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Revision as of 17:36, 21 October 2019
Part Improvement
We have upgraded LacI gene (BBa_C0012) to a better version (BBa_K3257045).
LacI is one of the genes in Lac operon encoding the inhibitor protein binding to LacO (BBa_K3257066) sites (cis-acting element). In response to IPTG, the inhibitor protein detaches from LacO and enables the transcription of downstream genes. We mutated some specific sites in the LacI gene to improve its sensibility to IPTG (Christopher Voigt, et al.). Using EGFP as a reporter, its fluorescence intensity demonstrates a lower level of leakage and the same level of expression before and after the induction of IPTG. Also, we induce the improved Lac operon by arabinose to verify its orthogonal response to IPTG.
With LacIq promoter (BBa_K3257003) and rrnB T1 terminator (BBa_K3257020), improved LacI protein can be expressed and function properly in the Escherichia coli BL21(DE3). We used EGFP as a reporter controlled by our improved Lac operon and measured its green fluorescence over time.
According to our experiment, our Lac operon is improved in the following three main aspects.
Lower response to arabinose, better orthogonality
Crosstalk between the response to IPTG and arabinose has been a defect of the wild type Lac operon. When 4 mM arabinose is added, a few lac inhibitors would detach from lac operator. This means that it is induced in a relatively low but unignorable level. According to the measurement of our experiment, our improved LacI can respond to IPTG with better orthogonality. As shown in Figure 1, when 4 mM arabinose is added, oLacI (wild-type LacI) is induced at a significantly higher level than iLacI (improved LacI).
Figure 1. The expression level of EGFP controlled by different versions of LacI and inducers, or under different promoters. The origin point indicates the time when different inducers are added (1 mM IPTG and/or 4 mM Arabinose). The title of the graph shows which kind of inducer is added to the culture. The horizontal axe shows the duration of time, the vertical axe shows the quantified level of EGFP expression. The fluorescence level (excitation wavelength: 485 nm; detection wavelength: 528 nm) is quantified by the concentration of fluorescein, and normalized by the measured OD600 equivalent to the number of beads in the system. oLacI stands for the wildtype LacI, iLacI stands for our improved version of LacI. +LacO indicates that the promoter constitutes a LacO sequence. Control is the negative control plasmid which does not constitute an EGFP sequence. Error bar in the two graphs on the first row indicates the SEM of three replicates. The second row showed only the mean amount of three replicate.
Higher induction level than the wild-type Lac operon when induced by IPTG
Our improved Lac operon does not malfunction and can be normally induced by IPTG. When 1 mM IPTG is added, EGFP controlled by both operons can be induced and expressed at relatively the same level (Figure 1), while the level of induction under the control of iLacI is significantly higher than that of oLacI (Figure 2).
Figure 2. The induction level of EGFP under different repressor and promoters. Induction level is calculated by dividing fluorescence level after 9 h of induction by 1 h afterwards. The fluorescence level is quantified as in Figure 1. oLacI stands for the wildtype LacI, iLacI stands for our improved version of LacI. +LacO indicates that the promoter constitutes a LacO sequence. t test analysis shows that the induction level of iLacI is significantly higher than oLacI, *** indicates that p=0.0002.
Lower uninduced leakage
The uninduced leakage level is also an important parameter of an operon. Improved LacI lowers the leakage level compared to the wild-type one. The figure below (Figure 3) is the measurement of the fluorescence of EGFP controlled by wild-type and improved Lac operon. When no IPTG or arabinose is added, the fluorescence of EGFP controlled by improved Lac operon much lower than the fluorescence of EGFP controlled by wild-type Lac operon (Figure 1 & 3).
Figure 3. The basal fluorescence level of EGFP controlled by different repressors. The bar indicates the mean fluorescence level during the 10 h with no inducer in the culture. The fluorescence level is quantified as in Figure 1. oLacI stands for the wildtype LacI, iLacI stands for our improved version of LacI. Control is below the detection level and not shown. Error bar indicates the SEM of fluorescence signal in the 10 h. Paired t test analysis shows that iLacI has a significantly lower of fluorescence than oLacI, p=0.0057 (**).
Project by Team:Fudan-TSI
Mutation library generation is critical for biological and medical research, but current methods cannot mutate a specific sequence continuously without manual intervention. We hereby present a toolbox for in vivo continuous mutation library construction. First, the target DNA is transcribed into RNA. Next, our reverse transcriptase (RT) reverts RNA into cDNA, during which the target is randomly mutated by our RT's enhanced error-prone ability. Finally, the mutated version replaces the original sequence through recombination. These steps will be carried out iteratively, generating a random mutation library of the target with high efficiency as mutations accumulate along with bacterial growth. Our toolbox is orthogonal and provides a wide range of applications among various species. R-Evolution could mutate coding sequences and regulatory sequences, which enables the evolution of individual proteins or multiple targets at a time, promotes high-throughput research, and serves as a foundational advance to synthetic biology.