Abstract
Soybean plants (Glycine max [L.] Merr. cv Williams), which were symbiotic with Bradyrhizobium japonicum, and which grew well upon reduced nitrogen supplied solely through N2 fixation processes, often exhibited excess accumulation of starch and sucrose and diminished soluble protein in their source leaves. Nitrate and ammonia, when supplied to the nodulated roots of N2-fixing plants, mediated a reduction of foliar starch accumulation and a corresponding increase in soluble protein in the source leaves. This provided an opportunity to examine the potential metabolic adjustments by which NO3− and NH4+ (N) sufficiency or deficiency exerted an influence upon soybean leaf starch synthesis. When compared with soybean plants supplied with N, elevated starch accumulation was focused in leaf palisade parenchyma tissue of N2-fixing plants. Foliar activities of starch synthesis pathway enzymes including fructose-1,6-bisphosphate phosphatase, phosphohexoisomerase, phosphoglucomutase (PGM), as well as adenosine diphosphate glucose pyrophosphorylase (in some leaves) exhibited highest activities in leaf extracts of N2-fixing plants when expressed on a leaf protein basis. This was interpreted to mean that there was an adaptation of these enzyme activities in the leaves of N2-fixing plants, and this contributed to an increase in starch accumulation. Another major causal factor associated with increased starch accumulation was the elevation in foliar levels of fructose-6-phosphate, glucose-6-phosphate, and glucose-1-phosphate (G1P), which had risen to chloroplast concentrations considerably in excess of the Km values for their respective target enzymes associated with starch synthesis, e.g. elevated G1P with respect to adenosine diphosphate glucose pyrophosphorylase (ADPG-PPiase) binding sites. The cofactor glucose-1,6-bisphosphate (G1,6BP) was found to be obligate for maximal PGM activity in soybean leaf extracts of N2-fixing as well as N-supplemented plants, and G1,6BP levels in N2-fixing plant leaves was twice that of levels in N-supplied treatments. However the concentration of chloroplastic G1,6BP in illuminated leaves was computed to be saturating with respect to PGM in both N2-fixing and N-supplemented plants. This suggested that the higher level of this cofactor in N2-fixing plant leaves did not confer any higher PGM activation and was not a factor in higher starch synthesis rates. Relative to plants supplied with NO3− and NH4+, the source leaf glycerate-3-phosphate (3-PGA) and orthophosphate (Pi) concentrations in leaves of N2-fixing plants were two to four times higher. Although Pi is a physiological competitive inhibitor of leaf chloroplast ADPG-PPiase, and hence, starch synthesis, elevated chloroplast 3-PGA levels in N2-fixing plant leaves apparently prevented interference of Pi with ADPG-PPiase catalysis and starch synthesis.
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- Baysdorfer C., Robinson J. M. Sucrose and Starch Synthesis in Spinach Plants Grown under Long and Short Photosynthetic Periods. Plant Physiol. 1985 Nov;79(3):838–842. doi: 10.1104/pp.79.3.838. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown M. S., Bethlenfalvay G. J. The Glycine-Glomus-Rhizobium Symbiosis : VII. Photosynthetic Nutrient-Use Efficiency in Nodulated, Mycorrhizal Soybeans. Plant Physiol. 1988 Apr;86(4):1292–1297. doi: 10.1104/pp.86.4.1292. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fredeen A. L., Rao I. M., Terry N. Influence of Phosphorus Nutrition on Growth and Carbon Partitioning in Glycine max. Plant Physiol. 1989 Jan;89(1):225–230. doi: 10.1104/pp.89.1.225. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Galloway C. M., Dugger W. M., Black C. C. In vitro activation of phosphoglucomutase by fructose 2,6-bisphosphate. Plant Physiol. 1985 Nov;79(3):920–922. doi: 10.1104/pp.79.3.920. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gerhardt R., Stitt M., Heldt H. W. Subcellular Metabolite Levels in Spinach Leaves : Regulation of Sucrose Synthesis during Diurnal Alterations in Photosynthetic Partitioning. Plant Physiol. 1987 Feb;83(2):399–407. doi: 10.1104/pp.83.2.399. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heldt H. W., Chon C. J., Maronde D. Role of orthophosphate and other factors in the regulation of starch formation in leaves and isolated chloroplasts. Plant Physiol. 1977 Jun;59(6):1146–1155. doi: 10.1104/pp.59.6.1146. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heldt W. H., Werdan K., Milovancev M., Geller G. Alkalization of the chloroplast stroma caused by light-dependent proton flux into the thylakoid space. Biochim Biophys Acta. 1973 Aug 31;314(2):224–241. doi: 10.1016/0005-2728(73)90137-0. [DOI] [PubMed] [Google Scholar]
- Itaya K., Ui M. A new micromethod for the colorimetric determination of inorganic phosphate. Clin Chim Acta. 1966 Sep;14(3):361–366. doi: 10.1016/0009-8981(66)90114-8. [DOI] [PubMed] [Google Scholar]
- Kaiser W. M., Bassham J. A. Light-Dark Regulation of Starch Metabolism in Chloroplasts: II. Effect of Chloroplastic Metabolite Levels on the Formation of ADP-Glucose by Chloroplast Extracts. Plant Physiol. 1979 Jan;63(1):109–113. doi: 10.1104/pp.63.1.109. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kerr P. S., Huber S. C., Israel D. W. Effect of N-source on soybean leaf sucrose phosphate synthase, starch formation, and whole plant growth. Plant Physiol. 1984 Jun;75(2):483–488. doi: 10.1104/pp.75.2.483. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Levi C., Preiss J. Amylopectin degradation in pea chloroplast extracts. Plant Physiol. 1978 Feb;61(2):218–220. doi: 10.1104/pp.61.2.218. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mathewson P. R., Pomeranz Y. Modified chromogenic alpha-amylase assay for sprouted wheat. J Assoc Off Anal Chem. 1979 Jan;62(1):198–200. [PubMed] [Google Scholar]
- Rao I. M., Fredeen A. L., Terry N. Leaf Phosphate Status, Photosynthesis, and Carbon Partitioning in Sugar Beet: III. Diurnal Changes in Carbon Partitioning and Carbon Export. Plant Physiol. 1990 Jan;92(1):29–36. doi: 10.1104/pp.92.1.29. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robinson J. M. Photosynthetic Carbon Metabolism in Leaves and Isolated Chloroplasts from Spinach Plants Grown under Short and Intermediate Photosynthetic Periods. Plant Physiol. 1984 Jun;75(2):397–409. doi: 10.1104/pp.75.2.397. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rufty T. W., Huber S. C., Volk R. J. Alterations in leaf carbohydrate metabolism in response to nitrogen stress. Plant Physiol. 1988 Nov;88(3):725–730. doi: 10.1104/pp.88.3.725. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schnarrenberger C., Krüger I. Distinction between Cytosol and Chloroplast Fructose-Bisphosphate Aldolases from Pea, Wheat, and Corn Leaves. Plant Physiol. 1986 Feb;80(2):301–304. doi: 10.1104/pp.80.2.301. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sharkey T. D., Vanderveer P. J. Stromal Phosphate Concentration Is Low during Feedback Limited Photosynthesis. Plant Physiol. 1989 Oct;91(2):679–684. doi: 10.1104/pp.91.2.679. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sicher R. C., Baysdorfer C., Kremer D. F. A comparative analysis of fructose 2,6-bisphosphate levels and photosynthate partitioning in the leaves of some agronomically important crop species. Plant Physiol. 1987 Apr;83(4):768–771. doi: 10.1104/pp.83.4.768. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sicher R. C. Evidence for a light dependent increase of phosphoglucomutase activity in isolated, intact spinach chloroplasts. Plant Physiol. 1989 Feb;89(2):557–563. doi: 10.1104/pp.89.2.557. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Silvius J. E., Kremer D. F., Lee D. R. Carbon assimilation and translocation in soybean leaves at different stages of development. Plant Physiol. 1978 Jul;62(1):54–58. doi: 10.1104/pp.62.1.54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith R. G., Vanlerberghe G. C., Stitt M., Turpin D. H. Short-Term Metabolite Changes during Transient Ammonium Assimilation by the N-Limited Green Alga Selenastrum minutum. Plant Physiol. 1989 Oct;91(2):749–755. doi: 10.1104/pp.91.2.749. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steup M., Peavey D. G., Gibbs M. The regulation of starch metabolism by inorganic phosphate. Biochem Biophys Res Commun. 1976 Oct 18;72(4):1554–1561. doi: 10.1016/s0006-291x(76)80191-x. [DOI] [PubMed] [Google Scholar]
- Turpin D. H., Botha F. C., Smith R. G., Feil R., Horsey A. K., Vanlerberghe G. C. Regulation of Carbon Partitioning to Respiration during Dark Ammonium Assimilation by the Green Alga Selenastrum minutum. Plant Physiol. 1990 May;93(1):166–175. doi: 10.1104/pp.93.1.166. [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Veau E. J., Robinson J. M., Warmbrodt R. D., van Berkum P. Photosynthesis and photosynthate partitioning in n(2)-fixing soybeans. Plant Physiol. 1990 Sep;94(1):259–267. doi: 10.1104/pp.94.1.259. [DOI] [PMC free article] [PubMed] [Google Scholar]