New stabilized FastPrep-CLEAs for sialic acid synthesis |
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Authors: | García-García María Inmaculada Sola-Carvajal Agustín Sánchez-Carrón Guiomar García-Carmona Francisco Sánchez-Ferrer Alvaro |
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Affiliation: | Department of Biochemistry and Molecular Biology-A, Faculty of Biology, University of Murcia, Campus Espinardo, E-30100 Murcia, Spain |
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Abstract: | N-acetyl-d-neuraminic acid aldolase, a key enzyme in the biotechnological production of N-acetyl-d-neuraminic acid (sialic acid) from N-acetyl-d-mannosamine and pyruvate, was immobilized as cross-linked enzyme aggregates (CLEAs) by precipitation with 90% ammonium sulfate and crosslinking with 1% glutaraldehyde. Because dispersion in a reciprocating disruptor (FastPrep) was only able to recover 40% of the activity, improved CLEAs were then prepared by co-aggregation of the enzyme with 10 mg/mL bovine serum albumin followed by a sodium borohydride treatment and final disruption by FastPrep (FastPrep-CLEAs). This produced a twofold increase in activity up to 86%, which is a 30% more than that reported for this aldolase in cross-linked inclusion bodies (CLIBs). In addition, these FastPrep-CLEAs presented remarkable biotechnological features for Neu5Ac synthesis, including, good activity and stability at alkaline pHs, a high KM for ManNAc (lower for pyruvate) and good operational stability. These results reinforce the practicability of using FastPrep-CLEAs in biocatalysis, thus reducing production costs and favoring reusability. |
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Keywords: | CLEAs, cross-linked enzyme aggregates AS, ammonium sulfate BSA, bovine serum albumin SB, sodium borohydride FP-CLEAs, FastPrep-CLEAs Neu5Ac, N-acetylneuraminic acid (sialic acid) NAL, N-acetylneuraminate lyase ManNAc, N-acetyl-d-mannosamine Pyr, pyruvate LpNAL, Lactobacillus plantarum NAL 7-ACA, 7-aminocephalosporanic acid |
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