Recombinant protein production and streptomycetes

J Biotechnol. 2012 Apr 30;158(4):159-67. doi: 10.1016/j.jbiotec.2011.06.028. Epub 2011 Jul 14.

Abstract

The biopharmaceutical market has come a long way since 1982, when the first biopharmaceutical product, recombinant human insulin, was launched. Just over 200 biopharma products have already gained approval. The global market for biopharmaceuticals which is currently valued at over US$99 billion has been growing at an impressive compound annual growth rate over the previous years. To produce these biopharmaceuticals and other industrially important heterologous proteins, different prokaryotic and eukaryotic expression systems are used. All expression systems have some advantages as well as some disadvantages that should be considered in selecting which one to use. Choosing the best one requires evaluating the options--from yield to glycosylation, to proper folding, to economics of scale-up. No host cell from which all the proteins can be universally expressed in large quantities has been found so far. Therefore, it is important to provide a variety of host-vector expression systems in order to increase the opportunities to screen for the most suitable expression conditions or host cell. In this overview, we focus on Streptomyces lividans, a Gram-positive bacterium with a proven excellence in secretion capacity, as host for heterologous protein production. We will discuss its advantages and disadvantages, and how with systems biology approaches strains can be developed to better producing cell factories.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biopharmaceutics / methods
  • Genetic Vectors / genetics
  • Humans
  • Recombinant Proteins / biosynthesis*
  • Recombinant Proteins / genetics*
  • Streptomyces lividans / genetics*
  • Streptomyces lividans / metabolism*

Substances

  • Recombinant Proteins