Difference between revisions of "Team:Aachen/Lab/Bioreactor/Hardware"
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=Overview= | =Overview= | ||
− | One of the vital elements of a Do-It-Yourself bioreactor is the hardware design which should be feasible as well as reliable. The most important point to be kept in mind while constructing a bioreactor is the sterility. At every step of the development of the bioreactor, we have fulfilled | + | One of the vital elements of a Do-It-Yourself bioreactor is the hardware design which should be feasible as well as reliable. The most important point to be kept in mind while constructing a bioreactor is the sterility. At every step of the development of the bioreactor, we have fulfilled these criteria. |
{{Team:Aachen/ReadMore|title=Construction Manuals|link=/Team:Aachen/Notebook/Construction_Manuals|picture=rmConstruction|url=/wiki/images/1/15/Aachen_tile_Lab_Bioreactor_Hardware_construction_manuals.JPG}} | {{Team:Aachen/ReadMore|title=Construction Manuals|link=/Team:Aachen/Notebook/Construction_Manuals|picture=rmConstruction|url=/wiki/images/1/15/Aachen_tile_Lab_Bioreactor_Hardware_construction_manuals.JPG}} | ||
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==Principle== | ==Principle== | ||
− | For our bioreactor, we | + | For our bioreactor, we need a peristaltic pump and it is necessary to use sterile tubings which requires the pumps to be assembled and disassembled in minimum possible time. Hence the pumps were built with different layers and a 3D structure that could be partly disassembled to position the tube. The tube was pressed between the 3D structure and the walls thereby generated the required pressure to pump the liquid from one side to another. |
A detailed construction manual is available at '''[[Team:Aachen/Notebook/Construction_Manuals/Pumps|pumps]]'''. | A detailed construction manual is available at '''[[Team:Aachen/Notebook/Construction_Manuals/Pumps|pumps]]'''. | ||
=Stirrer= | =Stirrer= | ||
− | {{Team:Aachen/Figure|Aachen_Reactor_Vortex.JPG|title=The vortex inside the reactor | + | {{Team:Aachen/Figure|Aachen_Reactor_Vortex.JPG|title=The vortex inside the reactor created by our stirrer|subtitle=The stirring range is between 200 rpm and 1400 rpm|size=medium}} |
We use a DC motor and a 3D printed structure holding 4 magnets as our stirrer. The Voltage to the circuit is controlled using Analog output values thus controlling the speed of the stirrer. The magnets are placed in such a way so that half of the structure is north and the other half is south. This increases the area of magnetism thus holding the stirrer firmly into its magnetic pull. | We use a DC motor and a 3D printed structure holding 4 magnets as our stirrer. The Voltage to the circuit is controlled using Analog output values thus controlling the speed of the stirrer. The magnets are placed in such a way so that half of the structure is north and the other half is south. This increases the area of magnetism thus holding the stirrer firmly into its magnetic pull. | ||
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=Continous OD Device= | =Continous OD Device= | ||
− | + | How can we find out if there is really bacteria growing in our reactor? The common way is doing OD measurements. But if there is only 10 ml of reactor volume, every measurement would disturb the conditions drastically and thereby influence the experiment itself. Therefore, we are required to take minimum possible sample volume. | |
− | How can we find out if there is really bacteria growing in our reactor? The common way is doing OD measurements. But if there is only 10 ml of reactor volume, every measurement would disturb the conditions drastically and thereby influence the experiment itself. | + | |
{{Team:Aachen/Figure|Aachen_ODCloseup.jpg|title=Optical Density Measurement device|subtitle=As shown the transmitter and receiver are placed opposite sides of the tube|size=large}} | {{Team:Aachen/Figure|Aachen_ODCloseup.jpg|title=Optical Density Measurement device|subtitle=As shown the transmitter and receiver are placed opposite sides of the tube|size=large}} | ||
− | It is | + | It is also important that the samples are taken in a sterile manner. Furthermore the OD should be measured automatically so that the experiment can run without the need of a person taking samples. Finally the device to measure to OD has to be cheap and easy to assemble while having a precision to compete with commercial spectrometers. |
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− | Light having wavelength 605 nm is emitted by a LED and is emitted in the medium. On the opposite side, we have a | + | Light having wavelength 605 nm is emitted by a LED and is emitted in the medium. On the opposite side, we have a phototransistor to measure the intensity of the light reaching it, through the sample. |
− | We have developed on iGEM Aachen 2014 OD device measurement principle to get live data, and built a device using optimum materials, along with use of calibration file to get as precise | + | We have developed on iGEM Aachen 2014 OD device measurement principle to get live data, and built a device using optimum materials, along with use of calibration file to get as precise values as possible. |
− | To obtain the cell concentration in the medium, a special transistor that converts light to frequency, TSL 235R<ref></ref>, is used. | + | To obtain the cell concentration in the medium, a special transistor that converts light to frequency, TSL 235R<ref>http://www.ti.com/lit/ds/symlink/tsl235.pdf</ref>, is used. |
To keep the whole measurement sterile, the medium with the bacteria flows through silicon tubes and a transparent glass structure through the device without getting in contact with the surrounding air, while the device itself is mounted around this tube. | To keep the whole measurement sterile, the medium with the bacteria flows through silicon tubes and a transparent glass structure through the device without getting in contact with the surrounding air, while the device itself is mounted around this tube. | ||
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− | To test if our continuous OD device can also be used to monitor batch fermentations, we set up a simple batch culture. We used a preculture of | + | To test if our continuous OD device can also be used to monitor batch fermentations, we set up a simple batch culture. We used a preculture of ''Eschererichia coli'' BL21 Gold (DE3) with plasmid pSB1KRDP in M9 medium with 40 mM glucose that was grown in a stirred flask. A pump was used to cycle the culture from the vessel through the continuous OD sensor and back into the vessel. This setup was far from being perfect from a bioprocess perspective, but the goal of this experiment was testing the OD sensor and not the generation of biologically relevant samples. |
{{Team:Aachen/Figure|Aachen_OnlineOD.png|title=Growth Curve Recorded with our Online OD Unit|subtitle=The growth rate is smoothed with a moving average over 150 data points.|size=large}} | {{Team:Aachen/Figure|Aachen_OnlineOD.png|title=Growth Curve Recorded with our Online OD Unit|subtitle=The growth rate is smoothed with a moving average over 150 data points.|size=large}} | ||
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+ | As shown in the figure above, our DIY online OD sensor capable of recording growth curves at a very high resolution. By building multiple sensor units it is certainly possible to increase the throughput and data quality of strain characterization experiments. | ||
=Assembly= | =Assembly= |
Latest revision as of 15:58, 5 October 2015