Clericuzio Marco, Novello Giorgia, Bivona Mattia, Gamalero Elisa, Bona Elisa, Caramaschi Alice, Massa Nadia, Asteggiano Alberto, Medana Claudio
Dipartimento di Scienze e Innovazione Tecnologica, Università del Piemonte Orientale, Viale T. Michel 11, 15121 Alessandria, Italy.
Dipartimento per lo Sviluppo Sostenibile e la Transizione Ecologica, Università del Piemonte Orientale, Piazza San Eusebio 5, 13100 Vercelli, Italy.
Antibiotics (Basel). 2024 Apr 3;13(4):326. doi: 10.3390/antibiotics13040326.
The World Health Organization (WHO) promotes research aimed at developing new drugs from natural compounds. Fungi are important producers of bioactive molecules, and they are often effective against other fungi and/or bacteria and are thus a potential source of new antibiotics. Basidiomycota crude extracts, which have previously been proven to be active against ATCC27853, were subjected to liquid chromatographic separation by RP-18, leading to six macro-fractions for each fungal extract. The various fractions were tested for their bioactivities against ATCC27853, and ten of them were characterized by HPLC-HRMS and NMR. Further chromatographic separations were performed for a few selected macro-fractions, yielding seven pure compounds. Bioactivity was mainly found in the lipophilic fractions containing fatty acids and their derivatives, such as hydroxy or keto C-18 unsaturated acids, and in various complex lipids, such as glycolipids and related compounds. More hydrophilic molecules, such as GABA, phenethylamine, two chromogenic anthraquinoids and pistillarin, were also isolated, and their antibacterial activities were recorded. The novelties of this research are as follows: (i) the genera and have never been investigated before for the synthesis of antibiotic compounds; (ii) the molecules produced by these genera are known, but their production has never been reported in the investigated fungi; (iii) the determination of bacterial siderophore synthesis inhibition by certain compounds from and .
世界卫生组织(WHO)推动旨在从天然化合物开发新药的研究。真菌是生物活性分子的重要生产者,它们通常对其他真菌和/或细菌有效,因此是新抗生素的潜在来源。先前已证明对ATCC27853有活性的担子菌粗提物,通过RP - 18进行液相色谱分离,每种真菌提取物得到六个大组分。测试了各个组分对ATCC27853的生物活性,其中十个通过HPLC - HRMS和NMR进行了表征。对一些选定的大组分进行了进一步的色谱分离,得到了七种纯化合物。生物活性主要存在于含有脂肪酸及其衍生物(如羟基或酮基C - 18不饱和酸)的亲脂性组分中,以及各种复杂脂质(如糖脂和相关化合物)中。还分离出了更多亲水性分子,如GABA、苯乙胺、两种显色蒽醌和 pistillarin,并记录了它们的抗菌活性。本研究的新颖之处如下:(i)以前从未研究过[具体属名缺失]属用于合成抗生素化合物;(ii)这些属产生的分子是已知的,但在被研究的真菌中从未有过其产生的报道;(iii)测定了[具体属名缺失]属某些化合物对细菌铁载体合成的抑制作用。