评估嗜卤属 Halarchaeum 的新陈代谢、系统发生学和分类学分类。

IF 2.2 4区 生物学 Q3 MICROBIOLOGY Fems Microbiology Letters Pub Date : 2024-01-09 DOI:10.1093/femsle/fnae001
Shuang Wang, Manik Prabhu Narsing Rao, Syed Raziuddin Quadri
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引用次数: 0

摘要

本研究采用基因组学方法来评估嗜卤属卤虫的代谢潜力和分类学分类。基因组分析表明,在高盐度环境中,与碳水化合物相比,卤虫属成员更倾向于以氨基酸作为主要能量来源。基因组分析揭示了与代谢途径相关的关键基因,包括恩伯登-梅耶霍夫途径、半磷酸化恩特纳-杜多罗夫途径和尿素循环。此外,基因组分析表明,半知菌目成员采用了多种渗透调节机制(包括盐入和盐出两种策略)。半知菌成员还编码缓解酸和热胁迫的基因。Halarchaeum solikamskense 和 Halarchaeum nitratireducens 之间的平均核苷酸同一性值超过了定义不同物种的既定阈值(95-96%)。这种高度相似性表明这两个物种之间关系密切,因此建议将 Halarchaeum solikamskense 重新分类为 Halarchaeum nitratireducens 的异型异名。这项研究的结果有助于我们了解分类学的分类方法,并揭示了卤虫物种在其特定生态位所采用的适应策略。
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Assessing the metabolism, phylogenomic, and taxonomic classification of the halophilic genus Halarchaeum.

In this study, a genomic approach was employed to evaluate the metabolic potentials and taxonomic classification of the halophilic genus Halarchaeum. Genomic analysis revealed that Halarchaeum members exhibit a predilection for amino acids as their primary energy source in high-salinity environments over carbohydrates. Genome analysis unveiled the presence of crucial genes associated with metabolic pathways, including the Embden-Meyerhof pathway, semi-phosphorylative Entner-Doudoroff pathway, and the urea cycle. Furthermore, the genomic analysis indicated that Halarchaeum members employ diverse mechanisms for osmotic regulation (encompassing both salt-in and salt-out strategies). Halarchaeum members also encode genes to alleviate acid and heat stress. The average nucleotide identity value between Halarchaeum solikamskense and Halarchaeum nitratireducens exceeded the established threshold (95%-96%) for defining distinct species. This high similarity suggests a close relationship between these two species, prompting the proposal to reclassify Halarchaeum solikamskense as a heterotypic synonym of Halarchaeum nitratireducens. The results of this study contribute to our knowledge of taxonomic classification and shed light on the adaptive strategies employed by Halarchaeum species in their specific ecological niches.

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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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