From 2008.igem.org

Revision as of 17:43, 28 October 2008

Week 1: from 07/21/08 to 07/27/08

General Preparations

1. Preparation of chemiocompetent cells from E. Coli DH5α, Top10 and DB 3.1
2. Preparation of antibiotic stocks for Ampicillin and Kanamicin
3. Preparation of LB medium and LB plates for cloning.

Week 2: from 07/28/08 to 08/03/08

• Eluition and Amplification from 2008 Registry Collection: [http://partsregistry.org/Part:BBa_R0082 R0082], [http://partsregistry.org/Part:BBa_R0083 R0083], [http://partsregistry.org/wiki/index.php/Part:BBa_M30109 M30109] in TOP10 strain to build and characterize the Light response system to be our spatial selective trigger.
  

• Eluition and Amplification from 2008 Registry Collection: [http://partsregistry.org/Part:BBa_E0240 E0240], [http://partsregistry.org/Part:BBa_P1010 pSB3K3_P1010]in DB3.1 and the Practice Promoter Set ([http://partsregistry.org/wiki/index.php?title=Part:BBa_J23103/ J23150, J23151, J23102]) to test and set up the new [http://partsregistry.org/Measurement Biobrick Standard Measurement Protocol]

• Transformation and Amplification from our Lab Stock of [http://partsregistry.org/Part:BBa_S0100 S0100], BBa_I763020, [http://partsregistry.org/wiki/index.php?title=Part:BBa_I763005 I763005] and [http://partsregistry.org/Part:BBa_C0051 C0051]

• Growth Curves of Dh5 Alpha, Top10 and XL1 Blue with Low Medium and High Copy Numbers to assay and define the different kinetics (Further Detail)

Week 3: from 08/04/08 to 08/10/08

08/04/08

• Digestion and Control Gel Run of the previous amplified constructs :

1.[http://partsregistry.org/Part:BBa_S0100 S0100] E/S
Consistent Part Length
2. PLAC-CI X/P
Consistent Part Length
3. R0083 S/P
Single Vector Band as Expexted. Is Hard to verify the Part length correctness given the small size
4. R0082 S/P
Single Vector Band as Expexted. Is Hard to verify the Part length correctness given the small size
5. C0051 X/P
Consistent Part Length.
7. M30105 E/S
The Part appears not consistent. The Gel has unexpected multiple bands.
8. RBS GFP TAG X/P
Consistent Part Length
9.Pλ GFP X/P
Consistent Part Length.

• Ligation of R0082 and R0083 with E0240 to obtain a Reporter for the Light Driven Trigger.

Week 4: from 08/11/08 to 08/17/08

HOLIDAY

Week 5: from 08/18/08 to 08/24/08

Starts the protein construct cloning

1. Ligations: [http://partsregistry.org/Part:BBa_I763020 I763020] + [http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_S0100 S0100] + [http://partsregistry.org/Part:BBa_B0015 B0015], TETR + [http://partsregistry.org/Part:BBa_B0015 B0015]
2. Trasformation of the ligations in E.coli
3. Inoculation and miniprep preparation
4. Enzymatic digestion and construct gel run: GFP T x\p, S0100 T x\p, TETR T x\p
5. Gel extraction of the parts

Week 6: from 08/25/08 to 08/31/08

1. Ligation: B0034 + TetR T , B0034 + GFP T
2. Trasformation in E.coli
3. Inoculation and miniprep preparation
4. Digestion and gel run of the constructs: RBS TETR T x\p, RBS GFP T x\p
5. Gel extraction of the parts
6. Ligation of RBS GFP T and S0100, RBS GFP T and RBS TetR
7. Trasformation in E.coli
8. Inoculation and miniprep preparation
9. Digestion and control gel run of the parts: RBS TETR RBS GFP T x\p, S0100 RBS GFP T x\p
10. Gel extraction

• Final cloning step:

1. Ligation of promotor J23118 and RBS GFP T, promotor J23105 and RBS GFP T, promotor J23100 and RBS GFP T
2. Trasformation in E.coli
3. Inoculation and preparation of Miniprep
4. Digestion and control gel run of the constructs:J23118 RBS GFP T, J23105 RBS GFP T, J23100 RBS GFP T
5. Gel extraction

Week 7: from 09/01/08 to 09/07/08

Arrival of the operator library (link) from GeneArt

• Implementation of the protocol to separate each Lac Operator from the library

1. Single digestion with Pst and control gel run (In this way we open the plasmid in 3 points,leaving free the Lac Operator1 and 2, remaining the plasmid with the lac Operator 3)
2. Gel extraction of the upper band containing Lac Operator3 inside the plasmid
3. Single digestion with Xba and control gel run
4. Gel extraction of the upper band containing Lac Operator1 inside the plasmid
5. Single digestion with EcoRI and control gel run (In this way we open the plasmid in 2 points,leaving free the Lac Operator3, remaining the plasmid with the lac Operator1 and 2)
6. Gel extraction of the upper band containing Lac Operator1 e Lac Operator2 inside the plasmid
7. Further single digestion with Pst and control gel run
8. Gel extraction of the upper band containing Lac Operator2

This protocol was executed for both Tet, Lex, Lambda operators library

Week 8: from 09/08/08 to 09/14/08

• Assembly of the constructs

1. Ligation of Lac2 operator and S0100 RBS GFP T, Lac2 operator and S0100, Lac1 operator and S0100, LexA2 operator and RBS GFP T
2. Trasformation in E.coli
3. Inoculation and preparation of Miniprep
4. Digestion and control gel run
5. Gel extraction of the constructs: LexA2 RBS GFP T x\p, Lac2 S0100 T x\p, Lac2 S0100 RBS GFP T x\p, Lac1 S0100 T x\p

Week 9: from 09/15/08 to 09/21/08

1. Ligation of the previous purified constructs and the promoters J23118, J23100
2. Trasformation in E.coli
3. Inoculation and preparation of Miniprep
4. Digestion and control gel run
5. Gel extraction of the constructs: J23118 S0100 RBS GFP T, J23118 Lac2 S0100 RBS GFP T, J23118 LexA2 RBS GFP T, J23100 LexA2 RBS GFP T, J23118 Lac2 S0100 T, J23118 Lac1 S0100 T

Week 10: from 09/22/08 to 09/28/08

Week 11: from 09/29/08 to 10/05/08

• Start preparing to LEXA_2 operator reporter construct:

1. digestion X/P of B0034-J04031-B0010-B0012
2. digestion S/P of LEXA_2 operator
3. Control Gel Run of B0034-J04031-B0010-B0012 digested X/P and LEXA_2 operator digested S/P
4. Gel extraction of B0034-J04031-B0010-B0012 digested X/P and LEXA_2 operator digested S/P
5. ligation of B0034-J04031-B0010-B0012 digested X/P with LEXA_2 operator digested S/P
6. trasformation of LEXA_2-B0034-J04031-B0010-B0012
7. inoculation of LEXA_2-B0034-J04031-B0010-B0012
8. miniprep of LEXA_2-B0034-J04031-B0010-B0012
9. digestion X/P of LEXA_2-B0034-J04031-B0010-B0012
10. digestion S/P of J23118
11. control gel run of LEXA_2-B0034-J04031-B0010-B0012 digested X/P and J23118 digested S/P
12. gel extraction of LEXA_2-B0034-J04031-B0010-B0012 digested X/P and J23118 digested S/P
13. ligation of LEXA_2-B0034-J04031-B0010-B0012 digested X/P with J23118 digested S/P
14. trasformation of J23118-LEXA_2-B0034-J04031-B0010-B0012
15. inoculation of J23118-LEXA_2-B0034-J04031-B0010-B0012
16. miniprep of J23118-LEXA_2-B0034-J04031-B0010-B0012
17. UV testing of J23118-LEXA_2-B0034-J04031-B0010-B0012

• since construct test was successful, we plan to prepare the same construct for the other two LEXA operator to test the affinity to LEXA, in order to choose one that best lends itself to the implementation of bistable toggle switch.

Week 12: from 10/06/08 to 10/12/08

Week 13: from 10/13/08 to 10/19/08

Week 14: from 10/20/08 to 10/26/08

Week 15: from 10/27/08 to 10/29/08

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