Team:BNU-China/Demonstrate
Results
Microtubule
Display module
Plasmid construction
We have accomplished the construction of two parts whose functions are described respectively in the previous design page (Microtubule module). They are (BBa_K2220019) and pYD1-β tubulin (BBa_K2220020), both parts have been validated by sequencing. The electrophoresis image of these two parts are shown as below (See Figure 1).
pYD1-β tubuiin was transfected into S. cerevisiae EBY100 by our team and validated its function by protein analysis, including Western blot and immunofluorescence microscopy(See Figure 2 and 3). Meanwhile, pYD1-α tubulin was transfected into S.cerevisiae EBY100 by FAFU-China, as part of collaboration works.(Click to see more details)
Figure 1 The electrophoresis image of 6 plasmids.
Protein expression analysis- Western blot
Recombinant S.cerevisiae EBY100 strain harbouring the pYD1-β tubulin plasmid was precultivated to mid-log growth phase and then induced by galactose. After 24h inducing，the supernatant from cell lysates of engineered EBY100-pYD1-β was analysed by Western blot.The image shows the results of a Western blot analysis carried out with an anti-V5 antibody.
Figure 2 The partly results of a Western blot analysis carried out with an anti-V5 antibody.
Function analysis- Immunofluorescence microscopy
Recombinant S. cerevisiae EBY100 strain harbouring the pYD1–β tubulin plasmid was precultivated to mid-log growth phase and then induced for 24 h at 20℃. During the inducing period, cells equaling to 2 OD600 units were collected every two hours from 8 h to 24 h. To detect the displayed protein, immunofluorescence microscopy was performed, with mouse IgG against βI tubulin and donkey anti-mouse IgG conjugated with Cy3 as primary and second antibody respectively. Results showed that optimal detection of β-tubulin occurred at 12 h.
Figure 3 Induced 12h in SG-CAA medium；
A,B recipient strain with empty plasmid;
C bright-field micrograph of S. cerevisiae EBY100 cells harbouring pYD1–β tubulin;
D immunofluorescence micrograph of S. cerevisiae EBY100 cells harbouring pYD1–β tubulin.
Secretory module
Plasmid construction
Four parts have been constructed, which are pYCα-α tubulin (BBa_K2220022), pYCα-β tubulin (BBa_K2220023), pYCα-mCherry-α tubulin (BBa_K2220024), pYCα-β-tubulin-mGFP (BBa_K2220025) and pYCα-mCherry (BBa_K2220021). All parts have been validated by sequencing.(See Figure 1)
Protein expression analysis- Western blot
Figure 4 An obvious color of mCherry produced by our engineered yeast harbouring vector pYCα-mCherry-α .
Recombinant S. cerevisiae INVSc1 strain harboring pYCα-α tubulin, pYCα-β tubulin, pYCα-mCherry and pYCα-mCherry-α tubulin plasmid were precultivated to mid-log growth phase respectively and then induced for 48 h at 30℃ in SG-Ura medium. The recombinant proteins were extracted and analysed by Western blot. The image shows the results of a Western blot analysis carried out with an anti-V5 antibody.
Figure 5 Western blot analysis of the supernatant from cell lysates of engineered yeasts mentioned above, carried out with an anti-V5 antibody.
Furthermore, it has been proven that our recombinant proteins can be secreted normally and worked as it expected. Firstly, the secretion function of part pYCα-mCherry have been proven by western blot analysis (See Figure 5). And then we tested the dynamic behavior of our recombinant proteins mCherry-α tubulin and β tubulin, described in the following functional analysis.
Figure 6 The results of Western blot analysis carried out with an anti-V5 antibody.
Lane A the purified supernatant of S.cerevisiae INVSc1 harboring pYCα-mCherry culture, induced for 12 hours in SG-Ura.
Lane B the supernatant from cell lysates of S.cerevisiae INVSc1 harboring pYCα-mCherry (without purified), induced for 12 hours in SG-Ura.
Protein expression analysis- Fluorescence microscopy
Recombinant S. cerevisiae INVSc1 strain harbouring the pYCα–mCherry-α tubulin or pYCα–mCherry plasmid was precultivated to mid-log growth phase respectively and then induced for 20 h at 30℃. To detect the protein expression of our engineered yeast, fluorescence microscopy was performed. As image shown below, the expression rate of mCherry is almost up to 100%.
Figure 7 Induced 20h in SG-Ura medium；
A,B recipient strain with empty plasmid;
C bright-field micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry-α;
D fluorescence micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry-α;
E bright-field micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry;
F fluorescence micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry.
Recombinant S. cerevisiae INVSc1 strain harbouring pYCα–β tubulin-mGFP plasmid was precultivated to mid-log growth phase and then induced for 18 h at 30℃ in SG-Ura medium. The expression of recombinant protein can be obviously observed from fluorescence microscope field.
Figure 8 Induced 18h in SG-Ura medium;
A,B recipient strain with empty plasmid;
C bright-field micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–β tubulin-mGFP;
D fluorescence micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–β tubulin-mGFP.
From the images above, we can conclude that all of our parts can work as it expected, including display or secretion of recombinant proteins. Then, we tested the function of our upgraded display system.
Protein function analysis- OD340 test & Electron microscopy
Tubulin polymerization assay is based on an adaption of the original method of Shelanski et al.(1973) and Lee at al.(1977). Light at wavelength of 340 nm is scattered by microtubules proportionally to the concentration of polymerized microtubule. Purified α and β tubulins secreted by engineered INVSc1 were mixed together and incubated at 37℃ for 1 h, and absorbance readings at 340 nm were conducted every minute. The results are shown in the image below.
Comparing the absorbance curves obtained, it was clear that the secreted tubulins had successfully polymerized into microtubules when GTP is added into the system.
Figure 9 Absorbance curve of polymerization reaction at 340 nm.
To get more definitive results, we observed samples with High Resolution Transmission Electron Microscopy (HRTEM). The following two images are polymerized microtubules observed in the system containing secreted mCherry-α-tubulin and β-tubulin. Several microtubules can be seen on these images.
Figure 10 Electron microscopy images of polymerized microtubules.
A Linear microtubule observed with HRTEM. The red arrows indicate the microtubules;
B Enlarged view of image A. The red arrows indicate the microtubules.
From the results we got with absorbance curves and electron microscopy images, the function of the secrete module can be verified.
Function verification of upgraded display system
As the function of the secrete module was verified, we experimented on the polymerization of microtubules at the surface of the yeast cells. Specifically, we did the polymerization reaction with tubulins extracted from the brain tissue of Sus scrofa domesticus and yeasts displaying β-tubulin. We did microscopic exam with HRTEM. Polymerized microtubules were observed on the cell wall of the yeasts, of which the quantity and length were consistent with our model prediction. The followings are the results.
Figure 11 Microscopic images of polymerized microtubules on yeast cell wall.
A Polymerization with tubulins extracted from the brain tissue of Sus scrofa domesticus and yeasts displaying β-tubulin. Considerable numbers of microtubule were displayed on the yeast cell wall;
B Control: Yeasts displaying β-tubulin without free tubulins. There were no observable microtubules on the yeast cell wall.
Figure 12 Enlarged view of microtubules on the yeast surface in Fig. 11A
The red arrows indicate the microtubules.
Figure 13 More enlarged view of microtubules on the yeast surface in Fig. 11A
The red arrows indicate the microtubules.
Figure 14 Microscopic image of a free microtubule, which is obviously longer than those polymerized on yeast surface.
Figure 15 Microscopic image of yeasts connected to each other through microtubules.
Flagellar Filament
Display module
Plasmid construction
We have successfully constructed the following 11 parts that have been described in detail in the previous design page. (Flagellar filament module)
In display module, we constructed and validated the following 6 parts. They are pYD1-FliC (BBa_K2220002), pYD1-XynA(BBa_K2220004), pYD1-PETase(BBa_K2220005), pYD1-BG(BBa_K2220007), pYD1-EG(BBa_K2220006), pYD1-CBH(BBa_K2220008), which means to fuse the target gene sequences with AGA2 gene respectively. And we also constructed pYD1-FilC(eGFP) (BBa_K2220003) as our positive control. The length and sequence of each parts have been validated by sequencing. The length validation are presented on the part registry page.
Protein expression analysis-Fluorescence Microscopy
Recombinant S. cerevisiae EBY100 strain harbouring pYD1-FliC(eGFP) plasmid was precultivated to mid-log growth phase and then induced for 24 h at 20℃ in SG-CAA medium. The expression of recombinant protein FliC(eGFP) can be obviously observed from fluorescence microscope field.
Figure 11 Induced for 24h in SG-CAA medium;
A,B recipient strain with empty plasmid;
C bright-field micrograph of S. cerevisiae EBY100 cells harbouring pYD1–FliC(eGFP);
D fluorescence micrograph of S. cerevisiae EBY100 cells harbouring pYD1–FliC(eGFP).
Function analysis- Enzyme activity assay
We then validated the function of our pYD1-FliC(XynA) by testing the enzyme activity of recombinant S. cerevisiae EBY100 harbouring pYD1-FliC(XynA). By culturing and inducing control group(EBY100-pYD1) and experimental group(EBY100-FliC(XynA)) in same initial concentration in SG-CAA medium (plus 5% xylan), the same volume supernatant were collected every two hours from 10h to 18h to examine the concentration of reducing sugar by DNS method. The results are shown as below.
Figure 12 Xylnase enzyme activity assay curve.
The value of OD540 are positive correlation with the concentration of reducing sugar under DNS method. So here we use the value of OD540 to estimate the concentration of reducing sugar .Before 14h, engineered yeast were consuming the galactose in medium, so the OD540 values of two groups are similarly decreasing. After 14h, the OD540 of Control group is still decrease, while the values of experimental group are change to increase, and decrease again after 16h, that means FliC(Xylanase) proteins have been displayed in certain quantity at the beginning of 14h, and degraded the xylan of culture medium to xylose, so the concentration of reducing sugar increased. After a period, yeast absorption rate of xylose and galactose was greater than that of xylan decomposed by enzyme, so the concentration of reducing sugar decreased again. Thus, from here we concluded that our FilC(XynA) are successfully displayed on the yeast surface.
Secretory module
In secretory module,we successfully constructed the following parts: pYCα-FliC-XynA (BBa_K2220011), pYCα-FliC-BG (BBa_K2220014), pYCα-FliC-EG (BBa_K2220013), pYCα-FliC-CBH (BBa_K2220015), and pYCα-FliC-eGFP (BBa_K2220003) as positive control. The lengths and sequences of each part has been validated by sequencing. The length validations are presented on the part registry page. The function of those parts were described on previous design page.
Protein expression analysis- Western blot
Figure 13 The results of a Western blot analysis carried out with an anti-His antibody
The image shows the results of a Western blot analysis carried out with an anti-His antibody. The recombinant proteins are expressed by S.cerevisiae INVSC1 pYCα-FilC(PETase) and pYCα-FliC(XynA) respectively. After 24h inducing，the recombinant proteins are extracted and analysed by Western blot
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