TEST-SYSTEMS FOR MONITORING OF CORROSION-RELEVANT SULFATE-REDUCING BACTERIA USING REAL-TIME PCR ASSAY
Journal: Biotechnologia Acta (Vol.9, No. 1)Publication Date: 2016-02-25
Authors : D. R. Аbdulina; L. М. Purish; G. А. Iutynska; М. М. Nikitin; A. G. Golikov;
Page : 48-54
Keywords : sulfate-reducing bacteria; dissimilatory sulfate-reduction genes; test-systems; real-time PCR.;
Abstract
The possibility of the designing test-systems for specific detection of corrosive-relevant sulfate-reducing bacteria using real-time PCR assay were investigated. This method of the bacteria identification is based on the detection of the functional genes, encoding key enzymes of dissimilatory sulfate-reduction pathway, i.e. dissimilatory sulfitreductase α subunit dsrA. It was established among the six test-systems specificity reveal only three designed on the base of Desulfotomaculum, Desulfovibrio, Desulfobulbus genera sequences. The most corrosive-relevant strain Desulfovibrio sp. UCM B-11503 dsrA gene detected more effectively (threshold cycle was 20,0), than less corrosive-relevant strains Desulfovibrio sp. UCM B-11504 (threshold cycle was 28,1) and for Desulfotomaculum sp. UCM B-11505 and Desulfomicrobium sp. UCМ B-11506 were 24,9 and 23,1 cycles, respectively. Test-systems allowed identifying corrosive-relevant sulfate-reducing bacteria faster and more effective. This approach will serve as a base for monitoring of these bacteria for estimating corrosion sites on the high-level dangerous man-caused objects.
Other Latest Articles
- INFLUENCE OF CULTIVATION CONDITIONS ON ANTIMICROBIAL PROPERTIES OF Nocardia vaccinii ІMV B-7405 SURFACTANTS
- IRE1 KNOCKDOWN MODIFIES GLUCOSE AND GLUTAMINE DEPRIVATION EFFECTS ON THE EXPRESSION OF PROLIFERATION RELATED GENES IN U87 GLIOMA CELLS
- PROBLEM OF GENETICALLY MODIFIED FOODS SAFETY: A TOXICOLOGIST’S VIEW
- NUTRIENT MEDIA FOR OBTAINING A PURE CULTURE OF FUNGI OF THE GENUS Pleurotus in vitro
- POSSIBILITY OF COMPUTER EXPERIMENT IN STUDY OF ANIMAL SPERMATOZOA HETEROGENEITY
Last modified: 2016-11-11 20:35:50