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新型脂肪酶-辛基琼脂糖生物催化 2-芳基丙酸衍生物的方法。

A New Approach in Lipase-Octyl-Agarose Biocatalysis of 2-Arylpropionic Acid Derivatives.

机构信息

Department of Laboratory Medicine, Faculty of Pharmacy, Ludwik Rydygier Collegium Medicum, Nicolaus Copernicus University in Toruń, 85-094 Bydgoszcz, Poland.

Department of Medicinal Chemistry, Faculty of Pharmacy, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, 85-089 Bydgoszcz, Poland.

出版信息

Int J Mol Sci. 2024 May 7;25(10):5084. doi: 10.3390/ijms25105084.

Abstract

The use of lipase immobilized on an octyl-agarose support to obtain the optically pure enantiomers of chiral drugs in reactions carried out in organic solvents is a great challenge for chemical and pharmaceutical sciences. Therefore, it is extremely important to develop optimal procedures to achieve a high enantioselectivity of the biocatalysts in the organic medium. Our paper describes a new approach to biocatalysis performed in an organic solvent with the use of CALB-octyl-agarose support including the application of a polypropylene reactor, an appropriate buffer for immobilization (Tris base-pH 9, 100 mM), a drying step, and then the storage of immobilized lipases in a climatic chamber or a refrigerator. An immobilized lipase B from (CALB) was used in the kinetic resolution of (,)-flurbiprofen by enantioselective esterification with methanol, reaching a high enantiomeric excess (ee = 89.6 ± 2.0%). As part of the immobilization optimization, the influence of different buffers was investigated. The effect of the reactor material and the reaction medium on the lipase activity was also studied. Moreover, the stability of the immobilized lipases: lipase from (CRL) and CALB during storage in various temperature and humidity conditions (climatic chamber and refrigerator) was tested. The application of the immobilized CALB in a polypropylene reactor allowed for receiving over 9-fold higher conversion values compared to the results achieved when conducting the reaction in a glass reactor, as well as approximately 30-fold higher conversion values in comparison with free lipase. The good stability of the CALB-octyl-agarose support was demonstrated. After 7 days of storage in a climatic chamber or refrigerator (with protection from humidity) approximately 60% higher conversion values were obtained compared to the results observed for the immobilized form that had not been stored. The new approach involving the application of the CALB-octyl-agarose support for reactions performed in organic solvents indicates a significant role of the polymer reactor material being used in achieving high catalytic activity.

摘要

将脂肪酶固定在辛基琼脂糖载体上,以在有机溶剂中进行的反应中获得手性药物的对映纯异构体,这对化学和制药科学来说是一个巨大的挑战。因此,开发最佳程序以实现生物催化剂在有机介质中的高对映选择性非常重要。我们的论文描述了一种在有机溶剂中进行生物催化的新方法,该方法使用了 CALB-辛基琼脂糖载体,包括使用聚丙烯反应器、合适的固定化缓冲液(Tris 碱,pH9,100mM)、干燥步骤,然后将固定化脂肪酶储存在气候室或冰箱中。使用来自 (CALB)的固定化脂肪酶 B 通过与甲醇的对映选择性酯化动力学拆分(,)-氟比洛芬,达到高对映过量(ee=89.6±2.0%)。作为固定化优化的一部分,研究了不同缓冲液的影响。还研究了反应器材料和反应介质对脂肪酶活性的影响。此外,还测试了固定化脂肪酶:来自 (CRL)和 CALB 的稳定性,在不同温度和湿度条件(气候室和冰箱)下储存。在聚丙烯反应器中应用固定化 CALB 可获得比在玻璃反应器中进行反应时高 9 倍以上的转化率值,并且与游离脂肪酶相比,转化率值高约 30 倍。证明了固定化 CALB-辛基琼脂糖载体具有良好的稳定性。在气候室或冰箱中储存 7 天(避免受潮)后,与未储存的固定化形式相比,获得了约 60%更高的转化率值。涉及在有机溶剂中进行反应时应用 CALB-辛基琼脂糖载体的新方法表明,使用聚合物反应器材料在实现高催化活性方面具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3737/11121684/ac7b375fde21/ijms-25-05084-g001.jpg

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