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                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;QsrR is a protein which can combine with Bap-1,6-quinone.[5]As Laccase,we put the</font></p>
 
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;QsrR is a protein which can combine with Bap-1,6-quinone.[5]As Laccase,we put the</font></p>
 
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;gene fragment in the E.coli.Let it produce itself.</font></p>
 
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;gene fragment in the E.coli.Let it produce itself.</font></p>
                                         <img src="https://static.igem.org/mediawiki/2015/7/7d/2015hsnu-benzo-a-pyrene_3.png" height="300" width="500">
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                                         <img src="https://static.igem.org/mediawiki/2015/7/7d/2015hsnu-benzo-a-pyrene_3.png" height="300" width="550">
 +
                                        <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;We design a gene part make QsrR repress sfRFP’s production.</font></p>
 +
                                        <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;Usually,QsrR is on the Binding Site,and red fluorescent protein will not be produced.</font></p>
 +
                                        <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;When QsrR combine with Bap-1,6-quinone, QsrR will be activated and go away.</font></p>
 +
                                        <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;And the transcription will carry on,then it will produce red fluorescent protein</font></p>
 +
                                        <img src="https://static.igem.org/mediawiki/2015/8/8e/2015hsnu-benzo-a-pyrene_4.png" height="400" width="550">
 
                                 </div>
 
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                                 <div>
 
                                         <h2><font color="#008b8b">&nbsp;&#10017; Reference</font></h2>
 
                                         <h2><font color="#008b8b">&nbsp;&#10017; Reference</font></h2>
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;(註1)Metabolism of mercury, administered as methylmercuric chloride or mercuric chloride, by lactating ruminants.</font></p>
+
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;[1] 黄靖芬,李来好,陈胜军,杨贤庆..烟熏食品中苯并(a)芘的产生机理及防止方法smoked foods  Mechanism of benzo (a) pyrene and prevention methods</font></p>
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;(註2)台北醫學大學公共衛生學系碩士班碩士論文Graduate Institute.</font></p>
+
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;[2] 降低食品中多環芳香族碳氫化合物含量之作業指引(草案) reduce operating guidelines in food polycyclic aromatic hydrocarbon content of the (draft)</font></p>
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;(註3)Brown, N. L., J. V. Stoyanov, et al. (2003). "The MerR family of transcriptional regulators." FEMS Microbiol Rev 27(2-3): 145-163.</font></p>
+
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;[3] Basic Information about Benzo(a)pyrene in Drinking Water</font></p>
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;(註4)Park, S. J., J. Wireman, et al. (1992). "Genetic analysis of the Tn21 mer operator-promoter." J Bacteriol 174(7): 2160-2171.</font></p>
+
                                        <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;[4] Hadibarata T, Kristanti RA. Identification of metabolites from benzo[a]pyrene oxidation by ligninolytic enzymes of Polyporus sp. S133. J Environ Manage. 2012 11/30;111(0):115-9.(2013 IGEM CUHK)</font></p>
 +
                                         <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;[5] Ji Q, Zhang L, Jones MB, Sun F, Deng X, Liang H, et al. Molecular mechanism of quinone signaling mediated through S-quinonization of a YodB family repressor QsrR. Proceedings of the National </font></p>
 +
                                        <p><font face="Comic Sans MS">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Academy of Sciences. 2013 March 26;110(13):5010-5. (2013 IGEM CUHK)</font></p>
 
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Latest revision as of 12:12, 30 August 2015

 Benzo[a]pyrene

 ✡ Introduction

   (1)Why do we detect benzo[a]pyrene?

   Because when food,such as fried food ,which is heated above 300 degrees

   celcius,food will release benzo[a]pyrene recycled oil usually contain

   benzo[a]pyrene[1].

   (2)Harm?

   Pathway:from skin,breathing in,eating Carcinogenic,environmental

   pollution, Skin irritation,eye irritation[1].

   (3)Taiwanese regulation

[2]

   (4)National regulation

   Europe:The same to Taiwanese regulation[2]

   American:The MCL has been set at 0.2 ppb[3]

 ✡ Circuit Design

   So far,we don’t find the protein which can combine with the Benzo[a]pyrene,so first

   we must degradate it by Laccase. And its product is Bap-1,6-quinone which can

   combine with the protein,in order that we can detect Benzo[a]pyrene. [4]

   We put the gene fragment which can produce the Laccase in the E.coli

   Let it produce itself.

   QsrR is a protein which can combine with Bap-1,6-quinone.[5]As Laccase,we put the

   gene fragment in the E.coli.Let it produce itself.

   We design a gene part make QsrR repress sfRFP’s production.

   Usually,QsrR is on the Binding Site,and red fluorescent protein will not be produced.

   When QsrR combine with Bap-1,6-quinone, QsrR will be activated and go away.

   And the transcription will carry on,then it will produce red fluorescent protein

 ✡ Result

 ✡ Reference

   [1] 黄靖芬,李来好,陈胜军,杨贤庆..烟熏食品中苯并(a)芘的产生机理及防止方法smoked foods Mechanism of benzo (a) pyrene and prevention methods

   [2] 降低食品中多環芳香族碳氫化合物含量之作業指引(草案) reduce operating guidelines in food polycyclic aromatic hydrocarbon content of the (draft)

   [3] Basic Information about Benzo(a)pyrene in Drinking Water

   [4] Hadibarata T, Kristanti RA. Identification of metabolites from benzo[a]pyrene oxidation by ligninolytic enzymes of Polyporus sp. S133. J Environ Manage. 2012 11/30;111(0):115-9.(2013 IGEM CUHK)

   [5] Ji Q, Zhang L, Jones MB, Sun F, Deng X, Liang H, et al. Molecular mechanism of quinone signaling mediated through S-quinonization of a YodB family repressor QsrR. Proceedings of the National

         Academy of Sciences. 2013 March 26;110(13):5010-5. (2013 IGEM CUHK)