Line 53: | Line 53: | ||
<br><br><br><br> | <br><br><br><br> | ||
<br><br><br><br> | <br><br><br><br> | ||
− | <br> | + | <br><br> |
<p>These growths were then scraped up and plated onto a LB+Spec plate.</p> | <p>These growths were then scraped up and plated onto a LB+Spec plate.</p> | ||
</html> | </html> |
Revision as of 16:14, 10 October 2016
Conjugation
We have attempted to conjugate GFP into both G. oxydans and G. hansenii with a Diaminopimelic Acid (DAP) auxotrophic strain of E. coli . The plasmid contains the vector pMMB67EH, the promoter PA-1, GFP and a spectinomycin resistance gene.
The first conjugation was done with KOM strains 4 (G. oxydans) 5 ( G. oxydans and 15 ( L. fermentati ). We attempted these conjugations before sequencing the recipient strains, so that is why we tried to conjugate into L. fermentati . First, a mixture between a KOM strain and the DAP auxotroph strain were plated on a LB+DAP solid medium to allow for conjugation to occur. After 24 hours of incubation, I scraped up the growth and plated each conjugation mixture onto a LB+Spec plate.
Next, we viewed the potential transconjugants on a fluorescence microscope.
We then picked these glowing colonies and then after streaking them out onto more LB+Spec plates, we attempted to use 16s sequencing to confirm successful conjugation. After troubleshooting our 16s procedure, we were finally able to obtain a viable sequencing result. However, all of the glowing colonies were identified as E. coli. For the next round of conjugation, we used a strain of both G. oxydans and Gluconacetobacter hansenii from the American Type Culture Collection (ATCC).
These growths were then scraped up and plated onto a LB+Spec plate.