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Team:Chalmers-Gothenburg
From 2012.igem.org
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== Biodetection of human chorionic gonadotropin hormone == | == Biodetection of human chorionic gonadotropin hormone == | ||
The aim of this project was to develop an idea for a biological construct that could be entered in the International Genetically Engineered Machine (iGEM) competition. For this reason, ''Saccharomyces cerevisiae'' have been planned to be modifed in such a way that the yeast cell should function as a biosensor for the human chorionic gonadotropin hormone (hCG). This hormone is produced in the body during pregnancy and consequently, the idea is for the biosensor to function as a simple pregnancy test. To construct the biosensor, the Ste2 receptor in the yeast pheromone signaling pathway will be replaced with the human luteinizing hormone receptor (LH/CG), which is the receptor that hCG binds to with high affnity. The yeast strain that will be used contains a yeast/human chimeric G-alpha subunit, enabling coupling of the receptor with the already existing pheromone pathway in yeast. Consequently, binding of hCG should result in activation of the pathway. The genes tnaA and fmo, encoding tryptophanase and avin-containing monooxygenas respectively, will also be introduced into the yeast strain. These enzymes catalyze the conversion of tryptophan to indigo. tnaA will be set under the control of the pheromone induced FIG1 promoter and fmo of the constitutive TEF1 promoter. Hence, detection of hCG should result in the production of bio-indigo. In order to ensure hCG to pass the yeast cell wall, the gene CWP2, encoding a cell wall protein, will also be deleted. | The aim of this project was to develop an idea for a biological construct that could be entered in the International Genetically Engineered Machine (iGEM) competition. For this reason, ''Saccharomyces cerevisiae'' have been planned to be modifed in such a way that the yeast cell should function as a biosensor for the human chorionic gonadotropin hormone (hCG). This hormone is produced in the body during pregnancy and consequently, the idea is for the biosensor to function as a simple pregnancy test. To construct the biosensor, the Ste2 receptor in the yeast pheromone signaling pathway will be replaced with the human luteinizing hormone receptor (LH/CG), which is the receptor that hCG binds to with high affnity. The yeast strain that will be used contains a yeast/human chimeric G-alpha subunit, enabling coupling of the receptor with the already existing pheromone pathway in yeast. Consequently, binding of hCG should result in activation of the pathway. The genes tnaA and fmo, encoding tryptophanase and avin-containing monooxygenas respectively, will also be introduced into the yeast strain. These enzymes catalyze the conversion of tryptophan to indigo. tnaA will be set under the control of the pheromone induced FIG1 promoter and fmo of the constitutive TEF1 promoter. Hence, detection of hCG should result in the production of bio-indigo. In order to ensure hCG to pass the yeast cell wall, the gene CWP2, encoding a cell wall protein, will also be deleted. | ||
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Revision as of 08:05, 22 May 2012
Biodetection of human chorionic gonadotropin hormone
The aim of this project was to develop an idea for a biological construct that could be entered in the International Genetically Engineered Machine (iGEM) competition. For this reason, Saccharomyces cerevisiae have been planned to be modifed in such a way that the yeast cell should function as a biosensor for the human chorionic gonadotropin hormone (hCG). This hormone is produced in the body during pregnancy and consequently, the idea is for the biosensor to function as a simple pregnancy test. To construct the biosensor, the Ste2 receptor in the yeast pheromone signaling pathway will be replaced with the human luteinizing hormone receptor (LH/CG), which is the receptor that hCG binds to with high affnity. The yeast strain that will be used contains a yeast/human chimeric G-alpha subunit, enabling coupling of the receptor with the already existing pheromone pathway in yeast. Consequently, binding of hCG should result in activation of the pathway. The genes tnaA and fmo, encoding tryptophanase and avin-containing monooxygenas respectively, will also be introduced into the yeast strain. These enzymes catalyze the conversion of tryptophan to indigo. tnaA will be set under the control of the pheromone induced FIG1 promoter and fmo of the constitutive TEF1 promoter. Hence, detection of hCG should result in the production of bio-indigo. In order to ensure hCG to pass the yeast cell wall, the gene CWP2, encoding a cell wall protein, will also be deleted.
