Difference between revisions of "Part:BBa K3332043"
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Fig.1 Circuit | Fig.1 Circuit | ||
− | To construct this part, we moved formaldehyde_derivative-1 promoter (BBa_ BBa_K3332042) and RBS_ECFP_T(BBa_E0420) into the expression vector pSB1C3 by standard assembly. Then the ligation mixture was transformed into E. coli | + | To construct this part, we moved formaldehyde_derivative-1 promoter (BBa_ BBa_K3332042) and RBS_ECFP_T(BBa_E0420) into the expression vector pSB1C3 by standard assembly. Then the ligation mixture was transformed into E. coli BL21(DE3) to compare the sensitivity of formaldehyde with other promoters.( formaldehyde_derivative-2 promoter, formaldehyde_derivative-3, formaldehyde promoter) |
===Characterization=== | ===Characterization=== |
Revision as of 10:25, 27 October 2020
Formaldehyde_derivative-2 promoter
An improvement of BBa_K1334002 by adding the binding sites.It's more sensitive to formaldehyde.We use it to test whether it has any improvement compared with BBa_K1334002.
Usage and Biology
As a DNA binding protein, hxlR is the transcriptional activator of the hxlAB operon from Bacillus subtilis. The possible mechanism of formaldehyde induced expression is that the formaldehyde changes the conformation of hxlR which stimulating RNA polymerase to open the transcription.
There are two binding sites (BRH1, BRH2) of hxlR, which are necessary for formaldehyde induced expression. Therefore, we increased the amount of binding sites to improve the sensitivity of the formaldehyde promoter. There are two BRH1 and two BRH2 in the formaldehyde_derivative-2 promoter, as opposed to one BRH1 and one BRH2 on the registry formaldehyde promoter (BBa_ K1334002).
Fig.1 Circuit
To construct this part, we moved formaldehyde_derivative-1 promoter (BBa_ BBa_K3332042) and RBS_ECFP_T(BBa_E0420) into the expression vector pSB1C3 by standard assembly. Then the ligation mixture was transformed into E. coli BL21(DE3) to compare the sensitivity of formaldehyde with other promoters.( formaldehyde_derivative-2 promoter, formaldehyde_derivative-3, formaldehyde promoter)
Characterization
We use Formaldehyde_derivative-2 promoter _B0034_E0020_B0015_pSB1C3 to characterize Formaldehyde_derivative-2 promoter.
The agarose gel electrophoresis images are below:
Fig.2 Formaldehyde_derivative-2 promoter _B0034_E0020_B0015_pSB1C3(BBa_K3332093) digested by Xba I and Pst I (about 1557 bp)
Protocol:
1.Culture glycerol bacteria containing the corresponding plasmid in test tube for 12h.
2.Add 4mL of the above bacterial solution into 200 mL LB medium and maintain the culture condition at 37 ℃ and 180 rpm.
3.Add 0.8mM formaldehyde into each group when OD600 increased to 0.6 and the culture condition is the same as before.
4.Then, sampling culture in 96-well plate reader every 3 hours to measure the fluorescence intensity (ECFP) and corresponding OD600, then calculate the fluorescence / OD value of each group.
Here is the result:
Fig.3 The curve of fluorescence intensity (ECFP) /OD by pHCHO (BBa_ K1334002) and formaldehyde_derivative-2 promoter
We discovered that formaldehyde_derivative-2 promoter is more sensitive to the registry formaldehyde promoter (BBa_ K1334002).
Reference
[1]Yurimoto, H., Hirai, R., Matsuno, N., Yasueda, H., Kato, N. and Sakai, Y. (2005), HxlR, a member of the DUF24 protein family, is a DNA‐binding protein that acts as a positive regulator of the formaldehyde‐inducible hxlAB operon in Bacillus subtilis. Molecular Microbiology, 57: 511-519. doi:10.1111/j.1365-2958.2005.04702.x
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]