Team:Edinburgh/Bacterial/Blue light producer
From 2010.igem.org
(31 intermediate revisions not shown) | |||
Line 48: | Line 48: | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/BioBricks#Genomic">submitted parts</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/BioBricks#Genomic">submitted parts</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Results#Genomic">results</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Results#Genomic">results</a></li> | ||
- | <li><a href="https://2010.igem.org/Team:Edinburgh/Project/Future">future | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Project/Future">the future</a></li> |
<li><a href="https://2010.igem.org/Team:Edinburgh/Project/References">references</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Project/References">references</a></li> | ||
</ul> | </ul> | ||
Line 55: | Line 55: | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial" class="dir">bacterial BRIDGEs</a> | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial" class="dir">bacterial BRIDGEs</a> | ||
<ul> | <ul> | ||
- | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Core_repressilator">the | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Core_repressilator">the project</a></li> |
<li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Red_light_producer">red light</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Red_light_producer">red light</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Red_light_sensor">red sensor</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Red_light_sensor">red sensor</a></li> | ||
Line 64: | Line 64: | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/BioBricks#Bacterial">submitted parts</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/BioBricks#Bacterial">submitted parts</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Results#Bacterial">results</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Results#Bacterial">results</a></li> | ||
- | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Future">future | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Future">the future</a></li> |
<li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/References">references</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/References">references</a></li> | ||
</ul> | </ul> | ||
Line 75: | Line 75: | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Bacterial">the bacterial model</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Bacterial">the bacterial model</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Signalling">the signalling model</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Signalling">the signalling model</a></li> | ||
+ | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Tools">tools</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Results#Modelling">results</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Results#Modelling">results</a></li> | ||
- | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Future">future | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Future">the future</a></li> |
<li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/References">references</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/References">references</a></li> | ||
</ul> | </ul> | ||
Line 83: | Line 84: | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Human" class="dir">human BRIDGEs</a> | <li><a href="https://2010.igem.org/Team:Edinburgh/Human" class="dir">human BRIDGEs</a> | ||
<ul> | <ul> | ||
- | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/ | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/Communication">communication of science</a></li> |
+ | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/Branding">iGEM survey</a></li> | ||
+ | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/Conversations">conversations</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Human/Epic">the epic</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/Epic">the epic</a></li> | ||
- | <li><a href="https://2010.igem.org/Team:Edinburgh/ | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/FutureApps">future applications</a></li> |
- | <li><a href="https://2010.igem.org/Team:Edinburgh/Human | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Results#Human">further thoughts</a></li> |
<li><a href="https://2010.igem.org/Team:Edinburgh/Human/References">references</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/References">references</a></li> | ||
</ul> | </ul> | ||
Line 93: | Line 96: | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Notebook" class="dir">lab notes </a> | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook" class="dir">lab notes </a> | ||
<ul> | <ul> | ||
- | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook">collaboration</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Collaboration">collaboration</a></li> |
+ | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Attribution">attribution</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/BRIDGE">BRIDGE</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/BRIDGE">BRIDGE</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Red_light_producer">red light</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Red_light_producer">red light</a></li> | ||
Line 99: | Line 103: | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Blue_light_producer">blue light</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Blue_light_producer">blue light</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Blue_light_sensor">blue sensor</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Blue_light_sensor">blue sensor</a></li> | ||
+ | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Green_light_producer">green light</a></li> | ||
+ | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Green_light_sensor">green sensor</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Modelling">modelling</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Modelling">modelling</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Safety">safety</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Safety">safety</a></li> | ||
Line 123: | Line 129: | ||
<br> | <br> | ||
- | <p> | + | <p>To produce blue light, we used two systems using the bacterial luciferase from <i>Xenorhabdus luminescens</i> (LuxAB). The standalone LuxAB has an emission peak of 495nm (<a href="https://static.igem.org/mediawiki/2010/0/09/Ed10-LuxABSpectra.gif">Figure 1</a>). According to <a href="#References">O'Kane and Lee (1985)</a> and others, the addition of lumazine protein LumP shifts the wavelength towards the blue spectrum (478 nm), such that it will be in the correct region to <b>activate</b> the <a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Blue_light_sensor">blue light sensor</a>. </p> |
+ | <center><br><br><p><img src="https://static.igem.org/mediawiki/2010/0/09/Ed10-LuxABSpectra.gif" border="0"/></p><br> | ||
+ | <p><b>Figure 1:</b> Emission spectra of LuxAB (in solid black line). The LuxAB depicted is that from <i>Vibrio campbellii</i>, but sources confirm that other bacterial luciferases produce similar spectral graphs.</p> | ||
+ | <p>Image: <a href="#References">Suadee et al. (2008)</a></p><br><br></center> | ||
+ | |||
+ | <a name="Strategy" id="Strategy"></a><h2>Strategy</h2> | ||
+ | <br> | ||
+ | <p><a href="https://2009.igem.org/Team:Edinburgh">Last year's Edinburgh team</a> already made both of these parts individually, so all we had to do was <b>fuse</b> them together and add a promoter. Individual parts were resubmitted in pSB1C3.</p> | ||
<br> | <br> | ||
<br> | <br> | ||
Line 130: | Line 143: | ||
<a name="Problems" id="Problems"></a><h2>Problems</h2> | <a name="Problems" id="Problems"></a><h2>Problems</h2> | ||
<br> | <br> | ||
- | |||
- | |||
- | |||
- | |||
- | <p></p> | + | <p>We were <b>experiencing</b> problems with last year’s <a href="http://partsregistry.org/Part:BBa_K216008">LuxAB</a> and <a href="http://partsregistry.org/Part:BBa_K216007">LumP</a> parts, in that blue and red colonies were growing when they should not be. This was another reason for <b>resubmitting</b> them, as the parts contained in the Registry may have the same problems.</p> |
+ | <p>We have also had issues with the instrument used to <b>measure</b> the spectral output. It could not pick up a signal from the tubes despite visible bioluminescence. Hopefully we will be able to characterise these parts more fully before the Jamboree.</p> | ||
<br> | <br> | ||
<br> | <br> | ||
- | <a name="BioBricks" id="BioBricks"></a><h2> | + | <a name="BioBricks" id="BioBricks"></a><h2>BioBricks</h2> |
<br> | <br> | ||
- | |||
- | |||
- | <p></p> | + | <p>Both <i>lumP</i> and <i>luxAB</i> have already been submitted as BioBricks in pSB1A3 by <a href="https://2009.igem.org/Team:Edinburgh">last year's Edinburgh team</a>, but we are re-submitting <b>corrected</b> variants in pSB1C3.</p> |
+ | <p>We are also submitting a luxAB-lumP fusion construct in pSB1C3 with a constitutive promoter which can be used for blue light production. We have confirmation of working luxAB with the promoter in question.</p><br> | ||
+ | |||
+ | <p><a href="http://partsregistry.org/Part:BBa_K322139">BBa_K322139</a>: bacterial luciferase <i>luxAB</i>, updated version of <a href="http://partsregistry.org/Part:BBa_K216008">BBa_K216008</a>.</p> | ||
+ | <p><a href="http://partsregistry.org/Part:BBa_K322312">BBa_K322312</a>: <i>luxCDE</i> (required for <i>luxAB</i> expression), updated version of <a href="http://partsregistry.org/Part:BBa_K216017">BBa_K216017</a>.</p> | ||
+ | <p><a href="http://partsregistry.org/Part:BBa_K322007">BBa_K322007</a>: <i>lumP</i> (shifts <i>luxAB</i> to blue), updated version of <a href="http://partsregistry.org/Part:BBa_K216007">BBa_K216007</a>.</p> | ||
+ | <p><a href="http://partsregistry.org/Part:BBa_K322140">BBa_K322140</a>: <i>luxAB</i> under <i>lac</i> promoter.</p> | ||
+ | <p><a href="http://partsregistry.org/Part:BBa_K322141">BBa_K322141</a>: <i>luxAB</i> and <i>luxCDE</i> under <i>lac</i> promoter.</p> | ||
+ | <p><a href="http://partsregistry.org/Part:BBa_K322149">BBa_K322149</a>: <i>luxAB</i> and <i>lumP</i> composite part.</p> | ||
+ | <p><a href="http://partsregistry.org/Part:BBa_K322150">BBa_K322150</a>: <i>luxAB</i> and <i>lumP</i> under <i>lac</i> promoter.</p><br> | ||
+ | <br> | ||
+ | |||
+ | </div> | ||
+ | |||
+ | <div id="body" style="padding: 0px 60px 10px 60px; height: 1356px"> | ||
+ | |||
+ | <br> | ||
+ | <br> | ||
+ | |||
+ | <a name="Characterisation" id="Characterisation"></a><h2>Characterisation</h2> | ||
+ | <br> | ||
+ | |||
+ | <center><br><br><p><img src="https://static.igem.org/mediawiki/2010/a/a4/Ed10-blue01.jpg" border="0" width="600px"/></p><br> | ||
+ | <p><b>Figure 2:</b> Emission output (blue light) of the <i>luxAB/lumP</i> fusion.</p><br><br></center> | ||
+ | |||
+ | <p><a href="https://static.igem.org/mediawiki/2010/a/a4/Ed10-blue01.jpg">Figure 2</a> shows the light output of the <i>luxAB/lumP</i> fusion, a distinctly blue colour. Unfortunately, we have been unable so far to get a spectrum reading from our samples, but hope to be able to achieve one by the Jamboree.</p> | ||
<br> | <br> | ||
Line 153: | Line 186: | ||
<br> | <br> | ||
- | <p></p> | + | <p><b>O'Kane, D. J. & Lee, J. (1985).</b> Chemical characterization of lumazine protein from Photobacterium leiognathi: comparison with lumazine protein from Photobacterium phosphoreum. <i>Biochemistry</i> <b>24</b>, 1467-1475.</p> |
+ | <p><b>Suadee, C., Nijvipakul, S., et al. (2008).</b> LuxG Is a Functioning Flavin Reductase for Bacterial Luminescence. <i>J. Bacteriol.</i> <b>190</b>(5): 1531-1538</p> | ||
+ | <p>Edinburgh 2009 team wiki, <i>https://2009.igem.org/Team:Edinburgh</i>.</p> | ||
<br> | <br> | ||
Line 160: | Line 195: | ||
<center><a href="#top" class="dir"><img width="100" src="https://static.igem.org/mediawiki/2010/9/9f/Ed10-RTT.png"></a></center> | <center><a href="#top" class="dir"><img width="100" src="https://static.igem.org/mediawiki/2010/9/9f/Ed10-RTT.png"></a></center> | ||
+ | </div> | ||
+ | |||
+ | <div id="windowbox" style="border: .2em solid #660000; padding: 5px; position:fixed; top:50%; right:30px; width:8%;"> | ||
+ | <span style="color:ivory;">Throughout this wiki there are words in <b>bold</b> that indicate a relevance to <b>human aspects</b>. It will become obvious that <b>human aspects</b> are a part of almost everything in <b>iGEM</b>.</span> | ||
+ | |||
</div> | </div> | ||
Latest revision as of 02:29, 28 October 2010
Overview: The blue light producer
To produce blue light, we used two systems using the bacterial luciferase from Xenorhabdus luminescens (LuxAB). The standalone LuxAB has an emission peak of 495nm (Figure 1). According to O'Kane and Lee (1985) and others, the addition of lumazine protein LumP shifts the wavelength towards the blue spectrum (478 nm), such that it will be in the correct region to activate the blue light sensor.
Figure 1: Emission spectra of LuxAB (in solid black line). The LuxAB depicted is that from Vibrio campbellii, but sources confirm that other bacterial luciferases produce similar spectral graphs.
Image: Suadee et al. (2008)
Strategy
Last year's Edinburgh team already made both of these parts individually, so all we had to do was fuse them together and add a promoter. Individual parts were resubmitted in pSB1C3.
Problems
We were experiencing problems with last year’s LuxAB and LumP parts, in that blue and red colonies were growing when they should not be. This was another reason for resubmitting them, as the parts contained in the Registry may have the same problems.
We have also had issues with the instrument used to measure the spectral output. It could not pick up a signal from the tubes despite visible bioluminescence. Hopefully we will be able to characterise these parts more fully before the Jamboree.
BioBricks
Both lumP and luxAB have already been submitted as BioBricks in pSB1A3 by last year's Edinburgh team, but we are re-submitting corrected variants in pSB1C3.
We are also submitting a luxAB-lumP fusion construct in pSB1C3 with a constitutive promoter which can be used for blue light production. We have confirmation of working luxAB with the promoter in question.
BBa_K322139: bacterial luciferase luxAB, updated version of BBa_K216008.
BBa_K322312: luxCDE (required for luxAB expression), updated version of BBa_K216017.
BBa_K322007: lumP (shifts luxAB to blue), updated version of BBa_K216007.
BBa_K322140: luxAB under lac promoter.
BBa_K322141: luxAB and luxCDE under lac promoter.
BBa_K322149: luxAB and lumP composite part.
BBa_K322150: luxAB and lumP under lac promoter.
Characterisation
Figure 2: Emission output (blue light) of the luxAB/lumP fusion.
Figure 2 shows the light output of the luxAB/lumP fusion, a distinctly blue colour. Unfortunately, we have been unable so far to get a spectrum reading from our samples, but hope to be able to achieve one by the Jamboree.
References
O'Kane, D. J. & Lee, J. (1985). Chemical characterization of lumazine protein from Photobacterium leiognathi: comparison with lumazine protein from Photobacterium phosphoreum. Biochemistry 24, 1467-1475.
Suadee, C., Nijvipakul, S., et al. (2008). LuxG Is a Functioning Flavin Reductase for Bacterial Luminescence. J. Bacteriol. 190(5): 1531-1538
Edinburgh 2009 team wiki, https://2009.igem.org/Team:Edinburgh.