180 related articles for article (PubMed ID: 18502859)
1. The production in vivo of microcin E492 with antibacterial activity depends on salmochelin and EntF.
Mercado G; Tello M; Marín M; Monasterio O; Lagos R
J Bacteriol; 2008 Aug; 190(15):5464-71. PubMed ID: 18502859
[TBL] [Abstract][Full Text] [Related]
2. Insight into siderophore-carrying peptide biosynthesis: enterobactin is a precursor for microcin E492 posttranslational modification.
Vassiliadis G; Peduzzi J; Zirah S; Thomas X; Rebuffat S; Destoumieux-Garzón D
Antimicrob Agents Chemother; 2007 Oct; 51(10):3546-53. PubMed ID: 17646411
[TBL] [Abstract][Full Text] [Related]
3. The Ferric uptake regulator (Fur) and iron availability control the production and maturation of the antibacterial peptide microcin E492.
Marcoleta AE; Gutiérrez-Cortez S; Hurtado F; Argandoña Y; Corsini G; Monasterio O; Lagos R
PLoS One; 2018; 13(8):e0200835. PubMed ID: 30071030
[TBL] [Abstract][Full Text] [Related]
4. The expression of genes involved in microcin maturation regulates the production of active microcin E492.
Corsini G; Baeza M; Monasterio O; Lagos R
Biochimie; 2002; 84(5-6):539-44. PubMed ID: 12423798
[TBL] [Abstract][Full Text] [Related]
5. Structure, organization and characterization of the gene cluster involved in the production of microcin E492, a channel-forming bacteriocin.
Lagos R; Baeza M; Corsini G; Hetz C; Strahsburger E; Castillo JA; Vergara C; Monasterio O
Mol Microbiol; 2001 Oct; 42(1):229-43. PubMed ID: 11679081
[TBL] [Abstract][Full Text] [Related]
6. Microcin e492 amyloid formation is retarded by posttranslational modification.
Marcoleta A; Marín M; Mercado G; Valpuesta JM; Monasterio O; Lagos R
J Bacteriol; 2013 Sep; 195(17):3995-4004. PubMed ID: 23836864
[TBL] [Abstract][Full Text] [Related]
7. Cooperative uptake of microcin E492 by receptors FepA, Fiu, and Cir and inhibition by the siderophore enterochelin and its dimeric and trimeric hydrolysis products.
Strahsburger E; Baeza M; Monasterio O; Lagos R
Antimicrob Agents Chemother; 2005 Jul; 49(7):3083-6. PubMed ID: 15980406
[TBL] [Abstract][Full Text] [Related]
8. Antibacterial and antitumorigenic properties of microcin E492, a pore-forming bacteriocin.
Lagos R; Tello M; Mercado G; García V; Monasterio O
Curr Pharm Biotechnol; 2009 Jan; 10(1):74-85. PubMed ID: 19149591
[TBL] [Abstract][Full Text] [Related]
9. Involvement of enterobactin synthesis pathway in production of microcin H47.
Azpiroz MF; Laviña M
Antimicrob Agents Chemother; 2004 Apr; 48(4):1235-41. PubMed ID: 15047525
[TBL] [Abstract][Full Text] [Related]
10. Parasitism of iron-siderophore receptors of Escherichia coli by the siderophore-peptide microcin E492m and its unmodified counterpart.
Destoumieux-Garzón D; Peduzzi J; Thomas X; Djediat C; Rebuffat S
Biometals; 2006 Apr; 19(2):181-91. PubMed ID: 16718603
[TBL] [Abstract][Full Text] [Related]
11. The activity of microcin E492 from Klebsiella pneumoniae is regulated by a microcin antagonist.
Orellana C; Lagos R
FEMS Microbiol Lett; 1996 Mar; 136(3):297-303. PubMed ID: 8867383
[TBL] [Abstract][Full Text] [Related]
12. Catecholate siderophore esterases Fes, IroD and IroE are required for salmochelins secretion following utilization, but only IroD contributes to virulence of extra-intestinal pathogenic Escherichia coli.
Caza M; Garénaux A; Lépine F; Dozois CM
Mol Microbiol; 2015 Aug; 97(4):717-32. PubMed ID: 25982934
[TBL] [Abstract][Full Text] [Related]
13. Reconstitution and characterization of the Escherichia coli enterobactin synthetase from EntB, EntE, and EntF.
Gehring AM; Mori I; Walsh CT
Biochemistry; 1998 Feb; 37(8):2648-59. PubMed ID: 9485415
[TBL] [Abstract][Full Text] [Related]
14. Dissection of the EntF condensation domain boundary and active site residues in nonribosomal peptide synthesis.
Roche ED; Walsh CT
Biochemistry; 2003 Feb; 42(5):1334-44. PubMed ID: 12564937
[TBL] [Abstract][Full Text] [Related]
15. The colicin G, H and X determinants encode microcins M and H47, which might utilize the catecholate siderophore receptors FepA, Cir, Fiu and IroN.
Patzer SI; Baquero MR; Bravo D; Moreno F; Hantke K
Microbiology (Reading); 2003 Sep; 149(Pt 9):2557-2570. PubMed ID: 12949180
[TBL] [Abstract][Full Text] [Related]
16. Assembly line enzymology by multimodular nonribosomal peptide synthetases: the thioesterase domain of E. coli EntF catalyzes both elongation and cyclolactonization.
Shaw-Reid CA; Kelleher NL; Losey HC; Gehring AM; Berg C; Walsh CT
Chem Biol; 1999 Jun; 6(6):385-400. PubMed ID: 10375542
[TBL] [Abstract][Full Text] [Related]
17. Investigations of the MceIJ-catalyzed posttranslational modification of the microcin E492 C-terminus: linkage of ribosomal and nonribosomal peptides to form "trojan horse" antibiotics.
Nolan EM; Walsh CT
Biochemistry; 2008 Sep; 47(35):9289-99. PubMed ID: 18690711
[TBL] [Abstract][Full Text] [Related]
18. Effect of norepinephrine on colonisation and systemic spread of Salmonella enterica in infected animals: role of catecholate siderophore precursors and degradation products.
Methner U; Rabsch W; Reissbrodt R; Williams PH
Int J Med Microbiol; 2008 Jul; 298(5-6):429-39. PubMed ID: 17888732
[TBL] [Abstract][Full Text] [Related]
19. Interdomain communication between the thiolation and thioesterase domains of EntF explored by combinatorial mutagenesis and selection.
Zhou Z; Lai JR; Walsh CT
Chem Biol; 2006 Aug; 13(8):869-79. PubMed ID: 16931336
[TBL] [Abstract][Full Text] [Related]
20. The synergistic triad between microcin, colibactin, and salmochelin gene clusters in uropathogenic Escherichia coli.
Massip C; Chagneau CV; Boury M; Oswald E
Microbes Infect; 2020 Apr; 22(3):144-147. PubMed ID: 31954842
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]