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The kinetics and mechanism of shear inactivation of lipase from Candida cylindracea
Author(s) -
Lee YuanKun,
Choo ChoonLiang
Publication year - 1989
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.260330207
Subject(s) - kinetics , lipase , mechanism (biology) , chemistry , enzyme kinetics , shear (geology) , enzyme , biophysics , biochemistry , biology , physics , paleontology , quantum mechanics , active site
Abstract Shearing experiments were conducted in a stirred tank reactor with 0.1% lipase solutions of Candida cylindracea. Inactivation of the lipase solutions were observed at various shear rates from 50 to 150 s −1 after continuous shearing for ca. 30‐240 min under optimal pH and temperature conditions. However, there was no shear stress denaturation of the lipase when it was subjected to shear stresses of 0.72‐109.2 kg/m/s 2 and shear rate of 100 s −1 . In the presence of polypropylene glycol, the rate of denaturation of the lipase decreased by 93%. When the lipase solution was filled to the brim, the rate of denaturation of the lipase decreased by 97% compared to that when reactor was half‐filled. The rate of denaturation of the lipase decreased by 61% when probes in the fermentor were removed. There was no significant difference in the rate of denaturation of the lipase under ambient conditions compared with that in the absence of oxygen, or in the absence of free metal ions. Recovery of lipase activity from the first hour of shearing was observed at a shear rate of 150 s −1 . The native lipase and the lipase which had recovered its activity showed similar pH profiles, temperature profiles, and activation energies. Temperature was found to have no effect in the rate of shear‐induced denaturation of the lipase in the range 20 to 30°C during shearing at 100 s −1 and optimal pH. Above 30°C, the rate of denaturation of the lipase increased drastically as a function of temperature. The significance of the findings in the de sign of reactor systems for hydrolysis or esterification of oils by lipase will be discussed.