喜玛拉雅西部农田土壤中高海拔、冷适应、代谢多样的aurulentdyadobacter sp. 11 .的描述。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Amit Yadav, Kiran Kirdat, Vipool Thorat, Ngangyola Tuikhar, Kirti Chundawat, Tushar Lodha, Bhavesh Tiwarekar, Umera Patwekar, Malad Mubarak, Shuchi Shastri, Saurabh Kumar, Yogesh Shouche, Reeta Goel
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引用次数: 0

摘要

从印度西喜马拉雅山脉甘戈特里地区寒冷的高海拔农田土壤中分离出一种新的细菌菌株,命名为UC10T。该菌株革兰氏染色阴性,需氧,不形成孢子,不运动,形成金色菌落,产生柔红素样色素。菌株UC10T生长在很宽的温度范围(5°C-30°C), pH(6-11)和盐度(高达4% NaCl),在30°C, pH 7.0和1% NaCl下生长最佳。接近全长的16S rRNA基因序列(MK743979)与luticola Dyadobacter具有98.95%的相似性,其次是与Dyadobacter crusticola的97.68%和与Dyadobacter koreensis的97.40%,系统发育分析将UC10基因序列定位在Dyadobacter属的一个不同分支中。全基因组系统发育分析显示,UC10T与线性Dyadobacter linearis、D. crusticola和D. luticola密切相关,但与它们明显不同的是,UC10T的平均核苷酸同源性较低(T为6.93 Mb, G+C含量为46.5 mol%),并编码多个冷适应相关基因,包括冷休克蛋白和脂肪酸去饱和酶。该菌株还含有降解芳香族化合物的基因,并证明了在以苯甲酸钠为唯一碳源的最小培养基中生长的能力。此外,UC10T的脂肪酸和极性脂质谱显示出独特的成分,进一步支持其分化。综合基因组学、表型和化学分类证据支持菌株UC10T代表一个新物种,因此建议将其命名为aurulentus Dyadobacter sp. nov.。型应变为UC10T (= MCC 4019T = KCTC 72455T = JCM 34514T)。重要性:高海拔、寒冷的栖息地,如西喜马拉雅山脉的甘戈特里地区,对可培养微生物多样性的探索仍然不足。在这里,我们描述了一种从这样的环境中分离出来的新型冷适应物种——aurulentus Dyadobacter sp. nov.。该菌株表现出独特的生态和代谢特性,包括在低温下生长和降解苯甲酸钠等芳香族化合物。基因组分析揭示了关键的冷适应特征,如冷休克蛋白、脂肪酸去饱和酶、硝酸盐同化途径和多药耐药基因,支持在营养有限的低温土壤中生存。该菌株独特的化学分类特征,以C16:0升高和独特的极性脂质为标志,强调了其生态专业化。总之,这些特征表明了它在生物修复和冷环境生物技术方面的潜在效用。该研究拓宽了我们对Dyadobacter spp.在极端环境下的适应策略和生态功能的认识,对生物勘探冷活性酶和了解高原微生物群落的抗性进化具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Description of high-altitude, cold-adaptive, metabolically versatile Dyadobacter aurulentus sp. nov. isolated from Western Himalayan farmland soils.

A novel bacterial strain, designated UC10T, was isolated from cold, high-altitude farmland soil in the Gangotri region of the Western Himalayas, India. The strain is Gram-stain-negative, aerobic, non-spore forming, and non-motile, forming golden colonies that produce a flexirubin-like pigment. Strain UC10T grows over a broad range of temperatures (5°C-30°C), pH (6-11), and salinities (up to 4% NaCl), with optimal growth at 30°C, pH 7.0, and 1% NaCl. The nearly full-length 16S rRNA gene sequence (MK743979) shares 98.95% similarity with Dyadobacter luticola, followed by 97.68% with Dyadobacter crusticola and 97.40% with Dyadobacter koreensis, and phylogenetic analysis places UC10ᵀ in a distinct clade within the genus Dyadobacter. Whole-genome phylogenetic analyses revealed that UC10T is closely related to Dyadobacter linearis, D. crusticola, and D. luticola but is clearly distinguished from them by low average nucleotide identity (<81%), digital DNA-DNA hybridization (<24%), and amino acid identity (<80%) values. The genome of UC10T is 6.93 Mb with a G+C content of 46.5 mol% and encodes multiple cold adaptation-related genes, including cold-shock proteins and fatty acid desaturases. The strain also harbors genes for aromatic compound degradation and demonstrated the ability to grow in minimal medium containing sodium benzoate as the sole carbon source. Additionally, fatty acid and polar lipid profiles of UC10T revealed unique compositions, further supporting its differentiation. The combined genomic, phenotypic, and chemotaxonomic evidence supports the designation of strain UC10T as representing a novel species, for which the name Dyadobacter aurulentus sp. nov. is proposed. The type strain is UC10T (= MCC 4019T = KCTC 72455T = JCM 34514T).

Importance: High-altitude, cold habitats such as the Gangotri region of the Western Himalayas remain underexplored for culturable microbial diversity. Here, we describe Dyadobacter aurulentus sp. nov., a novel cold-adapted species isolated from such an environment. This strain demonstrates unique ecological and metabolic traits, including growth at low temperatures and degradation of aromatic compounds like sodium benzoate. Genomic analysis revealed key cold adaptation features such as cold-shock proteins, fatty acid desaturases, nitrate assimilation pathways, and multidrug resistance genes, supporting survival in nutrient-limited, low-temperature soils. The strain's distinct chemotaxonomic profile, marked by elevated C16:0 and unique polar lipids, underscores its ecological specialization. Together, these features point to its potential utility in bioremediation and cold-environment biotechnology. This study broadens our understanding of the adaptive strategies and ecological functions of Dyadobacter spp. in extreme environments, with implications for bioprospecting cold-active enzymes and understanding resistance evolution in high-altitude microbial communities.

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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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