Team:Vanderbilt/Notebook

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*Re-did genomic extractions for those that produced less than 50 ng/ul of genomic DNA. Used this new template in further PCRs
*Re-did genomic extractions for those that produced less than 50 ng/ul of genomic DNA. Used this new template in further PCRs
*Extracted the Gal10 gene from our template plasmid and a kanomycin resitance gene bordered by LoxP sites.
*Extracted the Gal10 gene from our template plasmid and a kanomycin resitance gene bordered by LoxP sites.
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<div style="color:black;font-size:13pt">'''June'''</div>
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*All of the gene cassettes for plasmid construction that were successfully extracted so far were ligated together and inserted into the MCS of pUC19. This formed our first intermediate plasmid.
<div style="color:black;font-size:13pt">'''July'''</div>
<div style="color:black;font-size:13pt">'''July'''</div>
* Finally reached the point that all terpene genes were consistently amplifying with the synthase gene primers. The genomic DNA sample for sabinene was completely used before this point, although all other of the 8 terpenes showed clear bands.
* Finally reached the point that all terpene genes were consistently amplifying with the synthase gene primers. The genomic DNA sample for sabinene was completely used before this point, although all other of the 8 terpenes showed clear bands.
<html><img src="https://static.igem.org/mediawiki/parts/b/b8/VU_CadCarHumLnr.jpg" align="left" width="650" >
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<img src="https://static.igem.org/mediawiki/parts/b/bc/VU_LnsMyrSanZin.jpg" align="right" width="650" ></html><br>
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* The results of the genomic DNA PCR indicated each gene had a large fraction of introns. None of the genes had a distinct band at exactly the right weight corresponding with what the intron-less cDNA size would be.  
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* The results of the genomic DNA PCR indicated each gene had a large fraction of introns. None of the genes had a distinct band at exactly the right weight corresponding with what the intron-less cDNA size would be.
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==<b><font size="6">Fall 2014</font></b>==
==<b><font size="6">Fall 2014</font></b>==

Revision as of 23:09, 16 October 2014


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Lab Notebook



Spring 2014

An example of a gel showing high molecular weight (>10 kb) bands corresponding to successfully extracted plant Genomic DNA (in this case, samples LNS1 and LNS2 from Aradopsis DNA)

March 27th
  • Extracted genomic DNA from 100 mg of Arabidopsis thaliana leaves using a Viogene DNA extraction kit. Samples were labeled ZIN for zingiberene.
  • Two samples were prepared and nanodropped. The concentration of the first was 2.6 ng/ul, and the second was 3.5 ng/ul of DNA, indicating a minimal yield of DNA.
March 30th
  • Extracted genomic DNA from 100 mg of Picea abies needles using the same extraction kit and protocol. Samples were labeled CAR for carene.
  • Two samples were prepared and nanodropped. The concentration of the first was 0.9 ng/ul, and the second was 3.5 ng/ul of DNA, indicating a minimal yield of DNA.
March 31th
  • Ran a 0.6 % argarose gel on the DNA extracted from ZIN and CAR, as well as the column flow-through from the kit.
  • ZIN1, ZIN2, CAR1, and CAR2 all show a faint but distinct DNA band above the highest rung on the DNA ladder (>10kb), showing the presence of DNA. No bands were seen on the kit flow-through. Indicates successful genomic extraction.
  • Preformed a second genomic extraction on Picea abies to improve yield. Nanodrop shows CAR3 to be at 6.2 ng/ul and CAR4 to be 11.5 ng/ul.
  • Extracted genomic DNA from Gossypium hirsutum . Samples nanodroppped: CAD1 1.8 ng/ul and CAD2 7.8 ng/ul.
April 1st
  • Ran a gel on CAR3, CAR4, CAD1, and CAD2. Brighter genomic DNA bands were seen on the cadinene camples than before, but cadinene samples showed significant smearing near the top of the gel.
April 2nd
  • Extracted genomic DNA from Salvia officinalis . Samples nanodropped: SAB1 7.5 ng/ul, and SAB 11.4 ng/ul.
  • Extracted genomic DNA from Mentha citrata . Samples nanodropped: LNR1 3.4 ng/ul, LNR2 6.2 ng/ul, LNR3 7.3 ng/ul
  • E. coli containing p404GALS and pDZ207 from Addgene were grown on LB plates with ampicilin. These were miniprepped using a Viogen kit. Samples nanodropped: p404GALS (A) 130.2 ng/ul, p404GALS (B) 112.3 ng/ul, pDZ207 (A) 145.3 ng/ul, pDZ207 (B) 84.1 ng/ul.
April 3rd
  • Extracted genomic DNA again from Arabidopsis thaliana . Sample nanodropped: LNS1 53.4 ng/ul, LNS2 585.2 ng/ul
  • Ran gel on LNR1, LNR2, LNR3, LNS1, LNS2, SAB1, and SAB2. All show high weight DNA bands, with Linalool (S) samples having the brightest.

An example of a gel showing high molecular weight (>10 kb) bands corresponding to successfully extracted plant Genomic DNA (in this case, samples LNS1 and LNS2 from Aradopsis DNA)

April 4th
  • Extracted genomic DNA from Zingiber zermbet . Sample nanodropped: HUM1 31.9 ng/ul and HUM2 18.6 ng/ul
  • Extracted genomic DNA from Ocimum basilicum . Sample nanodropped: GER1 2.3 ng/ul
April 5th
  • Extracted genomic DNA from Santalum album seeds since the sapling was still not fully grown. Sample nanodropped: SAN1 53.8 ng/ul and SAN2 28.4 ng/ul
April 7th
  • Extracted genomic DNA from Perilla frutescens . Sample nanodropped: MYR1 632.8 ng/ul and MYR2 958.6 ng/ul
  • Ran gel on MYR1, MYR2, SAN1, and SAN2. Myrcene samples show bright band at high weight as well as smearing toward bottom. Santelene samples have visible but much fainter genomic DNA band.
April 24th
  • Preformed PCR using zingiberene synthase primers on LNS2 genomic DNA and using linalool (S) synthase primers on the sample template.
  • Ran gel on PCR product. Resulted in no visible bands formed.
April 25th
  • Took 1.8 ul of HUM1 genomic DNA and preformed a PCR with humelene synthase primers.
  • Ran gel on PCR product. Resulted in three total bands, one faint around 1.2 kb, and two bands very close in size just under 3.0 kb.
  • Both ~3 kb bands were gel extracted, combining across all four lanes. Samples nanodropped: HUM-top 8.5 ng/ul, HUM-bottom 10.6 ng/ul.

April 27th
  • Preformed PCR using linalool (R) synthase primers on LNR3 genomic DNA.
  • Ran gel on PCR product. Resulted in no visible bands formed.
April 29th
  • Preformed PCR using myrcene synthase primers on MYR2 genomic DNA.
  • Ran gel on PCR product. Smeared bands on gel but no distinct bands.
  • Preformed overlap-extension PCR on the gel extracted humelene samples (both HUM-top and HUM-bottom) to add epitope tag sequence
  • Ran gel on OE-PCR product. Only extremely faint bands were visible.


Summer 2014

May
  • Continued troubleshooting PCR reaction conditions for all of the terpenes that failed to amplify. Tried adjusting template concentration, adding DMSO, changing thermocycler program, hot start PCR, new polymerase and dNTPs
  • Re-did genomic extractions for those that produced less than 50 ng/ul of genomic DNA. Used this new template in further PCRs
  • Extracted the Gal10 gene from our template plasmid and a kanomycin resitance gene bordered by LoxP sites.
June
  • All of the gene cassettes for plasmid construction that were successfully extracted so far were ligated together and inserted into the MCS of pUC19. This formed our first intermediate plasmid.
July
  • Finally reached the point that all terpene genes were consistently amplifying with the synthase gene primers. The genomic DNA sample for sabinene was completely used before this point, although all other of the 8 terpenes showed clear bands.


  • The results of the genomic DNA PCR indicated each gene had a large fraction of introns. None of the genes had a distinct band at exactly the right weight corresponding with what the intron-less cDNA size would be.

Fall 2014

August 24th
  • Text
October 14th
  • Re-digested saved sample of Santelene gBlock with EcoRI and SpeI. PCR purified and ligated to saved sample of digested pVU14004
  • Transformed competent cells with San+pVU ligation mix. Plated on ampicillin plates.
October 15th
  • One colony grew on the San+pVU plate. Added to liquid culture with ampicillin and incubated at 37 degrees.

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