Difference between revisions of "Part:BBa K2617010"
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<partinfo>BBa_K2617010 short</partinfo> | <partinfo>BBa_K2617010 short</partinfo> | ||
− | + | Fre_adhE is the fermentation control element of Escherichia coli controls the expression,including the promoter, ribosome binding site (RBS) and the entire transcription factor (TF) binding site. | |
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<partinfo>BBa_K2617010 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2617010 SequenceAndFeatures</partinfo> | ||
+ | ==Characterization== | ||
+ | FRE_adhE is the transcriptional and translational regulatory element which contains the cassette of 5′ upstream region controlling the expression of the major fermentative gene adhE. For the function determination, we used the FRE_adhE to drive the synthetic 1-butanol production. And the plasmid piGEM2018-Module002 was constructed successfully(Fig. 1). | ||
+ | [[File:T--UESTC-China--plasmid.png|500px|thumb|center|'''Fig. 1''' piGEM2018-Module002]] | ||
+ | Theoretically, fermentation of 1-butanol will be triggered under anaerobic conditions because of FRE’s regulation. We detected the production of butanol in E. coli BL21(DE3) carrying the above plasmid by gas chromatography. | ||
+ | [[File:T--UESTC-China--butanol GC.png|500px|thumb|center|'''Fig. 2''' The production of butanol determined using GC. ]] | ||
+ | The result (Fig. 2) shows our fermentation regulatory element successfully worked. | ||
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Latest revision as of 09:55, 17 October 2018
FRE_adhE: The fermentation regulatory element of Escherichia coli controls the expression
Fre_adhE is the fermentation control element of Escherichia coli controls the expression,including the promoter, ribosome binding site (RBS) and the entire transcription factor (TF) binding site.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Characterization
FRE_adhE is the transcriptional and translational regulatory element which contains the cassette of 5′ upstream region controlling the expression of the major fermentative gene adhE. For the function determination, we used the FRE_adhE to drive the synthetic 1-butanol production. And the plasmid piGEM2018-Module002 was constructed successfully(Fig. 1).
Theoretically, fermentation of 1-butanol will be triggered under anaerobic conditions because of FRE’s regulation. We detected the production of butanol in E. coli BL21(DE3) carrying the above plasmid by gas chromatography.
The result (Fig. 2) shows our fermentation regulatory element successfully worked.