Evidence map›Paper›PMID 39496518›Full record

ArticleFEMS microbiology ecology2024

Genomic insights into key mechanisms for carbon, nitrogen, and phosphate assimilation by the acidophilic, halotolerant genus Acidihalobacter members.

Himel Nahreen Khaleque, Homayoun Fathollahzadeh, Anna H Kaksonen, Jorge Valdés, Eva Vergara, David S Holmes, Elizabeth L J Watkin

Abstract read
In one paragraph

Article in FEMS microbiology ecology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Himel Nahreen KhalequeSchool of Science, Edith Cowan University, Joondalup, WA 6027, Australia.ORCID 0000-0002-5737-9678
Homayoun FathollahzadehSchool of Science, Edith Cowan University, Joondalup, WA 6027, Australia.
Anna H KaksonenCSIRO, Environment, Floreat, WA 6014, Australia.
Jorge ValdésCenter for Bioinformatics and Integrative Biology, Facultad de Ciencias de la Vida, Universidad Andrés Bello, Av. República 330, Santiago 8370146, Chile.
Eva VergaraCenter for Bioinformatics and Genome Biology, Fundación Ciencia & Vida, Facultad de Medicina y Ciencia, Universidad San Sebastián, Santiago, 8420000, Chile.
David S HolmesCenter for Bioinformatics and Genome Biology, Fundación Ciencia & Vida, Facultad de Medicina y Ciencia, Universidad San Sebastián, Santiago, 8420000, Chile.ORCID 0000-0001-9555-138X
Elizabeth L J WatkinSchool of Science, Edith Cowan University, Joondalup, WA 6027, Australia.

Funding

CSIROCurtin University
6 · The paper itself

Abstract

In-depth comparative genomic analysis was conducted to predict carbon, nitrogen, and phosphate assimilation pathways in the halotolerant, acidophilic genus Acidihalobacter. The study primarily aimed to understand how the metabolic capabilities of each species can determine their roles and effects on the microbial ecology of their unique saline and acidic environments, as well as in their potential application to saline water bioleaching systems. All four genomes encoded the genes for the complete tricarboxylic acid cycle, including 2-oxoglutarate dehydrogenase, a key enzyme absent in obligate chemolithotrophic acidophiles. Genes for a unique carboxysome shell protein, csoS1D, typically found in halotolerant bacteria but not in acidophiles, were identified. All genomes contained lactate and malate utilization genes, but only A. ferrooxydans DSM 14175T contained genes for the metabolism of propionate. Genes for phosphate assimilation were present, though organized differently across species. Only A. prosperus DSM 5130T and A. aeolianus DSM 14174T genomes contained nitrogen fixation genes, while A. ferrooxydans DSM 14175T and A. yilgarnensis DSM 105917T possessed genes for urease transporters and respiratory nitrate reductases, respectively. The findings suggest that all species can fix carbon dioxide but can also potentially utilize exogenous carbon sources and that the non-nitrogen-fixing species rely on alternative nitrogen assimilation mechanisms.

Indexed as

CarbonGenome, BacterialNitrogenPhosphatesBacterial ProteinsCitric Acid CycleGenomicsPhylogenyBacterial ProteinsCarbonNitrogenPhosphatesacidophilesbioleachingcomparative genomicshalotolerantnutrient assimilation

Identifiers

PMID39496518
PMCPMC11585279

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.