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Team:Valencia/Notebook/Week12
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<div class=col_center_top><b>WEEK 12</b></div><!-- fin clase col_left_top--> | <div class=col_center_top><b>WEEK 12</b></div><!-- fin clase col_left_top--> | ||
<div class=col_center_center> | <div class=col_center_center> | ||
| - | <b> | + | <b>Engineering:</b> The prototype is finished and we are doing several trials to check that everything goes properly and yes it does! |
<br><br> | <br><br> | ||
| - | <b>pH-stat</b> | + | <b>pH-stat:</b> There was a large increase in the concentration of Synechocystis, especially in flasks 5 and 6, but also contamination from other microorganisms. |
| - | < | + | <p>We started two new 80 ml cultures to which 2 ml of fertilizer to each one was added. They finally began to develop favourably, increasing their concentration and also we could see a vast majority of growing cells against the cells which are not reproducing.</p> |
| - | <b>Colicin production</b> | + | <p>Once we obtained and established the culture under laboratory conditions, we measured the change in pH. Since the 24 hour light had caused serious damage to the culture, we measured the pH changes that occurred each hour in photoperiods of 4 hours of light and 4 of darkness.</p> |
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| + | <br> | ||
| + | <b>Colicin production:</b> We start growing the E.coli with microcin C51 in LB medium with ampicilin. And we perform a viable count and a plasmid extraction too.<br> | ||
</div><!-- fin clase col_left_top--> | </div><!-- fin clase col_left_top--> | ||
Latest revision as of 23:47, 21 September 2011
WEEK 12
Engineering: The prototype is finished and we are doing several trials to check that everything goes properly and yes it does!
pH-stat: There was a large increase in the concentration of Synechocystis, especially in flasks 5 and 6, but also contamination from other microorganisms.
Colicin production: We start growing the E.coli with microcin C51 in LB medium with ampicilin. And we perform a viable count and a plasmid extraction too.
pH-stat: There was a large increase in the concentration of Synechocystis, especially in flasks 5 and 6, but also contamination from other microorganisms.
We started two new 80 ml cultures to which 2 ml of fertilizer to each one was added. They finally began to develop favourably, increasing their concentration and also we could see a vast majority of growing cells against the cells which are not reproducing.
Once we obtained and established the culture under laboratory conditions, we measured the change in pH. Since the 24 hour light had caused serious damage to the culture, we measured the pH changes that occurred each hour in photoperiods of 4 hours of light and 4 of darkness.
Colicin production: We start growing the E.coli with microcin C51 in LB medium with ampicilin. And we perform a viable count and a plasmid extraction too.
