Search results for "Micrococcus"

showing 10 items of 30 documents

Combining in the melt physical and biological properties of poly(caprolactone) and chlorhexidine to obtain antimicrobial surgical monofilaments.

2012

Bacterial infections on a sutured wound represent a critical problem, and the preparation of suture threads possessing antimicrobial properties is valuable. In this work, poly(caprolactone) (PCL) monofilaments were compounded at the concentration of 1, 2 and 4 % (w/w), respectively, to the antiseptic chlorhexidine diacetate (CHX). The incorporation was carried out in the melt by a single-step methodology, i.e. “online” approach. Mechanical tests revealed that the incorporation of CHX does not significantly change tensile properties of PCL fibres as the thermal profile adopted to prepare the compounded fibres does not compromise the antibacterial activity of CHX. In fact, CHX confers to comp…

Thermoplasticmedicine.drug_classCell SurvivalPolyestersSettore BIO/19 - Microbiologia GeneraleApplied Microbiology and Biotechnologychemistry.chemical_compoundAntisepticTensile StrengthPolymer chemistryUltimate tensile strengthmedicineEscherichia coliHumanschemistry.chemical_classificationpoly(caprolactone)biologyChemistryChlorhexidinechlorhexidineChlorhexidineSuture TechniquesSpectrometry X-Ray EmissionGeneral MedicineFibroblastsbiology.organism_classificationAntimicrobialMicrococcus luteusSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiEquipment and Suppliessurgical monofilamentsAnti-Infective Agents LocalMicroscopy Electron ScanningMicrococcus luteusAntibacterial activityCaprolactoneBiotechnologyNuclear chemistrymedicine.drugBacillus subtilisApplied microbiology and biotechnology
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HSP70 gene expression in Mytilus galloprovincialis hemocytes is triggered by moderate heat shock and Vibrio anguillarum, but not by V. splendidus or …

2005

Complete sequence of HSP70 cDNA from the mussel, Mytilus galloprovincialis was established before quantifying its expression following moderate heat shock or injection of heat-killed bacteria. HSP70 cDNA is comprised of 2378 bp including one ORF of 654 aa, with a predicted 70 bp 5'-UTR and a 343 bp 3'-UTR (GenBank, 18 Jan 05, AY861684). Alignment identity ranged from 89% for Crassostrea ariakensis to 72% for C. virginica. Curiously, HSP70 gene and cDNA sequences from M. galloprovincialis, deposited later (03 and 27 May), show only 73% identity with the present sequence. Meanwhile, characteristic motifs of the HSP70 family were located in conserved positions. Expression of HSP70 gene was qua…

Untranslated regionVibrio anguillarumHemocytesMolecular Sequence DataImmunologyMicrococcusMicrobiologyComplementary DNAGene expressionAnimalsHSP70 Heat-Shock ProteinsAmino Acid SequenceCloning MolecularPhylogenyVibrioMytilusBase SequencebiologyReverse Transcriptase Polymerase Chain Reactionbiology.organism_classificationMytilusRandom Amplified Polymorphic DNA TechniqueHousekeeping geneHsp70RNA28S rRNA Gene expression Heat shock HSP70Sequence AlignmentHeat-Shock ResponseBacteriaDevelopmental BiologyDevelopmental & Comparative Immunology
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Differential involvement of mussel hemocyte sub-populations in the clearance of bacteria.

2008

Abstract Mussels are filter-feeders living in a bacteria-rich environment. We have previously found that numerous bacterial species are naturally present within the cell-free hemolymph, including several of the Vibrio genus, whereas the intra-cellular content of hemocytes was sterile. When bacteria were injected into the circulation of the mussel, the number of living intra-hemocyte bacteria dramatically increased in less than an hour, suggesting intense phagocytosis, then gradually decreased, with no viable bacteria remaining 12 h post-injection for Micrococcus lysodeikticus, 24 h for Vibrio splendidus and more than 48 h for V ibrio anguillarum. The total hemocyte count (THC) was dramatica…

Vibrio anguillarumHemocytesPhagocytosisAntimicrobial peptidesColony Count MicrobialMytiluAquatic ScienceFlow cytometryMicrobiologyMicrococcusHemolymphHemolymphHyalinocytemedicineEnvironmental ChemistryAnimalsVibrio anguillarumGram-Positive Bacterial InfectionsVibrioMytilusVibrio splendidubiologymedicine.diagnostic_testGranulocyteGeneral MedicineMusselMolluscsbiology.organism_classificationFlow CytometryMicrococcus lysodeikticuVibrioVibrio InfectionsClearanceBacteriaFishshellfish immunology
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Lysozyme gene expression and hemocyte behaviour in the Mediterranean mussel, Mytilus galloprovincialis, after injection of various bacteria or temper…

2008

The aim of the present study was to evaluate the expression of the Mytilus galloprovincialis lysozyme gene in different in vivo stress situations, including injection of bacteria Vibrio splendidus LGP32, Vibrio anguillarum or Micrococcus lysodeikticus, as well as heat shock at 30 C and cold stress at 5 C. Injection of V. splendidus LGP32 resulted in: (i) a general down-regulation of lysozyme gene expression, as quantified by Q-PCR; (ii) reduction in the number of circulating hemocytes; (iii) decrease in the percentage of circulating hemocytes expressing lysozyme mRNA which was now restricted to only small cells, as observed by ISH; and (iv) accumulation of hemocytes expressing lysozyme in t…

Vibrio anguillarumHemocytesPopulationLysozymeMytiluVibrio splendidusAquatic ScienceGene Expression Regulation EnzymologicMicrobiologyMicrococcus03 medical and health scienceschemistry.chemical_compoundISHGene expressionRNA Ribosomal 28SEnvironmental ChemistryMicrococcus lysodeikticusAnimalsVibrio anguillarumeducation030304 developmental biologyVibrioMytilus0303 health sciencesMessenger RNAeducation.field_of_studyVibrio splendidubiologyQ-PCRMusclesTemperature04 agricultural and veterinary sciencesGeneral MedicineMolluscsbiology.organism_classificationMicrococcus lysodeikticuMytilusReal-time polymerase chain reactionchemistryHeat shockQ PCR040102 fisheries0401 agriculture forestry and fisheriesMuramidaseGene expressionLysozymeBacteriaFishshellfish immunology
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Specific expression of antimicrobial peptide and HSP70 genes in response to heat-shock and several bacterial challenges in mussels

2007

Abstract Defensin, mytilin and myticin are antimicrobial peptides (AMP) involved in mussel innate immunity. Their in vitro antibacterial activity is different according to the targeted bacterial species. To determine if this specificity is correlated to different regulations of gene expressions, adult mussels were challenged in vivo with either Vibrio splendidus LGP32, Vibrio anguillarum , Micrococcus lysodeikticus or by heat shock. RNAs were isolated from circulating hemocytes and AMP mRNAs were quantified by Q-PCR using 28S rRNA as housekeeping gene. In addition, HSP70 gene expression was also quantified as representing non-specific response to stress. In naive mussels, the three AMP mRNA…

Vibrio anguillarumHot TemperatureTime Factorsantimicrobial peptidemusselAntimicrobial peptidesecological immunologyAquatic ScienceMicrococcusMicrobiologychemistry.chemical_compoundAnimalsEnvironmental ChemistryHSP70 Heat-Shock ProteinsRNA MessengerDefensinHSP70DNA PrimersVibrioMytilusRegulation of gene expressionbiologyReverse Transcriptase Polymerase Chain ReactionMytilinmolluskGeneral Medicinebiology.organism_classificationMyticinMolecular biologyImmunity InnateHousekeeping geneHsp70Gene Expression Regulationchemistrygene regulationAntimicrobial Cationic PeptidesFish & Shellfish Immunology
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Evidence for essential primary amino groups in a bacterial coupling factor F1ATPase.

1980

Abstract We have found that the binding of pyridoxal-5′-phosphate to 6 primary amino groups leads to the inactivation of the enzyme. A preferential reaction of pyridoxal-5′-phosphate with the α-subunits of this enzyme can be demonstrated. The reactivity of the amino groups is influenced by various effectors. In the presence of ATP the inhibition of the ATPase activity is noncompetitive.

chemistry.chemical_classificationAdenosine TriphosphatasesPrimary (chemistry)Binding SitesChemistryStereochemistryEffectorCell MembraneBiophysicsCell BiologyBiochemistryMicrococcusCoupling (electronics)Structure-Activity RelationshipEnzymeBiochemistrySolubilityPyridoxal PhosphateAtpase activityReactivity (chemistry)Amino AcidsMolecular BiologyBiochemical and biophysical research communications
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Ability of Kocuria varians LTH 1540 To Degrade Putrescine: Identification and Characterization of a Novel Amine Oxidase.

2015

This work describes the identification and characterization of an amine oxidase from Kocuria varians LTH 1540 (syn. Micrococcus varians) primarily acting on putrescine. Data from MALDI-TOF MS/MS and the identification of Δ(1)-pyrroline as degradation product from putrescine indicate that the enzyme is a flavin-dependent putrescine oxidase (PuO). Properties of partially purified enzyme have been determined. The enzyme oxidizes diamines, putrescine and cadaverine, and, to a lesser extent, polyamines, such as spermidine, but not monoamines. The kinetic constants (Km and Vmax) for the two major substrates were 94 ± 10 μM and 2.3 ± 0.1 μmol/min·mg for putrescine and 75 ± 5 μM and 0.15 ± 0.02 μmo…

chemistry.chemical_classificationAmine oxidaseCadaverineOxidoreductases Acting on CH-NH Group DonorsChromatographyKocuria variansGeneral ChemistryBiologyHydrogen-Ion ConcentrationAmine oxidase inhibitorsMicrococcusSpermidinePutrescine oxidasechemistry.chemical_compoundKineticsEnzymeBiodegradation EnvironmentalchemistryBacterial ProteinsEnzyme StabilityPutrescinePutrescineGeneral Agricultural and Biological SciencesJournal of agricultural and food chemistry
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3'-Arylazido-beta-alanyl-2-azido ATP, a cross-linking photoaffinity label for F1ATPases.

1989

Abstract The synthesis of the 3′-arylazido-2-azido ATP derivative 3′-O-{3-[N-(4-azido-2-nitrophenyl)-amino]propionyl}2-azido-adenosine 5′-triphosphate (2,3′-DiN3ATP) is described. The bifunc­ tional photoreactive ATP analog is characterized spectroscopically. Photoaffinity labeling of F, ATPase from Micrococcus luteus by this analog results in the inactivation of the enzyme and in the formation of higher molecular weight cross-links,

chemistry.chemical_classificationAzidesPhotoaffinity labelingbiologyLightStereochemistryAffinity Labelsbiology.organism_classificationGeneral Biochemistry Genetics and Molecular BiologyMicrococcuschemistry.chemical_compoundKineticsProton-Translocating ATPasesEnzymeAdenosine TriphosphatechemistryIndicators and ReagentsBifunctionalBeta (finance)Micrococcus luteusDerivative (chemistry)Zeitschrift fur Naturforschung. C, Journal of biosciences
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First evidence of antimicrobial activity of neurotoxin 2 from anemonia sulcata (Cnidaria)

2014

International audience; We investigated the antibacterial activity of Anemonia sulcata (Cnidaria, Anthozoa) tentacle and body acidic extracts. Biochemical purification consisted of first step on solid phase Sep-Pak C8 column followed by several HPLC runs on C18 column using different conditions. Anti-Micrococcus lysodeikticus activity has been detected in 40 % acetonitrile fractions. The resulting purified molecule from tentacles had a molecular mass determined by MALDI-TOF mass spectrum of 4946,299 Da and has been completely sequenced. Its aa sequence revealed identity with the Neurotoxin 2 (ATX-II), a Na + channel blocking toxins. Consequently, ATX-II appeared to display a dual role as to…

lcsh:Biology (General)antimicrobial peptideMicrococcus lysodeikticusneurotoxin[SDU.STU.HY]Sciences of the Universe [physics]/Earth Sciences/Hydrologylcsh:QH301-705.5antimicrobial peptide; Anemonia sulcata; ATX II; neurotoxin; Micrococcus lysodeikticusATX IIAnemonia sulcata
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Structure, Biosynthesis, and Bioactivity of Photoditritide from Photorhabdus temperata Meg1

2019

A new cyclic peptide photoditritide (1), containing two rare amino acid d-homoarginine residues, was isolated from Photorhabdus temperata Meg1 after the nonribosomal peptide synthetase encoding gene pdtS was activated via promoter exchange. The structure of 1 was elucidated by HR-MS and NMR experiments. The absolute configurations of amino acids were determined according to the advanced Marfey's method after hydrolysis of 1. Bioactivity testing of 1 revealed potent antimicrobial activity against Micrococcus luteus with an MIC value of 3.0 μM and weak antiprotozoal activity against Trypanosoma brucei rhodesiense with an IC50 value of 13 μM. Additionally, the biosynthetic pathway of 1 was als…

medicine.drug_classPharmaceutical Science01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundHydrolysisBiosynthesisNonribosomal peptideDrug DiscoverymedicinePharmacologychemistry.chemical_classificationbiology010405 organic chemistryOrganic ChemistryTrypanosoma brucei rhodesiensebiology.organism_classificationCyclic peptide0104 chemical sciencesAmino acid010404 medicinal & biomolecular chemistryComplementary and alternative medicinechemistryBiochemistryAntiprotozoalMolecular MedicineMicrococcus luteusJournal of Natural Products
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