Coding

Part:BBa_K1049001:Experience

Designed by: masahiro sano   Group: iGEM13_KIT-Kyoto   (2013-09-09)
Revision as of 04:13, 24 September 2013 by Okaeri007 (Talk | contribs) (Applications of BBa_K1049001)


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Applications of BBa_K1049001

Applications of BBa_K1049002

Our team KIT-Kyoto 2013 constructed this part for the purpose of measurement. T7 promoter is an IPTG-inducible promoter. We added 20uL IPTG (100mM) to our genetically modified E.coli after cultivation at 28 and 37 degree C. 2 hours after, we extracted soluble proteins from it by using FastBreak™ Cell Lysis Reagent and did SDS-polyacrylamide gel electrophoresis.

Figure.1 SDS-PAGE Starting from the left, marker, ATF2 at 28 degree C, ATF2 + IPTG at 28 degree C, marker, ATF2 at 37 degree C, ATF2 + IPTG at 37 degree C

ATF2 gene encodes AATase, which is about 62kDa. The consumption of protein marker is like this.

Myosin 200kDa β‐Galactosidase 120kDa Bovine Serum Albumin 95kDa Glutamine dehydrogenase 68kDa Ovalbumin 50kDa Carbonic Anhydrase 36kDa Myoglobin 27kDa Lysozyme 20kDa Aprotinin 10kDa

You can find the band at lanes which are added IPTG just beneath the band of 68kDa.

In addition, according to this previous study, the ability of ATF2 protein producing isoamyl acetate in yeast is higher than ATF1 protein. It is known that both ATF1 and ATF2 protein are involved in producing isoamyl acetate.

Earlystudy.png

In 2006, MIT iGEM team submitted ATF1 coding sequence. (BBa_J45006) Our new part, ATF2 coding sequence, fall under the category of the improvement of function existing BioBrick Part, BBa_J45006. Herewith, our team, KIT-Kyoto 2013 iGEM team, meets the additional requirements for a Gold Medal.

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