Direct Spectrophotometric Assay for Benzaldehyde Lyase Activity

  • Natalia D
  • Kohlmann C
  • Ansorge-Schumacher M
  • et al.
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Abstract

Benzaldehyde lyase from Pseudomonas fluorescens Biovar I. (BAL, EC 4.1.2.38) is a versatile catalyst for the organic synthesis of chiral α -hydroxy ketones. To allow fast assessment of enzyme activity, a direct spectrophotometric assay is desirable. Here, a new robust and easy-to-handle assay based on UV absorption is presented. The assay developed is based on the ligation of the α -hydroxy ketone (R)-2,2′-furoin from 2-furaldehyde. A robust assay with direct monitoring of the product is facilitated with a convenient concentration working range minimising experimental associated with low concentrations.

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Natalia, D., Kohlmann, C., Ansorge-Schumacher, M. B., & Greiner, L. (2011). Direct Spectrophotometric Assay for Benzaldehyde Lyase Activity. Biotechnology Research International, 2011, 1–4. https://doi.org/10.4061/2011/478925

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