Elizaveta Bonch-Osmolovskaya

Dr. Elizaveta Bonch-Osmolovskaya

Winogradsky Institute of Microbiology, Russian Academy of Sciences, Prospekt 60 Let Oktyabrya 7, Bldg 2, Moscow 117312, Russia

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2021 in Microbiology
Verified
Journal Article
Open access
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IKI. B. Kotova
I. B. Kotova
YTYu. V. Taktarova
Yu. V. Taktarova
ETE. A. Tsavkelova
E. A. Tsavkelova
MEM. A. Egorova
M. A. Egorova
IBI. A. Bubnov
I. A. Bubnov
EBElizaveta Bonch-Osmolovskaya
Elizaveta Bonch-Osmolovskaya
—: The growing worldwide production of synthetic plastics leads to increased amounts of plastic pollution. Even though microbial degradation of plastics is known to be a very slow process, this capacity has been found in many bacteria, including invertebrate symbionts, and microscopic fungi. Research in this field has been mostly focused on microbial degradation of polyethylene, polystyrene, and polyethylene terephthalate (PET). Quite an arsenal of different methods is available today for detecting processes of plastic degradation and measuring their rates. Given the lack of generally accepted protocols, it is difficult to compare results presented by different authors. PET degradation by recombinant hydrolases from thermophilic actinobacteria happens to be the most efficient among the currently known plastic degradation processes. Various approaches to accelerating microbial plastic degradation are also discussed.

27 December 2016 in Extremophiles
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Journal Article
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AMAlexander Yu. Merkel
Alexander Yu. Merkel
NPNikolay V. Pimenov
Nikolay V. Pimenov
IRIgor I. Rusanov
Igor I. Rusanov
ASAlexander I. Slobodkin
Alexander I. Slobodkin
GSGalina B. Slobodkina
Galina B. Slobodkina
EBElizaveta Bonch-Osmolovskaya
Elizaveta Bonch-Osmolovskaya

11 September 2021 in Life
Verified
Journal Article
Open access
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AMAlexander Yu Merkel
Alexander Yu Merkel
NCNikolay A. Chernyh
Nikolay A. Chernyh
NPNikolai Pimenov
Nikolai Pimenov
EBElizaveta Bonch-Osmolovskaya
Elizaveta Bonch-Osmolovskaya
ASAleksandr SLOBODKIN
Aleksandr SLOBODKIN
Terrestrial mud volcanoes (TMVs) are important natural sources of methane emission. The microorganisms inhabiting these environments remain largely unknown. We studied the phylogenetic composition and metabolic potential of the prokaryotic communities of TMVs located in the Taman Peninsula, Russia, using a metagenomic approach. One of the examined sites harbored a unique community with a high abundance of anaerobic methane-oxidizing archaea belonging to ANME-3 group (39% of all 16S rRNA gene reads). The high number of ANME-3 archaea was confirmed by qPCR, while the process of anaerobic methane oxidation was demonstrated by radioisotopic experiments. We recovered metagenome-assembled genomes (MAGs) of archaeal and bacterial community members and analyzed their metabolic capabilities. The ANME-3 MAG contained a complete set of genes for methanogenesis as well as of ribosomal RNA and did not encode proteins involved in dissimilatory nitrate or sulfate reduction. The presence of multiheme c-type cytochromes suggests that ANME-3 can couple methane oxidation with the reduction of metal oxides or with the interspecies electron transfer to a bacterial partner. The bacterial members of the community were mainly represented by autotrophic, nitrate-reducing, sulfur-oxidizing bacteria, as well as by fermentative microorganisms. This study extends the current knowledge of the phylogenetic and metabolic diversity of prokaryotes in TMVs and provides a first insight into the genomic features of ANME-3 archaea.

26 October 2019 in Genes
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ASAleksandr SLOBODKIN
Aleksandr SLOBODKIN
GSGalina Slobodkina
Galina Slobodkina
MAMaxime Allioux
Maxime Allioux
KAKarine Alain
Karine Alain
MJMohamed Jebbar
Mohamed Jebbar
EBElizaveta Bonch-Osmolovskaya
Elizaveta Bonch-Osmolovskaya
Information on the biochemical pathways of carbon and energy metabolism in representatives of the deep lineage bacterial phylum Deferribacteres are scarce. Here, we report the results of the sequencing and analysis of the high-quality draft genome of the thermophilic chemolithoautotrophic anaerobe Deferribacter autotrophicus. Genomic data suggest that CO2 assimilation is carried out by recently proposed reversible tricarboxylic acid cycle (“roTCA cycle”). The predicted genomic ability of D. autotrophicus to grow due to the oxidation of carbon monoxide was experimentally proven. CO oxidation was coupled with the reduction of nitrate to ammonium. Utilization of CO most likely involves anaerobic [Ni, Fe]-containing CO dehydrogenase. This is the first evidence of CO oxidation in the phylum Deferribacteres. The genome of D. autotrophicus encodes a Nap-type complex of nitrate reduction. However, the conversion of produced nitrite to ammonium proceeds via a non-canonical pathway with the participation of hydroxylamine oxidoreductase (Hao) and hydroxylamine reductase. The genome contains 17 genes of putative multiheme c-type cytochromes and “e-pilin” genes, some of which are probably involved in Fe(III) reduction. Genomic analysis indicates that the roTCA cycle of CO2 fixation and putative Hao-enabled ammonification may occur in several members of the phylum Deferribacteres.

27 August 2020 in Microorganisms
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TKTatiana Kochetkova
Tatiana Kochetkova
Stepan ToshchakovStepan Toshchakov
Stepan Toshchakov
KZKseniya S. Zayulina
Kseniya S. Zayulina
AEAlexander G. Elcheninov
Alexander G. Elcheninov
DZDaria G Zavarzina
Daria G Zavarzina
IKIlya Kublanov
Ilya Kublanov
Chukotka is an arctic region located in the continuous permafrost zone, but thermal springs are abundant there. In this study, for the first time, the microbial communities of the Chukotka hot springs (CHS) biofilms and sediments with temperatures 54–94 °C were investigated and analyzed by NGS sequencing of 16S rRNA gene amplicons. In microbial mats (54–75 °C), phototrophic bacteria of genus Chloroflexus dominated (up to 89% of all prokaryotes), while Aquificae were the most numerous at higher temperatures in Fe-rich sediments and filamentous “streamers” (up to 92%). The electron donors typical for Aquificae, such as H2S and H2, are absent or present only in trace amounts, and the prevalence of Aquificae might be connected with their ability to oxidize the ferrous iron present in CHS sediments. Armatimonadetes, Proteobacteria, Deinococcus-Thermus, Dictyoglomi, and Thermotogae, as well as uncultured bacteria (candidate divisions Oct-Spa1-106, GAL15, and OPB56), were numerous, and Cyanobacteria were present in low numbers. Archaea (less than 8% of the total community of each tested spring) belonged to Bathyarchaeota, Aigarchaeota, and Thaumarchaeota. The geographical location and the predominantly autotrophic microbial community, built on mechanisms other than the sulfur cycle-based ones, make CHS a special and unique terrestrial geothermal ecosystem.

1 October 2021 in Microorganisms
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Journal Article
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EFEvgenii N. Frolov
Evgenii N. Frolov
AGAlexandra Gololobova
Alexandra Gololobova
AKAlexandra A. Klyukina
Alexandra A. Klyukina
EBElizaveta Bonch-Osmolovskaya
Elizaveta Bonch-Osmolovskaya
NPNikolai Pimenov
Nikolai Pimenov
AMAlexander Yu Merkel
Alexander Yu Merkel
Microbial communities of the Kamchatka Peninsula terrestrial hot springs were studied using radioisotopic and cultural approaches, as well as by the amplification and sequencing of dsrB and 16S rRNA genes fragments. Radioisotopic experiments with 35S-labeled sulfate showed that microbial communities of the Kamchatka hot springs are actively reducing sulfate. Both the cultivation experiments and the results of dsrB and 16S rRNA genes fragments analyses indicated the presence of microorganisms participating in the reductive part of the sulfur cycle. It was found that sulfate-reducing prokaryotes (SRP) belonging to Desulfobacterota, Nitrospirota and Firmicutes phyla inhabited neutral and slightly acidic hot springs, while bacteria of phylum Thermodesulofobiota preferred moderately acidic hot springs. In high-temperature acidic springs sulfate reduction was mediated by archaea of the phylum Crenarchaeota, chemoorganoheterotrophic representatives of genus Vulcanisaeta being the most probable candidates. The 16S rRNA taxonomic profiling showed that in most of the studied communities SRP was present only as a minor component. Only in one microbial community, the representatives of genus Vulcanisaeta comprised a significant group. Thus, in spite of comparatively low sulfate concentrations in terrestrial hot springs of the Kamchatka, phylogenetically and metabolically diverse groups of sulfate-reducing prokaryotes are operating there coupling carbon and sulfur cycles in these habitats.