Difference between revisions of "Part:BBa K395702"

 
Line 6: Line 6:
 
It is necessary to add either beta-carotene or the synthesis operon.this part applies to ② and ④  
 
It is necessary to add either beta-carotene or the synthesis operon.this part applies to ② and ④  
  
[[Image:Tokyotech_registry_zeaxanthin.jpg|center|500px|thumb|Fig.2 zeaxanthin pellet and plate, TLC<br>These works are done by Yumiko Kinoshita]]
+
[[Image:Tokyotech_registry_zeaxanthin.jpg|center|650px|thumb|Fig.2 zeaxanthin pellet and plate, TLC<br>These works are done by Yumiko Kinoshita]]
  
 
These parts contain ''crtZ'' (&beta;-carotene hydroxylase) under inducible promoter control. This enzyme is responsible for the conversion of &beta;-carotene into zeaxanthin. Our team designed some BioBricks to do this conversion. Characterization of these BioBricks has been performed in ''E. coli'' strain MG1655.  (→[http://2010.igem.org/Team:Tokyo_Tech/Project/Apple_Reporter more information])
 
These parts contain ''crtZ'' (&beta;-carotene hydroxylase) under inducible promoter control. This enzyme is responsible for the conversion of &beta;-carotene into zeaxanthin. Our team designed some BioBricks to do this conversion. Characterization of these BioBricks has been performed in ''E. coli'' strain MG1655.  (→[http://2010.igem.org/Team:Tokyo_Tech/Project/Apple_Reporter more information])

Latest revision as of 23:48, 27 October 2010

rbs+crtZ under pBad promoter for double plasmids

This part contains crtZ, which works as the zeaxanthin biosynthesis pathway when add beta-carotene as a substrate.

It is necessary to add either beta-carotene or the synthesis operon.this part applies to ② and ④

Fig.2 zeaxanthin pellet and plate, TLC
These works are done by Yumiko Kinoshita

These parts contain crtZ (β-carotene hydroxylase) under inducible promoter control. This enzyme is responsible for the conversion of β-carotene into zeaxanthin. Our team designed some BioBricks to do this conversion. Characterization of these BioBricks has been performed in E. coli strain MG1655. (→[http://2010.igem.org/Team:Tokyo_Tech/Project/Apple_Reporter more information])


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1205
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1144
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 979
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 961