Part:BBa_K3823009
SQR-SDO-AprBA-SAT
Brief introduction
Tongji_China 2021 hope to solve the odor problem of waste food. According to the background we have researched, we found that hydrogen sulfide and ammonia are the two main odors that cause malodor in food waste, so we decided to convert these two malodor-emitting odors into non-toxic and odorless substances, so that we could solve the problem through engineered bacteria. After literature review and intense discussions, we decided to converse hydrogen sulfide into sulfate(figure 1)
We choose SQR, SDO, AprBA, SAT to oxidize sulfide, using J23110 as the promoter.
Construction
Characterization
1.The mRNA expression level of the target gene was detected by RT-qPCR
We extracted RNA of our engineered bacteria and wild-type bacteria for RT qPCR experiment. The relative content of target mRNA in each group was calculated based on 16s gene of E.coli. The experimental results can prove that our engineering bacteria can transcribe the mRNA of the introduced gene normally. (There is no target gene in the wild type, the relative expression of engineering bacteria is very high and the difference is large)
2.The expression level of the target protein was detected by SDS-PAGE
We first tried to introduce plasmids linked with 1/2/3/4 target genes into E.coli DH5α, and detected their protein expression levels. However, due to the low expression amount and the limitation of Spectrophotometry, we did not find significant differences between the engineered strain and the wild type protein strips.
Therefore, four target genes were added with efficient T7 promoter respectively and introduced into E.coli BL21(DE3).Under the condition of IPTG induction, all proteins of strain containing target genes and wild-type strain were extracted. SDS-PAGE experiment and Coomassie brilliant blue staining showed that the expression of each target protein could be realized in E.coli BL21(DE3).
We had hoped to construct plasmids with T7 promoter for all four genes, and then test the protein expression, but the construction process was very difficult. Finally, due to the limited time, we connected the four genes, but only the SQR gene was regulated by the T7 promoter. In the staining results, only the SQR band was obvious, but it was speculated that the other proteins should be able to express normally.
Protein function verification experiment
In view of the the limiting capacity of our laboratory to detect the intermediates in the sulfide oxidation pathway, we mainly verified the function of our engineered bacteria from the oxidation level of sulfide and the generation level of sulfate.
Characterization experiment of S2- oxidation amount
We configured a series of sodium sulfide solutions with concentration gradient and tested them with detection reagents according to certain methods. The standard curve obtained is ideal. It can be considered that our detection method can accurately reflect the relative content of sulfide in the solution within this concentration range.
We put the engineered bacteria and wild-type bacteria into a certain concentration of sodium sulfide solution, take out the bacterial solution every 30 min to detect the residual sulfide concentration. The results show that our engineered bacteria can oxidize sulfide better. (because the bacteria have a certain adsorption effect on sulfide, the initial sulfur ion concentration of the two groups of added bacterial solution is lower than blank)
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 3324
Illegal SpeI site found at 1797
Illegal PstI site found at 1514
Illegal PstI site found at 2726 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30
Illegal NheI site found at 1465
Illegal NheI site found at 1488
Illegal NheI site found at 2311
Illegal NheI site found at 2334
Illegal NheI site found at 3216
Illegal SpeI site found at 1797
Illegal PstI site found at 1514
Illegal PstI site found at 2726 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1997
Illegal BamHI site found at 1373
Illegal BamHI site found at 3529
Illegal BamHI site found at 4984 - 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 3324
Illegal SpeI site found at 1797
Illegal PstI site found at 1514
Illegal PstI site found at 2726 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 3324
Illegal SpeI site found at 1797
Illegal PstI site found at 1514
Illegal PstI site found at 2726
Illegal NgoMIV site found at 109
Illegal NgoMIV site found at 533
Illegal NgoMIV site found at 1723
Illegal NgoMIV site found at 4003
Illegal NgoMIV site found at 4174
Illegal NgoMIV site found at 4857
Illegal AgeI site found at 1028
Illegal AgeI site found at 1744
Illegal AgeI site found at 2537 - 1000COMPATIBLE WITH RFC[1000]
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