Team:Edinburgh/Bacterial/References
From 2010.igem.org
(9 intermediate revisions not shown) | |||
Line 9: | Line 9: | ||
<style type="text/css"> | <style type="text/css"> | ||
#body{ | #body{ | ||
- | background-image:url( | + | background-image:url(https://static.igem.org/mediawiki/2010/a/a8/Ed10-LargePaper.jpg); |
+ | background-repeat:repeat-y; | ||
} | } | ||
</style> | </style> | ||
Line 45: | Line 46: | ||
<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 52: | Line 53: | ||
<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 61: | Line 62: | ||
<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 74: | Line 75: | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Tools">tools</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 81: | Line 82: | ||
<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/Communication">communication of science</a></li> | <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/ | + | <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/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 125: | Line 118: | ||
<br> | <br> | ||
- | <div id="body" style="padding: 0px 60px 10px 60px; height: | + | <div id="body" style="padding: 0px 60px 10px 60px; height: 1356px"> |
<br> | <br> | ||
Line 138: | Line 131: | ||
<p><b>Garcia-Ojalvo, J., M. B. Elowitz, et al. (2004).</b> Modeling a synthetic multicellular clock: Repressilators coupled by quorum sensing. <i>Proceedings of the National Academy of Sciences of the United States of America</i> <b>101</b>(30): 10955-10960.</p> | <p><b>Garcia-Ojalvo, J., M. B. Elowitz, et al. (2004).</b> Modeling a synthetic multicellular clock: Repressilators coupled by quorum sensing. <i>Proceedings of the National Academy of Sciences of the United States of America</i> <b>101</b>(30): 10955-10960.</p> | ||
+ | |||
+ | <p><b>Seliger, H. H., & McElroy, W. D. (1964).</b> The Colors of Firefly Bioluminescence: Enzyme Configuration and Species Specificity. <i>PNAS</i> <b>52</b> (1) 75-81</p> | ||
+ | |||
+ | <p><b>Branchini, B. R., Southworth, T. L., Khattak, N. F., Michelini, E. & Roda, A. (2005).</b> Red- and green-emitting firefly luciferase mutants for bioluminescent reporter applications. <i>Analytical Biochemistry</i> <b>345</b>, 140-148.</p> | ||
+ | <p><b>Branchini, B. R., Ablamsky, D. M., Murtiashaw, M. H., Uzasci, L., Fraga, H. & Southworth, T. L. (2007).</b> Thermostable red and green light-producing firefly luciferase mutants for bioluminescent reporter applications. <i>Analytical Biochemistry</i> <b>361</b>, 253-262.</p> | ||
+ | <p><b>Moradi, A., Hosseinkhani, S., Naderi-Manesh, H., Sadeghizadeh, M. & Alipour, B. S. (2009).</b> Effect of Charge Distribution in a Flexible Loop on the Bioluminescence Color of Firefly Luciferases. <i>Biochemistry</i> <b>48</b>, 575-582.</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>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><b>Fujii, H., Noda, K., Asami, Y., Kuroda, A., Sakata, M. & Tokida, A. (2007).</b> Increase in bioluminescence intensity of firefly luciferase using genetic modification. <i>Analytical Biochemistry</i> <b>366</b>, 131-136.</p> | <p><b>Fujii, H., Noda, K., Asami, Y., Kuroda, A., Sakata, M. & Tokida, A. (2007).</b> Increase in bioluminescence intensity of firefly luciferase using genetic modification. <i>Analytical Biochemistry</i> <b>366</b>, 131-136.</p> | ||
+ | <p><b>Shapirol, E., Lu, C., Baneyx, F. (2009).</b> Design and characterization of novel trypsin-resistant firefly luciferases by site-directed mutagenesis. <i>Protein Eng Des Sel</i> <b>22</b>(11): 655-663.</p> | ||
Line 153: | Line 154: | ||
<p><b>Hirose, Y., Shimada, T., Narikawa, R., Katayama, M. & Ikeuchi, M. (2008).</b> Cyanobacteriochrome CcaS is the green light receptor that induces the expression of phycobilisome linker protein. <i>Proceedings of the National Academy of Sciences</i> <b>105</b>, 9528-9533.</p> | <p><b>Hirose, Y., Shimada, T., Narikawa, R., Katayama, M. & Ikeuchi, M. (2008).</b> Cyanobacteriochrome CcaS is the green light receptor that induces the expression of phycobilisome linker protein. <i>Proceedings of the National Academy of Sciences</i> <b>105</b>, 9528-9533.</p> | ||
+ | <p><b>Makino, K., Shinagawa, H., Amemura, M., Kawamoto, T., Yamada, M., Nakata, A. (1989).</b> Signal transduction in the phosphate regulon of Escherichia coli involves phosphotransfer between PhoR and PhoB proteins. <i>Journal of Molecular Biology</i> <b>210</b>(3), 551-559</p> | ||
+ | <p><b>Kalogeraki, V. S. and Winans, S. C. (1996).</b> Suicide plasmids containing promoterless reporter genes can simultaneously disrupt and create fusions to target genes of diverse bacteria. <i>Gene</i> <b>188</b>(1), 69-75</p> | ||
+ | |||
+ | <p>Edinburgh 2009 team wiki, <i>https://2009.igem.org/Team:Edinburgh</i>.</p> | ||
+ | <p>Ljubljana 2007 team wiki, <i>https://2007.igem.org/Ljubljana</i>.</p> | ||
+ | <p>UT Austin 2004 team wiki (Registry coliroid page), <i>http://partsregistry.org/Coliroid</i>.</p> | ||
+ | <p>Harvard 2008 team wiki, <i>https://2008.igem.org/Team:Harvard</i>.</p> | ||
+ | <p>EPF Lausanne 2009 team wiki, <i>https://2009.igem.org/Team:EPF-Lausanne</i>.</p> | ||
+ | <p>Tokyo-Nokogen 2009 team wiki, <i>https://2009.igem.org/Team:Tokyo-Nokogen</i>.</p> | ||
+ | <p>Cambridge 2010 team wiki, <i>https://2010.igem.org/Team:Cambridge</i>.</p> | ||
+ | <p>Mexico UNAM-Genomics 2010 team wiki, <i>https://2010.igem.org/Team:UNAM-Genomics_Mexico</i>.</p> | ||
</div> | </div> |
Latest revision as of 02:29, 28 October 2010
References
Elowitz, M. B. and S. Leibler (2000). A synthetic oscillatory network of transcriptional regulators. Nature 403(6767): 335-338.
Danino, T., O. Mondragon-Palomino, et al (2009). A synchronized quorum of genetic clocks. Nature 463(7279): 326-330.
Garcia-Ojalvo, J., M. B. Elowitz, et al. (2004). Modeling a synthetic multicellular clock: Repressilators coupled by quorum sensing. Proceedings of the National Academy of Sciences of the United States of America 101(30): 10955-10960.
Seliger, H. H., & McElroy, W. D. (1964). The Colors of Firefly Bioluminescence: Enzyme Configuration and Species Specificity. PNAS 52 (1) 75-81
Branchini, B. R., Southworth, T. L., Khattak, N. F., Michelini, E. & Roda, A. (2005). Red- and green-emitting firefly luciferase mutants for bioluminescent reporter applications. Analytical Biochemistry 345, 140-148.
Branchini, B. R., Ablamsky, D. M., Murtiashaw, M. H., Uzasci, L., Fraga, H. & Southworth, T. L. (2007). Thermostable red and green light-producing firefly luciferase mutants for bioluminescent reporter applications. Analytical Biochemistry 361, 253-262.
Moradi, A., Hosseinkhani, S., Naderi-Manesh, H., Sadeghizadeh, M. & Alipour, B. S. (2009). Effect of Charge Distribution in a Flexible Loop on the Bioluminescence Color of Firefly Luciferases. Biochemistry 48, 575-582.
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
Fujii, H., Noda, K., Asami, Y., Kuroda, A., Sakata, M. & Tokida, A. (2007). Increase in bioluminescence intensity of firefly luciferase using genetic modification. Analytical Biochemistry 366, 131-136.
Shapirol, E., Lu, C., Baneyx, F. (2009). Design and characterization of novel trypsin-resistant firefly luciferases by site-directed mutagenesis. Protein Eng Des Sel 22(11): 655-663.
Levskaya, A., Chevalier, A. A., Tabor, J. J. & other authors (2005). Synthetic biology: Engineering Escherichia coli to see light. Nature 438, 441-442.
Gambetta, G. A. & Lagarias, J. C. (2001). Genetic engineering of phytochrome biosynthesis in bacteria. Proceedings of the National Academy of Sciences of the United States of America 98, 10566-10571.
Levskaya, A., O. D. Weiner, et al. (2009). Spatiotemporal control of cell signalling using a light-switchable protein interaction. Nature Vol 461
Strickland, D., Moffat, K. & Sosnick, T. R. (2008). Light-activated DNA binding in a designed allosteric protein. Proceedings of the National Academy of Sciences 105, 10709-10714.
Schüttrigkeit, T. A., Kompa, C. K., Salomon, M., Rüdiger, W. & Michel-Beyerle, M. E. (2003). Primary photophysics of the FMN binding LOV2 domain of the plant blue light receptor phototropin of Avena sativa. Chemical Physics 294, 501-508.
Wu, Y. I., D. Frey, et al. (2009). A genetically encoded photoactivatable Rac controls the motility of living cells. Nature Vol 461
Hirose, Y., Shimada, T., Narikawa, R., Katayama, M. & Ikeuchi, M. (2008). Cyanobacteriochrome CcaS is the green light receptor that induces the expression of phycobilisome linker protein. Proceedings of the National Academy of Sciences 105, 9528-9533.
Makino, K., Shinagawa, H., Amemura, M., Kawamoto, T., Yamada, M., Nakata, A. (1989). Signal transduction in the phosphate regulon of Escherichia coli involves phosphotransfer between PhoR and PhoB proteins. Journal of Molecular Biology 210(3), 551-559
Kalogeraki, V. S. and Winans, S. C. (1996). Suicide plasmids containing promoterless reporter genes can simultaneously disrupt and create fusions to target genes of diverse bacteria. Gene 188(1), 69-75
Edinburgh 2009 team wiki, https://2009.igem.org/Team:Edinburgh.
Ljubljana 2007 team wiki, https://2007.igem.org/Ljubljana.
UT Austin 2004 team wiki (Registry coliroid page), http://partsregistry.org/Coliroid.
Harvard 2008 team wiki, https://2008.igem.org/Team:Harvard.
EPF Lausanne 2009 team wiki, https://2009.igem.org/Team:EPF-Lausanne.
Tokyo-Nokogen 2009 team wiki, https://2009.igem.org/Team:Tokyo-Nokogen.
Cambridge 2010 team wiki, https://2010.igem.org/Team:Cambridge.
Mexico UNAM-Genomics 2010 team wiki, https://2010.igem.org/Team:UNAM-Genomics_Mexico.