scholarly article | Q13442814 |
review article | Q7318358 |
P2093 | author name string | Ziqiang Guan | |
Janet M Wood | |||
Tatyana Romantsov | |||
P2860 | cites work | Hydrophobic acridine dyes for fluorescence staining of mitochondria in living cells. 1. Thermodynamic and spectroscopic properties of 10-n-alkylacridine orange chlorides | Q72720476 |
A second Escherichia coli protein with CL synthase activity | Q73352785 | ||
The modification of the membrane of Oceanomonas baumannii when subjected to both osmotic and organic solvent stress | Q74128375 | ||
The role of the carboxyl terminal alpha-helical coiled-coil domain in osmosensing by transporter ProP of Escherichia coli | Q74327613 | ||
Responses of E. coli to osmotic stress: large changes in amounts of cytoplasmic solutes and water | Q74537547 | ||
Visualization of membrane domains in Escherichia coli | Q77928045 | ||
A structural model for the osmosensor, transporter, and osmoregulator ProP of Escherichia coli | Q81637305 | ||
Solution structure of the C-terminal antiparallel coiled-coil domain from Escherichia coli osmosensor ProP | Q27642653 | ||
A new vital stain for visualizing vacuolar membrane dynamics and endocytosis in yeast | Q28131611 | ||
Specific covalent labeling of recombinant protein molecules inside live cells | Q28276029 | ||
Central mechanisms of osmosensation and systemic osmoregulation | Q28281823 | ||
Structure of the MscL homolog from Mycobacterium tuberculosis: a gated mechanosensitive ion channel | Q28291702 | ||
Cardiolipin domains in Bacillus subtilis marburg membranes | Q28488997 | ||
Culture medium for enterobacteria | Q29616466 | ||
Osmotic stress signaling and osmoadaptation in yeasts | Q29617597 | ||
Varying division planes of secondary constrictions in spheroidal Escherichia coli cells | Q30720370 | ||
Effects of lipid composition on the membrane activity and lipid phase behaviour of Vibrio sp. DSM14379 cells grown at various NaCl concentrations | Q30989044 | ||
A curvature-mediated mechanism for localization of lipids to bacterial poles | Q33263252 | ||
Osmosensing by bacteria: signals and membrane-based sensors | Q33538953 | ||
Purification and reconstitution of an osmosensor: transporter ProP of Escherichia coli senses and responds to osmotic shifts | Q33852610 | ||
The ion coupling and organic substrate specificities of osmoregulatory transporter ProP in Escherichia coli. | Q33870915 | ||
Mechanisms and significance of cell volume regulation | Q34007380 | ||
Biophysical characterization of changes in amounts and activity of Escherichia coli cell and compartment water and turgor pressure in response to osmotic stress | Q34172755 | ||
Protein stabilization by naturally occurring osmolytes | Q34253785 | ||
Isolation and sequencing of Escherichia coli gene proP reveals unusual structural features of the osmoregulatory proline/betaine transporter, ProP. | Q34359329 | ||
Bacterial osmosensing: roles of membrane structure and electrostatics in lipid-protein and protein-protein interactions | Q34363946 | ||
Biology of extremophilic and extremotolerant methanotrophs | Q34504320 | ||
Analysis of ubiquinones, dolichols, and dolichol diphosphate-oligosaccharides by liquid chromatography-electrospray ionization-mass spectrometry | Q34705078 | ||
Bacterial Membrane Lipids: Where Do We Stand? | Q35550561 | ||
Characterization of the Erwinia chrysanthemi osmoprotectant transporter gene ousA. | Q35601149 | ||
Anionic lipids enriched at the ExPortal of Streptococcus pyogenes | Q35634620 | ||
How lipids affect the activities of integral membrane proteins | Q35935383 | ||
Intracellular organic osmolytes: function and regulation | Q36512042 | ||
Cardiolipin synthesis for the assembly of bacterial and mitochondrial membranes | Q36745013 | ||
Lipid localization in bacterial cells through curvature-mediated microphase separation | Q36783773 | ||
Subcellular localization of Escherichia coli osmosensory transporter ProP: focus on cardiolipin membrane domains | Q36842817 | ||
Bacterial mechanosensitive channels: experiment and theory. | Q36896042 | ||
Molecular and genetic characterization of osmosensing and signal transduction in the nematode Caenorhabditis elegans | Q36974966 | ||
Mechanisms of salinity tolerance | Q37150358 | ||
Adaptive modifications in membranes of halotolerant and halophilic microorganisms | Q38619487 | ||
Lipid spirals in Bacillus subtilis and their role in cell division. | Q38783136 | ||
Visualization of phospholipid domains in Escherichia coli by using the cardiolipin-specific fluorescent dye 10-N-nonyl acridine orange | Q39499180 | ||
Lipid domains of mycobacteria studied with fluorescent molecular probes | Q39499294 | ||
Escherichia coli minicell membranes are enriched in cardiolipin. | Q39527523 | ||
Corynebacterium glutamicum is equipped with four secondary carriers for compatible solutes: identification, sequencing, and characterization of the proline/ectoine uptake system, ProP, and the ectoine/proline/glycine betaine carrier, EctP. | Q39568600 | ||
Peptidoglycan as a barrier to transenvelope transport | Q39842837 | ||
Metabolism and function of the membrane phospholipids of Escherichia coli | Q39913919 | ||
Disruption of the Escherichia coli cls gene responsible for cardiolipin synthesis | Q39951737 | ||
Quantification of cardiolipin by liquid chromatography-electrospray ionization mass spectrometry | Q40063841 | ||
Periplasmic space in Salmonella typhimurium and Escherichia coli | Q40820160 | ||
Fluorescent labeling of recombinant proteins in living cells with FlAsH. | Q40846769 | ||
Effect of some environmental factors on the content and composition of microbial membrane lipids | Q41506586 | ||
Cardiolipin synthase from Escherichia coli | Q41643588 | ||
Identification of N-acylphosphatidylserine molecules in eukaryotic cells | Q41867504 | ||
Osmolality, temperature, and membrane lipid composition modulate the activity of betaine transporter BetP in Corynebacterium glutamicum | Q42909811 | ||
Contribution of chemical changes in membrane lipids to the osmoadaptation of the halophilic bacterium Chromohalobacter salexigens | Q43018137 | ||
Anionic phospholipids affect the rate and extent of flux through the mechanosensitive channel of large conductance MscL. | Q43202528 | ||
Variations of the envelope composition of Bacillus subtilis during growth in hyperosmotic medium | Q43541888 | ||
10N-nonyl acridine orange interacts with cardiolipin and allows the quantification of this phospholipid in isolated mitochondria | Q43670813 | ||
Cardiolipin binds nonyl acridine orange by aggregating the dye at exposed hydrophobic domains on bilayer surfaces | Q43782760 | ||
Osmosensor ProP of Escherichia coli responds to the concentration, chemistry, and molecular size of osmolytes in the proteoliposome lumen | Q44276469 | ||
Combined solvent and water activity stresses on turgor regulation and membrane adaptation in Oceanimonas baumannii ATCC 700832. | Q44459917 | ||
Creation of a Fully Functional Cysteine-Less Variant of Osmosensor and Proton-Osmoprotectant Symporter ProP from Escherichia coli and Its Application to Assess the Transporter's Membrane Orientation | Q44608212 | ||
Lipid-protein interactions studied by introduction of a tryptophan residue: the mechanosensitive channel MscL. | Q44670399 | ||
Detection of alpha-helical coiled-coil dimer formation by spin-labeled synthetic peptides: a model parallel coiled-coil peptide and the antiparallel coiled coil formed by a replica of the ProP C-terminus | Q44702795 | ||
Osmotic response in Lactobacillus casei ATCC 393: biochemical and biophysical characteristics of membrane | Q44730001 | ||
Roles of K+, H+, H2O, and DeltaPsi in solute transport mediated by major facilitator superfamily members ProP and LacY. | Q46488318 | ||
Formation of an antiparallel, intermolecular coiled coil is associated with in vivo dimerization of osmosensor and osmoprotectant transporter ProP in Escherichia coli | Q46617415 | ||
Cardiolipin controls the osmotic stress response and the subcellular location of transporter ProP in Escherichia coli | Q46713999 | ||
The osmotic activation of transporter ProP is tuned by both its C-terminal coiled-coil and osmotically induced changes in phospholipid composition | Q46765778 | ||
Role of anionic phospholipids in the adaptation of Bacillus subtilis to high salinity | Q46973367 | ||
Biophysical compensation mechanisms buffering E. coli protein-nucleic acid interactions against changing environments | Q48014911 | ||
A Pseudomonas putida cardiolipin synthesis mutant exhibits increased sensitivity to drugs related to transport functionality | Q48079785 | ||
Mechanism of assembly of the outer membrane of Salmonella typhimurium. Isolation and characterization of cytoplasmic and outer membrane | Q50236593 | ||
Structure and function of transmembrane segment XII in osmosensor and osmoprotectant transporter ProP of Escherichia coli | Q50688737 | ||
Visualisation of the mechanosensitive channel of large conductance in bacteria using confocal microscopy. | Q50772655 | ||
Cardiolipin promotes polar localization of osmosensory transporter ProP in Escherichia coli | Q51003525 | ||
Core residue replacements cause coiled-coil orientation switching in vitro and in vivo: structure-function correlations for osmosensory transporter ProP. | Q54429514 | ||
10-N nonyl-acridine orange: a fluorescent probe which stains mitochondria independently of their energetic state. | Q54491447 | ||
The effects of phosphoglycerides on Escherichia coli cardiolipin synthase. | Q54626091 | ||
Active increase in cardiolipin synthesis in the stationary growth phase and its physiological significance in Escherichia coli. | Q54646503 | ||
Genetic regulation of cardiolipin synthase in Escherichia coli. | Q54687695 | ||
Effect of osmotic pressure on membrane energy-linked functions in Escherichia coli. | Q54701909 | ||
Heterogeneity in the Binding of Lipid Molecules to the Surface of a Membrane Protein: Hot Spots for Anionic Lipids on the Mechanosensitive Channel of Large Conductance MscL and Effects on Conformation† | Q57947812 | ||
Fatty acid membrane composition and activation of glycine-betaine transport in Lactococcus lactis subjected to osmotic stress | Q59807937 | ||
Biochemical and biophysical studies of Bacillus subtilis envelopes under hyperosmotic stress. | Q64992897 | ||
The effect of salt on phospholipid fatty acid composition in Escherichia coli K-12 | Q66901033 | ||
The effect of temperature and other growth conditions on the fatty acid composition of Escherichia coli | Q70188006 | ||
Membranes as a target for stress adaptation | Q71376966 | ||
Direct cardiolipin assay in yeast using the red fluorescence emission of 10-N-nonyl acridine orange | Q72612620 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2092-2100 | |
P577 | publication date | 2009-06-17 | |
P1433 | published in | Biochimica et Biophysica Acta | Q864239 |
P1476 | title | Cardiolipin and the osmotic stress responses of bacteria | |
P478 | volume | 1788 |
Q36207968 | A Cardiolipin-Deficient Mutant of Rhodobacter sphaeroides Has an Altered Cell Shape and Is Impaired in Biofilm Formation. |
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Q54474655 | Alternative cardiolipin synthase Cls1 compensates for stalled Cls2 function in Staphylococcus aureus under conditions of acute acid stress. |
Q64953344 | Amino acids and proteomic acclimation of Staphylococcus aureus when incubated in a defined minimal medium supplemented with 5% sodium chloride. |
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Q37872826 | An overview of molecular stress response mechanisms in Escherichia coli contributing to survival of Shiga toxin-producing Escherichia coli during raw milk cheese production |
Q37992166 | Bacterial mechanosensitive channels--MscS: evolution's solution to creating sensitivity in function |
Q38415713 | Bacterial membrane lipids: diversity in structures and pathways |
Q55287989 | Beyond Chloride Brines: Variable Metabolomic Responses in the Anaerobic Organism Yersinia intermedia MASE-LG-1 to NaCl and MgSO4 at Identical Water Activity. |
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Q64086052 | Caulobacter crescentus Adapts to Phosphate Starvation by Synthesizing Anionic Glycoglycerolipids and a Novel Glycosphingolipid |
Q36927203 | Cell-Envelope Remodeling as a Determinant of Phenotypic Antibacterial Tolerance in Mycobacterium tuberculosis |
Q53077639 | Comparative genomic analysis of Lactobacillus plantarum GB-LP4 and identification of evolutionarily divergent genes in high-osmolarity environment. |
Q51067991 | Comparative metagenomics reveals insights into the deep-sea adaptation mechanism of the microorganisms in Iheya hydrothermal fields |
Q36851350 | Contributions of Coulombic and Hofmeister Effects to the Osmotic Activation of Escherichia coli Transporter ProP. |
Q34386310 | Determinants of intrinsic aminoglycoside resistance in Pseudomonas aeruginosa |
Q53059090 | Discovery of a bifunctional cardiolipin/phosphatidylethanolamine synthase in bacteria. |
Q36339949 | Discovery of a cardiolipin synthase utilizing phosphatidylethanolamine and phosphatidylglycerol as substrates |
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Q34512877 | Electrostatics at the membrane define MscL channel mechanosensitivity and kinetics |
Q36115928 | Evolutionary history influences the salinity preference of bacterial taxa in wetland soils |
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Q45845924 | Functional reconstitution and osmoregulatory properties of the ProU ABC transporter from Escherichia coli |
Q35646845 | Genes Associated with Desiccation and Osmotic Stress in Listeria monocytogenes as Revealed by Insertional Mutagenesis. |
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Q35915356 | Global Metabolic Responses to Salt Stress in Fifteen Species |
Q38994591 | Global Transcriptional Responses to Osmotic, Oxidative, and Imipenem Stress Conditions in Pseudomonas putida |
Q41597989 | Helical jackknives control the gates of the double-pore K+ uptake system KtrAB |
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Q33774463 | Identification of unique cardiolipin and monolysocardiolipin species in Acinetobacter baumannii |
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Q46363832 | Knowns and unknowns of membrane lipid synthesis in streptomycetes. |
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