Difference between revisions of "Part:BBa K598011"
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This device can respond to different TPP concentration and behave a sensitive response when induced by 1mM arabinose. And it mainly inhibit the gene expression. The working curve is shown in fig.1. The inhibition ratio is the value of fluorescence intensity compared to that of without TPP. | This device can respond to different TPP concentration and behave a sensitive response when induced by 1mM arabinose. And it mainly inhibit the gene expression. The working curve is shown in fig.1. The inhibition ratio is the value of fluorescence intensity compared to that of without TPP. | ||
− | [[Image: | + | [[Image:PEKING-R PBAD-2.5.png|center|thumb|500px| '''Figure 1'''Working curve of BBa_K598011. The inhibition ratio is fluorescence intensity under given TPP concentrations compared to that of without TPP. Constructed plasmids were transformed into E. coli DH5acells and characterized in M9 medium with a TPP concentration gradient of 0.001, 0.003, 0.01, 0.03, 0.1, 0.3, 1, 3 uM with being induced by 1mM arabinose. |
]] | ]] |
Revision as of 15:55, 5 October 2011
pBAD+TPP Down-regulated Hammerhead Ribozyme 2.5 with Native RBS+E0040+B0015
This is a basic part that consists of pBAD promoter, thiamine pyrophosphate (TPP) ligand responsive hammerhead ribozyme numbered 2.5 with native RBS (AAGGAGAT), BBa_E0040 and BBa_B0015. This device can respond to different TPP concentration and behave a sensitive response when induced by 1mM arabinose. And it mainly inhibit the gene expression. The working curve is shown in fig.1. The inhibition ratio is the value of fluorescence intensity compared to that of without TPP.
This part is obtained by PCR from inactive TPP-HHAZ 2.5 [1] which is kindly provided by Markus Wieland et. al., and then inserted into pSB1C3 through standard assembly.
[1] Markus Wieland, Armin Benz, Benedikt Klauser, and Jörg S. Hartig. (2009). Artificial Ribozyme Switches Containing Natural Riboswitch Aptamer Domains. Angew. Chem. 121, 2753-2756
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 125
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 65
Illegal BamHI site found at 258 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 931