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Purification and characterization of nicotianamine synthase from Fe-deficient barley roots

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Iron Nutrition in Soils and Plants

Part of the book series: Developments in Plant and Soil Sciences ((DPSS,volume 59))

Abstract

Nicotianamine (NA), the key precursor of the mugineic acid family phytosiderophores (MAs), is synthesized from S-adenosylmethionine (SAM). The NA synthase was strongly induced by Fe-deficiency treatment, and the activity increased to the maximum level faster than the time of maximum level of MAs secretion and also before the appearance of severest chlorosis. The enzyme was mainly localized in the roots of barley. NA synthase had the optimum pH at 9.0, a molecular weight of about 40,000~50,000 estimated by gel filtration or about 30,000 by SDS-PAGE. Using hydrophobic chromatography, hydroxylapatite chromatography, and preparative SDS-PAGE, NA synthase was purified as one band on SDS-PAGE.

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References

  • Bienfait H F 1988 Mechanisms in Fe-efficiency reactions of higher plants. J. Plant Nutr. 11, 605–629.

    Article  CAS  Google Scholar 

  • Bowman W H, Tabo C W and Tabor H 1973 Spermidine biosynthesis. J. Biol. Chem. 248, 2480–2486.

    PubMed  CAS  Google Scholar 

  • Dzandu J K, Johnson J F and Wise G E 1988 Sodium Dodesyl Sulfate-Gel Electrophoresis: Staining of polypeptide using heavy metal salts. Anal. Biochem. 174, 157–167.

    Article  PubMed  CAS  Google Scholar 

  • Fushiya S, Takahashi K, Nakatsuyama S, Sato Y, Nozoe S and Takagi S 1982 Co-occurrence of nicotianamine and avenic acids in Avena sativa and Oryza sativa. Phytochemistry 21, 1907–1908.

    Article  CAS  Google Scholar 

  • Kanazawa K, Higuchi K, Fushiya S, Nozoe S, Nishizawa N K, Chino M and Mori S 1994 Induction of two enzyme activities involved in the biosynthesis of mugineic acid in Fe deficient barley roots. Plant and Soil (In press).

    Google Scholar 

  • Kawai S, Itoh K, Takagi S, Iwashita T and Nomoto K 1988a Studies on phytosiderophores: biosynthesis of mugineic acid and 2’-deoxymugineic acid in Hordeum vulgare L. var. Minorimugi. Tetrahedron Lett. 29, 1053–1056.

    Article  CAS  Google Scholar 

  • Kawai S, Takagi S and Sato Y 1988b Mugineic acid-family phytosiderophores in root-secretions of barley, corn and sorghum varieties. J. Plant Nutr. 11, 633–642.

    Article  CAS  Google Scholar 

  • Laemmli U K 1970 Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680.

    Article  PubMed  CAS  Google Scholar 

  • Ma J F and Nomoto K 1993 Two related biosynthetic pathway of mugineic acids in Gramineous plants. Plant Physiol. 102, 373–378.

    Article  PubMed  CAS  Google Scholar 

  • Marschner H, Römheld V and Kissel M 1987 Localization of phytosiderophore release and of iron uptake along intact barley roots. Physiol. Plant. 71, 157–172.

    Article  CAS  Google Scholar 

  • Mihashi S and Mori S 1989 Characterization of mugineic-acid-Fe transporter in Fe-deficient barley roots using the multicompartment transport box method. Biol. Metals 2, 146–154.

    Article  CAS  Google Scholar 

  • Mino Y, Ishida T, Ota N, Inoue M, Nomoto K, Takemoto T, Tanaka H and Sugiura Y 1983 Mugineic acid-iron (III) complex: characterization for absorption and transport of iron in gramineous plants. J. Am. Chem. Soc. 105, 4671–4676.

    Article  CAS  Google Scholar 

  • Mori S, Hachisuka M, Kawai S, Takagi S and Nishizawa N K 1988 Peptides related to phytosiderophore secretion by Fe-deficient barley roots. J. Plant Nutr. 11, 653–662.

    Article  CAS  Google Scholar 

  • Mori S and Nishizawa N 1987 Methionine as a dominant precursor of phytosiderophores in graminaceae plants. Plant Cell Physiol. 28, 1081–1092.

    CAS  Google Scholar 

  • Mori S, Nishizawa N, Kawai S, Sato S and Takagi S 1987 Dynamic state of mugineic acid and analogous phytosiderophores in Fedeficient barley. J. Plant Nutr. 10, 1003–1011.

    Article  CAS  Google Scholar 

  • Mudd S H and Cantoni G L 1958 Activation of methionine for transmethylation m. The methionine-activating enzyme of bakers’ yeast. J. Biol. Chem. 231, 481–492.

    PubMed  CAS  Google Scholar 

  • Nakanishi H, Okumura N, Umehara Y, Nishizawa N K, Chino M and Mori S 1993 Expression of a gene specific for iron deficiency (Ids 3) in the roots of Hordeum vulgare. Plant Cell Physiol. 34, 401–410.

    PubMed  CAS  Google Scholar 

  • Nishizawa N and Mori S 1987 The particular vesicle appearing in barley root cells and its relation to mugineic acid secretion. J. Plant Nutr. 10,1013–1020.

    Article  CAS  Google Scholar 

  • Nomoto K, Yoshioka H, Arima M, Fushiya S, Takagi S and Takemoto T 1981 Structure of 2’-deoxymugineic acid, a novel amino acid possessing an iron-chelating activity. Chimia 7, 249–250.

    Google Scholar 

  • Pajula R L, Raina A and Eloranta T 1979 Polyamine synthesis in mammalian tissues. Eur. J. Biochem. 101, 619–626.

    Article  PubMed  CAS  Google Scholar 

  • Romheld V 1987 Different strategies for iron acquisition in higher plants. Physiol. Plant. 70, 231–234.

    Article  Google Scholar 

  • Römheld V and Marschner H 1986 Evidence for a specific uptake system for iron phytosiderophores in roots of grasses. Plant Physiol. 70, 175–180.

    Article  Google Scholar 

  • Rudolph A, Becker R and Scholz G 1985 The occurrence of amino acid nicotianamine in plants and microorganisms. A reinvestigation. Biochem. Physiol. Pflanzen 180, 557–563.

    CAS  Google Scholar 

  • Samejima K and Yamada B 1982 Purification of spermidine synthase from rat ventral prostate by affinity chromatography on immobilized S-adenosyl (5’)-3-thiopropylamine. Arch. Biochem. Biophys. 216, 213–222.

    Article  PubMed  CAS  Google Scholar 

  • Scholz G, Becker R, Pich A and Stephan U W 1992 Nicotianamine — a common constituent of strategies I and II of iron-aquicition by plants: A review. J. Plant Nutr. 15, 1647–1665.

    Article  CAS  Google Scholar 

  • Scholz G, Becker R, Stephan U W, Rudolph A and Pich A 1988 The regulation of iron uptake and possible function of nicotianamine in higher plants. Biochem. Physiol. Pflanzen 183, 258–269.

    Google Scholar 

  • Shojima S, Nishizawa N K and Mori S 1989a Establishment of a cell-free system for the biosynthesis of nicotianamine. Plant Cell Physiol. 30, 673–677.

    CAS  Google Scholar 

  • Shojima S, Nishizawa N K, Fushiya S, Nozoe S, Kumashiro T, Nagata T, Ohata T and Mori S 1989b Biosynthesis of nicotianamine in the suspension — cultured cells of tobacco (Nicotiana megalosiphon). Biol. Metals 2, 142–145.

    Article  CAS  Google Scholar 

  • Shojima S, Nishizawa N K, Fushiya S, Nozoe S, Irifune T and Mori S 1990 Biosynthesis of phytosiderophores. Plant Physiol. 93, 1497–1503.

    Article  PubMed  CAS  Google Scholar 

  • Stephan U W and Scholz G 1990 Nicotianamine concentrations in iron sufficient and iron deficient sunflower and barley roots. J. Plant Physiol. 136, 631–634.

    Article  CAS  Google Scholar 

  • Stephan U W and Scholz G 1993 Nicotianamine: mediator of transport of iron and heavy metals in the phloem? Physiol. Plant. 88, 522–529.

    Article  CAS  Google Scholar 

  • Sugiura Y, Tanaka H, Mino Y, Ishida T, Ota N, Inoue M, Nomoto K, Yoshioka H and Takemoto T 1981 Structure, properties, and transport mechanism of iron (III) complex of mugineic acid, a possible phytosiderophore. J. Am. Chem. Soc. 103, 6979–6982.

    Article  CAS  Google Scholar 

  • Takagi S 1976 Naturally occurring iron-chelating compounds in oat-and rice-root washing. I. Activity measurement and preliminary characterization. Soil Sci. Plant Nutr. 22, 423–433.

    Article  CAS  Google Scholar 

  • Takagi S 1993 Production of phytosiderophores. In Iron Chelation in Plants and Soil Microorganisms, pp 111–131. Eds. L L Barton and H Hemming. Academic Press, San Diego.

    Google Scholar 

  • Takagi S, Nomoto K and Takemoto S 1984 Physiological aspect of mugineic acid, a possible phytosiderophore of graminaceous plants. J. Plant Nutr. 7, 469–477.

    Article  CAS  Google Scholar 

  • Takemoto T, Nomoto K, Fushiya S, Ouchi R, Kusano G, Hikino H, Takagi S, Matsuura Y and Kakudo M 1978 Structure of mugineic acid, a new amino acid possessing an iron-chelating activity from root washing of water-cultured Hordeum vulgare. Proc. Jpn. Acad. 54, 469–473.

    Article  CAS  Google Scholar 

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J. Abadía

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© 1995 Springer Science+Business Media Dordrecht

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Higuchi, K., Kanazawa, K., Nishizawa, NK., Chino, M., Mori, S. (1995). Purification and characterization of nicotianamine synthase from Fe-deficient barley roots. In: Abadía, J. (eds) Iron Nutrition in Soils and Plants. Developments in Plant and Soil Sciences, vol 59. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-0503-3_5

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  • DOI: https://doi.org/10.1007/978-94-011-0503-3_5

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-4224-6

  • Online ISBN: 978-94-011-0503-3

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