A method for 13C‐labeling of metabolic carbohydrates within French bean leaves (Phaseolus vulgaris L.) for decomposition studies in soils |
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Authors: | Cyril Girardin Daniel P. Rasse Philippe Biron Jaleh Ghashghaie Claire Chenu |
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Affiliation: | 1. INRA, UMR 7618 Bioemco, F‐78850 Thiverval Grignon, France;2. Norwegian Institute for Agricultural and Environmental Research, 1432 ?s, Norway;3. University of Paris VI, UMR 7618 Bioemco, F‐78850 Thiverval Grignon, France;4. Laboratoire Ecologie Systématique et Evolution, CNRS‐UMR 8079, Batiment 362, Université Paris‐Sud, F‐91405 Orsay cedex, France;5. Plateforme Métabolisme‐Métabolome, IFR 87 “La Plante et son Environnement”, Institut de Biotechnologie des Plantes (IBP), Batiment 630, Université Paris‐Sud, F‐91405 Orsay cedex, France;6. AgroParisTech, UMR 7618 Bioemco, F‐78850 Thiverval Grignon, France |
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Abstract: | The molecular composition of plant residues is suspected to largely govern the fate of their constitutive carbon (C) in soils. Labile compounds, such as metabolic carbohydrates, are affected differently from recalcitrant and structural compounds by soil‐C stabilisation mechanisms. Producing 13C‐enriched plant residues with specifically labeled fractions would help us to investigate the fate in soils of the constitutive C of these compounds. The objective of the present research was to test 13C pulse chase labeling as a method for specifically enriching the metabolic carbohydrate components of plant residues, i.e. soluble sugars and starch. Bean plants were exposed to a 13CO2‐enriched atmosphere for 0.5, 1, 2, 3 and 21 h. The major soluble sugars were then determined on water‐soluble extracts, and starch on HCl‐hydrolysable extracts. The results show a quick differential labeling between water‐soluble and water‐insoluble compounds. For both groups, 13C‐labeling increased linearly with time. The difference in δ13C signature between water‐soluble and insoluble fractions was 7‰ after 0.5 h and 70‰ after 21 h. However, this clear isotopic contrast masked a substantial labeling variability within each fraction. By contrast, metabolic carbohydrates on the one hand (i.e. soluble sugars + starch) and other fractions (essentially cell wall components) on the other hand displayed quite homogeneous signatures within fractions, and a significant difference in labeling between fractions: δ13C = 414 ± 3.7‰ and 56 ± 5.5‰, respectively. Thus, the technique generates labeled plant residues displaying contrasting 13C‐isotopic signatures between metabolic carbohydrates and other compounds, with homogenous signatures within each group. Metabolic carbohydrates being labile compounds, our findings suggest that the technique is particularly appropriate for investigating the effect of compound lability on the long‐term storage of their constitutive C in soils. Copyright © 2009 John Wiley & Sons, Ltd. |
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