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Plant Physiol, February 2001, Vol. 125, pp. 926-934

Sucrose Metabolism in Plastids1

Nathalie Gerrits, Stefan C.H.J. Turk,2 Kees P.M. van Dun, Stephan H.D. Hulleman, Richard G.F. Visser, Peter J. Weisbeek, and Sjef C.M. Smeekens*

Departments of Molecular Plant Physiology and Molecular Cell Biology, University of Utrecht, Padualaan 8, 3584 CH Utrecht, The Netherlands (N.G., S.C.H.J.T., P.J.W., S.C.M.S.); Advanta Seeds, P.O. Box 1, 4410 AA Rilland, The Netherlands (K.P.M.v.D.); Agrotechnological Research Institute, P.O. Box 17, 6700 AA Wageningen, The Netherlands (S.H.D.H.); and Laboratory of Plant Breeding, Wageningen Agricultural University, P.O. Box 386, 6700 AJ Wageningen, The Netherlands (R.G.F.V.)

The question whether sucrose (Suc) is present inside plastids has been long debated. Low Suc levels were reported to be present inside isolated chloroplasts, but these were argued to be artifacts of the isolation procedures used. We have introduced Suc-metabolizing enzymes in plastids and our experiments suggest substantial Suc entry into plastids. The enzyme levansucrase from Bacillus subtilis efficiently synthesizes fructan from Suc. Targeting of this enzyme to the plastids of tobacco (Nicotiana tabacum) and potato (Solanum tuberosum) plants leads to high-level fructan accumulation in chloroplasts and amyloplasts, respectively. Moreover, introduction of this enzyme in amyloplasts leads to an altered starch structure. Expression of the yeast invertase in potato tuber amyloplasts results in an 80% reduction of total Suc content, showing efficient hydrolysis of Suc by the plastidic invertase. These observations suggest that Suc can enter plastids efficiently and they raise questions as to its function and metabolism in this organelle.


1 This work was financially supported by the Ministry of Economic Affairs, by the Ministry of Education, Culture, and Science, and by the Ministry of Agriculture, Nature Management, and Fishery in the framework of an industrial relevant research program of the Netherlands Association of Biotechnology Centers in the Netherlands. S.T. was financially supported by the European Union-Food and Agro-Industrial Research (program no. PL-96-1896).

2 Present address: Keygene, P.O. Box 216, 6700 AE Wageningen, The Netherlands.

* Corresponding author; e-mail j.c.m.smeekens{at}bio.uu.nl; fax 31-30-2513655.

© 2001 American Society of Plant Physiologists



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