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. 1988 Dec;88(4):1229–1234. doi: 10.1104/pp.88.4.1229

Inhibition of Nodule Functioning in Cowpea by a Xanthine Oxidoreductase Inhibitor, Allopurinol

Craig A Atkins 1, Paul J Sanford 1, Paul J Storer 1, John S Pate 1
PMCID: PMC1055746  PMID: 16666449

Abstract

Allopurinol (1H-pyrazolo-[3,4-d]pyrimidine-4-ol), an inhibitor of xanthine oxidation in ureide-producing nodulated legumes, was taken up from the rooting medium, translocated in xylem, and transferred to nodules of both the ureide-forming cowpea (Vigna unguiculata L. Walp.) and the amide-forming white lupin (Lupinus albus L.). Cowpea suffered severe nitrogen deficiency, extreme chlorosis, and reduced growth, whereas lupin was unaffected by the inhibitor. Similar results were obtained with oxypurinol (1H-pyrazolo-[3,4-d]pyrimidine-4,6-diol). Xylem composition of symbiotic cowpea was markedly changed by allopurinol. Ureides fell to a very low level, but xanthine and, to a lesser extent, hypoxanthine increased markedly. Xylem glutamine was also reduced, but there was little change in other amino acids. Nitrogenase (EC 1.7.99.2) activity of intact nodulated plants or nodulated root segments of plants treated with allopurinol or oxypurinol for 24 hours or more was severely inhibited in cowpea but unaffected in lupin for periods of exposure up to 9 days. Nitrogenase activity of slices of nodules prepared from allopurinol-treated cowpea showed inhibition comparable to that of intact plants. Breis prepared from nodules of treated plants showed no reduction in nitrogenase, nor was there reduction in activity of breis following addition of allopurinol, xanthine, or a range of purine pathway intermediates. Increasing the O2 concentration in assays above 20% (volume/volume) reversed inhibition of nitrogenase by allopurinol in intact nodulated roots. It was concluded for cowpea that allopurinol not only inhibited ureide synthesis but also caused inhibition of nitrogenase activity, thereby leading to progressive dysfunction and eventual senescence of nodules. The mechanistic relationships between inhibition of ureide biosynthesis, changes in gaseous diffusion resistance, and reduced nitrogenase activity remain obscure.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Atkins C. A., Pate J. S., Griffiths G. J., White S. T. Economy of Carbon and Nitrogen in Nodulated and Nonnodulated (NO(3)-grown) Cowpea [Vigna unguiculata (L.) Walp.]. Plant Physiol. 1980 Nov;66(5):978–983. doi: 10.1104/pp.66.5.978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Atkins C. A., Ritchie A., Rowe P. B., McCairns E., Sauer D. De Novo Purine Synthesis in Nitrogen-Fixing Nodules of Cowpea (Vigna unguiculata [L.] Walp.) and Soybean (Glycine max [L.] Merr.). Plant Physiol. 1982 Jul;70(1):55–60. doi: 10.1104/pp.70.1.55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Atkins C. A., Storer P. J., Pate J. S. Pathways of Nitrogen Assimilation in Cowpea Nodules Studied using N(2) and Allopurinol. Plant Physiol. 1988 Jan;86(1):204–207. doi: 10.1104/pp.86.1.204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Das D. K., Engelman R. M., Clement R., Otani H., Prasad M. R., Rao P. S. Role of xanthine oxidase inhibitor as free radical scavenger: a novel mechanism of action of allopurinol and oxypurinol in myocardial salvage. Biochem Biophys Res Commun. 1987 Oct 14;148(1):314–319. doi: 10.1016/0006-291x(87)91112-0. [DOI] [PubMed] [Google Scholar]
  5. Fhaoláin I. N., Coughlan M. P. Effects of allopurinol and of oxypurinol on turkey liver xanthine dehydrogenase. FEBS Lett. 1978 Jun 15;90(2):305–308. doi: 10.1016/0014-5793(78)80392-5. [DOI] [PubMed] [Google Scholar]
  6. Peterson D. A., Kelly B., Gerrard J. M. Allopurinol can act as an electron transfer agent. Is this relevant during reperfusion injury? Biochem Biophys Res Commun. 1986 May 29;137(1):76–79. doi: 10.1016/0006-291x(86)91177-0. [DOI] [PubMed] [Google Scholar]
  7. Rainbird R. M., Thorne J. H., Hardy R. W. Role of amides, amino acids, and ureides in the nutrition of developing soybean seeds. Plant Physiol. 1984 Feb;74(2):329–334. doi: 10.1104/pp.74.2.329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Trijbels F., Vogels G. D. Degradation of allantoin by Pseudomonas acidovorans. Biochim Biophys Acta. 1966 Feb 14;113(2):292–301. doi: 10.1016/s0926-6593(66)80068-1. [DOI] [PubMed] [Google Scholar]
  9. Triplett E. W. Two indirect methods for detecting ureide synthesis by nodulated legumes. Plant Physiol. 1986 Jun;81(2):566–571. doi: 10.1104/pp.81.2.566. [DOI] [PMC free article] [PubMed] [Google Scholar]

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