β-Glucans occur in the bran of grasses (Gramineae) such as barley, oats, rye and wheat, generally in amounts of about 7%, 5%, 2% and less than 1% respectively..

β-Glucans consist of linear
unbranched polysaccharides of linked β-(1
3)-
and β-(1
4)-D-glucopyranose
units in a non-repeating but non-random order. [Back to Top
]
β-Glucans form 'worm'-like cylindrical
molecules containing up to about 250,000 glucose residues
that may produce cross-links between regular areas containing
consecutive cellotriose units. They agregate in solution
[1681] to form thermoreversible
infinite network gels. 90% of the β-(1
4)-
links are in cellotriosyl and cellotetraosyl units joined
by single β-(1
3)-links
with no single β-(1
4)-
or double β-(1
3)-links
[234]. The ratio of
cellotriosyl/cellotetraosyl is about 2.0-2.4 in oats, about
3.0 in barley and about 3.5 in wheat. A recent intervarietal
study of glucans from barley and oats has been completed [787]. [Back to Top
]
The main use of β-glucans is in texturizing as fat substitutes. They are recognized as having important positive health benefits centered around their benefits in coronary heart disease, cholesterol lowering and reducing the glycemic response. Such health benefits are linked to its high viscosity although it may be that some of these effects are due to appetite suppression. High molecular weight β-glucans are viscous due to labile cooperative associations whereas lower molecular weight β-glucans can form soft gels as the chains are easier to rearrange to maximize linkages. Barley β-glucan is highly viscous and pseudoplastic, both properties decreasing with increasing temperature [748]. These properties cause difficulty in the brewing industry, negatively affecting fermentation and filtration.
Note that the related hydrocolloid curdlan has only β-(1
3)-D-glucopyranose
units which form thermoreversible triple helical structures on heating
and become irreversibly linked as the concentration or temperature
increases.
Interactive structures are available (Jmol). [Back to Top
]
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This page was last updated by Martin Chaplin on 10 April, 2012