Alla Bryanskaya

Dr. Alla Bryanskaya

Institute of Cytology and Genetics, Novosibirsk, Novosibirskaya Oblast’, Russia
orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

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

Representative Publications

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23 November 2015 in Scientific Reports
Verified
Journal Article
Open access
KSKonstantin V. Starostin
Konstantin V. Starostin
EDEvgeny A. Demidov
Evgeny A. Demidov
ABAlla Bryanskaya
Alla Bryanskaya
VEVadim M. Efimov
Vadim M. Efimov
ARAlexey S. Rozanov
Alexey S. Rozanov
SPSergey E. Peltek
Sergey E. Peltek
Microorganism identification by MALDI TOF mass-spectrometry is based on the comparison of the mass spectrum of the studied organism with those of reference strains. It is a rapid and reliable method. However, commercial databases and programs are mostly designed for identification of clinically important strains and can be used only for particular mass spectrometer models. The need for open platforms and reference databases is obvious. In this study we describe a geometric approach for microorganism identification by mass spectra and demonstrate its capabilities by analyzing 24 strains belonging to theBacillus pumilusgroup. This method is based on representing mass spectra as points on a multidimensional space, which allows us to use geometric distances to compare the spectra. Delimitation of microorganisms performed by geometric approach correlates well with the results of molecular phylogenetic analysis and clustering using Biotyper 3.1. All three methods used allowed us to reliably divide the strains into two groups corresponding to closely related species,Bacillus pumilusandBacillus altitudinis. The method developed by us will be implemented in a Web interface designed for using open reference databases for microorganism identification. The data is available athttp://www.bionet.nsc.ru/mbl/database/database.html.

1 June 2015 in Russian Geology and Geophysics
Verified
Journal Article
Closed access
ELE.V. Lazareva
E.V. Lazareva
SZS.M. Zhmodik
S.M. Zhmodik
NDN.L. Dobretsov
N.L. Dobretsov
ATA.V. Tolstov
A.V. Tolstov
BSB.L. Shcherbov
B.L. Shcherbov
ABAlla Bryanskaya
Alla Bryanskaya

1 November 2015 in Algal Research
Verified
Journal Article
Closed access
APA.V. Piligaev
A.V. Piligaev
KSK.N. Sorokina
K.N. Sorokina
ABAlla Bryanskaya
Alla Bryanskaya
SPS.E. Peltek
S.E. Peltek
Nikolay KolchanovNikolay Kolchanov
Nikolay Kolchanov
VPV.N. Parmon
V.N. Parmon

7 February 2024 in Microorganisms
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Journal Article
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TKTamara M. Khlebodarova
Tamara M. Khlebodarova
NBNatalia V. Bogacheva
Natalia V. Bogacheva
AZAndrey V. Zadorozhny
Andrey V. Zadorozhny
ABAlla Bryanskaya
Alla Bryanskaya
AVAsya Rifhatovna Vasilieva
Asya Rifhatovna Vasilieva
SPS. Peltek
S. Peltek
In the 1980s, Escherichia coli was the preferred host for heterologous protein expression owing to its capacity for rapid growth in complex media; well-studied genetics; rapid and direct transformation with foreign DNA; and easily scalable fermentation. Despite the relative ease of use of E. coli for achieving the high expression of many recombinant proteins, for some proteins, e.g., membrane proteins or proteins of eukaryotic origin, this approach can be rather ineffective. Another microorganism long-used and popular as an expression system is baker’s yeast, Saccharomyces cerevisiae. In spite of a number of obvious advantages of these yeasts as host cells, there are some limitations on their use as expression systems, for example, inefficient secretion, misfolding, hyperglycosylation, and aberrant proteolytic processing of proteins. Over the past decade, nontraditional yeast species have been adapted to the role of alternative hosts for the production of recombinant proteins, e.g., Komagataella phaffii, Yarrowia lipolytica, and Schizosaccharomyces pombe. These yeast species’ several physiological characteristics (that are different from those of S. cerevisiae), such as faster growth on cheap carbon sources and higher secretion capacity, make them practical alternative hosts for biotechnological purposes. Currently, the K. phaffii-based expression system is one of the most popular for the production of heterologous proteins. Along with the low secretion of endogenous proteins, K. phaffii efficiently produces and secretes heterologous proteins in high yields, thereby reducing the cost of purifying the latter. This review will discuss practical approaches and technological solutions for the efficient expression of recombinant proteins in K. phaffii, mainly based on the example of enzymes used for the feed industry.

28 December 2017 in BMC Ecology and Evolution
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Journal Article
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ARAleksei Rozanov
Aleksei Rozanov
ABAlla Bryanskaya
Alla Bryanskaya
TITimofey Vladimirovich Ivanisenko
Timofey Vladimirovich Ivanisenko
TMTatyana Konstantinovna Malup
Tatyana Konstantinovna Malup
SPSergey Evgenievich Peltek
Sergey Evgenievich Peltek
Microbial mats are a good model system for ecological and evolutionary analysis of microbial communities. There are more than 20 alkaline hot springs on the banks of the Barguzin river inflows. Water temperature reaches 75 °C and pH is usually 8.0–9.0. The formation of microbial mats is observed in all hot springs. Microbial communities of hot springs of the Baikal rift zone are poorly studied. Garga is the biggest hot spring in this area. In this study, we investigated bacterial and archaeal diversity of the Garga hot spring (Baikal rift zone, Russia) using 16S rRNA metagenomic sequencing. We studied two types of microbial communities: (i) small white biofilms on rocks in the points with the highest temperature (75 °C) and (ii) continuous thick phototrophic microbial mats observed at temperatures below 70 °C. Archaea (mainly Crenarchaeota; 19.8% of the total sequences) were detected only in the small biofilms. The high abundance of Archaea in the sample from hot springs of the Baikal rift zone supplemented our knowledge of the distribution of Archaea. Most archaeal sequences had low similarity to known Archaea. In the microbial mats, primary products were formed by cyanobacteria of the genus Leptolyngbya. Heterotrophic microorganisms were mostly represented by Actinobacteria and Proteobacteria in all studied samples of the microbial mats. Planctomycetes, Chloroflexi, and Chlorobi were abundant in the middle layer of the microbial mats, while heterotrophic microorganisms represented mostly by Firmicutes (Clostridia, strict anaerobes) dominated in the bottom part. Besides prokaryotes, we detect some species of Algae with help of detection their chloroplasts 16 s rRNA. High abundance of Archaea in samples from hot springs of the Baikal rift zone supplemented our knowledge of the distribution of Archaea. Most archaeal sequences had low similarity to known Archaea. Metagenomic analysis of microbial communities of the microbial mat of Garga hot spring showed that the three studied points sampled at 70 °C, 55 °C, and 45 °C had similar species composition. Cyanobacteria of the genus Leptolyngbya dominated in the upper layer of the microbial mat. Chloroflexi and Chlorobi were less abundant and were mostly observed in the middle part of the microbial mat. We detected domains of heterotrophic organisms in high abundance (Proteobacteria, Firmicutes, Verrucomicrobia, Planctomicetes, Bacteroidetes, Actinobacteria, Thermi), according to metabolic properties of known relatives, which can form complete cycles of carbon, sulphur, and nitrogen in the microbial mat. The studied microbial mats evolved in early stages of biosphere formation. They can live autonomously, providing full cycles of substances and preventing live activity products poisoning.

19 December 2014 in BMC Genomics
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Journal Article
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ARAlexey S Rozanov
Alexey S Rozanov
ABAlla Bryanskaya
Alla Bryanskaya
TMTatiana K Malup
Tatiana K Malup
IMIrina Mescheryakova
Irina Mescheryakova
ELElena V Lazareva
Elena V Lazareva
SPS. Peltek
S. Peltek
Geothermal areas are of great interest for the study of microbial communities. The results of such investigations can be used in a variety of fields (ecology, microbiology, medicine) to answer fundamental questions, as well as those with practical benefits. Uzon caldera is located in the Uzon-Geyser depression that is situated in the centre of the Karym-Semyachin region of the East Kamchatka graben-synclinorium. The microbial communities of Zavarzin spring are well studied; however, its benthic microbial mat has not been previously described.