Flow-based biocatalysis: Application to peracetylated arabinofuranosyl-1, 5-arabinofuranose synthesis. (September 2018)

• Record Type: Journal Article
• Authors: Bavaro, Teodora; Pinto, Andrea; Dall'Oglio, Federica; Hernáiz, María J.; Morelli, Carlo F.; Zambelli, Paolo; De Micheli, Carlo; Conti, Paola; Tamborini, Lucia; Terreni, Marco
• Is Part Of: Process biochemistry. Volume 72(2018)
• Page Start: 112
• Page End: 118
• Publication Date: 2018-09
• Subjects: Lipases -- Enzymatic hydrolysis -- Flow chemistry -- Immobilized enzymes -- Disaccharides -- Tuberculosis; Biochemical engineering -- Periodicals; Biotechnology -- Periodicals; Biochemistry -- periodicals; Biotechnology -- periodicals; Chemical Engineering -- periodicals; Génie biochimique -- Périodiques; Biotechnologie -- Périodiques; Biochemical engineering; Biotechnology; Periodicals; 660.63
• DOI: 10.1016/j.procbio.2018.06.026
• Languages: English
• ISSNs: 1359-5113

Abstract

Graphical abstract: Highlights: Novozym® 435 catalyzed the regioselective hydrolysis in C5 of the peracetylated α-arabinose. Immobilized lipase TL catalyzed the regioselective hydrolysis in C1 of the peracetylated β-arabinose. The lipase-catalyzed hydrolysis of acetylated arabinose was performed in flow. Flow-based biocatalysis resulted in an improvement of the specific reaction rates. Abstract: The lipase-catalyzed regioselective hydrolysis of peracetylated arabinose was performed in a packed bed flow reactor (PBR). In particular, the hydrolysis of the α anomer of peracetylated arabinose catalyzed by Novozym® 435 resulted in the monodeprotection of C5 in only 5 min and 91% yield. By using the immobilized Pseudomonas stutzeri lipase, the regioselective hydrolysis of the β anomer was also accomplished affording the C1 deacetylated derivative in 30 min with good yields. The high local concentration of the immobilized biocatalyst in the PBR allow for a significant reduction of the reaction time; moreover, repeated re-use, and easy downstream processing increase the efficiency and the productivity of the process, if compared to the classical batch procedure. In fact, under optimized conditions, the specific reaction rate of the biocatalyzed flow reaction showed an increase of more than 300 times compared to the batch one. The obtained building blocks were prepared in gram scale and then used for the synthesis of peracetylated arabinofuranosyl-1, 5-arabinofuranose.