Curdlan gum is a microbial fermentation extracellular polymer prepared
commercially from a mutant strain of Alcaligenes faecalis var. myxogenes. It is relatively expensive by weight but becoming
rather less so.

Curdlan gum is an a moderate molecular weight (DP~450) unbranched
linear 1
3 β-D
glucan (M.Wt. ~100K) with no side-chains. [Back to Top
]
Curdlan gum has junction zones consisting of parallel in-phase triple
right-handed six-fold helices (fibre repeat 18.78 Å) [503]
forming an uncharged rigid rod-like conformation. The chains are
held by intra-helix hydrogen bonding between the 2-OH groups; each
such group hydrogen bonding by donation to one chain and acceptance
from the other chain on the inside of the helix axis. As single
stranded curdlan forms a six-fold helix stabilized by a chain of
intramolecular hydrogen bonds between neighboring 2-OH groups, the
change from single to triple helices involves these 2-OH groups
changing their hydrogen bonding allegiance from intramolecular to
intermolecular. [Back to Top
]
Curdlan gum is tasteless and produces retortable freezable food elastic gels. It is insoluble in cold watera but aqueous suspensions plasticize and briefly dissolve before producing reversible gels (that is, curdling, hence its name) on heating to around 55°C [504]. Heating at higher temperatures produces more resilient irreversible gels, which then remain on cooling, by the aggregation of the triple-helical structures and syneresis. The 'curds' consist of mixtures of single and triple helices. Salts tend to prevent curdlan from gelling and their presence weakens the final gels [504].
Scleroglucan (from Sclerotinia sclerotiorum) is also a
1
3 β-D
glucan but has additional 1
6 β-links
that confer solubility under ambient conditions but do not significantly
interfere with a triple helix gelling process similar to curdlan.
Similar polysaccharides can be also extracted from other sources
such as waste yeast.
Interactive structures are available (Chime). [Back to Top
]
a Curdlan is soluble in dimethylsufoxide []. [Back]
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This page was last updated by Martin Chaplin on 23 June, 2008