Difference between revisions of "Part:BBa K4390100"
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<partinfo>BBa_K4390100 short</partinfo> | <partinfo>BBa_K4390100 short</partinfo> | ||
| − | + | ==Improvement of part BBa_K3380600== | |
| + | This part is an improvement of [[Part:BBa_K3380600]], as it expands the possibility of usage to detecting lead. | ||
| + | The Edinburgh-UHAS_Ghana team for 2022 designed a construct to detect lead in contaminated water. This construct is composed of a fluorescent RNA aptamer iSpinach flanked by the F30 tRNA scaffolds (BBa_K4390094) which under a strong T7 RNA promoter (BBa_I712074), downstream of the promotor there is the lead promotor which acts as the binding site for the pbrR repressor (BBa_K346002) as to allow transcriptional repression of the T7 promotor. This construct is designed to be cell-free and only requires transcription of the RNA aptamer to produce fluorescence. It should be noted that T7 RNA polymerase, chemical energy (ATP), NTPs and DFHBI or DFHO are also required in the cell-free reaction so that fluorescence is observed. | ||
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| + | ===Usage and Biology=== | ||
| + | This biosensor should be used with a cell-free lysate which contains the pbrR repressor T7 RNA polymerase, chemical energy (ATP), NTPs and DFHBI or DFHO to induce fluorescence in the presence of arsenic ions. The pbrR repressor will bind to the pbrR binding site on the lead promotor when lead ions are not present in the reaction. This causes transcriptional repression of the RNA aptamer as the T7 polymerase is physically occluded from reading the linear construct. When lead ions are present in the reaction the pbrR repressor will then bind to the lead ions and it will allow the transcription of the RNA aptamer, this aptamer can then bind to the DFHBI or DFHO which will induce fluorescence. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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Latest revision as of 13:44, 12 October 2022
pbrR controlled iSpinach biosensor
Improvement of part BBa_K3380600
This part is an improvement of Part:BBa_K3380600, as it expands the possibility of usage to detecting lead.
The Edinburgh-UHAS_Ghana team for 2022 designed a construct to detect lead in contaminated water. This construct is composed of a fluorescent RNA aptamer iSpinach flanked by the F30 tRNA scaffolds (BBa_K4390094) which under a strong T7 RNA promoter (BBa_I712074), downstream of the promotor there is the lead promotor which acts as the binding site for the pbrR repressor (BBa_K346002) as to allow transcriptional repression of the T7 promotor. This construct is designed to be cell-free and only requires transcription of the RNA aptamer to produce fluorescence. It should be noted that T7 RNA polymerase, chemical energy (ATP), NTPs and DFHBI or DFHO are also required in the cell-free reaction so that fluorescence is observed.
Usage and Biology
This biosensor should be used with a cell-free lysate which contains the pbrR repressor T7 RNA polymerase, chemical energy (ATP), NTPs and DFHBI or DFHO to induce fluorescence in the presence of arsenic ions. The pbrR repressor will bind to the pbrR binding site on the lead promotor when lead ions are not present in the reaction. This causes transcriptional repression of the RNA aptamer as the T7 polymerase is physically occluded from reading the linear construct. When lead ions are present in the reaction the pbrR repressor will then bind to the lead ions and it will allow the transcription of the RNA aptamer, this aptamer can then bind to the DFHBI or DFHO which will induce fluorescence. 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 SapI.rc site found at 134