Team:UNIPV-Pavia/Notebook/Week2Jul

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''Experiment with Tecan F200 (continues the next day)''
 
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* <html><u>Description</u></html>
 
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* <html><u>Purpose:</u></html>
 
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* <html><u>Materials & Methods</u></html>
 
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* <html><u>Protocol</u></html>
 
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* <html><u>Results</u></html>
 
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*We transformed about 40 pg of the overnight ligation and 1 ul of the resuspended F2620 BioBrick. We plated transformed bacteria and incubated the two plates overnight at 37°C.
*We transformed about 40 pg of the overnight ligation and 1 ul of the resuspended F2620 BioBrick. We plated transformed bacteria and incubated the two plates overnight at 37°C.
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''End of experiment with Tecan F200 (last measurement)''
 
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Latest revision as of 23:24, 21 October 2009

EthanolPVanimation.gif

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Week from July 6th, to July 12nd, 2009

Previous Week Next Week

July, 6th

  • We planned to dedicate this week to the assembly of an IPTG/lactose->PoPS device in order to have a lactose sensor for our project, but also a useful inducible system for general purpose applications.


  • We already had R0011 and BOL1 purified plasmids stored at -20°C. Digestion for:
R0011(E-X) BOL1(E-S)
  • Gel run/cut and band purification.
  • The purified DNA gave a good result at Nanodrop, but we decided to perform the entire work on BOL1 again because we were not sure that we had extracted a pure band.
  • We stored R0011(E-X) DNA at -20°C.
  • We infected 5 ml of LB + Amp with 8 ul of BOL1 glycerol stock to grow two identical overnight cultures (37°C, 220 rpm).



Preparation of experiment with Tecan F200

  • We picked a colony of B0030 plate (stored at +4°C) and infected 5 ml of LB + Amp.
  • We also infected 5 ml of LB + Amp with 10 ul of A1 and J23100 glycerol stocks.
  • We incubated the inocula overnight at 37°C, 220 rpm.

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July, 7th

  • Miniprep for BOL1 (X2).
  • Digestion for BOL1(E-S)(X2).
  • Gel run/cut/purification: none of the two BOL1 samples gave a good results in DNA quantification...we decided to cut the miniprepped plasmids again, but this time through an overnight digestion (both plasmids E-S).
  • In case of failure, we also infected 5 ml of LB + Amp with 8 ul of BOL1 glycerol stock to grow an overnight culture at 37°C, 220 rpm.
  • We prepared 0.5 l of LB + Amp.
  • We received sequencing results for:
    • T9002 - long part, but SEQUENCE CONFIRMED! while MIT results were "INCONSISTENT".
    • A10 - results showed a good chromatogram, but K117000 had not been correctly ligated. We will repeat this ligation one of the next weeks.


Preparation of experiment with Tecan F200

  • We diluted 1:100 the overnight cultures of A1, B0030 and J23100.
  • We incubated the diluted cultures for 5 hours (37°C, 220 rpm).



Experiment with Tecan F200



Preparation of tomorrow's experiment with Tecan F200

  • We picked a colony from B0030 native plate (stored ad +4°C) and infected 5 ml of LB + Amp. We incubated the inoculum at 37°C, 220 rpm overnight.


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July, 8th

  • Gel run/cut/band purification for BOL1(E-S) overnight digestion. Results: gel showed that the enzymes had cut very well and this time also the purification gave a good quantification at Nanodrop.
  • We took R0011(E-X) stored ad -20°C and we were ready to ligate;)
  • Ligation:
    • A11: BOL1(E-S) + R0011(E-X) in pSB1A2
  • We incubated the ligation overnight at 16°C.



Preparation of experiment with Tecan F200

  • We diluted 1:100 the overnight culture of B0030.


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July, 9th

  • We resuspended F2620 BioBrick from iGEM 2009 plates.
  • We transformed about 40 pg of the overnight ligation and 1 ul of the resuspended F2620 BioBrick. We plated transformed bacteria and incubated the two plates overnight at 37°C.


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July, 10th

  • A11 and F2620 overnight plates showed colonies!
  • Colony PCR for 6 colonies of A11 plate: the picked colonies were inoculated in 1 ml of LB + Amp and incubated at 37°C, 220 rpm waiting for PCR results.
  • We also picked a colony from F2620 to infect 1 ml of LB + Amp. We incubated this inoculum with the others.

Colony PCR for A11 plate: all the colonies showed the correct plasmid. We kept the 1st, 3rd and 6th colonies.

  • Gel results: all the picked colonies showed the expected amplicon of a correctly ligated plasmid! We decided to prepare a glycerol stock for:
    • A11-1
    • A11-3
    • A11-6
  • Next week, only A11-1 will be used, but the other colonies will be used in case of failure.
  • We also prepared a glycerol stock for F2620 culture.


  • We contacted iGEM HQ to request these BioBricks:
K116001 K116002 K112405
P0412 I746902 I746903
K101017 F2620

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