# Characterization of a Boron-Tolerant Nocardia niigatensis Isolated from Boron-Rich Soils: Physiological, Enzymatic, and Genomic Insights

**Authors:** Kerem Özdemir

PMC · DOI: 10.3390/microorganisms14020306 · Microorganisms · 2026-01-28

## TL;DR

A boron-tolerant Nocardia niigatensis strain was isolated from boron-rich soils and shown to have potential for bioremediation and industrial applications.

## Contribution

The study provides a comprehensive characterization of a boron-tolerant Nocardia niigatensis strain with physiological, enzymatic, and genomic insights.

## Key findings

- The strain exhibited robust growth at boron concentrations up to 50 mM, indicating potential for bioremediation.
- The strain showed positive L-glutaminase activity and a broad enzymatic profile, suggesting industrial relevance.
- Metagenomic analysis revealed differences in microbial communities linked to mineral types in boron-rich soils.

## Abstract

In this study, a Nocardia niigatensis strain was isolated from boron-rich mining soils in the Bigadiç region of Türkiye and comprehensively characterized. The primary aim of this study was to isolate boron-tolerant Nocardia species and evaluate their physiological, enzymatic, and biochemical profiles. Selective isolation techniques were employed to obtain Nocardia isolates, and species-level identification was achieved using both 16S rRNA gene sequencing and MALDI-TOF MS analysis, which consistently confirmed the isolate as N. niigatensis. In addition to molecular identification, the morphological, physiological, and biochemical characteristics of the strain were extensively investigated. The strain demonstrated notable boron tolerance, exhibiting robust growth at concentrations up to 50 mM, highlighting its potential applicability in the bioremediation of boron-contaminated environments. Physiological assays further revealed moderate halotolerance and a mesophilic growth profile, with optimal growth observed at 27–37 °C. Enzymatic screening indicated positive L-glutaminase activity, an enzyme of considerable industrial relevance. Moreover, API ZYM profiling revealed a broad enzymatic spectrum, including esterases, arylamidases, phosphatases, and glucosidases, suggesting substantial metabolic versatility. Antibiotic susceptibility testing showed sensitivity to doxycycline, tobramycin, and erythromycin, whereas resistance was observed against imipenem and several β-lactam antibiotics. Metagenomic analysis of boron-rich soils from two distinct mining sites revealed marked differences in microbial community composition, with variations in Actinobacteria abundance associated with mineral type. Overall, these findings emphasize the adaptive capacity and biotechnological potential of environmental Nocardia strains inhabiting chemically stressful ecosystems, warranting further genomic and metabolomic investigations.

## Linked entities

- **Chemicals:** boron (PubChem CID 5462311), doxycycline (PubChem CID 54671203), tobramycin (PubChem CID 36294), erythromycin (PubChem CID 12560), imipenem (PubChem CID 104838)
- **Species:** Nocardia niigatensis (taxon 209249)

## Full-text entities

- **Diseases:** lung disease (MESH:D008171), injury to (MESH:D014947), multidrug (MESH:D018088), infections (MESH:D007239), HIV (MESH:D015658), Nocardia (MESH:D009617)
- **Chemicals:** N (MESH:D009584), agar (MESH:D000362), boric acid (MESH:C032688), Doxycycline (MESH:D004318), NaCl (MESH:D012965), PR (MESH:D011221), formic acid (MESH:C030544), P (MESH:D010758), Salt (MESH:D012492), Oleandomycin (MESH:D009827), Tobramycin (MESH:D014031), ethanol (MESH:D000431), asparagine (MESH:D001216), Erythromycin (MESH:D004917), Boron (MESH:D001895), E (MESH:D004540), water (MESH:D014867), phenol (MESH:D019800), Clindamycin (MESH:D002981), Vancomycin (MESH:D014640), xylan (MESH:D014990), Enoxacin (MESH:D015365), starch (MESH:D013213), Congo red (MESH:D003224), Rifampicin (MESH:D012293), oil (MESH:D009821), carbohydrate (MESH:D002241), Ca2B6O11 5H2O (-), Penicillin (MESH:D010406), glycerol (MESH:D005990), Nitrofurantoin (MESH:D009582), Sulbactam (MESH:D013407), Lugol's iodine (MESH:C010389), beta-lactam (MESH:D047090), Tween 80 (MESH:D011136), cycloheximide (MESH:D003513), Rhodamine B (MESH:C029773), heavy-metal (MESH:D019216), Neomycin (MESH:D009355), Imipenem (MESH:D015378), Ampicillin (MESH:D000667), carboxymethyl cellulose (MESH:D002266), glutamine (MESH:D005973), phenolphthalein (MESH:D020113), borate (MESH:D001881), novobiocin (MESH:D009675), FM (MESH:D005286), nystatin (MESH:D009761)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Nocardia sp. (species) [taxon 1821], Nocardia cyriacigeorgica (species) [taxon 135487], Nocardia (genus) [taxon 1817], Bacillus cereus (species) [taxon 1396], Escherichia coli (E. coli, species) [taxon 562], Meleagris gallopavo (common turkey, species) [taxon 9103], Actinomycetota (actinobacteria, phylum) [taxon 201174], Enterococcus faecalis (species) [taxon 1351], Pseudomonadota (proteobacteria, phylum) [taxon 1224], Nocardia otitidiscaviarum (species) [taxon 1823], Staphylococcus aureus (species) [taxon 1280], Collinsella (genus) [taxon 102106], Bifidobacterium (genus) [taxon 1678], Homo sapiens (human, species) [taxon 9606], Bacteroidota (Bacteroides-Cytophaga-Flexibacter group, phylum) [taxon 976], Nocardia farcinica (species) [taxon 37329], Enterococcus faecalis ATCC 29212 (strain) [taxon 1201292], Actinomycetes (high G+C Gram-positive bacteria, class) [taxon 1760], Streptomyces (genus) [taxon 1883], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Nocardia niigatensis (species) [taxon 209249]
- **Cell lines:** ATCC 29212 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), BR005 — Homo sapiens (Human), Finite cell line (CVCL_H556)

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943181/full.md

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Source: https://tomesphere.com/paper/PMC12943181