Team:Groningen/Notebook/7 August 2009

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Latest revision as of 09:39, 11 August 2009

Wet

GVP Cluster

→ DONE isolate plasmids from overnight precultures

→ DONE perform a restriction on isolated plasmid (should result in 6000 and 3000bp fragments)

→ TODO plate on cultures for pure colony over the weekend

→ TODO cut pSB3K3 plasmid and GVP containing plasmid for ligation

→ TODO purify wanted fragments

www.sigmaaldrich.com

Plasmid Purification

Plasmid isolation was performed on the cultures of E.coli TOP10 containing plasmids [http://partsregistry.org/wiki/index.php?title=Part:pSB1AC3 pSB1AC3] with high, medium and low constitutive promoters and [http://partsregistry.org/wiki/index.php?title=Part:BBa_I750016 GVP] with the "Sygma-Aldrich™ [http://www.sigmaaldrich.com/life-science/molecular-biology/dna-and-rna-purification/plasmid-miniprep-kit.html GenElute™] Plasmid Miniprep Kit".

• From each tube 4mL of culture was collected in a 2.0mL cup, and the cells were pelleted by centrifugation for 1 min. at max. speed and the supernatant discarded.
• Plasmids were eluted with 20μL MQ and stored in the fridge

Concentration of Plasmids

GVP+Metal dependent promotors
Plasmids suspected to be positive for the metal dependent promotors in front of the GVP cluster were restricted for 1 h @ 37 °C using [http://fermentas.com/catalog/re/fastnoti.htm NotI]. No enzyme was present anymore to do restriction of sample 4 1x (Paul code).
Samples were put on 1% (TBE) agarose gel with a 1 kB DNA marker. Postive signals should be seen a ~6000 & ~2000, negative (first lane after marker) at ~7000 & ~2500.

Transporters

GlpF

The GlpF PCRs done yesterday (PCR 1 and2) were run on gel (lanes 2,3). Also the restriction done yesterday in order to check the ligations are shown on the gel below. The restriction was performed with HaeII for details see the notebook of 06-08-09.

a band of 105 was expected for GlpF PCR1 which could not be seen on the above 1% agarose gel. Therefor 1uL of PCR1 (with 4 uL MQ and 1 uL 6x orange loading dye) was loaded to a 2% gel as shown below (arrow), since the amount of loaded DNA is low the band is not very dark.

Metal Accumulation

• 2nd PCR to amplify SmtA and GST-SmtA
  • Use pGEX-3X-GST-SmtA to amplify SmtA-GST and SmtA
  • Use pET29a-SmtA to amplify SmtA
  • Program: MT NIENKE (Left PCR machine)
    • Globally: 10cycles touchdown from 65-50°C, 25 cycles with Tm gradient from 60-50°C (4steps), elongation time of 1:20.
  • Mix

MM NH4 21uL

Primer fw [10mM] 1uL

Primer rev [10mM] 1uL

Vector 1uL

HomeTaq pol 1uL

• • Run program o/n
  • Check on gel
    • No bands seen on gel, except for SmtA-GST nr 4 (highest Tm) which gave a band around 900bp... Which is too small for SmtA-GST...

--> The tubes where unfortunately not put in the correct position, so the Tm at the gradient step was ~45-55°C....

• Transform E. coli with pGB68 (mymT)
  • Use pGB68 from filter resuspended in 40uL MQ.
  • As neg control use pSB1AC3 (incl ccdB), as pos control use pSB1AC3-low promoter.
  • Mix 2-4uL of vector with 50uL chemically competent cells (prepared 31 aug)
  • Transform using heat-shock @ 37°C

Vectors

Dry

We (Jasper and Annelies) looked at using figure 1 from Singh2008. So far it looks like it shows problems similar to those we encountered with figure 3A from Kostal2004. Specifically, if we plug in the constants for GlpF we determined earlier it looks like either the export rate or the concentration at which it reaches half its maximum rate should be negative... We weren't able to get Mathematica to use Minimize on our cost function, so we couldn't try fitting all four parameters at once, we should try this with figure 3A from Kostal2004 as soon as Klaas Bernd is back.