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δ-Lactones—A New Class of Compounds That Are Toxic to E. coli K12 and R2–R4 Strains
Lactones are among the well-known organic substances with a specific taste and smell. They are characterized by antibacterial, antiviral, anti-inflammatory, and anti-cancer properties. In recent years, among this group of compounds, new biologically active substances have been searched by modifying...
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/PMC8199173/ https://www.ncbi.nlm.nih.gov/pubmed/34070884 http://dx.doi.org/10.3390/ma14112956 |
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author | Kowalczyk, Paweł Gawdzik, Barbara Trzepizur, Damian Szymczak, Mateusz Skiba, Grzegorz Raj, Stanisława Kramkowski, Karol Lizut, Rafał Ostaszewski, Ryszard |
author_facet | Kowalczyk, Paweł Gawdzik, Barbara Trzepizur, Damian Szymczak, Mateusz Skiba, Grzegorz Raj, Stanisława Kramkowski, Karol Lizut, Rafał Ostaszewski, Ryszard |
author_sort | Kowalczyk, Paweł |
collection | PubMed |
description | Lactones are among the well-known organic substances with a specific taste and smell. They are characterized by antibacterial, antiviral, anti-inflammatory, and anti-cancer properties. In recent years, among this group of compounds, new biologically active substances have been searched by modifying the main (leading) structure with new analogs with stronger or different responses that may have a toxic effect on the cells of pathogenic bacteria and constitute an alternative to commonly used antibiotics. A preliminary study of δ-lactone derivatives as new potential candidates for antibacterial drugs was conducted. Particular emphasis was placed on the selection of the structure of lactones with the highest biological activity, especially those with fluorine in their structure as a substituent in terms of action on bacterial lipopolysaccharide (LPS) in the model strains of Escherichia coli K12 (without LPS in its structure) and R2–R4 (LPS of different lengths in its structure). In the presented studies, on the basis of the conducted MIC and MBC tests, it was shown that the antibacterial (toxic) activity of lactones depends on their structure and the length of the bacterial LPS in the membrane of specific strains. Moreover, oxidative damage of bacterial DNA isolated from bacteria after modification with newly synthesized compounds after application of the repair enzyme Fpg glycosylase was analyzed. The analyzed damage values were compared with the modification with appropriate antibiotics: ciprofloxacin, bleomycin, and cloxacillin. The presented research clearly shows that lactone derivatives can be potential candidates as substitutes for drugs, e.g., the analyzed antibiotics. Their chemical and biological activity is related to coumarin derivatives and the corresponding δ-lactone groups in the structure of the substituent. The observed results are of particular importance in the case of increasing bacterial resistance to various drugs and antibiotics, especially in nosocomial infections and neoplasms, and in the era of a microbial pandemic. |
format | Online Article Text |
id | pubmed-8199173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81991732021-06-14 δ-Lactones—A New Class of Compounds That Are Toxic to E. coli K12 and R2–R4 Strains Kowalczyk, Paweł Gawdzik, Barbara Trzepizur, Damian Szymczak, Mateusz Skiba, Grzegorz Raj, Stanisława Kramkowski, Karol Lizut, Rafał Ostaszewski, Ryszard Materials (Basel) Article Lactones are among the well-known organic substances with a specific taste and smell. They are characterized by antibacterial, antiviral, anti-inflammatory, and anti-cancer properties. In recent years, among this group of compounds, new biologically active substances have been searched by modifying the main (leading) structure with new analogs with stronger or different responses that may have a toxic effect on the cells of pathogenic bacteria and constitute an alternative to commonly used antibiotics. A preliminary study of δ-lactone derivatives as new potential candidates for antibacterial drugs was conducted. Particular emphasis was placed on the selection of the structure of lactones with the highest biological activity, especially those with fluorine in their structure as a substituent in terms of action on bacterial lipopolysaccharide (LPS) in the model strains of Escherichia coli K12 (without LPS in its structure) and R2–R4 (LPS of different lengths in its structure). In the presented studies, on the basis of the conducted MIC and MBC tests, it was shown that the antibacterial (toxic) activity of lactones depends on their structure and the length of the bacterial LPS in the membrane of specific strains. Moreover, oxidative damage of bacterial DNA isolated from bacteria after modification with newly synthesized compounds after application of the repair enzyme Fpg glycosylase was analyzed. The analyzed damage values were compared with the modification with appropriate antibiotics: ciprofloxacin, bleomycin, and cloxacillin. The presented research clearly shows that lactone derivatives can be potential candidates as substitutes for drugs, e.g., the analyzed antibiotics. Their chemical and biological activity is related to coumarin derivatives and the corresponding δ-lactone groups in the structure of the substituent. The observed results are of particular importance in the case of increasing bacterial resistance to various drugs and antibiotics, especially in nosocomial infections and neoplasms, and in the era of a microbial pandemic. MDPI 2021-05-30 /pmc/articles/PMC8199173/ /pubmed/34070884 http://dx.doi.org/10.3390/ma14112956 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 Kowalczyk, Paweł Gawdzik, Barbara Trzepizur, Damian Szymczak, Mateusz Skiba, Grzegorz Raj, Stanisława Kramkowski, Karol Lizut, Rafał Ostaszewski, Ryszard δ-Lactones—A New Class of Compounds That Are Toxic to E. coli K12 and R2–R4 Strains |
title | δ-Lactones—A New Class of Compounds That Are Toxic to E. coli K12 and R2–R4 Strains |
title_full | δ-Lactones—A New Class of Compounds That Are Toxic to E. coli K12 and R2–R4 Strains |
title_fullStr | δ-Lactones—A New Class of Compounds That Are Toxic to E. coli K12 and R2–R4 Strains |
title_full_unstemmed | δ-Lactones—A New Class of Compounds That Are Toxic to E. coli K12 and R2–R4 Strains |
title_short | δ-Lactones—A New Class of Compounds That Are Toxic to E. coli K12 and R2–R4 Strains |
title_sort | δ-lactones—a new class of compounds that are toxic to e. coli k12 and r2–r4 strains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199173/ https://www.ncbi.nlm.nih.gov/pubmed/34070884 http://dx.doi.org/10.3390/ma14112956 |
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