Team:UNIPV-Pavia/Calendar/July/settimana3

From 2011.igem.org

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Revision as of 13:31, 27 July 2011

UNIPV TEAM 2011

March
M T W T F S S
  1 2 3 4 5 6
7 8 9 10 11 12 13
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30 31    

April
M T W T F S S
        1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30

May
M T W T F S S
            1
2 3 4 5 6 7 8
9 10 11 12 13 14 15
16 17 18 19 20 21 22
23 24 25 26 27 28 29
30 31

June
M T W T F S S
    1 2 3 4 5
6 7 8 9 10 11 12
13 14 15 16 17 18 19
20 21 22 23 24 25 26
27 28 29 30

July
M T W T F S S
        1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30 31

August
M T W T F S S
1 2 3 4 5 6 7
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 28
29 30 31

September
M T W T F S S
      1 2 3 4
5 6 7 8 9 10 11
12 13 14 15 16 17 18
19 20 21 22 23 24 25
26 27 28 29 30

October
M T W T F S S
          1 2
3 4 5 6 7 8 9
10 11 12 13 14 15 16
17 18 19 20 21 22 23
24 25 26 27 28 29 30
31

JULY: WEEK 3

July, 11th

Digestions of previously purified plasmids were performed for ligations:

Plasmid Kind DNA (μl) H2O (μl) Enzyme 1 (μl) Enzyme 2 (μl) Buffer H (μl) Final Volume (μl)
E1-2 Insert 18 2.5 1 XbaI 1 PstI 2.5 25
E2-2 Insert 18 2.5 1 XbaI 1 PstI 2.5 25
E3-1 Insert 18 2.5 1 XbaI 1 PstI 2.5 25
E4-2 Insert 18 2.5 1 XbaI 1 PstI 2.5 25
E5-2 Insert 18 2.5 1 XbaI 1 PstI 2.5 25
E6-1 Insert 11 9.5 1 XbaI 1 PstI 2.5 25
E7-2 Insert 18 2.5 1 XbaI 1 PstI 2.5 25
E8-3 Vector 20.5 0 1 SpeI 1 PstI 2.5 25
BBa_R0040 Vector 14.5 6 1 SpeI 1 PstI 2.5 25
BBa_C0261 Insert 18 2.5 1 XbaI 1 PstI 2.5 25
BBa_I13507 Insert 10 10.5 1 XbaI 1 PstI 2.5 25
BBa_B0034 Vector 10 10.5 1 SpeI 1 PstI 2.5 25

Reactions were incubated at 37°C for three hours while two medium-size agarose gels were prepared according to protocols.

In the afternoon gel electrophoresis was performed.

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As shown, in figure all clones were positive, so we cut and purified the bands of interest.

After gel extraction, cut DNA was quantified:

Plasmid DNA (ng/μl)
E1 (X-P) 4.2
E2 (X-P) 3.8
E3 (X-P) 4.1
E4 (X-P) 3.7
E5 (X-P) 5.6
E6 (X-P) 7.8
E7 (X-P) 6.4
E8 (S-P) 3.4
BBa_C0261 (X-P) 4.8
BBa_R0040 (S-P) 7.9
BBa_B0034 (S-P) 11.0
BBa_I13507 (X-P) 6.8


Then ligations were performed in a final volume of 10 μl:

Ligation Name Vector Vector volume (μl) Insert Insert volume (μl) Buffer (μl) T4 Ligase (μl)
E9 BBa_B0030 (S-P) 1 E1 (X-P) 7 1 1
E10 BBa_B0031 (S-P) 1 E1 (X-P) 7 1 1
E11 BBa_B0032 (S-P) 1 E1 (X-P) 7 1 1
E12 BBa_B0034 (S-P) 1 E1 (X-P) 7 1 1
E13 BBa_R0040 (S-P) 1.5 E2 (X-P) 6.5 1 1
E14 BBa_R0040 (S-P) 1.5 E3 (X-P) 6.5 1 1
E15 BBa_R0040 (S-P) 1.5 E4 (X-P) 6.5 1 1
E16 BBa_R0040 (S-P) 2 BBa_C0261 (X-P) 6 1 1
E17 E8 (S-P) 4.5 E5 (X-P) 3.5 1 1
E18 E8 (S-P) 5 E6 (X-P) 3 1 1
E19 E8 (S-P) 5 E7 (X-P) 3 1 1
E20 E8 (S-P) 5 BBa_I13507 (X-P) 3 1 1
E21 BBa_R0040 (S-P) 2 E5 (X-P) 6 1 1
E22 BBa_R0040 (S-P) 2.5 E6 (X-P) 5.5 1 1
E23 BBa_R0040 (S-P) 2 E7 (X-P) 6 1 1

Ligations were incubated ON at 16°C.

July, 12th

E9, E10, E11, E12, E13, E14, E15, E16, E17, E18, 19, E20, E21, E22 and E23 were transformed in 100 μl of TOP10 competent cells according to protocols. Plates were incubated ON at 37°C.

July, 13th

All plates showed a lot of colonies, except for E13, E16 (one colony),while for E14, E15 no colony was observed. Because of RFP, E21 was red, E22 and E23 a little bit less. Two colonies for E9, E10, E11, E12, E17, E18, E19, E20, E21, E22, E23 plates were picked. 500 ml of LB with Ampicillin were prepared. ???????????glicerolo stock. diciamo dei reinoculi????????????

July, 14th

A glycerol stock for E21-2, E23-2. E11-1 was prepared. Cultures grew overnight; plasmid purification and quantification were carried out:

Plasmid DNA (ng/μl)
E9-1 114
E10-1 72
E11-1 78.5
E12-1 151.7
E13-1 133
E16-1 134.4
E17-1 27.8
E18-1 25.5

For E9-1, E9-2, E10-1, E10-2, E11-1, E11-2, E12-1, E12-2, E17-1, E18-2, E19-1, E19-2, E21-1, E20-2, E21-1, E21-2, E22-1, E22-2, E23-1, E23-2 PCR was performed. ??????????????????????????????????primer? da scrivere???????????????????????????????????????

In order to screen the DNA, a digestion for each ligation was performed.

DNA (μl) H2O (μl) Enzyme 1 (μl) Enzyme 2 (μl) Buffer H (μl) Final Volume (μl)
3 18.5 0.5 EcoRI 0.5 PstI 2.5 25

Reactions were incubated at 37°C for three hours while two medium-size agarose gels were prepared according to protocols.

BBa_B0032 were transformed in 100 μl of MGZ1 competent cells to test the competence according to protocols. Plates were incubated ON at 37°C.

In the afternoon gel electrophoresis was performed.

link alle 2 img dei gel con ling wiki

As shown in figure, all clones were positive, except for E9-1,E17-2, E18-1, E18-2, E19-1 which didn' t show any DNA band. E9-2, E17-2, E18-2, E19-2, E20-2, E21-1, E22-2, E23-1 purification was carried out for sequencing.

Plasmid DNA (ng/μl)
E9-2 66
E17-2 28
E18-2 26.3
E19-2 39.1
E20-2 22.1
E21-1 143.1
E22-2 70.4
E23-1 80.9
BBa_I13521 79

Cells harbouring E9-2, E10-1, E11-1, E12-1, E13, E16, E21-1, E22-2, E23-1 were inoculated in???? 5 ml???? LB + Amp.

July, 15th

All plates showed a lot of colonies, but the plate containing MGZ1 transformed with BBa_B0032 also showed a lot of satellities.

In order to screen the DNA, digestionS for E17-1, E17-2, E18-1, E18-2 ligation were performed.

Ligation Name DNA (μl) H2O (μl) Enzyme 1 (μl) Enzyme 2 (μl) Buffer H (μl) Final Volume (μl)
E17-1 6 15.5 0.5 EcoRI 0.5 PstI 2.5 25
E17-2 6 15.5 0.5 EcoRI 0.5 PstI 2.5 25
E18-1 6 15.5 0.5 EcoRI 0.5 PstI 2.5 25
E18-2 6 15.5 0.5 EcoRI 0.5 PstI 2.5 25