"Enzyme Test Bench," a High-Throughput Enzyme Characterization Technique Including the Long-Term Stability

被引:13
|
作者
Rachinskiy, Kirill [1 ]
Schultze, Hergen [2 ]
Boy, Matthias [2 ]
Bornscheuer, Uwe [3 ]
Buechs, Jochen [1 ]
机构
[1] Rhein Westfal TH Aachen, Dept Biochem Engn, D-52074 Aachen, Germany
[2] BASF AG, Ludwigshafen, Germany
[3] Inst Biochem, Greifswald, Germany
关键词
microtiter plate; online monitoring; fluorescent assay; high throughput; esterase; pH-shift; long term stability; experimental design; parameter estimation; modeling; MICROTITER PLATES; LYSOZYME INACTIVATION; THERMAL INACTIVATION; DIRECTED EVOLUTION; TEMPERATURE; BIOCATALYSTS; KINETICS; SHEAR; THERMOSTABILITY; DEACTIVATION;
D O I
10.1002/bit.22242
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A new high throughput technique for enzyme characterization with specific attention to the long term stability, called "Enzyme Test Bench," is presented. The concept of the Enzyme Test Bench consists of short term enzyme tests in 96-well microtiter plates under partly extreme conditions to predict the enzyme long term stability under moderate conditions. The technique is based on the mathematical modeling of temperature dependent enzyme activation and deactivation. Adapting the temperature profiles in sequential experiments at optimal non-linear experimental design, the long term deactivation effects can be purposefully accelerated and detected within hours. During the experiment the enzyme activity is measured online to estimate the model parameters from the obtained data. Thus, the enzyme activity and long term stability can be calculated as a function of temperature. The engineered instrumentation provides for simultaneous automated assaying by fluorescent measurements, mixing and homogenous temperature control in the range of 10-85 +/- 0.5 degrees C. A universal fluorescent assay for online acquisition of ester hydrolysis reactions by pH-shift is developed and established. The developed instrumentation and assay are applied to characterize two esterases. The results Of the characterization, carried out in microtiter plates applying short term experiments of hours, are in good agreement with the results of long term experiments at different temperatures in 1 L stirred tank reactors of a week. Thus, the new technique allows for both: the enzyme screening with regard to the long term stability and the choice of the optimal process temperature regarding Such process parameters as turn over number, space time yield or optimal process duration. The comparison of the temperature dependent behavior of both characterized enzymes clearly demonstrates that the frequently applied estimation of long term stability at moderate temperatures by simple activity measurements after exposing the enzymes to elevated temperatures may lead to suboptimal enzyme selection. Thus, temperature dependent enzyme characterization is essential in primary screening to predict its long term behavior. Biotechnol. Bioeng. 2009;103: 305-322. (C) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:305 / 322
页数:18
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