Abstract

High cell density cultivation necessitates cell division and biomass formation, the mechanisms of which remain poorly understood, especially from the cellular energetics perspective. Specifically, the sensing of energy abundance and the channelling of nutritional energy into biomass formation and cell maintenance remains enigmatic at the sensory, effector and decision levels. Thus, optimization of cell growth remains an iterative trial and error process where the principal parameters are growth medium composition and incubation temperature. In this study, a new semidefined formulated medium was shown to be useful for high cell density cultivation of Escherichia coli DH5α (ATCC 53868). Comprising K2HPO4, 12.54; KH2PO4, 2.31; D-Glucose, 4.0; NH4Cl, 1.0; Yeast extract, 12.0; NaCl, 5.0; MgSO4, 0.24; the medium possessed a high capacity phosphate buffer able to moderate pH fluctuations during cell growth known to be detrimental to biomass formation. With glucose and NH4Cl providing the nutrients for initial growth, followed by a lag phase of 3 hours, a maximal optical density of 12.0 was obtained after 27 hours of cultivation at 37 oC and 230 rpm. Yeast extract provides a secondary source of carbon and nitrogen. Maximal optical density obtained in formulated medium was higher than the 10.1, 4.2, and 3.4 obtained in Tryptic Soy Broth, M9 with 1 g/L of yeast extract, and LB Lennox, respectively. Cultivation of E. coli DH5α in formulated medium with 6 g/L of glucose resulted in a longer lag phase of 8 hours and a longer time (68 hours) to attainment of maximal optical density, which marked the upper limit of glucose concentration beyond which biomass formation would be reduced. Specifically, glucose concentration above 6 g/L markedly reduced biomass formation possibly due to the environmental stress arising from low pH in the culture broth. Glucose concentration below 4 g/L, on the other hand, reduced biomass formation through a smaller pool of nutrients serving as biomass building blocks. Deviation from 1:1 molar ratio between glucose and NH4Cl was not detrimental to biomass formation and growth rates. Collectively, a semi-defined formulated medium could increase optical density of E. coli DH5α beyond that of LB Lennox and Tryptic Soy Broth, and may find use in cultivation of cells for applied microbiology research.

Highlights

  • Lack of biomass formation is a critical problem of many commercially available media in cultivation of common bacteria for applied microbiology studies

  • This study demonstrated the utility of a new semidefined formulated medium in enabling high cell density aerobic cultivation of Escherichia coli DH5α (ATCC 53868) in shake flasks

  • Growth of E. coli DH5α in formulated medium with 6 g/L of glucose and 1.5 g/L of ammonium chloride resulted in a longer lag phase of 8 hours and a longer time period to attainment of maximal optical density of 12.0 at 68 hours (Figure 4a)

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Summary

Introduction

Lack of biomass formation is a critical problem of many commercially available media in cultivation of common bacteria for applied microbiology studies. Such studies typically require relatively large amount of biomass for various characterization studies and experiments. The holy grail in microbial cell culture is in tailoring growth medium composition to the specific microbial physiology and metabolism of the microbial species. While a multitude of media are available for the cultivation of various microorganisms, growth medium formulation remains an art, where specific design rules for an optimal medium with respect to a particular species of microbe are lacking. Trial and error approaches remain the norm in the formulation of medium for bacterial culture [8]

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