L.B. liquid culture medium dry powder, agar powder
Glucose
Kanamycin
1,2-distearoyl-sn-glycero-3-phosphoethanolamine
1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol (DSPE-PEG)
Lecithin
calcium chloride
SDS-PAGE pre-made gel kit
His antibody (rabbit)
Flag antibody (rabbit)
anti-rabbit secondary antibody
agarose (dry powder)
lasmid DNA extraction kit
restriction endonuclease kit
bacterial viability staining kit
bacterial viability (CCK-8) kit
GLP-1 ELISA kit
First, prepare sterile L.B. liquid medium and solid agar plates. The L.B. liquid medium (dry powder) is mixed with deionized water at a concentration of 25 g/L and different concentrations of glucose (0, 2, 5, 8, 11 mmol/L), then brought to a final volume of 500 mL and sterilized at 121°C under high pressure for 30 minutes to obtain sterile medium. For solid agar plates, add 15 g/L of agar powder to the previously described liquid medium solution, sterilize it for the same amount of time, and pour the hot medium into plates, allowing it to cool before use.
Since our laboratory has stored the ENC1917 strain (purchased from a commercial cell bank in 2023), we thaw the strain according to the protocol and inoculate it into L.B. liquid medium containing 11 mmol/L glucose, followed by incubating at a constant temperature with shaking for 8 hours. After that, we dilute the culture by a factor of 10^7 and spread the diluted solution onto L.B. solid agar plates, then incubate at a constant temperature for 48 hours to amplify the colonies. In the subsequent experiments, we will obtain the required ECN1917 bacteria from these plates.
Dilute the electroporated bacterial suspension after 12 hours of culture and spread it onto L.B. solid agar plates (with 200 µg/ml kanamycin), then incubate for 48 hours to observe the colonies. Afterward, pick individual colonies surviving on the antibiotic plates for restriction enzyme identification.
For the identification of recombinant plasmids, we extracted plasmids from previously amplified recombinant bacteria using a bacterial DNA extraction kit, following the provided protocol. Subsequently, the plasmid solution was incubated with the restriction endonucleases BspDI and PuvI at 37°C for 5 minutes. The digested plasmids were then separated by agarose gel electrophoresis to verify the presence of the expected plasmid structure in the recombinant bacteria.
Preparation and characterization of nanovesicles. Nanovesicles was prepared according to the previously reported method. In detail, Engineered was grown in LB medium overnight at 37 ℃ and then centrifuged at 5000 rpm for 5 min. The cell precipitates were rinsed twice with sterile PBS and suspended in 1 mL sterile PBS to achieve the desired concentration. After that, the lipid membrane was prepared by thin film dispersion method. 2 mL of cholesterol (1.24 mg mL-1 ), DLPC (3 mg mL-1 ) and DSPE-PEG2000 (1 mg mL-1 ) were mixed in chloroform. Then, the solution was dried at room temperature by a rotary evaporator and the transparent lipid film was obtained. The bacterial solution containing 12.5 mM CaCl2 was hydrated in the lipid film, and was incubated for 30 min at 37 ℃.
In this project, we used the CCK-8 bacterial viability assay and the DMAO/PI bacterial viability and death staining method for bacterial activity assessment. Specifically, we cultured the chassis bacteria and engineered bacteria for the same duration until the logarithmic growth phase. We then added 90 µL of the bacterial suspension and 10 µL of CCK-8 solution to a 96-well cell culture plate and incubated it in the dark at 37°C for 30 minutes. After incubation, we measured the absorbance at 450 nm using a microplate reader.
For the viability and death staining, the logarithmic phase bacterial suspension was diluted 1:1,000,000 and mixed with DMAO and PI solution (at a 1:1000 dilution ratio). After incubating in the dark at 37°C for 30 minutes, we used a laser confocal microscope to capture images in both the red and green channels.
We diluted the DLPC-encapsulated engineered bacteria to a concentration of 10,000 CFU/mL. Then, we took 10 µL of the bacterial suspension and dropped it onto a copper grid suitable for electron microscopy. After allowing it to air dry naturally, we added 10 µL of a 1 mg/mL tungsten phosphoric acid solution and let it air dry again. Microscopic images were captured using an F-30 transmission electron microscope.