ABSTRACTThe polysaccharides, such as κ-carrageenan, ι-carrageenan, aga dịch - ABSTRACTThe polysaccharides, such as κ-carrageenan, ι-carrageenan, aga Việt làm thế nào để nói

ABSTRACTThe polysaccharides, such a

ABSTRACT
The polysaccharides, such as κ-carrageenan, ι-carrageenan, agarose (agar), gellan gum, amylose, curdlan, algi-
nate, and deacetylated rhamsan gum, in water changed into an ice-like structure with hydrogen bonding between
polymer and water molecules, and between water-water molecules even at a concentration range of 0.1% - 1.0%
(W/V) at room temperature, resulting in gelation. Such dramatic changes from liquid into gels have been un-
derstood at the molecular level in principles. In this review, we describe the structure-function relationship of
starch on the view point of rheological aspects and discuss gelatinization and retrogradation mechanism includ-
ing water molecules at molecular level. The starch molecules (amylose and amylopectin) play a dominant role in
the center of the tetrahedral cavities occupied by water molecules, and the arrangement is partially similar to a
tetrahedral structure in a gelatinization process. The arrangement should lead to a cooperative effect stabilizing
extended regions of ice-like water with hydrogen bonding on the surface of the polymer molecules, where he-
miacetal oxygen and hydroxyl groups might participate in hydrogen bonding with water molecules. Thus, a
more extended ice-like hydrogen bonding within water molecules might be achieved in a retrogradation process.
Though many investigations not only include starch gelatinization and retrogradaion, but also the gelling prop-
erties of the polysaccharides have been undertaken to elucidate the structure-function relationship, no other re-
searchers have established mechanism at the molecular level. There is reasonable consistency in our investiga-
tions.
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ABSTRACTThe polysaccharides, such as κ-carrageenan, ι-carrageenan, agarose (agar), gellan gum, amylose, curdlan, algi-nate, and deacetylated rhamsan gum, in water changed into an ice-like structure with hydrogen bonding between polymer and water molecules, and between water-water molecules even at a concentration range of 0.1% - 1.0% (W/V) at room temperature, resulting in gelation. Such dramatic changes from liquid into gels have been un-derstood at the molecular level in principles. In this review, we describe the structure-function relationship of starch on the view point of rheological aspects and discuss gelatinization and retrogradation mechanism includ-ing water molecules at molecular level. The starch molecules (amylose and amylopectin) play a dominant role in the center of the tetrahedral cavities occupied by water molecules, and the arrangement is partially similar to a tetrahedral structure in a gelatinization process. The arrangement should lead to a cooperative effect stabilizing extended regions of ice-like water with hydrogen bonding on the surface of the polymer molecules, where he-miacetal oxygen and hydroxyl groups might participate in hydrogen bonding with water molecules. Thus, a more extended ice-like hydrogen bonding within water molecules might be achieved in a retrogradation process. Though many investigations not only include starch gelatinization and retrogradaion, but also the gelling prop-erties of the polysaccharides have been undertaken to elucidate the structure-function relationship, no other re-searchers have established mechanism at the molecular level. There is reasonable consistency in our investiga-tions.
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