Difference between revisions of "Team:TU Darmstadt/Notebook/sec1/K1602012"

(Created page with "{{:Team:TU_Darmstadt/Templates/CSS}} <h3>K1602003 - cis-aconitate decarboxylase (cadA)</h3> <html><div class="contentSection"> <figure class="rightFig" style="width:30%">...")
 
 
(10 intermediate revisions by 3 users not shown)
Line 1: Line 1:
 
{{:Team:TU_Darmstadt/Templates/CSS}}
 
{{:Team:TU_Darmstadt/Templates/CSS}}
−
<h3>K1602003 - cis-aconitate decarboxylase (cadA)</h3>
+
<h3>K1602012 - D-Xylonic Acid Dehydratases (yjhG)</h3>
  
  
 
<html><div class="contentSection">
 
<html><div class="contentSection">
 
<figure class="rightFig"  style="width:30%">
 
<figure class="rightFig"  style="width:30%">
−
<img src="https://static.igem.org/mediawiki/2015/8/86/Agar_gel_c3_cadA.png" width=100% height=100%>
+
<img class="transparent" alt="https://static.igem.org/mediawiki/2015/1/12/TU_Darmstadt_PCR_xylB_xylC_yjhG_yagE_yqhD.png" src="https://static.igem.org/mediawiki/2015/1/12/TU_Darmstadt_PCR_xylB_xylC_yjhG_yagE_yqhD.png">
−
<figcaption><br><b>Figure 1</b> PCR of cadA (X). The size of the amplified product was around 1.5 kbp. DNA marker: 2-Log DNA Ladder (NEB).</figcaption>
+
<figcaption><br><b>Figure 1</b> PCR of <i>yjhG</i>. The size of the amplified product was around 2,2 kbp. DNA marker: 2-Log DNA Ladder (NEB).</figcaption>
 
</figure>
 
</figure>
−
The <em>cadA</em>-gene was synthesized by GeneArt and amplified through PCR using the cadA (FW) and cadA (REV) oligonucleotides. The PCR product was verified by agarose gel electrophoresis and subsequently purified. The <em>cadA </em>amplicon was cut with EcoRI and PstI and ligated into a pSB1C3 vector using T4-ligase. The ligation product was transformed into <em>E.coli </em>Top 10 by heat shock transformation and the cells were spread out on a CMP agar plate. Clones were screened with colony PCR using VF2 and VR oligonucleotides. Plasmid DNA was isolated from positive clones which were verified by Sanger sequencing.
+
 
 +
<p align="justify">
 +
The <i>yjhG</i>-gene was isolated from K12 <i>E. coli</i> and amplified by colony PCR using the <i>yjhG</i> (FW) and <i>yjhG</i> (REV) oligonucleotides. The PCR product was verified by agarose gel electrophoresis, digested with <i>Dpn</i>I for 120 minutes and subsequently purified. The <i>yjhG</i> amplicon was cut with <i>EcoR</i>I and <i>Pst</i>I and ligated into a pSB1C3 vector using T4-ligase. <i>E. coli</i> Top 10 has been transformed with the ligation product by heat shock transformation and the cells were spread out on a CMP agar plate. Clones were screened with colony PCR using VF2 and VR oligonucleotides. Plasmid DNA was isolated from positive clones which were verified by sanger sequencing.
 +
</p>
 
</div></html>
 
</div></html>

Latest revision as of 19:41, 18 September 2015

K1602012 - D-Xylonic Acid Dehydratases (yjhG)


https://static.igem.org/mediawiki/2015/1/12/TU_Darmstadt_PCR_xylB_xylC_yjhG_yagE_yqhD.png

Figure 1 PCR of yjhG. The size of the amplified product was around 2,2 kbp. DNA marker: 2-Log DNA Ladder (NEB).

The yjhG-gene was isolated from K12 E. coli and amplified by colony PCR using the yjhG (FW) and yjhG (REV) oligonucleotides. The PCR product was verified by agarose gel electrophoresis, digested with DpnI for 120 minutes and subsequently purified. The yjhG amplicon was cut with EcoRI and PstI and ligated into a pSB1C3 vector using T4-ligase. E. coli Top 10 has been transformed with the ligation product by heat shock transformation and the cells were spread out on a CMP agar plate. Clones were screened with colony PCR using VF2 and VR oligonucleotides. Plasmid DNA was isolated from positive clones which were verified by sanger sequencing.