Difference between revisions of "Team:Virginia/Results"

With only 5 weeks of lab, there was a rush to verify sequences with restriction enzyme digests, build any of the preliminary parts, and visualize E. coli with BMCs in them. Unfortunately, the time limitation prevented us from succesfully completing most of the steps we planned for in the last 10 months, but shown below are results from one series of procedures we performed to produce BMCs in E. coli BL21(DE3). With the generous help of Dr. Criswell at UVA, we were able to successfully culture the cells, fixate them, and take pictures of 6 different samples using a Transmission Electron Microscope (TEM).

The series of TEM Setup procedures are described in the Notebook page for 10/20 and 10/21. We transfected the BL21(DE3) cells with with pdu-ABJKNU and pdu-ABJKNUT, and then prepared 5 plates as follows:

1. BL21(DE3) control
2. pdu-ABJKNU
3. pdu-ABJKNU, diluted cell concentration
4. pdu-ABJKNUT
5. pdu-ABJKNUT, diluted cell concentration

Plates 1, 2, and 5 are pictured below and were the cultured cells we used for preparing TEM samples. As seen in Figure 1, the higher concentration of pdu-ABJKNU cells grew at a similar rate to the control cells and the diluted pduABJKNUT.

The following 6 cultures were fixated for TEM use as follows:

1. BL21(DE3)
2. BL21(DE3) + IPTG
3. pdu-ABJKNU
4. pdu-ABJKNU + IPTG
5. pdu-ABJKNUT
6. pdu-ABJKNUT + IPTG

A sample picture has been selected from each of the samples and is shown in Figure 2. We were not able to determine any significant difference between the samples, suggesting that there was a problem with the production of BMCs. The most likely reason for this is a deviation from the protocol we intended to follow due to a time limitation. Instead of allowing the samples to sit at room temperature overnight, we only allowed them to sit for a few hours, which led us to fix the cells before enough time for BMC formation had passed.