Difference between revisions of "Part:BBa K1590009"
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<partinfo>BBa_K1590009 short</partinfo> | <partinfo>BBa_K1590009 short</partinfo> | ||
| − | Escherichia coli PotD sequence, encoding Spermidine/putrescine-binding periplasmic protein. | + | <i>Escherichia coli</i> PotD sequence, encoding Spermidine/putrescine-binding periplasmic protein. |
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K1590009 SequenceAndFeatures</partinfo> | <partinfo>BBa_K1590009 SequenceAndFeatures</partinfo> | ||
| − | + | ===Usage and Biology=== | |
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| + | For semen detection our main target ligand is the polyamine spermidine which is found in relatively high concentrations in seminal fluid (5-15 mM). Spermidine is made from another polyamine called putrescine and is the precursor of spermine. Regulation of polyamine synthesis, degradation and transport is tightly controlled in bacteria. In E. coli, two of three identified transport systems are ABC transporters composed of a periplasmic binding protein, a pair of transmembrane proteins and a membrane protein possessing ATPase catalytic activity. Out of these three components, we were interested in investigating the periplasmic binding protein PotD which specifically binds spermidine. The fact that this protein is responsible for transportation of spermidine and lacking in enzymatic activity meant that it was an ideal candidate for use in FluID for semen detection. | ||
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| + | 6-His - PotD was purified by Ni-affinity chromatography and subsequently blotted against. | ||
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| + | https://static.igem.org/mediawiki/2015/7/70/Semen-fig3.png | ||
| + | <br> | ||
| + | Chromatogram showing the purification profile of the his-tagged bacterial protein, PotD. The fractions corresponding to the two peaks observed on the chromatograph were further analysed on SDS page gel. B) Coomassie Stain of the purified fractions (A12 + B12). 10 µl of each fraction was mixed with 10 µl of 2x Laemmli buffer and loaded onto an SDS gel which was ran for 1 hour at 100V and then stained. These were then western blotted to confirm the presence of our target protein PotD-His. | ||
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===Functional Parameters=== | ===Functional Parameters=== | ||
<partinfo>BBa_K1590009 parameters</partinfo> | <partinfo>BBa_K1590009 parameters</partinfo> | ||
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Revision as of 20:04, 18 September 2015
Spermidine/putrescine-binding periplasmic protein
Escherichia coli PotD sequence, encoding Spermidine/putrescine-binding periplasmic protein.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 429
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 148
- 1000COMPATIBLE WITH RFC[1000]
Usage and Biology
For semen detection our main target ligand is the polyamine spermidine which is found in relatively high concentrations in seminal fluid (5-15 mM). Spermidine is made from another polyamine called putrescine and is the precursor of spermine. Regulation of polyamine synthesis, degradation and transport is tightly controlled in bacteria. In E. coli, two of three identified transport systems are ABC transporters composed of a periplasmic binding protein, a pair of transmembrane proteins and a membrane protein possessing ATPase catalytic activity. Out of these three components, we were interested in investigating the periplasmic binding protein PotD which specifically binds spermidine. The fact that this protein is responsible for transportation of spermidine and lacking in enzymatic activity meant that it was an ideal candidate for use in FluID for semen detection.
6-His - PotD was purified by Ni-affinity chromatography and subsequently blotted against.
Chromatogram showing the purification profile of the his-tagged bacterial protein, PotD. The fractions corresponding to the two peaks observed on the chromatograph were further analysed on SDS page gel. B) Coomassie Stain of the purified fractions (A12 + B12). 10 µl of each fraction was mixed with 10 µl of 2x Laemmli buffer and loaded onto an SDS gel which was ran for 1 hour at 100V and then stained. These were then western blotted to confirm the presence of our target protein PotD-His.