NOVEMBER 5-9, 2000    KANSAS CITY, MISSOURI

A A C C   2 0 0 0   A n n u a l   M e e t i n g

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Molecular bases of kernel hardness as probed by confocal Raman microspectroscopy: An investigation on the role of endosperm cell walls.
O. PIOT (1), J. C. Autran (2), and M. Manfait (1). (1) Laboratoire de Spectroscopie Biomoléculaire, Université de Reims; (2) Unité de Technologie des Céréales et des Agropolymères, INRA Montpellier.

In order to optimize the milling of Triticum aestivum wheat grains, we have undertaken to study the molecular bases of the grain cohesion. After having characterized the starch granule - protein matrix interface within the central starchy endosperm, and established a correlation between the a helical secondary structure of interstitial proteins (protein content between starch granules) and kernel hardness, we are presently looking more into the role of endosperm cell walls in the adhesive forces which maintain the kernel structure. To do so, we are employing confocal Raman microspectroscopy. We have shown that arabinoxylans chains (main component of the cell walls ramified by esterified ferulic acid) could be linked to proteins and, more surprisingly to lipids (phospholipids), via ferulic esters. Furthermore, by following the evolution of cell walls at different maturation stages (during the period of ripening and desiccation of the grain,), we have observed that, within the cell walls, the ferulic content increases while the protein content decreases when the kernel hardens. The modification of the molecular organization in the walls would reflect their reinforcement upon ripening. These results show that Raman microspectroscopy is a very efficient technique in establishing certain bases of the grain cohesion, implicating the central endosperm cell walls.

 


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