Team:UNIPV-Pavia/Calendar/September/week1

From 2011.igem.org

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R0040 in J61002-1C3 and J101-31N-1C3 showed colonies while E3N-1C3 did not grow; two colonies were picked for each plate and inoculated in Lb + Cm34, 5 ml.
R0040 in J61002-1C3 and J101-31N-1C3 showed colonies while E3N-1C3 did not grow; two colonies were picked for each plate and inoculated in Lb + Cm34, 5 ml.
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E3-1C3-2 was purified and quantified:
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2 &mu;l of the purified plasmidic DNA of E3-1C3-2 were digested with 0.5 &mu;l EcoRI and PstI restriction enzymes in a 25 &mu;l final volume; a small size agarose gel was prepared.
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2 &mu;l of the purified plasmidic DNA were digested with 0.5 &mu;l EcoRI and PstI restriction enzymes in a 25 &mu;l final volume; a small size agarose gel was prepared.
 
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Revision as of 10:41, 4 September 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

SEPTEMBER: WEEK 1

September, 2nd

E3-1C3-2 was purified in order to screen the part length.

Plasmid DNA (ng/μl)
E2-1C3-2 82.1

R0040 in J61002-1C3, E3N-1C3 and J101-31N-1C3 were transformed in 200 μl of TOP10 competent cells.
Inoculum of E24-2, E25-1, E26-2, E27-2 and RBS32 in M9 + Amp to collect supernatant after 3OC6-HSL supplementation.
Inoculum in M9 + Cm12.5 of T9002-ENTERO and ENTERO-RBS to measure 3OC6-HSL concentration in supernatants at different pHs collected on August, 31st.

September, 3rd

All the cultures were diluted 1:200 in M9 with the proper antibiotic. After two hours T9002-ENTERO and ENTERO-RBS were aliquoted in 96-well microplate and induced with known concentrations of 3OC6-HSL and with the supernatants collected on August, 31st.
E24-2, E25-1, E26-2, E27-2, RBS32 and sterile M9 were supplemented with 100 nM 3OC6-HSL. Supernatants were collected at t = 0 h, t = 7 h and t = 24 h from all of these tubes.
R0040 in J61002-1C3 and J101-31N-1C3 showed colonies while E3N-1C3 did not grow; two colonies were picked for each plate and inoculated in Lb + Cm34, 5 ml.
2 μl of the purified plasmidic DNA of E3-1C3-2 were digested with 0.5 μl EcoRI and PstI restriction enzymes in a 25 μl final volume; a small size agarose gel was prepared.

The gel did not show the correct band.
500 ml M9 and 1 l LB were prepared.