Abstract
Shoot/root grafting studies showed organ and host cultivar effects on net H2 evolution from Pisum sativum L. root nodules. Net H2 evolution from those nodules represents the sum of H2 formed by Rhizobium nitrogenase and H2 oxidized by any uptake hydrogenase present in the bacteria. Grafts between pea cultivars `JI1205' or `Alaska' and `Feltham First' in symbioses with R. leguminosarum 128C53 showed that shoots of both JI1205 and Alaska increased H2 uptake significantly (P ≤ 0.05) in Feltham First root nodules. The same plants also had less net H2 evolution at similar rates of C2H2 reduction than plants formed by grafting Feltham First shoots on Feltham First roots. Although JI1205 and Alaska shoots increased H2-uptake activity of Feltham First root nodules 28 days after the graft was made, intermediate to high levels of H2 uptake activity were still present in nodules on roots of both JI1205 and Alaska grafted to Feltham First shoots. These results indicate the presence of a transmissible shoot factor(s) which can increase uptake hydrogenase activity in a Rhizobium symbiont and show that root genotype also can influence that parameter.
Parallel grafting experiments using the same pea cultivars in symbioses with R. leguminosarum strain 300, which lacks uptake hydrogenase activity, suggested that a transmissible shoot factor(s) altered H2 formation from nitrogenase by changing the electron allocation coefficient of that enzyme complex.
The root and shoot factor(s) detected in this study had no permanent effect on strain 128C53. Bacterial cells isolated from Feltham First nodules with low H2 uptake activity formed root nodules on JI1205 and Alaska with high H2 uptake activity. Bacteroids isolated from nodules on intact JI1205, Alaska, or Feltham First plants with high, medium, or low H2 uptake activity, respectively, maintained those phenotypes during in vitro assays.
Full text
PDF




Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bedmar E. J., Edie S. A., Phillips D. A. Host Plant Cultivar Effects on Hydrogen Evolution by Rhizobium leguminosarum. Plant Physiol. 1983 Aug;72(4):1011–1015. doi: 10.1104/pp.72.4.1011. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bergersen J. F., Turner G. L. Nitrogen fixation by the bacteroid fraction of breis of soybean root nodules. Biochim Biophys Acta. 1967 Aug 29;141(3):507–515. doi: 10.1016/0304-4165(67)90179-1. [DOI] [PubMed] [Google Scholar]
- Bethlenfalvay G. J., Phillips D. A. Effect of Light Intensity on Efficiency of Carbon Dioxide and Nitrogen Reduction in Pisum sativum L. Plant Physiol. 1977 Dec;60(6):868–871. doi: 10.1104/pp.60.6.868. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bethlenfalvay G. J., Phillips D. A. Variation in nitrogenase and hydrogenase activity of alaska pea root nodules. Plant Physiol. 1979 May;63(5):816–820. doi: 10.1104/pp.63.5.816. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bulen W. A., LeComte J. R. The nitrogenase system from Azotobacter: two-enzyme requirement for N2 reduction, ATP-dependent H2 evolution, and ATP hydrolysis. Proc Natl Acad Sci U S A. 1966 Sep;56(3):979–986. doi: 10.1073/pnas.56.3.979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carter K. R., Jennings N. T., Hanus J., Evans H. J. Hydrogen evolution and uptake by nodules of soybeans inoculated with different strains of Rhizobium japonicum. Can J Microbiol. 1978 Mar;24(3):307–311. doi: 10.1139/m78-051. [DOI] [PubMed] [Google Scholar]
- Dejong T. M., Phillips D. A. Nitrogen Stress and Apparent Photosynthesis in Symbiotically Grown Pisum sativum L. Plant Physiol. 1981 Aug;68(2):309–313. doi: 10.1104/pp.68.2.309. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dixon R. O. Hydrogenase in legume root nodule bacteroids: occurrence and properties. Arch Mikrobiol. 1972;85(3):193–201. doi: 10.1007/BF00408844. [DOI] [PubMed] [Google Scholar]
- Dixon R. O. Hydrogenase in pea root nodule bacterioids. Arch Mikrobiol. 1968;62(3):272–283. doi: 10.1007/BF00413898. [DOI] [PubMed] [Google Scholar]
- Edie S. A., Phillips D. A. Effect of the host legume on acetylene reduction and hydrogen evolution by Rhizobium nitrogenase. Plant Physiol. 1983 May;72(1):156–160. doi: 10.1104/pp.72.1.156. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hageman R. V., Burris R. H. Electron allocation to alternative substrates of Azotobacter nitrogenase is controlled by the electron flux through dinitrogenase. Biochim Biophys Acta. 1980 Jun 10;591(1):63–75. doi: 10.1016/0005-2728(80)90220-0. [DOI] [PubMed] [Google Scholar]
- Keyser H. H., van Berkum P., Weber D. F. A Comparative Study of the Physiology of Symbioses Formed by Rhizobium japonicum with Glycine max, Vigna unguiculata, and Macroptilium atropurpurem. Plant Physiol. 1982 Dec;70(6):1626–1630. doi: 10.1104/pp.70.6.1626. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Koch B., Evans H. J., Russell S. Reduction of acetylene and nitrogen gas by breis and cell-free extracts of soybean root nodules. Plant Physiol. 1967 Mar;42(3):466–468. doi: 10.1104/pp.42.3.466. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lim S. T., Shanmugam K. T. Regulation of hydrogen utilisation in Rhizobium japonicum by cyclic AMP. Biochim Biophys Acta. 1979 May 16;584(3):479–492. doi: 10.1016/0304-4165(79)90121-1. [DOI] [PubMed] [Google Scholar]
- Nelson L. M., Salminen S. O. Uptake hydrogenase activity and ATP formation in Rhizobium leguminosarum bacteroids. J Bacteriol. 1982 Aug;151(2):989–995. doi: 10.1128/jb.151.2.989-995.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]