Difference between revisions of "Part:BBa K2922029"
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===Summary=== | ===Summary=== | ||
Abbreviated as Nkil, lysis protein for Colicin-N is a 5.6 kDa protein, which is encoded by gene <i>cnl</i>. The lysis protein is required for both Colicin-E1 release and partial cell lysis[1]. (Fig.1) | Abbreviated as Nkil, lysis protein for Colicin-N is a 5.6 kDa protein, which is encoded by gene <i>cnl</i>. The lysis protein is required for both Colicin-E1 release and partial cell lysis[1]. (Fig.1) | ||
− | <table><tr><th>[[File:Ndesign.png|thumb| | + | <table><tr><th>[[File:Ndesign.png|thumb|720px|Fig.1 Nkil helps Colicin-N release and makes partial cell lysis.]]</th><th></table> |
===Identification=== | ===Identification=== | ||
− | When we | + | When we were building this circuit, we did the nucleic acid gel electrophoresis experiment to verify. After the circuit is built, we sent the plasmid to sequence, and got the correct sequencing. |
− | After new molecular cloning experiments, we | + | 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-159bp. (Fig.2) |
− | <table><tr><th>[[File:Nkil-Ekil.png|thumb| | + | <table><tr><th>[[File:Nkil-Ekil.png|thumb|720px|Fig.2 The result of this plasmid cut with enzyme <i>Xba</i>I and <i>Pst</i>I.]]</th><th></table> |
===Reference=== | ===Reference=== | ||
[1] A. P. Pugsley, The immunity and lysis genes of ColN plasmid pCHAP4. Molecular & General Genetics Mgg 211, 335-341 (1988). | [1] A. P. Pugsley, The immunity and lysis genes of ColN plasmid pCHAP4. Molecular & General Genetics Mgg 211, 335-341 (1988). |
Revision as of 02:53, 20 October 2019
Lysis protein for colicin-N coding region
Summary
Abbreviated as Nkil, lysis protein for Colicin-N is a 5.6 kDa protein, which is encoded by gene cnl. The lysis protein is required for both Colicin-E1 release and partial cell lysis[1]. (Fig.1)
Identification
When we were building this circuit, we did the nucleic acid gel electrophoresis experiment to verify. After the circuit is 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-159bp. (Fig.2)
Reference
[1] A. P. Pugsley, The immunity and lysis genes of ColN plasmid pCHAP4. Molecular & General Genetics Mgg 211, 335-341 (1988).
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 118
- 1000COMPATIBLE WITH RFC[1000]