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The aim of this paper was to investigate the effects of microwave radiation on the viability of Paenibacillus larvae spores and to study the relationship between the microwave power consumption, the exposure time and the number of spores in the examined suspensions. Sterile distilled water suspensions were made using larval detritus, to contain tens, hundreds and thousands of spores. The suspensions of all the dilutions were gradually exposed to a microwave radiation power of 170, 510 and 850 W. In all the cases, the exposure time was 1, 2, 3, 4, 5, 10, 15, 20, 25 and 30 minutes. After cooling, 0.1 ml of each exposed suspension was inoculated onto three modified MYP (mannitol egg yolk polymyxin) agar plates and incubated aerobically at 37 ± 1 °C for 120 hours. The statistical evaluation of the spore counts decreasing with time was performed with the use of the nonparametric Friedman's variance test using the Unistat Statistical Package v6.5. The results showed that the rate of devitalisation of the spores is dependent on the microwave oven power consumption, but independent of the number of spores. Using a power consumption of 170, 510 and 850 W, the devitalisation of the spores occurred after 15, 3 and 2 min of exposure, respectively.

The aim of this paper was to investigate the effects of microwave radiation on the viability of Paenibacillus larvae spores and to study the relationship between the microwave power consumption, the exposure time and the number of spores in the examined suspensions. Sterile distilled water suspensions were made using larval detritus, to contain tens, hundreds and thousands of spores. The suspensions of all the dilutions were gradually exposed to a microwave radiation power of 170, 510 and 850 W. In all the cases, the exposure time was 1, 2, 3, 4, 5, 10, 15, 20, 25 and 30 minutes. After cooling, 0.1 ml of each exposed suspension was inoculated onto three modified MYP (mannitol egg yolk polymyxin) agar plates and incubated aerobically at 37 ± 1 °C for 120 hours. The statistical evaluation of the spore counts decreasing with time was performed with the use of the nonparametric Friedman's variance test using the Unistat Statistical Package v6.5. The results showed that the rate of devitalisation of the spores is dependent on the microwave oven power consumption, but independent of the number of spores. Using a power consumption of 170, 510 and 850 W, the devitalisation of the spores occurred after 15, 3 and 2 min of exposure, respectively. [ABSTRACT FROM AUTHOR]

Ktedonobacter racemifer corrig. Cavaletti et al. 2007 is the type species of the genus Ktedonobacter, which in turn is the type genus of the family Ktedonobacteraceae, the type family of the order Ktedonobacterales within the class Ktedonobacteria in the phylum 'Chloroflexi'. Although K. racemifer shares some morphological features with the actinobacteria, it is of special interest because it was the first cultivated representative of a deep branching unclassified lineage of otherwise uncultivated environmental phylotypes tentatively located within the phylum 'Chloroflexi'. The aerobic, filamentous, non-motile, spore-forming Gram-positive heterotroph was isolated from soil in Italy. The 13,661,586 bp long non-contiguous finished genome consists of ten contigs and is the first reported genome sequence from a member of the class Ktedonobacteria. With its 11,453 protein-coding and 87 RNA genes, it is the largest prokaryotic genome reported so far. It comprises a large number of over-represented COGs, particularly genes associated with transposons, causing the genetic redundancy within the genome being considerably larger than expected by chance. This work is a part of the Genomic Encyclopedia of Bacteria and Archaea project.

Desulfotomaculum acetoxidans Widdel and Pfennig 1977 was one of the first sulfate-reducing bacteria known to grow with acetate as sole energy and carbon source. It is able to oxidize substrates completely to carbon dioxide with sulfate as the electron acceptor, which is reduced to hydrogen sulfide. All available data about this species are based on strain 5575(T), isolated from piggery waste in Germany. Here we describe the features of this organism, together with the complete genome sequence and annotation. This is the first completed genome sequence of a Desulfotomaculum species with validly published name. The 4,545,624 bp long single replicon genome with its 4370 protein-coding and 100 RNA genes is a part of the Genomic Encyclopedia of Bacteria and Archaea project.

Studies in all three agroclimatic regions of Belarus have allowed us to obtain more then 100 isolates of B. cinerea causing gray mold of many plants. The isolates were shown to belong to the three cultural-morphological groups such as mycelial, sporulating and sclerotial. Mycelial isolates (48.5%) concerned by some researchers as the high pathogenic group prevail over other two groups. Nutritive substrate was proved not to determine the formation of strictly definite morphotype. The rate of radial growth of B. cinerea colonies reveals no correlation with morphological peculiarities of these. Strict regularities in the forming of spores and sclerotia were not established when characterizing isolates from different cultural groups what indicates the presence of transitional forms between detected ones. Thus, population of B. cinerea in Belarus conditions is morpho-physiologically diverse.

Desulfotomaculum ruminis Campbell and Postgate 1965 is a member of the large genus Desulfotomaculum which contains 30 species and is contained in the family Peptococcaceae. This species is of interest because it represents one of the few sulfate-reducing bacteria that have been isolated from the rumen. Here we describe the features of D. ruminis together with the complete genome sequence and annotation. The 3,969,014 bp long chromosome with a total of 3,901 protein-coding and 85 RNA genes is the second completed genome sequence of a type strain of the genus Desulfotomaculum to be pub-lished, and was sequenced as part of the DOE Joint Genome Institute Community Sequencing Program 2009. [ABSTRACT FROM AUTHOR]

Desulfotomaculum ruminis Campbell and Postgate 1965 is a member of the large genus Desulfotomaculum which contains 30 species and is contained in the family Peptococcaceae. This species is of interest because it represents one of the few sulfate-reducing bacteria that have been isolated from the rumen. Here we describe the features of D. ruminis together with the complete genome sequence and annotation. The 3,969,014 bp long chromosome with a total of 3,901 protein-coding and 85 RNA genes is the second completed genome sequence of a type strain of the genus Desulfotomaculum to be pub-lished, and was sequenced as part of the DOE Joint Genome Institute Community Sequencing Program 2009. [ABSTRACT FROM AUTHOR]

Desulfotomaculum ruminis Campbell and Postgate 1965 is a member of the large genus Desulfotomaculum which contains 30 species and is contained in the family Peptococcaceae. This species is of interest because it represents one of the few sulfate-reducing bacteria that have been isolated from the rumen. Here we describe the features of D. ruminis together with the complete genome sequence and annotation. The 3,969,014 bp long chromosome with a total of 3,901 protein-coding and 85 RNA genes is the second completed genome sequence of a type strain of the genus Desulfotomaculum to be published, and was sequenced as part of the DOE Joint Genome Institute Community Sequencing Program 2009.