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From 2009.igem.org

Revision as of 22:20, 21 October 2009 (view source) Jurquiza (Talk | contribs) (→Uriel Urquiza) ← Older edit		Revision as of 22:24, 21 October 2009 (view source) Nandomgu (Talk | contribs) (→Fernando Montaño) Newer edit →
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	====Assembly of the P4 vector.====<br>		====Assembly of the P4 vector.====<br>
-	* I must create an eternal bacterial source of P4 sid1. Therefore I must Infect C1a with it.	+
-	*I need to develop a good protocol for P4 sid1 lysate production.	+	We want P4 to work as a [[Team:LCG-UNAM-Mexico/Description#Delivery|transduction vector for biobricks]]. Several things need to be done, which include individual amplification of P4 sid1 essential region, which we expect to be sufficient for a stable permanence of the biobrick inside the cell. To test this, the first biobrick added will be a reporter gene, which is intended to permanently stay with our P4 version. This is enough to further produce our P4 viral particles and assess functionality of the delivery by transduction into several wild-type bacterial strains as reported in literature.
-	* I must obtain the essential region of P4 sid1 by PCR. This will add the preffix and suffix to the region.<br>	+
-	3) I need to ligate the "biobricked" P4 region to a reporter; better off RFP or a hard-resistance antibiotic.<br> Then, I have to transform to produce P4 (preferably with our stock producing bacterium) and infect wild-type strains to look for reporter-associated colonies. <br>(Also try in many bacterial strains)<br>	+	====Checking functionality for the Kamikaze system====
-	4) When the kamikaze system is ready, I need to ligate the P4sid1 region to it and transform an E.coli C1a strain with it. <br>	+
-	5) then we can start testing the system!<br>	+	Now we will be ready to ligate the entire device. Many things have to be assessed, as the complete packaging and delivery of the vector into the host cells, and of course, the functionality of the system. This involves checking for presence and reaction to AHL, production of antisense RNAs and many parameter calculations.
-	6) ultimate goal: standardize P4 as an iGEM vector.	+
		+	====P2 control system functionality====
		+
		+	The cox/ogr control system in which [[Team:LCG-UNAM-Mexico/Wet lab/Objectives#Uriel Urquiza|Uriel]] is working needs experimental validation of functionality. I intend to transform P2 lysogenic strains and expect lysis through activation of such genes. This will prove the construction works.
		+
		+	====P4 as an iGEM Plasmid====
		+
		+	P4 will have to suffer many more modifications in order that it functions as an iGEM standard vector. The design automatically eliminated forbidden restriction sites, but we also need transcription terminators and universal primers. After addition of such sequences, functionality has to be assessed again.
	====Testing for activity of the control system====		====Testing for activity of the control system====

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Revision as of 22:24, 21 October 2009

Wet Lab!!

General objectives

Uriel Laura Nando Abraham Paz

The final aim is to get and test the following device.

I. Biobrick Assembly of the Kamikaze system

Many cuts, pastes and clones for biobrick organization into the suicide system!!
In the hands of:
Abraham and Paz

II. Construction of the standardized P4 vector

An incredible and challenging fight against PCR and logical thinking!!In charge:
Nando and Paz

III. Construction of the P4-producing strain

A passionate struggle with natural selection and recombination!!
leading:
Uriel, Laura, and Miguel

IV. System testing and parameter obtention

The integrative side of the bite back
In the hands of: Laura (and Everyone else soon!)

Are you ready 2 rumble??

Personal Objectives

Uriel Urquiza

Journal

• • Construction of the phage production control system.

  In order to produce a grate amount of P4 phage particles that have our death system, we want to avoid the natural
  early lysis that occur when WT P4 and P2 interact. This avoidance will be achieved by taking the control of the 
  two major regulators of P2 morphopoietic genes and deleting them form lysogenic P2; this will yield a P2 phage 
  which only has capsid and tail genes.  The control system that is going to be implemented is constituted by a 
  promoter inducible by IPTG in conjunction with transactivators cox and ogr from phage P2. All this will 
  allow us to grow bacteria in great quantities, induce lysis whenever we want and consequently a stock amount
  of modified P2. 

• • Qualitative characterization of T7/T3 multipromter.

  The multi-promoter that we have designed has the capacity to respond specifically to T7/T3 RNA polymerases
  so if one or both polymerases are present in the cell the genes downstream of this promoter will be active. 
  A first characterization approach is the introduction of a plasmid carrying our promoter in the E. coli strain
  BL21(DE3)pLysS that has a T7 RNA polymerase inducible by IPTG and then perform assays with and without this 
  inductor, finally microscope visualization with suitable filter and light will be performed to see a GFP that 
  is under control of the multipromoter.

Laura Gomez

• • To obtain all the relevant experimental information about T7 and T3.

 Model validation needs some critical parameters like strain(C1a) growth rate and the T3 and T7 burst sizes. The 
 parameters found in the literature correspond to k12 strain however we used a k12 derivative strain, C1a, for this 
 reason it was indispensable to obtain experimentally a C1a growth plot. In the same way, simulations
 showed us that the burst size is a critical parameter to determine the efficiency of our system.

• • Generation of data to feedback the infection model.

 The experimental data would be used to feedback the model in order to obtain the most accurate model as possible.

Abraham Avelar

• • Ensamble the kamikaze construction

 Clone the colicines with the multipromoter, design and Clone the asRNA and help in the ensamble of all the device.

• • Test the construction

 Obtain the time that E3 takes to kill E. coli, this parameter will be provided to the model. The preference 
 for E3 above E9 is due to a modeling suggestion that shows the effectivity of our system when the translation
 machinery is disrupted, test the efficience of plaquing with the asRNA by itself and the efficience of all the
 device.

Fernando Montaño

====Assembly of the P4 vector.====

We want P4 to work as a transduction vector for biobricks. Several things need to be done, which include individual amplification of P4 sid1 essential region, which we expect to be sufficient for a stable permanence of the biobrick inside the cell. To test this, the first biobrick added will be a reporter gene, which is intended to permanently stay with our P4 version. This is enough to further produce our P4 viral particles and assess functionality of the delivery by transduction into several wild-type bacterial strains as reported in literature.

Checking functionality for the Kamikaze system

Now we will be ready to ligate the entire device. Many things have to be assessed, as the complete packaging and delivery of the vector into the host cells, and of course, the functionality of the system. This involves checking for presence and reaction to AHL, production of antisense RNAs and many parameter calculations.

P2 control system functionality

The cox/ogr control system in which Uriel is working needs experimental validation of functionality. I intend to transform P2 lysogenic strains and expect lysis through activation of such genes. This will prove the construction works.

P4 as an iGEM Plasmid

P4 will have to suffer many more modifications in order that it functions as an iGEM standard vector. The design automatically eliminated forbidden restriction sites, but we also need transcription terminators and universal primers. After addition of such sequences, functionality has to be assessed again.

Testing for activity of the control system

Uriel's cox and ogr construction needs to be tested experimentally to assureThe procedure will be:

1) Transform a P2 lysogenic strain with the construction. 2)assess IPTG induced lysis activation

Enrique Paz

• • Desingn of our modified version of bacteriophage P4

What we need to do over P4 genome and how to do it in order to construct a bacteriophage compatible with standards
in synthetic biology. 

• • Construction and test of the gossip device (quorum sensing)

Some -a lot- restrictions, ligations, transformations, tests, etc. To achieve a high quality device for quorum
sensing that we will use for construction of our "alarm" system.

• • Test the host range of our modified P4

According to litterature bacteriophage P4 has an unusual host-range. We would like to test it so we can transport
easily synthetic construction to another interesting bacteria species!

Work Journals

• Nando's Lab Journal

• Uriel's Lab Journal

• Abraham's Lab Journal

• Laura's Lab Journal

• Enrique's Lab Journal

Retrieved from "http://2009.igem.org/Team:LCG-UNAM-Mexico/Wet_Lab/Objectives"