Line 61: | Line 61: | ||
</td> | </td> | ||
<th> | <th> | ||
− | <b>pET29B in BL21 (Negative control)</b> | + | <b>pET29B in BL21 (Negative control)</b></th> |
+ | <td> | ||
<ul> | <ul> | ||
<li> 10 ml O/Ns in LB+Kan</li> | <li> 10 ml O/Ns in LB+Kan</li> | ||
Line 70: | Line 71: | ||
<li> 5 uL 1M IPTG</li> | <li> 5 uL 1M IPTG</li> | ||
</ul> | </ul> | ||
− | </ | + | </td> |
</tr> | </tr> | ||
− | <tr><th><b>Fermented "syn poo" supernatant</b> | + | <tr><th><b>Fermented "syn poo" supernatant</b></th></tr> |
+ | <tr> | ||
+ | <td> | ||
<ul> | <ul> | ||
<li> 10 ml O/Ns in LB+Kan</li> | <li> 10 ml O/Ns in LB+Kan</li> | ||
Line 82: | Line 85: | ||
<li> 23 ml dH<sub>2</sub>O</li> | <li> 23 ml dH<sub>2</sub>O</li> | ||
</ul> | </ul> | ||
− | </ | + | </td> |
− | <th><b>Pure VFAs</b> | + | <th><b>Pure VFAs</b></th> |
+ | <td> | ||
<ul> | <ul> | ||
<li> 10 ml O/Ns in LB+Kan</li> | <li> 10 ml O/Ns in LB+Kan</li> | ||
Line 99: | Line 103: | ||
<li> 30 ml dH<sub>2</sub>O</li> | <li> 30 ml dH<sub>2</sub>O</li> | ||
</ul> | </ul> | ||
+ | </td> | ||
</tr> | </tr> | ||
</table> | </table> |
Revision as of 00:09, 24 October 2017
Beta Oxidation
Insert beta-oxidation pathway only image here
Aim
...bla bla bla
Volatile fatty acids & beta-oxidation pathway
…
Gene construct
Insert gene construct image here
…
Chassis and vector
…
Experiment
Glucose (Positive control) | ||
---|---|---|
|
pET29B in BL21 (Negative control) |
|
Fermented "syn poo" supernatant | ||
|
Pure VFAs |
|
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:
pET29B in BL21 (Negative control)- 10 ml O/Ns in LB+Kan
- "Syn poo" fermented supernatant {..!!hyperlink to eng page for syn poo protocol..}
- 100 uL MgSO4
- 5 uL CaCl2
- 10 ml M9 salts
- 5 uL 1M IPTG
{..........what else was added was supernatant added....}
Glucose (Positive control)- 10 ml O/Ns in LB+Kan
- 7 ml 20% Glucose {..!!cite why this conc chosen..}
- 100 uL MgSO4
- 5 uL CaCl2
- 10 ml M9 salts
- 5 uL 1M IPTG
- 20 ml dH2O
- 10 ml O/Ns in LB+Kan
- 10 ml "Syn poo" fermented supernatant {..!!hyperlink to eng page for syn poo protocol..}
- 100 uL MgSO4
- 5 uL CaCl2
- 10 ml M9 salts
- 5 uL 1M IPTG
- 23 ml dH2O
- 10 ml O/Ns in LB+Kan
- VFAs
- 410 uL propionic acid
- 118 uL acetic acid
- 55 uL butyric acid
- 100 uL MgSO4
- 5 uL CaCl2
- 10 ml M9 salts
- 5 uL 1M IPTG
- 30 ml dH2O
The OD600 readings of .....???? were taken and recorded:
Condition | OD600 of replicate 1 | OD600 of replicate 2 | OD600 of replicate 3 |
---|---|---|---|
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 |
---|---|---|---|
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 |