Metabolic and evolutionary patterns in the extremely acidophilic archaeon Ferroplasma acidiphilum YT

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Metabolic and evolutionary patterns in the extremely acidophilic archaeon Ferroplasma acidiphilum YT. / Golyshina, Olga; Hai, Tran; Reva, Olga N. et al.
In: Scientific Reports, Vol. 7, 3682, 16.06.2017.

Research output: Contribution to journalArticlepeer-review

HarvardHarvard

Golyshina, O, Hai, T, Reva, ON, Lemak, S, Yakunin, AF, Goesmann, A, Nechitaylo, TY, LaCono, V, Smedile, F, Slesarev, A, Rojo, D, Barbas, C, Ferrer, M, Yakimov, MM & Golyshin, P 2017, 'Metabolic and evolutionary patterns in the extremely acidophilic archaeon Ferroplasma acidiphilum YT', Scientific Reports, vol. 7, 3682. https://doi.org/10.1038/s41598-017-03904-5

APA

Golyshina, O., Hai, T., Reva, O. N., Lemak, S., Yakunin, A. F., Goesmann, A., Nechitaylo, T. Y., LaCono, V., Smedile, F., Slesarev, A., Rojo, D., Barbas, C., Ferrer, M., Yakimov, M. M., & Golyshin, P. (2017). Metabolic and evolutionary patterns in the extremely acidophilic archaeon Ferroplasma acidiphilum YT. Scientific Reports, 7, Article 3682. https://doi.org/10.1038/s41598-017-03904-5

CBE

Golyshina O, Hai T, Reva ON, Lemak S, Yakunin AF, Goesmann A, Nechitaylo TY, LaCono V, Smedile F, Slesarev A, et al. 2017. Metabolic and evolutionary patterns in the extremely acidophilic archaeon Ferroplasma acidiphilum YT. Scientific Reports. 7:Article 3682. https://doi.org/10.1038/s41598-017-03904-5

MLA

VancouverVancouver

Golyshina O, Hai T, Reva ON, Lemak S, Yakunin AF, Goesmann A et al. Metabolic and evolutionary patterns in the extremely acidophilic archaeon Ferroplasma acidiphilum YT. Scientific Reports. 2017 Jun 16;7:3682. Epub 2017 Jun 16. doi: 10.1038/s41598-017-03904-5

Author

Golyshina, Olga ; Hai, Tran ; Reva, Olga N. et al. / Metabolic and evolutionary patterns in the extremely acidophilic archaeon Ferroplasma acidiphilum YT. In: Scientific Reports. 2017 ; Vol. 7.

RIS

TY - JOUR

T1 - Metabolic and evolutionary patterns in the extremely acidophilic archaeon Ferroplasma acidiphilum YT

AU - Golyshina, Olga

AU - Hai, Tran

AU - Reva, Olga N.

AU - Lemak, Sofia

AU - Yakunin, Alexander F.

AU - Goesmann, Alexander

AU - Nechitaylo, Taras Y.

AU - LaCono, Violetta

AU - Smedile, Francesco

AU - Slesarev, Alexei

AU - Rojo, David

AU - Barbas, Coral

AU - Ferrer, Manuael

AU - Yakimov, Michail M.

AU - Golyshin, Peter

PY - 2017/6/16

Y1 - 2017/6/16

N2 - Ferroplasmaceae represent ubiquitous iron-oxidising extreme acidophiles with a number of unique physiological traits. In a genome-based study of Ferroplasma acidiphilum YT, the only species of the genus Ferroplasma with a validly published name, we assessed its central metabolism and genome stability during a long-term cultivation experiment. Consistently with physiology, the genome analysis points to F. acidiphilum YT having an obligate peptidolytic oligotrophic lifestyle alongside with anaplerotic carbon assimilation. This narrow trophic specialisation abridges the sugar uptake, although all genes for glycolysis and gluconeogenesis, including bifunctional unidirectional fructose 1,6-bisphosphate aldolase/phosphatase, have been identified. Pyruvate and 2-oxoglutarate dehydrogenases are substituted by ‘ancient’ CoA-dependent pyruvate and alpha-ketoglutarate ferredoxin oxidoreductases. In the lab culture, after ~550 generations, the strain exhibited the mutation rate of ≥1.3 × 10−8 single nucleotide substitutions per site per generation, which is among the highest values recorded for unicellular organisms. All but one base substitutions were G:C to A:T, their distribution between coding and non-coding regions and synonymous-to-non-synonymous mutation ratios suggest the neutral drift being a prevalent mode in genome evolution in the lab culture. Mutations in nature seem to occur with lower frequencies, as suggested by a remarkable genomic conservation in F. acidiphilum YT variants from geographically distant populations.

AB - Ferroplasmaceae represent ubiquitous iron-oxidising extreme acidophiles with a number of unique physiological traits. In a genome-based study of Ferroplasma acidiphilum YT, the only species of the genus Ferroplasma with a validly published name, we assessed its central metabolism and genome stability during a long-term cultivation experiment. Consistently with physiology, the genome analysis points to F. acidiphilum YT having an obligate peptidolytic oligotrophic lifestyle alongside with anaplerotic carbon assimilation. This narrow trophic specialisation abridges the sugar uptake, although all genes for glycolysis and gluconeogenesis, including bifunctional unidirectional fructose 1,6-bisphosphate aldolase/phosphatase, have been identified. Pyruvate and 2-oxoglutarate dehydrogenases are substituted by ‘ancient’ CoA-dependent pyruvate and alpha-ketoglutarate ferredoxin oxidoreductases. In the lab culture, after ~550 generations, the strain exhibited the mutation rate of ≥1.3 × 10−8 single nucleotide substitutions per site per generation, which is among the highest values recorded for unicellular organisms. All but one base substitutions were G:C to A:T, their distribution between coding and non-coding regions and synonymous-to-non-synonymous mutation ratios suggest the neutral drift being a prevalent mode in genome evolution in the lab culture. Mutations in nature seem to occur with lower frequencies, as suggested by a remarkable genomic conservation in F. acidiphilum YT variants from geographically distant populations.

U2 - 10.1038/s41598-017-03904-5

DO - 10.1038/s41598-017-03904-5

M3 - Article

VL - 7

JO - Scientific Reports

JF - Scientific Reports

SN - 2045-2322

M1 - 3682

ER -