Team:ECUST/Biocide

BIOCIDE

Description

We insert fragment of Cecropin AD into vector pET-28a(Figure 1)

Figure 1. The vector pET-28a Vector is cut by NcoI and BamHI. Sequence of AD was chemically synthesized and amplified by PCR, then ligated with linearized vector by Ezmax.

Design

The plasmid was transformed to E. coli BL21 and cultured at 37 °C for 12 h. positive monoclonal bacteria were cultured and verified by PCR(Figure 2).

Figure 2. 1% Agarose Gel Electrophoresis of PCR, which shows that our vector was successfully constructed.

Result

We verified the expression of Cecropin AD by SDS-PAGE(Figure 3).

Figure 3. The SDS-PAGE of Cecropin AD Lane 1 :before induction Lane 2,3:after induction

To test the effect of cecropin AD, we measured the growth curve of iron bacteria adding with different concentration of cecropin AD.

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