Green Production of Cladribine by Using Immobilized 2'-Deoxyribosyltransferase from Lactobacillus delbrueckii Stabilized through a Double Covalent/Entrapment Technology

Biomolecules. 2021 Apr 29;11(5):657. doi: 10.3390/biom11050657.

Abstract

Nowadays, enzyme-mediated processes offer an eco-friendly and efficient alternative to the traditional multistep and environmentally harmful chemical processes. Herein we report the enzymatic synthesis of cladribine by a novel 2'-deoxyribosyltransferase (NDT)-based combined biocatalyst. To this end, Lactobacillus delbrueckii NDT (LdNDT) was successfully immobilized through a two-step immobilization methodology, including a covalent immobilization onto glutaraldehyde-activated biomimetic silica nanoparticles followed by biocatalyst entrapment in calcium alginate. The resulting immobilized derivative, SiGPEI 25000-LdNDT-Alg, displayed 98% retained activity and was shown to be active and stable in a broad range of pH (5-9) and temperature (30-60 °C), but also displayed an extremely high reusability (up to 2100 reuses without negligible loss of activity) in the enzymatic production of cladribine. Finally, as a proof of concept, SiGPEI 25000-LdNDT-Alg was successfully employed in the green production of cladribine at mg scale.

Keywords: antineoplastic drug; biomimetic silica; calcium alginate; entrapment; enzyme immobilization; glutaraldehyde.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / metabolism
  • Biocatalysis
  • Cladribine / metabolism*
  • Enzyme Stability
  • Enzymes, Immobilized / chemistry
  • Enzymes, Immobilized / metabolism
  • Glutaral / chemistry
  • Green Chemistry Technology
  • Hydrogen-Ion Concentration
  • Lactobacillus delbrueckii / enzymology*
  • Silicon Dioxide / chemistry
  • Temperature
  • Transferases / chemistry*
  • Transferases / metabolism*

Substances

  • Bacterial Proteins
  • Enzymes, Immobilized
  • Cladribine
  • Silicon Dioxide
  • Transferases
  • Glutaral