Abstract

Cupriavidus necator H16 is gaining significant attention as a microbial chassis for range of biotechnological applications. While the bacterium is a major producer of bioplastics, its lithoautotrophic and versatile metabolic capabilities make the bacterium a promising microbial chassis for biofuels and chemicals using renewable resources. It remains necessary to develop appropriate experimental resources to permit controlled bioengineering and system optimization of this microbe. In this study, we employed statistical design of experiments to gain understanding of the impact of components of defined media on C. necator growth and built a model that can predict the bacterium's cell density based on medium components. This highlighted medium components, and interaction between components, having the most effect on growth: fructose, amino acids, trace elements, CaCl2, and Na2HPO4 contributed significantly to growth (t values of <-1.65 or >1.65); copper and histidine were found to interact and must be balanced for robust growth. Our model was experimentally validated and found to correlate well (r2 = 0.85). Model validation at large culture scales showed correlations between our model-predicted growth ranks and experimentally determined ranks at 100 ml in shake flasks (ρ = 0.87) and 1 liter in a bioreactor (ρ = 0.90). Our approach provides valuable and quantifiable insights on the impact of medium components on cell growth and can be applied to model other C. necator responses that are crucial for its deployment as a microbial chassis. This approach can be extended to other nonmodel microbes of medical and industrial biotechnological importance.IMPORTANCE Chemically defined media (CDM) for cultivation of C. necator vary in components and compositions. This lack of consensus makes it difficult to optimize new processes for the bacterium. This study employed statistical design of experiments (DOE) to understand how basic components of defined media affect C. necator growth. Our growth model predicts that C. necator can be cultivated to high cell density with components held at low concentrations, arguing that CDM for large-scale cultivation of the bacterium for industrial purposes will be economically competitive. Although existing CDM for the bacterium are without amino acids, addition of a few amino acids to growth medium shortened lag phase of growth. The interactions highlighted by our growth model show how factors can interact with each other during a process to positively or negatively affect process output. This approach is efficient, relying on few well-structured experimental runs to gain maximum information on a biological process, growth.

Highlights

  • Cupriavidus necator H16 is gaining significant attention as a microbial chassis for range of biotechnological applications

  • While C. necator has been reported to have broad substrate range, its ability to utilize carbohydrates as a carbon source during heterotrophic growth appears to be limited to fructose and N-acetylglucosamine [8, 11, 29]

  • Utilization of fructose by C. necator is most likely to occur via substrate import by an ATP-binding cassette (ABC)-type transporter, followed by catabolism via 2-keto-3deoxy-6-phosphogluconate (KDPG), the Entner-Doudoroff pathway

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Summary

Introduction

Cupriavidus necator H16 is gaining significant attention as a microbial chassis for range of biotechnological applications. We employed statistical design of experiments to gain understanding of the impact of components of defined media on C. necator growth and built a model that can predict the bacterium’s cell density based on medium components. Our approach provides valuable and quantifiable insights on the impact of medium components on cell growth and can be applied to model other C. necator responses that are crucial for its deployment as a microbial chassis This approach can be extended to other nonmodel microbes of medical and industrial biotechnological importance. The development of C. necator as an industrial chassis requires appropriate tools for studying and engineering the organism One of these resources is the availability of a characterized, chemically defined growth medium. Understanding the impact of each component of a chemically defined medium on C. necator growth is a fundamental tool for controlled exploration of the biotechnological potential of this important bacterium

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