Hu Wen-Jin, Deng Li-Xian, Huang Yi-Ying, Wang Xiao-Chun, Qing Jin-Ling, Zhu Hao-Jun, Zhou Xing, Zhou Xiao-Ying, Chu Jie-Mei, Pan Xinli
Institute of Eco-Environmental Research, Guangxi Academy of Sciences, No. 98 Daling Road, Nanning, 530007, China.
Life Science Institute, Guangxi Medical University, No. 22 Shuangyong Road, Nanning, 530021, China.
BMC Microbiol. 2025 Feb 28;25(1):103. doi: 10.1186/s12866-025-03801-2.
The genus Microbacterium in the phylum Actinomycetota contains over 100 species to date that little is known about their bioactive metabolites production. In this study, a mangrove sediment-derived strain B2969 was identified as a novel type strain within the genus Microbacterium due to the low 16S rRNA gene sequence similarity (< 99%), and low overall genome relatedness indices (ANI, 75.4%-79.5%; dDDH, 18.5%-22.7%, AAI, 68.7%-76.3%; POCP, 48.3%-65.0%) with the validly named species of the genus. The type strain B2969 (= MCCC 1K099113 = JCM 36707) is proposed to represent Microbacterium alkaliflavum sp. nov.. The crude extracts of strain B2969 showed weak cytotoxicity against NPC cell lines TW03 and 5-8F, with IC values of ranging from 3.5 µg/µL to 2.4 µg/µL respectively. Genome analysis of strain B2969 found 8 clusters of genes responsible for secondary metabolite biosynthesis, including cytotoxic compounds desferrioxamines. In addition, the application of liquid chromatography tandem mass spectrometry (LC-MS/MS)-based molecular networking strategy led to the identification of 10 compounds with potent cytotoxic activity in ethyl acetate extracts of strain B2969. Results from the cytotoxicity assay, genome mining, and metabolite profiling based on LC-MS/MS analysis revealed its ability to produce bioactive compounds.BackgroundMangrove ecosystems are largely unexplored sources of Actinomycetota, which represent potential important reservoirs of bioactive compounds. The genus Microbacterium in the phylum Actinomycetota contains over 100 species to date that little is known about their bioactive metabolites production. In this study, a novel species, namely B2969, within the genus Microbacterium that showed cytotoxicity against nasopharyngeal carcinoma (NPC) cell lines was isolated from mangrove sediments. Genome mining and metabolic profiling analyses were explored here to assess its biosynthetic potential of metabolites with cytotoxic properties.ResultsHere, a mangrove sediment-derived strain B2969 was identified as a novel species within the genus Microbacterium due to the low 16S rRNA gene sequence similarity (< 99.0%), and low overall genome relatedness indices (ANI, 75.4%-79.5%; dDDH, 18.5%-22.7%, AAI, 68.7%-76.3%; POCP, 48.3%-65.0%) with the type strains of this genus. We proposed that strain B2969 represents a new species, in which the name Microbacterium alkaliflavum sp. nov. is proposed. The strain showed weak cytotoxicity against NPC cell lines TW03 and 5-8F, with IC values of ranging from 3.512 µg/µL to 2.428 µg/µL respectively. Genome analysis of strain B2969 found 8 clusters of genes responsible for secondary metabolite biosynthesis, including desferrioxamines. In addition, the application of liquid chromatography tandem mass spectrometry (LC-MS/MS)-based molecular networking strategy led to the identification of 10 potent cytotoxic compounds in ethyl acetate extracts of strain B2969.ConclusionsThis study confirmed the taxonomy status of type strain B2969 (= MCCC 1K099113 = JCM 36707) within the genus Microbacterium, in which the name Microbacterium alkaliflavum sp. nov.. Results from the cytotoxicity assay, genome mining, and metabolite profiling based on LC-MS/MS analysis revealed its ability to produce bioactive substances, providing sufficient evidence for the potential of Microbacterium species in the discovery of novel pharmaceuticals.
放线菌门中的微杆菌属至今已包含100多个物种,但人们对它们生物活性代谢产物的产生知之甚少。在本研究中,一株源自红树林沉积物的菌株B2969,因其16S rRNA基因序列相似性较低(<99%),以及与该属有效命名物种的整体基因组相关性指数较低(ANI,75.4%-79.5%;dDDH,18.5%-22.7%,AAI,68.7%-76.3%;POCP,48.3%-65.0%),被鉴定为微杆菌属内的一个新型菌株。模式菌株B2969(=MCCC 1K099113 = JCM 36707)被提议代表新种嗜碱黄微杆菌。菌株B2969的粗提物对鼻咽癌细胞系TW03和5-8F显示出较弱的细胞毒性,IC值分别为3.5 μg/μL至2.4 μg/μL。对菌株B2969的基因组分析发现了8个负责次生代谢物生物合成的基因簇,包括细胞毒性化合物去铁胺。此外,基于液相色谱串联质谱(LC-MS/MS)的分子网络策略的应用,使得在菌株B2969的乙酸乙酯提取物中鉴定出10种具有强细胞毒性活性的化合物。细胞毒性测定、基因组挖掘以及基于LC-MS/MS分析的代谢物谱分析结果揭示了其产生生物活性化合物的能力。
背景
红树林生态系统在很大程度上是放线菌门尚未被探索的来源,放线菌门是生物活性化合物潜在的重要储存库。放线菌门中的微杆菌属至今已包含100多个物种,但人们对它们生物活性代谢产物的产生知之甚少。在本研究中,从红树林沉积物中分离出了微杆菌属内的一个新物种,即B2969,它对鼻咽癌(NPC)细胞系显示出细胞毒性。在此进行了基因组挖掘和代谢物谱分析,以评估其产生具有细胞毒性特性的代谢物的生物合成潜力。
结果
在此,一株源自红树林沉积物的菌株B2969,因其16S rRNA基因序列相似性较低(<99.0%),以及与该属模式菌株的整体基因组相关性指数较低(ANI,75.4%-79.5%;dDDH,18.5%-22.7%,AAI,68.7%-76.3%;POCP,48.3%-65.0%),被鉴定为微杆菌属内的一个新物种。我们提议菌株B2969代表一个新物种,并提议将其命名为嗜碱黄微杆菌。该菌株对鼻咽癌细胞系TW03和5-8F显示出较弱的细胞毒性,IC值分别为3.512 μg/μL至2.428 μg/μL。对菌株B2969的基因组分析发现了8个负责次生代谢物生物合成的基因簇,包括去铁胺。此外,基于液相色谱串联质谱(LC-MS/MS)的分子网络策略的应用,使得在菌株B2969的乙酸乙酯提取物中鉴定出10种具有强细胞毒性的化合物。
结论
本研究确定了模式菌株B2969(=MCCC 1K099113 = JCM 36707)在微杆菌属内的分类地位,即嗜碱黄微杆菌新种。细胞毒性测定、基因组挖掘以及基于LC-MS/MS分析的代谢物谱分析结果揭示了其产生生物活性物质的能力,为微杆菌属物种在发现新型药物方面的潜力提供了充分证据。