scholarly article | Q13442814 |
P50 | author | Kai-Uwe Hinrichs | Q26923527 |
P2093 | author name string | Stefan Häusler | |
Miriam Sollich | |||
Marcos Y Yoshinaga | |||
Roy E Price | |||
Solveig I Bühring | |||
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Fungal diversity in deep-sea hydrothermal ecosystems | Q24650682 | ||
Cell proliferation at 122 degrees C and isotopically heavy CH4 production by a hyperthermophilic methanogen under high-pressure cultivation | Q24653236 | ||
Functional rafts in cell membranes | Q27860768 | ||
Methane-consuming archaebacteria in marine sediments | Q28143355 | ||
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Cardiolipin domains in Bacillus subtilis marburg membranes | Q28488997 | ||
Production of α-galactosylceramide by a prominent member of the human gut microbiota | Q28534671 | ||
Impacts of temperature and pH on the distribution of archaeal lipids in Yunnan hot springs, China | Q28661967 | ||
The distribution and abundance of archaeal tetraether lipids in U.S. Great Basin hot springs | Q28681405 | ||
Stability and proton-permeability of liposomes composed of archaeal tetraether lipids | Q43022955 | ||
Effect of growth temperature on ether lipid biochemistry in Archaeoglobus fulgidus. | Q43023860 | ||
Cultivation of a thermophilic ammonia oxidizing archaeon synthesizing crenarchaeol | Q43023988 | ||
Ion permeability of the cytoplasmic membrane limits the maximum growth temperature of bacteria and archaea | Q43024161 | ||
The major lipid cores of the archaeon Ignisphaera aggregans: implications for the phylogeny and biosynthesis of glycerol monoalkyl glycerol tetraether isoprenoid lipids | Q43031489 | ||
Archaeal and bacterial diversity in an arsenic-rich shallow-sea hydrothermal system undergoing phase separation | Q43101584 | ||
Molecular mechanisms of water and solute transport across archaebacterial lipid membranes | Q43617496 | ||
Microbial lipids reveal carbon assimilation patterns on hydrothermal sulfide chimneys | Q44484167 | ||
Structural analysis of sphingophospholipids derived from Sphingobacterium spiritivorum, the type species of genus Sphingobacterium | Q44732196 | ||
Intact polar membrane lipids in prokaryotes and sediments deciphered by high-performance liquid chromatography/electrospray ionization multistage mass spectrometry--new biomarkers for biogeochemistry and microbial ecology. | Q44820864 | ||
Effect of Headgroups on Small-Ion Permeability across Archaea-Inspired Tetraether Lipid Membranes. | Q45936333 | ||
Effect of growth temperature and growth phase on the lipid composition of the archaeal membrane from Thermococcus kodakaraensis | Q46171708 | ||
Metabolic control of the membrane fluidity in Bacillus subtilis during cold adaptation | Q46836579 | ||
Life at high temperatures. Evolutionary, ecological, and biochemical significance of organisms living in hot springs is discussed | Q47777366 | ||
More, smaller bacteria in response to ocean's warming? | Q51351302 | ||
A novel ether core lipid with H-shaped C80-isoprenoid hydrocarbon chain from the hyperthermophilic methanogen Methanothermus fervidus. | Q51524761 | ||
Homeostasis of the membrane proton permeability in Bacillus subtilis grown at different temperatures. | Q54001789 | ||
Processes influencing extreme As enrichment in shallow-sea hydrothermal fluids of Milos Island, Greece | Q54087727 | ||
Distribution of betaine lipids in marine algae | Q56083121 | ||
An Amperometric Microsensor for the Determination of H2S in Aquatic Environments | Q56611321 | ||
The organic geochemistry of glycerol dialkyl glycerol tetraether lipids: A review | Q56680920 | ||
Hydrothermal studies in the aegean sea | Q56993819 | ||
Bacterial and archaeal phylotypes associated with distinct mineralogical layers of a white smoker spire from a deep-sea hydrothermal vent site (9 degrees N, East Pacific Rise) | Q57087885 | ||
Relative abundance of Archaea and Bacteria along a thermal gradient of a shallow-water hydrothermal vent quantified by rRNA slot-blot hybridization | Q57088137 | ||
Effect of Methyl-Branched Fatty Acids on the Structure of Lipid Bilayers | Q57204643 | ||
Omega-3 Fatty Acids and the DHA Principle | Q57235136 | ||
Fossilization and degradation of intact polar lipids in deep subsurface sediments: A theoretical approach | Q58063000 | ||
Microstructure of diffusive boundary layers and the oxygen uptake of the sea floor | Q59080547 | ||
Systematic fragmentation patterns of archaeal intact polar lipids by high-performance liquid chromatography/electrospray ionization ion-trap mass spectrometry | Q59920953 | ||
Archaebacterial lipids: highly proton-impermeable membranes from 1,2-diphytanyl-sn-glycero-3-phosphocoline | Q64356651 | ||
Molecular arrangements in sphingolipids. Conformation and hydrogen bonding of ceramide and their implication on membrane stability and permeability | Q67877167 | ||
The isolation and characterization of a mutant strain of Saccharomyces cerevisiae that requires a long chain base for growth and for synthesis of phosphosphingolipids | Q70275555 | ||
Bacterial membranes and lipid packing theory | Q70767432 | ||
Proton and carbon-13 nuclear magnetic resonance studies of the polar lipids of Halobacterium halobium | Q71848419 | ||
Molecular modeling of archaebacterial bipolar tetraether lipid membranes | Q73818477 | ||
Involvement of yeast sphingolipids in the heat stress response of Saccharomyces cerevisiae | Q73956113 | ||
Characterization of glycolipids from Meiothermus spp | Q77905427 | ||
Sphingolipid composition in Bacteroides species | Q80056866 | ||
Unsaturated diether lipids in the psychrotrophic archaeon Halorubrum lacusprofundi | Q81398334 | ||
A ring to rule them all: the effect of cyclopropane Fatty acids on the fluidity of lipid bilayers | Q86984856 | ||
Turnover of microbial lipids in the deep biosphere and growth of benthic archaeal populations | Q28709071 | ||
Intact polar and core glycerol dibiphytanyl glycerol tetraether lipids of group I.1a and I.1b thaumarchaeota in soil | Q28727505 | ||
Lipid rafts as a membrane-organizing principle | Q29615727 | ||
Molecular basis of bacterial outer membrane permeability revisited | Q29616208 | ||
Molecular basis of bacterial outer membrane permeability | Q29617897 | ||
A proton shelter inspired by the sugar coating of acidophilic archaea | Q30460554 | ||
Eicosapentaenoic acid plays a beneficial role in membrane organization and cell division of a cold-adapted bacterium, Shewanella livingstonensis Ac10. | Q30485419 | ||
Membrane sphingolipids as essential molecular signals for Bacteroides survival in the intestine | Q30499062 | ||
Conformational studies of sphingolipids by NMR spectroscopy. II. Sphingomyelin | Q30616800 | ||
Thermoflavifilum aggregans gen. nov., sp. nov., a thermophilic and slightly halophilic filamentous bacterium from the phylum Bacteroidetes. | Q30733773 | ||
Hydrogen-bonding propensities of sphingomyelin in solution and in a bilayer assembly: a molecular dynamics study | Q30773070 | ||
A natural view of microbial biodiversity within hot spring cyanobacterial mat communities | Q31961145 | ||
Variation in molecular species of polar lipids from thermoplasma acidophilum depends on growth temperature | Q32051239 | ||
Structural elucidation of phosphoglycolipids from strains of the bacterial thermophiles Thermus and Meiothermus | Q33242342 | ||
Rapid discrimination of archaeal tetraether lipid cores by liquid chromatography-tandem mass spectrometry. | Q33441072 | ||
Extending the known range of glycerol ether lipids in the environment: structural assignments based on tandem mass spectral fragmentation patterns | Q33455724 | ||
Detection of microbial biomass by intact polar membrane lipid analysis in the water column and surface sediments of the Black Sea. | Q33485501 | ||
Humboldt's spa: microbial diversity is controlled by temperature in geothermal environments | Q33647148 | ||
Life in extreme environments | Q33936544 | ||
Do sterols reduce proton and sodium leaks through lipid bilayers? | Q33951999 | ||
Molecular mechanisms for proton transport in membranes | Q33955973 | ||
Identification of 16S ribosomal DNA-defined bacterial populations at a shallow submarine hydrothermal vent near Milos Island (Greece) | Q33987283 | ||
CHARMM all-atom additive force field for sphingomyelin: elucidation of hydrogen bonding and of positive curvature. | Q33990999 | ||
Crenarchaeol: the characteristic core glycerol dibiphytanyl glycerol tetraether membrane lipid of cosmopolitan pelagic crenarchaeota | Q34153045 | ||
Hydration and molecular motions in synthetic phytanyl-chained glycolipid vesicle membranes | Q34177037 | ||
The archaeal cell envelope | Q34185088 | ||
Extending the upper temperature limit for life | Q34222898 | ||
Cold adaptation in the Antarctic Archaeon Methanococcoides burtonii involves membrane lipid unsaturation | Q34373070 | ||
Sphingobacterium thermophilum sp. nov., of the phylum Bacteroidetes, isolated from compost | Q34384027 | ||
Thermonema rossianum sp. nov., a new thermophilic and slightly halophilic species from saline hot springs in Naples, Italy | Q34413406 | ||
The origin of methanethiol in midocean ridge hydrothermal fluids | Q34413960 | ||
Microbial diversity of Loki's Castle black smokers at the Arctic Mid-Ocean Ridge. | Q34420363 | ||
Comparison of intact polar lipid with microbial community composition of vent deposits of the Rainbow and Lucky Strike hydrothermal fields. | Q34508658 | ||
Adaptations to energy stress dictate the ecology and evolution of the Archaea | Q34576774 | ||
Temperature and pH controls on glycerol dibiphytanyl glycerol tetraether lipid composition in the hyperthermophilic crenarchaeon Acidilobus sulfurireducens | Q34625550 | ||
Spatial heterogeneity of bacterial populations along an environmental gradient at a shallow submarine hydrothermal vent near Milos Island (Greece). | Q39527602 | ||
Distribution and diversity of sulfur-oxidizing Thiomicrospira spp. at a shallow-water hydrothermal vent in the Aegean Sea (Milos, Greece). | Q39527609 | ||
Lipid and protein composition of membranes of Bacillus megaterium variants in the temperature range 5 to 70 degrees C | Q39618591 | ||
A lipid-phase separation model of low-temperature damage to biological membranes | Q39846282 | ||
Changes in fatty acid branching and unsaturation of Streptomyces griseus and Brevibacterium fermentans as a response to growth temperature | Q39894298 | ||
Effect of temperature on the fatty acid composition of the extreme thermophiles, Bacillus caldolyticus and Bacillus caldotenax | Q40098060 | ||
Ether polar lipids of methanogenic bacteria: structures, comparative aspects, and biosyntheses | Q40693496 | ||
Effects of pH and temperature on the composition of polar lipids in Thermoplasma acidophilum HO-62. | Q41340573 | ||
Betaine ether-linked glycerolipids: chemistry and biology | Q41352591 | ||
Molecular basis for membrane phospholipid diversity: why are there so many lipids? | Q41550195 | ||
Occurrence of a bacterial membrane microdomain at the cell division site enriched in phospholipids with polyunsaturated hydrocarbon chains | Q41887671 | ||
Thermococcus kodakarensis modulates its polar membrane lipids and elemental composition according to growth stage and phosphate availability | Q41899645 | ||
Structural analysis by reductive cleavage with LiAlH4 of an allyl ether choline-phospholipid, archaetidylcholine, from the hyperthermophilic methanoarchaeon Methanopyrus kandleri | Q42134035 | ||
The effect of temperature on the growth and lipid composition of the extremely halophilic coccus, Sarcina marina | Q42268532 | ||
Tetraether membrane lipids of Candidatus "Aciduliprofundum boonei", a cultivated obligate thermoacidophilic euryarchaeote from deep-sea hydrothermal vents | Q42920394 | ||
The effect of growth temperature on the thermotropic behavior of the membranes of a thermophilic Bacillus. Composition-structure-function relationships | Q43019571 | ||
Sulfolipids dramatically decrease phosphorus demand by picocyanobacteria in oligotrophic marine environments | Q34695245 | ||
The Upper Temperature Limit for Eukaryotic Organisms | Q34725615 | ||
Spatial and temporal variability of biomarkers and microbial diversity reveal metabolic and community flexibility in Streamer Biofilm Communities in the Lower Geyser Basin, Yellowstone National Park | Q34974940 | ||
Methanothermobacter thermautotrophicus modulates its membrane lipids in response to hydrogen and nutrient availability | Q34999565 | ||
Biosynthesis of phosphatidylcholine in bacteria. | Q35053477 | ||
Critical role of anteiso-C15:0 fatty acid in the growth of Listeria monocytogenes at low temperatures | Q35205271 | ||
Sphingolipid and glycosphingolipid metabolic pathways in the era of sphingolipidomics | Q35324757 | ||
Lipids, curvature, and nano-medicine | Q35590501 | ||
SAR11 lipid renovation in response to phosphate starvation. | Q35796061 | ||
Omega-3 fatty acids in cellular membranes: a unified concept | Q35905744 | ||
Archaeal and bacterial glycerol dialkyl glycerol tetraether lipids in hot springs of yellowstone national park | Q36137032 | ||
The Effects of Temperature and Growth Phase on the Lipidomes of Sulfolobus islandicus and Sulfolobus tokodaii | Q36138760 | ||
Proportions of diether, macrocyclic diether, and tetraether lipids in Methanococcus jannaschii grown at different temperatures | Q36147278 | ||
Temperature dependence of structure, bending rigidity, and bilayer interactions of dioleoylphosphatidylcholine bilayers | Q36259570 | ||
Lipids and lipid metabolism in eukaryotic algae | Q36402813 | ||
Biophysics of sphingolipids I. Membrane properties of sphingosine, ceramides and other simple sphingolipids. | Q36637060 | ||
Sediment microbial communities in Great Boiling Spring are controlled by temperature and distinct from water communities | Q36708769 | ||
Factors controlling the distribution of archaeal tetraethers in terrestrial hot springs | Q36710516 | ||
Oxygen Microelectrode That Is Insensitive to Medium Chemical Composition: Use in an Acid Microbial Mat Dominated by Cyanidium caldarium | Q36712217 | ||
The role of tetraether lipid composition in the adaptation of thermophilic archaea to acidity | Q36736427 | ||
Effect of Growth Temperature on the Lipid Composition of Thermus aquaticus | Q36773710 | ||
Diversity and phylogenetic analyses of bacteria from a shallow-water hydrothermal vent in Milos island (Greece) | Q36989075 | ||
Effects of ceramide and other simple sphingolipids on membrane lateral structure | Q37291700 | ||
Nonmarine crenarchaeol in Nevada hot springs. | Q37552909 | ||
Mycobacterial outer membrane is a lipid bilayer and the inner membrane is unusually rich in diacyl phosphatidylinositol dimannosides | Q37687576 | ||
The role of alterations in membrane lipid composition in enabling physiological adaptation of organisms to their physical environment | Q37840225 | ||
Lipids of mitochondria | Q38134492 | ||
Proton flux mechanisms in model and biological membranes | Q38201819 | ||
Biophysical properties of sphingosine, ceramides and other simple sphingolipids | Q38252307 | ||
Phospholipids and glycolipids mediate proton containment and circulation along the surface of energy-transducing membranes | Q38905810 | ||
Identification and significance of unsaturated archaeal tetraether lipids in marine sediments. | Q39213944 | ||
Crenarchaeol dominates the membrane lipids of Candidatus Nitrososphaera gargensis, a thermophilic group I.1b Archaeon | Q39358505 | ||
Important roles for membrane lipids in haloarchaeal bioenergetics. | Q39449911 | ||
Glycolipid function | Q39509688 | ||
P921 | main subject | marine sediment | Q1898474 |
P304 | page(s) | 1550 | |
P577 | publication date | 2017-08-22 | |
P1433 | published in | Frontiers in Microbiology | Q27723481 |
P1476 | title | Heat Stress Dictates Microbial Lipid Composition along a Thermal Gradient in Marine Sediments | |
P478 | volume | 8 |
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