Difference between revisions of "Part:BBa K3740008"

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Constructed J23100-RBS009-sfGFP-rrnB T1 (<partinfo>BBa_K3740060</partinfo>) was transformed into E. coli DH5α. We quantified the  
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Constructed J23100-RBS009-sfGFP-rrnB T1 (<partinfo>BBa_K3740060</partinfo>) was transformed into <i>E. coli</i> DH5α. We quantified the  
 
fluorescence intensity when the optical absorbance of bacterial culture at 600nm was around 0.2.
 
fluorescence intensity when the optical absorbance of bacterial culture at 600nm was around 0.2.
 
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Revision as of 16:29, 18 October 2021


RBS009

Description

Modulation of protein expression level.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE 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).

Significance analysis of the average fluorescence intensity of sfGFP between B0034 and RBS009