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Team:Colombia
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{{https://2012.igem.org/User:Tabima}} | {{https://2012.igem.org/User:Tabima}} | ||
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==='''Our Project'''=== | ==='''Our Project'''=== | ||
Our objective is to generate a genetically-modified bacteria "detect and alert" system, particularly as a defense aid for coffee plantations against plant pathogens. Bacteria are built such that they can detect chitin, an organic compound found in fungal cell walls, amplify this initial signal, and finally alert the plant by stimulating an early hypersensitive response against infection. We have also included a way for the bacteria to control their own population density. Using the bacteria ''Escherichia coli'' K12, the system will use two differently-modified plasmids. The first one will detect the presence of chitin and weigh such input for intensity and duration. If significant, it will also produce a signal molecule to engage the response of the second plasmid. Upon exposure to enough concentration of the molecule, the second plasmid will produce a systemic acquired response triggering hormone (Salicylic Acid) to activate the plant defenses, both attacking the fungi as well as controlling the bacterial population growth. We're currently investigating whether or not we can expand our detection plasmid for other plant pathogens such as ''Ralstonia sp.'' We strongly believe this biocontrol method may prove to become a powerful tool for farmers and crop workers everywhere. In addition, our constructed "detect and alert" biobricks could be useful to plentiful synthetic biology experiments and future iGEM teams. | Our objective is to generate a genetically-modified bacteria "detect and alert" system, particularly as a defense aid for coffee plantations against plant pathogens. Bacteria are built such that they can detect chitin, an organic compound found in fungal cell walls, amplify this initial signal, and finally alert the plant by stimulating an early hypersensitive response against infection. We have also included a way for the bacteria to control their own population density. Using the bacteria ''Escherichia coli'' K12, the system will use two differently-modified plasmids. The first one will detect the presence of chitin and weigh such input for intensity and duration. If significant, it will also produce a signal molecule to engage the response of the second plasmid. Upon exposure to enough concentration of the molecule, the second plasmid will produce a systemic acquired response triggering hormone (Salicylic Acid) to activate the plant defenses, both attacking the fungi as well as controlling the bacterial population growth. We're currently investigating whether or not we can expand our detection plasmid for other plant pathogens such as ''Ralstonia sp.'' We strongly believe this biocontrol method may prove to become a powerful tool for farmers and crop workers everywhere. In addition, our constructed "detect and alert" biobricks could be useful to plentiful synthetic biology experiments and future iGEM teams. | ||
Revision as of 17:38, 14 July 2012
Team Colombia @ 2012 iGEM
Template:Https://2012.igem.org/User:Tabima
Our Project
Our objective is to generate a genetically-modified bacteria "detect and alert" system, particularly as a defense aid for coffee plantations against plant pathogens. Bacteria are built such that they can detect chitin, an organic compound found in fungal cell walls, amplify this initial signal, and finally alert the plant by stimulating an early hypersensitive response against infection. We have also included a way for the bacteria to control their own population density. Using the bacteria Escherichia coli K12, the system will use two differently-modified plasmids. The first one will detect the presence of chitin and weigh such input for intensity and duration. If significant, it will also produce a signal molecule to engage the response of the second plasmid. Upon exposure to enough concentration of the molecule, the second plasmid will produce a systemic acquired response triggering hormone (Salicylic Acid) to activate the plant defenses, both attacking the fungi as well as controlling the bacterial population growth. We're currently investigating whether or not we can expand our detection plasmid for other plant pathogens such as Ralstonia sp. We strongly believe this biocontrol method may prove to become a powerful tool for farmers and crop workers everywhere. In addition, our constructed "detect and alert" biobricks could be useful to plentiful synthetic biology experiments and future iGEM teams.
