation of bovine coronary artery and activation of coronary arterial guanylate cyclase by nitric oxide, nitroprusside and a carcinogenic nitrosamine. Adv Cyclic Nucl Res 9: 221–224

    Google Scholar 

  • Henri Y, Lepoivre m, Drapier J-C, Baricos WH, Ducrocq C, Boucher J-L and Guissani A (1993) EPR characterization of molecular targets for NO in mammalian cells and organelles. FASEB J 7: 1124–1134

    Google Scholar 

  • Jain DK and Patriquin DG (1985) Characterization of a substance produced by Azospirillum which causes branching of wheat root hairs. Can J Microbiol 31: 206–210

    Google Scholar 

  • Johannes E, Brosnan JM and Sanders D (1991) Calcium channels and signal transduction in plant cells. BioEssays 13: 331–336

    Google Scholar 

  • Leone AM, Palmer RMJ, Knowles RG, Francis PL, Ashton DS and Moncada S (1991) Constitutive and inducible nitric oxide synthases incorporate molecular oxygen into both nitric oxide and citruline. J Biol Chem 266: 23790–23795

    Google Scholar 

  • Leshem YY (1996) Nitric oxide in biological systems. Plant Growth Reg 18: 155–159

    Google Scholar 

  • Madison DV (1993) Pass the nitric oxide. Proc Natl Acad Sci USA 90: 4329–4331

    Google Scholar 

  • Martin R, Martinez-Murillo R, Bentura ML, Rodrigo J and Golvano MP (1995) Presence of the enzyme nitric oxide synthase in root nodules of lupine plants (Lupinus albus cv. Multolupa). Plant Microbe Inter 19: S335

    Google Scholar 

  • Mathews RW and Kerr SW (1993) Biological activity of Snitrosothiols: the role of nitric oxide. J Pharmacol Exp Ther 267: 1529–1537

    Google Scholar 

  • Mayer B, John M, Heinzel B, Werner ER, Wachter H, Schultz G and Bohme E (1991) Brain nitric oxide synthase is a biopterin-and flavin-containing multi-functional oxido-reductase. FEBS Lett 288: 187–191

    Google Scholar 

  • Noritake T, Kawakita K and Doke N (1996) Nitric oxide induces phytoalexin accumulation in potato tuber tissues. Plant Cell Physiol 37: 113–116

    Google Scholar 

  • Olbe m and Somarin m (1991) ATP-dependent Ca2+ transport in wheat root plasma membrane vesicles. Physiol Plant 83: 535–543

    Google Scholar 

  • Prince RC and Gunson DE (1993) Rising interest in nitric oxide synthase. TIBS 18: 35–36

    Google Scholar 

  • Rayle DL and Cleland RE (1992) The acid growth theory of auxininduced cell elongation is alive and well. Plant Physiol 99: 1271–1274

    Google Scholar 

  • Sen S and Cheema R (1995) Nitric oxide synthase and calmodulin immunoreactivity in plant embryonic tissue. Biochem Arch 11: 221–227

    Google Scholar 

  • Suzuki T, Tabata H and Nakamura A (1994) The inhibition of growth by gravitropic stimulation in darkness in agravitropic primary roots of Zea and role of calcium. Plant Cell Physiol 35: 1029–1035

    Google Scholar 

  • Wellburn AR (1990) Why are atmospheric oxides of nitrogen usually phytotoxic and not alternative fertilizers? New Phytol 115: 395–429

    Google Scholar 

  • Zimmer W, Rocben K and Bothe H (1998) An alternative explanation for growth promotion by bacteria of genus Azospirillum. Planta 176: 333–342

    Google Scholar 

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Gouvêa, C., Souza, J., Magalhães, A. et al. NO·–releasing substances that induce growth elongation in maize root segments. Plant Growth Regulation 21, 183–187 (1997). https://doi.org/10.1023/A:1005837012203

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