广泛的基因组研究确定了三个副球藻科种群的特征,并揭示了 Pseudogemmobacter lacusdianii sp.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2024-11-05 Epub Date: 2024-09-27 DOI:10.1128/spectrum.01088-24
Yang Deng, Cong-Jian Li, Jing Zhang, Wei-Hong Liu, Li-Yan Yu, Yu-Qin Zhang
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引用次数: 0

摘要

副球孢科细菌在各个领域的应用潜力巨大,备受研究关注。研究人员分别从淡水、纸莎草根圈土壤和植物圈等不同环境中分离出三株革兰氏染色阴性菌 CPCC 101601T、CPCC 101403T 和 CPCC 100767。对它们的 16S rRNA 基因序列进行分析,并与 GenBank 数据库中的序列进行比较,结果表明它们属于副球藻科,与所有具有有效分类名称的副球藻科成员的核苷酸相似度为 92.5%-99.9%。基于 16S rRNA 基因和全基因组序列的系统发育研究确定 CPCC 101601T 属于假革膜杆菌属,CPCC 101403T 属于副球菌属,CPCC 100767 属于宝石菌属。值得注意的是,利用平均核苷酸同一性(ANI)进行的基因组分析显示,T 和 CPCC 101403T 代表各自属中的新物种。相反,CPCC 100767 与 Gemmobacter fulvus con5T 的 ANI(98.5%)和 dDDH(87.4%)值都很高,表明它属于这一已被确认的物种。深入的基因组分析表明,CPCC 101601T、CPCC 101403T 和 CPCC 100767 菌株含有与反硝化、MA 利用和多羟基烷酸生物合成途径相关的关键基因。此外,基因分型和表型分析证实,菌株 CPCC 100767 具有将大气中的氮转化为氨和产生 5-氨基乙酰丙酸的能力,而 CPCC 101601T 只能进行前一种生物处理。这拓展了我们对副球孢科的了解,并为进一步研究提供了新的微生物材料。现代基因组学技术,如平均核苷酸同一性和数字 DNA-DNA 杂交,被用来确定物种归属。与主要基于 16S rRNA 基因分析的传统分类方法相比,这些方法能提供更精确的结果。除了对这些菌株进行分类外,研究人员还深入研究了它们的基因组,发现了与反硝化、MA 利用和多羟基烷酸生物合成有关的关键基因。这些基因的鉴定为了解这些菌株的环境作用提供了分子基础。特别是,菌株 CPCC 100767 展示了将大气中的氮转化为氨和生产 5-氨基乙酰丙酸的能力。这些生物加工能力具有重要的实用价值,例如在农业生产中用作生物肥料或生物刺激剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extensive genomic study characterizing three Paracoccaceae populations and revealing Pseudogemmobacter lacusdianii sp. nov. and Paracoccus broussonetiae sp. nov.

Bacteria within the family Paracoccaceae show promising potential for applications in various fields, garnering significant research attention. Three Gram stain-negative bacteria, strains CPCC 101601T, CPCC 101403T, and CPCC 100767, were isolated from diverse environments: freshwater, rhizosphere soil of Broussonetia papyrifera, and the phycosphere, respectively. Analysis of their 16S rRNA gene sequences, compared with those in the GenBank database, indicated that they belong to the family Paracoccaceae, with nucleotide similarities of 92.5%-99.9% to all of the Paracoccaceae members with valid taxonomic names. Phylogenetic studies based on 16S rRNA gene and whole-genome sequences identified CPCC 101601T as a member of the genus Pseudogemmobacter, CPCC 101403T belonging to the genus Paracoccus, and CPCC 100767 as part of the genus Gemmobacter. Notably, genomic analysis using average nucleotide identity (ANI; <95%) and digital DNA-DNA hybridization (dDDH; <70%) with their closely related strains suggested that CPCC 101601T and CPCC 101403T represent new species within their respective genera. Conversely, CPCC 100767 exhibited high ANI (98.5%) and dDDH (87.4%) values with Gemmobacter fulvus con5T, indicating it belongs to this already recognized species. The in-depth genomic analysis revealed that strains CPCC 101601T, CPCC 101403T, and CPCC 100767 harbor key genes related to the pathways for denitrifying, MA utilization, and polyhydroxyalkanoate biosynthesis. Moreover, genotyping and phenotyping analysis confirmed that strain CPCC 100767 has the ability to convert atmospheric nitrogen into ammonia and produce 5-aminolevulinic acid, whereas CPCC 101601T can only perform the former bioprocess.IMPORTANCEBased on polyphasic taxonomic study, two new species, Pseudogemmobacter lacusdianii and Paracoccus broussonetiae, affiliated with the family Paracoccaceae were identified. This expands our understanding of the family Paracoccaceae and provides new microbial materials for further studies. Modern genomic techniques such as average nucleotide identity and digital DNA-DNA hybridization were utilized to determine species affiliations. These methods offer more precise results than traditional classification mainly based on 16S rRNA gene analysis. Beyond classification of these strains, the research delved into their genomes and discovered key genes related to denitrification, MA utilization, and polyhydroxyalkanoate biosynthesis. The identification of these genes provides a molecular basis for understanding the environmental roles of these strains. Particularly, strain CPCC 100767 demonstrated the ability to convert atmospheric nitrogen into ammonia and produce 5-aminolevulinic acid. These bioprocess capabilities are of significant practical value, such as in agricultural production for use as biofertilizers or biostimulants.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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