Barley for Food and Health: Science, Technology, and Products
Barley for Food and Health: Science, Technology, and Products
Barley for Food and Health: Science, Technology, and Products
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64 BARLEY: GENETICS AND NUTRIENT COMPOSITION<br />
In the endosperm they comprise 20 to 25% of the cell wall material <strong>and</strong> 86% in<br />
the aleurone. <strong>Barley</strong> arabinoxylans vary considerably with respect to the ratio of<br />
xylose to arabinose. In hulls, ratios of about 1 : 9 have been observed (Aspinall<br />
<strong>and</strong> Ferrier 1957), whereas in starchy endosperm or aleurone tissues, ratios of<br />
1 : 3 were reported in a number of studies reviewed by MacGregor <strong>and</strong> Fincher<br />
(1993). From the literature it appears that the ratios reported are very dependent<br />
on the solvent used to solubilize the molecules. Arabinoxylans found in<br />
barley generally have a (1-4)-β-xylopyranosyl backbone that supports one or<br />
two α-l-arabinofuranosyl residues. Most arabinose is found as monomeric substituents<br />
but with a small proportion of oligomeric sidechains, consisting of two<br />
or more arabinosyl residues or an arabinosyl residue with a terminal xylosyl<br />
residue (Voragen et al. 1992; Viëtor et al. 1993). Galactosyl, glucosyl, <strong>and</strong> xylosyl<br />
can be present as terminal residues, but are quantitatively minor; however,<br />
glucuronopryanosyl terminal residues may constitute up to 4% by weight of the<br />
arabinoxylan in the hull (Aspinall <strong>and</strong> Ross 1963).<br />
Estimates of arabinoxylan contents of barley grain range from 4 to 7% by<br />
weight, being concentrated in the outer layers of the caryopsis <strong>and</strong> the hull<br />
(Hashimoto et al. 1987). It was reported by Henry (1987) that less than 25%<br />
of total barley arabinoxylan is found in the endosperm, constituting about 1.5%<br />
by weight. Henry (1986) concluded that total arabinoxylan content <strong>and</strong> xylose–<br />
arabinose ratios varied somewhat with genotype but that content varied more,<br />
due to environmental factors. For example, thin or small kernels with low starch<br />
content contain higher amounts of arabinoxylans than large or plump kernels<br />
containing high levels of starch. This is presumed to be because most arabinoxylan<br />
is located in the outer layers of the grain, <strong>and</strong> small thin grains contain<br />
relatively less endosperm than plump large grains. According to MacGregor <strong>and</strong><br />
Fincher (1993), there have been no comprehensive studies on the genetic basis<br />
<strong>for</strong> arabinoxylan levels in barley, nor is there in<strong>for</strong>mation on the number of genes<br />
involved or their location in the genome.<br />
Of all the components of TDF in barley, β-glucans are probably the most<br />
important in terms of human diet <strong>and</strong> health benefits. β-Glucans consist of<br />
high-molecular-weight linear chains of β-glucosyl residues polymerized through<br />
both β-(1,3) <strong>and</strong> β-(1,4) linkages. <strong>Barley</strong> β-glucans are members of a family<br />
of polysaccharides that is heterogeneous with respect to molecular size, solubility,<br />
<strong>and</strong> molecular structure (MacGregor <strong>and</strong> Fincher 1993). Although it is not<br />
possible to show a single structure <strong>for</strong> β-glucan, it has been demonstrated that<br />
blocks of two or three contiguous (1,4)-linked β-glucosyl residues are separated<br />
by single β-(1,3) linkages along the polysaccharide chain (Parrish et al. 1960;<br />
Woodward et al. 1983a). The β-glucosyl units are referred to as cellotriosyls<br />
(trisaccharides) <strong>and</strong> cellotetraosyls (tetrasaccharides). A schematic representation<br />
of barley β-glucan is shown in Figure 4.1.<br />
1,3 : 1,4 - Beta - GLUCAN<br />
FIGURE 4.1<br />
β-Glucan structure.