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Development of a recovery and recycle process for a pseudomonas lipase used for large‐scale enzymatic synthesis
Author(s) -
Junker B. H.,
Bhupathy M.,
Buckland B. C.
Publication year - 1993
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.260420412
Subject(s) - chemistry , lipase , catalysis , substrate (aquarium) , hydrolysis , chromatography , enzyme , ultrafiltration (renal) , immobilized enzyme , triacylglycerol lipase , aqueous solution , organic chemistry , oceanography , geology
Enzymes are potential catalysts for a wide range of large‐scale chemical synthesis steps, particularly when the creation of a specific chiral center is desired. The efficient recycling of the enzyme catalyst and the removal of carryover impurities were crucial factors in the improvement of a stereoselective ester hydrolysis step used in the synthesis of a selective leukotriene antagonist. In this enzymatic reaction step, the substrate and product were both largely insoluble, while the enzyme was soluble in the aqueous reaction mixture. Microfiltration and ultrafiltration of the slurry reaction mother liquor indicated near 100% enzyme protein recovery, while activity recovery was about 70% to 80%. These activity losses might be accounted for by enzyme degradation (1 to 2 mg/L · h) during the 40‐hour reaction period. Dissolved impurities, principally a diacid byproduct, in the enzyme recycling stream were reduced 60% to 70% by either lowering the solution pH to 4.0 or raising the solution ionic strength to 1 M . © 1993 John Wiley & Sons, Inc.