Difference between revisions of "Part:BBa K200018:Experience"
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<partinfo>BBa_K200018 1</partinfo> | <partinfo>BBa_K200018 1</partinfo> | ||
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+ | <br> | ||
[[Image:II09_CRP-GFP fluor different media.jpg|500px|right]] | [[Image:II09_CRP-GFP fluor different media.jpg|500px|right]] | ||
Cells with BBa_K200018 were grown overnight in various different media, and the GFP fluorescence was measured. <br> | Cells with BBa_K200018 were grown overnight in various different media, and the GFP fluorescence was measured. <br> | ||
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For all the other secondary carbon sources, 10% Casamino Acids in M9 shows the highest corrected fluorescence at 22000.<br> | For all the other secondary carbon sources, 10% Casamino Acids in M9 shows the highest corrected fluorescence at 22000.<br> | ||
− | [[Image:II09_CRP-GFP abs different media.jpg|500px|right]] | + | <br> |
+ | <br> | ||
+ | [[Image:II09_CRP-GFP abs different media.jpg|500px|right]]<br> | ||
For effective gene expression, not only must the promoter activity be strong, but there must also be enough cells expressing the genes. Therefore, OD600 is also a critical factor.<br> | For effective gene expression, not only must the promoter activity be strong, but there must also be enough cells expressing the genes. Therefore, OD600 is also a critical factor.<br> | ||
<br> | <br> | ||
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+ | [http://2012.igem.org/Team:University_College_London The 2012 iGem UCL team] further characterized the cstA promoter ([https://parts.igem.org/Part:BBa_K118011 Part:BBa_K118011]) using GFP as a reporter gene ([https://parts.igem.org/Part:BBa_E0040 Part:BBa_E0040]). | ||
+ | ''E. coli'' transformed with cstA promoter fused with GFP was grown overnight in LB media, in order to induce the starvation response cells were centrifuged and resuspended in minimal M9 media supplemented with different glucose concentrations (0%, 0.2%, 0.5%, 1.0%, 2.0%, 5%) and chloramphenicol (15 μg/mL). The tested cultures incubated at different concentrations of glucose shown a trend of decreasing GFP expression with raising glucose concentration. Fluorescence was highest at 0% added glucose and lowest at 5%, which implies that the starvation response increases the cstA promoter activity. | ||
+ | [[Image:UCL2012-chart.jpg|thumb|center|700px|]] | ||
<partinfo>BBa_K200018 EndReviews</partinfo> | <partinfo>BBa_K200018 EndReviews</partinfo> |
Latest revision as of 16:20, 13 September 2012
This experience page is provided so that any user may enter their experience using this part.
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how you used this part and how it worked out.
Applications of BBa_K200018
User Reviews
UNIQf8c0a589e2a3235a-partinfo-00000000-QINU UNIQf8c0a589e2a3235a-partinfo-00000001-QINU
UNIQf8c0a589e2a3235a-partinfo-00000002-QINU
BBa_K200018 1 Not understood Kun |
Cells with BBa_K200018 were grown overnight in various different media, and the GFP fluorescence was measured. For effective gene expression, not only must the promoter activity be strong, but there must also be enough cells expressing the genes. Therefore, OD600 is also a critical factor.
|
[http://2012.igem.org/Team:University_College_London The 2012 iGem UCL team] further characterized the cstA promoter (Part:BBa_K118011) using GFP as a reporter gene (Part:BBa_E0040). E. coli transformed with cstA promoter fused with GFP was grown overnight in LB media, in order to induce the starvation response cells were centrifuged and resuspended in minimal M9 media supplemented with different glucose concentrations (0%, 0.2%, 0.5%, 1.0%, 2.0%, 5%) and chloramphenicol (15 μg/mL). The tested cultures incubated at different concentrations of glucose shown a trend of decreasing GFP expression with raising glucose concentration. Fluorescence was highest at 0% added glucose and lowest at 5%, which implies that the starvation response increases the cstA promoter activity. UNIQf8c0a589e2a3235a-partinfo-00000004-QINU |