| Literature DB >> 33947162 |
Cintia Wanda Rivero1,2, Natalia Soledad García1, Jesús Fernández-Lucas3,4, Lorena Betancor5, Gustavo Pablo Romanelli6, Jorge Abel Trelles1,2.
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.Entities:
Keywords: antineoplastic drug; biomimetic silica; calcium alginate; entrapment; enzyme immobilization; glutaraldehyde
Year: 2021 PMID: 33947162 DOI: 10.3390/biom11050657
Source DB: PubMed Journal: Biomolecules ISSN: 2218-273X