Difference between revisions of "Part:BBa K1412007"
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<partinfo>BBa_K1412007 short</partinfo> | <partinfo>BBa_K1412007 short</partinfo> | ||
− | This part is | + | This part is derived from [https://parts.igem.org/Part:BBa_K1412005 BBa_K1412005] by taking RBS out. |
+ | As iGEM14_[http://2014.igem.org/Team:XMU-China# XMU-China] has developed a system to characterize the strength of different promoter and RBS, this part provides an easier assembly path to contruct new devices to characterize the strength of promoters and RBSs which is unknown. | ||
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+ | =='''Method'''== | ||
− | + | Contructing new device by this part, then characterize the device in <i>E.coli (CL-1)</i>(knock <i>CheZ</i> gene out of genome). In order to take reference, we need to choose appropriate reference parts(see the wiki from iGEM14_[http://2014.igem.org/Team:XMU-China# XMU-China]) which has only one portion(RBS or promoter) different from the new contructed device. As the expression strength from reference part is already known, we can spot both kinds of device on the same semi-solid culture medium. By comparing the chemotaxis diameter of both devices, we can tell unknown expression strength of unknown promoters or RBSs. | |
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<partinfo>BBa_K1412007 parameters</partinfo> | <partinfo>BBa_K1412007 parameters</partinfo> | ||
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=='''Reference'''== | =='''Reference'''== | ||
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[2] [http://pubs.acs.org/doi/abs/10.1021/bi00561a015 Chelsky D and Dahlquist FW (1980) Chemotaxis in Escherichia coli: association of protein components. Biochemistry 19: 4633–4639 ]. | [2] [http://pubs.acs.org/doi/abs/10.1021/bi00561a015 Chelsky D and Dahlquist FW (1980) Chemotaxis in Escherichia coli: association of protein components. Biochemistry 19: 4633–4639 ]. | ||
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+ | <I><B>More information, click here: [http://2014.igem.org/Team:XMU-China# XMU-China] |
Latest revision as of 17:00, 14 October 2014
CheZ-TT
This part is derived from BBa_K1412005 by taking RBS out.
As iGEM14_[http://2014.igem.org/Team:XMU-China# XMU-China] has developed a system to characterize the strength of different promoter and RBS, this part provides an easier assembly path to contruct new devices to characterize the strength of promoters and RBSs which is unknown.
Method
Contructing new device by this part, then characterize the device in E.coli (CL-1)(knock CheZ gene out of genome). In order to take reference, we need to choose appropriate reference parts(see the wiki from iGEM14_[http://2014.igem.org/Team:XMU-China# XMU-China]) which has only one portion(RBS or promoter) different from the new contructed device. As the expression strength from reference part is already known, we can spot both kinds of device on the same semi-solid culture medium. By comparing the chemotaxis diameter of both devices, we can tell unknown expression strength of unknown promoters or RBSs.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Reference
[1] [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0011915#pone-0011915-g006 Paungfoo-Lonhienne C et al. (2010) Turning the table: plants consume microbes as a source of nutrients. PLoS One 5(7): e11915 ].
[2] [http://pubs.acs.org/doi/abs/10.1021/bi00561a015 Chelsky D and Dahlquist FW (1980) Chemotaxis in Escherichia coli: association of protein components. Biochemistry 19: 4633–4639 ].
More information, click here: [http://2014.igem.org/Team:XMU-China# XMU-China]