Sulfate-reducing bacteria in marine sediments

The occurrence of hydrogen sulfide in the waters of certain seas, fjords, and basins, as well as the presence of black or blue stinking sediments, can hardly escape the notice of any marine scientist. It is not surprising, therefore, that the eminent oceanographer Murray (Murray and Irvine, 1895) concerned himself with the nature of these materials and postulated their bacterial origin even before bacteriologists had described the specific organisms involved

Ökologische Untersuchungen zur Nitrifikation in Nord-und Ostsee

Ammonia, nitrite and nitrate were regularly estimated at several stations in the Kieler Bucht (western Baltic Sea) since November 1964. There are considerable seasonal changes in the contents of these 3 nitrogen compounds with impressive maxima of nitrite and nitrate in February or at the beginning of March. The great increase of nitrite and nitrate during the winter and also a smaller increase in summer are mainly caused by oxidation of ammonia, first to nitrite and then to nitrate, by nitrifying bacteria. In consequence chemoautotrophic nitrite- and nitratebacteria could be found in the water as well as in sediments all over the Kieler Bucht and also in the North Sea around the isle of Helgoland. These nitrifying bacteria are able to oxidize ammonia or nitrite in salinity conditions typical for the western Baltic Sea and the North Sea

Occurrence and population densities of yeast species in a fresh-water lake

Quantitative studies of yeasts present in surface and deep water samples from a fresh water body (Douglas Lake, Michigan) revealed 12 species ( Candida parapsilosis, C. pulcherrima, Cryptococcus albidus, Cr. diffluens, Cr. gastricus, Cr. laurentii, Rhodotorula glutinis, R. pilimanae, R. rubra, Trichosporon cutaneum, Debaryomyces sp., “black yeasts”). In two regions of surface sampling the population densities averaged 39.6 and 5.5 cells per 100 ml respectively, whereas the average deep water count was 40.3 cells per 100 ml. Yeasts of the genus Rhodotorula predominated.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/41778/1/10482_2005_Article_BF02046074.pd

Identification and Characterization of a Mef2 Transcriptional Activator in Schistosome Parasites

Myocyte enhancer factor 2 protein (Mef2) is an evolutionarily conserved activator of transcription that is critical to induce and control complex processes in myogenesis and neurogenesis in vertebrates and insects, and osteogenesis in vertebrates. In Drosophila, Mef2 null mutants are unable to produce differentiated muscle cells, and in vertebrates, Mef2 mutants are embryonic lethal. Schistosome worms are responsible for over 200 million cases of schistosomiasis globally, but little is known about early development of schistosome parasites after infecting a vertebrate host. Understanding basic schistosome development could be crucial to delineating potential drug targets. Here, we identify and characterize Mef2 from the schistosome worm Schistosoma mansoni (SmMef2). We initially identified SmMef2 as a homolog to the yeast Mef2 homolog, Resistance to Lethality of MKK1P386 overexpression (Rlm1), and we show that SmMef2 is homologous to conserved Mef2 family proteins. Using a genetics approach, we demonstrate that SmMef2 is a transactivator that can induce transcription of four separate heterologous reporter genes by yeast one-hybrid analysis. We also show that Mef2 is expressed during several stages of schistosome development by quantitative PCR and that it can bind to conserved Mef2 DNA consensus binding sequences