Slalom chromatography is an alternative chromatographic procedure for the a
nalysis of relatively large double-stranded DNA molecules and is based on a
hydrodynamic principle. The retardation of the DNA fragments from the clea
vage of the Lambda DNA by the KpnI restriction enzyme was studied using an
acetonitrile-phosphate buffer as a mobile phase (flow rate equal to 0.3 ml/
min) and a C1 column as a stationary phase at various temperatures. It was
shown that the temperature constituted an important parameter for the separ
ation of the DNA fragments in slalom chromatography. The DNA hydrodynamic b
ehavior with the temperature was related to the variation in the fluid visc
osity and the modification of the elastic properties of the biopolymer. (C)
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