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首页> 外文期刊>Chemical Engineering Science >Model-based characterization of operational stability of multimeric enzymes with complex deactivation behavior: An in-silico investigation
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Model-based characterization of operational stability of multimeric enzymes with complex deactivation behavior: An in-silico investigation

机译:具有复杂失活行为的多聚酶的操作稳定性的基于模型的表征:计算机模拟研究

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摘要

A comprehensive characterization of the enzyme kinetics and stability is required in order to design biotransformation processes efficiently. In particular, the characterization of the operational stability (stability under process conditions) of biocatalysts lacks established procedures and the few reported procedures have hardly been evaluated by transfer to reactor scale. In the scope of this modeling study three potentially applicable characterization methods were tested: (i) progress curves recorded at different temperatures; (ii) isothermal continuous reactor operation at different (elevated) temperatures; and (iii) continuous reactor operation with a temperature gradient. Input data from those procedures were generated in-silico by introducing two virtual dimeric enzymes with defined, complex deactivation mechanisms. The applied degradation pathways account for experimentally proven phenomena, which were neglected in operational stability descriptions so far, such as multiple intermediate unfolding state and subunit dissociation. By introducing a random normal error data sets with typical experimental variance were generated. On the basis of these data a model-based experimental analysis for parameter estimation was applied which included the testing of different simplified models (with increasing complexity until over-parameterization became evident). The obtained fits were evaluated by the lack of fit variance and the significance level of the F-statistics. Both criteria indicated a dimeric model with two intermediate unfolding states as best description, which was the model with the highest similarity to the models that had been applied to produce the data in the first place. When subjecting the obtained parameterization to a virtual process design task the quality of the prediction could be easily tested by comparison with the prediction from the original mechanistic model that was used to produce the input data. The obtained results clearly indicate that the often used Lumry-Eyring type models should not be used as empiric description for potentially complex multimeric enzyme deactivation mechanisms as it is done in current operational stability investigations. Next, for the continuous reactor procedures a nice correlation between the obtained significance level of the F-statistics and the accuracy of process prediction was found demonstrating the usefulness of these experimental procedures for parameter estimation. Further, it was possible to estimate a specific threshold significance level that can be used as an indicator for reliable parameterizations with respect to process design.
机译:为了有效设计生物转化过程,需要对酶动力学和稳定性进行全面表征。特别是,生物催化剂的操作稳定性(在工艺条件下的稳定性)的表征缺乏既定的程序,几乎没有报道的程序已通过转移至反应器规模进行评估。在该建模研究的范围内,测试了三种可能适用的表征方法:(i)在不同温度下记录的进度曲线; (ii)等温连续反应器在不同(升高)温度下的运行; (iii)具有温度梯度的连续反应器操作。通过引入两种具有定义的复杂失活机制的虚拟二聚酶,从计算机上获得了来自那些程序的输入数据。应用的降解途径解释了经过实验证明的现象,这些现象在到目前为止的操作稳定性描述中都被忽略,例如多个中间展开状态和亚基解离。通过引入随机正态误差,产生了具有典型实验方差的数据集。基于这些数据,进行了基于模型的参数估计实验分析,其中包括对不同简化模型的测试(随着复杂性的增加,直到出现过度参数化为止)。通过缺乏拟合方差和F统计量的显着性水平来评估获得的拟合。这两个标准都表明一个具有两个中间展开状态的二聚体模型是最好的描述,该模型是与最初用于生成数据的模型具有最高相似性的模型。当对获得的参数化进行虚拟过程设计任务时,可以通过与用于生成输入数据的原始机械模型的预测进行比较,轻松地测试预测的质量。所获得的结果清楚地表明,不应将常用的Lumry-Eyring类型模型用作潜在的复杂多聚酶失活机制的经验描述,因为它已在当前的操作稳定性研究中完成。接下来,对于连续反应器程序,发现所获得的F统计量的显着性水平与过程预测的准确性之间存在良好的相关性,这证明了这些实验程序对于参数估计的有用性。此外,可以估计特定的阈值显着性水平,该阈值显着性水平可以用作针对过程设计进行可靠参数化的指标。

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