Direct spectrophotometric assay for benzaldehyde lyase activity

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Dessy Natalia - , RWTH Aachen University (First author)
  • Christina Kohlmann - (Author)
  • Marion Bettina Ansorge-Schumacher - , Technical University of Berlin (Author)
  • Lasse Greiner - (Author)

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.

Details

Original languageEnglish
Number of pages4
JournalBiotechnology research international
Volume2011
Issue numberArticle ID 478925
Publication statusPublished - 2011
Peer-reviewedYes
Externally publishedYes

External IDs

ORCID /0000-0002-2912-546X/work/171551975

Keywords

Keywords

  • Biokatalyse, Benzaldehydlyase, C-C-Knüpfung, Aktivitätsassay