Difference between revisions of "Part:BBa K2922027"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K2922027 short</partinfo> | <partinfo>BBa_K2922027 short</partinfo> | ||
− | + | ===Summary=== | |
− | + | As a kind of bacteriocin secreted by <i>E.coli</i>, colicin can kill other related bacteria that can’t secret specific immunity proteins. | |
− | + | Similar to Colicin-E1, Colicin-N is also a type of pore-forming colicin, encoded by gene <i>cna</i>. This class of transmembrane toxins depolarize the cytoplasmic membrane, leading to dissipation of cellular energy.[1] (Fig.1) | |
− | + | <table><tr><th>[[File:Ndesign.png|thumb|300px|Fig.1 Colicin-N can kill other bacteria.]]</th><th></table> | |
− | === | + | ===Identification=== |
− | + | When we are building this circuit, we are doing the nucleic acid gel electrophoresis experiment to verify. After the circuit is built, we send the plasmid to sequence, and get the correct sequencing. | |
− | + | After new molecular cloning experiments, we do Enzyme-Cut identification to certify the plasmid is correct. We use the <i>Xba</i>I and <i>Pst</i>I to cut the plasmid, then we getting the target separate fragment-1168bp. (Fig.2) | |
− | + | <table><tr><th>[[File:E1 N.png|thumb|300px|Fig.2 The result of this plasmid cut with enzyme <i>Xba</i>I and <i>Pst</i>I.]]</th><th></table> | |
+ | ===Reference=== | ||
+ | [1] E. Cascales et al., Colicin biology. Microbiol Mol Biol Rev 71, 158-229 (2007). | ||
+ | ===Sequence and Features=== | ||
<partinfo>BBa_K2922027 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2922027 SequenceAndFeatures</partinfo> | ||
Revision as of 13:09, 19 October 2019
Colicin-N coding region
Summary
As a kind of bacteriocin secreted by E.coli, colicin can kill other related bacteria that can’t secret specific immunity proteins. Similar to Colicin-E1, Colicin-N is also a type of pore-forming colicin, encoded by gene cna. This class of transmembrane toxins depolarize the cytoplasmic membrane, leading to dissipation of cellular energy.[1] (Fig.1)
Identification
When we are building this circuit, we are doing the nucleic acid gel electrophoresis experiment to verify. After the circuit is built, we send the plasmid to sequence, and get the correct sequencing. After new molecular cloning experiments, we do Enzyme-Cut identification to certify the plasmid is correct. We use the XbaI and PstI to cut the plasmid, then we getting the target separate fragment-1168bp. (Fig.2)
Reference
[1] E. Cascales et al., Colicin biology. Microbiol Mol Biol Rev 71, 158-229 (2007).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 931
- 1000COMPATIBLE WITH RFC[1000]