Difference between revisions of "Part:BBa K526000"
(13 intermediate revisions by the same user not shown) | |||
Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K526000 short</partinfo> | <partinfo>BBa_K526000 short</partinfo> | ||
− | ''' | + | |
− | fim inversion system''' | + | '''fim inversion system''' |
fimE is a invertase,by function,that is capable of inverting any DNA sequence that is flanked by fimE recognition site. | fimE is a invertase,by function,that is capable of inverting any DNA sequence that is flanked by fimE recognition site. | ||
− | When fimE recognition sequences are flanked to a promoter element we can ensure that there is no leaky expression as the promoter can be maintained in the opposite orientation till the presence of inducer. Thus, fim inversion promoters ensures that there is | + | When fimE recognition sequences are flanked to a promoter element we can ensure that there is no leaky expression as the promoter can be maintained in the opposite orientation till the presence of inducer. Thus, fim inversion promoters ensures that there is a tight regulation of target gene expression (Fig 1). |
− | [[Image:SKL7.jpg | + | |
+ | [[Image:SKL7.jpg|250px]] | ||
'''Light Receptor''' | '''Light Receptor''' | ||
− | Pompc is a promoter sequence that is regulated by the | + | Pompc is a promoter sequence that is regulated by the hybrid light receptor, Cph8. Unfortunately we need to have the continous presence of darkness in order to induce the gene expression. Maintenance of complete darkness (especially on an industrial scale) for a longer duration is impossible. Hence, many researchers tried to introduce an invertor (usually the lambda repressor, cI). But even this system demands the continous presence of light which is again practically difficult. Hence, we propose a light mediated pulse inducer using the fimE processor. <br/><br/> |
+ | '''A Novel Light Based Pulse Induction System''' | ||
+ | <p>We made an attempt to introduce a light based pulse induction system using the fimE processor. | ||
+ | In this biobrick part, we have made an attempt to regulate the expression of fimE based on light so that we could precisely turn on a previously uninduced gene. The system would be permanently on when all of the promoter is inverted indicating need for no further inducer. This system would also ensure more tight control of target gene expression. This combination would be potentially useful for toxic gene expression as the basal level of the toxic gene would be kept as low as possible. </p> | ||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 04:27, 6 October 2011
Pompc promoter coding fimE
fim inversion system
fimE is a invertase,by function,that is capable of inverting any DNA sequence that is flanked by fimE recognition site. When fimE recognition sequences are flanked to a promoter element we can ensure that there is no leaky expression as the promoter can be maintained in the opposite orientation till the presence of inducer. Thus, fim inversion promoters ensures that there is a tight regulation of target gene expression (Fig 1).
Light Receptor
Pompc is a promoter sequence that is regulated by the hybrid light receptor, Cph8. Unfortunately we need to have the continous presence of darkness in order to induce the gene expression. Maintenance of complete darkness (especially on an industrial scale) for a longer duration is impossible. Hence, many researchers tried to introduce an invertor (usually the lambda repressor, cI). But even this system demands the continous presence of light which is again practically difficult. Hence, we propose a light mediated pulse inducer using the fimE processor.
A Novel Light Based Pulse Induction System
We made an attempt to introduce a light based pulse induction system using the fimE processor. In this biobrick part, we have made an attempt to regulate the expression of fimE based on light so that we could precisely turn on a previously uninduced gene. The system would be permanently on when all of the promoter is inverted indicating need for no further inducer. This system would also ensure more tight control of target gene expression. This combination would be potentially useful for toxic gene expression as the basal level of the toxic gene would be kept as low as possible.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 750
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 750
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 750
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 750
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 750
- 1000COMPATIBLE WITH RFC[1000]