Coding

Part:BBa_K2365034

Designed by: yuanqi jia   Group: iGEM17_NAU-CHINA   (2017-10-14)
Revision as of 15:59, 31 October 2017 by 1314 (Talk | contribs)


ZHD101--Zearalenone degrading enzyme

In our developed assay, the gene encoding ZHD101(a ZEN-degrading enzyme)was cloned. ZHD101, a lactonohydrolase produced by the fungal species Clonostachys rosea, converts ZEN into 1-(3,5-dihydroxy-phenyl)-10-hydroxy-1-undecen- 6-one, which is a markedly less toxic product. In previous studies, ZHD101 has been shown to be successfully expressed by Escherichia coli, Saccharomyces cerevisiae, and rice plants, and the recombinant ZHD101 produced by these genetically modifed organisms efectively degraded ZEN .


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 772


PCR Result

ZHD101 DNA.jpg


ZHD101 uv.png

This is our Uv mapping result,for this result we set four time point ,Z2 as our time point 1 which are taken after 2 hours’culturation ,shown in pink colour line on the figure and Z4 as time point 2 which are taken after 4 hours’culturation,shown in dark blue line while Z6 as our time point 3 which are taken after 6 hours’culturation shown in pretty blue line. the bottom of the figure is the point 4 which are taken after 8 hours’culturation. We added zearalenone by 1ug/ml and the degrading enzyme start to work.the ZEN is degraded as time goes by.The obvious degrading effect is proved by the height of Uv mapping

Fig3 shows that we use the MSD to analyze the degrading effects of our ZEN degrading enzyme


Uv.png

We use the High Performance Liquid Chromatography(HPLC) to analyze the ability of acetylation of ZHD101

[edit]
Categories
Parameters
None