New Gene of Aminoglycoside Phosphotransferase aph(3'')-Id from Streptomyces rimosus ATCC10970, Encoding Streptomycin Resistance
- Authors: Alekseeva M.G.1, Rudakova N.N.1, Zakharevich N.V.1, Mavletova D.A.1, Boyko K.M.2,3, Nikolaeva A.Y.3, Korzhenevskiy D.A.3, Danilenko V.N.1
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Affiliations:
- Vavilov Institute of General Genetics, Russian Academy of Sciences
- Bach Institute of Biochemistry, Federal Research Centre of Biotechnology, Russian Academy of Sciences
- National Research Center Kurchatov Institute
- Issue: Vol 54, No 10 (2018)
- Pages: 1254-1258
- Section: Short Communications
- URL: https://journal-vniispk.ru/1022-7954/article/view/188635
- DOI: https://doi.org/10.1134/S1022795418100034
- ID: 188635
Cite item
Abstract
Previously, in the strain Streptomyces rimosus ATCC10970 (producer of oxytetracycline), the aminoglycoside phosphotransferase AphVIII, determining kanamycin, neomycin, and paromomycin resistance, was identified and characterized. Recently, the authors obtained the 3D structure of AphVIII. The 14 aph genes, including gene aphVIII, were annotated when the genome of S. rimosus ATCC10970 was sequenced. In the present study, a new aph(3'')-Id (aphSR3) gene encoding streptomycin phosphotansferase was first identified in the strain of S. rimosus ATCC10970 using bioinformatic and comparative phylogenetic analysis of the aphSR1-aphSR14 genes with the previously known aph genes from clinical isolates and producer strains of aminoglycoside antibiotics belonging to seven subfamilies. When cloning, it was found that the gene aphSR3 (aph(3'')-Id) in Escherichia coli causes resistance to streptomycin at a concentration of 150 μg/mL. The obtained data can be used in practical terms to study the distribution and features of the functions of genes that determine the natural resistance to aminoglycoside antibiotics in actinobacteria of the genus Streptomyces.
About the authors
M. G. Alekseeva
Vavilov Institute of General Genetics, Russian Academy of Sciences
Email: valerid@vigg.ru
Russian Federation, Moscow, 119991
N. N. Rudakova
Vavilov Institute of General Genetics, Russian Academy of Sciences
Email: valerid@vigg.ru
Russian Federation, Moscow, 119991
N. V. Zakharevich
Vavilov Institute of General Genetics, Russian Academy of Sciences
Email: valerid@vigg.ru
Russian Federation, Moscow, 119991
D. A. Mavletova
Vavilov Institute of General Genetics, Russian Academy of Sciences
Email: valerid@vigg.ru
Russian Federation, Moscow, 119991
K. M. Boyko
Bach Institute of Biochemistry, Federal Research Centre of Biotechnology,Russian Academy of Sciences; National Research Center Kurchatov Institute
Email: valerid@vigg.ru
Russian Federation, Moscow, 119071; Moscow, 123182
A. Y. Nikolaeva
National Research Center Kurchatov Institute
Email: valerid@vigg.ru
Russian Federation, Moscow, 123182
D. A. Korzhenevskiy
National Research Center Kurchatov Institute
Email: valerid@vigg.ru
Russian Federation, Moscow, 123182
V. N. Danilenko
Vavilov Institute of General Genetics, Russian Academy of Sciences
Author for correspondence.
Email: valerid@vigg.ru
Russian Federation, Moscow, 119991
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