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Structure of cellulose II hydrate
Author(s) -
Lee David M.,
Blackwell John
Publication year - 1981
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.1981.360201010
Subject(s) - hydrate , chemistry , cellulose , crystallography , molecule , monoclinic crystal system , crystal structure , organic chemistry
A hydrate of cellulose II can be formed by swelling Fortisan fibers in hydrazine and then washing in water. The hydrate is stable at 93% relative humidity and has a monoclinic unit cell with dimensions a = 9.02 Å, b = 9.63 Å, c = 10.34 Å, and γ = 116.0°; the space group is P 2 1 . The unit cell contains disaccharide sections of two chains and approximately four water molecules. The structure was refined using the LALS method, based on 10 observed and 10 unobserved reflections. An antiparallel arrangement of adjacent chains was assumed, since this occurs in cellulose II (the starting material), and the hydrate also reverts to cellulose II on dehydration. Refinement of the positions and side‐chain conformations of the chains shows that the chains are stacked in the same way as in cellulose II, and the hydrate is formed by insertion of water molecules between the stacks. However, all efforts to arrange the water molecules in crystallographically regular positions led to unsatisfactory agreement between the observed and calculated intensities. These results suggest an irregular arrangement of the water molecules, which was modeled using water‐weighted atomic scattering factors. The analysis resulted in two refined models with relative chain staggers of ∼ + c /4 and ∼ ‐ c /4, which are indistinguishable in terms of the x‐ray agreement. Our preference is for the + c /4 model, for which the stacks of chains are analogous to those in cellulose II.

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