Strain and Fermentation Development Services

Yields Are Number One

We offer you our strong expertise in developing strains based on E. coli host systems to produce peptides, proteins (soluble and insoluble), plasmid DNA products, and vaccines.

Richter-Helm BioLogics provides strain development modules for protein-based products with your choice of amino acid sequence or expression construct, or even using your candidate seed strain. Chemical and heat induction systems are available. We are also able to screen strains to determine which is most appropriate for producing your plasmid-DNA product.

Our strain development activities can be flexibly configured to suit your needs. The possibilities include:

  • Construct design and cloning
  • Strain screening and expression parameter testing
  • Feasibility fermentation runs
  • RCB production

Strain development is very closely coordinated with fermentation development, with both being handled by the experienced process development team of Richter-Helm BioLogics.

“Since launching our joint development project, we have been able to rely fully and consistently on Richter-Helm BioLogics.”

(customer)

USP development at Richter-Helm BioLogics covers a wide range of leading-edge batch and fed-batch fermentation strategies based on microbial hosts such as E. coli and yeasts.

We can flexibly vary USP development components depending on your needs. The portfolio includes feasibility studies, complete USP development, and fermentation adaptation and/or optimization studies. The available general fermentation development services include:

  • A process design phase performed at a small scale (e.g. of one liter) in batch or fed-batch mode
  • An intermediate process scale-up to 10 liters
  • A process engineering/adaptation phase (which can include a robustness study)
  • A process reproducibility study (e.g. for preclinical animal studies etc.)

From Parameter Screening to Robustness Testing

Various process parameters can be investigated to establish the most appropriate and productive fermentation approach, e.g.

  • Growth rate, growth temperature, pH, DO level
  • Induction mode, induction point/OD600, expression time
  • Feeding profiles, media composition, etc.

In addition, cell harvesting techniques such as centrifugation or crossflow filtration can be selected. Rapid at-line and offline PD analyses are available throughout the development phase, e.g.:

  • OD600, cell wet weight, cell dry weight
  • Expression kinetics, EoF yield
  • Substrate/byproducts
Contour plot of USP parameter screening
Contour plot of USP parameter screening

Design of experiment (DoE) tools applying full or fractional factorial design modules are routinely used to assist in developing and optimizing processes or, if applicable, to supplement parameter screenings etc.