Team:Chiba/Sender
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(New page: English:Each species has their own LuxI-type proteins,which synthesize their specific autoinducers,AHLs.AHLs produced by different LuxI-type proteins differ only in the length of the acyl-...) |
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+ | <html><link rel="stylesheet" href="https://2008.igem.org/wiki/index.php?title=User:Maiko/chiba.css&action=raw&ctype=text/css" type="text/css" /></html> | ||
+ | [[Image:Chiba-U.gif]] | ||
+ | {| style="color:white;background-color:Maroon" cellpadding="3" cellspacing="3" border="1" bordercolor="white" width="100%" align="center" | ||
+ | !align="center"|[[Team:Chiba|Home]] | ||
+ | !align="center"|[[Team:Chiba/Team|The Team]] | ||
+ | !align="center"|[[Team:Chiba/Project|The Project]] | ||
+ | !align="center"|[[Team:Chiba/Parts|Parts Submitted to the Registry]] | ||
+ | !align="center"|[[Team:Chiba/Reference|Reference]] | ||
+ | !align="center"|[[Team:Chiba/Notebook|Notebook]] | ||
+ | !align="center"|[[Team:Chiba/Acknowledgements|Acknowledgements]] | ||
+ | |} | ||
+ | __NOTOC__ | ||
+ | ==Signal molecule sender== | ||
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English:Each species has their own LuxI-type proteins,which synthesize their specific autoinducers,AHLs.AHLs produced by different LuxI-type proteins differ only in the length of the acyl-chain moiety and substitution at position C-3.LuxR,which is original for Vibrio fischeri,is activated by its cognate autoinducer,3OC6HSL.However,LuxR is also activated by non-endogenous molecules,C4HSL,C6HSL,and 3OC12HSL.Activation by non-endogenous molecules requires a higher signal concentration(2).This results in slower activation of receivers,when AHL concentration is increasing. | English:Each species has their own LuxI-type proteins,which synthesize their specific autoinducers,AHLs.AHLs produced by different LuxI-type proteins differ only in the length of the acyl-chain moiety and substitution at position C-3.LuxR,which is original for Vibrio fischeri,is activated by its cognate autoinducer,3OC6HSL.However,LuxR is also activated by non-endogenous molecules,C4HSL,C6HSL,and 3OC12HSL.Activation by non-endogenous molecules requires a higher signal concentration(2).This results in slower activation of receivers,when AHL concentration is increasing. | ||
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+ | ===Design=== | ||
+ | ===Experiment=== | ||
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+ | |||
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+ | |||
+ | {| style="color:white;background-color:Maroon" cellpadding="3" cellspacing="3" border="1" bordercolor="white" width="100%" align="center" | ||
+ | !align="center"|[[Team:Chiba|Home]] | ||
+ | !align="center"|[[Team:Chiba/Team|The Team]] | ||
+ | !align="center"|[[Team:Chiba/Project|The Project]] | ||
+ | !align="center"|[[Team:Chiba/Parts|Parts Submitted to the Registry]] | ||
+ | !align="center"|[[Team:Chiba/Reference|Reference]] | ||
+ | !align="center"|[[Team:Chiba/Notebook|Notebook]] | ||
+ | !align="center"|[[Team:Chiba/Acknowledgements|Acknowledgements]] | ||
+ | |} |
Revision as of 18:18, 26 October 2008
Home | The Team | The Project | Parts Submitted to the Registry | Reference | Notebook | Acknowledgements |
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Signal molecule sender
English:Each species has their own LuxI-type proteins,which synthesize their specific autoinducers,AHLs.AHLs produced by different LuxI-type proteins differ only in the length of the acyl-chain moiety and substitution at position C-3.LuxR,which is original for Vibrio fischeri,is activated by its cognate autoinducer,3OC6HSL.However,LuxR is also activated by non-endogenous molecules,C4HSL,C6HSL,and 3OC12HSL.Activation by non-endogenous molecules requires a higher signal concentration(2).This results in slower activation of receivers,when AHL concentration is increasing.
Design
Experiment
Home | The Team | The Project | Parts Submitted to the Registry | Reference | Notebook | Acknowledgements |
---|