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Chemoenzymatic Synthesis of Sialic Acid Derivatives Using Immobilized N‐Acetylneuraminate Lyase in a Continuous Flow Reactor

机译:在连续流动反应器中使用固定化的N-乙酰神经氨酸裂解酶化学酶促合成唾液酸衍生物

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摘要

The synthesis of N‐acetylneuraminic acid (Neu5Ac) derivatives is drawing more and more attention in glycobiology research because of the important role of sialic acids in e. g. cancer, bacterial, and healthy cells. Chemical preparation of these carbohydrates typically relies on multistep synthetic procedures leading to low overall yields. Herein we report a continuous flow process involving N‐acetylneuraminate lyase (NAL) immobilized on Immobead 150P (Immobead‐NAL) to prepare Neu5Ac derivatives. Batch experiments with Immobead‐NAL showed equal activity as the native enzyme. Moreover, by using a fivefold excess of either N‐acetyl‐D‐mannosamine (ManNAc) or pyruvate the conversion and isolated yield of Neu5Ac were significantly improved. To further increase the efficiency of the process, a flow setup was designed providing a chemoenzymatic entry into a series of N‐functionalized Neu5Ac derivatives in conversions of 48–82%, and showing excellent stability over 1 week of continuous use.
机译:N-乙酰神经氨酸(Neu5Ac)衍生物的合成由于在唾液酸中的重要作用而在糖生物学研究中越来越受到关注。 G。癌症,细菌和健康细胞。这些碳水化合物的化学制备通常依赖于多步合成程序,导致总产率低。在此,我们报道了一个连续的流动过程,其中涉及固定在Immobead 150P(Immobead-NAL)上的N-乙酰神经氨酸裂解酶(NAL)以制备Neu5Ac衍生物。用Immobead-NAL进行的批量实验显示出与天然酶相同的活性。此外,通过使用五倍过量的N-乙酰基-D-甘露糖胺(ManNAc)或丙酮酸,Neu5Ac的转化率和分离产率得到了显着提高。为了进一步提高该过程的效率,设计了一种流程装置,以化学酶法将一系列N功能化的Neu5Ac衍生物转化为48-82%的化合物,并在连续使用1周内显示出出色的稳定性。

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