PRK

Achievements:

1. Construction and digestion of DNA gel shows that the size of it was right
2. The SDS-PAGE of PRK showed that the expression of PRK in the expected protein size
3. PRK toxicity test proves that the function of it varies when cloned into different plasmid

We constructed PRK fragments from IDT DNA synthesis. After PCR amplification, PRK is then cloned into pSB1C3 and transformed into DH5α. SDS-PAGE ensured that the protein expression was as expected. The results are shown below:

Fig. 1: Confirmation of prk digestion.
Fig. 2: Confirmation of PRK expression in DH5˚α. The expected protein size is 37.7kDa.

We initially decided to test its function by HPLC to measure the amount of RuBP inside the cell. Our instructors pointed out some difficulties in HPLC measurement such as excessive noise signal in our sample.We therefore determined to test its function with a toxicity test. The product of PRK-RuBP cannot be metabolite by wild type E. coli. The accumulation of RuBP depletes the sugar from the native pentose phosphate pathway. Lack of carbon source, the growth of that strain may be repressed. We incubate the PRK expressing strain and control stain that contains no plasmid in M9 medium and altered M9 medium with 0.4% xylose as its sole carbon source. In normal M9 medium, glucose will not be converted into RuBP. In altered M9 medium, xylose will go through the native pathway and be converted into RuBP. Growth arrest of PRK strain should be observed.

We tested PRK in different strains. We first cloned prk into pSB1C3 and transformed into BL21(DE3). After 12 hours, the strain without plasmid could grow up to 1.4 O.D.600 in altered M9 xylose medium. The strain that contains PRK can grew up to 0.75 O.D.600 in normal M9 medium either. In contrast, the PRK strain that grew in altered M9 xylose medium showed no growth at all. The result shows that PRK can suppress/inhibit the growth, which matches to our expectation.

Fig. 3 The result of PRK test in BL21(DE3). The PRK expressing strain is incubated in both normal M9 medium and altered M9 xylose medium to compare with the strain without plasmid. The PRK expressing strain grown in altered M9 xylose showed merely no growth, which proves the function of PRK.

Although the function of PRK have been confirmed, we would like to lower the expression of it to minimize the growth arrest. We thus cloned the part into pSB3K3, a low copy number plasmid to lower its protein expression. We then compare the growth under high and low copy number plasmid. We found out that pSB3K3 shows a little growth arrest comparing to the strain without plasmid. The growth of it exceed that of PRK expressed in pSB1C3. We can regulate the expression of PRK via high or low copy number plasmid to optimize the growth and carbon fixation efficiency of the bacteria.

Fig. 4 Compares the growth in M9 xylose medium of PR K expressing strain in high and low copy number plasmid. The low copy number plasmid, pSB3K3, shows a little bit of growth retard compare to non-PRK expressing strain. However, the toxicity is much less than high copy number expressing strain.

We also transformed pSB3K3-prk into W3110 strain. W3110 is reported to have higher pressure tolerance. The trend of the results is similar to that of the BL21(DE3) but there is no statistically significant between the experiment and the control group. We deduce that PRK can still function in W3110 since the trend matches our expectation. As pSB3K3 is a low copy number plasmid, the expression of protein may be lower than that of high copy number plasmid. The pressure tolerance of W3110 strain may also lessen the toxicity influence by PRK.

CA

Achievements:

1. Construct the ca and transform it into BL21(DE3)
2. Run the SDS-PAGE to confirm its expression
3. Measure the activity of CA enzyme

We cloned the DNA fragments into pSB1C3 plasmid after the gene is amplified with PCR. We transform the plasmid into DH5-alpha and BL21(DE3). Next, we confirm its protein expression with SDS-PAGE.

Fig. 5 Confirmation of ca digestion
Fig. 6 Confirmation of CA expression in BL21(DE3). The expected protein size is 27.9kDa.

We then ran the activity test of CA. In our bypass pathway, the function of CA is to convert proton and bicarbonate into water and carbon dioxide. During the reaction, the concentration of proton can be easily observed by the pH meter. By measuring the time interval between the pH shift and compare with the sample without CA, we can determine the activity of that specific enzyme. The enzyme activity of our CA is 21.8 unit/liter. To confirm the contribution of the CA to the whole pathway, we also ran the total solution which will be described in the following content.

Rubisco

Achievements:

1. Construction and digestion of DNA gel shows that the size of it was right
2. The SDS-PAGE of PRK showed that the expression of PRK in the expected size

We constructed PRK fragments from IDT DNA synthesis. After PCR amplification of the three subunits, rubisco is then cloned into pSB1C3 and transformed into DH5α. SDS-PAGE ensured that the protein expression was as expected. The results are shown below:

Fig. 7 Confirmation of rbcL digestion.
Fig. 8 Confirmation of rbcL expression in DH5˚α. The expected protein size is 52.37kDa.

After mining a lot of information from the publications, we found out a method to determine the activity of rubisco by thin-layer chromatographic has been reported. However, due to time concern, we are not capable of measuring the enzyme activity of Rubisco with this method. We finally confirm its function from the results of total solution test.

Rubisco

Achievements:

1. Develop an index to evaluate the carbon fixation ability of each constructed strain
2. Confirm the importance of Rubisco enzyme in bypass pathway
3. Check the growth and carbon fixation enhancement of CA enzyme
4. Compare the carbon fixation rate of W3110 and BL21(DE3) E. coli strains
5. Compare different CO2 incubation environment

Overview

In the total solution experiment, we strive to measure the carbon fixation amount of each sample. After reading numerous publications, we found out that previous researches determine the efficiency of carbon fixation via measuring the decrease of carbon dioxide concentration in the closed system or measure the weight percentage of C14 radioisotope in the dry cell. However, due to biosafety constrain of our lab, we can barely use the radioisotope. Measuring the decrease of carbon dioxide concentration in the closed system is also impractical for us since we have too much test samples. A new method to measure multiple samples in the short period of time is developed by our team. We are able to evaluate the fixation efficiency of each sample with optical density O.D. 600 and xylose consumption. We have measure various construction to prove that the enzyme of our construction is necessary for carbon fixation.

The test samples below were incubated in an altered M9 medium which substitute glucose to xylose. 1/1000 of LB medium was added to support some rare elements. Since the concentration of LB medium is too low, it doesn’t contribute the carbon source of the bacteria.

We defined a new index, Xylose Utilization Index, to describe the potential of carbon fixation. We can compare this index of each strain to find out the strain that has highest capacity of carbon fixing.

To define the XUI index, we firstly made two assumptions:

1. O.D. 600 of the sample has linear relationship to dry cell weight (biomass). Optical density is frequently used as a means of describing the cell density in the broth. We measured the dry cell weight of samples in different O.D. value and discovered that it has linear relationship. We conclude that we can utilize O.D. value to estimate the dry cell weight. 1 0.D. of BL21(DE3) strain per litter yields the dry cell weight of 0.8 gram.

Fig. 9 shows the dry cell weight of BL21(DE3) incubated in altered M9 xylose medium. A linear relationship between O.D. and dry cell weight is observed.

2. The elemental formula of E. coli should be fixed or varies within a small range. Although there may exist slightly different in different growth condition, we assume that such error can be ignore during the following calculation.

After these two assumptions, the Xylose Consumption Index is designed to evaluate the carbon fixation ability of each strain. The definition of the index is xylose consumption over O.D. 600. O.D. 600 measurement can be viewed as the weight of carbon of the bacteria. The index shows the ratio of xylose consumption per biomass. For wild type E. coli, it only consumes xylose (the sole carbon source provided in our medium) as its carbon source. Although some native E. coli pathway may utilize CO2 (such as lipid synthesis), the amount is too small to consider. As for engineered strain, carbon dioxide can be utilized as it’s carbon source. By producing same amount of carbon biomass, it requires less xylose. We can thus compare the XUI of each strain to determine the possible strain that fix carbon. The less the XUI in the sample, the more possibility that it fix carbon.

We use the Dinitrosalicylic Acid (DNS) reducing sugar assay to measure the xylose concentration in the medium. Under base solution, DNS will turn to brown color while reacting with reductive sugar in high temperature. In the specific temperature range, the color will have linear relationship with the reductive sugar concentration. We can thus measure the xylose concentration at O.D.540.

Fig. 10 Shows the calibration line of DNS assay kit.

Before measuring the XUI, we observe the growth curve of each strain. We found out that W3110(L5T7) constructed strain cannot grow in altered M9 solution. W3110(L5T7) is a newly constructed strain, we are not quite certain its characteristic. We eliminate this strain from the following experiment. BL21(DE3) and W3110 constructed strains show little growth after 24 hours.

Fig. 11 shows the growth of W3110(L5T7), BL21(DE3), W3110 incubated in normal incubator for 24 hours. The growth of W3110(L5T7) is not obvious while other strains shows growth after 24hours.

Total solution check: Function of Rubisco

We then utilized XUI to evaluate the function of each enzyme in the pathway. We first check the function of Rubisco in BL21(DE3) strain. Rubisco enzyme with promoter P_T7 (BBa_K2762011) was cloned into pSB1C3 and PRK with promoter P_LacI (BBa_K2762007)was cloned into pSB3K3. Both plasmids were then co-transformed into BL21(DE3). We measure the XUI of the strain and compare to the control that IPTG was not added and BL21(DE3) without plasmid. IPTG can induce the promoter P_T7 to produce the downstream enzyme. The growth of each strain is first examined. The IPTG induced strain showed growth retard. We assume the cause of growth retard is due to the pressure from overexpressing the protein rubisco. The control strain without IPTG induction produce less rubisco enzyme than the experiment and had less pressure. We then compare the XUI of each strain and discovered that control strain without IPTG induction produce less rubisco enzyme than the experiment. Without rubisco, the bypass pathway is not capable of using CO2. We found out that the strain without Rubisco has higher XUI, symbolizing that rubisco is essential in carbon fixation pathway.

Fig. 12 Shows the growth and XUI measured in 5% CO2 incubation of 12 hours respectively. Lower growth of the strain that contains. The XUI of the strain that contains both Rubisco and PRK shows statistically significant decrease compare to strain without both enzymes.

We developed a closed bioreactor system and implemented online monitoring system which can live monitoring several environmental parameters. Here is the detail of our bioreactor.

Gas inlet port are located on the bioreactor’s lower part while outlet port are located on the bioreactor’s upper lid. As low concentration CO2 enters the bioreactor, it flows through the diffuser refiner and dissolves in the buffered medium to form acid. A pH sensor and temperature sensor is installed to monitor the bioreactor tank for further control implementation. Besides, the CO2 concentration level of exhaust gas is monitored by a CO2 gas sensor, which is mounted on the upper lid. These sensor’s output is connected to an Arduino analog input and sensor readings are displayed on a serial LCD which is attached on the lid of bioreactor. The data is then uploaded in real time to a web server via WiFi by using Arduino WiFi Shield.

To prevent sedimentation of cells at the bottom of bioreactor, we build our own 3D printed slow speed magnetic stirrer which permits gentle mixing of microcarrier cell cultures. The 3D printed magnet bed is designed specifically for two magnets and can be fitted on the DC motor. The stirrer works by using a DC motor to spin two magnets with opposite polarity, which could create a magnetic field in the bioreactor and cause the stir bar to spin and mix the contents. For controlling the speed of the DC motor, we use Arduino and L298N to control the input voltage to the motor by using PWM signal.

Besides, we also implemented fed-batch culture system in our design. Nutrients are fed to the bioreactor during cultivation to prevent nutrient depletion. The nutrients are pumped into the growth chamber at a rate proportional to the growth factor of the culture, which is determined experimentally through the doubling time of the particular bacterial strain.

• Acrylic Sheet
• Arduino UNO
• Power Supply
• Batteries
• Rotameter
• pH meter
• Thermometer(DS18B20)
• CO2 sensor(MG811)
• Wi-fi sensor(ESP8266 NodeMcu)
• Geared DC Motor
• Tubes
• Magnets
• 3D Printed Structure
• Nuts and Screws
• Wires
• Pumps