Strain identifier

BacDive ID: 4969

Type strain: No

Species: Klebsiella pneumoniae

Strain history: CIP <- 1994, ATCC <- E.C. Robertson, Escherichia coli var. communior

NCBI tax ID(s): 573 (species)

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For citation purpose refer to the digital object identifier (doi) of the current version.
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General

@ref: 447

BacDive-ID: 4969

DSM-Number: 789

keywords: genome sequence, Bacteria, aerobe, mesophilic, Gram-negative

description: Klebsiella pneumoniae CCUG 58866 is an aerobe, mesophilic, Gram-negative bacterium that was isolated from cow's milk.

NCBI tax id

  • NCBI tax id: 573
  • Matching level: species

strain history

@refhistory
447<- ATCC; ATCC 4352 <- E.C. Robertson; (Escherichia coli var. communior)
67770IAM 12015 <-- ATCC 4352 <-- E. C. Robertson ("Escherichia coli subsp. communior").
121885CIP <- 1994, ATCC <- E.C. Robertson, Escherichia coli var. communior

doi: 10.13145/bacdive4969.20230509.8.1

Name and taxonomic classification

LPSN

  • @ref: 20215
  • description: domain/bacteria
  • keyword: phylum/pseudomonadota
  • domain: Bacteria
  • phylum: Pseudomonadota
  • class: Gammaproteobacteria
  • order: Enterobacterales
  • family: Enterobacteriaceae
  • genus: Klebsiella
  • species: Klebsiella pneumoniae
  • full scientific name: Klebsiella pneumoniae (Schroeter 1886) Trevisan 1887 (Approved Lists 1980)

  • synonyms

    • @ref: 20215
    • synonym: Hyalococcus pneumoniae

@ref: 447

domain: Bacteria

phylum: Proteobacteria

class: Gammaproteobacteria

order: Enterobacteriales, not validated

family: Enterobacteriaceae

genus: Klebsiella

species: Klebsiella pneumoniae

full scientific name: Klebsiella pneumoniae (Schroeter 1886) Trevisan 1887

type strain: no

Morphology

cell morphology

@refgram stainconfidencecell shapemotility
69480negative99.985
121885negativerod-shapedno

Culture and growth conditions

culture medium

@refnamegrowthlinkcomposition
447COLUMBIA BLOOD MEDIUM (DSMZ Medium 693)yeshttps://mediadive.dsmz.de/medium/693Name: COLUMBIA BLOOD MEDIUM (DSMZ Medium 693) Composition: Defibrinated sheep blood 50.0 g/l Columbia agar base
41831MEDIUM 3 - Columbia agaryesColumbia agar (39.000 g);distilled water (1000.000 ml)
447TRYPTICASE SOY YEAST EXTRACT MEDIUM (DSMZ Medium 92)yeshttps://mediadive.dsmz.de/medium/92Name: TRYPTICASE SOY YEAST EXTRACT MEDIUM (DSMZ Medium 92) Composition: Trypticase soy broth 30.0 g/l Agar 15.0 g/l Yeast extract 3.0 g/l Distilled water
121885CIP Medium 3yeshttps://catalogue-crbip.pasteur.fr/fiche_milieu.xhtml?crbip=3
121885CIP Medium 72yeshttps://catalogue-crbip.pasteur.fr/fiche_milieu.xhtml?crbip=72

culture temp

@refgrowthtypetemperaturerange
447positivegrowth37mesophilic
41831positivegrowth30mesophilic
61767positivegrowth30mesophilic
67770positivegrowth37mesophilic
121885positivegrowth30-41
121885nogrowth5psychrophilic
121885nogrowth10psychrophilic

Physiology and metabolism

oxygen tolerance

@refoxygen tolerance
61767aerobe
121885facultative anaerobe

antibiogram

@refmediumincubation temperatureincubation timeoxygen conditionPenicillin Goxacillinampicillinticarcillinmezlocillincefalotincefazolincefotaximeaztreonamimipenemtetracyclinechloramphenicolgentamycinamikacinvancomycinerythromycinlincomycinofloxacinnorfloxacincolistinpipemidic acidnitrofurantoinbacitracinpolymyxin bkanamycinneomycindoxycyclineceftriaxoneclindamycinfosfomycinmoxifloxacinlinezolidnystatinquinupristin/dalfopristinteicoplaninpiperacillin/tazobactam
447Mueller-Hinton Agar371aerob068122232304238323236-382224618-2010-1240401432240162418-20303816244026012032
447Mueller-Hinton Agar30aerob08610203028-30403830-3232382022020-22104038-40142822016221830-3236202438-4022014030
447Mueller-Hinton Agar30aerob08610203028-30403830-3232382022020-22104038-40142822016221830-3236202438-4022014030

spore formation

@refspore formationconfidence
69481no100
69480no99.894

metabolite utilization

@refChebi-IDmetaboliteutilization activitykind of utilization tested
6836830849L-arabinose+fermentation
6836827613amygdalin+fermentation
6836828053melibiose+fermentation
6836817992sucrose+fermentation
6836862345L-rhamnose+fermentation
6836830911sorbitol+fermentation
6836817268myo-inositol-fermentation
6836816899D-mannitol+fermentation
6836817634D-glucose+fermentation
683685291gelatin-hydrolysis
6836827897tryptophan-energy source
6836816199urea+hydrolysis
6836818257ornithine-degradation
6836825094lysine+degradation
6836829016arginine-hydrolysis
12188529864mannitol+fermentation
12188517234glucose+fermentation
12188517716lactose+fermentation
12188517632nitrate+reduction
12188516301nitrite+reduction
121885132112sodium thiosulfate-builds gas from
12188517234glucose+degradation
6837418257ornithine-degradation
6837429016arginine-hydrolysis
6837425094lysine+degradation
6837416199urea-hydrolysis
6837418403L-arabitol-builds acid from
6837418024D-galacturonic acid+builds acid from
68374Potassium 5-ketogluconate-builds acid from
6837416899D-mannitol+builds acid from
6837417306maltose+builds acid from
6837415963ribitol+builds acid from
6837418394palatinose+builds acid from
6837415792malonate-assimilation
6837427897tryptophan-energy source
6837417634D-glucose+builds acid from
6837417992sucrose+builds acid from
6837430849L-arabinose+builds acid from
6837418333D-arabitol+builds acid from
6837427082trehalose+builds acid from
6837462345L-rhamnose+builds acid from
6837417268myo-inositol-builds acid from
6837417057cellobiose+builds acid from
6837430911sorbitol+builds acid from

metabolite production

@refChebi-IDmetaboliteproduction
6837435581indoleno
6836815688acetoinno
6836835581indoleno
6836816136hydrogen sulfideno
12188535581indoleno

metabolite tests

@refChebi-IDmetaboliteindole testvoges-proskauer-test
6837435581indole-
6836815688acetoin-
6836835581indole-

enzymes

@refvalueactivityec
68382alpha-fucosidase-3.2.1.51
68382alpha-mannosidase-3.2.1.24
68382N-acetyl-beta-glucosaminidase-3.2.1.52
68382beta-glucosidase+3.2.1.21
68382alpha-glucosidase+3.2.1.20
68382beta-glucuronidase-3.2.1.31
68382beta-galactosidase+3.2.1.23
68382alpha-galactosidase+3.2.1.22
68382naphthol-AS-BI-phosphohydrolase+
68382acid phosphatase+3.1.3.2
68382alpha-chymotrypsin-3.4.21.1
68382trypsin-3.4.21.4
68382cystine arylamidase-3.4.11.3
68382valine arylamidase-
68382leucine arylamidase+3.4.11.1
68382lipase (C 14)-
68382esterase lipase (C 8)+
68382esterase (C 4)+
68382alkaline phosphatase+3.1.3.1
68374L-aspartate arylamidase-3.4.11.21
68374alpha-maltosidase-
68374alpha-galactosidase+3.2.1.22
68374alpha-glucosidase-3.2.1.20
68374beta-galactosidase+3.2.1.23
68374N-acetyl-beta-glucosaminidase-3.2.1.52
68374beta-glucuronidase-3.2.1.31
68374beta-glucosidase+3.2.1.21
68374lipase-
68374urease-3.5.1.5
68374lysine decarboxylase+4.1.1.18
68374arginine dihydrolase-3.5.3.6
68374ornithine decarboxylase-4.1.1.17
68368cytochrome oxidase-1.9.3.1
68368gelatinase-
68368tryptophan deaminase-4.1.99.1
68368urease+3.5.1.5
68368ornithine decarboxylase-4.1.1.17
68368lysine decarboxylase+4.1.1.18
68368arginine dihydrolase-3.5.3.6
68368beta-galactosidase+3.2.1.23
121885oxidase-
121885beta-galactosidase+3.2.1.23
121885alcohol dehydrogenase-1.1.1.1
121885catalase+1.11.1.6
121885lysine decarboxylase+4.1.1.18
121885ornithine decarboxylase-4.1.1.17
121885urease+3.5.1.5

API zym

@refControlAlkaline phosphataseEsteraseEsterase LipaseLipaseLeucine arylamidaseValine arylamidaseCystine arylamidaseTrypsinalpha- ChymotrypsinAcid phosphataseNaphthol-AS-BI-phosphohydrolasealpha- Galactosidasebeta- Galactosidasebeta- Glucuronidasealpha- Glucosidasebeta- GlucosidaseN-acetyl-beta- glucosaminidasealpha- Mannosidasealpha- Fucosidase
121885-+++-+----++++-++---

API 20E

@refONPGADH ArgLDC LysODCCITH2SURETDA TrpINDVPGELGLUMANINOSorRHASACMELAMYARAOX
447+-+-+-+----++-++++++-
447+-+---+----++-++++++-
447+-+---+----++-++++++-

API ID32E

@refODCADH ArgLDC LysURELARLGAT5KGLIPRPbeta GLUMANMALADOPLEbeta GURMNTINDbeta NAGbeta GALGLUSACLARADARLalpha GLUalpha GALTRERHAINOCELSORalphaMALAspA
61767--+--+---+++++----+++++-+++-++--

API biotype100

@refGLUFRUGALTREMNESBEMELSACRAFMTEMALLACLTEMbGaMaGaCELGENMbGuESCRIBARAXYLPLERHAFUCMLZDARLLARLXLTDULTAGGLYINOMANMTLTURSORADOHBGLYXERYMDG3MDGSATMUCLTATDTATMTATDMLTLMLTCATETATETTECITGRTGAT2KG5KGTRYNAGGNTPACPATpOBEQATGTEmOBEBATPPATCMTTGEBETPCEABTHINLATCAPCYTHISSUCFUMGREGYTAVTETNTTNGLNITA3OBUAPTGTTPRODALALALASERMNTPROPTYR2KT
121885+++++++++++++++++++++++++-+-+--+++++++---+-+++-+++++-++++--++++++--+-+---+-+---++-+++-+-+++++++----

Isolation, sampling and environmental information

isolation

@refsample type
447cow's milk
61767Milk,cow
67770Cow's milk
121885Food, Cow, milk

isolation source categories

Cat1Cat2Cat3
#Host#Mammals#Bovinae (Cow, Cattle)
#Host Body Product#Fluids#Milk

Safety information

risk assessment

@refbiosafety levelbiosafety level comment
4472Risk group (German classification)
1218852Risk group (French classification)

Sequence information

Genome sequences

@refdescriptionaccessionassembly leveldatabaseNCBI tax ID
66792Klebsiella pneumoniae ATCC 4352GCA_010374885scaffoldncbi573
66792Klebsiella pneumoniae strain ATCC 4352573.30826wgspatric573

Genome-based predictions

predictions

traitpredictionconfidencetraining_data
spore-formingno100no
motileno84.049no
flagellatedno94.05no
gram-positiveno97.426no
anaerobicno97.434yes
aerobicyes87.231no
halophileno89.06no
spore-formingno93.92no
glucose-utilyes94.832no
thermophileno99.659yes
glucose-fermentyes91.166no

External links

@ref: 447

culture collection no.: CCUG 58866, DSM 789, ATCC 4352, NCIB 10341, WDCM 00192, JCM 20348, CIP 104216, IAM 12015, IFO 13277, NBRC 13277, NCIMB 10341, CECT 8453, NCTC 13635

straininfo link

  • @ref: 74465
  • straininfo: 125696

literature

topicPubmed-IDtitleauthorsjournalDOIyearmeshtopic2
Phylogeny4553806Corrected identification of a test organism (ATCC 4352) previously thought to be Escherichia coli.Brown CP, Wilson FHAppl Microbiol10.1128/am.23.3.661-661.19721972Bacteriological Techniques, Escherichia coli/*classification, Klebsiella/*classification, Klebsiella pneumoniae/classification
Pathogenicity10918953Synthesis and antimicrobial activity of 4-carbethoxymethyl-2-[(alpha-haloacyl)amino] thiazoles and 5-nonsubstituted/substituted 2-[(4-carbethoxymethylthiazol-2-yl)imino]-4-thiazolidinones.Ates O, Altintas H, Otuk GArzneimittelforschung10.1055/s-0031-13002512000Anti-Bacterial Agents, Anti-Infective Agents/*chemical synthesis/pharmacology, Antitubercular Agents/chemical synthesis/pharmacology, Bacteria/drug effects, Candida/drug effects, Magnetic Resonance Spectroscopy, Microbial Sensitivity Tests, Mycobacterium tuberculosis/drug effects, Structure-Activity Relationship, Thiazoles/*chemical synthesis/pharmacology
Pathogenicity11268772Synthesis of Mannich bases of some 2,5-disubstituted 4-thiazolidinones and evaluation of their antimicrobial activities.Kocabalkanli A, Ates O, Otuk GArch Pharm (Weinheim)10.1002/1521-4184(200102)334:2<35::aid-ardp35>3.0.co;2-42001Anti-Bacterial Agents/*chemical synthesis/chemistry/pharmacology, Antifungal Agents/chemical synthesis/chemistry/pharmacology, Gram-Negative Bacteria/drug effects, Gram-Positive Bacteria/drug effects, Mannich Bases/*chemical synthesis/chemistry/pharmacology, Microbial Sensitivity Tests, Structure-Activity Relationship, Thiazoles/*chemical synthesis/chemistry/pharmacology
Pathogenicity11829115Synthesis and antimicrobial activity of some 1,2,4-triazole-3-mercaptoacetic acid derivatives.Ulusoy N, Gursoy A, Otuk GFarmaco10.1016/s0014-827x(01)01128-42001Anti-Bacterial Agents/*chemical synthesis/pharmacology, Bacteria/drug effects/growth & development, Microbial Sensitivity Tests, Mycobacterium tuberculosis/drug effects, Structure-Activity Relationship, Thioglycolates/chemical synthesis/*pharmacology, Triazoles/chemical synthesis/*pharmacology
Pathogenicity11829119Synthesis and evaluation of antibacterial activity of some 2-[[alpha-(4-substituted benzoyloxy)-alpha-phenylacetyl or methylacetyl]amino]-5-(4-methoxyphenyl)- 1,3,4-oxadiazoles.Kocabalkanli A, Ates O, Otuk GFarmaco10.1016/s0014-827x(01)01158-22001Anti-Bacterial Agents, Anti-Infective Agents/*chemical synthesis/pharmacology, Bacteria/drug effects, Fungi/drug effects, Microbial Sensitivity Tests, Oxadiazoles/chemical synthesis/*pharmacology, Structure-Activity Relationship
Pathogenicity12666252Synthesis and antimicrobial activity of [2-[2-(N, N-disubstituted thiocarbamoyl-sulfanyl)-acylamino] thiazol-4-yl]acetic acid ethyl esters.Ates O, Gursoy A, Altintas H, Otuk G, Birteksoz SArch Pharm (Weinheim)10.1002/ardp.2003900022003Anti-Bacterial Agents/*chemical synthesis/chemistry/pharmacology, Antitubercular Agents/*chemical synthesis/chemistry/pharmacology, Microbial Sensitivity Tests, Mycobacterium tuberculosis/*drug effects, Structure-Activity Relationship, Thiazoles/*chemical synthesis/chemistry/pharmacology
Pathogenicity15038463Synthesis of some new 6-methylimidazo[2,1-b]thiazole-5-carbohydrazide derivatives and their antimicrobial activities.Ur F, Cesur N, Birteksoz S, Otuk GArzneimittelforschung10.1055/s-0031-12969472004Anti-Infective Agents/*chemical synthesis/*pharmacology, Bacteria/drug effects, Chemical Phenomena, Chemistry, Physical, Fungi/drug effects, Hydrazines/*chemical synthesis/*pharmacology, Indicators and Reagents, Magnetic Resonance Spectroscopy, Microbial Sensitivity Tests, Spectrometry, Mass, Electrospray Ionization, Spectrophotometry, Ultraviolet, Spectroscopy, Fourier Transform Infrared, Thiazoles/*chemical synthesis/*pharmacology
Pathogenicity16129517Synthesis and antimicrobial activity of some novel derivatives of benzofuran: part 1. Synthesis and antimicrobial activity of (benzofuran-2-yl)(3-phenyl-3-methylcyclobutyl) ketoxime derivatives.Koca M, Servi S, Kirilmis C, Ahmedzade M, Kazaz C, Ozbek B, Otuk GEur J Med Chem10.1016/j.ejmech.2005.07.0042005Anti-Infective Agents/*chemical synthesis/chemistry/*pharmacology, Bacteria/drug effects, Benzofurans/*chemical synthesis/chemistry/*pharmacology, Microbial Sensitivity Tests, Molecular Structure, Oximes/*chemical synthesis/chemistry/*pharmacology, Structure-Activity Relationship
Pathogenicity16618017Synthesis and evaluation of antimicrobial and anticonvulsant activities of some new 3-[2- (5-aryl-1,3,4-oxadiazol-2-yl/4-carbethoxymethylthiazol-2-yl) imino-4-thiazolidinon-5-ylidene]-5-substituted/nonsubstituted 1H-indole-2-ones and investigation of their structure-activity relationships.Altintas H, Ates O, Uyde-Dogan BS, Alp FI, Kaleli D, Ozdemir O, Birteksoz S, Otuk G, Atana D, Uzun MArzneimittelforschung2006Anti-Infective Agents/*chemical synthesis/*pharmacology, Anticonvulsants/*chemical synthesis/*pharmacology, Antifungal Agents/chemical synthesis/pharmacology, Bacteria/drug effects, Fungi/drug effects, Gas Chromatography-Mass Spectrometry, Indicators and Reagents, Indoles/*chemical synthesis/*pharmacology, Magnetic Resonance Spectroscopy, Microbial Sensitivity Tests, Pentylenetetrazole/antagonists & inhibitors, Seizures/chemically induced/prevention & control, Spectrometry, Mass, Electrospray Ionization, Spectrophotometry, Infrared, Spectrophotometry, Ultraviolet, Structure-Activity Relationship, Thiazoles/*chemical synthesis/*pharmacology
18472907Synthesis, Characterization and Antimicrobial Activity of d Metal Complexes of some 2-Substituted-1H-Benzimidazoles.Ulkuseven B, Tavman A, Otuk GMet Based Drugs10.1155/MBD.1999.1631999
Pathogenicity22852470Hydroxyapatites and europium(III) doped hydroxyapatites as a carrier of silver nanoparticles and their antimicrobial activity.Wiglusz RJ, Kedziora A, Lukowiak A, Doroszkiewicz W, Strek WJ Biomed Nanotechnol10.1166/jbn.2012.14242012Anti-Bacterial Agents/administration & dosage/*pharmacology, Drug Carriers/administration & dosage/chemistry/pharmacology, Escherichia coli/drug effects, Europium/administration & dosage/*chemistry, Hydroxyapatites/administration & dosage/*chemistry, Ions/chemistry, Klebsiella pneumoniae/drug effects, Luminescence, Metal Nanoparticles/administration & dosage/*chemistry, Microbial Sensitivity Tests, Microscopy, Electron, Transmission, Nanocomposites/administration & dosage/*chemistry/ultrastructure, Silver/administration & dosage/*chemistry/*pharmacology, Staphylococcus aureus/drug effects, X-Ray Diffraction
Pathogenicity24192397Activity of the antiseptic polyhexanide against gram-negative bacteria.Fabry WH, Kock HJ, Vahlensieck WMicrob Drug Resist10.1089/mdr.2013.01132013Anti-Bacterial Agents/pharmacology, Anti-Infective Agents, Local/*pharmacology, Biguanides/*pharmacology, Ciprofloxacin/pharmacology, Drug Combinations, Escherichia coli/*drug effects/growth & development, Gentamicins/pharmacology, Haemophilus influenzae/*drug effects/growth & development, Klebsiella pneumoniae/*drug effects/growth & development, Microbial Sensitivity Tests, Microbial Viability/drug effects, Moraxella catarrhalis/*drug effects/growth & development, Pseudomonas aeruginosa/*drug effects/growth & development, beta-Lactams/pharmacology
Pathogenicity24377177[Use of the materials based on partially reduced graphene-oxide with silver nanoparticle as bacteriostatic and bactericidal agent].Kedziora A, Gerasymchuk Y, Sroka E, Bugla-Ploskonska G, Doroszkiewicz W, Rybak Z, Hreniak DC, Wilgusz R, Strek WAPolim Med2013Anti-Bacterial Agents/*chemical synthesis/*pharmacology, Escherichia coli/drug effects, Gram-Negative Bacteria/*drug effects, Gram-Positive Bacteria/*drug effects, Graphite/chemistry/*pharmacology, Klebsiella pneumoniae/drug effects, Microbial Sensitivity Tests, Nanocomposites/*chemistry, Nanoparticles, Silver/chemistry/*pharmacology, Staphylococcus aureus/drug effects
Pathogenicity27930849Searching for a potential antibacterial lead structure against bacterial biofilms among new naphthoquinone compounds.Moreira CS, Silva AC, Novais JS, Sa Figueiredo AM, Ferreira VF, da Rocha DR, Castro HCJ Appl Microbiol10.1111/jam.133692017Anti-Bacterial Agents/*pharmacology, Biofilms/*drug effects, Enterobacter cloacae, Enterococcus faecalis/drug effects, Escherichia coli/drug effects, Gram-Positive Bacteria/drug effects, Humans, Klebsiella pneumoniae/drug effects, Methicillin-Resistant Staphylococcus aureus/*drug effects, Microbial Sensitivity Tests, Naphthoquinones/chemistry/*pharmacology, Proteus mirabilis/drug effects, Pseudomonas aeruginosa/drug effects, Staphylococcus/drug effects, Vancomycin
Pathogenicity28004034Klebsiella pneumoniae Planktonic and Biofilm Reduction by Different Plant Extracts: In Vitro Study.Paula-Ramos L, da Rocha Santos CE, Camargo Reis Mello D, Nishiama Theodoro L, De Oliveira FE, Back Brito GN, Junqueira JC, Jorge AOC, de Oliveira LDScientificWorldJournal10.1155/2016/35214132016Amaranthaceae/chemistry, Anti-Bacterial Agents/*pharmacology, *Biofilms, Juglans/chemistry, Klebsiella pneumoniae/*drug effects/growth & development, Microbial Sensitivity Tests, Plant Extracts/*pharmacology, Rosmarinus/chemistry
Pathogenicity28671568Antibacterial Activities of Pyrenylated Coumarins from the Roots of Prangos hulusii.Tan N, Yazici-Tutunis S, Bilgin M, Tan E, Miski MMolecules10.3390/molecules220710982017Anti-Bacterial Agents/*chemistry/pharmacology, Bacillus subtilis/drug effects, Coumarins/chemistry/pharmacology, Gram-Negative Bacteria/*drug effects, Klebsiella pneumoniae/drug effects, Methylene Chloride/chemistry/pharmacology, Microbial Sensitivity Tests, Molecular Structure, Plant Extracts/*chemistry/pharmacology, Plant Roots/*chemistry
Pathogenicity29202138Effects and time-kill assessment of amoxicillin used in combination with chloramphenicol against bacteria of clinical importance.Olajuyigbe OO, Coopoosamy RM, Afolayan AJActa Biochim Pol10.18388/abp.2016_14952017Amoxicillin/*pharmacology, Anti-Bacterial Agents/*pharmacology, Bacteria/*drug effects/isolation & purification, Chloramphenicol/*pharmacology, Drug Resistance, Bacterial/drug effects, Drug Synergism, Microbial Sensitivity Tests, Time FactorsEnzymology
Pathogenicity29550501Antibacterial naphthoquinone derivatives targeting resistant strain Gram-negative bacteria in biofilms.Novais JS, Moreira CS, Silva ACJA, Loureiro RS, Sa Figueiredo AM, Ferreira VF, Castro HC, da Rocha DRMicrob Pathog10.1016/j.micpath.2018.03.0242018Anti-Bacterial Agents/chemical synthesis/chemistry/*pharmacology/toxicity, Biofilms/*drug effects, Ciprofloxacin/pharmacology, Erythrocytes/drug effects, Gram-Negative Bacteria/*drug effects, Gram-Positive Bacteria/drug effects, Humans, Materials Testing, Microbial Sensitivity Tests, Naphthoquinones/chemical synthesis/chemistry/*pharmacology/toxicity
Pathogenicity31820692Efficient Synthesis and Antibacterial Profile of Bis(2-hydroxynaphthalene- 1,4-dione).Novais JS, Rosandiski AC, de Carvalho CM, de Saules Silva LS, Dos S Velasco de Souza LC, Santana MV, Martins NRC, Castro HC, Ferreira VF, Gonzaga DTG, de Resende GO, de C da Silva FCurr Top Med Chem10.2174/15680266196661912101603422020Anti-Bacterial Agents/*chemical synthesis/chemistry/*pharmacology, Dose-Response Relationship, Drug, Gram-Negative Bacteria/*drug effects, Gram-Positive Bacteria/*drug effects, Humans, Microbial Sensitivity Tests, Molecular Structure, Naphthols/*chemical synthesis/chemistry/*pharmacology, Structure-Activity Relationship
35267830Sustainable Antibacterial and Antiviral High-Performance Copper-Coated Filter Produced via Ion Beam Treatment.Jung S, Yang JY, Jang D, Kim T, Baek KH, Yoon H, Park JY, Kim SK, Hong J, Ryoo S, Jang HW, Lee SPolymers (Basel)10.3390/polym140510072022

Reference

@idauthorscataloguedoi/urltitle
447Curators of the DSMZLeibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSM 789)https://www.dsmz.de/collection/catalogue/details/culture/DSM-789
20215Parte, A.C., Sardà Carbasse, J., Meier-Kolthoff, J.P., Reimer, L.C. and Göker, M.10.1099/ijsem.0.004332List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ
41831Curators of the CIPhttps://brclims.pasteur.fr/brcWeb/souche/detail/1/16100
61767Curators of the CCUGCulture Collection University of Gothenburg (CCUG) (CCUG 58866)https://www.ccug.se/strain?id=58866
66792Julia Koblitz, Joaquim Sardà, Lorenz Christian Reimer, Boyke Bunk, Jörg Overmannhttps://diaspora-project.de/progress.html#genomesAutomatically annotated for the DiASPora project (Digital Approaches for the Synthesis of Poorly Accessible Biodiversity Information)
67770Curators of the JCMhttps://jcm.brc.riken.jp/en/
68368Automatically annotated from API 20E
68374Automatically annotated from API ID32E
68382Automatically annotated from API zym
69480Julia Koblitz, Joaquim Sardà, Lorenz Christian Reimer, Boyke Bunk, Jörg Overmannhttps://diaspora-project.de/progress.html#genomesPredictions based on genome sequence made in the Diaspora project (Digital Approaches for the Synthesis of Poorly Accessible Biodiversity Information)
69481Xiao-Yin To, René Mreches, Martin Binder, Alice C. McHardy, Philipp C. Münch10.21203/rs.3.rs-2527258/v1Predictions based on the model GenomeNet Sporulation v. 1
74465Reimer, L.C., Lissin, A.,Schober, I., Witte,J.F., Podstawka, A., Lüken, H., Bunk, B.,Overmann, J.10.60712/SI-ID125696.1StrainInfo: A central database for resolving microbial strain identifiers
121885Curators of the CIPCollection of Institut Pasteur (CIP 104216)https://catalogue-crbip.pasteur.fr/fiche_catalogue.xhtml?crbip=CIP%20104216