Device

Part:BBa_K302018:Experience

Designed by: Steven Woodhouse, Alan Koh, Rachel May Boyd, Philip Hall   Group: iGEM10_Newcastle   (2010-08-18)
Revision as of 03:49, 26 September 2022 by SinubilovesCola (Talk | contribs) (Contribution from iGEM2022 ZJU-China)

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Applications of BBa_K302018

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UNIQe1ab52f9e3cce343-partinfo-00000000-QINU UNIQe1ab52f9e3cce343-partinfo-00000001-QINU

User Reviews

Liaoliao_Gao
In 2022, ZJU-China iGEM team has characterized the output of this part in a novel chassis E. coli BL21(DE3). The result was documented in the experience page and the main page of (BBa_K302018).

Contribution from iGEM2022 ZJU-China

The sequence of (BBa_K302018) was synthesized and cloned into the PHY-plasmid to obtain the recombinant expression vector

We first tested the inhibitory concentration of subtilisin by zone of inhibition experiment, using BL21 transformed by PHY-Immunity plasmid or PHY-Empty plasmid as control. The concentration of subtilisin were 100mg/ml, 50mg/ml, 25mg/ml, 12.5mg/ml.

GLL-2.png
Fig1 Zone of inhibition experiment for subtilisin in BL21.

Then, we prepared normal LB culture plates with different concentration of subtilisin, including 0.1mg/ml, 0.2mg/ml, 1mg/ml and 10mg/ml, in individual dishes. Then we inoculated BL21 transformed by immunity plasmid or PHY-empty plasmid as control in the plates. <p>Results:For the immunity group, some colonies grew on the surface of the media with 1mg/ml subtilisin, while the control group didn’t. This suggested that the PHY-Immunity plasmid worked well in BL21.

GLL-1.png
Fig2 The colonies growth condition in plates with different concentration of subtilisin