Beta Oxidation
Aim
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Volatile fatty acids & beta-oxidation pathway
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Gene construct
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Chassis and vector
The part was inserted into pET29b vector downstream a T7 promoter and lac operon. Thus, the expression of the operon was induced using Isopropyl β-D-1-thiogalactopyranoside (IPTG). E. coli (BL21) was chosen as the chassis because of its ability in better protein expression. After transforming the bacteria with plasmid, colonies were selected and screened for presence of plasmid. A successful colony was then selected for experiments.
Experiment
The O/Ns were grown in the respective media for ~24 hours. The flasks containing different media was inoculated with the O/Ns after adjusting the OD600. The composition of each of the replicate in the flasks is shown below:Glucose (Positive control) | pET29B in BL21 (Negative control) |
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Fermented "syn poo" supernatant | Pure VFAs |
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The OD600 readings of .....???? were taken and recorded:
Condition | OD600 of replicate 1 | OD600 of replicate 2 | OD600 of replicate 3 |
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pET29b in BL21 (Negative control) | 0.571 | 0.531 | 0.487 |
Glucose (Positive control) | 0.190 | 0.195 | 0.139 |
Pure VFAs | 0.140 | 0.134 | 0.146 |
Fermented "syn poo" supernatant | 0.135 | 0.107 | 0.144 |
After spinning down the culture in flasks, the cells were resuspended in 1x PBS. The OD600 readings were taken:
Condition | OD600 of replicate 1 | OD600 of replicate 2 | OD600 of replicate 3 |
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pET29b in BL21 (Negative control) | 2.659 | 2.001 | 2.899 |
Glucose (Positive control) | 1.934 | 1.887 | 1.919 |
Pure VFAs | 0.510 | 0.571 | 0.532 |
Fermented "syn poo" supernatant | 2.533 | 2.559 | 2.349 |