Skip to main content
Log in

Respiration and nitrogenase activity in nodules ofCasuarina cunninghamiana and cultures ofFrankia sp. HFP020203: Effects of temperature and partial pressure of O2

  • Published:
Plant and Soil Aims and scope Submit manuscript

Abstract

The effects of time after exposure to acetylene and of nodule excision were examined using a flow-through system. After a transient depression in the rate of acetylene reduction that began about 1.5 min after exposure to acetylene, the rate recovered to 98% of the initial maximum value after 40 min. After nodule excision the rate stabilized to 90% of the initial maximum value observed in the intact plant.

Excised nodules, measured at 6-min intervals in a closed system, with frequent changes of the gas mixture, were used for the remaining experiments. Acetylene reduction by the nodules increased rapidly as temperature was increased between 6 and 26°C. Between 26 and 36°C there was relatively little effect of temperature on acetylene reduction.

Nodules and cultures ofFrankia were compared with respect to the effect of temperature and pO2 (partial pressure of oxygen) on oxygen uptake. Cultures ofFrankia were grown on a nitrogen-free medium at either 0.3 kPa O2 (vesicles absent) or 20 kPa O2 (vesicles present). Oxygen uptake by nodules (vesicles absent) and by vesicle-containing cultures was strongly dependent on pO2 at values below 20 kPa. This suggests the presence of a barrier to oxygen diffusion. Oxygen uptake was dependent on temperature as well as on pO2, but the Q10 was much larger for the cultures than for the nodules. This suggests that vesicles or related structures are not the source of the diffusion barrier in Casuarina nodules. Respiration by cultures ofFrankia lacking vesicles became O2-saturated at low pO2 values. Thus these cultures did not have a significant diffusion barrier. From these results it is concluded that nodules ofCasuarina cunninghamiana have a barrier to oxygen diffusion supplied by the host tissue and not byFrankia.

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

  • Appleby C A 1984 Leghemoglobin and Rhizobium respiration. Annu. Rev. Plant Physiol. 35, 443–478.

    Google Scholar 

  • Abdel Wahab A M 1980 Nitrogen-fixing nonlegumes in Egypt. I. Nodulation and N2 (C2H2) fixation byCasuarina equisetifolia. Z. Allg. Mikrobiologie 20, 3–12.

    Google Scholar 

  • Berg R H 1983 Preliminary evidence for the involvement of suberization in infection ofCasuarina. Can. J. Bot. 61, 2910–2918.

    Google Scholar 

  • Berg R H and McDowell L 1987 Endophyte differentiation inCasuarina actinorhizae. Protoplasma 136, 104–117.

    Google Scholar 

  • Berg R H and McDowell L 1988 Cytochemistry of the wall of infected cells inCasuarina actinorhizae. Can. J. Bot. 66, 2038–2047.

    Google Scholar 

  • Bond G 1956 A feature of the root nodules ofCasuarina. Nature 177, 191–192.

    Google Scholar 

  • Bond G 1961 The oxygen relation of nitrogen fixation in root nodules. Z. Allg. Mikrobiologie 1, 93–99.

    Google Scholar 

  • Fleming A I, Wittenberg J B, Wittenberg B A, Dudman W F and Appleby C A 1987 The purification, characterization and ligand-binding kinetics of hemoglobins from root nodules of the non-leguminousCasuarina glauca-Frankia symbiosis. Biochim. Biophys. Acta 911, 209–220.

    Google Scholar 

  • Minchin F R, Sheehy J E and Witty J E 1986 Further errors in the acetylene reduction assay: Effects of plant disturbance. J. Exp. Bot. 37, 1581–1591.

    Google Scholar 

  • Murry M A, Zhang Z and Torrey J G 1985 Effect of O2 on vesicle formation, acetylene reduction, and O2-uptake kinetics inFrankia sp. HFPCcI3 isolated fromCasuarina cunninghamiana. Can. J. Bot. 31, 804–809.

    Google Scholar 

  • Parsons R, Silvester W B, Harris S, Gruijters W T M and Bullivant S 1987Frankia vesicles provide inducible and absolute oxygen protection for nitrogenase. Plant Physiol. 83, 728–731.

    Google Scholar 

  • Reddell P, Bowen G D and Robson A D 1985 The effects of soil temperature on plant growth, nodulation and nitrogen fixation inCasuarina cunninghamiana MIQ. New Phytol. 101, 441–450.

    Google Scholar 

  • Rogers C, Meyer J A, Stannett V and Szwarc M 1956 Studies in the gas and vapor permeability of plastic films and coated papers. Part II. Some factors affecting the permeability constant. TAPPI 39, 741–747.

    Google Scholar 

  • Sheehy J E, Minchin F R and Witty J F 1985 Control of nitrogen fixation in a legume nodule: an analysis of the role of oxygen diffusion in relation to nodule structure. Ann. Bot. 55, 549–562.

    Google Scholar 

  • Ting I P 1982 Plant Physiology. Addison Wesley Publishing Company, Reading, Massachusetts, 642 p.

    Google Scholar 

  • Tjepkema J D 1983 Hemoglobins in the nitrogen-fixing root nodules of actinorhizal plants. Can. J. Bot. 61, 2949–2929.

    Google Scholar 

  • Tjepkema J D and Asa D J 1987 Total and CO-reactive heme content of actinorhizal nodules and the roots of some nonnodulated plants. Plant and Soil 100, 225–236.

    Google Scholar 

  • Tjepkema J D, Pathirana M S and Zeng S 1988a The gas diffusion pathway and hemoglobin content in actinorhizal nodules.In Nitrogen Fixation: Hundred Years After — Proc. 7th Intern. Congress on Nitrogen Fixation. Eds. H Bothe, F J de Bruin and W E Newton. p 701. Gustav Fisher, Stuttgart, FRG.

    Google Scholar 

  • Tjepkema J D, Schwintzer C R and Monz C A 1988b Time course of acetylene reduction in nodules of five actinorhizal genera. Plant Physiol. 86, 581–583.

    Google Scholar 

  • Tjepkema J D and Winship L J 1980 Energy requirement for nitrogen fixation in actinorhizal and legume root nodules. Science 209, 279–281.

    PubMed  Google Scholar 

  • Tjepkema J D and Yocum C S 1973 Respiration and oxygen transport in soybean nodules. Planta 115, 59–72.

    Google Scholar 

  • Tyson J H and Silver W S 1979 Relationship of ultrastructure to acetylene reduction (N2 fixation) in root nodules ofCasuarina. Bot. Gaz. 140 (suppl.), S44-S48.

    Google Scholar 

  • Waughman G J 1977 The effect of temperature on nitrogenase activity. J. Exp. Bot. 28, 949–960.

    Google Scholar 

  • Winship L J and Tjepkema J D 1982 Simultaneous measurement of acetylene reduction and respiratory gas exchange of attached root nodules. Plant Physiol. 70, 361–365.

    Google Scholar 

  • Winship L J and Tjepkema J D 1985 Nitrogen fixation and respiration by root nodules ofAlnus rubra Bong.: Effects of temperature and oxygen concentration. Plant and Soil 87, 91–107.

    Google Scholar 

  • Zhang Z, Lopez M F and Torrey J G 1984 A comparison of cultural characteristics and infectivity ofFrankia isolates from root nodules ofCasuarina species. Plant and Soil 78, 79–90.

    Google Scholar 

  • Zhang Z and Torrey J G 1985 Biological and cultural characteristics of the effectiveFrankia strain HFPCcI3 (Actinomycetales) fromCasuarina cunninghamiana (Casuarinaceae). Ann. Bot. 56, 367–378.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tjepkema, J.D., Murry, M.A. Respiration and nitrogenase activity in nodules ofCasuarina cunninghamiana and cultures ofFrankia sp. HFP020203: Effects of temperature and partial pressure of O2 . Plant Soil 118, 111–118 (1989). https://doi.org/10.1007/BF02232795

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02232795

Key words

Navigation