Vera Safronova

Dr. Vera Safronova

All-Russia Research Institute for Agricultural Microbiology (ARRIAM)
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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1 January 2014 in Plant Physiology and Biochemistry
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Journal Article
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ABAndrey Belimov
Andrey Belimov
ICIan C.Dodd
Ian C.Dodd
VSVera Safronova
Vera Safronova
VDValentina A. Dumova
Valentina A. Dumova
ASAlexander Shaposhnikov
Alexander Shaposhnikov
WDWilliam J. Davies
William J. Davies

22 January 2015 in Antonie van Leeuwenhoek
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Journal Article
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VSVera Safronova
Vera Safronova
IKIrina G. Kuznetsova
Irina G. Kuznetsova
ASAnna L. Sazanova
Anna L. Sazanova
Anastasiia KimeklisAnastasiia Kimeklis
Anastasiia Kimeklis
ABAndrey A. Belimov
Andrey A. Belimov
ITIgor A. Tikhonovich
Igor A. Tikhonovich

31 July 2020 in Plants
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Journal Article
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ABAndrey Belimov
Andrey Belimov
ASAlexander Shaposhnikov
Alexander Shaposhnikov
TATatiana S. Azarova
Tatiana S. Azarova
NMNatalia M. Makarova
Natalia M. Makarova
VSVera Safronova
Vera Safronova
ITIgor A. Tikhonovich
Igor A. Tikhonovich
Cadmium (Cd) is one of the most widespread and toxic soil pollutants that inhibits plant growth and microbial activity. Polluted soils can be remediated using plants that either accumulate metals (phytoextraction) or convert them to biologically inaccessible forms (phytostabilization). The phytoremediation potential of a symbiotic system comprising the Cd-tolerant pea (Pisum sativum L.) mutant SGECdt and selected Cd-tolerant microorganisms, such as plant growth-promoting rhizobacterium Variovorax paradoxus 5C-2, nodule bacterium Rhizobium leguminosarum bv. viciae RCAM1066, and arbuscular mycorrhizal fungus Glomus sp. 1Fo, was evaluated in comparison with wild-type pea SGE and the Cd-accumulating plant Indian mustard (Brassica juncea L. Czern.) VIR263. Plants were grown in pots in sterilized uncontaminated or Cd-supplemented (15 mg Cd kg−1) soil and inoculated or not with the microbial consortium. Cadmium significantly inhibited growth of uninoculated and particularly inoculated SGE plants, but had no effect on SGECdt and decreased shoot biomass of B. juncea. Inoculation with the microbial consortium more than doubled pea biomass (both genotypes) irrespective of Cd contamination, but had little effect on B. juncea biomass. Cadmium decreased nodule number and acetylene reduction activity of SGE by 5.6 and 10.8 times, whereas this decrease in SGECdt was 2.1 and 2.8 times only, and the frequency of mycorrhizal structures decreased only in SGE roots. Inoculation decreased shoot Cd concentration and increased seed Cd concentration of both pea genotypes, but had little effect on Cd concentration of B. juncea. Inoculation also significantly increased concentration and/or accumulation of nutrients (Ca, Fe, K, Mg, Mn, N, P, S, and Zn) by Cd-treated pea plants, particularly by the SGECdt mutant. Shoot Cd concentration of SGECdt was twice that of SGE, and the inoculated SGECdt had approximately similar Cd accumulation capacity as compared with B. juncea. Thus, plant–microbe systems based on Cd-tolerant micro-symbionts and plant genotypes offer considerable opportunities to increase plant HM tolerance and accumulation.

1 January 2017 in International Journal of Systematic and Evolutionary Microbiology
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Journal Article
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VSVera Safronova
Vera Safronova
IKIrina G. Kuznetsova
Irina G. Kuznetsova
ASAnna L. Sazanova
Anna L. Sazanova
ABAndrey A. Belimov
Andrey A. Belimov
EAEvgeny Andronov
Evgeny Andronov
ITIgor A. Tikhonovich
Igor A. Tikhonovich
Gram-stain-negative strains V5/3MT, V5/5K, V5/5M and V5/13 were isolated from root nodules of Vicia alpestris plants growing in the North Ossetia region (Caucasus). Sequencing of the partial 16S rRNA gene (rrs) and four housekeeping genes (dnaK, gyrB, recA and rpoB) showed that the isolates from V. alpestris were most closely related to the species Microvirga zambiensis (order Rhizobiales , family Methylobacteriaceae ) which was described for the single isolate from root nodule of Listia angolensis growing in Zambia. Sequence similarities between the Microvirga -related isolates and M. zambiensis WSM3693T ranged from 98.5 to 98.7 % for rrs and from 79.7 to 95.8 % for housekeeping genes. Cellular fatty acids of the isolates V5/3MT, V5/5K, V5/5M and V5/13 included important amounts of C18 : 1ω7c (54.0–67.2 %), C16 : 0 (6.0–7.8 %), C19 : 0 cyclo ω8c (3.1–10.2 %), summed feature 2 (comprising one or more of iso-C16 : 1 I, C14 : 0 3-OH and unknown ECL 10.938, 5.8–22.5 %) and summed feature 3 (comprising C16 : 1ω7c and/or iso-C15 : 02-OH, 2.9–4.0 %). DNA–DNA hybridization between the isolate V5/3MT and M. zambiensis WSM3693T revealed DNA–DNA relatedness of 35.3 %. Analysis of morphological and physiological features of the novel isolates demonstrated their unique phenotypic profile in comparison with reference strains from closely related species of the genus Microvirga . On the basis of genotypic and phenotypic analysis, a novel species named Microvirga ossetica sp. nov. is proposed. The type strain is V5/3MT (=LMG 29787T=RCAM 02728T). Three additional strains of the species are V5/5K, V5/5M and V5/13.

29 January 2022 in Biomolecules
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EMElena Martynenko
Elena Martynenko
TATatiana Arkhipova
Tatiana Arkhipova
VSVera Safronova
Vera Safronova
OSOksana Seldimirova
Oksana Seldimirova
IGIlshat Galin
Ilshat Galin
Guzel KudoyarovaGuzel Kudoyarova
Guzel Kudoyarova
Inoculation with plant growth-promoting rhizobacteria can increase plant salt resistance. We aimed to reveal bacterial effects on the formation of apoplastic barriers and hormone concentration in relation to maintaining ion homeostasis and growth of salt-stressed plants. The rhizosphere of a durum wheat variety was inoculated with cytokinin-producing Bacillus subtilis and auxin-producing Pseudomonas mandelii strains. Plant growth, deposition of lignin and suberin and concentrations of sodium, potassium, phosphorus and hormones were studied in the plants exposed to salinity. Accumulation of sodium inhibited plant growth accompanied by a decline in potassium in roots and phosphorus in shoots of the salt-stressed plants. Inoculation with both bacterial strains resulted in faster appearance of Casparian bands in root endodermis and an increased growth of salt-stressed plants. B. subtilis prevented the decline in both potassium and phosphorus concentrations and increased concentration of cytokinins in salt-stressed plants. P. mandelii decreased the level of sodium accumulation and increased the concentration of auxin. Growth promotion was greater in plants inoculated with B. subtilis. Increased ion homeostasis may be related to the capacity of bacteria to accelerate the formation of Casparian bands preventing uncontrolled diffusion of solutes through the apoplast. We discuss the relative impacts of the decline in Na accumulation and maintenance of K and P content for growth improvement of salt-stressed plants and their possible relation to the changes in hormone concentration in plants.

25 February 2021 in Biomolecules
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OYOleg Yuzikhin
Oleg Yuzikhin
NGNatalia Gogoleva
Natalia Gogoleva
ASAlexander Shaposhnikov
Alexander Shaposhnikov
TKTatiana Konnova
Tatiana Konnova
EOElena V. Osipova
Elena V. Osipova
YGYuri Gogolev
Yuri Gogolev
The phytohormone abscisic acid (ABA) plays an important role in plant growth and in response to abiotic stress factors. At the same time, its accumulation in soil can negatively affect seed germination, inhibit root growth and increase plant sensitivity to pathogens. ABA is an inert compound resistant to spontaneous hydrolysis and its biological transformation is scarcely understood. Recently, the strain Rhodococcus sp. P1Y was described as a rhizosphere bacterium assimilating ABA as a sole carbon source in batch culture and affecting ABA concentrations in plant roots. In this work, the intermediate product of ABA decomposition by this bacterium was isolated and purified by preparative HPLC techniques. Proof that this compound belongs to ABA derivatives was carried out by measuring the molar radioactivity of the conversion products of this phytohormone labeled with tritium. The chemical structure of this compound was determined by instrumental techniques including high-resolution mass spectrometry, NMR spectrometry, FTIR and UV spectroscopies. As a result, the metabolite was identified as (4RS)-4-hydroxy-3,5,5-trimethyl-4-[(E)-3-oxobut-1-enyl]cyclohex-2-en-1-one (dehydrovomifoliol). Based on the data obtained, it was concluded that the pathway of bacterial degradation and assimilation of ABA begins with a gradual shortening of the acyl part of the molecule.