Rapid expression and purification of 100 nmol quantities of active protein using cell-free protein synthesis

Biotechnol Prog. 2004 Jan-Feb;20(1):102-9. doi: 10.1021/bp0341693.

Abstract

Two strategies for ATP regeneration during cell-free protein synthesis were applied to the large-scale production and single-column purification of active chloramphenicol acetyl transferase (CAT). Fed-batch reactions were performed on a 5-10 mL scale, approximately 2 orders of magnitude greater than the typical reaction volume. The pyruvate oxidase system produced 104 nmol of active CAT in a 5 mL reaction over the course of 5 h. The PANOx system produced 261 +/- 42 nmol, about 7 mg, of active CAT in a 10 mL reaction over the course of 4 h. The reaction product was purified to apparent homogeneity with approximately 70% yield by a simple affinity chromatography adsorption and elution. To our knowledge, this is the largest amount of actively expressed protein to be reported in a simple, fed-batch cell-free protein synthesis reaction.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / chemistry
  • Cell-Free System / chemistry*
  • Chloramphenicol O-Acetyltransferase / chemical synthesis*
  • Chloramphenicol O-Acetyltransferase / isolation & purification*
  • Chromatography / methods*
  • Enzyme Activation
  • Feasibility Studies
  • Microchemistry / methods*
  • Molecular Weight
  • Oxidation-Reduction
  • Pyruvate Oxidase / chemistry*

Substances

  • Adenosine Triphosphate
  • Pyruvate Oxidase
  • Chloramphenicol O-Acetyltransferase