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PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 7, p. e22143
Copper is an essential cofactor for many enzymes but at high concentrations it is toxic for the cell. Copper ion concentrations >= 50 mu M inhibited growth of... 
MYCOBACTERIUM-TUBERCULOSIS | RESPIRATORY-CHAIN | ACID-PRODUCING BACTERIA | HOMEOSTASIS | TRANSCRIPTIONAL REGULATORS | PSEUDOMONAS-AERUGINOSA | ESCHERICHIA-COLI K-12 | BIOLOGY | GENE-EXPRESSION | COMPARATIVE GENOMIC ANALYSES | MOLECULAR ANALYSIS | Protein Kinases - metabolism | Corynebacterium glutamicum - drug effects | Protein Kinases - genetics | Corynebacterium glutamicum - genetics | DNA, Bacterial - metabolism | Genes, Bacterial - genetics | Nucleotide Motifs - genetics | Adaptation, Physiological - drug effects | Corynebacterium glutamicum - cytology | Phosphorylation - genetics | Adaptation, Physiological - genetics | Base Sequence | Stress, Physiological - drug effects | Homeostasis - drug effects | Phosphorylation - drug effects | Copper - toxicity | Binding Sites | Stress, Physiological - genetics | Bacterial Proteins - genetics | Signal Transduction - genetics | Corynebacterium glutamicum - physiology | Gene Expression Regulation, Bacterial - drug effects | Gene Expression Regulation, Bacterial - genetics | DNA, Bacterial - genetics | Histidine Kinase | Signal Transduction - drug effects | Bacterial Proteins - metabolism | Mutation | Homeostasis - genetics | Oxidases | DNA microarrays | RNA | Analysis | Genes | Genomics | Cellular signal transduction | Genetic transcription | Adenosine triphosphatase | Cytochrome | Transcription | Homeostasis | Genomes | Glucose | Kinases | DNA repair | Proteins | Signal transduction | Reporter gene | Histidine | Clonal deletion | Corynebacterium glutamicum | Deletion | Bacteria | Copper | Deoxyribonucleic acid--DNA | Stresses | Gene clusters | RNA polymerase | Metabolism | Gene expression | Heavy metals | Stress | Histidine kinase | Multicopper oxidase | Tuberculosis | Electrophoretic mobility | Transduction | Deoxyribonucleic acid | DNA
Journal Article
BMC Genomics, ISSN 1471-2164, 12/2010, Volume 11, Issue 1, pp. 728 - 728
Background: Corynebacterium pseudotuberculosis is generally regarded as an important animal pathogen that rarely infects humans. Clinical strains are... 
MYCOBACTERIUM-TUBERCULOSIS | GRAM-POSITIVE BACTERIA | OXIDATIVE STRESS | PHOSPHOLIPASE-D | TRANSCRIPTIONAL REGULATORS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | NONRIBOSOMAL PEPTIDE SYNTHETASES | GENETICS & HEREDITY | HIDDEN MARKOV-MODELS | DNA-BINDING PROTEIN | SIDEROPHORE BIOSYNTHESIS | CU,ZN SUPEROXIDE-DISMUTASE | Virulence Factors - genetics | Genes, Bacterial - genetics | Corynebacterium pseudotuberculosis - physiology | Zinc - metabolism | Humans | Fimbriae, Bacterial - genetics | Corynebacterium pseudotuberculosis - genetics | Corynebacterium pseudotuberculosis - pathogenicity | Virulence - genetics | Base Sequence | Female | Transcription, Genetic | Child | Histiocytic Necrotizing Lymphadenitis - microbiology | Regulon - genetics | Gene Regulatory Networks - genetics | Molecular Sequence Annotation | Iron - metabolism | Sequence Analysis, DNA | Genome, Bacterial - genetics | Histiocytic Necrotizing Lymphadenitis - genetics | Manganese - metabolism | Bacterial Adhesion - genetics | Virulence Factors - metabolism | Corynebacterium pseudotuberculosis - isolation & purification | Corynebacteria | Usage | Genes | Physiological aspects | Genetic aspects | Research | Nucleotide sequencing | Health aspects | Animals | Hospitals | Antibiotics | Goats | Taxonomy | Genomics | Bacteria | Genomes | Binding sites | Genes, Bacterial | Fimbriae, Bacterial | Genome, Bacterial | Virulence | Biochemistry, Molecular Biology | Iron | Gene Regulatory Networks | Virulence Factors | Histiocytic Necrotizing Lymphadenitis | Zinc | Bacterial Adhesion | Corynebacterium pseudotuberculosis | Regulon | Life Sciences | Manganese
Journal Article
BMC Biology, ISSN 1741-7007, 05/2014, Volume 12, Issue 1, pp. 41 - 41
Journal Article
Applied Microbiology and Biotechnology, ISSN 0175-7598, 10/2014, Volume 98, Issue 20, pp. 8641 - 8655
Inducible expression is a versatile genetic tool for controlling gene transcription, determining gene functions and other uses. Herein, we describe our... 
Life Sciences | Biotechnology | Microbiology | Resorcinol switch | Ribozyme | Microbial Genetics and Genomics | Cumate switch | Inducible systems | Strong inducible promoter | SECONDARY METABOLISM | ESCHERICHIA-COLI | PSEUDOMONAS-PUTIDA F1 | ALBUS J1074 GENOME | COMPLETE GENOME SEQUENCE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | PROTEIN EXPRESSION | GENE-EXPRESSION | BETA-GLUCURONIDASE | SYNTHETIC BIOLOGY | CORYNEBACTERIUM-GLUTAMICUM | Corynebacterium glutamicum - genetics | Benzoates - metabolism | RNA, Catalytic - metabolism | Transcriptional Activation - drug effects | Molecular Sequence Data | Lac Repressors - genetics | Molecular Biology - methods | Actinobacteria - drug effects | Isopropyl Thiogalactoside - metabolism | Glucuronidase - analysis | Actinobacteria - genetics | Actinobacteria - metabolism | Operator Regions, Genetic | Lac Repressors - metabolism | Genes, Reporter | Resorcinols - metabolism | Promoter Regions, Genetic | Pseudomonas putida - genetics | Escherichia coli Proteins - metabolism | Transcription Factors - genetics | Sequence Analysis, DNA | Glucuronidase - genetics | Escherichia coli Proteins - genetics | Genetics, Microbial - methods | RNA, Catalytic - genetics | Genetic Vectors | Streptomyces | Physiological aspects | Genetic aspects | Research | Resorcinols | Analysis | Studies | Bacteria | Genetic engineering | Ribozymes
Journal Article
Journal Article
Applied Microbiology and Biotechnology, ISSN 0175-7598, 4/2010, Volume 86, Issue 4, pp. 1057 - 1066
Journal Article
Journal Article
Journal Article
Applied Microbiology and Biotechnology, ISSN 0175-7598, 5/2014, Volume 98, Issue 9, pp. 4083 - 4094
In this study, a recently sequenced 9.8-kb plasmid, pLAtc1, from Acidithiobacillus caldus strain SM-1 was characterized and developed into an expression... 
Life Sciences | pLAtc1 | Biotechnology | Succinate dehydrogenase | Microbiology | Microbial Genetics and Genomics | Acidithiobacillus caldus SM-1 | α-Ketoglutarate dehydrogenase | pLAtcE | IncQ-like plasmid | SEQUENCE-ANALYSIS | MUTAGENESIS | alpha-Ketoglutarate dehydrogenase | ESCHERICHIA-COLI | ADDICTION SYSTEMS | INCQ | GRAM-NEGATIVE BACTERIA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | THIOBACILLUS | COPY NUMBER | PERSPECTIVES | HOST-RANGE PLASMID | Conjugation, Genetic | Corynebacterium glutamicum - genetics | Drug Resistance, Bacterial | Molecular Sequence Data | DNA, Bacterial - chemistry | Green Fluorescent Proteins - genetics | Multilocus Sequence Typing | Plasmids - classification | Transcription Termination, Genetic | Acidithiobacillus - genetics | Cloning, Molecular | Genes, Reporter | Genetic Engineering - methods | Genes, Bacterial | Promoter Regions, Genetic | Gene Expression | Green Fluorescent Proteins - analysis | Selection, Genetic | DNA Replication | Genotype | Plasmids - isolation & purification | Genetic Vectors - isolation & purification | DNA, Bacterial - genetics | Genetic Vectors - classification | Comamonas testosteroni - genetics | Escherichia coli - genetics | Replication Origin | Bacillus (Bacteria) | Genetic aspects | Research | Genetic vectors | Plasmids | Studies | Bacteria | Gene expression | Analysis
Journal Article
Molecular Microbiology, ISSN 0950-382X, 11/2009, Volume 74, Issue 3, pp. 724 - 741
P>We previously showed that the 2-oxoglutarate dehydrogenase inhibitor protein OdhI of Corynebacterium glutamicum is phosphorylated by PknG at Thr14, but that... 
MYCOBACTERIUM-TUBERCULOSIS | SER/THR KINASE | AMINO-ACIDS | FHA DOMAINS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CORYNEFORM BACTERIA | REGULATORY NETWORK | MICROBIOLOGY | IDENTIFICATION | EXPRESSION | DEHYDROGENASE | MOLECULAR ANALYSIS | Phosphorylation | Corynebacterium glutamicum - genetics | DNA, Bacterial - metabolism | Phosphoprotein Phosphatases - metabolism | Ketoglutarate Dehydrogenase Complex - metabolism | Threonine - metabolism | Ketoglutarate Dehydrogenase Complex - genetics | Corynebacterium glutamicum - metabolism | Cell Division | Threonine - genetics | Cytoskeletal Proteins - metabolism | Mycobacterium tuberculosis - metabolism | Protein-Serine-Threonine Kinases - metabolism | Amino Acid Sequence | Genes, Bacterial | Genome, Bacterial | Bacterial Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Corynebacterium glutamicum - enzymology | Protein Structure, Tertiary - genetics | Signal Transduction - genetics | Binding Sites - genetics | Substrate Specificity - genetics | Sequence Homology, Amino Acid | Sequence Alignment | DNA, Bacterial - genetics | Phosphoprotein Phosphatases - genetics | Bacterial Proteins - metabolism | Protein-Serine-Threonine Kinases - chemistry | Ketoglutaric Acids | Gene Expression Regulation, Bacterial | Mycobacterium tuberculosis - genetics | Mycobacterium tuberculosis - growth & development | Proteins | Genetic research | Phosphatases | Protein kinases | Serine | Glutamine
Journal Article
Journal of Biotechnology, ISSN 0168-1656, 09/2017, Volume 258, pp. 69 - 78
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2012, Volume 7, Issue 3, p. e31709
Corynebacterium diphtheriae and Corynebacterium glutamicum each have one gene (cat) encoding catalase. In-frame Delta cat mutants of C. diphtheriae and C.... 
OXIDATIVE STRESS | GENE | SOXR PROTEIN | TOXIN | ESCHERICHIA-COLI | NEISSERIA-MENINGITIDIS | BIOLOGY | INTRACELLULAR HYDROGEN-PEROXIDE | SUPEROXIDE-DISMUTASE | EXPRESSION | POSITIVE CONTROL | Corynebacterium glutamicum - drug effects | Corynebacterium glutamicum - genetics | Oxidative Stress | Species Specificity | Escherichia coli - drug effects | Corynebacterium diphtheriae - metabolism | Genetic Complementation Test | Corynebacterium glutamicum - metabolism | Base Sequence | Corynebacterium diphtheriae - genetics | Escherichia coli - metabolism | Repressor Proteins - metabolism | Recombinant Proteins - metabolism | Genes, Bacterial | Promoter Regions, Genetic | Catalase - genetics | Bacterial Proteins - genetics | Corynebacterium diphtheriae - drug effects | Hydrogen Peroxide - pharmacology | Repressor Proteins - genetics | Escherichia coli Proteins - metabolism | Recombinant Proteins - genetics | DNA, Bacterial - genetics | Escherichia coli - genetics | Escherichia coli Proteins - genetics | Bacterial Proteins - metabolism | Mutation | Catalase - biosynthesis | Animal genetics | Cysteine | Genetic aspects | Genetic transcription | Bacterial proteins | Escherichia coli | Oxidative stress | Transcription factors | Hydrogen peroxide | Transcription | Amino acids | Homology | Genomes | Gene deletion | Proteins | CAT gene | Clonal deletion | E coli | Catalase | Corynebacterium glutamicum | Deletion | Bacteria | Oxidation | Inhibition | Gram-negative bacteria | Dithiothreitol | Deoxyribonucleic acid--DNA | Stationary phase | Killing | Deoxyribonuclease | Cloning | Gene expression | Diphtheria | OxyR gene | Mutants | Strain | Studies | Plasmids | Electrophoretic mobility | Deoxyribonucleic acid | DNA
Journal Article