Imperial/Cell-Free/Comparison
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+ | <li><a href="https://2007.igem.org/Imperial/Cell-Free/Whatis" title=""><span>What is Cell-Free?</span></a></li> | ||
+ | <li><a class="current" href="https://2007.igem.org/Imperial/Cell-Free/Comparison" title=""><span>Advantages of CFS</span></a></li> | ||
+ | <li><a href="https://2007.igem.org/Imperial/Cell-Free/Contribution" title=""><span>Our Contributions</span></a></li> | ||
+ | <li><a href="https://2007.igem.org/Imperial/Cell-Free/Characterisation" title=""><span>Characterisation</span></a></li> | ||
+ | <li><a href="https://2007.igem.org/Imperial/Cell-Free/Applications" title=""><span>CFS Applications</span></a></li> | ||
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+ | = Cell-Free: Advantages and Disadvantages of CFS = | ||
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+ | {| border="1" | ||
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+ | |width=50%|<center>'''Advantages'''</center> | ||
+ | |width=50%|<center>'''Disadvantages'''</center> | ||
+ | |- | ||
+ | |style="background:#eeffee"|System is not an organism and is not restricted by the policies imposed on genetically modified organisms (GMO) | ||
+ | |style="background:#ffeeee"|Short expression lifespan because of limited energy of the system even in the presence of an ATP regenerating system | ||
+ | |- | ||
+ | |style="background:#eeffee"|Process is quick and simple requiring only preparation of cell extract and feeding solution and subsequent addition of DNA template | ||
+ | |style="background:#ffeeee"|Expensive system has no sustained metabolism to convert cheap energy (like sugars) into useable one for the gene expression machinery | ||
+ | |- | ||
+ | |style="background:#eeffee"|No concurrent expression of existing genome, therefore your genetically engineered device is more energy efficient | ||
+ | |style="background:#ffeeee"|Less characterization and experience of use in the laboratories compared to ''E. coli'' | ||
+ | |- | ||
+ | |style="background:#eeffee"|No DNA mutation of your genetically engineered device because there is no DNA replication | ||
+ | |style="background:#ffeeee"| | ||
+ | |- | ||
+ | |style="background:#eeffee"|No selective pressue on your genetically engineered device because the system is non-living and does not undergo natural selection | ||
+ | |style="background:#ffeeee"| | ||
+ | |- | ||
+ | |style="background:#eeffee"|No self-replication of your genetically engineered device leads to a fixed amount of DNA being expressed and more control over the rate of expression | ||
+ | |style="background:#ffeeee"| | ||
+ | |- | ||
+ | |style="background:#eeffee"|Expression system can be quality-controlled by manipulating adjustable parameters e.g. buffers are added to maintain optimum magnesium concentrations for efficient translation; protease inhibitors can be added to minimize degradation of synthesized proteins | ||
+ | |style="background:#ffeeee"| | ||
+ | |} | ||
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+ | <center> [https://2007.igem.org/Imperial/Cell-Free/Whatis << What is Cell-Free?] | Advantages of CFS | [https://2007.igem.org/Imperial/Cell-Free/Contribution Our Contributions >>] | ||
+ | </center> |
Latest revision as of 20:57, 26 October 2007
Cell-Free: Advantages and Disadvantages of CFS
System is not an organism and is not restricted by the policies imposed on genetically modified organisms (GMO) | Short expression lifespan because of limited energy of the system even in the presence of an ATP regenerating system |
Process is quick and simple requiring only preparation of cell extract and feeding solution and subsequent addition of DNA template | Expensive system has no sustained metabolism to convert cheap energy (like sugars) into useable one for the gene expression machinery |
No concurrent expression of existing genome, therefore your genetically engineered device is more energy efficient | Less characterization and experience of use in the laboratories compared to E. coli |
No DNA mutation of your genetically engineered device because there is no DNA replication | |
No selective pressue on your genetically engineered device because the system is non-living and does not undergo natural selection | |
No self-replication of your genetically engineered device leads to a fixed amount of DNA being expressed and more control over the rate of expression | |
Expression system can be quality-controlled by manipulating adjustable parameters e.g. buffers are added to maintain optimum magnesium concentrations for efficient translation; protease inhibitors can be added to minimize degradation of synthesized proteins |