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全球生物合成基因簇分析揭示了青霉属物种中次级代谢产物产生的巨大潜力。

Global analysis of biosynthetic gene clusters reveals vast potential of secondary metabolite production in Penicillium species.

机构信息

Department of Biology and Biological Engineering, Chalmers University of Technology, SE412 96 Gothenburg, Sweden.

Department of Biotechnology and Biomedicine, Technical University of Denmark, DK2800 Kgs. Lyngby, Denmark.

出版信息

Nat Microbiol. 2017 Apr 3;2:17044. doi: 10.1038/nmicrobiol.2017.44.

Abstract

Filamentous fungi produce a wide range of bioactive compounds with important pharmaceutical applications, such as antibiotic penicillins and cholesterol-lowering statins. However, less attention has been paid to fungal secondary metabolites compared to those from bacteria. In this study, we sequenced the genomes of 9 Penicillium species and, together with 15 published genomes, we investigated the secondary metabolism of Penicillium and identified an immense, unexploited potential for producing secondary metabolites by this genus. A total of 1,317 putative biosynthetic gene clusters (BGCs) were identified, and polyketide synthase and non-ribosomal peptide synthetase based BGCs were grouped into gene cluster families and mapped to known pathways. The grouping of BGCs allowed us to study the evolutionary trajectory of pathways based on 6-methylsalicylic acid (6-MSA) synthases. Finally, we cross-referenced the predicted pathways with published data on the production of secondary metabolites and experimentally validated the production of antibiotic yanuthones in Penicillia and identified a previously undescribed compound from the yanuthone pathway. This study is the first genus-wide analysis of the genomic diversity of Penicillia and highlights the potential of these species as a source of new antibiotics and other pharmaceuticals.

摘要

丝状真菌产生广泛的具有重要药用应用的生物活性化合物,如抗生素青霉素和降胆固醇他汀类药物。然而,与细菌来源的次级代谢产物相比,真菌次级代谢产物的研究关注较少。在这项研究中,我们对 9 种青霉属物种的基因组进行了测序,并与 15 个已发表的基因组一起,研究了青霉属的次级代谢产物,并鉴定了该属产生次级代谢产物的巨大、未开发的潜力。共鉴定出 1317 个推定的生物合成基因簇 (BGC),并将基于聚酮合酶和非核糖体肽合酶的 BGC 分组为基因簇家族,并映射到已知途径。BGC 的分组使我们能够根据 6-甲基水杨酸 (6-MSA) 合酶研究途径的进化轨迹。最后,我们将预测的途径与次级代谢产物产生的已发表数据进行交叉引用,并在青霉属中实验验证了抗生素 yanuthones 的产生,并从 yanuthone 途径中鉴定出一种以前未描述的化合物。这项研究是青霉属基因组多样性的首次全属分析,突出了这些物种作为新型抗生素和其他药物来源的潜力。

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