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Publication DateMICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, ISSN 1092-2172, 03/2016, Volume 80, Issue 1, pp. 1 - 43
Actinobacteria are Gram-positive bacteria with high G + C DNA content that constitute one of the largest bacterial phyla, and they are ubiquitously distributed...
FACTOR REGULATORY CASCADE | A-FACTOR | AERIAL MYCELIUM FORMATION | COMPLETE GENOME SEQUENCE | BIOSYNTHETIC GENE-CLUSTER | SECONDARY METABOLISM | STREPTOMYCES-COELICOLOR A3 | MORPHOLOGICAL-DIFFERENTIATION | BACTERIAL-CELL-DIVISION | MICROBIOLOGY | ANTIBIOTIC PRODUCTION
FACTOR REGULATORY CASCADE | A-FACTOR | AERIAL MYCELIUM FORMATION | COMPLETE GENOME SEQUENCE | BIOSYNTHETIC GENE-CLUSTER | SECONDARY METABOLISM | STREPTOMYCES-COELICOLOR A3 | MORPHOLOGICAL-DIFFERENTIATION | BACTERIAL-CELL-DIVISION | MICROBIOLOGY | ANTIBIOTIC PRODUCTION
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Loading RightsJournal of General Physiology, ISSN 0022-1295, 07/2010, Volume 136, Issue 1, pp. 47 - 62
Mutations in GJB2, which encodes Cx26, are one of the most common causes of inherited deafness in humans. More than 100 mutations have been identified...
GJB2 ENCODING CONNEXIN-26 | CX46 HEMICHANNELS | GAP-JUNCTION CHANNELS | PHYSIOLOGY | EPIDERMAL DIFFERENTIATION | EXTRACELLULAR LOOP DOMAIN | PORE-LINING RESIDUES | SKIN-DISEASE | CALCIUM REGULATION | SUPPORTING CELLS | CELL-DEATH | Deafness - genetics | Chloride Channels - drug effects | Calcium - metabolism | Connexins - physiology | Humans | Oocytes | Cysteine - genetics | Ion Channel Gating - physiology | Transfection | Keratitis - genetics | Calcium - pharmacology | Streptomyces - genetics | Connexins - drug effects | RNA, Messenger - genetics | Xenopus laevis | Electrophysiological Phenomena - physiology | Barium - pharmacology | Chelating Agents - pharmacology | Permeability | Membrane Potentials - physiology | Ethylenediamines - pharmacology | Syndrome | Connexin 26 | Mutation, Missense - physiology | Animals | Gap Junctions - physiology | Amino Acid Substitution - physiology | Mesylates - pharmacology | Cell Line, Tumor | Sulfhydryl Reagents - pharmacology | Mice | Chloride Channels - physiology | Electrophysiological Phenomena - drug effects | Ion Channel Gating - drug effects
GJB2 ENCODING CONNEXIN-26 | CX46 HEMICHANNELS | GAP-JUNCTION CHANNELS | PHYSIOLOGY | EPIDERMAL DIFFERENTIATION | EXTRACELLULAR LOOP DOMAIN | PORE-LINING RESIDUES | SKIN-DISEASE | CALCIUM REGULATION | SUPPORTING CELLS | CELL-DEATH | Deafness - genetics | Chloride Channels - drug effects | Calcium - metabolism | Connexins - physiology | Humans | Oocytes | Cysteine - genetics | Ion Channel Gating - physiology | Transfection | Keratitis - genetics | Calcium - pharmacology | Streptomyces - genetics | Connexins - drug effects | RNA, Messenger - genetics | Xenopus laevis | Electrophysiological Phenomena - physiology | Barium - pharmacology | Chelating Agents - pharmacology | Permeability | Membrane Potentials - physiology | Ethylenediamines - pharmacology | Syndrome | Connexin 26 | Mutation, Missense - physiology | Animals | Gap Junctions - physiology | Amino Acid Substitution - physiology | Mesylates - pharmacology | Cell Line, Tumor | Sulfhydryl Reagents - pharmacology | Mice | Chloride Channels - physiology | Electrophysiological Phenomena - drug effects | Ion Channel Gating - drug effects
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Loading RightsJournal of Internal Medicine, ISSN 0954-6820, 02/2012, Volume 271, Issue 2, pp. 131 - 141
. Bordbar A, Palsson BO (University of California San Diego, La Jolla, CA, USA). Using the reconstructed genome‐scale human metabolic network to study...
human metabolism | systems biology | constraints‐based modelling | Constraints-based modelling | Systems biology | Human metabolism | constraints-based modelling | COMMUNITY APPROACH | IN-SILICO | DRUG TARGETS | MEDICINE, GENERAL & INTERNAL | MATHEMATICAL-MODEL | HUMAN-ERYTHROCYTES | BACILLUS-SUBTILIS | STREPTOMYCES-COELICOLOR | SALMONELLA-TYPHIMURIUM | FLUX BALANCE ANALYSIS | Systems Biology - methods | Phenotype | Models, Biological | Chromosome Mapping - methods | Computer Simulation | Humans | Metabolic Diseases - genetics | Metabolomics - methods | Genome, Human - genetics | Metabolism - genetics | Physiological aspects | Medicine, Experimental | Medical research | Computer-generated environments | Computer simulation | constraints-based modeling
human metabolism | systems biology | constraints‐based modelling | Constraints-based modelling | Systems biology | Human metabolism | constraints-based modelling | COMMUNITY APPROACH | IN-SILICO | DRUG TARGETS | MEDICINE, GENERAL & INTERNAL | MATHEMATICAL-MODEL | HUMAN-ERYTHROCYTES | BACILLUS-SUBTILIS | STREPTOMYCES-COELICOLOR | SALMONELLA-TYPHIMURIUM | FLUX BALANCE ANALYSIS | Systems Biology - methods | Phenotype | Models, Biological | Chromosome Mapping - methods | Computer Simulation | Humans | Metabolic Diseases - genetics | Metabolomics - methods | Genome, Human - genetics | Metabolism - genetics | Physiological aspects | Medicine, Experimental | Medical research | Computer-generated environments | Computer simulation | constraints-based modeling
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Loading RightsAnnual Reviews in Microbiology, ISSN 0066-4227, 10/2003, Volume 57, Issue 1, pp. 441 - 466
Promoter recognition in eubacteria is carried out by the initiation factor sigma, which binds RNA polymerase and initiates transcription. Cells have one...
RNA polymerase | Bacillus subtilis | Streptomyces coelicolor | Escherichia coli | cyanobacteria | Cyanobacteria | COLI RNA-POLYMERASE | CRYSTAL-STRUCTURE | ESCHERICHIA-COLI | MORPHOLOGICAL-DIFFERENTIATION | EXTRACYTOPLASMIC STRESS-RESPONSE | MICROBIOLOGY | BACILLUS-SUBTILIS SIGMA(W) | AERIAL MYCELIUM FORMATION | STREPTOMYCES-COELICOLOR A3 | HEAT-SHOCK RESPONSE | GENE-EXPRESSION | Cyanobacteria - genetics | Amino Acid Sequence | Streptomyces - physiology | Streptomyces - genetics | Models, Molecular | Molecular Sequence Data | Phylogeny | Bacillus subtilis - genetics | Cyanobacteria - physiology | Sequence Alignment | Transcription, Genetic - physiology | Bacillus subtilis - physiology | Sigma Factor - physiology | Escherichia coli - genetics | Conserved Sequence | Escherichia coli - physiology | Bacteria | Research | Cell division | Ribonucleic acid--RNA | Ribonucleic acid
RNA polymerase | Bacillus subtilis | Streptomyces coelicolor | Escherichia coli | cyanobacteria | Cyanobacteria | COLI RNA-POLYMERASE | CRYSTAL-STRUCTURE | ESCHERICHIA-COLI | MORPHOLOGICAL-DIFFERENTIATION | EXTRACYTOPLASMIC STRESS-RESPONSE | MICROBIOLOGY | BACILLUS-SUBTILIS SIGMA(W) | AERIAL MYCELIUM FORMATION | STREPTOMYCES-COELICOLOR A3 | HEAT-SHOCK RESPONSE | GENE-EXPRESSION | Cyanobacteria - genetics | Amino Acid Sequence | Streptomyces - physiology | Streptomyces - genetics | Models, Molecular | Molecular Sequence Data | Phylogeny | Bacillus subtilis - genetics | Cyanobacteria - physiology | Sequence Alignment | Transcription, Genetic - physiology | Bacillus subtilis - physiology | Sigma Factor - physiology | Escherichia coli - genetics | Conserved Sequence | Escherichia coli - physiology | Bacteria | Research | Cell division | Ribonucleic acid--RNA | Ribonucleic acid
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Loading RightsApplied and Environmental Microbiology, ISSN 0099-2240, 2016, Volume 82, Issue 17, pp. 5132 - 5143
Copper sulfate (CuSO4) has been widely used as an algicide to control harmful cyanobacterial blooms (CyanoHABs) in freshwater lakes. However, there are...
2 ANTIBIOTIC CONTAMINANTS | AERUGINOSA | CYANOBACTERIA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | FRESH-WATERS | ANTIALGAL COMPOUND | CLASSIFICATION | MICROBIOLOGY | SP-NOV | EMENDED DESCRIPTION | IDENTIFICATION | JIUJIANGENSIS JXJ 0074(T) | Malondialdehyde - metabolism | Streptomyces - metabolism | Harmful Algal Bloom - drug effects | Tryptamines - pharmacology | Streptomyces - chemistry | Tryptamines - metabolism | Carbolines - metabolism | Chlorophyll - metabolism | Microcystis - drug effects | Microcystis - physiology | Carbolines - pharmacology | Streptomyces | Physiological aspects | Genetic aspects | Research | Metabolites | Microcystis | Index Medicus
2 ANTIBIOTIC CONTAMINANTS | AERUGINOSA | CYANOBACTERIA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | FRESH-WATERS | ANTIALGAL COMPOUND | CLASSIFICATION | MICROBIOLOGY | SP-NOV | EMENDED DESCRIPTION | IDENTIFICATION | JIUJIANGENSIS JXJ 0074(T) | Malondialdehyde - metabolism | Streptomyces - metabolism | Harmful Algal Bloom - drug effects | Tryptamines - pharmacology | Streptomyces - chemistry | Tryptamines - metabolism | Carbolines - metabolism | Chlorophyll - metabolism | Microcystis - drug effects | Microcystis - physiology | Carbolines - pharmacology | Streptomyces | Physiological aspects | Genetic aspects | Research | Metabolites | Microcystis | Index Medicus
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Loading RightsNature Reviews Microbiology, ISSN 1740-1526, 01/2014, Volume 12, Issue 11, pp. 724 - 725
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Loading RightsNature Reviews Microbiology, ISSN 1740-1526, 12/2008, Volume 6, Issue 12
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Loading RightsFEMS Microbiology Reviews, ISSN 0168-6445, 01/2008, Volume 32, Issue 1, pp. 107 - 146
Abstract The bacterial cell envelope is the first and major line of defence against threats from the environment. It is an essential and yet vulnerable...
two‐component system | stress response | cell wall | signal transduction | antibiotic resistance | extracytoplasmic function (ECF) σ factor | Signal transduction | Two-component system | Extracytoplasmic function (ECF) σ factor | Stress response | Cell wall | Antibiotic resistance | 2-COMPONENT SIGNAL-TRANSDUCTION | BETA-LACTAM RESISTANCE | LISTERIA-MONOCYTOGENES MUTANTS | MICROBIOLOGY | extracytoplasmic function (ECF) sigma factor | BACILLUS-SUBTILIS SIGMA(W) | REGULATED INTRAMEMBRANE PROTEOLYSIS | MICROARRAY-BASED IDENTIFICATION | EXTRACYTOPLASMIC-FUNCTION SIGMA(X) | STREPTOMYCES-COELICOLOR A3 | PENICILLIN-BINDING PROTEINS | CATIONIC ANTIMICROBIAL PEPTIDES | two-component system | Gram-Negative Bacteria - ultrastructure | Gram-Positive Bacteria - physiology | Transcription Factors - physiology | Gram-Positive Bacteria - drug effects | Cell Wall - physiology | Gram-Negative Bacteria - drug effects | Cell Wall - drug effects | Drug Resistance, Bacterial - physiology | Signal Transduction - physiology | Anti-Bacterial Agents - pharmacology | Gene Expression Regulation, Bacterial | Gram-Positive Bacteria - ultrastructure | Gram-Negative Bacteria - physiology
two‐component system | stress response | cell wall | signal transduction | antibiotic resistance | extracytoplasmic function (ECF) σ factor | Signal transduction | Two-component system | Extracytoplasmic function (ECF) σ factor | Stress response | Cell wall | Antibiotic resistance | 2-COMPONENT SIGNAL-TRANSDUCTION | BETA-LACTAM RESISTANCE | LISTERIA-MONOCYTOGENES MUTANTS | MICROBIOLOGY | extracytoplasmic function (ECF) sigma factor | BACILLUS-SUBTILIS SIGMA(W) | REGULATED INTRAMEMBRANE PROTEOLYSIS | MICROARRAY-BASED IDENTIFICATION | EXTRACYTOPLASMIC-FUNCTION SIGMA(X) | STREPTOMYCES-COELICOLOR A3 | PENICILLIN-BINDING PROTEINS | CATIONIC ANTIMICROBIAL PEPTIDES | two-component system | Gram-Negative Bacteria - ultrastructure | Gram-Positive Bacteria - physiology | Transcription Factors - physiology | Gram-Positive Bacteria - drug effects | Cell Wall - physiology | Gram-Negative Bacteria - drug effects | Cell Wall - drug effects | Drug Resistance, Bacterial - physiology | Signal Transduction - physiology | Anti-Bacterial Agents - pharmacology | Gene Expression Regulation, Bacterial | Gram-Positive Bacteria - ultrastructure | Gram-Negative Bacteria - physiology
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