Team:UNICAMP-Brazil/Notebooks/October 14

(Difference between revisions)

Revision as of 19:32, 21 October 2009

Now that we have PY1 promoter + RFP inserted in a plasmid with kanamycin resistance we are able to transform the conjugative strain. As we said before, this conjugative strain already has ampicilin resistance, which is why we inserted our construction in a plasmid with a different resistance.

Before transforming this strain we need to prepair electrocompetent cells. So today we inoculated a colony of this strain in liquid LB-AMP at 37ºC to prepare the competent cells tomorrow.

Fabi and Léo

We digested the Adh1+Lysozyme/biofusion minipreps in order to connect it to the yeast expression vector (YEP358). We used the XbaI and PstI enzymes. 9 of 10 digestions worked! =) The expected fragment size is 2000bp.

We chose two fragments and purified them from the agarose gel. We ligated them to YEP358. We will transform it tomorrow.

Raíssa and Taís

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 ==== PY Promoter - Preparation of electrocompetent cells of the conjugative strain ====
-*<p style=”text-align:justify;”>Now that we have PY1 promoter + RFP inserted in a plasmid with kanamycin resistance we are able to transform the conjugative strain. As we said before, this conjugative strain already has ampicilin resistance, that is why we inserted our construction in a plasmid with a different resistance.</p>
+*<p style=”text-align:justify;”>Now that we have PY1 promoter + RFP inserted in a plasmid with kanamycin resistance we are able to transform the conjugative strain. As we said before, this conjugative strain already has ampicilin resistance, which is why we inserted our construction in a plasmid with a different resistance.</p>
 *<p style=”text-align:justify;”>Before transforming this strain we need to prepair electrocompetent cells. So today we inoculated a colony of this strain in liquid LB-AMP at 37ºC to prepare the competent cells tomorrow.</p>