1. Field of the Invention
The invention generally relates to the process productivity in fermentors, and more specifically to a system and method for controlling the addition of oxygen in fermentations to achieve an improved oxygen consumption and substrate yield in microorganisms.
2. Description of the Related Art
Biochemical engineering is a branch of chemical engineering which deals with the design and construction of unit processes involving microorganisms. Fermentation is one example of a process involving the bulk growth of microorganisms on a growth medium. Fermentation is one of the most important processes used in biochemical engineering, and the products of fermentations are extensively used in the pharmaceutical, biotechnology, brewing, and water treatment industries. Fermentations are typically conducted in a fermentor, or bioreactor, which may refer to any vessel or system that supports a biologically active environment. Industrial bioreactors can employ a variety of microorganisms, including bacteria and animal cells, ranging in complexity and response to sheer.
The design of a fermentation system is quite a complex engineering task. Under optimum conditions the microorganisms or cells are able to perform their desired function with great efficiency. The bioreactors environmental conditions, such as gas (i.e., air, oxygen (O2), nitrogen (N2), carbon dioxide (CO2)) flow rates, temperature, pH, dissolved oxygen levels, and/or agitation speed/circulation rate need to be closely monitored and controlled. To this end, most industrial bioreactor manufacturers use vessels, sensors, and controllers as components of fermentation systems.
Optimal oxygen transfer during a fermentation is perhaps the most difficult task to accomplish. Oxygen solubility in water is extremely low (at the parts per million level), and the solubility is even less in presence of solutes such as nutrients and other additions in broths. Oxygen is also only 20.9% by volume in air. Oxygen transfer in bioreactors can be enhanced by agitation in mechanical fermentors. Agitation is also needed to mix nutrients and to keep the fermentation homogeneous. However, there are limits to the speed of agitation, as it can induce high stress in organisms leading to cell death. High agitation speed also results in higher power consumption, increasing product unit costs. The dissolved oxygen (DO) in the growth media is usually measured to help determine the amount of oxidant gas that should be added to the fermentor.
Many different fermentation systems and their control of oxygen have been documented. One method attempts to improve the oxygen utilization in continuous fermentation of single cells by recycling fermentation liquid. In this approach either air, enriched oxygen, or pure oxygen is used during fermentations. However, the only control applied in this method is the level of liquid in the fermentor. Another method focuses specifically on one type of microorganism (Escherichia coli bacteria), but methods of controlling the oxygen supply are not provided. Instead, the method teaches the regulation of the carbon source as a function of the oxygen uptake rate of the microorganism. Yet another method describes a method of increasing the oxygen transfer in a fermentation system by introducing oxygen in only one portion of the broth that is sent back to the fermentor. Still another method describes a method of utilizing high pressure in the fermentor to promote oxygen dissolution and low pressure to remove CO2. Still other methods teach a method of enriching bubble fermentors with oxygen while using air bubbles to agitate the growth media and eliminate CO2 accumulated in the media.
However, the foregoing methods each fail to provide a method to regulate the real-time oxygen supply in agitation and bubble fermentors to improve oxygen utilization and maximize the productivity of the fermentation, leading to favorable system economics.
Therefore, there remains a need for a method to optimize the use of pure oxygen in fermentation systems to maximize productivity, substrate yield, and oxygen utilization of the fermentation cell culture.
Aspects of the invention generally provide a method for controlling the addition of oxygen in fermentations to achieve a desired oxygen consumption and substrate yield in fermentations. In one aspect, the invention provides a method for regulating the addition of oxygen (O2) to a fermentor during a fermentation process, comprising measuring real-time dissolved oxygen (DO) in a fermentation broth, measuring real-time O2 concentration in the fermentor exhaust and providing the real-time DO measurement and real-time O2 measurement to an adaptive controller configured to regulate O2 flow into the fermentor responsive to the real-time DO measurement and real-time O2 measurement.
In another aspect, the invention provides a method for regulating the addition of O2 in a fermentor during a fermentation process, comprising measuring real-time dissolved oxygen (DO) in a fermentation broth, measuring real-time O2 concentration in the fermentor exhaust, and providing the real-time DO measurement and real-time O2 measurement to an adaptive controller, wherein the adaptive controller is configured to regulate incoming O2 flow and agitation speed in the fermentor responsive to the real-time DO measurement and real-time O2 measurement.
In another aspect, the invention provides a method for regulating the addition of O2 to a fermentor during a fermentation process, comprising measuring real-time dissolved oxygen (DO) in a fermentation broth, measuring real-time O2 concentration in the fermentor exhaust, measuring an additional real-time parameter in the fermentation broth and providing the real-time DO measurement, real-time O2 measurement, and additional real-time parameter measurement to an adaptive controller, wherein the adaptive controller is configured to regulate incoming O2 flow and agitation speed in the fermentor responsive to the real-time DO measurement, real-time O2 measurement and additional real-time parameter measurement.
In another aspect, the invention provides a method for regulating the addition of O2 to a fermentor during a fermentation process, comprising measuring real-time dissolved oxygen (DO) in a fermentation broth, measuring real-time O2 concentration in the fermentor exhaust, and providing the real-time DO measurement and real-time O2 measurement to an adaptive controller configured to regulate O2 and N2 flow into the fermentor responsive to the real-time DO measurement and real-time O2 measurement.
In another aspect, the invention provides a system for regulating addition of O2 during a fermentation process, comprising a fermentor, a first measuring device configured for measuring real-time dissolved oxygen (DO) in a fermentation broth, a second measuring device configured for measuring real-time O2 concentration in the fermentor exhaust, and an adaptive controller configured to regulate O2 flow into the fermentor responsive to the real-time DO measurement and real-time O2 measurement.
In another aspect, the invention provides a system for regulating addition of O2 during a fermentation process, comprising a fermentor, a first measuring device configured for measuring real-time dissolved oxygen (DO) in a fermentation broth, a second measuring device configured for measuring real-time O2 concentration in the fermentor exhaust, and an adaptive controller configured to regulate incoming O2 flow and agitation speed in the fermentor responsive to the real-time DO measurement and real-time O2 measurement.
In another aspect, the invention provides a system for regulating addition of O2 during a fermentation process, comprising a fermentor, a first measuring device configured for measuring real-time dissolved oxygen (DO) in a fermentation broth, a second measuring device configured for measuring real-time O2 concentration in the fermentor exhaust, a third measuring device configured for measuring an additional real-time parameter in the fermentation broth, and an adaptive controller configured to regulate incoming O2 flow and agitation speed in the fermentor responsive to the real-time DO measurement, real-time O2 measurement and additional real-time parameter measurement.
In another aspect, the invention provides a system for regulating addition of O2 during a fermentation process, comprising a fermentor, a first measuring device configured for measuring real-time dissolved oxygen (DO) in a fermentation broth, a second measuring device configured for measuring real-time O2 concentration in the fermentor exhaust, and an adaptive controller configured to regulate O2 and N2 flow into the fermentor responsive to the real-time DO measurement and real-time O2 measurement.
For a further understanding of the nature and objects of the present invention, reference should be made to the following detailed description, taken in conjunction with the accompanying drawings, in which like elements are given the same or analogous reference numbers and wherein:
The words and phrases used herein should be given their ordinary and customary meaning in the art by one skilled in the art unless otherwise further defined.
Aerobic fermentation is an important biochemical process typically conducted in a controlled reaction vessel. The environmental conditions in the vessel, such as gas exhaust content, temperature, pH, dissolved oxygen levels, and agitation speed rate need to be closely monitored and controlled to promote larger cell growth and product formation rates. The presence of pure oxygen in the fermentor promotes a high oxygen transfer rate to the microorganisms, enhancing growth and production formation. Embodiments of the present invention provide a system for manipulating the oxygen flow rate during an aerobic fermentation such that the productivity, yield and the oxygen transfer efficiency are maximized. The embodiments described herein offer methods and systems to accurately calculate the amount of pure oxygen to supply in an agitated fermentor based on real-time measurements of DO and O2 exhaust concentrations, while maintaining desired agitation speed for desired pH levels or CO2 removal. In bubble and airlift fermentors, the N2 supply is controlled in addition to O2 supply. Illustrative embodiments of the present invention include batch and fed-batch fermentations but other modes of operation are also contemplated.
The embodiments of the invention include various process control systems to control the amount of pure oxygen supplied to a fermentor.
In one embodiment, the process control system 100 described above is applied to a fermentor.
As noted above, an embodiment of the process control system 300 described above can be applied to a mechanically agitated fermentor.
The agitation speed of a rotor inside a fermentor can affect the amount of DO and O2 exhaust during a fermentation. Accordingly, in another embodiment, the agitation speed of the rotor is controlled.
Additional variables such as pH, cell density, and cell product formation can help determine the optimum amount of O2 to be supplied during a fermentation.
Addition of pure oxygen to bubble type or airlifted fermentors may require the removal of excess CO2. To accomplish this, an additional injection of N2 may be utilized to remove CO2 and provide extra mixing, according to one embodiment. Therefore, the manipulated variables in the bubble fermentor are the O2 and N2 flow rates.
The following example is presented for a further understanding of the nature and objects of the present invention. The example is illustrative only and other embodiments of the integrated processes and apparatus may be employed without departing from the true scope of the invention.
This example describes one model that can be used to control oxygen flow into a fermentor during an aerobic fermentation. The model can consist of following equations, which reflect the most important interactions during the fermentation process when a gas flow rate into the fermentor is controlled by an adaptive controller:
Equation 1 represents a typical microorganism growth rate represented by the Monod Equation. The microorganism growth rate can be influenced by O2 as a substrate in a fermentor, and Equation 1 can be modified to Equation 2 to include the addition of O2. The overall cell mass concentration can be represented as the multiplicative contribution of the substrate and the oxygen concentrations. Equation 3 represents the change in cell mass concentration as a function of the substrate growth rate and oxygen growth rate. Equation 4 represents the substrate consumption and Equation 5 represents the product formation during a fermentation. Both the substrate consumption and product formation rates are limited by the corresponding yields. Equation 6 reflects the overall O2 available in the media, which is a function of the oxygen transferred from the gas phase to the media (OTR) and the oxygen consumed by the microorganisms (OCR).
There is a continuous supply and removal of gas from the fermentor in this model. Using a material balance, the amount of gas exiting the fermentor is calculated as the difference of the gas supply and the oxygen transferred to the media (OTR) as shown in Equation 7, the OTR being calculated in Equation 8. In reality, the mass transfer coefficient, kla, is a function of the inlet gas flow rate as it changes the size of gas bubbles. The mass transfer coefficient can also change with time due to physical properties of the media during the fermentation, and an example of a time varying kla is given by Equation 10:
kla=1e−06*t2−0.0001*t+0.0038; (10)
In order to perform a control experiment, a control algorithm is needed. A controller that can be used in this model is known as a proportional plus integral controller (PI). Equation 9 represents a controller in discrete form, in which M is the manipulating variable, in this case the gas inlet flow, Fi, and E is the error between the set point and the controlled variable, the O2 in the media. The constants bo and b1 are the controller tuning parameters, and k represents the time interval. The parameters in Equation 9 are constant parameters that are satisfactory for processes that do not change significantly with time. However, as shown in Equation 10, fermentation processes can change significantly with time. Therefore, the controller parameters, bo and b1, are not necessarily kept constant. An example of a simple adaptive controller is given by Equation 11, which shows that the controller parameter changes as the O2 measurement changes:
bo=−21.55*O2+2.1664 (11)
Processes and apparatus for practicing the present invention have been described. It will be understood and readily apparent to the skilled artisan that many changes and modifications may be made to the above-described embodiments without departing from the spirit and the scope of the present invention. The foregoing is illustrative only and other embodiments of the integrated processes and apparatus may be employed without departing from the true scope of the invention defined in the following claims.
This application claims the benefit under 35 U.S.C. § 119(e) to provisional application No. 60/686,730, filed Jun. 02, 2005, the entire contents of which are incorporated herein by reference.
Number | Date | Country | |
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60686730 | Jun 2005 | US |