Microcalorimetric studies on the complex formation between cellobiohydrolase I (CBH I) from Trichoderma reesei and the (R)- and (S)-enantiomers of the β-receptor blocking agent alprenolol
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- 作者：Hedeland ; Mikael ; Henriksson ; Hongbin ; Bä ; ckman ; Per ; Isaksson ; Roland ; Pettersson ; Gö ; ran
- 关键词：Calorimetry ; Association constant ; R- and S-alprenolol ; Cellobiohydrolase I ; Complex formation
- 刊名：Thermochimica Acta
- 出版年：2000
- 出版时间：August 7, 2000
- 年：2000
- 卷：356
- 期：1-2
- 页码：153-158
- 全文大小：126 K
文摘
The thermodynamic quantities for the complex formation between the enantiomers of the β-blocking drug alprenolol and cellobiohydrolase I (CBH I), that earlier has been used as a chiral selector for aminoalcohols, revealed positive ΔH0 — values in all cases implying an entropy driven process. Association constants (Ka) for cellulase and the (R)- and (S)-enantiomers of alprenolol were determined by isothermal titration microcalorimetry and the inhibition constants (Ki) by enzyme inhibition experiments. Both inhibition experiments and microcalorimetry revealed that the affinity between the enantiomers of alprenolol and CBH I was higher in sodium phosphate buffer than in potassium phosphate buffer. This result was in agreement with previously reported liquid chromatographic separations of enantiomers using a chiral stationary phase based on CBH I immobilized to silica particles. The best fit of the isothermal titration data corresponded to a 1:1 binding isotherm.