Difference between revisions of "Part:BBa K2922024"
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<partinfo>BBa_K2922024 short</partinfo> | <partinfo>BBa_K2922024 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. | ||
+ | For Colicin-E1, it is a type of pore-forming colicin encoded by gene <i>cea</i>.This class of transmembrane toxins depolarize the cytoplasmic membrane, leading to dissipation of cellular energy.<ref>[1]https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847374/</ref>.(Fig.1) | ||
+ | <table><tr><th>[[File:E1design.png|thumb|720px|Fig.1 Colicin-E1 can kill other bacteria.]]</th><th></table> | ||
+ | ===Identification=== | ||
+ | When we were building this circuit, we did the nucleic acid gel electrophoresis experiment to verify. After the circuit was built, we sent the plasmid to sequence, and got the correct sequencing. | ||
+ | After new molecular cloning experiments, we did Enzyme-Cut identification to certify the plasmid was correct. We used the <i>Xba</i>I and <i>Pst</i>I to cut the plasmid, then we got the target separate fragment-1569bp. (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> | ||
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− | + | ===Sequence and Features=== | |
− | === | + | |
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<partinfo>BBa_K2922024 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2922024 SequenceAndFeatures</partinfo> | ||
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<partinfo>BBa_K2922024 parameters</partinfo> | <partinfo>BBa_K2922024 parameters</partinfo> | ||
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+ | ===Reference=== |
Latest revision as of 17:47, 20 October 2019
Colicin-E1 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. For Colicin-E1, it is a type of pore-forming colicin encoded by gene cea.This class of transmembrane toxins depolarize the cytoplasmic membrane, leading to dissipation of cellular energy.[1].(Fig.1)
Identification
When we were building this circuit, we did the nucleic acid gel electrophoresis experiment to verify. After the circuit was built, we sent the plasmid to sequence, and got the correct sequencing. After new molecular cloning experiments, we did Enzyme-Cut identification to certify the plasmid was correct. We used the XbaI and PstI to cut the plasmid, then we got the target separate fragment-1569bp. (Fig.2)
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 1312
Illegal AgeI site found at 1369
Illegal AgeI site found at 1501 - 1000COMPATIBLE WITH RFC[1000]