Search results for "Corynebacterium"

showing 10 items of 21 documents

Relevance of NADH Dehydrogenase and Alternative Two-Enzyme Systems for Growth of Corynebacterium glutamicum With Glucose, Lactate, and Acetate

2021

The oxidation of NADH with the concomitant reduction of a quinone is a crucial step in the metabolism of respiring cells. In this study, we analyzed the relevance of three different NADH oxidation systems in the actinobacterial model organism Corynebacterium glutamicum by characterizing defined mutants lacking the non-proton-pumping NADH dehydrogenase Ndh (Δndh) and/or one of the alternative NADH-oxidizing enzymes, L-lactate dehydrogenase LdhA (ΔldhA) and malate dehydrogenase Mdh (Δmdh). Together with the menaquinone-dependent L-lactate dehydrogenase LldD and malate:quinone oxidoreductase Mqo, the LdhA-LldD and Mdh-Mqo couples can functionally replace Ndh activity. In glucose minimal medium…

0301 basic medicineHistologylcsh:Biotechnologyrespiratory chain030106 microbiologyMutantBiomedical EngineeringRespiratory chainmalate dehydrogenaseBioengineeringDehydrogenaseMalate dehydrogenaseCorynebacterium glutamicum03 medical and health scienceschemistry.chemical_compoundNAD+/NADH ratioddc:570lcsh:TP248.13-248.65Lactate dehydrogenaseOriginal ResearchbiologyWild typeNADH dehydrogenaseBioengineering and BiotechnologyNADH dehydrogenaselactate dehydrogenaseSugR030104 developmental biologyBiochemistrychemistrybiology.proteinmalate:quinone oxidoreductaseBiotechnologyFrontiers in Bioengineering and Biotechnology
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The wasted chewing gum bacteriome

2020

Here we show the bacteriome of wasted chewing gums from five different countries and the microbial successions on wasted gums during three months of outdoors exposure. In addition, a collection of bacterial strains from wasted gums was set, and the biodegradation capability of different gum ingredients by the isolates was tested. Our results reveal that the oral microbiota present in gums after being chewed, characterised by the presence of species such as Streptococcus spp. or Corynebacterium spp., evolves in a few weeks to an environmental bacteriome characterised by the presence of Acinetobacter spp., Sphingomonas spp. and Pseudomonas spp. Wasted chewing gums collected worldwide contain …

0301 basic medicineTime Factors030106 microbiologyCorynebacteriumlcsh:MedicineSolid WasteArticleApplied microbiologyChewing Gum03 medical and health sciencesFood sciencelcsh:ScienceBiotransformationMultidisciplinarybiologyEnvironmental microbiologyBacteriaMicrobiotaPseudomonaslcsh:RBiofilmBacteriomeAcinetobacterbiology.organism_classificationSphingomonasChewing gum3. Good healthKocuria030104 developmental biologylcsh:QScientific Reports
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2020

Lsr2-like nucleoid-associated proteins play an important role as xenogeneic silencers (XS) of horizontally acquired genomic regions in actinobacteria. In this study, we systematically analyzed the in vivo constraints underlying silencing and counter-silencing of the Lsr2-like protein CgpS in Corynebacterium glutamicum Genome-wide analysis revealed binding of CgpS to regions featuring a distinct drop in GC profile close to the transcription start site (TSS) but also identified an overrepresented motif with multiple A/T steps at the nucleation site of the nucleoprotein complex. Binding of specific transcription factors (TFs) may oppose XS activity, leading to counter-silencing. Following a sy…

0303 health sciences030306 microbiologyEffectorVirulencePromoterComputational biologyBiologyMicrobiologyCorynebacterium glutamicum03 medical and health sciencesVirologyHorizontal gene transferGene silencingGeneTranscription factor030304 developmental biologymBio
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Corynebacterium aquatimens sp. nov., a lipophilic Corynebacterium isolated from blood cultures of a patient with bacteremia

2012

An unknown lipophilic coryneform bacterium isolated from the blood cultures of a patient with bacteremia was characterized by phenotypic and molecular genetic methods. Chemical analysis revealed the presence of short chain mycolic acids consistent with the genus Corynebacterium. The DNA G+C content was 60.8 mol%. Comparative 16S rRNA gene sequence analysis demonstrated that the isolate represents a new subline within the genus Corynebacterium. The closely phylogenetic relative of the unknown bacterium was found to be C. tuscaniense (97.8% sequence similarity). Partial rpoB gene sequence revealed that strain IMMIB L-2475(T) exhibited 13.5% sequence divergence with C. tuscaniense. The unknown…

AdultDNA BacterialMaleMolecular Sequence DataCorynebacteriumBacteremiaCorynebacteriumPolymerase Chain ReactionRibotypingApplied Microbiology and BiotechnologyMicrobiologylaw.inventionMycolic acidMicrobiologyRibotypingBacterial ProteinslawRNA Ribosomal 16SHumansPhylogenyEcology Evolution Behavior and SystematicsPolymerase chain reactionchemistry.chemical_classificationBase CompositionCorynebacterium InfectionsbiologyDNA–DNA hybridizationRibosomal RNAbiology.organism_classification16S ribosomal RNArpoBMolecular biologyMycolic AcidschemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationSystematic and Applied Microbiology
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A rare case of sepsis due to Corynebacterium macginleyi from central venous catheter in an elderly woman

2011

Corynebacterium macginleyi is a gram positive rod that causes especially ocular infections: since now only six elderly cases of extraocular infection are described. A 76 years old bedridden woman with a central venous catheter was hospitalized for 10 days of persistent fever. She was treated before with vancomicin and then with imipenem. The clinical conditions improved and the patient was discharged after two weeks of hospitalization. Among recognised risk factors for this infection the advanced age, indwelling devices and immunosuppression seem the most important. On the other hand, the antibiotics of choice are glycopeptides while the association of another antibiotic is recommended in o…

Catheterization Central VenousTreatment OutcomeBacterial ProteinsCorynebacterium InfectionsRNA Ribosomal 16SSepsisHumansCorynebacterium macginleyi Sepsis Elderly ImmunosuppressionFemaleCorynebacteriumAgedAnti-Bacterial Agents
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Bioconversion of Gibberellin Fermentation Residue into Feed Supplement and Organic Fertilizer Employing Housefly (Musca domestica L.) Assisted by Cor…

2014

The accumulation of a considerable quantity of gibberellin fermentation residue (GFR) during gibberellic acid A3 (GA3) production not only results in the waste of many resources, but also poses a potential hazard to the environment, indicating that the safe treatment of GFR has become an urgent issue for GA3 industry. The key to recycle GFR is converting it into an available resource and removing the GA3 residue. To this end, we established a co-bioconversion process in this study using house fly larvae (HFL) and microbes (Corynebacterium variabile) to convert GFR into insect biomass and organic fertilizer. About 85.5% GA3 in the GFR was removed under the following optimized solid-state fer…

Crop residueBioconversionlcsh:MedicineEnvironmental pollutionBiologyCorynebacteriumWaste ManagementHousefliesAnimalsDry matterOrganic matterFood scienceBiomasslcsh:ScienceFertilizerschemistry.chemical_classificationMultidisciplinarylcsh:Rfood and beveragesStrawAnimal FeedGibberellinschemistryAgronomyFermentationFermentationlcsh:QOrganic fertilizerResearch ArticlePloS one
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Identification of Gip as a novel phage‐encoded gyrase inhibitor protein of Corynebacterium glutamicum

2021

By targeting key regulatory hubs of their host, bacteriophages represent a powerful source for the identification of novel antimicrobial proteins. Here, a screening of small cytoplasmic proteins encoded by the CGP3 prophage of Corynebacterium glutamicum resulted in the identification of the gyrase-inhibiting protein Cg1978, termed Gip. Pull-down assays and surface plasmon resonance revealed a direct interaction of Gip with the gyrase subunit A (GyrA). The inhibitory activity of Gip was shown to be specific to the DNA gyrase of its bacterial host C. glutamicum. Overproduction of Gip in C. glutamicum resulted in a severe growth defect as well as an induction of the SOS response. Furthermore, …

DNA Replicationendocrine systemProtein subunitProphagesBiologyMicrobiologyDNA gyraseCorynebacterium glutamicum03 medical and health scienceschemistry.chemical_compoundViral Proteinsddc:570Topoisomerase II InhibitorsSOS responseMolecular BiologyProphage030304 developmental biology0303 health sciences030306 microbiologyDNA replicationAnti-Bacterial AgentsHigh-Throughput Screening AssaysCorynebacterium glutamicumchemistryBiochemistrybacteriaTopoisomerase-II InhibitorDNAhormones hormone substitutes and hormone antagonistsMolecular Microbiology
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Deciphering the rules underlying xenogeneic silencing and counter-silencing of Lsr2-like proteins

2019

ABSTRACTLsr2-like nucleoid-associated proteins play an important role as xenogeneic silencers (XS) of horizontally acquired genomic regions in actinobacteria. In this study, we systematically analyzed the in vivo constraints underlying silencing and counter-silencing of the Lsr2-like protein CgpS inCorynebacterium glutamicum. Genome-wide analysis revealed binding of CgpS to regions featuring a distinct drop in GC-profile close to the transcription start site (TSS), but also identified an overrepresented motif with multiple A/T steps at the nucleation site of the nucleoprotein complex. Binding of specific transcription factors (TFs) may oppose XS activity leading to counter-silencing. Follow…

EffectorGene silencingVirulencePromoterComputational biologyBiologyGeneTranscription factorCorynebacterium glutamicumNucleoprotein
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Lysine synthesis control in Corynebacterium glutamicum RC 115 in mixed substrate (glucose-acetate) medium.

2003

The effect of acetate as a glucose co-substrate on growth, lysine synthesis and experimental lysine yield from carbon substrates by Corynebacterium glutamicum RC 115 was investigated. It was found that low amounts of acetate, injected with a glucose-acetate pulse into the steady-state continuous culture in bioreactor, caused a slight decrease in the specific rates of glucose uptake and bacterial growth, but a significant increase in the cell specific rate of lysine synthesis and an increase in lysine yield. In contrast, acetate injected in high amounts was followed by a drastic decrease in the values of these parameters. A strong increase in experimental lysine yield under the latter condit…

Glucose uptakeLysineCell Culture TechniquesBioengineeringBacterial growthBiologyAcetatesCorynebacteriumcomplex mixturesApplied Microbiology and BiotechnologyCorynebacterium glutamicumFeedbackchemistry.chemical_compoundBioreactorsBiosynthesisBioreactorHomeostasisLysineSubstrate (chemistry)General MedicineAdaptation PhysiologicalGlucoseBiochemistrychemistryYield (chemistry)Flow Injection AnalysisbacteriaCell DivisionBiotechnologyJournal of biotechnology
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Quantitative studies of the secretion of complement component C3 by resident, elicited and activated macrophages. Comparison with C2, C4 and lysosoma…

1982

To quantitate the secretion of complement component C3 by guinea pig peritoneal macrophages an enzyme-linked immunosorbent assay was developed. C3 secretion was studied in resident, elicited and activated macrophages and compared with release of hemolytically active C2 and C4, as well as the lysosomal enzyme β-D-2-acetamido-2-deoxyglucosidase. Resident macrophages secreted about 6 ng C3/106 cells/h into culture supernatants over a period of 12 h. Corynebacterium parvum-activated cells were found to secrete 3 times that amount at nearly constant rates. There was a stepwise increase in secretion of functional C2 and C4 when comparing resident, elicited and activated macrophages; secretion was…

ImmunologyEnzyme releaseGuinea PigsCorynebacteriumEnzyme-Linked Immunosorbent AssayHemolysisGuinea pigAcetylglucosaminidaseImmunology and AllergyAnimalsHumansSecretionPropionibacterium acnesSerum Albuminchemistry.chemical_classificationbiologyMacrophagesComplement C4Complement C3Complement C2Macrophage Activationbiology.organism_classificationMolecular biologyKineticsEnzymechemistryCell culture supernatantLysosomesEuropean journal of immunology
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