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A Fluorescent Teixobactin Analogue
Author(s) -
Michael A. Morris,
Melody Malek,
Mohammad H Hashemian,
Betty T Nguyen,
Sylvie Manuse,
Kim Lewis,
James S. Nowick
Publication year - 2020
Publication title -
acs chemical biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.899
H-Index - 111
eISSN - 1554-8937
pISSN - 1554-8929
DOI - 10.1021/acschembio.9b00908
Subject(s) - biochemistry , bacteria , biology , fluorescence , peptide , depsipeptide , chemistry , genetics , physics , quantum mechanics
This report describes the first synthesis and application of a fluorescent teixobactin analogue that exhibits antibiotic activity and binds to the cell walls of Gram-positive bacteria. The teixobactin analogue, Lys(Rhod) 9 ,Arg 10 -teixobactin, has a fluorescent tag at position 9 and an arginine in place of the natural allo -enduracididine residue at position 10. The fluorescent teixobactin analogue retains partial antibiotic activity, with minimum inhibitory concentrations of 4-8 μg/mL across a panel of Gram-positive bacteria, as compared to 1-4 μg/mL for the unlabeled Arg 10 -teixobactin analogue. Lys(Rhod) 9 ,Arg 10 -teixobactin is prepared by a regioselective labeling strategy that labels Lys 9 with an amine-reactive rhodamine fluorophore during solid-phase peptide synthesis, with the resulting conjugate tolerating subsequent solid-phase peptide synthesis reactions. Treatment of Gram-positive bacteria with Lys(Rhod) 9 ,Arg 10 -teixobactin results in septal and lateral staining, which is consistent with an antibiotic targeting cell wall precursors. Concurrent treatment of Lys(Rhod) 9 ,Arg 10 -teixobactin and BODIPY FL vancomycin results in septal colocalization, providing further evidence that Lys(Rhod) 9 ,Arg 10 -teixobactin binds to cell wall precursors. Controls with either Gram-negative bacteria, or an inactive fluorescent homologue with Gram-positive bacteria, showed little or no staining in fluorescence micrographic studies. Lys(Rhod) 9 ,Arg 10 -teixobactin can thus serve as a functional probe to study Gram-positive bacteria and their interactions with teixobactin.

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