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Halogenated Metal-Binding Compounds from Shipworm Symbionts
[Image: see text] Bacteria use small molecules to impose strict regulation over the acquisition, uptake, and sequestration of transition metal ions. Low-abundance nutrient metals, such as Fe(III), need to be scavenged from the environment by high-affinity chelating molecules called siderophores. Con...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society and American Society of Pharmacognosy
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961882/ https://www.ncbi.nlm.nih.gov/pubmed/35196451 http://dx.doi.org/10.1021/acs.jnatprod.1c01049 |
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author | Miller, Bailey W. Schmidt, Eric W. Concepcion, Gisela P. Haygood, Margo G. |
author_facet | Miller, Bailey W. Schmidt, Eric W. Concepcion, Gisela P. Haygood, Margo G. |
author_sort | Miller, Bailey W. |
collection | PubMed |
description | [Image: see text] Bacteria use small molecules to impose strict regulation over the acquisition, uptake, and sequestration of transition metal ions. Low-abundance nutrient metals, such as Fe(III), need to be scavenged from the environment by high-affinity chelating molecules called siderophores. Conversely, metal ions that become toxic at high concentrations need to be sequestered and detoxified. Often, bacteria produce a suite of compounds that bind various metal ions at different affinities in order to maintain homeostasis. Turnerbactin, a triscatecholate siderophore isolated from the intracellular shipworm symbiont Teredinibacter turnerae T7901, is responsible for iron regulation and uptake. Herein, another series of compounds are described that complex with iron, copper, and molybdenum in solution. Teredinibactins belong to a class of metal-binding molecules that utilize a phenolate-thiazoline moiety in the coordination of metal ions. In contrast to other compounds in this class, such as yersiniabactin, the phenyl ring is decorated with a 2,4-dihydroxy-3-halo substitution pattern. UV–vis absorption spectroscopy based titration experiments with CuCl(2) show the formation of an intermediate complex at substoichiometric concentrations and conversion to a copper-bound complex at 1:1 molar equiv. |
format | Online Article Text |
id | pubmed-8961882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society and American Society of Pharmacognosy |
record_format | MEDLINE/PubMed |
spelling | pubmed-89618822022-03-30 Halogenated Metal-Binding Compounds from Shipworm Symbionts Miller, Bailey W. Schmidt, Eric W. Concepcion, Gisela P. Haygood, Margo G. J Nat Prod [Image: see text] Bacteria use small molecules to impose strict regulation over the acquisition, uptake, and sequestration of transition metal ions. Low-abundance nutrient metals, such as Fe(III), need to be scavenged from the environment by high-affinity chelating molecules called siderophores. Conversely, metal ions that become toxic at high concentrations need to be sequestered and detoxified. Often, bacteria produce a suite of compounds that bind various metal ions at different affinities in order to maintain homeostasis. Turnerbactin, a triscatecholate siderophore isolated from the intracellular shipworm symbiont Teredinibacter turnerae T7901, is responsible for iron regulation and uptake. Herein, another series of compounds are described that complex with iron, copper, and molybdenum in solution. Teredinibactins belong to a class of metal-binding molecules that utilize a phenolate-thiazoline moiety in the coordination of metal ions. In contrast to other compounds in this class, such as yersiniabactin, the phenyl ring is decorated with a 2,4-dihydroxy-3-halo substitution pattern. UV–vis absorption spectroscopy based titration experiments with CuCl(2) show the formation of an intermediate complex at substoichiometric concentrations and conversion to a copper-bound complex at 1:1 molar equiv. American Chemical Society and American Society of Pharmacognosy 2022-02-23 2022-03-25 /pmc/articles/PMC8961882/ /pubmed/35196451 http://dx.doi.org/10.1021/acs.jnatprod.1c01049 Text en © 2022 The Authors. Published by American Chemical Society and American Society of Pharmacognosy https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Miller, Bailey W. Schmidt, Eric W. Concepcion, Gisela P. Haygood, Margo G. Halogenated Metal-Binding Compounds from Shipworm Symbionts |
title | Halogenated Metal-Binding Compounds from Shipworm
Symbionts |
title_full | Halogenated Metal-Binding Compounds from Shipworm
Symbionts |
title_fullStr | Halogenated Metal-Binding Compounds from Shipworm
Symbionts |
title_full_unstemmed | Halogenated Metal-Binding Compounds from Shipworm
Symbionts |
title_short | Halogenated Metal-Binding Compounds from Shipworm
Symbionts |
title_sort | halogenated metal-binding compounds from shipworm
symbionts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961882/ https://www.ncbi.nlm.nih.gov/pubmed/35196451 http://dx.doi.org/10.1021/acs.jnatprod.1c01049 |
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