Difference between revisions of "Part:BBa K3740008"
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<h3>Characterization</h3> | <h3>Characterization</h3> | ||
| − | <p>The average fluorescence intensity of sfGFP induced by RBS009 (<partinfo>BBa_K3740008</partinfo>), was less than 3% of B0034 (<partinfo>BBa_B0034</partinfo>),<b>which means reducing the pressure to the host bacteria</b>.</p> | + | <p>The average fluorescence intensity of sfGFP induced by RBS009 (<partinfo>BBa_K3740008</partinfo>), was less than 3% of B0034 (<partinfo>BBa_B0034</partinfo>),<b> which means reducing the pressure to the host bacteria</b>.</p> |
[[File:szpt0.png|300px|thumb|center|Significance analysis of the average fluorescence intensity of sfGFP between B0034 and RBS009]] | [[File:szpt0.png|300px|thumb|center|Significance analysis of the average fluorescence intensity of sfGFP between B0034 and RBS009]] | ||
Revision as of 17:47, 20 October 2021
RBS009
Description
Modulation of protein expression level.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
2021 SZPT-China
Biology
Mutagenesis at specific position of RBS (BBa_B0034) was achieved RBS009 (BBa_K3740008) using random primers and PCR, and the constructed plasmid J23100-RBS009-sfGFP-rrnB T1 (BBa_K3740060). Compare the fluorescence intensity of sfGFP induced by J23100-B0034-sfGFP-rrnB T1 (BBa_K3740058).
Usage
Constructed J23100-RBS009-sfGFP-rrnB T1 (BBa_K3740060) was transformed into E. coli DH5α. We quantified the
fluorescence intensity when the optical absorbance of bacterial culture at 600nm was around 0.2.
Characterization
The average fluorescence intensity of sfGFP induced by RBS009 (BBa_K3740008), was less than 3% of B0034 (BBa_B0034), which means reducing the pressure to the host bacteria.
