Project description:This study compared the genome of Streptomyces rimosus rimosus against that of Streptomyces coelicolor. It also compared 4 strains with changes in oxytetracycline production and derived from G7, the type strain, against G7. Keywords: Comparative genomic hybridization
Project description:Background: Hypovirulent fungal strain Gibellulopsis nigrescens Vn-1 cross-protects sunflower against Verticillium wilt. To discover the mechanism of cross-protection by this hypovirulent strain, we analyzed defense enzyme activities and transcriptomes of root samples infected with virulent and hypovirulent strains. Results: Defense enzyme activities increased after inoculation, with the highest levels observed 24 h post-inoculation. At the same time, defense enzyme gene expressions were upregulated, and H2O2 accumulation decreased. A comparative transcriptome analysis revealed that there are 23 GO terms significantly enriched in the Vn-1 group compared with the control, including three specific oxidoreductase-related and four signaling related GO terms. In addition, there were 7 KEGG pathway only enriched in V33 group compared with the control, and 3 KEGG pathway (Alanine, aspartate and glutamate metabolism, Cutin, suberine and wax biosynthesis and Ribosome) only enriched in Vn-1 compared with the control. Conclusions: According to our results, both hypovirulent strain G. nigrescens Vn-1 and virulent strain V. dahliae V33 can reduce levels of reactive oxygen species in sunflower seedling by regulating HaCAT and HaPOD expression. Twenty three GO terms and three KEGG pathway contribute to the formation of specific resistance against virulent strain V. dahliae V33.
Project description:In this study, we describe the isolation and identification of Streptomyces isolates collected from traditional medicinal plants’ rhizosphere during a campaign in Hamedan Province, Iran. Traditional medicinal plants represent a rich and unique source for the isolation of Streptomyces and new antimicrobial compounds. This strain was isolated from the rhizosphere of Helichrysum rubicundum
Project description:To identify unique gene expression in cAMP supplemented Streptomyces coelicolor M1146 strain. The genes with different gene expression might be key genes to understand the effects of cAMP supplementation on the transcriptome of Streptomyces coelicolor M1146.
Project description:To identify unique gene expression in cAMP supplemented Streptomyces coelicolor M145 strain. The genes with different gene expression might be key genes to understand the effects of cAMP supplementation on the transcriptome of Streptomyces coelicolor M145.
Project description:Two component sensor-response regulator systems (TCSs) are very common in the genomes of the Streptomyces species that have been fully sequenced to date. It has been suggested that this large number is an evolutionary response to the variable environment that Streptomyces encounter in soil. Notwithstanding this, TCSs are also more common in the sequenced genomes of other Actinomycetales when these are compared to the genomes of most other eubacteria. In this study, we have used DNA/DNA genome microarray analysis to compare fourteen Streptomyces species and one closely related genus to Streptomyces coelicolor in order to identify a core group of such systems. This core group is compared to the syntenous and non-syntenous TCSs present in the genome sequences of other Actinomycetales in order to separate the systems into those present in Actinomycetales in general, the Streptomyces specific systems and the species specific systems. Horizontal transfer does not seem to play a very important role in the evolution of the TCS complement analyzed in this study. However, cognate pairs do not necessarily seem to evolve at the same pace, which may indicate the evolutionary responses to environmental variation may be reflected differently in sequence changes within the two components of the TCSs. The overall analysis allowed subclassification of the orphan TCSs and the TCS cognate pairs and identification of possible targets for further study using gene knockouts, gene overexpression, reporter genes and yeast two hybrid analysis.
