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Arabinoxylan
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Arabinoxylan is a form of the found in both the primary and secondary of plants which in addition to contains substantial amounts of another , .Scheller, H. V., & Ulvskov, P. (2010). Hemicelluloses. Annual Review of Plant Biology, 61, 263-289. The term arabinoxylan usually refers to feruloyl-arabinoxylan from and other containing moieties of the phenolic that can undergo oxidative coupling (in the same way as units) forming between arabinoxylan chains and with lignin. Whilst arabinose has been found linked to xylan in non-commelinid plants, ferulic acid has not been reported on these and unlike feruloyl-arabinoxylan these arabinoxylans are not . The remainder of this article refers to feruloyl-arabinoxylan from cell walls of and other species.


Structure
As with all xylan, the backbone of arabinoxylan chains is composed of a large number of 1,4-linked β-D-xylopyranosyl units. In arabinoxylan many of these xylose units are 3-linked with single α-L-arabinofuranosyl units and some of these arabinose in turn have ester-linked ferulic acid residues. These feruloyl units can undergo radical oxidative coupling forming ferulic acid dehydrodimers and possibly higher oligomers that covalently crosslink arabinoxylan chains. This mode of cross-linking is a key feature of both primary and secondary cell walls in and other species.

Due to its importance in food, the structure of arabinoxylan from wheat grain and other cereals has been intensively studied. In particular, the arabinoxylan from wheat endosperm that gives rise to white flour has a simpler structure than that from most tissues. Apart from the structural features described above, it has xylose units di-substituted with 2 and 3-linked residues. Due to a low degree of crosslinking into the cell wall, some of this endosperm arabinoxylan is extractable in water, giving rise to soluble dietary fiber.

Arabinoxylans from tissues other than endosperm are structurally more complex. The xylan backbone is often heavily substituted with resides and other sugars and these arabinoxylan polymers are sometimes termed glucuronarabinoxylans or heteroxylans. Both backbone and sidechain sugar residues can be acetylated. Arabinosyl residues can be acylated with phenolics other than ferulic acid, in particular but also and others. These acylated arabinosyl residues are frequently additionally substituted with 2-linked sugars. In lignified cell walls, there is strong evidence that feruloyl residues on arabinoxylan can be crosslinked into the lignin polymer, increasing recalcitrance to digestion.


Functions
Arabinoxylans chiefly serve a structural role in the .Wakabayashi K, et al (2005). Physiologia Plantarum. 125:127–134 They are also the reservoirs of large amounts of and other which are to them. Phenolic acids may also be involved in defense including protection against .

Arabinoxylans are one of the main components of soluble and insoluble which are shown to exert various health benefits. In addition, arabinoxylans, owing to their bound phenolic acids, are shown to have activity. Their ion exchange capacity and viscosity are also partly responsible for their beneficial metabolic effects.

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