Team:ZJU-China/Project

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You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2008.igem.org/Help:Template/Examples">HERE</a>.
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{|align="justify"
 
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|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
 
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|[[Image:ZJU-China_logo.png|200px|right|frame]]
 
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''Tell us more about your project.  Give us background.  Use this is the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
 
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!align="center"|[[Team:ZJU-China/Team|Team]]
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!align="center"|[https://igem.org/Team.cgi?year=2010&team_name=ZJU-China Official Team Profile]
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!align="center"|[[Team:ZJU-China/Project|Project]]
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!align="center"|[[Team:ZJU-China/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:ZJU-China/Modeling|Modeling]]
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!align="center"|[[Team:ZJU-China/Notebook|Notebook]]
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Your abstract
 
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<h4 class="current" id="try">Biofilm</h4>
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<div class="pane" style="display: block;"><a
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href="https://2011.igem.org/Team:ZJU-China/Project.html">Background</a> <a
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href="https://2011.igem.org/Team:ZJU-China/bio-Design.html">Design</a> <a
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href="https://2011.igem.org/Team:ZJU-China/bio-modeling.html">Modeling</a> <a
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href="https://2011.igem.org/Team:ZJU-China/bio-results.html">Results</a></div>
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<h4>Rainbofilm</h4>
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<a href="https://2011.igem.org/Team:ZJU-China/rainbo-Design.html">Design</a> <a
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href="https://2011.igem.org/Team:ZJU-China/rainbo-modeling-v1.html">Modeling</a> <a
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href="https://2011.igem.org/Team:ZJU-China/rainbo-Results.html">Results</a><a href="https://2011.igem.org/Team:ZJU-China/rainbo-Extension.html">Extension</a></div>
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<h4>Xfilm</h4>
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<div class="pane">
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<a href="https://2011.igem.org/Team:ZJU-China/X-Overview.html">Overview</a>
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<a href="https://2011.igem.org/Team:ZJU-China/X-Sugarfilm.html">Sugarfilm</a><a href="https://2011.igem.org/Team:ZJU-China/X-Sensorfilm.html">Sensorfilm</a><a href="https://2011.igem.org/Team:ZJU-China/X-Gluefilm.html">Gluefilm</a></div>
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<h4>Parts</h4>
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<div class="pane"><a
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href="https://2011.igem.org/Team:ZJU-China/BBa_I13602.html">BBa_I13602</a> <a
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href="https://2011.igem.org/Team:ZJU-China/BBa_K561000.html">BBa_K561000</a> <a
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href="https://2011.igem.org/Team:ZJU-China/BBa_K561002.html">BBa_K561002</a> <a
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href="https://2011.igem.org/Team:ZJU-China/BBa_K561003.html">BBa_K561003</a></div>
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<h4>Achievements</h4>
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== Project Details==
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<div class="pane"><a href="https://2011.igem.org/Team:ZJU-China/data.html">Data
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Page</a> <a href="https://2011.igem.org/Team:ZJU-China/judging.html">Judging Form</a> <a
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href="https://2011.igem.org/Team:ZJU-China/attribution.html">Attribution and
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Contributions</a></div>
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<h4>Tools</h4>
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<h1>Background</h1>
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</div>
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<p></p>
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<p>Biofilm is a multi-cellular bacteria community, which is
 +
prevalent in diverse natural and artificial settings. It is best known
 +
for its robust adaptability and strong resistance to environmental
 +
stress. We intended to utilize and modify this natural multicellular
 +
structure to develop a new kind of extracellular scaffold, constructing
 +
a stratified protein expression system using the naturally formed graded
 +
oxygen concentration within the bacteria biofilm.<br />
 +
</p>
 +
<p></p>
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<p>Biofilm formation process can be roughly divided into four
 +
stages: bacteria attachment, micro colony formation, biofilm maturation
 +
and biofilm dispersion. The best sample for the observation is the
 +
matured biofilm, which, according to previous studies, was formed after
 +
48 hours after inoculation with only exception in bubbling method
 +
(Bandara HM et al. 2009; Klausen M. et al. 2003.). <br />
 +
</p>
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<p></p>
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<p>Based on the references (Almeida C. et al. 2011; Rani SA et al.
 +
2007), we’ve developed three different biofilm formation methods:
 +
Bubbling method, Rubber tube method and cell culture plate method. The
 +
biofilm formed in the two former ways were observed through
 +
cryo-sectioning coupled with normal fluorescence microscopy while
 +
confocal laser scanning microscope was employed to obtain the biofilm
 +
images of the third method. In addition to the above, we’ve tested
 +
different material’s applicability in biofilm formation experiments and
 +
introduced autoinducer AI-2 as an accelerator molecule.</p>
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<img src="https://static.igem.org/mediawiki/2011/9/9d/ZjuYU1.gif"
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=== Part 2 ===
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<div class="footer" id="footer"><a href="https://2011.igem.org/">
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iGem 2011 Home Page</a> <a href="http://ung.igem.org/Special:Upload/">
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Upload Files</a> <a
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=== The Experiments ===
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=== Part 3 ===
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== Results ==
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Latest revision as of 18:22, 28 October 2011

<!DOCTYPE html PUBLIC "-//W3C//DTD XHTML 1.0 Transitional//EN" "http://www.w3.org/TR/xhtml1/DTD/xhtml1-transitional.dtd"> Biofilm Background

Biofilm

Rainbofilm

Xfilm

Parts

Achievements

Tools

Background

Biofilm is a multi-cellular bacteria community, which is prevalent in diverse natural and artificial settings. It is best known for its robust adaptability and strong resistance to environmental stress. We intended to utilize and modify this natural multicellular structure to develop a new kind of extracellular scaffold, constructing a stratified protein expression system using the naturally formed graded oxygen concentration within the bacteria biofilm.

Biofilm formation process can be roughly divided into four stages: bacteria attachment, micro colony formation, biofilm maturation and biofilm dispersion. The best sample for the observation is the matured biofilm, which, according to previous studies, was formed after 48 hours after inoculation with only exception in bubbling method (Bandara HM et al. 2009; Klausen M. et al. 2003.).

Based on the references (Almeida C. et al. 2011; Rani SA et al. 2007), we’ve developed three different biofilm formation methods: Bubbling method, Rubber tube method and cell culture plate method. The biofilm formed in the two former ways were observed through cryo-sectioning coupled with normal fluorescence microscopy while confocal laser scanning microscope was employed to obtain the biofilm images of the third method. In addition to the above, we’ve tested different material’s applicability in biofilm formation experiments and introduced autoinducer AI-2 as an accelerator molecule.