Skip to main content
Log in

Iron uptake and metabolism in the rhizobia/legume symbioses

  • Published:
Plant and Soil Aims and scope Submit manuscript

Abstract

Iron-containing proteins figure prominently in the nitrogen-fixing symbioses between bacteria of the genera Azorhizovium, Bradyrhizobium and Rhizobium and their respective plant hosts. Although iron is abundant in the soil, the acquisition of iron is problematic due to its low solubility at biological pH under aerobic conditions. The study of iron acquisition as it pertains to these economically important symbioses is directed at answering three questions: 1) how do rhizobial cells acquire iron as free-living microorganisms where they must compete for this nutrient with other soil inhabitants 2) how do the plant hosts acquire enough iron for the symbiosis and 3) how do rhizobia acquire iron as symbionts? Production and/or utilization of ferric-specific ligands (siderophores) has now been documented in the laboratory for a number of rhizobial species, but there is limited information on whether production and/or untilization occurs either in the soil or in planta. Studies with rhizobial mutants which can no longer produce and/or utilize siderophores should address whether siderophores contribute to functional symbioses. In addition, the ability to produce and/or utilize siderophores may affect the outcome of both interstrain and interspecific competition in the rhizosphere and in bulk soil. Some progress has been made at documenting the effects of iron deficiency on nodule development. Studies are also underway to determine whether, in addition to its central structural role, iron may also play a regulatory role in the symbioses. This review is an attempt to give an overview of the field, and hopefully will stimulate further research on the iron nutrition of these symbioses which account for such a significant proportion of the world's biologically fixed nitrogen.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ames-Gottfred N P, Christie B R and Jordan D C 1989 Use of the chrome azurol S agar plate technique to differentiate strains and field isolates of Rhizobium leguminosarum biovar trifolii. Appl. Environ. Microbiol. 55, 707–710.

    Google Scholar 

  • Appanna V D 1988 A comparative study of exopolysaccharide synthesis in Rhizobium meliloti JJ-1 exposed to aluminum and iron. Microbios 55, 33–39.

    Google Scholar 

  • Bagg A and Neilands J B 1987 Molecular mechanisms of regulation of siderophore-mediated iron assimilation. Microbiol. Rev. 51, 509–518.

    Google Scholar 

  • Bergersen F J 1963 Iron in the developing soybean nodule. Aust. J. Biol. Sci. 16, 916–19.

    Google Scholar 

  • Bosch I, Meidl E J, Hoult M, Plessner O and Guerinot M L 1988 Iron uptake and metabolism in the Bradyrhizobium/soybean symbiosis. In Nitrogen Fixation: Hundred Years After. Eds. H.Bothe, F JdeBruijn and W ENewton, p. 652. Gustav Fischer, New York.

    Google Scholar 

  • Braun V, Hantke K, Eick-Helmerick K, Köster W, PreBler U, Sauer M, Schäffer S, Schöffler H, Staudenmaier H and Zimmermann L 1987 Iron transport systems in Escherichia coli. In Iron Transport in Microbes, Plants and Animals. Eds. GWinkelmann, Dvan derHelm and J BNeilands. pp 35–51. VCH Publishers, New York, NY.

    Google Scholar 

  • Brown J C and Chaney R L 1971 Effect of iron on the transport of citrate into the xylem of soybeans and tomatoes. Plant Physiol. 47, 836–840.

    Google Scholar 

  • Buyer J S, Sikora L J and Chaney R L 1989 A new growth medium for the study of siderophore-mediated interactions. Biol. Fertil. Soil 8, 97–101.

    Google Scholar 

  • Carrillo-Castaneda G and Peralta J R V 1988 Siderophore-like activities in Rhizobium phaseoli. J. Plant Nutr. 11, 935–944.

    Google Scholar 

  • Chaney R L, Brown J C and Tiffin L O 1972 Obligatory reduction of ferric chelates in iron uptake by soybeans. Plant Physiol. 50, 208–213.

    Google Scholar 

  • Crichton R R, Ponce-Ortiz Y, Koch M H J, Parfait R and Stuhrmann H B 1978. Isolation and characterization of phytoferritin from pea (Pisum sativum) and lentil (Lens esculenta). Biochem J. 171, 349–256.

    Google Scholar 

  • Crowley D E, Reid C P P and Szaniszlo P J 1987 Microbial siderophores as iron sources for plants. In Iron Transport In Microbes, Plants and Animals. Eds. GWinkelmann, D van derHelm and J BNeilands. pp 375–386. VCH Publishers, New York, NY.

    Google Scholar 

  • Dart P J 1977 Infection and development of leguminous nodules. In A Treatise on Dinitrogen Fixation. Eds. R W F Hardy and W SSilver. pp 367–472. John Wiley and Sons, New York.

    Google Scholar 

  • deLorenzo V, Wee S, Herrero M and Neilands J B 1987 Operator sequences of the aerobactin operon of plasmid ColV-K30 binding the ferric uptake regulation (fur) repressor. J. Bacteriol. 169, 2624–2630.

    Google Scholar 

  • Djordjevic M A, Gabriel D W and Rolfe B G 1987 Rhizobium — the refined parasite of legumes. Annu. Rev. Phytopathol. 25, 145–168.

    Google Scholar 

  • Enard C, Diolez A and Expert D 1988 Systemic virulence of Erwinia chrysanthemi 3937 requires a functional iron assimilation system. J. Bacteriol. 170, 2419–2426.

    Google Scholar 

  • Ferrala N F, Champlin A K, and Fekete F A 1986 Morphological differences in the capsular polysaccharide of nitrogen-fixing Azotobacter chroococcum B-8 as a function of iron and molybdenum starvation. FEMS Microbiol. Lett. 33, 137–142.

    Google Scholar 

  • Fischer H M, Alvarez-Morales and Hennecke H 1986 The pleiotropic nature of symbiotic regulatory mutants: Bradyrhizobium japonium nifA gene is involved in control of nif gene expression and formation of determinate symbiosis. Mol. Gen. Genet. 209, 621–626.

    Google Scholar 

  • Fischer H M, Bruderer T and Hennecke H 1988 Essential and non-essential domains in the Bradyrhizobium japonicum NifA protein: Identification of indispensable cysteine residues potentially involved in redox and/or metal binding. Nucleic Acids Res. 16, 2207–2224.

    Google Scholar 

  • Fuhrmann J and Wollum A GII 1989a In vitro growth responses of Bradyrhizobium japonicum to soybean rhizosphere bacteria. Soil Biol. Biochem. 21, 131–135.

    Google Scholar 

  • Fuhrmann J and Wollum A GII 1989b Nodulation competition among Bradyrhizobium japonicum strains as influenced by rhizophere bacteria and iron availability. Biol. Fertil. Soils 7, 108–112.

    Google Scholar 

  • Gardner W K, Barber D A and Parbery D G 1983 The acquisition of phosphorus by Lupinus albus L. III. The probable mechanism by which phosphorus movement in the soil/root interface is enhanced. Plant and Soil 70, 107–124.

    Google Scholar 

  • Gill P R and Neilands J B 1989 Cloning of a genomic region required for a high affinity iron uptake system in Rhizobium meliloti 1021. Mol. Microbiol. 3, 1183–1189.

    Google Scholar 

  • Gill P R, Barton L L, Scoble M D and Neilands J B 1990 A high affinity iron transport system of Rhizobium meliloti may be required for efficient nitrogen fixation in planta. Plant and Soil 130, 211–217.

    Google Scholar 

  • Griggs D W and Konisky J 1989 Mechanism for iron-regulated transcription of the Escherichia coli cir gene: Metal-dependent binding of Fur protein to the promoters. J. Bacteriol. 171, 1048–1054.

    Google Scholar 

  • Guerinot M L and Chelm B K 1986 Bacterial Δ-aminolevulinic acid synthase activity is not essential for leghemoglobin formation in the soybean/Bradyrhizobium japonicum symbiosis. Proc. Natl. Acad. Sci. USA 83, 1837–1841.

    Google Scholar 

  • Guerinot M L, Meidl E J and Plessner O 1990 Citrate as a siderophore in Bradyrhizobium japonicum. J. Bacteriol. 172, 3298–3303.

    Google Scholar 

  • Hantke K 1982 Negative control of iron uptake systems in Escherichia coli. FEMS Microbiol. Lett. 15, 83–86.

    Google Scholar 

  • Henderson N, Austin S and Dixon R A 1983 Role of metal ions in negative regulation of nitrogen fixation by the nifL gene product from Klebsiella pneumoniae. Mol. Gen. Genet. 216, 484–491.

    Google Scholar 

  • John T R and Nadler K D 1983 Characterization of a Rhizobium leguminosarum mutant strain deficient in heme biosynthesis. Plant Physiol. 72S, 109.

    Google Scholar 

  • Jurkevitch E, Hadar Y and Chen Y 1988 Involvement of bacterial siderophores in the remedy of lime-induced chlorosis in peanut. Soil Sci. Soc. Am. J. 52, 1032–1037.

    Google Scholar 

  • Ko M P, Huang P-Y, Huang J-S and Barker K R 1987 The occurrence of phytoferritin and its relationship to effectiveness of soybean nodules. Plant Physiol. 83, 299–305.

    Google Scholar 

  • Laudenbach D E and Straus N A 1988 Characterization of a cyanobacterial iron stress-induced gene similar to psbC. J. Bacteriol. 170, 508–5026.

    Google Scholar 

  • Leong J 1986 Siderophores: Their biochemistry and possible role in the biocontrol of plant pathogens. Annu. Rev. Phytopathol. 24, 187–209.

    Google Scholar 

  • Leong S A, Williams P H and Ditta G S 1985 Analysis of the 5′ regulatory region of the gene for Δ-aminolevulinic acid synthetase of Rhizobium meliloti. Nucleic Acid Res. 13, 5965–5976.

    Google Scholar 

  • McClung C R, Somerville J E, Guerinot M L and Chelm B K 1987 Structure of the Bradyrhizobium japonicum gene hemA encoding 5-aminolevulinic acid synthase. Gene 54, 133–139.

    Google Scholar 

  • Miller J F, Mekalanos J J and Falkow S 1989 Coordinate regulation and sensory transduction in the control of bacterial virulence. Science 243, 916–922.

    Google Scholar 

  • Modi M, Shah K S and Modi V V 1985 Isolation and characterisation of catechol-like siderophore from cowpea Rhizobium RA-1. Arch. Microbiol. 141, 156–158.

    Google Scholar 

  • Moshiri F, Stults L, Novak P and Maier R J 1983 Nif -Hup- mutants of Rhizobium japonicum. J. Bacteriol. 155, 926–929.

    Google Scholar 

  • Nadler K D, Johnston A W B, Chen J-W and John T R 1990 A Rhizobium leguminosarum mutant defective in symbiotic iron acquisition. J. Bacteriol. 172, 670–677.

    Google Scholar 

  • Nambiar P T C and Sivaramakrishnan S 1987 Detection and assay of siderophores in cowpea rhizobia (Bradyrhizobium) using radioactive Fe (59Fe). Lett. Appl. Microbiol. 4, 37–40.

    Google Scholar 

  • Neilands J B and Leong S A 1986 Siderophores in relation to plant growth and disease. Annu. Rev. Plant Physiol. 37: 187–208.

    Google Scholar 

  • Neilands J B 1989 Siderophore systems of bacteria and fungi. In Metal Ions and Bacteria. Eds. T JBeveridge and R J Doyle. pp 141–163. John Wiley and Sons, New York.

    Google Scholar 

  • Noel K D, Stacey G, Tandon S R, Silver L E and Brill W J 1982 Rhizobium japonicum mutants defective in symbiotic nitrogen fixation. J. Bacteriol. 152, 485–494.

    Google Scholar 

  • O'Hara G W, Dilworth M J, Boonkerd N and Parkpian P 1988a Iron-deficiency specifically limits nodule development in peanut inoculated with Bradyrhizobium sp. New Phytol. 108, 51–57.

    Google Scholar 

  • O'Hara G W, Hartzook A, Bell R W and Loneragan J F 1988b Response to Bradyrhizobium strain of peanut cultivars grown under iron stress. J. Plant Nutr. 11, 843–852.

    Google Scholar 

  • Patel H N, Chakraborty R N and Desai S B 1988 Isolation and partial characterization of phenolate siderophore from Rhizobium leguminosarum IARI 102. FEMS Microbiol. Lett. 56, 131–134.

    Google Scholar 

  • Payne S M 1988 Iron and virulence in the family enterobacteriaceae. CRC Microbiol. Rev. 16, 81–111.

    Google Scholar 

  • Poole K and Braun V 1988 Iron regulation of Serratia marcescens hemolysin gene expresison. Infect. Immun. 56, 2967–2971.

    Google Scholar 

  • Reigh G and O'Connell M 1988 Siderophore production is strain specific in Rhizobium. In Nitrogen Fixation: Hundred Years After. Eds. HBothe, F JdeBruijn and W E Newton. p. 826. Gustav Fischer, New York.

    Google Scholar 

  • Redinbaugh M G and Campbell W H 1983 Reduction of ferric citrate catalyzed by NADH: nitrate reductase. Biochem. Biophys. Res. Commun. 114, 1182–1188.

    Google Scholar 

  • Rioux C R, Jordan D C and Rattray J B M 1986a Iron requirement of Rhizobium leguminosarum and secretion of anthranilic acid during growth on an iron-deficient medium. Arch. Biochem. Biophys. 248, 175–182.

    Google Scholar 

  • Rioux C R, Jordan D C and Rattray J B M 1986b Anthranilate-promoted iron uptake in Rhizobium leguminosarum. Arch. Biochem. Biophys. 248, 183–189.

    Google Scholar 

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

    Google Scholar 

  • Roessler P G and Nadler K D 1982 Effects of iron deficiency on heme biosynthesis in Rhizobium japonicum. J. Bacteriol. 149, 1021–1026.

    Google Scholar 

  • Salinas P C, Tolmasky M E and Crosa J H 1989 Regulation of the iron uptake system in Vibrio anguillarum: Evidence for a cooperative effect between two transcriptional activators. Proc. Natl. Acad. Sci. USA 86, 3529–3533.

    Google Scholar 

  • Schwyn B and Neilands J B 1987a Universal chemical assay for the detection and determination of siderophores. Anal. Biochem. 160, 47–56.

    Google Scholar 

  • Schwyn B and Neilands K B 1987b Siderophores from agronomically important species of the Rhizobiaceae. Comments Agric. Food Chem. 1, 95–114.

    Google Scholar 

  • Skorupska A, Choma A, Derylo M and Lorkiewicz Z 1988 Siderophore containing 2,3-dihydroxybenzoic acid and threonine formed by Rhizobium trifolii. Acta Biochim. Pol. 35, 119–130.

    Google Scholar 

  • Skorupska A, Derylo M and Lorkiewicz Z 1989 Siderophore production and utilization by Rhizobium trifolii. Biol. Metals 2, 45–49.

    Google Scholar 

  • Smith M J and Neilands J B 1984 Rhizobactin, a siderophore from Rhizobium meliloti. J. Plant Nutr. 7, 449–458.

    Google Scholar 

  • Smith M J and Neilands J B 1987 Rhizobactin, a structurally novel siderophore biochemically related to the opines. In Molecular Strategies For Crop Protection. Eds. C J Arntzen and CRyan. pp 157–168. Alan R. Liss, Inc., New York.

    Google Scholar 

  • Smith M J, Shoolery J N, Schwyn B, Holden I and Neilands J B 1985 Rhizobactin, a structurally novel siderophore from Rhizobium meliloti. J. Am. Chem. Soc. 107, 1739–1743.

    Google Scholar 

  • Spiro S, Roberts R E and Guest J R 1989 FNR-dependent repression of the ndh gene of Escherichia coli and metal ion requirement for FNR-regulated gene expresison. Mol. Microbiol. 3, 601–608.

    Google Scholar 

  • Soerensen K U, Terry R E, Jolley V D, Brown J C and Vargas M E 1988 The interaction of iron-stress response and root nodules in iron efficient and inefficient soybeans. J. Plant Nutr. 1, 853–862.

    Google Scholar 

  • Soerensen K U, Terry R E, Jolley V D and Brown J C 1989 Iron-stress response of inoculated and non-inoculated roots of an iron inefficient soybean cultivar in a split-root system. J. Plant Nutr. 12, 437–447.

    Google Scholar 

  • Stoebner J A and Payne S M 1988 Iron-regulated hemolysin production and utilization of heme and hemoglobin by Vibrio cholerae. Infect. Immun. 56, 2891–2895.

    Google Scholar 

  • Terry R E, Hartzook A, Jolley V D and Brown J C 1988 Interactions of iron nutrition and symbiotic nitrogen fixation in peanuts. J Plant Nutr. 11, 811–820.

    Google Scholar 

  • Tiffin L O 1970 Translocation of iron citrate and phosphorus in xylem exudate of soybean. Plant Physiol. 45, 280–283.

    Google Scholar 

  • Trageser M and Unden G 1989 Role of cysteine residues and of metal ions in the regulatory functioning of FNR, the transcriptional regulator of anaerobic respiration in Escherichia coli. Mol. Microbiol. 3, 593–599.

    Google Scholar 

  • Udvardi M K, Price G D, Gresshoff P M and Day D A 1988 A dicarboxylate transporter on the peribacteroid membrane of soybean nodules. FEBS Lett. 231, 36–40.

    Google Scholar 

  • Van derMark F and Van derBriel W 1985 Purification and partial characterization of ferritin from normal and iron-loaded leaves of Phaseolus vulgaris. Plant Sci. 39, 55–60.

    Google Scholar 

  • Verma D P S and Long S 1983 The molecular biology of Rhizobium-legume symbiosis. Int. Rev. Cytol. Suppl. 14, 211–245.

    Google Scholar 

  • Verma D P S, Kazazian V, Zogbi V and Bal A K 1978 Isolation and characterization of the membrane envelope enclosing the bacteroids in soybean root nodules. J. Cell Biol. 78, 919–936.

    Google Scholar 

  • Winkelmann G 1979 Surface polymers and hydroxy acids: A model of iron supply in sideramine-free fungi. Arch. Microbiol. 121, 43–51.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Rhizobia will be used to refer collectively to the genera Azorhizobium, Bradyrhizobium and Rhizobium throughout this article.

Rhizobia will be used to refer collectively to the genera Azorhizobium, Bradyrhizobium and Rhizobium throughout this article.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Guerinot, M.L. Iron uptake and metabolism in the rhizobia/legume symbioses. Plant Soil 130, 199–209 (1991). https://doi.org/10.1007/BF00011874

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00011874

Key words

Navigation