Mutarotation

mutarotation [¦myüd·ə·rō′tā·shən]

(chemistry)

A change in the optical rotation of light that takes place in the solutions of freshly prepared sugars.

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Mutarotation 

a gradual change in the optical activity of freshly prepared solutions of monosaccharides and some other optically active compounds. Mutarotation is a result of the inter-conversion of tautomeric forms of monosaccharides, leading to the establishment of a dynamic equilibrium between the forms. Thus, upon completion of mutarotation a solution of glucose has a specific rotation [α ]_p²⁰ of +52.5° and consists of 37 percent α-glucose with [α]_p²⁰ of +112° and 63 percent β-glucose with [a]_p²⁰ of +18.7°.

The rate of mutarotation depends on the temperature and nature of the solvent; it increases in the presence of acids and bases and particularly in the presence of bifunctional acid-base catalysts such as 2-oxypyridine. In living organisms, the mutarotation of monosaccharides and disaccharides is catalyzed by the enzyme aldose 1-epimerase.

REFERENCE

Khimiia uglevodov. Moscow, 1967.