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An apparatus (see illustration) for the continuous cultivation of microorganisms or plant cells. The nutrients required for cell growth are supplied continuously to the culture vessel by a pump connected to a medium reservoir. The cells in the vessel grow continuously on these nutrients. Residual nutrients and cells are removed from the vessel (fermenter) at the same rate by an overflow, thus maintaining the culture in the fermenter at a constant volume.

Schematic representation of chemostat apparatusenlarge picture
Schematic representation of chemostat apparatus

An important feature of chemostat cultivation is the dilution rate, defined as the volume of nutrient medium supplied per hour divided by the volume of the culture. During chemostat cultivation, an equilibrium is established (steady state) at which the growth rate of the cells equals the dilution rate. The higher the dilution rate, the faster the organisms are allowed to grow. Above a given dilution rate the cells will not be able to grow any faster, and the culture will be washed out of the fermenter. The chemostat thus offers the opportunity to study the properties of organisms at selected growth rates. See Fermentation

The nutrient medium which is fed to the fermenter contains an excess of all growth factors except one, the growth-limiting nutrient. The concentration of the cells (biomass) in the fermenter is dependent on the concentration of the growth-limiting nutrient in the medium feed. Upon entering the fermenter, the growth-limiting nutrient is consumed almost to completion, and only minute amounts of it may be found in the culture and the effluent. Initially, when few cells have been inoculated in the growth vessel, even the growth-limiting nutrient is in excess. Therefore, the microorganisms can grow at a rate exceeding their rate of removal. This growth of cells causes a fall in the level of the growth-limiting nutrient, gradually leading to a lower specific growth rate of the microorganisms. Once the specific rate of growth balances the removal of cells by dilution, a steady state is established in which both the cell density and the concentration of the growth-limiting nutrient remain constant. Thus the chemostat is a tool for the cultivation of microorganisms almost indefinitely in a constant physiological state.

To achieve a steady state, parameters other than the dilution rate and culture volume must be kept constant (for example, temperature and pH). The fermenter is stirred to provide a homogeneous suspension in which all individual cells in the culture come into contact with the growth-limiting nutrient immediately, and to achieve optimal distribution of air (oxygen) in the fermenter when aerobic cultures are in use.

Laboratory chemostats usually contain 0.5 to 10.5 quarts (0.5 to 10 liters) of culture, but industrial chemostat cultivation can involve volumes up to 343,000 gal (1300 m3) for the continuous production of microbial biomass.

The chemostat can be used to grow microorganisms on very toxic nutrients since, when kept growth-limiting, the nutrient concentration in the culture is very low. The chemostat can be used to select mutants with a higher affinity to the growth-limiting nutrient or, in the case of a mixed population, to select the species that are optimally adapted to the growth limitation and culture conditions. The chemostat is of great use in such fields as physiology, ecology, and genetics of microorganisms. See Bacterial genetics, Bacterial physiology and metabolism, Microbiology


An apparatus, and a principle, for the continuous culture of bacterial populations in a steady state.
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The heterogeneous distribution of clumps of bacterial cells we observed was also inconsistent with the model of a well-mixed chemostat, although more complex models of unmixed chemo-stats could apply (Smith and Waltman, 1995).
In contrast to a chemostat in which the entire volume is occupied by microbial cells utilizing available resources to support their growth, our imaging of the zebrafish intestine revealed bacterial colonization to be spatially highly heterogeneous, with punctate colonies and nonuniform distribution of colonies along the length of the gut (Fig.
Although mortality in this case is not predetermined by the chemostat flow rate (only natural mortality is involved), the equilibrium food concentration results from the resource uptake of the daphniids.
All experiments were run with the same unialgal food source, the chlorococcal Scenedesmus acutus Meyen taken directly from the outlet of a chemostat and diluted to the appropriate concentration with membrane-filtered (0.
The labeling technique produced mean C:P ratios (mean [+ or -] 1 SE) of 1240 [+ or -] 40 for P- Scenedesmus and 160 for P+ Scenedesmus, values comparable to means ([+ or -] 1 SE) of 1070 [+ or -] 70 and 225 [+ or -] 9 for algae taken directly from the respective chemostats (see Table 2).
Van Donk and Hessen (1993) used two of the same Daphnia species and a different species of Scenedesmus, and grew algae in batch cultures rather than chemostats.
In the first chemostat experiment with 1 mg glucose/L in the input medium, two flagellate chemostats were run in parallel and supplied with bacterial suspension (mean [+ or -] 1 SD, 3.
This outcome is similar to results obtained in chemostat culture (Lundquist and Levin 1986).
Coexistence of two competitors on one resource and one inhibitor: a chemostat model based on bacteria and antibiotics.
The other selective regime was chemostat culture, in which fresh medium flowed into the culture vessels at a constant rate; the bacterial populations maintained a high equilibrium density while holding the limiting resource to a low concentration.
The consortium of organisms is assumed to grow in a continuously illuminated chemostat with dilution rate D and reservoir concentration [N.