Colicin: Difference between revisions
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**[[4v5k]] – EcColE3 cytotoxic domain (mutant) + Tt30S ribosome – ''Thermos thermophilus''<br /> | **[[4v5k]] – EcColE3 cytotoxic domain (mutant) + Tt30S ribosome – ''Thermos thermophilus''<br /> | ||
**[[2zld]] - EcColE3 cytotoxic domain + outer membrane protein F<br /> | **[[2zld]] - EcColE3 cytotoxic domain + outer membrane protein F<br /> | ||
**[[1jch]] – EcColE3 + EcColE3 immunity protein<br /> | **[[1jch]], [[4udm]] – EcColE3 + EcColE3 immunity protein<br /> | ||
**[[2b5u]] – EcColE3 (mutant) + EcColE3 immunity protein<br /> | **[[2b5u]] – EcColE3 (mutant) + EcColE3 immunity protein<br /> | ||
**[[1e44]] – EcColE3 nuclease domain + EcColE3 immunity protein<br /> | **[[1e44]] – EcColE3 nuclease domain + EcColE3 immunity protein<br /> | ||
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**[[2wpt]] – EcColE9 (mutant) + EcColE2 immunity protein<br /> | **[[2wpt]] – EcColE9 (mutant) + EcColE2 immunity protein<br /> | ||
**[[2k5x]], [[1emv]], [[1bxi]] – EcColE9 DNase domain + EcColE9 immunity protein<br /> | **[[2k5x]], [[1emv]], [[1bxi]] – EcColE9 DNase domain + EcColE9 immunity protein<br /> | ||
**[[2vln]], [[2vlo]], [[2vlp]], [[2vlq]] - EcColE9 DNase domain (mutant) + EcColE9 immunity protein<br /> | **[[2vln]], [[2vlo]], [[2vlp]], [[2vlq]], [[5ew5]] - EcColE9 DNase domain (mutant) + EcColE9 immunity protein<br /> | ||
**[[2gze]], [[2gzg]], [[2gzi]], [[2gzj]], [[2gzf]], [[2gyk]], [[1fr2]] - EcColE9 DNase domain + EcColE9 immunity protein (mutant)<br /> | **[[2gze]], [[2gzg]], [[2gzi]], [[2gzj]], [[2gzf]], [[2gyk]], [[1fr2]] - EcColE9 DNase domain + EcColE9 immunity protein (mutant)<br /> | ||
**[[2ivz]] - EcColE9 T domain + TolB<br /> | **[[2ivz]], [[4jml]] - EcColE9 T domain + TolB<br /> | ||
**[[3o0e]] - EcColE9 fragment + outer membrane porin 1A | **[[3o0e]] - EcColE9 fragment + outer membrane porin 1A | ||
Revision as of 10:08, 3 April 2017
Colicins are a type of bacteriocin - peptide and protein antibiotics released by bacteria to kill other bacteria of the same species, in order to provide a competitive advantage for nutrient acquisition [1]. Bacteriocins are named after their species of origin; colicins are so-called because they are produced by E. Coli[2]. Because of their narrow killing spectrum which focuses primarily on the species which has made the peptide (or occasionally closely related species[3]), bacteriocins are important in microbial biodiversity and the stable co-existence of the bacterial populations[4][5]. Colicin peptides are plasmid-encoded. The peptide is released by the cell into the area surrounding it, and then parasitises proteins present in the host cell membrane to translocate across into the host cell. Many protein-protein interactions are involved in the cell entry, and the main system is involved in the grouping of colicins into two families: Group A colicins use the Tol system to enter the host cell, and Group B use the Ton system. Once inside the host cell, the cell killing follows 1st order kinetics - ie one molecule is theoretically sufficient to kill the cell[6]. The structure of all colicins, of which over 20 have been identified, follows a 3 domain design:
Some colicins exhibit DNase Activity and others TRNase activity. For more details see also ContentsSynthesis, Production and ReleaseSynthesis of many colicins is repressed by the LexA protein, which is part of the SOS regulon[8]. Targeting and ReceptorsColicins vary significantly in the receptors that they target to initiate their uptake. The majority of the group A colicins use the BtuB receptor, which is present on E. coli as a vitamin B12 uptake receptor. Once bound to the receptor, the coiled-coil receptor binding domain unfolds, in an essential step that removes the immunity protein and triggers translocation[9]. Other colicins use other receptors - generally involved in the uptake of small metabolite growth factors. Colicin UptakeColicins are divided into two groups depending on the method of uptake which they target. Group A colicins use the Tol system to bind to and enter the target cell, and group B use the Ton system. The Tol system consists of 5 proteins - TolA, TolB, TolR, TolQ and Pal[10], and group A proteins using this often recruit a second co-receptor involved in translocation, usually OmpF or TolC, but could be OmpC and PhoE[11]. The Ton system consists of TonB, ExbB and ExbD[12], and no known co-receptor is utilised in translocation[13].It could be possible that Ton-dependent colicins are indiscriminate in use of coreceptors, or that the colicins move down the outside wall of a β barrel protein[14]. It is known that colicins do unfold during translocation, but the peptides resulting from this exceed the diameter of pores formed by any of the molecules mentioned above[15][16]. However, while unfolding does occur, this is not induced by receptor binding in either Tol or Ton dependent colicins[17]. Understanding how the colicins can cross the membrane is highly important, as if this could be targeted and exploited it could be useful for novel therapeutic agents[18]. It is also estimated that a single colicin molecule is sufficient to kill the bacterial cell, following first order kinetics[19]. Killing ActivitiesColicins kill their target cell through a variety of different methods. The main killing activities are carried out through Pore Formation, DNase Activity and 16s rRNase activity, and some colicins also exhibit tRNase activity. The killing activities carried out by colicins could be used medicinally as an alternative to antibiotics in the case where the specific strain of E. coli can be identified[20], and as potential natural replacements for food preservatives[21].
Table taken from [51] except where indicated. SEE ALSO
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3D structure of Colicin
Updated on 03-April-2017
- Colicin-A
- Tol, Ton – CfColA translocation domain + EcTolB – Citrobacter freundii
- Translocation domain – EcColA pore-forming domain
- Tol, Ton – CfColA translocation domain + EcTolB – Citrobacter freundii
- Colicin-B
- DNase Activity - EcColB
- Colicin-D
- TRNase activity, Pore Formation, Translocation domain - EcColD catalytic domain + EcColD immunity protein
- TRNase activity, Pore Formation, Translocation domain - EcColD catalytic domain + EcColD immunity protein
- Colicin-E1
- H-N-H motif – EcColE1 channel-forming domain
- Colicin-E2
- Colicin A – EcColE2 receptor-binding domain + BtuB
- 16s rRNase activity – EcColE2 nuclease domain + EcColE2 immunity protein
- Colicin A – EcColE2 receptor-binding domain + BtuB
- Colicin-E3
- Colicin Ia – EcColE3 cytotoxic domain (mutant) + Tt30S ribosome – Thermos thermophilus
- BtuB - EcColE3 cytotoxic domain + outer membrane protein F
- TolA, TolB – EcColE3 + EcColE3 immunity protein
- TolR – EcColE3 (mutant) + EcColE3 immunity protein
- TolQ – EcColE3 nuclease domain + EcColE3 immunity protein
- Pal – EcColE3 receptor-binding domain + BtuB
- Colicin Ia – EcColE3 cytotoxic domain (mutant) + Tt30S ribosome – Thermos thermophilus
- Colicin-E5
- Colicin-E7
- ExbD - EcColE7
- Pore Formation - EcColE7 translocation domain
- DNase Activity, 16s rRNase activity - EcColE7 nuclease domain
- tRNase activity, Colicin A, Tol – EcColE7 (mutant) + DNA
- Colicin_Immunity_Protein - EcColE7 nuclease domain + DNA
- Colicin E1, ImmE1 - EcColE7 nuclease domain + EcColE7 immunity protein
- Colicin E2 - EcColE7 nuclease domain + EcColE9 immunity protein (mutant)
- Im2 - EcColE7 nuclease domain (mutant) + EcColE9 immunity protein (mutant)
- Colicin E3, Im3, Colicin E4, Im4 - EcColE7 nuclease domain (mutant) + EcColE7 immunity protein
- Colicin E5, ImmE5 - EcColE7 (mutant) + EcColE7 immunity protein (mutant)
- ExbD - EcColE7
- Colicin-E9
- Colicin E6 - EcColE9 DNase domain
- ImmE6 - EcColE9 DNase domain (mutant)
- Colicin E7, Im7 - EcColE9 DNase domain (mutant) + DNA
- Colicin E8 – EcColE9 (mutant) + EcColE2 immunity protein
- Im8, Colicin E9, Im9 – EcColE9 DNase domain + EcColE9 immunity protein
- Colicin N, Cni, Colicin S4, Csi, Colicin K - EcColE9 DNase domain (mutant) + EcColE9 immunity protein
- Cloacin DF13, Colicin U, Cui, Colicin 5, Ton, ExbB, Cfi - EcColE9 DNase domain + EcColE9 immunity protein (mutant)
- Colicin 6, Colicin 7 - EcColE9 T domain + TolB
- Colicin 8 - EcColE9 fragment + outer membrane porin 1A
- Colicin E6 - EcColE9 DNase domain
- Colicin-Ia
- Colicin 9 - EcColIa
- Colicin 10 – EcColIA R domain + ColI receptor
- Colicin 9 - EcColIa
- Colicin-M
- Cti, Colicin Ia, Iia – EcColM
- Colicin Ib, Imm – EcColM (mutant)
- Cti, Colicin Ia, Iia – EcColM
- Colicin-N
- Colicin B – EcColN receptor-binding domain
- Colicin-S4
- Cbi – EcColS4
References
Proteopedia Page Contributors and Editors (what is this?)
Gemma McGoldrick, Michal Harel, Jaime Prilusky, Alexander Berchansky

