Team:UNITN-Trento/Project/Blue light

We decided to develop a photo-inducible genetic circuit that triggers the production of Ethylene in the presence of blue light (470 nm), and blocks it in the dark.

We thought to use blue light as our inducer because it would fit perfectly to our very own B. fruity vending machine, being the easiest way to control a genetic device in a totally automated scaffold. All parts have been transformed and characterized in E. coli (strain NEB10b).

We wanted to produce ethylene with blue light (470 nm) and have an off state in the dark, so we designed of a blue light dependent device that includes an inverter cassette.

We engineered in E. coli a blue-light sensor composed by:

• Anderson promoter BBa_J23100;
• the blue light receptor YF1, which consist of YtvA from B. subtilis fused to a kinase domain (fixL) from B. japonicum ("Möglich A., J Mol Biol. 2009, 385(5): 1433–1444)(Ohlendorf R., J Mol Biol. 2012, 414: 534-542);
• its response regulator, FixJ;
• a downstream promoter PfixK2, which is turned off by phosphorylated FixJ;
• an inverter cassette composed of cI and Plambda;
• a reporter (chromoprotein amilCP), which was later substituted by EFE (our ethylene forming enzyme).

To assemble this device we used the following parts from the registry:

• Bba_J23100 from Berkeley 2006 iGEM team;
• Bba_K592016 from Uppsala 2011 iGEM team;
• BBa_K592020 from Uppsala 2011 iGEM team.

We characterized this circuit along with the version without the inverter cassette (activated at dark and inhibited by blue light). Thus we also created the part:

We first assembled the “inverted circuit” with a blue chromo-protein (AmilCP) downstream instead of EFE to obtain easy-to-watch and clear characterization results.
At first we compared the induction power of several light sources:

• 1 LED blue light;
• 1 blue light bulb;
• 1 white light bulb.

Then we decided to use only blue LED and normal light as inducers in further tests.

Moreover, AmilCP has an absorbance peak at 588 nm so we measured the absorbance peak at the UV-VIS spectrometer (PerkinElmer lambda 25)in order to have concrete data. We sonicated samples for 10 seconds and resuspended the pellets in 2 ml of PBS.

We carried out several tests in order to demonstrate the reproducibility of the behavior, although sometimes we observed amilCP production even in the dark control, so we could assume that the circuit doesn’t act like a perfectly controlled switch. We can make a speculation on the cause: probably the inverter cassette presence is responsible of this flawed behavior; Plambda is actually a strong promoter but CI transcription is at the end of a pretty long cascade that is likely to produce low CI; this means that there isn’t enough inhibitor to block Plambda activity. In order to confirm our theory we tested also the circuit without the inverter. This device, on the contrary, is designed to get switched on at dark and to be inhibited by blue light though. We extracted the part BBa_k952003, the circuit with the reporter AMILGFP (yellow fluorescent protein).

The part extracted from the registry missed a RBS sequence, resulting in a nonfunctional part. We decided to improve this part by inserting the missing RBS with a mutagenesis PCR. The mutagenesis was successfull.

In order to have it tested and characterized, we also added the pLac promoter ahead as already shown (BBa_K1065302).

The test involved the induction of both, the improved circuit and the original part, in order to demonstrate the actual enhancement of the device. So we compared samples depending on two factors: induction/non induction & RBS/no RBS. We also took some quantitative measurements with a Cary Eclipse Varian fluorimeter considering that amilGFP is a fluorescent protein that emits at 512 nm and absorbs at 503 nm. For measurements we resuspended sonicated samples' pellets in 2 ml of PBS.

We achieved a successful characterization of both circuit with or without the inverter, noticing a substantial difference between controls and induced samples; Nevertheless we couldn’t appreciate this for every test performed on Bba_k1065310. Comparing the behavior of the 2 devices, we can notice that, under the conditions that we used, the one without the inverter definitely shows a sharper switch.
Supposed causes:

• as already explained probably the genetic cascade in BBa_K1065310 that brings the activation of cI isn’t strong enough, resulting in a limited production of inverter thus in the subsequent production of AmilCP;
• furthermore, we believe that the absence of a terminator after pFixK2 could cause the transcription of several different-sized segments, sometimes including the inverter cassette.
• a remaining element probably involved in the different behaviors is the different upstream promoters used.

We believe that more improvements need to be provided to the system in order to get it perfected and satisfying:

• add a terminator after pFixK2;
• substitute J23100 with pLac promoter;
• improve the transcription of CI;

To this day we are in the process of improving it and hopefully have some great enhancements for the championships!!!

However we were able to produce ethylene by placing EFE (BBa_K1065000) downstream the circuits. Please go ahead to our ethylene measurements section for these data.