Team:Valencia/Notebook/July

From 2010.igem.org

(Difference between revisions)
 
(24 intermediate revisions not shown)
Line 88: Line 88:
|  5 ||  6 ||  7 || [[Team:Valencia/Notebook/July#July 8th|8]] ||[[Team:Valencia/Notebook/July#July 9th|9]] || [[Team:Valencia/Notebook/July#July 10th|10]] || [[Team:Valencia/Notebook/July#July 11th|11]] ||  
|  5 ||  6 ||  7 || [[Team:Valencia/Notebook/July#July 8th|8]] ||[[Team:Valencia/Notebook/July#July 9th|9]] || [[Team:Valencia/Notebook/July#July 10th|10]] || [[Team:Valencia/Notebook/July#July 11th|11]] ||  
|-
|-
-
| [[Team:Valencia/Notebook/July#July 12th|12]] || [[Team:Valencia/Notebook/July#July 13th|13]] || 14 || 15 || 16 || 17 || 18 ||  
+
| [[Team:Valencia/Notebook/July#July 12th|12]] || [[Team:Valencia/Notebook/July#July 13th|13]] || [[Team:Valencia/Notebook/July#July 14th|14]] || [[Team:Valencia/Notebook/July#July 15th|15]] || 16 || 17 || 18 ||  
|-
|-
| 19 || 20 || 21 || 22 || 23 || 24 || 25 ||  
| 19 || 20 || 21 || 22 || 23 || 24 || 25 ||  
Line 170: Line 170:
|}
|}
<br>
<br>
-
 
-
=July 8th=
 
-
 
-
==WETLab meeting==
 
-
 
-
We start to put together all the thing, to begin working in the Lab!!
 
-
We also made plans for the future.
 
-
 
-
We prepared the culture medium for growing our yeasts.
 
-
 
-
[[Image:valencia_gabi.jpg|Gabi with the super yeast culture medium|200px|thumb]]
 
-
 
-
 
-
==Social Event==
 
-
We got together in Serranos Towers, to chill out a litle bit after the "hard work" in the lab.
 
-
[[Image:valencia_serranos.jpg|Gettin' together in Serranos Tower|200px|thumb]]
 
-
 
-
 
-
=July 9th=
 
-
- We filled up the petri dishes with the yeast liquid culture medium.
 
-
 
-
- Then we planted the yeasts onto the petri dishes.
 
-
 
-
- We prepared an overnight culture at 37ºC into a stove with the bacteria having the plasmids pG1 and pLZ in order to purificate them next Monday.
 
-
 
-
=July 10th=
 
-
We transferred the bacterial culture from the stove (37ºC) to the fridge (4ºC).
 
-
 
-
 
-
=July 11th=
 
-
Spain won the World cup!!!!
 
-
 
=July 12th=
=July 12th=
Line 207: Line 175:
[[Image:miniprepGZ_12-7_3.jpg|center|thumb|200px|Dani reading the protocol and Gabi moral support for the first miniprep!!]]
[[Image:miniprepGZ_12-7_3.jpg|center|thumb|200px|Dani reading the protocol and Gabi moral support for the first miniprep!!]]
But before you start any procedure, you have to read the protocol!!!!
But before you start any procedure, you have to read the protocol!!!!
-
[[Image:miniprepGZ_12-7_5.jpg|center|thumb|200px|Gabi, Jose, Juan Angel and Dani's red hair doing the miniprep, almost done!!]]
 
- Then we carried out a digestion and the following electrophoresis to verify whether we had the constructions in the plasmids and to evaluate their concentration.
- Then we carried out a digestion and the following electrophoresis to verify whether we had the constructions in the plasmids and to evaluate their concentration.
-
[[Image:gel_ready_12-7_2.jpg|center|thumb|200px|Gabi and the high-tech device for run the gel!!]]
+
<gallery widths=200px heights=150px perrow=2>
-
First good result!! Here a picture of the electrophoresis. From left to right: Marker, pLZ and pG1.
+
Image:miniprepGZ_12-7_5.jpg|Gabi and the high-tech device for run the gel!!
-
[[Image:electroforesisGZfoto_12-7_2_c.jpg|center|thumb|400px| We have the constructions and in a good concentration!]]
+
Image:gel_ready_12-7_2.jpg|Gabi, Jose, Juan Angel and Dani's red hair doing the miniprep, almost done!!
 +
</gallery>
 +
First good result!! Here a picture of the electrophoresis. From left to right: Marker, pLZ and pG1.
 +
[[Image:electroforesisGZfoto_12-7_2_c.jpg|center|thumb|260px| We have the constructions and in a good concentration!]]
- We stored the non-digested plasmids in the refrigerator (we want to use it later on)
- We stored the non-digested plasmids in the refrigerator (we want to use it later on)
- We made (Jose made) a liquid culture of ''E. coli'' with the LEA gene, and puted it into the stove at 37ºC.
- We made (Jose made) a liquid culture of ''E. coli'' with the LEA gene, and puted it into the stove at 37ºC.
-
[[Image:Ecoli_liq_12-7_2.jpg|center|thumb|200px|Jose putting the liquid medium in the tube]]
+
Ale saying Jose what to do :D!!
-
[[Image:Ecoli_liq_12-7_1.jpg|center|thumb|200px|Ale saying Jose what to do :D!!]]
+
<gallery widths=200px heights=200px perrow=2>
 +
Image:Ecoli_liq_12-7_1.jpg|Ale saying Jose what to do :D!
 +
Image:Ecoli_liq_12-7_2.jpg|and Jose putting the liquid medium in the tube
 +
</gallery>
- We recieved a filter paper soaked with a plasmid from Kausik Li containing an ''Aplysia'' prion fused with the GR domain. Then we put the paper containing the plasmid in water in order to transform and clone it in ''E. coli'' later on.
- We recieved a filter paper soaked with a plasmid from Kausik Li containing an ''Aplysia'' prion fused with the GR domain. Then we put the paper containing the plasmid in water in order to transform and clone it in ''E. coli'' later on.
Line 229: Line 202:
- Then we carried out a digestion and the following electrophoresis to verify whether we had the constructions in the plasmids and to evaluate their concentration.
- Then we carried out a digestion and the following electrophoresis to verify whether we had the constructions in the plasmids and to evaluate their concentration.
-
 
+
[[Image:electropho_13-7.jpg|center|thumb|200px|Electrophoresis of the purified pM2 plasmid.]]
- We performed a  transformation of plasmid DNA containing a prionic gene into E.coli following a heat shock protocol.
- We performed a  transformation of plasmid DNA containing a prionic gene into E.coli following a heat shock protocol.
=July 14th=
=July 14th=
-
- We prepared some minimum culture medium for our future yeast cultures. We also elaborated five amino acid solutions our competent yeast strains are metabolic mutants for. We will use them in order to differentiate between plasmid transformed and non transformed yeast colonies (Only those yeast cells carrying the plasmid with the metabolic genes that our auxotrophic mutants lack will grow).
+
- We prepared 600ml of yeast minimum culture medium (SD) for our future yeast cultures.<br />
 +
SD Composition: <br />
 +
{|
 +
|YNB w/o a.a.
 +
|.............
 +
|6.7 g (1.7 + 5(NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub> )
 +
|-
 +
|Glucosa
 +
|.............
 +
|20 g
 +
|-
 +
|Agar
 +
|.............
 +
|20 g
 +
|-
 +
|H<sub>2</sub>O
 +
|.............
 +
|c.s.p. 1 L
 +
|}
 +
:
 +
- We also elaborated five amino acid and nitrogen bases solutions (Leu, His, Trp, Adenine, Uracil) for which our competent yeast strains are metabolic mutants.<br />
 +
Solutions Composition: <br />
 +
{|
 +
|a.a. / b.n.
 +
|.............
 +
|100 mg
 +
|-
 +
|H<sub>2</sub>O d.d.
 +
|.............
 +
|50 ml
 +
|}
 +
:
 +
We will use them in order to differentiate between plasmid transformed and non transformed yeast colonies (Only those yeast cells carrying the plasmid with the metabolic genes that our auxotrophic mutants lack will grow).
 +
 
 +
- No bacterial growth was observed on the dishes we planted yesterday. Therefore we re-cultured the two plasmid transformed ''E.coli'' strains (with the ''Aplysia'' and yeast prion genes) we worked on July 12th with.
 +
 
 +
- We started a culture of SC 5523 and SC 2606 yeasts strains (PSI+ and PSI-) in 5 ml of YPD. Overnight incubation at 30ºC in Emilia's Lab.
 +
 
 +
=July 15th=
 +
 
 +
- We prepared 0.5 L of YPD for stock. Four matraces of 250 ml with 50 ml each and one bottle of 0.5 L with 300 ml.
 +
 
 +
YPD Concentration
 +
{|
 +
|Yeast extract
 +
|.............
 +
|10 g
 +
|-
 +
|Peptone
 +
|.............
 +
|20 g
 +
|-
 +
|Dextrosa (D-glucosa)
 +
|.............
 +
|20 g
 +
|-
 +
|Agar
 +
|.............
 +
|10 g
 +
|-
 +
|H<sub>2</sub>O
 +
|.............
 +
|c.s.p. 1 L
 +
|}
 +
 
 +
 
 +
 
 +
- One colony was observed in the pG1-APC dish and non in the pG1-NMG1 one. We re-planted the colony (single strip) and left it in the 37ºC stove.
 +
 
 +
- The LiAc transformation protocol for Yeasts was started
-
- Finally, we re-cultured the two plasmid transformed ''E.coli'' strains (with the ''Aplysia'' and yeast prion genes) we worked the day before yesterday with.
+
The yeast strains are going to be transformed with the pL2/GZ plasmid (GRE domain and LacZ reporter).
 +
We planted tha yeasts in dishes with SD medium + Adenine, His. Also 200 µl of Try and Uracil were added in each one of the dishes, because the selection marker of the plasmid is the Leu synthesis gene.
 +
LiAc Protocol
 +
#Plant a colony in a petri dish with 5ml of YPD medium. Then overnight incubate at 30ºC. 
 +
#Inoculate at 0.4 OD a flask with 20 ml of YPD at ambient temperature. Inbubate at 30ºC with agitation until 1.6 OD.
 +
#Pick up the cells in a 50 ml corning. Spin at 3500 rpm 3'.
 +
#Discard the supernadant, and re-suspended the cell pack in a 10 ml of sterile water. Spin.
 +
#Discard the water content. Re-suspended in 0.4 ml of LiAc 100mM and pass to a Eppendorf. Spin at 13000 rpm 15s.
 +
#Discard LiAc. Re-suspend in 160 µl of LiAc 100mM in the vortex (Total aprox. volume 500 µl).
 +
#Separate in 75 µl aliquots (each one can be used for one transformation). Spin at 13000 rpm 15s and discard LiAc.
 +
#Add (important to follow the order)
 +
#* 240 µl PEG 50% (p/v).
 +
#* 36 µl LiAc 1 M.
 +
#* 50 µl DMA carrier (2 mg/ml).
 +
#*  3 µl of plasmidic DNA (with a previous bath of 5' at 100ºC, and 5' on ice).
 +
#* 31 µl sterile water.
 +
#Agigate in the vortex 1', until total re-suspension.
 +
#Incubate at 30ºC, 30' without agitation. Then add 33µl '''something magic'''.
 +
#Heat shock in 42ºC water bath for 20'.
 +
#Spin at 8000 rpm for 1'. Discard supernadant.
 +
#Re-suspend in 200µl of YPD and grow directly in dishes.
<html>
<html>

Latest revision as of 08:27, 19 July 2010

Time goes by... (El tiempo pasa...)

Follow us:
Valencia iGEM Team Facebook Valencia iGEM Team Twitter

Our main sponsors:


Our institutions:


Visitor location:

April
Mo Tu We Th Fr Sa Su
29 30 31 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  1  2
May
Mo Tu We Th Fr Sa Su
26 27 28  29 30  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 1 2 3 4 5 6
June
Mo Tu We Th Fr Sa Su
31  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  1 2 3 4
July
Mo Tu We Th Fr Sa Su
28 29 30   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  1
August
Mo Tu We Th Fr Sa Su
26 27 28  29 30 31  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  1  2  3  4  5
September
Mo Tu We Th Fr Sa Su
30 31  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  1  2  3
October
Mo Tu We Th Fr Sa Su
27 28 29 30  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
November
Mo Tu We Th Fr Sa Su
 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  1   2  3  4  5


Contents

July 12th

- We made a miniprep to purify the plasmids pG1 and pLZ.

Dani reading the protocol and Gabi moral support for the first miniprep!!

But before you start any procedure, you have to read the protocol!!!!

- Then we carried out a digestion and the following electrophoresis to verify whether we had the constructions in the plasmids and to evaluate their concentration.

Gabi and the high-tech device for run the gel!!

Gabi, Jose, Juan Angel and Dani's red hair doing the miniprep, almost done!!

First good result!! Here a picture of the electrophoresis. From left to right: Marker, pLZ and pG1.

We have the constructions and in a good concentration!

- We stored the non-digested plasmids in the refrigerator (we want to use it later on)

- We made (Jose made) a liquid culture of E. coli with the LEA gene, and puted it into the stove at 37ºC. Ale saying Jose what to do :D!!

Ale saying Jose what to do :D!

and Jose putting the liquid medium in the tube

- We recieved a filter paper soaked with a plasmid from Kausik Li containing an Aplysia prion fused with the GR domain. Then we put the paper containing the plasmid in water in order to transform and clone it in E. coli later on.

July 13th

- We carried out a miniprep to purify the pM2 plasmid containing the LEA gene.

- Then we carried out a digestion and the following electrophoresis to verify whether we had the constructions in the plasmids and to evaluate their concentration.

Electrophoresis of the purified pM2 plasmid.

- We performed a transformation of plasmid DNA containing a prionic gene into E.coli following a heat shock protocol.

July 14th

- We prepared 600ml of yeast minimum culture medium (SD) for our future yeast cultures.
SD Composition:

YNB w/o a.a. ............. 6.7 g (1.7 + 5(NH4)2SO4 )
Glucosa ............. 20 g
Agar ............. 20 g
H2O ............. c.s.p. 1 L

- We also elaborated five amino acid and nitrogen bases solutions (Leu, His, Trp, Adenine, Uracil) for which our competent yeast strains are metabolic mutants.
Solutions Composition:

a.a. / b.n. ............. 100 mg
H2O d.d. ............. 50 ml

We will use them in order to differentiate between plasmid transformed and non transformed yeast colonies (Only those yeast cells carrying the plasmid with the metabolic genes that our auxotrophic mutants lack will grow).

- No bacterial growth was observed on the dishes we planted yesterday. Therefore we re-cultured the two plasmid transformed E.coli strains (with the Aplysia and yeast prion genes) we worked on July 12th with.

- We started a culture of SC 5523 and SC 2606 yeasts strains (PSI+ and PSI-) in 5 ml of YPD. Overnight incubation at 30ºC in Emilia's Lab.

July 15th

- We prepared 0.5 L of YPD for stock. Four matraces of 250 ml with 50 ml each and one bottle of 0.5 L with 300 ml.

YPD Concentration

Yeast extract ............. 10 g
Peptone ............. 20 g
Dextrosa (D-glucosa) ............. 20 g
Agar ............. 10 g
H2O ............. c.s.p. 1 L


- One colony was observed in the pG1-APC dish and non in the pG1-NMG1 one. We re-planted the colony (single strip) and left it in the 37ºC stove.

- The LiAc transformation protocol for Yeasts was started

The yeast strains are going to be transformed with the pL2/GZ plasmid (GRE domain and LacZ reporter). We planted tha yeasts in dishes with SD medium + Adenine, His. Also 200 µl of Try and Uracil were added in each one of the dishes, because the selection marker of the plasmid is the Leu synthesis gene.

LiAc Protocol

  1. Plant a colony in a petri dish with 5ml of YPD medium. Then overnight incubate at 30ºC.
  2. Inoculate at 0.4 OD a flask with 20 ml of YPD at ambient temperature. Inbubate at 30ºC with agitation until 1.6 OD.
  3. Pick up the cells in a 50 ml corning. Spin at 3500 rpm 3'.
  4. Discard the supernadant, and re-suspended the cell pack in a 10 ml of sterile water. Spin.
  5. Discard the water content. Re-suspended in 0.4 ml of LiAc 100mM and pass to a Eppendorf. Spin at 13000 rpm 15s.
  6. Discard LiAc. Re-suspend in 160 µl of LiAc 100mM in the vortex (Total aprox. volume 500 µl).
  7. Separate in 75 µl aliquots (each one can be used for one transformation). Spin at 13000 rpm 15s and discard LiAc.
  8. Add (important to follow the order)
    • 240 µl PEG 50% (p/v).
    • 36 µl LiAc 1 M.
    • 50 µl DMA carrier (2 mg/ml).
    • 3 µl of plasmidic DNA (with a previous bath of 5' at 100ºC, and 5' on ice).
    • 31 µl sterile water.
  9. Agigate in the vortex 1', until total re-suspension.
  10. Incubate at 30ºC, 30' without agitation. Then add 33µl something magic.
  11. Heat shock in 42ºC water bath for 20'.
  12. Spin at 8000 rpm for 1'. Discard supernadant.
  13. Re-suspend in 200µl of YPD and grow directly in dishes.

Retrieved from "http://2010.igem.org/Team:Valencia/Notebook/July"