Here's what I've been up to:
Week 1Week 1 started fairly slowly, which gave me a chance to read up on several papers about research already carried on PcaK and the AAHS family. I began by culturing E. Coli which had been transformed with a plasmid containing the PcaK gene of the extremophile Haemophilus ducreyi, and then induced these via addition of arabinose (to turn on T7 RNA polymerase expression) and IPTG (to turn on protein expression). Unfortunately, the cells started to die on induction of protein expression - a possible explanation for this being that the protein is toxic to E. coli growth. This may lead to a low final concentration once purified, as it's possible that the cells that survived were those that were not expressing the protein! I proceeded to harvest the cells via centrifugation and then resuspend the pellets in PBS buffer and TCEP (reduces disulphide bonds). Next I got to use a cell disrupter to lyse the cells and, after an inital centrifugation to remove debris and unlysed cells, I pelleted the membranes via ultracentrifugation. These were then resuspended in detergent.
|HisTrap column for protein purifcation|
From here the real fun began as I purified PcaK via a HisTrap column - this contains nickel Sepharose beads which bind the ten histidine tag that PcaK was expressed with. Having learnt about this process in undergrad lectures, it was interesting to put the theory into practice! After measuring the absorbance of the purified protein at 280 nm, I calculated that a final protein concentration of 0.27 mg/ml had been achieved - alas, too low for crystal trials.
As a final 'polishing step' we performed size exclusion chromatography
|Size exclusion chromatography|
Unfortunately it seemed most of my protein eluted in the column void (this usually indicates aggregation) and due to the low concentration no visible peak was observed. Nevertheless, it was a good opportunity to use equipment I hadn't seen before. Finally, I ran an SDS PAGE gel of fractions from the purification process, which verified the low protein concentration I'd achieved - only a very faint band (see below) of purified protein can be seen on the gel.
All in all, a really interesting and enjoyable week. It feels like I've learnt a LOT already and I'm looking forward to what the next few weeks will involve.
|Dave the autoclave - my nemesis|
Luckily, one can never do enough reading so this gave me an opportunity to further research aromatic transporters and also look in more detail at the mechanisms of the equipment I'm using. I'm not in the lab tomorrow as am off to do the National Three Peaks Challenge (eek) so will update next week on how the purification process comes along.
For now, I'll leave you with this review (Cao, B., K. Nagarajan, and K.-C. Loh, Appl. Microbiol. Biotechnol.) on the biodegradation of aromatic compounds if you fancy a read - I think it offers a great insight into the mechanisms and possible applications of bioremediation.