College of Clinical Medicine, HuBei University of Science and Technology, Xianning, 437000, Hubei, China.
College of Chemical and Biological Engineering, Hechi University, Hechi, 546300, China.
Curr Microbiol. 2021 Jul;78(7):2569-2576. doi: 10.1007/s00284-021-02513-w. Epub 2021 May 12.
After separation of bacterial colonies on solid plates, purification, and screening through the agar cup-plate method, an antibiotic-resistant bacterial isolate was obtained, and named strain L20190601, the 16S rRNA gene sequence data of strain L20190601 to GenBank, NCBI have provided GenBank accession number MW931615. 16S rRNA gene sequencing revealed that this isolate was highly similar to a number of Streptomyces species. Among them, the homology with S. spectabilis was the highest, reaching 99.9, together with curved hyphal morphology and biochemical tests, allowed us to identify strain L20190601 as S. spectabilis. The red pigment produced by S. spectabilis strain L20190601 was structurally identified. An acid-base color reaction assay showed that when this pigment was dissolved in a solution at pH 3.0 and 9.0, the color of the solution was red and yellow, respectively. In addition, the analysis of absorption spectra revealed that at pH 8.0 and 3.0, the maximum absorption peaks were at 466 and 531 nm, respectively. These results are consistent with the spectral absorption characteristics of metacycloprodigiosin reported in the literature. Moreover, the retention time of purified pigments was identical to those of standard metacycloprodigiosin solutions. Mass spectrometry analysis revealed that the molecular weight of the red compound was 392.2 [M + H]. Finally, metacycloprodigiosin was found to be effective against eight clinically common pathogens: Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Streptococcus pyogenes, Pseudomonas aeruginosa, Bacillus typhi, Candida albicans, and Trichophyton rubrum. In summary, metacycloprodigiosin exhibited strong antibacterial activity and a broad antibacterial spectrum, and thus is a promising compound for the development of a new type of antibacterial drug.
在固体平板上分离细菌菌落、纯化和通过琼脂杯碟法筛选后,获得了一株抗生素抗性细菌分离株,并将其命名为 L20190601 菌株,该菌株的 16S rRNA 基因序列数据已提交给 GenBank,NCBI 提供的 GenBank 登录号为 MW931615。16S rRNA 基因测序表明,该分离株与许多链霉菌属物种高度相似。其中,与壮观链霉菌的同源性最高,达到 99.9%,结合弯曲菌丝形态和生化试验,我们将 L20190601 菌株鉴定为壮观链霉菌。壮观链霉菌 L20190601 产生的红色色素进行了结构鉴定。酸碱颜色反应试验表明,当该色素溶解在 pH 值为 3.0 和 9.0 的溶液中时,溶液的颜色分别为红色和黄色。此外,吸收光谱分析表明,在 pH 值为 8.0 和 3.0 时,最大吸收峰分别位于 466nm 和 531nm。这些结果与文献中报道的变环素光谱吸收特征一致。此外,纯化色素的保留时间与标准变环素溶液的保留时间相同。质谱分析表明,红色化合物的分子量为 392.2[M+H]+。最后,发现变环素对 8 种临床常见病原体有效:金黄色葡萄球菌、枯草芽孢杆菌、大肠杆菌、化脓性链球菌、铜绿假单胞菌、伤寒杆菌、白色念珠菌和红色毛癣菌。总之,变环素表现出较强的抗菌活性和较宽的抗菌谱,因此是开发新型抗菌药物的有前途的化合物。