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101. Effect of Long-Term Farming Practices on Agricultural Soil Microbiome Members Represented by Metagenomically Assembled Genomes (MAGs) and Their Predicted Plant-Beneficial Genes.

102. Plant species identity and soil characteristics determine rhizosphere soil bacteria community composition in European temperate forests.

103. Effect of intestinal tapeworms on the gut microbiota of the common carp, Cyprinus carpio.

104. Effect of Drought Stress and Developmental Stages on Microbial Community Structure and Diversity in Peanut Rhizosphere Soil.

105. The origin of aerobic methanotrophy within the Proteobacteria.

106. Gut bacteria of the cowpea beetle mediate its resistance to dichlorvos and susceptibility to Lippia adoensis essential oil.

107. Diversity of the microbial community and cultivable protease-producing bacteria in the sediments of the Bohai Sea, Yellow Sea and South China Sea.

108. The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives.

109. A comparison of dynamic distributions of intestinal microbiota between Large White and Chinese Shanxi Black pigs.

110. Assessing the spatial and temporal variability of bacterial communities in two Bardenpho wastewater treatment systems via Illumina MiSeq sequencing.

111. Exploring the bacteriome in anthropophilic ticks: To investigate the vectors for diagnosis.

112. Using formalin fixed paraffin embedded tissue to characterize the preterm gut microbiota in necrotising enterocolitis and spontaneous isolated perforation using marginal and diseased tissue.

113. Effects of Panax ginseng polysaccharides on the gut microbiota in mice with antibiotic-associated diarrhea.

114. Relic DNA does not obscure the microbial community of paddy soil microbial fuel cells.

115. Soil microbial community composition closely associates with specific enzyme activities and soil carbon chemistry in a long-term nitrogen fertilized grassland.

116. Community diversity and potential functions of rhizosphere-associated bacteria of nickel hyperaccumulators found in Albania.

117. Bacterial community changes in a glacial-fed Tibetan lake are correlated with glacial melting.

118. The soil microbial community of turf: linear and nonlinear changes of taxa and N-cycling gene abundances over a century-long turf development.

119. Analysis of Bacterial Communities in White Clover Seeds via High-Throughput Sequencing of 16S rRNA Gene.

120. Seasonal and spatial variation in the sediment bacterial community and diversity of Lake Bosten, China.

121. Impacts of heavy metals and soil properties at a Nigerian e-waste site on soil microbial community.

122. Methylotrophs and Methylotroph Populations for Chloromethane Degradation.

123. Specialized Metabolites from Methylotrophic Proteobacteria.

124. Microbial community composition and diversity in the Indian Ocean deep sea REY-rich muds.

125. Characterization of microbial communities of soils from gold mine tailings and identification of mercury-resistant strain.

126. 16S Metagenomic Comparison of Plasmodium falciparum -Infected and Noninfected Anopheles gambiae and Anopheles funestus Microbiota from Senegal.

127. Primary Colonizing Betaproteobacteriales Play a Key Role in the Growth of Legionella pneumophila in Biofilms on Surfaces Exposed to Drinking Water Treated by Slow Sand Filtration.

128. Exploring the rearrangement of sensory intelligence in proteobacteria: insight of Pho regulon.

129. Biofilm and planktonic bacterial communities in a drinking water distribution system supplied with untreated groundwater.

130. Structural and functional shifts of bacterioplanktonic communities associated with spatiotemporal gradients in river outlets of the subtropical Pearl River Estuary, South China.

131. Increasing Dietary Fiber Intake Is Associated with a Distinct Esophageal Microbiome.

132. Modernized Tools for Streamlined Genetic Manipulation and Comparative Study of Wild and Diverse Proteobacterial Lineages.

133. [Microbial Community Characteristics of Shortcut Nitrification Start-up in Different MBR-Inoculated Sludges].

134. Burn injury alters the intestinal microbiome's taxonomic composition and functional gene expression.

135. High PAH degradation and activity of degrading bacteria during alfalfa growth where a contrasted active community developed in comparison to unplanted soil.

136. Halobacteriovorax isolated from marine water of the Adriatic sea, Italy, as an effective predator of Vibrio parahaemolyticus, non-O1/O139 V. cholerae, V. vulnificus.

137. Hydrocarbon degradation and response of seafloor sediment bacterial community in the northern Gulf of Mexico to light Louisiana sweet crude oil.

138. Phylogenetic analyses of bacteria associated with the processing of iru and ogiri condiments.

139. Metagenomics reveals niche partitioning within the phototrophic zone of a microbial mat.

140. Microbiota dysbiosis and its pathophysiological significance in bowel obstruction.

141. Environmental Controls on Soil Microbial Communities in a Seasonally Dry Tropical Forest.

142. Diversity, specificity, co-occurrence and hub taxa of the bacterial-fungal pollen microbiome.

143. The Microbial Community of Tardigrades: Environmental Influence and Species Specificity of Microbiome Structure and Composition.

144. The Bacterial Population of Neutral Mine Drainage Water of Elizabeth's Shaft (Slovinky, Slovakia).

145. Comparative Analysis of the Gut Bacterial Community of Four Anastrepha Fruit Flies (Diptera: Tephritidae) Based on Pyrosequencing.

146. Taxonomical Resolution and Distribution of Bacterioplankton Along the Vertical Gradient Reveals Pronounced Spatiotemporal Patterns in Contrasted Temperate Freshwater Lakes.

147. Influence of Darkness and Aging on Marine and Freshwater Biofilm Microbial Communities Using Microcosm Experiments.

148. Iron-oxidizing bacteria in marine environments: recent progresses and future directions.

149. Nitrogen-fixing populations of Planctomycetes and Proteobacteria are abundant in surface ocean metagenomes.

150. Proteobacteria and Bacteroidetes are major phyla of filterable bacteria passing through 0.22 μm pore size membrane filter, in Lake Sanaru, Hamamatsu, Japan.

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