多糖降解古细菌主导酸性温泉:基因组和培养的见解到一个新的热变形菌谱系。

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-22 DOI:10.1128/msystems.00710-25
Maria I Prokofeva, Alina I Karaseva, Adolf S Tulenkov, Alexandra A Klyukina, Natalia E Suzina, Nicole J Bale, Anchelique Mets, Christa Schleper, Alexander G Elcheninov, Tatiana V Kochetkova
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引用次数: 0

摘要

测序技术和生物信息学的发展极大地促进了我们对微生物“暗物质”的理解,然而,纯培养物的分离,特别是古生菌的分离,仍然是罕见的和具有挑战性的。培养对于微生物代谢的可靠表征仍然至关重要,这是元基因组学和其他基于组学的方法无法完全取代的。在这里,我们报告了深分支古细菌谱系的第一个培养代表,以前被称为Candidatus Marsarchaeota。我们的系统发育分析将这些分离物置于热变形门内,作为一个新的目,Tardisphaerales。在70°C以下的酸性温泉中,Tardisphaerales的成员在原核生物群落中占主导地位,占微生物总数的40%,强调了它们的生态意义。功能基因组学和培养实验揭示了一种嗜热嗜酸、厌氧的生活方式,其能量代谢基于碳水化合物发酵,特别是多糖。这种代谢能力是由大量的糖苷酶编码基因和前所未有的代谢多功能性的热嗜酸菌支持。分离物具有完整的糖酵解、enterner - doudoroff和戊糖-磷酸途径,使它们能够利用不同的糖。多糖水解的专业化可能为这些生长缓慢的古菌提供了适应优势,因为大多数其他异养型嗜热酸菌更喜欢肽或单糖。此外,针对活性氧的强大防御机制和在酸性条件下的持久性使Tardisphaerales在这些极端栖息地中胜过其他异养生物并保持优势地位。这一新目的发现和培育扩大了原核生物分类,揭示了酸性地热生态系统碳循环的关键角色。自然环境中的大多数优势原核生物仍然未被培育,它们的代谢潜力和生态作用只能通过宏基因组学来推断。然而,培育是全面功能鉴定和新性状鉴定的必要条件。在这里,我们描述了在酸性温泉中丰富的新纲Tardisphaeria(温热变形门)中新的古细菌目Tardisphaerales的第一个培养代表。通过全基因组重建和纯培养的微生物学实验,我们证明了这些古细菌在代谢方面与已知的热嗜酸菌不同,使它们成为高温酸性环境中复杂有机物的关键降解者。它们的基因组编码多种糖苷酶,可以在高温和低pH下有效分解多糖,这是一种有前景的生物技术应用特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polysaccharide-degrading archaea dominate acidic hot springs: genomic and cultivation insights into a novel Thermoproteota lineage.

The expansion of sequencing technologies and bioinformatics has greatly advanced our understanding of microbial "dark matter," yet the isolation of pure cultures, especially among Archaea, remains rare and challenging. Cultivation is still essential for the reliable characterization of microbial metabolism, which cannot be fully replaced by metagenomics and other omics-based approaches. Here, we report the first cultivated representatives of a deep-branching archaeal lineage previously known as Candidatus Marsarchaeota. Our phylogenomic analyses place these isolates within the phylum Thermoproteota as a novel order, Tardisphaerales. Members of Tardisphaerales dominate the prokaryotic communities in acidic hot springs below 70°C, comprising up to 40% of the total microbial population, underscoring their ecological significance. Functional genomics and culture experiments reveal a thermoacidophilic, anaerobic lifestyle, with energy metabolism based on carbohydrate fermentation, particularly of polysaccharides. This metabolic capability is supported by numerous glycosidase-encoding genes and by unprecedented metabolic versatility among thermoacidophiles. The isolates possess complete glycolysis, Entner-Doudoroff, and pentose-phosphate pathways, allowing them to utilize different sugars. Specialization in polysaccharide hydrolysis presumably provides an adaptive advantage for these slow-growing archaea, as most other heterotrophic thermoacidophiles prefer peptides or simple sugars. Furthermore, robust defense mechanisms against reactive oxygen species and persistence in acidic conditions enable Tardisphaerales to outcompete other heterotrophs and maintain dominance in these extreme habitats. The discovery and cultivation of this new order expand prokaryotic taxonomy and reveal the key players in carbon cycling in acidic geothermal ecosystems.IMPORTANCEMost of the dominant prokaryotes in natural environments remain uncultivated, and their metabolic potential and ecological role can be inferred solely from metagenomics. However, cultivation is essential for comprehensive functional characterization and identification of novel traits. Here, we describe the first cultivated representatives of the new archaeal order Tardisphaerales within the novel class Tardisphaeria (phylum Thermoproteota), a lineage abundant in acidic hot springs. Through the whole-genome reconstruction and microbiological experiments in pure cultures, we demonstrate that these archaea are metabolically distinct from the known thermoacidophiles, making them the key degraders of the complex organic matter in hot, acidic environments. Their genomes encode a diverse set of glycosidases that allow efficient polysaccharide breakdown at high temperatures and low pH, a trait with promising biotechnological applications.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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