Difference between revisions of "Part:BBa K1122680"
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<partinfo>BBa_K1122680 short</partinfo> | <partinfo>BBa_K1122680 short</partinfo> | ||
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This part enables expression of ferric uptake repressor (Fur) using IPTG induction | This part enables expression of ferric uptake repressor (Fur) using IPTG induction | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K1122680 SequenceAndFeatures</partinfo> | <partinfo>BBa_K1122680 SequenceAndFeatures</partinfo> | ||
+ | ===Cloning=== | ||
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+ | Part was cloned from ''B. subtilis'' gDNA. Reaction product was analysed on an agarose gel (Figure 1) | ||
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+ | Figure 1. Agarose gel shows a PCR product of a desired size | ||
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+ | ===Functional analysis=== | ||
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+ | It was assumed that over-expression of Fur could increase bacterial tolerance to increased iron concentration due to enhanced perception of environmental [iron]. This was analysed experimentally be culturing cells induced and not induced to express Fur in LB nmedium supplemented with increasing concentrations of iron. Results obtained (figure 2)indicate that indeed the cells that contain more copies of Fur protein survive better in medium with increased iron levels | ||
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+ | [[File:Fur_graph]] | ||
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+ | Figure 2. Survival of cells induce and noninduced to express Fur in varying iron concentrations. | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Revision as of 16:26, 4 October 2013
Plac - LacZ - Fur
This part enables expression of ferric uptake repressor (Fur) using IPTG induction
Usage and Biology
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 769
Cloning
Part was cloned from B. subtilis gDNA. Reaction product was analysed on an agarose gel (Figure 1)
Figure 1. Agarose gel shows a PCR product of a desired size
Functional analysis
It was assumed that over-expression of Fur could increase bacterial tolerance to increased iron concentration due to enhanced perception of environmental [iron]. This was analysed experimentally be culturing cells induced and not induced to express Fur in LB nmedium supplemented with increasing concentrations of iron. Results obtained (figure 2)indicate that indeed the cells that contain more copies of Fur protein survive better in medium with increased iron levels
Figure 2. Survival of cells induce and noninduced to express Fur in varying iron concentrations.