Difference between revisions of "Part:BBa K4271001"

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Revision as of 10:58, 7 October 2022

T7 Promoter + Lac operator + RBS + OPH + T7 terminator

This sequence is responsible for the regulation and expression of the OPH gene. The T7 promoter, transcribed by only the T7 RNA polymerase, identifies the sequence downstream and enables fast and effective transcription. We further designed a lac operon, so that upon IPTG induction, the lacI repressor protein will be detached from the lacI gene, leading to the transcription and translation of our target oph gene. The ribosome binding site (RBS) is where the ribosome bind on the mRNA for translation. This RBS is taken from the pET22B vector. OPH a gene that encodes organophosphate hydrolase, paraoxon, a type of organic phosphate and insecticide. The product of the paraoxon degradation, pNP, will be detected to evaluate the efficacy of the gene. The T7 terminator identifies the end of the transcription sequence.

Usage and Biology

Build:

Synthetic oph gene we used in this study is derived from the opd (organophosphate degradation) gene in Agrobacterium tumefaciens and performed with codon usage optimization for E. coli heteroexpression. We digested the oph gene with BamHI and HindIII, subcloned it to pET22b vectors that underwent the same restriction enzyme digestion, then transformed the recombinant into E. coli DH5α. The transformation was conducted by plasmid extraction through mini-prep.

We later confirmed the insertion of our oph gene into the enzyme plasmid by enzyme digestion, cutting the recombinant DNA with BamHI and HindIII respectively, and observing the same band sizes of 6.5 kilobases after gel electrophoresis (left). We later digested our pET22b::OPH again with both BamHI and HindIII, two of resulting DNA bands include the 1071 base-long oph and the 5479 base-long pET22b vector (right). Finally, the plasmid was transformed into the competent cells E.coli BL21(DE3) via heat shock, which we later used to examine the level of paraoxon degradation by our enzyme plasmid.

Test:

To confirm the efficiency of our pNP sensor in determining the amount of pNP produced, we measure the GFP fluorescence of E. coli BL21 (DE3) with and without pNP sensor in the presence and absence of pNP.

Analysis of Result:

The result we acquired from the experiment is not consistent with the data previously published (Jha, Ramesh K., et al.). The difference in the level of GFP fluorescence with and without adding 125 µM of pNP is not significant enough to prove the effectiveness of our pNP sensor (Jha, Ramesh K., et al.). Given that the genetic organization and sequence of our pNP sensor is identical to the plasmid design in the research paper, we went back to further examine and check the pNP sensor design. As a result, we discovered the lack of commonly used RBS sequence in front of pNPmut1-1 in the sensor plasmid, from which we inferred that the poor transcription of pNPmut1-1 might be the reason behind the relatively weak and undetectable green fluorescence signals. In Redesign, we are planning to insert RBS by flanking 4 bases apart from the start codon of pNPmut1-1 in the pNP sensor backbone (Fig.5) to further observe if GFP expression will increase in the presence of the same amount of pNP.

	% of protein
	Truncated	Non-Truncated
1. BL2(DE3) (negative control)	0	0
2. BL2(DE3) +paraoxon (experimental)	0.2323266987	0.3905284832
Replicate 3	35.8	64.2
3. BL2(DE3) +pNP (positive control)	8.905950096	9.966890595
4. PET::OPH +IPTG induction (negative control)	0	0
5. PET::OPH +paraoxon +IPTG induction (experimental)	6.720481928	6.916144578
6. PET::OPH +pNP +IPTG induction (positive control)	11.83912249	12.51005484

Sequence and Features