Putz Sebastian, Teetz Niklas, Abt Michael, Jerono Pascal, Meurer Thomas, Franzreb Matthias
Department for Bioengineering and Biosystems, Karlsruhe Institute of Technology (KIT), Institute of Functional Interfaces (IFG), Eggenstein-Leopoldshafen, Germany.
Department for Electrobiotechnology, Karlsruhe Institute of Technology (KIT), Institute of Process Engineering in Life Sciences (BLT), Karlsruhe, Germany.
Biotechnol Bioeng. 2025 Nov;122(11):3018-3036. doi: 10.1002/bit.70038. Epub 2025 Aug 4.
Optimizing enzymatic catalysis is crucial for enhancing the efficiency and scalability of many bioprocesses such as biotransformations, pharmaceutical synthesis, and food processing, as well as for improving the performance of analytical applications, including assays and biosensors. However, optimizing these reactions is challenging due to the multitude of interacting parameters such as pH, temperature, and cosubstrate concentration that require precise adjustment for maximum enzyme activity. Current optimization methods are often labor-intensive and time-consuming, especially when accounting for complex parameter interactions in highly dimensional parameter spaces. To overcome these challenges, we present a machine learning-driven laboratory platform that enables rapid, data-informed optimization of enzymatic reaction conditions in a fully automated environment. By conducting over 10,000 simulated optimization campaigns on a surrogate model generated via linear interpolation of experimentally obtained data, we identified and fine-tuned the most efficient machine learning algorithm for optimizing enzymatic reactions. This allows the platform to autonomously determine optimal reaction conditions with minimal experimental effort and without human intervention. The effectiveness of our approach is demonstrated by the accelerated optimization of reaction conditions in a five-dimensional design space across multiple enzyme-substrate pairings. In conclusion, our self-driving lab platform, equipped with a tailored optimization algorithm, offers a novel and superior alternative to traditional optimization methods. Moreover, the methodology for selecting the most efficient problem-specific optimization algorithm can be extended to self-driving lab platforms with broader applications.
优化酶催化对于提高许多生物过程(如生物转化、药物合成和食品加工)的效率和可扩展性至关重要,对于改善包括分析测定和生物传感器在内的分析应用性能也很关键。然而,由于存在众多相互作用的参数,如pH值、温度和共底物浓度,需要精确调整以实现最大酶活性,因此优化这些反应具有挑战性。当前的优化方法通常劳动强度大且耗时,尤其是在考虑高维参数空间中复杂的参数相互作用时。为了克服这些挑战,我们提出了一个机器学习驱动的实验室平台,该平台能够在全自动环境中对酶促反应条件进行快速、基于数据的优化。通过对通过实验获得的数据进行线性插值生成的替代模型进行超过10000次模拟优化活动,我们识别并微调了用于优化酶促反应的最有效机器学习算法。这使得该平台能够以最少的实验工作量且无需人工干预自主确定最佳反应条件。我们的方法的有效性通过在跨多个酶-底物对的五维设计空间中加速反应条件优化得到了证明。总之,我们配备定制优化算法的自动驾驶实验室平台为传统优化方法提供了一种新颖且优越的替代方案。此外,选择最有效问题特定优化算法的方法可以扩展到具有更广泛应用的自动驾驶实验室平台。