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Production of N-Acetyl-d-Neuraminic Acid by Use of an Efficient Spore Surface Display System

机译:通过使用高效的孢子表面展示系统生产N-乙酰基-d-神经氨酸

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Production of N -acetyl-d-neuraminic acid (Neu5Ac) via biocatalysis is traditionally conducted using isolated enzymes or whole cells. The use of isolated enzymes is restricted by the time-consuming purification process, whereas the application of whole cells is limited by the permeability barrier presented by the microbial cell membrane. In this study, a novel type of biocatalyst, Neu5Ac aldolase presented on the surface of Bacillus subtilis spores, was used for the production of Neu5Ac. Under optimal conditions, Neu5Ac at a high concentration (54.7 g liter~(?1)) and a high yield (90.2%) was obtained under a 5-fold excess of pyruvate over N -acetyl-d-mannosamine. The novel biocatalyst system, which is able to express and immobilize the target enzyme simultaneously on the surface of B. subtilis spores, represents a suitable alternative for value-added chemical production.
机译:传统上,通过生物催化生产N-乙酰基-d-神经氨酸(Neu5Ac)是使用分离的酶或整个细胞进行的。分离的酶的使用受到费时的纯化过程的限制,而整个细胞的应用受到微生物细胞膜呈现的通透性屏障的限制。在这项研究中,枯草芽孢杆菌孢子表面上出现的新型生物催化剂Neu5Ac醛缩酶被用于生产Neu5Ac。在最佳条件下,丙酮酸比N-乙酰基-d-甘露糖胺高5倍,可获得高浓度(54.7 g升(?1))和高产率(90.2%)的Neu5Ac。能够同时在枯草芽孢杆菌孢子表面上表达和固定目标酶的新型生物催化剂系统代表了增值化学生产的合适替代方法。

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