Difference between revisions of "Part:BBa K2587009"
Line 5: Line 5:
 
ptxD is coding for the phosphonate dehydrogenase, that catalyses the oxidation of phosphite (phosphonate) using NAD+ and H20 to Phosphate and NADH. pH optimum is pH = 7.25-7.75.
 
ptxD is coding for the phosphonate dehydrogenase, that catalyses the oxidation of phosphite (phosphonate) using NAD+ and H20 to Phosphate and NADH. pH optimum is pH = 7.25-7.75.
  
−
<!-- Add more about the biology of this part here
+
<h4><strong>Usage and Biology</strong></h4>
−
===Usage and Biology===
+
 
<p>Most of the microorganisms, espacially common used modelorgansims like <i>Escherichia coli</i> or <i>Saccharomyces cerevisiae</i> grow only very slow on phosphite as phosphorus source. As a result the ptxD gene together with a phosphite media could be used as a selection marker. Without a permanent usage of antibiotics a screening and a decrease of the contamination risk could be achieved. </p>
 
<p>Most of the microorganisms, espacially common used modelorgansims like <i>Escherichia coli</i> or <i>Saccharomyces cerevisiae</i> grow only very slow on phosphite as phosphorus source. As a result the ptxD gene together with a phosphite media could be used as a selection marker. Without a permanent usage of antibiotics a screening and a decrease of the contamination risk could be achieved. </p>
  

Revision as of 09:27, 2 October 2018


ptxD_opt

ptxD is coding for the phosphonate dehydrogenase, that catalyses the oxidation of phosphite (phosphonate) using NAD+ and H20 to Phosphate and NADH. pH optimum is pH = 7.25-7.75.

Usage and Biology

Most of the microorganisms, espacially common used modelorgansims like Escherichia coli or Saccharomyces cerevisiae grow only very slow on phosphite as phosphorus source. As a result the ptxD gene together with a phosphite media could be used as a selection marker. Without a permanent usage of antibiotics a screening and a decrease of the contamination risk could be achieved.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 93
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 6
    Illegal BamHI site found at 1044
    Illegal XhoI site found at 216
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 714
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 22
    Illegal BsaI.rc site found at 1051