未开发岩溶生态系统沉积物微生物亚群落的生物合成潜力及其生态影响

IF 3.9 3区 生物学 Q2 MICROBIOLOGY MicrobiologyOpen Pub Date : 2024-04-09 DOI:10.1002/mbo3.1407
Pablo Suárez-Moo, Alejandra Prieto-Davó
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引用次数: 0

摘要

人们研究了各种环境中的微生物群落,以寻找新的天然产品,这些产品在医学和生物技术领域有着广泛的应用。我们采用富集方法和基因组挖掘工具,研究了墨西哥尤卡坦半岛喀斯特生态系统中沿海天坑沉积物中微生物群落的生物合成潜力。通过研究,我们在这些亚群落的 35 个高质量元基因组组装基因组(MAGs)中发现了 203 个生物合成基因簇(BGCs)和 55 个次级代谢产物(SMs)。最丰富的 BGC 类型是萜烯、非核糖体肽合成酶和 III 型多酮合成酶。以前曾有报道称,一些在硅学中鉴定出的 BGCs 和 SMs 具有抗病原菌和真菌的生物活性。其他一些则可能在水坑生态系统中发挥重要作用,如铁增溶和渗透压保护。有趣的是,75%的BGCs与MiBIG数据库中之前报道的细菌BGCs没有序列同源性。这表明,这种环境中的微生物群落可能是编码新型特化化合物基因的一个尚未开发的来源。大多数 BGCs 都是在 Virgibacillus 属的途径中发现的,其次是 Sporosarcina、Siminovitchia、Rhodococcus 和 Halomonas。后者与副梭菌和溶血芽孢杆菌一起,拥有数量最多的已鉴定 BGC 类型。这项研究对未开发环境中沉积物微生物群落中的 SMs 的潜在生态作用提供了新的见解,强调了它们作为新型天然产品来源的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Biosynthetic potential of the sediment microbial subcommunities of an unexplored karst ecosystem and its ecological implications

Microbial communities from various environments have been studied in the quest for new natural products with a broad range of applications in medicine and biotechnology. We employed an enrichment method and genome mining tools to examine the biosynthetic potential of microbial communities in the sediments of a coastal sinkhole within the karst ecosystem of the Yucatán Peninsula, Mexico. Our investigation led to the detection of 203 biosynthetic gene clusters (BGCs) and 55 secondary metabolites (SMs) within 35 high-quality metagenome-assembled genomes (MAGs) derived from these subcommunities. The most abundant types of BGCs were Terpene, Nonribosomal peptide-synthetase, and Type III polyketide synthase. Some of the in silico identified BGCs and SMs have been previously reported to exhibit biological activities against pathogenic bacteria and fungi. Others could play significant roles in the sinkhole ecosystem, such as iron solubilization and osmotic stress protection. Interestingly, 75% of the BGCs showed no sequence homology with bacterial BGCs previously reported in the MiBIG database. This suggests that the microbial communities in this environment could be an untapped source of genes encoding novel specialized compounds. The majority of the BGCs were identified in pathways found in the genus Virgibacillus, followed by Sporosarcina, Siminovitchia, Rhodococcus, and Halomonas. The latter, along with Paraclostridium and Lysinibacillus, had the highest number of identified BGC types. This study offers fresh insights into the potential ecological role of SMs from sediment microbial communities in an unexplored environment, underscoring their value as a source of novel natural products.

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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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