Team:UNIPV-Pavia/Notebook/Week2Oct

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m (pH sensor)
(October, 11th)
 
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<div>
<div>
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<html><a name="week_start"></a></html>
= Week from October 5th, to October 11st, 2009 =
= Week from October 5th, to October 11st, 2009 =
<html>
<html>
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<tr>
<tr>
<td align="left" width="50%">
<td align="left" width="50%">
-
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week5Sep">
+
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week5Sep#week_start">
  <img src="https://2009.igem.org/Special:FilePath?file=Left_arrow.png"/>
  <img src="https://2009.igem.org/Special:FilePath?file=Left_arrow.png"/>
</a>
</a>
-
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week5Sep">Previous Week</a>
+
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week5Sep#week_start">Previous Week</a>
</td>
</td>
<td align="right" width="50%">  
<td align="right" width="50%">  
-
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week3Oct">Next Week</a>
+
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week3Oct#week_start">Next Week</a>
-
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week3Oct">
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<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week3Oct#week_start">
  <img src="https://2009.igem.org/Special:FilePath?file=Right_arrow.png"/>
  <img src="https://2009.igem.org/Special:FilePath?file=Right_arrow.png"/>
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== <html><font class="dayw_style">October, 5th</font></html> ==
== <html><font class="dayw_style">October, 5th</font></html> ==
 +
 +
*Miniprep for:
 +
**A19-2
 +
**F2620MIT1
 +
**B5new2-3
 +
**A8pg
 +
 +
*Digestion for:
 +
**A19-2(S-P)
 +
**F2620MIT1(E-S)
 +
**B5new2-3(X-P-ClaI)
 +
**A8pg(E-X)
 +
 +
*Gel run/cut/band purification for all.
 +
 +
*Ligations:
 +
**A20 = F2620(E-S) + A8pg(E-X) in pSB1A2
 +
**A21 = A19-2(S-P) + B5new2-3(X-P-ClaI) in pSB4C5
 +
*We incubated the ligations at 16°C overnight.
 +
 +
 +
*Team Meeting
*Team Meeting
 +
 +
 +
===== pH sensor =====
===== pH sensor =====
*Infection of 4 ml LB + Amp with 8 ul from glycerol stock of:
*Infection of 4 ml LB + Amp with 8 ul from glycerol stock of:
Line 37: Line 63:
== <html><font class="dayw_style">October, 6th</font></html> ==
== <html><font class="dayw_style">October, 6th</font></html> ==
 +
 +
*We transformed 1 ul of the 1:20 dilutions of A20 and A21 ligations. We incubated the plated bacteria at 37°C overnight.
 +
===== pH sensor =====
===== pH sensor =====
''4th experiment''
''4th experiment''
*We put 50 ul into 5 ml LB NaCl 250 mM + Amp pH 6,6 falcon for each of the overnight cultures RBS33 - A2 - pNhaA and incubated them for four five hours  at 37°C, 220 rpm.
*We put 50 ul into 5 ml LB NaCl 250 mM + Amp pH 6,6 falcon for each of the overnight cultures RBS33 - A2 - pNhaA and incubated them for four five hours  at 37°C, 220 rpm.
-
*OD measure of the three falcon with TECAN in order to make dilutions with a final volume of 3 ml and an OD equal to 0,02.
+
*OD measure of the three falcons with TECAN in order to make dilutions with a final volume of 3 ml and an OD equal to 0,02.
*We diluted:
*We diluted:
**RBS into:
**RBS into:
Line 57: Line 86:
*** LB NaCl 250 mM + Amp pH 7,5
*** LB NaCl 250 mM + Amp pH 7,5
*** LB NaCl 250 mM + Amp pH 8,5
*** LB NaCl 250 mM + Amp pH 8,5
-
*We started this 24 hours experiment that performed absorbance and fluorescence measures (on three different wells) for each sample every 5 minutes.
+
*We started this 21 hours' experiment that performed absorbance and fluorescence measures (on three different wells) for each sample every 5 minutes.
<div align="right">
<div align="right">
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== <html><font class="dayw_style">October, 7th</font></html> ==
== <html><font class="dayw_style">October, 7th</font></html> ==
-
===== pH sensor =====
 
-
Qui risultati?
 
 +
*We inoculated 3 colonies of A20 plate (in 5 ml of LB + Amp) and 4 colonies of A21 plate (in 5 ml of LB + Cm). We incubated these inocula at 37°C, 220 rpm overnight.
<div align="right">
<div align="right">
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== <html><font class="dayw_style">October, 8th</font></html> ==
== <html><font class="dayw_style">October, 8th</font></html> ==
 +
 +
*Glycerol stocks, miniprep and digestion screening for A20 (3 samples) and A21 (4 samples): all of them were positive!
 +
 +
*Over-day experiment on beta-gal activity using BioVision Lactose Assay kit: we diluted 1:100 the overnight cultures of B0033, A5 and V1022 in 30 ml of LB + Amp + 4.5% lactose for B0033 and A5 and in 30 ml of LB + 4.5% lactose without antibiotic for V1022. Then we incubated the three cultures (in 50 ml falcon tubes) at 37°C, 220 rpm; every 2 hours we measured the OD600 and the lactose using the commercial kit.
 +
 +
*All the streaked plates were grown and all the unshaken falcon tubes confirmed the phenotypes: B9-2, B9new-1, B9new-2 were cloudy, while B5new2-3 and F2620 were normal. This phenotype was not confirmed on the plates, which looked equal.
 +
===== pH sensor =====
===== pH sensor =====
*Infection of 4 ml LB + Amp with 8 ul from glycerol stock of:
*Infection of 4 ml LB + Amp with 8 ul from glycerol stock of:
Line 86: Line 121:
== <html><font class="dayw_style">October, 9th</font></html> ==
== <html><font class="dayw_style">October, 9th</font></html> ==
 +
 +
*Sequencing results for:
 +
**A19-1 sequence ok!
 +
**A19-2 very noisy (NNNNN)
 +
*We will try to repeat the A21 assembly using A19-1 instead of A19-2 to be sure that the sequence is correct.
 +
 +
*LB + 2% glucose and LB + 10% glucose preparation (0.5 l for each).
 +
 +
*Experiment on B9-2 and F2620TOP10: we inoculated 8 ul of their glycerol stocks in 8 ml of LB + Amp (without glucose) to see if the strange phenotype of B9 happened in this conditions. We incubated the 15 ml falcon tubes at 37°C without shaking (anaerobic).
 +
 +
*We inoculated 8 ul of these glycerol stocks:
 +
**B9-2 (X2) Amp
 +
**B5new2-3 Amp
 +
**F2620TOP10 Amp
 +
**A21 Cm
 +
**A21 + 3OC6HSL 1uM Cm
 +
*in 8 ml of LB + indicated antibiotic + 2% glucose and incubated them at 37°C, 220 rpm for 24 hours.
 +
 +
*We also inoculated 8 ul of these glycerol stocks:
 +
**F2620TOP10 Amp
 +
**B3
 +
**B4
 +
**A19-1 Cm
 +
**A1 Amp
 +
*in 5 ml of LB + suitable antibiotic.
 +
===== pH sensor =====
===== pH sensor =====
''5th experiment'' (with this experiment we try to give E.coli a pH and sodium shock to see if something happens).
''5th experiment'' (with this experiment we try to give E.coli a pH and sodium shock to see if something happens).
-
*We put 50 ul into 5 ml LB NaCl 70 mM + Amp pH 6,6 falcon for each of the overnight cultures RBS33 - A2 - pNhaA and incubated them for four four hours and a half at 37°, 220 rpm.
+
*We put 50 ul into 5 ml LB NaCl 70 mM + Amp pH 6,6 falcon for each of the overnight cultures RBS33 - A2 - pNhaA and incubated them for four four hours and a half at 37°C, 220 rpm.
-
*OD measure of the three falcon with TECAN in order to make dilutions with a final volume of 3 ml and an OD equal to 0,02.
+
*OD measure of the three falcons with TECAN in order to make dilutions with a final volume of 3 ml and an OD equal to 0,02.
*We diluted:
*We diluted:
**RBS into:
**RBS into:
Line 100: Line 161:
*** LB NaCl 600 mM + Amp pH 10
*** LB NaCl 600 mM + Amp pH 10
*** LB NaCl 600 mM + Amp pH 11,2
*** LB NaCl 600 mM + Amp pH 11,2
-
*We started this 6 hours experiment that performed absorbance and fluorescence measures (on three different wells) for each sample every 5 minutes.
+
*We started this 6 hours' experiment that performed absorbance and fluorescence measures (on three different wells) for each sample every 5 minutes.
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== <html><font class="dayw_style">October, 10th</font></html> ==
== <html><font class="dayw_style">October, 10th</font></html> ==
-
===== pH sensor =====
 
-
Qui risultati?
 
 +
*Experiment with Tecan F200 using A1 construct.
 +
 +
*After 24 hours from the inoculum, we inoculated 50 ul of:
 +
**B9-2
 +
**B9-2 bis
 +
**B5new2-3
 +
**F2620TOP10
 +
**A21
 +
**A21 + 3OC6HSL 1uM
 +
*in 30 ml of LB + suitable antibiotic + 10% glucose (anaerobic) in order to begin fermentation. We added 3OC6HSL 1 uM to A21 and 1%w/v of ethanol to B9-2 bis cultures.
 +
 +
*We incubated the fermentations at 37°C, 220 rpm for 24 hours.
 +
 +
*Before incubation, we aliquoted 200 ul of all these cultures (except B9-2 + 1%EtOH) in the microplate reader (samples in triplicate). We incubated them for 24 hours.
 +
 +
 +
*Miniprep for:
 +
**A19-1
 +
**B3
 +
**B4
 +
**B5new2-3
 +
 +
*Digestion:
 +
**A19-1 (S-P)
 +
**B3 (X-P)
 +
**B4 (X-P)
 +
**B5new2-3 (X-P-ClaI)
 +
 +
*Gel run: unfortunately B5new2-3 had some undigested bands near the band of interest, so we decided to repeat this digestion on Monday. Moreover, F2620TOP10 had a bright band with high molecular weight (nicked DNA) and the band of interest looked a bit smeared, maybe digestion failed. We decided to repeat this digestion on Monday as well.
 +
 +
*Gel cut for B3(X-P), B4(X-P) and A19-1(S-P). We stored the cut gel at +4°C.
<div align="right">
<div align="right">
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== <html><font class="dayw_style">October, 11th</font></html> ==
== <html><font class="dayw_style">October, 11th</font></html> ==
 +
*End of fermentation: we measured the pH and then we centrifuged the falcon tubes at 9000 rpm for 10 minutes. We stored the supernatant at +4°C.
 +
 +
 +
''Experiment with Tecan F200''
 +
*<html><a href="http://aimed11.unipv.it/iGEM2009/TestTECANInfiniteF200/PiatraEtanolo_11_09_09.pdf" target="_blank">Download Protocol</a></html>
<div align="right">
<div align="right">
[[#top|Top]]
[[#top|Top]]
</div>
</div>
 +
 +
<html>
<html>
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<tr>
<tr>
<td align="left" width="50%">
<td align="left" width="50%">
-
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week5Sep">
+
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week5Sep#week_start">
  <img src="https://2009.igem.org/Special:FilePath?file=Left_arrow.png"/>
  <img src="https://2009.igem.org/Special:FilePath?file=Left_arrow.png"/>
</a>
</a>
-
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week5Sep">Previous Week</a>
+
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week5Sep#week_start">Previous Week</a>
</td>
</td>
<td align="right" width="50%">  
<td align="right" width="50%">  
-
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week3Oct">Next Week</a>
+
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week3Oct#week_start">Next Week</a>
-
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week3Oct">
+
<a href="https://2009.igem.org/Team:UNIPV-Pavia/Notebook/Week3Oct#week_start">
  <img src="https://2009.igem.org/Special:FilePath?file=Right_arrow.png"/>
  <img src="https://2009.igem.org/Special:FilePath?file=Right_arrow.png"/>
</a>
</a>

Latest revision as of 15:12, 20 October 2009

EthanolPVanimation.gif

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Week from October 5th, to October 11st, 2009

Previous Week Next Week

October, 5th

  • Miniprep for:
    • A19-2
    • F2620MIT1
    • B5new2-3
    • A8pg
  • Digestion for:
    • A19-2(S-P)
    • F2620MIT1(E-S)
    • B5new2-3(X-P-ClaI)
    • A8pg(E-X)
  • Gel run/cut/band purification for all.
  • Ligations:
    • A20 = F2620(E-S) + A8pg(E-X) in pSB1A2
    • A21 = A19-2(S-P) + B5new2-3(X-P-ClaI) in pSB4C5
  • We incubated the ligations at 16°C overnight.


  • Team Meeting


pH sensor
  • Infection of 4 ml LB + Amp with 8 ul from glycerol stock of:
    • RBS33
    • A2
    • pNhaA
  • Overnight incubation of these three cultures at 37°C, 220 rpm.

Top

October, 6th

  • We transformed 1 ul of the 1:20 dilutions of A20 and A21 ligations. We incubated the plated bacteria at 37°C overnight.
pH sensor

4th experiment

  • We put 50 ul into 5 ml LB NaCl 250 mM + Amp pH 6,6 falcon for each of the overnight cultures RBS33 - A2 - pNhaA and incubated them for four five hours at 37°C, 220 rpm.
  • OD measure of the three falcons with TECAN in order to make dilutions with a final volume of 3 ml and an OD equal to 0,02.
  • We diluted:
    • RBS into:
      • LB NaCl 250 mM + Amp pH 5,5
      • LB NaCl 250 mM + Amp pH 6,6
      • LB NaCl 250 mM + Amp pH 7,5
      • LB NaCl 250 mM + Amp pH 8,5
    • pNhaA into:
      • LB NaCl 250 mM + Amp pH 5,5
      • LB NaCl 250 mM + Amp pH 6,6
      • LB NaCl 250 mM + Amp pH 7,5
      • LB NaCl 250 mM + Amp pH 8,5
    • A2 into:
      • LB NaCl 250 mM + Amp pH 5,5
      • LB NaCl 250 mM + Amp pH 6,6
      • LB NaCl 250 mM + Amp pH 7,5
      • LB NaCl 250 mM + Amp pH 8,5
  • We started this 21 hours' experiment that performed absorbance and fluorescence measures (on three different wells) for each sample every 5 minutes.

Top

October, 7th

  • We inoculated 3 colonies of A20 plate (in 5 ml of LB + Amp) and 4 colonies of A21 plate (in 5 ml of LB + Cm). We incubated these inocula at 37°C, 220 rpm overnight.

Top

October, 8th

  • Glycerol stocks, miniprep and digestion screening for A20 (3 samples) and A21 (4 samples): all of them were positive!
  • Over-day experiment on beta-gal activity using BioVision Lactose Assay kit: we diluted 1:100 the overnight cultures of B0033, A5 and V1022 in 30 ml of LB + Amp + 4.5% lactose for B0033 and A5 and in 30 ml of LB + 4.5% lactose without antibiotic for V1022. Then we incubated the three cultures (in 50 ml falcon tubes) at 37°C, 220 rpm; every 2 hours we measured the OD600 and the lactose using the commercial kit.
  • All the streaked plates were grown and all the unshaken falcon tubes confirmed the phenotypes: B9-2, B9new-1, B9new-2 were cloudy, while B5new2-3 and F2620 were normal. This phenotype was not confirmed on the plates, which looked equal.
pH sensor
  • Infection of 4 ml LB + Amp with 8 ul from glycerol stock of:
    • RBS33
    • A2
    • pNhaA
  • Overnight incubation of these three cultures at 37°C, 220 rpm.


Top

October, 9th

  • Sequencing results for:
    • A19-1 sequence ok!
    • A19-2 very noisy (NNNNN)
  • We will try to repeat the A21 assembly using A19-1 instead of A19-2 to be sure that the sequence is correct.
  • LB + 2% glucose and LB + 10% glucose preparation (0.5 l for each).
  • Experiment on B9-2 and F2620TOP10: we inoculated 8 ul of their glycerol stocks in 8 ml of LB + Amp (without glucose) to see if the strange phenotype of B9 happened in this conditions. We incubated the 15 ml falcon tubes at 37°C without shaking (anaerobic).
  • We inoculated 8 ul of these glycerol stocks:
    • B9-2 (X2) Amp
    • B5new2-3 Amp
    • F2620TOP10 Amp
    • A21 Cm
    • A21 + 3OC6HSL 1uM Cm
  • in 8 ml of LB + indicated antibiotic + 2% glucose and incubated them at 37°C, 220 rpm for 24 hours.
  • We also inoculated 8 ul of these glycerol stocks:
    • F2620TOP10 Amp
    • B3
    • B4
    • A19-1 Cm
    • A1 Amp
  • in 5 ml of LB + suitable antibiotic.
pH sensor

5th experiment (with this experiment we try to give E.coli a pH and sodium shock to see if something happens).

  • We put 50 ul into 5 ml LB NaCl 70 mM + Amp pH 6,6 falcon for each of the overnight cultures RBS33 - A2 - pNhaA and incubated them for four four hours and a half at 37°C, 220 rpm.
  • OD measure of the three falcons with TECAN in order to make dilutions with a final volume of 3 ml and an OD equal to 0,02.
  • We diluted:
    • RBS into:
      • LB NaCl 600 mM + Amp pH 10
      • LB NaCl 600 mM + Amp pH 11,2
    • pNhaA into:
      • LB NaCl 600 mM + Amp pH 10
      • LB NaCl 600 mM + Amp pH 11,2
    • A2 into:
      • LB NaCl 600 mM + Amp pH 10
      • LB NaCl 600 mM + Amp pH 11,2
  • We started this 6 hours' experiment that performed absorbance and fluorescence measures (on three different wells) for each sample every 5 minutes.


Top

October, 10th

  • Experiment with Tecan F200 using A1 construct.
  • After 24 hours from the inoculum, we inoculated 50 ul of:
    • B9-2
    • B9-2 bis
    • B5new2-3
    • F2620TOP10
    • A21
    • A21 + 3OC6HSL 1uM
  • in 30 ml of LB + suitable antibiotic + 10% glucose (anaerobic) in order to begin fermentation. We added 3OC6HSL 1 uM to A21 and 1%w/v of ethanol to B9-2 bis cultures.
  • We incubated the fermentations at 37°C, 220 rpm for 24 hours.
  • Before incubation, we aliquoted 200 ul of all these cultures (except B9-2 + 1%EtOH) in the microplate reader (samples in triplicate). We incubated them for 24 hours.


  • Miniprep for:
    • A19-1
    • B3
    • B4
    • B5new2-3
  • Digestion:
    • A19-1 (S-P)
    • B3 (X-P)
    • B4 (X-P)
    • B5new2-3 (X-P-ClaI)
  • Gel run: unfortunately B5new2-3 had some undigested bands near the band of interest, so we decided to repeat this digestion on Monday. Moreover, F2620TOP10 had a bright band with high molecular weight (nicked DNA) and the band of interest looked a bit smeared, maybe digestion failed. We decided to repeat this digestion on Monday as well.
  • Gel cut for B3(X-P), B4(X-P) and A19-1(S-P). We stored the cut gel at +4°C.

Top

October, 11th

  • End of fermentation: we measured the pH and then we centrifuged the falcon tubes at 9000 rpm for 10 minutes. We stored the supernatant at +4°C.


Experiment with Tecan F200

Top



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