Part:BBa_K3018000
Bacterial flavin-containing monooxydase, codon-optimized
This part encodes a bacterial flavin-containing monooxygenase(bFMO), which can catalyze the oxidation of indole. We had the codon-optimized for E. coli. You can use this part to produce indigo through indoxyl and leucoindigo in E. coli. Indigo is a hydrophobic blue dye; the expression of functional FMO can be estimated by the color of culture solution. Clones on LB plates should be blue when it works.
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]
Tongji_China 2019 Characterization
All characterizations are performed in plasmid pET-28a(+), strain E. coli BL21(DE3).
Function Validation
To validate the function of this part in E. coli BL21(DE3), we transformed pET-28a(+)-bFMO into E. coli BL21(DE3). Bacte and induced with IPTG (final concentration: 0.5mM) . Culture without induction was used as control.
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Tongji-China 2024: The characterization of bFMO produces a blue gradient.
We quantitatively characterized the bFMO gene, providing future iGEM teams with characterization conditions and possibilities for indigo color gradients, and offering a broader range of color options for fields such as bioart and fashion.
We have chosen E. coli BL21(DE3) as the chassis strain, which is capable of efficiently expressing T7 promoters under IPTG induction. The plasmids we constructed are shown in the following figure. Initially, we selected Kana as the resistance screening gene, 6xHis as the purification tag, and T7 promoter.
Figure 1: Design Map of bFMO-pET28a
After gene synthesis at Genewiz, we amplified the gene, extracted the plasmid, and transformed it into BL21(DE3). Upon colony formation, we observed color changes, indicating leaky expression.
Figure 2: Leaky Expression of Indigo in Solid Medium
To prevent leaky expression, we replaced the T7 promoter with the medium-strength promoter J23110.
Figure 3: Promoter J23110 and Design of Primers
After the ligation reaction, we successfully replaced the T7 promoter with the J23110 promoter and obtained monoclones through transformation.
Figure 4: Monoclonal Selection of E. coli after Promoter Replacement through Spread Plating
Subsequently, we proceeded to validate the expression in liquid medium. After picking the successfully transformed monoclones, we cultured them in 12ml shake flasks for 12 hours before adding IPTG (final concentration of 0.5mM) and prepared L-tryptophan (final concentration of 5mg/ml) to the culture. The culture was then incubated at 37°C for 18 hours to observe color development. However, the final coloration failed.
Addressing the above issues, we devised the following experimental plan improvements based on their ease of verification:
1. Directly prepare a tryptophan-containing medium.
2. Measure the OD600 growth curves of cultures in liquid media with different substrate concentrations (5.0/2.5/1/0g/L) before adding the inducer.
3. After obtaining the growth curves, add IPTG during the early logarithmic growth phase to induce expression.
4. Initially, reduce the characterization temperature to 30°C.
Figure 5: Growth Curve and Indigo Color Development
Our constructed plasmid successfully demonstrated indigo coloration in the medium, as evident from the growth curve and the visible color change.
Figure 6: Expression of Indigo in Liquid LB Medium
1. Characterization in Liquid Medium
Figure 7: Visualization of Changes in Blue Color Over Time in Liquid Medium
Figure 8: Changes in Solution Purity and Brightness Over Time in Liquid Medium
2. Characterization in Solid Medium
Figure 9: Box Plot of Univariate Analysis
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