Difference between revisions of "Part:BBa K1963010"
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<partinfo>BBa_K1963010 short</partinfo> | <partinfo>BBa_K1963010 short</partinfo> | ||
− | This is a multi-sequence system for small RNA (sRNA) production in an E. coli host - or especially with co-expression of E. coli Hfq BBa_K1963000. The system is based on the BBa_K1963002 template and has the proD strong promoter, followed by a short antisense sequence targeting the RBS and 5' end of the fliC transcript, followed by the E. coli micC hairpin, followed by the strong terminator sequence T1/TE. The anti fliC sRNA is placed after C-193. The system should impair motility of E. coli. | + | This is a multi-sequence system for small RNA (sRNA) production in an <i>E. coli</i> host - or especially with co-expression of <i>E. coli</i> Hfq <partinfo>BBa_K1963000</partinfo>. The system is based on the <partinfo>BBa_K1963002</partinfo> template and has the <i>proD</i> strong promoter, followed by a short antisense sequence targeting the RBS and 5' end of the <i>E. coli</i> <i>fliC</i> transcript, followed by the <i>E. coli micC</i> hairpin, followed by the strong terminator sequence T1/TE. The anti RBS-<i>fliC</i> sRNA is placed after C-193. The system should impair motility of <i>E. coli</i> as a proof-of-concept. |
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+ | <b>Note that this part differs from <partinfo>BBa_K1963004</partinfo> slightly in that the sRNA for this one covers the <i>fliC</i> RBS</b> | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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+ | The motile <i>E. coli</i> host strain MG1655 was tranformed with <partinfo>BBa_K1963010</partinfo> and subjected to a plate-based swimming assay (Figure 1). The <partinfo>BBa_K1963010</partinfo> contains a sRNA that will target the RBS and initial codons of the <i>fliC</i> transcript that encodes flagellin - the principle component of the flagellum. The data related to this biobrick are labelled <b><i>spiRNA-fliC-RBS-CDS</i></b> in Figure 1. | ||
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+ | Experimental procedures needed. | ||
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+ | https://static.igem.org/mediawiki/parts/f/f6/Ecoliflicfrulhuq2.png | ||
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+ | <b>Figure 1. sRNA Devices can Inhibit Swimming in an <i>E. coli</i> Test System.</b> | ||
+ | Photographs representative of motility assays with MG1655 transformed with <partinfo>BBa_K1963002</partinfo> (control), <partinfo>BBa_K1963004</partinfo> (<i>spiRNA-fliC-CDS</i>)and <partinfo>BBa_K1963010</partinfo> (<i>spiRNA-fliC-RBS-CDS</i>). Bar graph showing average swimming/spreading area and standard deviation of replicates. | ||
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Latest revision as of 15:20, 23 October 2016
An sRNA system for down-regulation of E. coli fliC encoding flagellin
This is a multi-sequence system for small RNA (sRNA) production in an E. coli host - or especially with co-expression of E. coli Hfq BBa_K1963000. The system is based on the BBa_K1963002 template and has the proD strong promoter, followed by a short antisense sequence targeting the RBS and 5' end of the E. coli fliC transcript, followed by the E. coli micC hairpin, followed by the strong terminator sequence T1/TE. The anti RBS-fliC sRNA is placed after C-193. The system should impair motility of E. coli as a proof-of-concept.
Note that this part differs from BBa_K1963004 slightly in that the sRNA for this one covers the fliC RBS
Usage and Biology
The motile E. coli host strain MG1655 was tranformed with BBa_K1963010 and subjected to a plate-based swimming assay (Figure 1). The BBa_K1963010 contains a sRNA that will target the RBS and initial codons of the fliC transcript that encodes flagellin - the principle component of the flagellum. The data related to this biobrick are labelled spiRNA-fliC-RBS-CDS in Figure 1.
Experimental procedures needed.
Figure 1. sRNA Devices can Inhibit Swimming in an E. coli Test System. Photographs representative of motility assays with MG1655 transformed with BBa_K1963002 (control), BBa_K1963004 (spiRNA-fliC-CDS)and BBa_K1963010 (spiRNA-fliC-RBS-CDS). Bar graph showing average swimming/spreading area and standard deviation of replicates.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 101