From 2006.igem.org
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| - | [[NCBS_Bangalore_2006#The_Living_Networks_Wiki|IGEM Bangalore HOME]]
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| - | ===The projects===
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| - | [[X-Y_chemotaxis|Regulation of Bacterial Chemotaxis]]
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| - | * Use two attractants whose receptors are inducible (serine with Tar, aspartate with Tsr). These define two orthogonal axes. Use a default attractant along a diagonal to establish '-' movement. Immediate goals: To establish substrate geometries upon which multiple reproducible, stable, quantitative chemical gradients can be established; to validate default chemotaxis in the absence of MCP receptors.
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| - | [[Image:ncbs_igem2006_net1.jpg|thumb|none|160 px]] <br/>
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| - | [[Synchronization_of_Cell_Cycle|Synchronization of bacterial cell cycles]]
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| - | *Synchronization of bacterial cell cycles. Use a cell cycle-dependent promoter to drive a LuxI-LuxR based cell-cell signal. Use regulation of replication initiator DnaA to modulate cell cycle in receiver cells. Immediate goals: To determine if candidate promoters oscillate; to regulate DnaA levels.
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| - | [[Image:ncbs_igem2006_net2.jpg|thumb|none|160 px]]
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| - | [[Memory_effects_of_UV_exposure|Monitoring long-term effects of UV exposure]]
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| - | *Analysis of stress responses in biofilms. Connect stress response system to a lac based bistable GFP reporter. This allows transient expression at a stress-response promoter to trigger persistent expression of GFP. Immediate goals: To standardize biofilm assay; to design other experiments in which such a construct would be useful, especially using a cell-sorter.
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| - | [[Image:ncbs_igem2006_net3.jpg|thumb|none|160 px]]
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Latest revision as of 10:58, 28 October 2006
