Manipulation of carrier proteins in antibiotic biosynthesis

Chem Biol. 2004 Feb;11(2):195-201. doi: 10.1016/j.chembiol.2004.02.010.

Abstract

Engineering biosynthetic pathways into suitable host organisms has become an attractive venue for the design, evaluation, and production of small molecule therapeutics. Polyketide (PK) and nonribosomal peptide (NRP) synthases have been of particular interest due to their modular structure, yet routine cloning and expression of these enzymes remains challenging. Here we describe a method to covalently label carrier proteins from PK and NRP synthases using the enzymatic transfer of a modified coenzyme A analog by a 4'-phosphopantetheinyltransferase. Using this method, carrier proteins can be loaded with single fluorescent or affinity reporters, providing novel entry for protein visualization, Western blot identification, and affinity purification. Application of these methods provides an ideal tool to track and quantify metabolically engineered pathways. Such techniques are valuable to measure protein expression, solubility, activity, and native posttranslational modification events in heterologous systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / biosynthesis*
  • Blotting, Western
  • Carrier Proteins / chemistry*
  • Carrier Proteins / metabolism
  • Chromatography, Affinity
  • Coenzyme A / biosynthesis
  • Drug Design*
  • Fluorescent Dyes / analysis
  • Peptide Synthases / chemistry*
  • Protein Engineering
  • Protein Processing, Post-Translational

Substances

  • Anti-Bacterial Agents
  • Carrier Proteins
  • Fluorescent Dyes
  • Peptide Synthases
  • non-ribosomal peptide synthase
  • Coenzyme A