HaloTag™: Evaluation of a covalent one-step immobilization for biocatalysis

J Biotechnol. 2017 Jan 10:241:170-174. doi: 10.1016/j.jbiotec.2016.12.004. Epub 2016 Dec 5.

Abstract

Easy, fast and gentle immobilization for the efficient reuse of important biocatalysts is highly demanded. We used the commercially available HaloTag™ technology (Promega), so far relatively unknown in the context of biocatalysis, to immobilize the benzaldehyde lyase from P. fluorescence (PfBAL). Immobilization mediated by this fusion tag proceeds rapidly within minutes from crude extracts yielding covalently attached enzymes in high purity, making expensive and laborious previous chromatographic purification steps obsolete, which strongly reduces the costs for biocatalyst immobilization. Further, we introduce a novel design of HaloTag fusions and demonstrate the positive effect of the tag on soluble expression and activity of PfBAL. The immobilized biocatalyst was stable at 4°C for months and was successfully reused in several repetitive batches for the carboligation of aggressive aldehydes.

Keywords: Benzaldehyde lyase; CC bond formation; Covalent enzyme immobilization; Economizing production process; Enzyme fusion; Repetitive batch.

MeSH terms

  • Aldehyde-Lyases / chemistry
  • Aldehyde-Lyases / metabolism
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / metabolism
  • Biotechnology / methods*
  • Enzymes, Immobilized / chemistry*
  • Enzymes, Immobilized / metabolism
  • Genetic Engineering
  • Pseudomonas fluorescens / enzymology
  • Recombinant Proteins / chemistry*
  • Recombinant Proteins / metabolism
  • Rhodococcus

Substances

  • Bacterial Proteins
  • Enzymes, Immobilized
  • Recombinant Proteins
  • Aldehyde-Lyases
  • benzaldehyde lyase