Team:LCG-UNAM-Mexico/Notebook/2008-June 2

Final design

Scheme

The first plasmid contains the efflux pump for Nickel (rcnA), which will maintain its natural regulation dependent of metal (by RcnR) and additionally, it will contain a promoter regulated by the repressor of lambda phage, cI. Besides, of course, a resistance as a marker of the plasmid.

The second contains everything needed for regulating the power down from an external signal (AHL). Both luxR as aiiA will occur constitutively, the first one, with a strong promoter (pTetR), as we do not want the presence of LuxR to be limiting, and the second one, having a moderate promoter or weak (pLacZ), to give us space to play with concentrations of AHL without aiiA always wining. And cI *, cI modified with a queue of LVA for rapid degradation, regulated by a promoter dependent of LuxR + AHL. It will also contain an equal resistance as a marker.

In the presence of AHL, this joins with LuxR and induces the production of cI *, which in turn represses the transcription of rcnA. Like cI *, signal AHL has to be short-lived since aiiA is degradating constantly, so the system quickly returns to its initial state once it ceases to manage AHL.

Parts

Defining bioparts we will use or where to get what is necessary.

Part: BBa_I729006

Part of Quorum sensing used by the team Chiba in iGEM2007. Both tetR and LacI + pL are constitutive promoters, but since LacI + pL is a very strong promoter, it will probably be replaced. This biopart will be responsible for the regulation by luxR and the action of the system by AHL. Instead of GFP (Subpart E0040), the BBa_C0051 part that codes for the protein cI + LVA will be inserted, which will join the regulatory region of cI (biopart BBa_R0051) in the other plasmid.

(Previous experience: none)

Part:BBa_C0051

Region coding for the repressor cI based on the repressor cI of lambda phage with modified LVA with a queue for rapid degradation. cI joins the regulator cI (BBa_R0051)

(Previous experience: none)

Part:BBa_R0051

Promoter regulated by cI based on the pR promoter of lambda phage. The promoter has two binding sites to cI repressor of lambda phage (BBa_C0051). The union of cI results in the suppression of the transcript.

(Previous experience: it works)

Of the previous 3 bioparts, the sequence is in the registration of biological parts and according to this page, DNA is available.

Part: BBa_G00510

This is the forward primer of C0051 that has 24 pb.
(No DNA in the bank, but we know that it works)
gatttctgcatagccagacttggg

Part: BBa_G00511

Reverse primer for C0051 that has 26 pb.
cactgactagcgataactttccccac
(No DNA in the bank but we know that it works)

Vectors

We need to define the vectors we can use.

Possibilities:
*The ones recorded in the spreadsheet (courses).

In bioparts:

Primers

Build or find oligos that we could use for our constructions.

We need:
• rcnA (with its regulatory region; no promoter).
• cI *.
• Constitutive promoter for luxR (tetR is proposed, it is a strong promoter).
• Constitutive promoter for aiiA (lacZ is proposed, it is a moderate promoter).
• aiiA.
• Promoter dependent of cI.
~ In all cases, we have to check whether they already exist (in biopartes or something) and evaluate them.

Promoters

Investigate a little more about the proposed promoters and define whether they are the most optimal.

Facts about kinetics & other things...

Investigate a little more about the parties involved in the system to begin with an outline of modeling and defining how the design is theoretically feasible.

Note: To join HSLwith LuxR and enable the transcription of cI, HLS should be at a concentration of micromolar order.
Note (2): Not all bioparts have been used previously, most DNA is available but still there is no record of it working. We need to check the quality of DNA to ensure that there will be no problems.

Modeling

Variables
Concentrations of:

• LuxR (constant).
• aiiA (constant).
• AHL (arbitrary).
• cI* (according to aiiA, AHL & LuxR).
• RcnA (according to cI*).

Knowing the initial concentrations and lifetime of proteins involved, as well as the efficiency action of aiiA (kinetics in general).
* The concentration of Nickel (NiCl2) in the medium which supports the cell according to Rodrigue et al. (2005) before inhibiting growth is 4 μ M for the strain lacking rcnA, 10 μ M in the wildtype and up to 100 times more in a strain with a multicopy gene.

Assumption 1: Once there is nickel in the medium, RcnR does not matter for the pump regulation. This because there will be large concentrations of metal, so we can assume that RcnR will always be linked to a molecule and it will therefore be unable to suppress the transcript of rcnA; the noise that the few RcnR free molecules can cause, will be indistinguishable from normal behaviour of the pump.

Assumption 2: Any decrease in the concentration of AHL is due to aiiA. It is believed that the natural degradation of this is irrelevant in the time scale analysis. Either way, a process will not be distinguishable from the other and even when the first is estimated, it would not be very informative for the analysis, so we intend to take this assumption as true.

Assumption 3: The transcription of cI * depends solely on the concentration of AHL. LuxR is not a limiting step, ie, it is in constant concentration and in sufficient quantity to be always available to associate with AHL. Only to simplify the analysis, at least as a first approximation.

Initial outline:

(v1) AHL0
(v2) aiiA + AHL -> aiiA
(v3) AHL + LuxR -> cI*
(v4,v5) ρ + cI* <--> ρ.cI*
ρ -> ρ +RcnA
RcnA + Ni -> RcnA
RcnA -> Ø

Experimental work

1. Take the sequences (fasta format)
2. Once you have the sequence find appropriate reading frames
3. Make the restriction map
-- Nedcutter, check the page for NewEngland Biolabs (because we are going to use enzymes from that company)
For rcnA and rcnR, the regulatory region that was among the two genes was not explained.
We have to take the whole sequence in fasta format and use it in a program called Gene Construction Kit. This shows reading frames and restriction sites.

In fruitfly.org: 9005/seq_tools/promoter.html we can look for primers and we can adjust parameters. We can also analyze the stability energy, and seek the lowest point of stability. This point is generally the -10box. To find inverted repeats, we shall use the program StemLoop of the parcel of GCG (genetics computer group). This program calls in the sequence in a GCG format. To find direct repeats we will use the program "repeat". For rcnR and rcnA we found three direct repeats between the -10 box and the translation start of rcnA.We suggest that this is a regulatory region. Based on this, we designed the primers, trying to preserve the regulatory region and changing its promoter.

Primer design. The region should be rich in GC, of about 20 nucleotides with a 50% GC content at least and it should finish in G. The program can also show the double chain to facilitate the design of oligo lower. If they are rich in AT, they can be longer primers to increase its Tm.

The most popular program at the center is Oligo. Here we open a new window and paste the sequence. This will open two windows. The first one with the Tm, and the other one with the free energy. The program can calculate all oligos and show potential couples with its parameters. We can also specify were we want the oligo to be located. Once the program generates it, we can analyze its biochemical properties.

Trying to k Delta G so it won't be lower than -10.

The differences between the TMS should not be greater than 5 degrees. Enzymes used in PCR use magnesium chloride. The most reliable and processed use magnesium acetate. It is said that 10mM of dinucleotidos is an optimal concentration for PCR, .4 mM is used in the lab. Once we have the oligo, we add a site at the far restraining 5 '. And add nucleotides in the 5 'end to ensure that the enzyme is positioned correctly and efficiently cut. These nucleotides are different for each enzyme, and they also protect the 5' end.

Two plasmids are used as a basis prK415 P. Our advisor, Miguel, already has isolated DNA and this DNA will be used to transform and to have a the plasmid reserved. 2ul of the plasmid and competent cells treated with calcium chloride. The theory says that positive ions are attached to the membrane, so the membrane has a positive charge. As DNA has a negative charge, once they are mixed at 4 degrees Celsius for 20 minutes, we are going to take the tube and put it at 42 degrees centigrade. This stress produces holes in the membrane and many things will be capable or entering or exiting through the membrane, including DNA. Then it remains 2 more minutes at this temperature. The we return it to ice for 5 more minutes to recover. Later, the cells are placed in 1ml of rich medium (LB) were they are allowed to grow at 37 degrees for one hour at 300 revolutions per minute (this allows them to recover).

100ul are taken and used to plate in petri dishes with the antibiotic. It is left to grow for an entire day and at the end, isolated colonies should appear.
Bacteria with kanamycin 5ml of two strains, one with a deletion in rcnA and another one with any deletion except for rcnA . For 6 hours, the bacteria will have an exponential growth. Genomic DNA will be extracted.

The contents of the tube will be put in an eppendorf, we centrifuge and then we withdraw the liquid medium with a syringe. Before we lyse de cells, we need to wash with TE 10 1 (Tris 10uM EDTA 1uM), with pH 8. Vortex, to separate and disintegrate. Again, we centrifuge and remove supernatant. To lyse, we add 400-450 ul TE5020pH8 and SDS 10% and K proteinase. We leave it at 37 degrees for 20 minutes. The medium goes from an opaque color to a light color when lysis happens. We add ethanol 100% once we have lysed the cells and we vortex. In the presence of ethanol DNA is precipitated, so we add 1ml of ethanol. Then we centrifuge for a few minutes and we have pellet. We wash three times with ethanol 70%, which solubilised salts and the small molecules (including RNA). We remove all the ethanol, this tube is placed in a specific centrifuge. The vacuum from this centrifuge will remove the remain solvent. It is necessary to remove all the ethanol, because this affects the pH. TE 10 1 RNAs 10mg per ml, this Stock solution is divided 1000 times and 50ul approx are added. To check the quality of the DNA extracted, we use an agarose gel.

Transforming bioparts: Bacteria needed to extract DNA plasmid. Centrifuge, wash and put solution 1. Glucose, TRIS, EDTA and sometimes RNAs 1. Sodium hydroxide and SDS in the solution 2, sodium hydroxide denatures the DNA. Solution 3 with sodium acetate neutralizes the base. Wash and dry every time.