Team:DTU-Denmark/Notebook/14 August 2013

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(Conclusion)
(PCR for Nir2 extraction from PAO1)
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program: touchdown PCR (called U2 on Eppendorf)
program: touchdown PCR (called U2 on Eppendorf)
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The table shows the composition of each reaction:
The table shows the composition of each reaction:

Revision as of 18:24, 14 August 2013

14 August 2013

Contents

lab 208


Main purpose


  • PCR for extraction of Nir2 from PAO1
  • extract fragments for SPL and perform USER ligation

Who was in the lab


Gosia, Kristian, Julia, Henrike

Procedure


PCR for Nir2 extraction from PAO1

We tried to reproduce the successful extraction of Nir2 from PAO1. The extracted Nir2 fragment will be used as template for a screening PCR with USER primers.


primers: 42a and 42b

template: 1 colony of P. aeruginosa cells resuspended in 100 uL milliQ water

program: touchdown PCR (called U2 on Eppendorf)


The table shows the composition of each reaction:

component (per reaction) without additives 5% DMSO 2mM MgCl2 5% DMSO + 2mM MgCl2 Negative control
dNTPs 1uL 1uL 1uL 1uL 1uL
GC buffer 10uL 10uL 10uL 10uL 10uL
Phusion polymerase 0.5uL 0.5uL 0.5uL 0.5uL 0.5uL
MilliQ water 31.5uL 29uL 29.5uL 27uL 32.5uL
template 1uL 1uL 1uL 1uL -
FW primer 3uL 3uL 3uL 3uL 3uL
RV primer 3uL 3uL 3uL 3uL 3uL
DMSO - 2.5uL - 2.5uL -
MgCl2 - - 2uL 2uL -

PCR for Nir2 with USER endings

We are still trying to amplify Nir2 with endings that are suitable for USER cloning with Nir1. The same reaction mix as yesterday was run on two new programs.

Sample 1-6: 63C annealing temperature

Sample 7-12: ramp from 65C-57C

If this PCR is not successful we suggest to try touchdown.

Gel purification

gel purify PCR products from constitutive promoter SPL and constitutive promoter ref

Results


Purification gel

  • 1 kb ladder
  • constitutive promoter SPL
  • constitutive promoter SPL
  • constitutive promoter reference
  • constitutive promoter reference
  • araBAD promoter reference
  • araBAD promoter reference
  • 1 kb ladder

2013-08-14 const spl ref ara-ref.jpg


Gel on todays PCR

  • 1kb ladder
  • Nir2 extraction PCR without additives
  • Nir2 extraction PCR without additives
  • Nir2 extraction PCR with 5% DMSO
  • Nir2 extraction PCR with 5% DMSO
  • Nir2 extraction PCR with MgCl
  • Nir2 extraction PCR with MgCl
  • Nir2 extraction PCR with 5% DMSO and MgCl2
  • Nir2 extraction PCR with 5% DMSO and MgCl2
  • negative from Nir2 extraction PCR
  • sample 1 Nir2 User PCR
  • sample 2 Nir2 User PCR
  • sample 3 Nir2 User PCR
  • sample 4 Nir2 User PCR
  • sample 5 Nir2 User PCR
  • sample 6 Nir2 User PCR
  • sample 7 Nir2 User PCR
  • sample 8 Nir2 User PCR
  • 1 kb ladder

2013-08-14 nir2extraction nir2user.jpg

Conclusion


We were able to amplify the Nir2 by extracting it from genomic DNA from P. aeruginosa and will purify tomorrow. The PCR of Nir2 with USER endings was not successful and will be repeated with a touchdown program before doing a gradient PCR.

lab 115


Main purpose


  • Distinguish the proper amount of glucose substrate for DM minimal medium in order to grow the E.coli cells

Who was in the lab


Ariadni, Helen, Natalia

Procedure


Calculate different concentrations of DM Minimal medium with NH4Cl and glucose for overnight growing E.coli cells.

First we make one NH4Cl 0.916 M solution

  1. 2.45 gr of NH4Cl
  2. 50 ml of DM minimal medium


The table shows the composition of each tube before we add some cells:

Concentration of glucose (%) Glucose (gr) NH4Cl (uL) DM minimal medium (uL) Total volume (mL)
0.5 0 50 9950 10
1 0.0489 100 9900 10
5 0.4401 500 9500 10
10 0.9291 1000 9000 10

Results

Conclusion



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