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稀有放线菌:生物活性聚酮化合物和肽的潜在来源。

Rare actinobacteria: a potential source of bioactive polyketides and peptides.

机构信息

Hislop School of Biotechnology, Hislop College, Nagpur, Maharashtra, 440001, India.

Department of Biochemistry, Dr. Ambedkar College, Deekshabhoomi, Nagpur, Maharashtra, 440001, India.

出版信息

World J Microbiol Biotechnol. 2019 Jun 11;35(6):92. doi: 10.1007/s11274-019-2668-z.

Abstract

Polyketides and peptides obtained from actinobacteria are important therapeutic compounds which include front line antibiotics and anticancer drugs. Many screening programs are directed towards isolation of bioactive compounds from these organisms but the chances of finding novel antimicrobial leads among common actinobacteria are fast dwindling. As a result, the focus has shifted to the members of less exploited genera of rare actinobacteria. Three isolates, MMS8, MMS16 and KCR3 found to be potent polyketide and peptide producers were identified by 16S rRNA gene sequencing and their sequences deposited in the GenBank under the accession numbers MG407702, MG372012 and MG430204 respectively. MMS8 identified as Micromonospora auratinigra, yielded one potent compound determined to be chloroanthraquinone with an minimum inhibitory concentration (MIC) of 8 µg/ml against Bacillus subtilis and an IC value of 10 µg/ml and 4 μg/ml against HeLa and IMR cell lines respectively. This is the first report of the production of chloroanthraquinone by M. auratinigra. MMS16, identified as a member of the family Micromonosporaceae, yielded a potent compound MMS16B analyzed to be a novel bafilomycin analogue. The MIC of the compound was found to be 7 μg/ml against B.subtilis and IC value against HeLa and IMR was observed to be 9 μg/ml and 14 μg/ml respectively. MMS16B was also found to exhibit anti-quorum sensing (AQS) activity at sublethal concentrations. KCR3 identified as Kocuria kristinae yielded a novel antimicrobial peptide with antibacterial, antifungal and AQS activity. To the best of our knowledge, no antimicrobial activity has ever been reported from K. kristinae.

摘要

放线菌产生的聚酮类化合物和肽类化合物是重要的治疗化合物,包括一线抗生素和抗癌药物。许多筛选计划都针对这些生物体内生物活性化合物的分离,但在常见放线菌中发现新型抗菌先导化合物的机会正在迅速减少。因此,研究重点已经转移到开发利用较少的稀有放线菌属成员上。通过 16S rRNA 基因测序鉴定了三个分离株,MMS8、MMS16 和 KCR3,它们被鉴定为强效聚酮类化合物和肽类化合物的产生菌,其序列分别保存在 GenBank 中,登录号为 MG407702、MG372012 和 MG430204。MMS8 被鉴定为 Micromonospora auratinigra,产生了一种强效化合物,确定为氯蒽醌,对枯草芽孢杆菌的最小抑菌浓度 (MIC) 为 8μg/ml,对 HeLa 和 IMR 细胞系的 IC 值分别为 10μg/ml 和 4μg/ml。这是首次报道 M. auratinigra 产生氯蒽醌。MMS16 被鉴定为 Micromonosporaceae 家族的成员,产生了一种强效化合物 MMS16B,分析为新型巴弗洛霉素类似物。该化合物的 MIC 对枯草芽孢杆菌的抑制浓度为 7μg/ml,对 HeLa 和 IMR 的 IC 值分别为 9μg/ml 和 14μg/ml。MMS16B 还表现出亚致死浓度的抗群体感应 (AQS) 活性。KCR3 被鉴定为 Kocuria kristinae,产生了一种具有抗菌、抗真菌和 AQS 活性的新型抗菌肽。据我们所知,K. kristinae 从未报道过抗菌活性。

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