Enzymatic Synthesis of Sialic Acids in Microfluidics to Overcome Cross-Inhibitions and Substrate Supply Limitations

ACS Appl Mater Interfaces. 2021 Oct 20;13(41):49433-49444. doi: 10.1021/acsami.1c12307. Epub 2021 Oct 6.

Abstract

Multienzymatic cascade reactions are a powerful strategy for straightforward and highly specific synthesis of complex materials, such as active substances in drugs. Cross-inhibitions and incompatible reaction steps, however, often limit enzymatic activity and thus the conversion. Such limitations occur, e.g., in the enzymatic synthesis of the biologically active sialic acid cytidine monophosphate N-acetylneuraminic acid (CMP-Neu5Ac). We addressed this challenge by developing a confinement and compartmentalization concept of hydrogel-immobilized enzymes for improving the efficiency of the enzyme cascade reaction. The three enzymes required for the synthesis of CMP-Neu5Ac, namely, N-acyl-d-glucosamine 2-epimerase (AGE), N-acetylneuraminate lyase (NAL), and CMP-sialic acid synthetase (CSS), were immobilized into bulk hydrogels and microstructured hydrogel-enzyme-dot arrays, which were then integrated into microfluidic devices. To overcome the cytidine triphosphate (CTP) cross-inhibition of AGE and NAL, only a low CTP concentration was applied and continuously conveyed through the device. In a second approach, the enzymes were compartmentalized in separate reaction chambers of the microfluidic device to completely avoid cross-inhibitions and enable the use of higher substrate concentrations. Immobilization efficiencies of up to 25% and pronounced long-term activity of the immobilized enzymes for several weeks were realized. Moreover, immobilized enzymes were less sensitive to inhibition and the substrate-channeling effect between immobilized enzymes promoted the overall conversion in the trienzymatic cascade reaction. Based on this, CMP-Neu5Ac was successfully synthesized by immobilized enzymes in noncompartmentalized and compartmentalized microfluidic devices. This study demonstrates the high potential of immobilizing enzymes in (compartmentalized) microfluidic devices to perform multienzymatic cascade reactions despite cross-inhibitions under continuous flow conditions. Due to the ease of enzyme immobilization in hydrogels, this concept is likely applicable for many cascade reactions with or without cross-inhibition characteristics.

Keywords: biocatalysis; cascade reaction; compartmentalization; enzyme immobilization; incompatibility; microfluidic reactor; microstructured hydrogel; sialic acid.

MeSH terms

  • Carbohydrate Epimerases / chemistry
  • Carrier Proteins / chemistry
  • Cytidine Monophosphate / analogs & derivatives*
  • Cytidine Monophosphate / chemical synthesis
  • Enzymes, Immobilized / chemistry*
  • Hydrogels / chemistry*
  • Lab-On-A-Chip Devices
  • Microfluidics / instrumentation
  • Microfluidics / methods
  • N-Acylneuraminate Cytidylyltransferase / chemistry
  • Oxo-Acid-Lyases / chemistry
  • Polyethylene Glycols / chemistry
  • Sialic Acids / chemical synthesis*

Substances

  • Carrier Proteins
  • Enzymes, Immobilized
  • Hydrogels
  • Sialic Acids
  • cytidine-5'-monophosphosialic acid
  • Polyethylene Glycols
  • N-Acylneuraminate Cytidylyltransferase
  • Oxo-Acid-Lyases
  • N-acetylneuraminate lyase
  • Carbohydrate Epimerases
  • N-acyl-D-glucosamine 2-epimerase
  • Cytidine Monophosphate