Method

To check whether our bacteria successfully secret GLP-1 to the environment, we collect the bacterial media and measure its GLP-1 concentration. After centrifugation of bacterial culture, we collect supernatant and pass it through 0.22 um filter to exclude bacteria. We then concentrate the solution by 5 kDa ultra centrifugal filter tubes. We also collect the bacterial pellet and lyze E. coli delicately by adding lysis buffer, followed by freeze and thaw the media to free GLP-1 inside bacteria. Both Immunoblotting and ELISA are used to detect GLP-1 concentration inside and outside bacteria.

Protocol

A. Sample Preparation

1. 10 μL bacterial culture was cultured in 5mL LB at 37℃, with suitable concentration of antibiotics shaking till 600 nm absorbance in cuvette is 1.5 (usually it takes about 18hr).
2. Centrifuge the bacterial culture at 12000 rpm for 3 min.
3. Pass the supernatant through 0.22 μm filter. Transfer the supernatant to 5 kDa ultra centrifugal filter tubes and centrifuge at 10000 rpm for 40 min.
4. Add 250μL of E. coli lysis buffer to the pellet and use liquid Nitrogen to freeze-thaw for three cycles.
5. Heat the samples at 95℃ for 10 min before immune-blotting.

B. Dot-Blotting

1. Soak the PVDF membrane in ethanol for 5min to activate the membrane.
2. Drop every 2 μL sample in a very small area on the membrane.
3. Blocking with 5% de-fat milk (in PBST) for 1hr.
4. Wash with PBST for 10 min, repeat 3 times.
5. Add primary antibody (1:1000 dilution in PBST) and incubate at 4℃overnight.
6. Wash with PBST for 10 min, repeat 3 times.
7. Add secondary antibody (1:5000 dilution in PBST) and incubate at 25℃ 2hr.
8. Wash with PBST for 10 min, repeat 3 times.
9. Mix 2 mL ECL with 2mL substrate, add to the membrane and let stand for 5 min.
10. Expose the membrane to the film in dark room.

C. ELISA

1. Wash the wells with 250 μL Wash Buffer.
2. Add 100 μL Assay Buffer to each well, and add 100 μL standards in ascending orders to wells, and add samples in the remaining wells.
3. Incubate at 4℃ overnight.
4. Decant liquid from plate.
5. Wash 5 times with 250 μL Wash Buffer.
6. Add 200 μL Detection Conjugate in each well. Incubate 2hr at room temperature.
7. Wash 3 times with 250 μL Wash Buffer.
8. Add 200 μL diluted substrate and incubate for 20 min.
9. Read plate on fluorescence plate reader with excitation/emission wavelength of 355 nm/460 nm.