Autotrophic production of stable-isotope-labeled arginine in Ralstonia eutropha strain H16

Appl Environ Microbiol. 2012 Nov;78(22):7884-90. doi: 10.1128/AEM.01972-12. Epub 2012 Aug 31.

Abstract

With the aim of improving industrial-scale production of stable-isotope (SI)-labeled arginine, we have developed a system for the heterologous production of the arginine-containing polymer cyanophycin in recombinant strains of Ralstonia eutropha under lithoautotrophic growth conditions. We constructed an expression plasmid based on the cyanophycin synthetase gene (cphA) of Synechocystis sp. strain PCC6308 under the control of the strong P(cbbL) promoter of the R. eutropha H16 cbb(c) operon (coding for autotrophic CO(2) fixation). In batch cultures growing on H(2) and CO(2) as sole sources of energy and carbon, respectively, the cyanophycin content of cells reached 5.5% of cell dry weight (CDW). However, in the absence of selection (i.e., in antibiotic-free medium), plasmid loss led to a substantial reduction in yield. We therefore designed a novel addiction system suitable for use under lithoautotrophic conditions. Based on the hydrogenase transcription factor HoxA, this system mediated stabilized expression of cphA during lithoautotrophic cultivation without the need for antibiotics. The maximum yield of cyanophycin was 7.1% of CDW. To test the labeling efficiency of our expression system under actual production conditions, cells were grown in 10-liter-scale fermentations fed with (13)CO(2) and (15)NH(4)Cl, and the (13)C/(15)N-labeled cyanophycin was subsequently extracted by treatment with 0.1 M HCl; 2.5 to 5 g of [(13)C/(15)N]arginine was obtained per fed-batch fermentation, corresponding to isotope enrichments of 98.8% to 99.4%.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arginine / metabolism*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Bioreactors / microbiology
  • Carbon Dioxide / metabolism
  • Cupriavidus necator / metabolism*
  • Fermentation
  • Gene Expression
  • Hydrogen / metabolism
  • Isotope Labeling / methods*
  • Metabolic Engineering
  • Peptide Synthases / genetics
  • Peptide Synthases / metabolism
  • Plasmids
  • Promoter Regions, Genetic
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Synechocystis / enzymology
  • Synechocystis / genetics

Substances

  • Bacterial Proteins
  • Recombinant Proteins
  • cyanophycin
  • Carbon Dioxide
  • Hydrogen
  • Arginine
  • Peptide Synthases
  • cyanophycin synthase, bacteria