4.5 Article

Shift of the reaction equilibrium at high pressure in the continuous synthesis of neuraminic acid

Journal

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
Volume 18, Issue -, Pages 567-579

Publisher

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.18.59

Keywords

aldolase; continuous fixed-bed reactor; enzyme; epimerase; GlcNAc; high pressure; immobilization; ManNAc; Neu5Ac; pyruvate

Funding

  1. Federal Ministry of Education and Research [031B0405A]

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The importance of a compound that fights against influenza is self-evident during a pandemic. Continuous flow reactors in chemical industry are considered the next stepping stone for large scale production of these compounds. This study investigates the synthesis of N-acetylneuraminic acid in a continuous fixed-bed reactor using immobilized enzymes, and shows the potential of a high-pressure circular reactor for increasing reaction equilibrium conversion and yield.
The importance of a compound that helps fight against influenza is, in times of a pandemic, self-evident. In order to produce these compounds in vast quantities, many researchers consider continuous flow reactors in chemical industry as next stepping stone for large scale production. For these reasons, the synthesis of N-acetylneuraminic acid (Neu5Ac) in a continuous fixed-bed reactor by an immobilized epimerase and aldolase was investigated in detail. The immobilized enzymes showed high stability, with half-life times > 173 days under storage conditions (6 degrees C in buffer) and reusability over 50 recycling steps, and were characterized regarding the reaction kinetics (initial rate) and scalability (different lab scales) in a batch reactor. The reaction kinetics were studied in a continuous flow reactor. A high-pressure circular reactor (up to 130 MPa) was applied for the investigation of changes in the position of the reaction equilibrium. By this, equilibrium conversion, selectivity, and yield were increased from 57.9% to 63.9%, 81.9% to 84.7%, and 47.5% to 54.1%, respectively. This indicates a reduction in molar volume from N-acetyl-D-glucosamine (GlcNAc) and pyruvate (Pyr) to Neu5Ac. In particular, the circular reactor showed great potential to study reactions at high pressure while allowing for easy sampling. Additionally, an increase in affinity of pyruvate towards both tested enzymes was observed when high pressure was applied, as evidenced by a decrease of K-I for the epimerase and K-M for the aldolase from 108 to 42 mM and 91 to 37 mM, respectively.

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