Difference between revisions of "Part:BBa K3457055"

Latest revision as of 03:05, 27 October 2020

Arac-Pbad-CAHS 106094

    This biological part is the expression sequence of Cytosolic-abundant heat soluble protein 106094, also called CAHS 106094.

Contribution

Group: QHFZ-China iGEM 2020

Author: Yixian Yang

     TDPs (Tardigrade intrinsically Disordered Proteins) show protective effect to bacteria. However, ralated studies are all use T7 promoter and E. coli BL21 (DE3) strain. This year, we used the Inducible pBad/araC promoter to express a TDP, CAHS 106094, in another starin. For all the experiments below, we use E. coli DH5α strain. The part is constructed by Gibson technique assembly on the basis of BBa_K3457037 Arac-Pbad-GFP, which was givren by iGEM Team NEFU-China 2020.

Design

Figure 1. The Schematic cartoon of the DNA construct.

Documentation:

Protocol:

Figure 2. Experiment protocol.

【Day 1】Induction culture
(1) Pick clones which are in good condition and put them into 500 μL LB medium containing antibiotics. Shake them to grow at 37℃ for 5~7 hours until the bacteria solution becomes turbid.
(2) Add 0.2% L-arabinose into 3 mL LB medium containing antibiotics. Add 3 μL of the bacteria solution mentioned in step 1 to dilute the bacteria by the ratio of 1:1000. Shake the solution to grow the bacteria at 37℃ overnight.
【Day 2】Freeze-dried
(1) If fluorescence induced by the iPTG is detectable in the control group (GFP), continue conducting the experiment.
(2) Use spectrophotometer to measure the OD₆₀₀ of the bacteria solution, OD₆₀₀ = 1 equals to 10⁹ cells. If the OD₆₀₀ value is between 0.1 and 1, There is a linear relationship between OD₆₀₀ and bacterial density. Calculate the volume of bacterial solution for 10⁹ cells by using the formula V = 100 / (OD₆₀₀ × Dilution ratio).
(3) Take out a measured amount of 10⁹ cells and centrifuge it at 8000 rpm for 3 min. Then pour out the supernatant.
(4) Resuspend the bacteria in a 15 mL tube with pre-refrigerated 100 μL 3% glucose solution.
(5) Take off the cover of the tube and put the bacteria into the cold trap. Open the compressor of the lyophilization machine and freeze the shake tube for 2 h at -70℃.
(6) Put the caky bacteria solution into the drying chamber of the lyophilization machine. Open the vacuum pump to dry it in vacuum for 6h at 1 Pa vacuum degree.
(7) Turn off the vacuum pump, place it at seal box filled with silica-gel desiccant a for 2 days at room temperature.
【Day 3】Room temperature storage
【Day 4】Detect the survival rate
(1) Add 1 mL of sterile water to the tube, vortex for 15 s, placed it at room temperature for 10 min.
(2) Adjust the density of the bacteria solution by gradient dilution, then spread 100 μL of the bacteria solution on the LB plate.
(3) If the density above is not suitable, take 100μL of the solution and spread it on the LB plate after several gradient dilutions.
(4) Culture the bacteria overnight at 37℃.
【Day 5】Cell Count
(1) Take out the LB plate and take photos to record experimental results.
(2) Use the automatic cell counting function of Image J to count the colone number on the LB plate, then compare the results between each group.

Result

Figure 3. The Cfu of bacteria expressing CAHS 106094 after freeze-drying.

    As expected, the bacteria with an Arabinose promoter and CAHS 106094 exhibited a higher survival rate, which indicated that the promoter and L-arabinose could successfully induce the expression of CAHS 106094 at enough level in E. coli DH5α strain.

Sequence and Features