Difference between revisions of "Part:BBa K2365515"

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                                           Fluorescence intensity was measured by flow cytometry
 
                                           Fluorescence intensity was measured by flow cytometry
 
Measurements of specific fluorescence were performed using cells harvested from the logarithmic phase during growth in shake flasks.
 
Measurements of specific fluorescence were performed using cells harvested from the logarithmic phase during growth in shake flasks.
 +
[[File:启动子全部.jpeg|700px|center]]
 +
Figure.The fluorescence of the four test devices and control transformed into Saccharomyces cerevisiae and inoculated in YPD broth was measured after 8h. 
 +
Nevertheless, the attractiveness of yeast as a platform organism (especially for metabolic engineering applications) needs continued efforts to expand the set of tools available.

Revision as of 00:47, 2 November 2017


Mutant of TEF1

Mutant of TEF1 Yeast promoter; Constitutive expression

Transcription elongation factor gene promoter of Saccharomyces cerevisiae constitutive expression promoter in the commonly used system. According to the element and registry and database of synthetic biology database bioparts for synthetic biology (http://npbiosys.scbit.org/regulatoryelementdetails/00007) design and synthesis of tef1 mutations.

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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 166


Tef mutant.jpeg
                                          Fluorescence intensity was measured by flow cytometry

Measurements of specific fluorescence were performed using cells harvested from the logarithmic phase during growth in shake flasks.

启动子全部.jpeg

Figure.The fluorescence of the four test devices and control transformed into Saccharomyces cerevisiae and inoculated in YPD broth was measured after 8h. Nevertheless, the attractiveness of yeast as a platform organism (especially for metabolic engineering applications) needs continued efforts to expand the set of tools available.