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Dual Agents: Fungal Macrocidins and Synthetic Analogues with Herbicidal and Antibiofilm Activities
Eight analogues of the bioherbicides macrocidin A (1) and Z (2) with structural variance in the size of the macrocycle, its para- or meta-cyclophane character, and its functional groups were synthesized on two modular routes and tested for herbicidal, antibiotic, and antibiofilm activities. Apart fr...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388955/ https://www.ncbi.nlm.nih.gov/pubmed/34439072 http://dx.doi.org/10.3390/antibiotics10081022 |
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author | Treiber, Laura Pezolt, Christine Zeng, Haoxuan Schrey, Hedda Jungwirth, Stefan Shekhar, Aditya Stadler, Marc Bilitewski, Ursula Erb-Brinkmann, Maike Schobert, Rainer |
author_facet | Treiber, Laura Pezolt, Christine Zeng, Haoxuan Schrey, Hedda Jungwirth, Stefan Shekhar, Aditya Stadler, Marc Bilitewski, Ursula Erb-Brinkmann, Maike Schobert, Rainer |
author_sort | Treiber, Laura |
collection | PubMed |
description | Eight analogues of the bioherbicides macrocidin A (1) and Z (2) with structural variance in the size of the macrocycle, its para- or meta-cyclophane character, and its functional groups were synthesized on two modular routes and tested for herbicidal, antibiotic, and antibiofilm activities. Apart from the lead compounds 1 and 2, the structurally simplified dihydromacrocidin Z (3) and normacrocidin Z (4) showed high herbicidal activity in either thistles, dandelions or in both. The derivatives 2, 3, and dibromide 9 also inhibited the growth of Staphylococcus aureus biofilms by ca 70% when applied at subtoxic concentrations as low as ca 20 µM, which are unlikely to induce bacterial resistance. They also led to the dispersion of preformed biofilms of S. aureus, exceeding a similar effect by microporenic acid A, a known biofilm inhibitor. Compounds 3 and 9 showed no noticeable cytotoxicity against human cancer and endothelial cells at concentrations below 50 µM, making them conceivable candidates for application as anti-biofilm agents in a medicinal context. |
format | Online Article Text |
id | pubmed-8388955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83889552021-08-27 Dual Agents: Fungal Macrocidins and Synthetic Analogues with Herbicidal and Antibiofilm Activities Treiber, Laura Pezolt, Christine Zeng, Haoxuan Schrey, Hedda Jungwirth, Stefan Shekhar, Aditya Stadler, Marc Bilitewski, Ursula Erb-Brinkmann, Maike Schobert, Rainer Antibiotics (Basel) Article Eight analogues of the bioherbicides macrocidin A (1) and Z (2) with structural variance in the size of the macrocycle, its para- or meta-cyclophane character, and its functional groups were synthesized on two modular routes and tested for herbicidal, antibiotic, and antibiofilm activities. Apart from the lead compounds 1 and 2, the structurally simplified dihydromacrocidin Z (3) and normacrocidin Z (4) showed high herbicidal activity in either thistles, dandelions or in both. The derivatives 2, 3, and dibromide 9 also inhibited the growth of Staphylococcus aureus biofilms by ca 70% when applied at subtoxic concentrations as low as ca 20 µM, which are unlikely to induce bacterial resistance. They also led to the dispersion of preformed biofilms of S. aureus, exceeding a similar effect by microporenic acid A, a known biofilm inhibitor. Compounds 3 and 9 showed no noticeable cytotoxicity against human cancer and endothelial cells at concentrations below 50 µM, making them conceivable candidates for application as anti-biofilm agents in a medicinal context. MDPI 2021-08-23 /pmc/articles/PMC8388955/ /pubmed/34439072 http://dx.doi.org/10.3390/antibiotics10081022 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Treiber, Laura Pezolt, Christine Zeng, Haoxuan Schrey, Hedda Jungwirth, Stefan Shekhar, Aditya Stadler, Marc Bilitewski, Ursula Erb-Brinkmann, Maike Schobert, Rainer Dual Agents: Fungal Macrocidins and Synthetic Analogues with Herbicidal and Antibiofilm Activities |
title | Dual Agents: Fungal Macrocidins and Synthetic Analogues with Herbicidal and Antibiofilm Activities |
title_full | Dual Agents: Fungal Macrocidins and Synthetic Analogues with Herbicidal and Antibiofilm Activities |
title_fullStr | Dual Agents: Fungal Macrocidins and Synthetic Analogues with Herbicidal and Antibiofilm Activities |
title_full_unstemmed | Dual Agents: Fungal Macrocidins and Synthetic Analogues with Herbicidal and Antibiofilm Activities |
title_short | Dual Agents: Fungal Macrocidins and Synthetic Analogues with Herbicidal and Antibiofilm Activities |
title_sort | dual agents: fungal macrocidins and synthetic analogues with herbicidal and antibiofilm activities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388955/ https://www.ncbi.nlm.nih.gov/pubmed/34439072 http://dx.doi.org/10.3390/antibiotics10081022 |
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