Team:Imperial College/PHB production
From 2013.igem.org
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|[[File:Nilered.JPG|thumbnail|right|400px|<b>left</b> control cells <b>right phaCAB transformed MG1655</b>]] <br><br><br> | |[[File:Nilered.JPG|thumbnail|right|400px|<b>left</b> control cells <b>right phaCAB transformed MG1655</b>]] <br><br><br> | ||
- | |[[File:27-9-13phaCABall.jpg|thumbnail|right|400px| | + | |[[File:27-9-13phaCABall.jpg|thumbnail|right|400px|MG1655 constructs synthesising plastic. Strains were grown on Nile red plates, which stain the PHB strongly and fluoresce in presence of PHB. On the left are MG1655 cells with an empty vector (no fluorescence; no plastic), at the bottom is the native promoter (i.e. low fluorescence, some plastic). At the top and right we have our constitutive and hybrid promoter (respectively), which both show high expression and thus fluoresce very clearly.]] |
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O/N cutures of MG1655 transformed with either control or phaCAB plasmid were spread onto LB-agar plates with 3% glucose and Nile red staining. The staining indicates the production of P3HB. | O/N cutures of MG1655 transformed with either control or phaCAB plasmid were spread onto LB-agar plates with 3% glucose and Nile red staining. The staining indicates the production of P3HB. |
Revision as of 12:23, 28 September 2013
PHB production
Nile red staining
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O/N cutures of MG1655 transformed with either control or phaCAB plasmid were spread onto LB-agar plates with 3% glucose and Nile red staining. The staining indicates the production of P3HB.
Purification of P3HB