iBet uBet web content aggregator. Adding the entire web to your favor.
iBet uBet web content aggregator. Adding the entire web to your favor.



Link to original content: https://doi.org/10.1007/bf00397660
Distribution of photorespiratory enzymes between bundle-sheath and mesophyll cells in leaves of the C3−C4 intermediate species Moricandia arvensis (L.) DC | Planta Skip to main content
Log in

Distribution of photorespiratory enzymes between bundle-sheath and mesophyll cells in leaves of the C3−C4 intermediate species Moricandia arvensis (L.) DC

  • Published:
Planta Aims and scope Submit manuscript

Abstract

In order to study the location of enzymes of photorespiration in leaves of the C3−C4 intermediate species Moricandia arvensis (L.). DC, protoplast fractions enriched in mesophyll or bundlesheath cells have been prepared by a combination of mechanical and enzymic techniques. The activities of the mitochondrial enzymes fumarase (EC 4.2.1.2) and glycine decarboxylase (EC 2.1.2.10) were enriched by 3.0- and 7.5-fold, respectively, in the bundle-sheath relative to the mesophyll fraction. Enrichment of fumarase is consistent with the larger number of mitochondria in bundle-sheath cells relative to mesophyll cells. The greater enrichment of glycine decarboxylase indicates that the activity is considerably higher on a mitochondrial basis in bundle-sheath than in mesophyll cells. Serine hydroxymethyltransferase (EC 2.1.2.1) activity was enriched by 5.3-fold and glutamate-dependent glyoxylate-aminotransferase (EC 2.6.1.4) activity by 2.6-fold in the bundle-sheath relative to the mesophyll fraction. Activities of serine- and alanine-dependent glyoxylate aminotransferase (EC 2.6.1.45 and EC 2.6.1.4), glycollate oxidase (EC 1.1.3.1), hydroxypyruvate reductase (EC 1.1.1.81), glutamine synthetase (EC 6.3.1.2) and phosphoribulokinase (EC 2.7.1.19) were not significantly different in the two fractions. These data provide further independent evidence to complement earlier immunocytochemical studies of the distribution of photorespiratory enzymes in the leaves of this species, and indicate that while mesophyll cells of M. arvensis have the capacity to synthesize glycine during photorespiration, they have only a low capacity to metabolize it. We suggest that glycine produced by photorespiratory metabolism in the mesophyll is decarboxylated predominantly by the mitochondria in the bundle sheath.

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

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

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

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

RuBP:

ribulose 1,5-bisphosphate

References

  • Arnon, D.I. (1949) Copper enzymes in isolated chloroplasts. Polyphenol oxidase in Beta vulgaris. Plant Physiol. 24, 1–15

    Google Scholar 

  • Cossins, E.A. (1980) One-carbon metabolism. In: The biochemistry of plants. vol. 2, pp. 365–418, Davies, D.D., ed. Academic Press, New York, London

    Google Scholar 

  • Douce, R. (1985) Mitochondria in higher plants. Structure, function and biogenesis. Academic Press, New York, London

    Google Scholar 

  • Edwards, G.E., Ku, M.S.B. (1987) Biochemistry of C3−C4 intermediates. In: The biochemistry of plants, vol. 10, pp. 275–325, Hatch, M.D. and Boardman, N.K., eds. Academic Press, San Diego, London

    Google Scholar 

  • Edwards, G.E., Robinson, S.P., Tyler, N.J.C., Walker, D.A. (1978) Photosynthesis by isolated protoplasts, protoplast extracts, and chloroplasts of wheat. Influence of orthophosphate, pyrophosphate, and adenylates. Plant Physiol. 62, 313–319

    Google Scholar 

  • Hill, R.L., Bradshaw, R.A. (1969) Fumarase. Methods Enzymol. 13, 91–99

    Google Scholar 

  • Hunt, S., Smith, A.M., Woolhouse, H.W. (1987) Evidence for a light-dependent system for reassimilation of photorespiratory CO2, which does not include a C4 cycle, in the C3−C4 intermediate species Moricandia arvensis. Planta 171, 227–234

    Google Scholar 

  • Hylton, C.M., Rawsthorne, S., Smith, A.M., Jones, D.A., Woolhouse, H.W. (1988) Glycine decarboxylase is confined to the bundle-sheath cells of leaves of C3−C4 intermediate species. Planta 175, 452–459

    Google Scholar 

  • Kohn, L.D., Utting, J.M. (1982) Hydroxypyruvate reductase (D-glycerate dehydrogenase) from Pseudomonas. Methods Enzymol. 89, 341–345

    Google Scholar 

  • Ku, M.S.B., Edwards, G.E., Kanai, R. (1976) Distribution of enzymes related to C3 and C4 pathway of photosynthesis between mesophyll and bundle sheath cell of Panicum hians and Panicum milioides. Plant Cell Physiol. 17, 615–620

    Google Scholar 

  • O'Neal, D. and Joy, K.W. (1973) Glutamine synthetase of pea leaves. I. Purification, stabilization, and pH optima. Arch. Biochem. Biophys. 159, 113–122

    Google Scholar 

  • Rawsthorne, S., Hylton, C.M., Smith, A.M., Woolhouse, H.W. (1988) Photorespiratory metabolism and immunogold localization of photorespiratory enzymes in leaves of C3 and C3−C4 intermediate species of Moricandia. Planta 173, 298–308

    Google Scholar 

  • Smith, A.M., Woolhouse, H.W., Jones, D.A. (1982) Photosynthetic carbon metabolism of the cool-temperate C4 grass Spartina anglica Hubb. Planta 156, 441–448

    Google Scholar 

  • Taylor, R.T., Weissbach, H. (1965) Radioactive assay for serine transhydroxymethylase. Anal. Biochem. 13, 80–84

    Google Scholar 

  • Walton, N.J., Woolhouse, H.W. (1986) Enzymes of serine and glycine metabolism in leaves and non-photosynthetic tissues of Pisum sativum L. Planta 167, 119–128

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rawsthorne, S., Hylton, C.M., Smith, A.M. et al. Distribution of photorespiratory enzymes between bundle-sheath and mesophyll cells in leaves of the C3−C4 intermediate species Moricandia arvensis (L.) DC. Planta 176, 527–532 (1988). https://doi.org/10.1007/BF00397660

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00397660

Key words

Navigation