## ABSTRACX A recently developed semiempirical model of saccharide optical activity is used to calculate the Nan rotation of methyl @-xylobioside in solution as a function of its conformation. Combining the results with published conformational-energy calculations leads to a picture in which folde
Lactose conformation in aqueous solution from optical rotation
โ Scribed by Christopher A. Duda; Eugene S. Stevens
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 313 KB
- Volume
- 206
- Category
- Article
- ISSN
- 0008-6215
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โฆ Synopsis
A newly developed calculational model for saccharide optical rotation'+ has recently been extended to disaccharides, with applications to cellobiose and maltose'.
Here we apply the model to /?-lactose v-D-galactopyranosyl-( 1+4)-p-D-glucopyranose]. The purpose in doing so is to demonstrate that the model can account for the large difference in optical activity between two disaccharides, lactose and cellobiose, having the same chemical structure in the linkage region, and to develop a picture of the conformational variations of lactose in aqueous solution compatible with calculated potential-energy surfaces,6'7 n.m.r. studies,8,9 and measured optical rotation".
The calculational method, previously described in detaillm5, is based on a coupledoscillator model which requires the solution of the secular equations:
๐ SIMILAR VOLUMES
A chiroptical method of conformational analysis is applied to linear ( 1 + 3 ) -p-D-glucans and the dimeric analogues pand a-laminaribioside. The method is based on a recently developed semiempirical calculational model for saccharide optical activity. We conclude that disaccharide conformational en
The bulk crystallization of a-lactose monohydrate from aqueous solution by primary nucleation has been studied under controlled conditions of supersaturation, temperature, and pH. The induction times to nucleation were extremely long compared with those generally observed for other materials, even a
1,6-Anhydro-o-pyranoses and methyl 3,6-anhydro-o-pyranosides (Fig. 1) take up crystal structures'-4 in which the ring form approximates 'C,. We have applied a recently developed calculational model of saccharide optical activity to a series of anhydro sugars with the aim of interpreting observed sol