Difference between revisions of "Team:Macquarie Australia/Description"

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<a href="https://2015.igem.org/Team:Macquarie_Australia">Home</a></td>
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<a href="https://2015.igem.org/Team:Macquarie_Australia/ProjectOverview">Project</a></td>
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<a href="https://2015.igem.org/Team:Macquarie_Australia/Modeling">Modelling</a></td>
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<a href="https://2015.igem.org/Team:Macquarie_Australia/Practices">Human Practices</a></td>
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<a href="https://2015.igem.org/Team:Macquarie_Australia/Team">Team</a></td>
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<a href="https://2015.igem.org/Team:Macquarie_Australia/Attributions">Attributions</a></td>
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<h2>Project Description</h2>
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<p>Our project has its focus on photosynthesis - the natural process where plants and algae convert sunlight into useable energy. By developing artificial photosynthesis in a biological system we can better harvest the unlimited supply of solar energy. The long-term goal is to engineer bacteria that can produce hydrogen gas on an industrial scale.</p>
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<p>This year the aim of our team is to engineer bacteria to manufacture chlorophyll, the primary molecule of photosynthesis. Chlorophyll harvests light and is involved in the excitation transfer of energy. Chlorophyll-<i>a</i> can be synthesised via a pathway from the protoporphyrin-IX molecule. By placing 13 genes into 4 biobrick vectors we can recreate the pathway in <i>Escherichia coli</i>.</p>
  
<h2>Project Description</h2>
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<h4>Experimental Organism</h4>
<p>Our project has its focus on photosynthesis - the natural process where plants and algae convert sunlight into useable energy. By developing artificial photosynthesis in a biological system we can better harvest the unlimited supply of solar energy. The long-term goal is to engineer bacteria that can produce hydrogen gas on an industrial scale.</p>
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<p>Why did we choose <i>Escherichia coli</i> (<i>E.coli</i>) as a chassis?</p>
<p>This year the aim of our team is to engineer bacteria to manufacture chlorophyll, the primary molecule of photosynthesis. Chlorophyll harvests light and is involved in the excitation transfer of energy. Chlorophyll-<i>a</i> can be synthesised via a pathway from the protoporphyrin-IX molecule. By placing 13 genes into 4 biobrick vectors we can recreate the pathway in <i>Escherichia coli</i>.</p>
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<p>One reason is that <i>E.coli</i> is a well-categorised species with an abundance of literature and stocks world-wide.</p>
  
<h4>Experimental Organism</h4>
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<h4>Ideas Explored</h4>
<p>Why did we choose <i>Escherichia coli</i> (<i>E.coli</i>) as a chassis?</p>
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<p>The two different ideas that our project explores are the academic basis of photosynthesis and the potential applications.</p>
<p>One reason is that <i>E.coli</i> is a well-categorised species with an abundance of literature and stocks world-wide.</p>
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<p>Academically we want to learn more about the photosystems that enable photosynthesis. However, we also want to investigate real-world applications to help the public engage with the topic.</p>
  
<h4>Ideas Explored</h4>
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<h4>What is new from last year?</h4>
<p>The two different ideas that our project explores are the academic basis of photosynthesis and the potential applications.</p>
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<p>We intend on completing the Chlorophyll biosynthesis pathway within <i>E.coli</i>.</p>
<p>Academically we want to learn more about the photosystems that enable photosynthesis. However, we also want to investigate real-world applications to help the public engage with the topic.</p>
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<p>A completely new aspect is the construction of Photosystem-II.</p>
  
<h4>What is new from last year?</h4>
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<p>We intend on completing the Chlorophyll biosynthesis pathway within <i>E.coli</i>.</p>
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<p>A completely new aspect is the construction of Photosystem-II.</p>
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Revision as of 02:40, 8 September 2015

Project Description
Link to Project page

Project Description

Our project has its focus on photosynthesis - the natural process where plants and algae convert sunlight into useable energy. By developing artificial photosynthesis in a biological system we can better harvest the unlimited supply of solar energy. The long-term goal is to engineer bacteria that can produce hydrogen gas on an industrial scale.

This year the aim of our team is to engineer bacteria to manufacture chlorophyll, the primary molecule of photosynthesis. Chlorophyll harvests light and is involved in the excitation transfer of energy. Chlorophyll-a can be synthesised via a pathway from the protoporphyrin-IX molecule. By placing 13 genes into 4 biobrick vectors we can recreate the pathway in Escherichia coli.

Experimental Organism

Why did we choose Escherichia coli (E.coli) as a chassis?

One reason is that E.coli is a well-categorised species with an abundance of literature and stocks world-wide.

Ideas Explored

The two different ideas that our project explores are the academic basis of photosynthesis and the potential applications.

Academically we want to learn more about the photosystems that enable photosynthesis. However, we also want to investigate real-world applications to help the public engage with the topic.

What is new from last year?

We intend on completing the Chlorophyll biosynthesis pathway within E.coli.

A completely new aspect is the construction of Photosystem-II.