Frontiers in microbiology

mBio

Biochemical Society transactions

[1] YtrA, a GntR-Family Transcription Factor, Represses Two Genetic Loci Encoding Membrane Proteins in .

[2] Microbial Communities of Red Sea Coral Reefs

[3] the effect of dna extraction methods on observed microbial communities from fibrous and liquid rumen fractions of dairy cows

[4] study of genetics, phenotypic and behavioral properties of eubacteria and archaebacteria

[5] computational exploration of putative luxr solos in archaea and their functional implications in quorum sensing

[6] nitrification is a primary driver of nitrous oxide production in laboratory microcosms from different land-use soils

[7] evaluation of 16s rrna gene primer pairs for monitoring microbial community structures showed high reproducibility within and low comparability between datasets generated with multiple archaeal and bacterial primer pairs

[8] deep subsurface mine stalactites trap endemic fissure fluid archaea, bacteria and nematoda possibly originating from ancient (inland) seas.

[9] putative archaeal viruses from the mesopelagic ocean

[10] “altiarchaeales”: uncultivated archaea from the subsurface

[11] diversity and subcellular distribution of archaeal secreted proteins

[12] tandem-repeat protein domains across the tree of life

[13] bacterial and archaeal α-amylases: diversity and amelioration of the desirable characteristics for industrial applications

[14] phylogenetic and functional analysis of metagenome sequence from high-temperature archaeal habitats demonstrate linkages between metabolic potential and geochemistry

[15] efficient crispr-mediated post-transcriptional gene silencing in a hyperthermophilic archaeon using multiplexed crrna expression

[16] the human-associated archaeon methanosphaera stadtmanae is recognized through its rna and induces tlr8-dependent nlrp3 inflammasome activation

[17] quantification of ammonia oxidation rates and the distribution of ammonia-oxidizing archaea and bacteria in marine sediment depth profiles from catalina island, california

[18] the distribution and abundance of archaeal tetraether lipids in u.s. great basin hot springs

[19] distribution, abundance, and diversity patterns of the thermoacidophilic deep-sea hydrothermal vent euryarchaeota 2 (dhve2).

[20] replication slippage of the thermophilic dna polymerases b and d from the euryarchaeota pyrococcus abyssi

[21] differences in the composition of archaeal communities in sediments from contrasting zones of lake taihu

[22] Comprehensive glycoproteomics shines new light on the complexity and extent of glycosylation in archaea

[23] A Well-Conserved Archaeal B-Family Polymerase Functions as an Extender in Translesion Synthesis.

[24] Enzymatic Switching Between Archaeal DNA Polymerases Facilitates Abasic Site Bypass.

[25] Form and function of archaeal genomes.

[26] Protein Adaptations in Archaeal Extremophiles

[27] Ammonia-Oxidizing Archaea (AOA) Play with Ammonia-Oxidizing Bacteria (AOB) in Nitrogen Removal from Wastewater

[28] Diversity and Niche of Archaea in Bioremediation

[29] Structural insights into the mechanism of internal aldimine formation and catalytic loop dynamics in an archaeal Group II decarboxylase.

[30] Robust Archaeal and Bacterial Communities Inhabit Shallow Subsurface Sediments of the Bonneville Salt Flats.

[31] Factors controlling the distribution of archaeal tetraethers in terrestrial hot springs.

[32] Diversity and spatial distribution of amoA-encoding archaea in the deep-sea sediments of the tropical West Pacific Continental Margin.

[33] Archaeology of Archaea: geomicrobiological record of Pleistocene thermal events concealed in a deep-sea subseafloor environment.

[34] Effects of applying inorganic fertilizer and organic manure for 35 years on the structure and diversity of ammonia-oxidizing archaea communities in a Chinese Mollisols field.

[35] Corrigendum to “Natrachaeobius chitinivorans gen. nov., sp. nov., and Natrarchaeobius haloalkaliphilus sp. nov., alkaliphilic, chitin-utilizing haloarchaea from hypersaline alkaline lakes” (Systematic and Applied Microbiology (2019) 42(3) (309–318), (S0723202018304387), (10.1016/j.syapm.2019.01.001))

[36] Bacteria, fungi and archaea domains in rhizospheric soil and their effects in enhancing agricultural productivity

[37] Characterizing Chemoautotrophy and Heterotrophy in Marine Archaea and Bacteria With Single-Cell Multi-isotope NanoSIP

[38] Abstract P-11: Conformational Study of an Archaeal Photoreceptor/Transducer Complex from Natronomonas pharaonis Assembled in Styrene-Maleic Acid Lipid Particles Using Electron Paramagnetic Resonance Spectroscopy

[39] Organic Matter Regulates Ammonia-Oxidizing Bacterial and Archaeal Communities in the Surface Sediments of Aquaculture Ponds.

[40] Altered Gut Archaea Composition and Interaction with Bacteria are Associated with Colorectal Cancer.

[41] Levels of heavy metal concentrations and their effect on net nitrification rates and nitrifying archaea/bacteria in paddy soils of Bangladesh

[42] Green manuring inhibits nitrification in a typical paddy soil by changing the contributions of ammonia-oxidizing archaea and bacteria

[43] Novel insights into plant-associated archaea and their functioning in arugula (Eruca sativa Mill.)

[44] Anaerobic treatment of municipal wastewater at ambient temperature: Analysis of archaeal community structure and recovery of dissolved methane

[45] close encounters of the third domain: the emerging genomic view of archaeal diversity and evolution

[46] monitoring physiological changes in haloarchaeal cell during virus release

[47] metaviromics of namib desert salt pans: a novel lineage of haloarchaeal salterproviruses and a rich source of ssdna viruses

[48] s-layer glycoproteins and flagellins: reporters of archaeal posttranslational modifications

[49] understanding dna repair in hyperthermophilic archaea: persistent gaps and other reasons to focus on the fork

[50] computational exploration of putative luxr solos in archaea and their functional implications in quorum sensing

[51] amoa-encoding archaea and thaumarchaeol in the lakes on the northeastern qinghai-tibetan plateau, china

[52] evaluation of 16s rrna gene primer pairs for monitoring microbial community structures showed high reproducibility within and low comparability between datasets generated with multiple archaeal and bacterial primer pairs

[53] deep subsurface mine stalactites trap endemic fissure fluid archaea, bacteria and nematoda possibly originating from ancient (inland) seas.

[54] putative archaeal viruses from the mesopelagic ocean

[55] “altiarchaeales”: uncultivated archaea from the subsurface

[56] diversity and subcellular distribution of archaeal secreted proteins

[57] higher-level classification of the archaea: evolution of methanogenesis and methanogens

[58] bacterial and archaeal α-amylases: diversity and amelioration of the desirable characteristics for industrial applications

[59] phylogenetic and functional analysis of metagenome sequence from high-temperature archaeal habitats demonstrate linkages between metabolic potential and geochemistry

[60] the lrp family of transcription regulators in archaea

[61] quantification of ammonia oxidation rates and the distribution of ammonia-oxidizing archaea and bacteria in marine sediment depth profiles from catalina island, california

[62] ribonucleoproteins in archaeal pre-rrna processing and modification

[63] archaeal and bacterial diversity in an arsenic-rich shallow-sea hydrothermal system undergoing phase separation

[64] getting on target: the archaeal signal recognition particle

[65] phylogenomic investigation of phospholipid synthesis in archaea

[66] thaumarchaeal ammonium oxidation and evidence for a nitrogen cycle in a subsurface radioactive thermal spring in the austrian central alps

[67] biotechnological uses of archaeal proteins

[68] temporal eukarya, bacteria, and archaea biodiversity during cultivation of an alkaliphilic algae, chlorella vulgaris, in an outdoor raceway pond

[69] biofilm formation of mucosa-associated methanoarchaeal strains

[70] adp-dependent kinases from the archaeal order methanosarcinales adapt to salt by a non-canonical evolutionarily conserved strategy

[71] the distribution and abundance of archaeal tetraether lipids in u.s. great basin hot springs

[72] archaeal ubiquitin-like proteins: functional versatility and putative ancestral involvement in trna modification revealed by comparative genomic analysis

[73] assembly of the complex between archaeal rnase p proteins rpp30 and pop5

[74] selenocysteine, pyrrolysine, and the unique energy metabolism of methanogenic archaea

[75] roles of thermophilic thiosulfate-reducing bacteria and methanogenic archaea in the biocorrosion of oil pipelines

[76] reverse methanogenesis and respiration in methanotrophic archaea

[77] horizontal gene transfer, dispersal and haloarchaeal speciation

[78] archaeal clusters of orthologous genes (arcogs): an update and application for analysis of shared features between thermococcales, methanococcales, and methanobacteriales

[79] protoliths of enigmatic archaean gneisses established from zircon inclusion studies: case study of the caozhuang quartzite, e. hebei, china

[80] differences in the composition of archaeal communities in sediments from contrasting zones of lake taihu

[81] Comprehensive glycoproteomics shines new light on the complexity and extent of glycosylation in archaea

[82] Comprehensive glycoproteomics shines new light on the complexity and extent of glycosylation in archaea

[83] RNA-Guided RNA modification: functional organization of the archaeal H/ACA RNP

[84] A Well-Conserved Archaeal B-Family Polymerase Functions as an Extender in Translesion Synthesis.

[85] Enzymatic Switching Between Archaeal DNA Polymerases Facilitates Abasic Site Bypass.

[86] Form and function of archaeal genomes.