Reporter

Part:BBa_I715039

Designed by: Oyinade Adefuye   Group: iGEM07_Davidson_Missouri_W   (2007-08-01)
Revision as of 18:58, 21 October 2019 by UOH4 (Talk | contribs)

pLac-RBS-RFP


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
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 781
    Illegal AgeI site found at 893
  • 1000
    COMPATIBLE WITH RFC[1000]

Measured by BIT-China 2019

The function of BBa_I715039 is confirmed by our 2019 team. We successfully constructed pUC19-mRFP plasmid and pUC19 plasmid expressing plasmid and measured the activity of these parts quantitatively. In this time,we introduced both of mRFP expressing plasmid and control group expressing plasmid into the same strain, difference in mRFP expression was observed dependent on cultivation time. The culture of the strain with pUC19-mRFP at 37℃ showed about 70 folds higher fluorescence intensity than control group, While the culture of the strain with pUC19-mRFP and control group at 37℃ at Initial stage of fermentation showed almost the same fluorescence intensity. No inducer was added during the entire fermentation process.This result indicates that the lac promoter is leaked without the addition of IPTG induction.

Fig.Fluorescent fermentation results of I715039.



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