Difference between revisions of "Part:BBa K4621150"
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===Testing and validation=== | ===Testing and validation=== | ||
− | We ligated the chi18A hypothetical promoter with EctOperon and overexpressed it in Streptomyces SCUT-3 using an integrated plasmid. The modified strain was inoculated in 40 mL LB medium and fermented at 40℃ and 220 rpm for | + | We ligated the chi18A hypothetical promoter with EctOperon and overexpressed it in Streptomyces SCUT-3 using an integrated plasmid. The modified strain was inoculated in 40 mL LB medium and fermented at 40℃ and 220 rpm for 48h. The production of Ectoine and 5-Hydroxyectoin in the presence or without chitin (the first day of fermentation) was detected to evaluate the chitin inducability of the promoter. The results are shown in FIG. 1. |
https://static.igem.wiki/teams/4621/wiki/parts/effect-of-different-promoters-on-yield.png | https://static.igem.wiki/teams/4621/wiki/parts/effect-of-different-promoters-on-yield.png | ||
− | Fig.1 Fermentation of products with or without the addition of an inducer(chitin) (a).Ectoine (b).5-Hydroxyectoin( | + | Fig.1 Fermentation of products with or without the addition of an inducer(chitin) (a).Ectoine (b).5-Hydroxyectoin(48h) |
Latest revision as of 18:19, 10 October 2023
It consists of the chi18A hypothetical promoter and EctOperon
Usage and Biology
EctOperon contains ectA, ectB, ectC and ectD and can produce 5-Hydroxyectoine from lysine.
chi18A hypothetical promoter is a whole functional sequence including the promoter of chitinase Chi18A gene, which was cloned from SCUT-3 gene. In our project, through transcriptome analysis, qPCR and other means, we found that the gene expression of chitinase Chi18A was up-regulated when SCUT-3 was in chitin medium, and we speculated that its promoter chi18A hypothetical promoter may have properties that can be induced by chitin.
Testing and validation
We ligated the chi18A hypothetical promoter with EctOperon and overexpressed it in Streptomyces SCUT-3 using an integrated plasmid. The modified strain was inoculated in 40 mL LB medium and fermented at 40℃ and 220 rpm for 48h. The production of Ectoine and 5-Hydroxyectoin in the presence or without chitin (the first day of fermentation) was detected to evaluate the chitin inducability of the promoter. The results are shown in FIG. 1.
Fig.1 Fermentation of products with or without the addition of an inducer(chitin) (a).Ectoine (b).5-Hydroxyectoin(48h)
The performance test indicated that ectoine production showed almost no significant difference between induced condition and non-induced condition, but hydroxyectoine varies in production level and severity of inducibility. ProP, a nickname for promoter of LPMO, and ProC, a nickname for promoter of chi19C, presented the two most strict inducibility among four promoters tested. Besides, ProP and ProA, a nickname for promoter of chi18A, shows two greatest strength.
From our results, it’s easy to assume that ProP is the most applicable promoter to continue studying. At the same time, we gave the runner-up to ProC. ProA, with great leakage of expression, was insufficient for further engineering, considering that the chemical we aim to produce could be harmful for host cells’ growth, so we put severity over strength when assessing performance of promoters.
The production of ectoine and hydroxyectoine tested in this experiment was relative limited, up to about 60-70mg/L. Further optimization and scale-up attempts could be made to ensure the strains can effectively valorize shrimp shell in industrial processing.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 3369
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 3369
Illegal NotI site found at 713
Illegal NotI site found at 1598
Illegal NotI site found at 1916 - 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 123
Illegal XhoI site found at 895
Illegal XhoI site found at 1069 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 3369
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 3369
Illegal NgoMIV site found at 930
Illegal NgoMIV site found at 1336
Illegal NgoMIV site found at 1342
Illegal NgoMIV site found at 1633
Illegal NgoMIV site found at 2682
Illegal NgoMIV site found at 2874
Illegal NgoMIV site found at 3384 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 518
Illegal BsaI.rc site found at 698
Illegal BsaI.rc site found at 1480
Illegal BsaI.rc site found at 2008
Illegal BsaI.rc site found at 2263
Illegal BsaI.rc site found at 2353
Illegal BsaI.rc site found at 2428
Illegal SapI site found at 556