Process for stereoselectively hydrolyzing, transesterifying or esterifying with immobilized isozyme of lipase from candida rugosa

作者: Carrington S. Cobbs , Adrien P. Malick , Gary J. Calton , Animesh Goswami , John P. Hamman

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摘要: An immobilized isozyme of Lipase MY or AY from Candida rugosa is used for stereoselectively hydrolyzing racemic mixtures esters 2-substituted acids, other than 2-halo propionic transesterifying acids esterify alcohols, at high enantiomeric excess, in an organic solvent. Immobilization the may be carried out presence acid such as stearic acid. The with a fatty ester that increases stereoselectivity rate hydrolysis mixture esters.

参考文章(26)
Takaharu Matsuo, Norio Sawamura, Kazunobu Tsumura, Yoshitaka Ebihara, Process for preparing enzyme preparation ,(1987)
Takaharu Matsuo, Norio Sawamura, Wataru Hashida, Yukio Hashimoto, Method for enzymatic transesterification of lipid and enzyme used therein ,(1981)
Frank J. Smith, Jerry M. Roper, (S) α-(cyano-3-phenoxy-benzyl acetate ,(1985)
Samun K. Dahod, Patricia Siuta-Mangano, Carbon tetrachloride-promoted stereo selective hydrolysis of methyl-2-chloropropionate by lipase. Biotechnology and Bioengineering. ,vol. 30, pp. 995- 999 ,(1987) , 10.1002/BIT.260300813
G. Benzonana, S. Esposito, On the positional and chain specificities of Candida cylindracea lipase Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. ,vol. 231, pp. 15- 22 ,(1971) , 10.1016/0005-2760(71)90251-7
John Caldwell, Andrew J. Hutt, Sylvie Fournel-Gigleux, The metabolic chiral inversion and dispositional enantioselectivity of the 2-arylpropionic acids and their biological consequences Biochemical Pharmacology. ,vol. 37, pp. 105- 114 ,(1988) , 10.1016/0006-2952(88)90762-9