Team:Exeter/lab book/1gp/wk6

From 2012.igem.org

Revision as of 11:31, 26 September 2012 by On7h33dg3 (Talk | contribs)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

ExiGEM2012 Lab Book 1GP wk6


Protocols \| Single Gene Plasmids and Enzyme Characterisation \| Showcasing Polysaccharide Production \| The 3-Gene Inducible Plasmid Operon Construction \| Glycobase
9th - 13th July - 16th - 20th July - 23rd - 27th July - 30th July - 3rd August - 6th - 10th August - 13th - 17th August - 20th - 24th August - 27th - 31st August - 3rd - 7th September - 10th - 14th September - 17th - 21st September - 24th - 28th September - Results
	Single Gene Plasmids and Enzyme Characterisation: 13th - 17th August 2012 Monday 13th August (9.00) • PCR amplification of WbbC from E.coli BL21(DE3) using 3-step PCR • Adding cultures with ligated WbnK-terminator and WclY-terminator in liquid medium overnight Tuesday 14th August (9.00) • Mini-Prepping of ligated WbnK-terminator and WclY-terminator • Gel Electrophoresis to check fragment sizes of ligated WbnK-terminator, WclY-terminator and PCR product generated from yesterday's PCR attempt Gel Electrophoresis showed that WbnK-terminator mini-prep 1 had worked, WbnK-terminator mini-prep 2 and all WclY-terminator mini-preps plus the PCR product were not discovered. For the PCR product, it was thought that the annealing temperature was too high. Lane 1 = DNA hyperladder, Lane 2 = WbnK-terminator mini-prep 1 (expected: 2 bands at 1003bp and 2070bp), Lane 3 = WbnK-terminator mini-prep 2 (expected: 2 bands at 1003bp and 2070bp), Lane 4 = WclY-terminator mini-prep 1 (expected: 2 bands at 1156bp and 2070bp), Lane 5 = WclY-terminator mini-prep 2 (expected: 2 bands at 1156bp and 2070bp), Lane 6 = WbbC PCR attempt, Lane 7 = DNA hyperladder. Wednesday 15th August (11.00) • PCR amplification of WbbC from E.coli BL21(DE3) using 3-step PCR • Send off WbnK-terminator for sequencing • Gel Electrophoresis to check fragment sizes of PCR product PCR amplification of WbbC was followed using the same protocol but the annealing temperature was taken down from 65°C to 60°C. Gel Electrophoresis did not show a PCR product and it was thought that the annealing temperature was too high again. Thursday 16th August (13.00) • PCR amplification of WbbC from E.coli BL21(DE3) using 3-step PCR • Adding cultures with ligated WclY-terminator in liquid medium overnight PCR amplification of WbbC was followed using the same protocol but the annealing temperature was taken down from 65°C to 55°C. Gel Electrophoresis did not show a PCR product and it was thought that there was an issue with the BL21 genomic DNA template. Friday 17th August (10.00) • PCR amplification of WbbC and FadR from E.coli BL21(DE3) using 3-step PCR FadR is a transcription factor involved in fatty acid metabolism and was used as a false-positive. Gel Electrophoresis did not show any PCR products and it was thought that there was an issue with the BL21 genomic DNA template. No cultures containing ligated WclY-terminator were found.