Team:Cambridge/Lab book/Week 6

From 2012.igem.org

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===Friday===
===Friday===
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'''[[Team:Cambridge/Protocols/PCRProtocol|PCR of split Mg2+ vector]]'''
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[[File:split Mg2+ 1.jpg|right|250px|thumb|results of split magnesium vector PCR. None of the products worked]]
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*PCR of magnesium riboswitch vector repeated with primers to split plasmid (kindly provided by [[Team:Cambridge/Special_thanks|P.J.Steiner]]).
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*Lanes 2 + 3: Fragment A (center - cut site (promotor side))
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*Lanes 4 + 5: Fragment B (without 8 codon substitution) (cut site (lac I side) - center)
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*Lanes 6 + 7: Fragment B (with 8 codon substitution) (cut stie (lac I side) - center)
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*Gels run, found PCR was unsuccessful.
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Revision as of 12:09, 6 August 2012

Week: 3 4 5 6 7

Contents

Monday

PCR of vectors and mOrange


mOrange PCR run at multiple temperatures, every two lanes increacing the temperature of the annealing step by 2 °C. No lanes worked.
Top: Fusion, lux containing vector gel. Lanes 2-4, Vector DNA. Lane 5, +ve control. Lane 6, -ve control. Bottom: Vector gel. Lanes 1-3, Fluorescent contruct vector DNA. Lanes 4-6, Riboswitch construct vector DNA.
  • Not all products were obtained during Friday's PCR. Most of these missing products were large vector backbones. They are being run again, with a much longer extension time of 300s. If that fails, primers will be ordered to split the vectors into manageable chunks, and the PCR reattempted when they arrive.
  • PCR cycle x35:
  • 15s Denaturing at 95 C
  • 45s Annealing at 60 C
  • 300s Extension at 72 C
  • Remaining stray product had a slightly tricky secondary structure at the 3' end. It will be run at a series of annealing temperatures in a PCR machine capable of a temperature gradient.
  • mOrange PCR run at many different temperatures, from 62 °C to 76 °C. Hopefully this should resolve the difficulties we have been having.

Separation of vector and mOrange DNA


  • Positive control produced no band. No primer smear - primers may not be in mix for some reason.
  • Realized correct lux vector template was not added during PCR preparation, consequently no amplification occured. Still appears to be a primer smear.
  • Fluorescent construct produced several bands. Appears to be due to mis-priming during PCR. Either changing the primers or raising the annealing temperature should solve this problem, but may mean that we have to do this PCR separately.
  • Riboswitch vector also failed. However, the extraction from the previous PCR run may have worked. We will try producing a functional plasmid with this extraction before running this PCR again.

Construction of riboswitch plasmid with Gibson Assembly


  • DNA from lanes 27+28, 27+29, 27+30 from gels run on Friday fused together with Gibson assembly to produce riboswitch construct. This does not have replacement of the first 8 codons of lac I with the 8 codons native to the gene downstream of the riboswitch.
  • DNA from lanes 22,23 and 24 fused with riboswitch DNA produced two weeks ago to produce riboswitch construct. This has replacement of the first 8 codons of lac I with the 8 codons native to the gene downstream of the riboswitch.

Transformation of Bacillus with riboswitch construct


  • Plasmids made by Gibson transformed into bacillus cells made two weeks ago and transformants plated out on 5μg/ml chloramphenicol plates.

Tuesday

New biobricks

  • E.coli containing biobricks ordered were plated out on kanomycin plates (50μg/ml).

Transformation of Bacillus with riboswitch construct


  • Plasmids made by Gibson transformed into bacillus cells made two weeks ago and transformants plated out on 5μg/ml chloramphenicol plates.

Transformation of E.coli with riboswitch construct


  • Plasmids made by Gibson transformed into TOP10 e.coli cells and transformants plated out on 100μg/ml ampicillin plates.

Wednesday

Mg2+ Riboswitch


  • Successful colonies produced from transformations two days ago streaked out onto chloramphenicol (5 μg/ml) containing plates.
  • Colonies also grown up in 10ml of medium A for use with plate reader later.

PCR of vector DNA


  • Standard PCR rerun, this time splitting fluorescent vector into two separate sections, one of 3kb and one of 4.5kb.
  • New primers used:
  • Fragment 1 reverse:
  • Fragment 2 forward:

Thursday

Friday

PCR of split Mg2+ vector

results of split magnesium vector PCR. None of the products worked
  • PCR of magnesium riboswitch vector repeated with primers to split plasmid (kindly provided by P.J.Steiner).
  • Lanes 2 + 3: Fragment A (center - cut site (promotor side))
  • Lanes 4 + 5: Fragment B (without 8 codon substitution) (cut site (lac I side) - center)
  • Lanes 6 + 7: Fragment B (with 8 codon substitution) (cut stie (lac I side) - center)
  • Gels run, found PCR was unsuccessful.