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Abstracts now available online - Euro Fed Lipid

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P4<br />

Carbohydrate metabolism in developing linseed embryos<br />

Stéphanie Troufflard 1 , Stephen Rawsthorne 2 , Jean-Charles Portais 3 , Albrecht Roscher 1<br />

1<br />

Génie Enzymatique et Cellulaire UMR CNRS 6022, Université de Picardie, Amiens,<br />

France<br />

2<br />

Department of Metabolic Biology, John Innes Centre, Norwich, UK<br />

3 Laboratoire de Biotechnologies-Bioprocédés UMR CNRS-INSA 5504 INRA 792, INSA,<br />

Toulouse, France<br />

<strong>Lipid</strong> accumulation in oilseeds depends on the efficient conversion of photosynthetic<br />

sugars into fatty acids. However, offer and demand to not always coincide, due to daynight<br />

cycles on the one hand and to developmental shifts on the other hand.<br />

Discrepancies between offer and demand can be buffered by temporary carbohydrate<br />

stores inside the embryo. For example, it has been shown that developing rapeseed<br />

(Brassica napus L.) embryos accumulate starch in the days prior to the onset of<br />

maximal lipid synthesis, and that this starch subsequently disappears in favour of<br />

storage lipids [1].<br />

We first analysed carbohydrate dynamics in developing linseed (Linum usitatissimum<br />

L.) embryos on a developmental timescale by measuring the storage product contents<br />

over time. Contrary to rapeseed, linseed accumulates very little starch, and the rate of<br />

net starch degradation is about a hundredfold lower than the rate of lipid synthesis [2].<br />

In a second approach, the capacity of isolated linseed plastids to synthesise starch was<br />

tested. When fed with [1- 14 C]-glucose 6-phosphate, the isolated plastids surprisingly<br />

synthesise starch at a rate which is nearly a hundred times higher than the net rate of<br />

synthesis in planta [2].<br />

Thirdly, the metabolism of [1- 13 C]-glucose by excised linseed embryos was directly<br />

followed by in vivo NMR. The label was incorporated into sucrose allowing to assess the<br />

rate of sucrose synthesis and the sucrose pool turnover. Label incorporation into fatty<br />

acids however occurred much faster suggesting that most of the incoming sugar<br />

bypasses the sucrose pool, and the latter might rather serve as a buffer on a timescale<br />

of several hours. Label analysis in the starch pool after the incubation period showed<br />

that the starch pool, too, is renewed in less than a day.<br />

[1] P.J. Eastmond and S. Rawsthorne, Plant Physiol. 122, 767 (2000)<br />

[2] S. Troufflard et al., Proceedings 16 th Intern. Symp. Plant <strong>Lipid</strong>s, Budapest (2004)

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