Institute for Microbial Biotechnology and Metagenomics (IMBM), Department of Biotechnology, University of the Western Cape, Robert Sobukwe Road, Bellville, Cape Town 7535, South Africa.
Marbio, UiT-The Arctic University of Norway, N-9037 Tromsø, Norway.
Mar Drugs. 2022 Dec 20;21(1):2. doi: 10.3390/md21010002.
Bacterial symbionts of marine invertebrates are rich sources of novel, pharmaceutically relevant natural products that could become leads in combatting multidrug-resistant pathogens and treating disease. In this study, the bioactive potential of the marine invertebrate symbiont was investigated. Bioactivity screening of the strain revealed Gram-positive specific antibacterial activity as well as cytotoxic activity against a human melanoma cell line (A2058). The dereplication of the active fraction using HPLC-MS led to the isolation and structural elucidation of cholic acid and 3-oxo cholic acid. is one of three type species belonging to the genus . The ability to generate cholic acid was assessed for all three species using thin-layer chromatography and was confirmed by LC-MS. The re-sequencing of all three type species using long-read Oxford Nanopore Technology (ONT) and Illumina data produced complete genomes, enabling the bioinformatic assessment of the ability of the strains to produce cholic acid. Although a complete biosynthetic pathway for cholic acid synthesis in this genus could not be determined based on sequence-based homology searches, the identification of putative penicillin or homoserine lactone acylases in all three species suggests a mechanism for the hydrolysis of conjugated bile acids present in the growth medium, resulting in the generation of cholic acid and 3-oxo cholic acid. With little known currently about the bioactivities of this genus, this study serves as the foundation for future investigations into their bioactive potential as well as the potential ecological role of bile acid transformation, sterol modification and quorum quenching by sp. in the marine environment.
海洋无脊椎动物的共生细菌是新型、具有药用相关性的天然产物的丰富来源,这些产物可能成为对抗多药耐药病原体和治疗疾病的先导化合物。在本研究中,研究了海洋无脊椎动物共生菌的生物活性潜力。该菌株的生物活性筛选显示出革兰氏阳性菌特异性的抗菌活性以及对人黑色素瘤细胞系(A2058)的细胞毒性活性。使用 HPLC-MS 对活性部分进行去重发现,分离并确定了胆酸和 3-氧胆酸的结构。 是属于 属的三个模式种之一。使用薄层层析法评估了所有三个物种产生胆酸的能力,并通过 LC-MS 进行了验证。使用长读长 Oxford Nanopore Technology (ONT) 和 Illumina 数据对所有三个 模式种进行重新测序,生成了完整的基因组,从而能够从生物信息学角度评估菌株产生胆酸的能力。尽管无法基于序列同源性搜索确定该属中胆酸合成的完整生物合成途径,但在所有三个物种中鉴定出青霉素或同型半胱氨酸内酯酰基酶表明存在一种机制用于水解存在于生长培养基中的结合胆汁酸,从而生成胆酸和 3-氧胆酸。由于目前对该属的生物活性知之甚少,本研究为进一步研究其生物活性潜力以及 属在海洋环境中通过胆汁酸转化、固醇修饰和群体感应淬灭的潜在生态作用奠定了基础。