Corynebacterium urealyticum (DSM 7110, ATCC 43043, Bajo)

Name: Corynebacterium urealyticum (DSM 7110, ATCC 43043, Bajo)
Creator: BacDive
License: http://creativecommons.org/licenses/by/4.0/

BacDive ID 3149

Type strain

Strain Designation Bajo

Culture col. no. DSM 7110 ATCC 43043 Bajo CIP 103425

NCBI tax ID(s) 43771

Special Collections DSMZ CIP

Links

Corynebacterium urealyticum Bajo is an obligate aerobe, mesophilic, Gram-positive human pathogen that was isolated from urine.

Gram-positive rod-shaped obligate aerobe mesophilic human pathogen genome sequence

Name and taxonomic classification

SI-ID 41613

ATCC 43043,CIP 103425,DSM 7110,CECT 4143

@ref 20215

Last LPSN update 2025-12-16 09:47:29

Domain Bacillati

Phylum Actinomycetota

Class Actinomycetes

Order Mycobacteriales

Family Corynebacteriaceae

Genus Corynebacterium

Species Corynebacterium urealyticum

Full scientific name Corynebacterium urealyticum Pitcher et al. 1992

BacDive ID	Other strains from **Corynebacterium urealyticum** (43)	Type strain
3148	C. urealyticum Armendariz, 1, DSM 7109, ATCC 43042, NCTC ... (type strain)
3150	C. urealyticum Garcia, DSM 7111, ATCC 43044, CCUG 18159
134904	C. urealyticum 721.86, CIP 102730
135000	C. urealyticum 105.87, CIP 102843
135241	C. urealyticum A21397, CIP 103276
136070	C. urealyticum 266-85, CIP 102292
136094	C. urealyticum 448-86, CIP 102444
137638	C. urealyticum 195-87, CIP 102949
137819	C. urealyticum 386.84, CIP 100873
137860	C. urealyticum 823.85, CIP 101943
137961	C. urealyticum 269-86, CIP 102316
137963	C. urealyticum 298-86, CIP 102319
137984	C. urealyticum CIP 102375
138002	C. urealyticum 457-86, CIP 102449
138003	C. urealyticum 455-86, CIP 102450
138004	C. urealyticum 459-86, CIP 102451
138605	C. urealyticum 486-86, CIP 102488
138760	C. urealyticum 131.87, CIP 102875
139205	C. urealyticum 493.85, CIP 101698
139593	C. urealyticum 136.87, CIP 102879
143107	C. urealyticum CCUG 17231
143123	C. urealyticum CCUG 17286
143227	C. urealyticum CCUG 17882
143333	C. urealyticum CCUG 18441
143386	C. urealyticum CCUG 18829
143636	C. urealyticum CCUG 20684
143659	C. urealyticum CCUG 20855
144969	C. urealyticum CCUG 27323
145011	C. urealyticum CCUG 27400 A
146987	C. urealyticum CCUG 32602
147007	C. urealyticum CCUG 32635
147463	C. urealyticum CCUG 33614
147717	C. urealyticum CCUG 34075
147718	C. urealyticum CCUG 34076
148170	C. urealyticum CCUG 34966
148212	C. urealyticum CCUG 35044
148223	C. urealyticum CCUG 35067
148569	C. urealyticum CCUG 35650
149423	C. urealyticum CCUG 37702
151852	C. urealyticum CCUG 45051
151948	C. urealyticum CCUG 45302
152685	C. urealyticum CCUG 47356
156105	C. urealyticum CCUG 60386

Morphology

Cell morphology

@ref	Gram stain	Cell shape
123740	positive	rod-shaped
125439	positive
125439
125438
125438	positive

Colony morphology

Culture and growth conditions

Culture medium

@ref	Name	Medium link	Composition
2987	TRYPTICASE SOY YEAST EXTRACT MEDIUM (DSMZ Medium 92)	Medium recipe at MediaDive	Name: TRYPTICASE SOY YEAST EXTRACT MEDIUM (DSMZ Medium 92; with strain-specific modifications) Composition: Trypticase soy broth 30.0 g/l Agar 15.0 g/l Yeast extract 3.0 g/l Tween 80 2.0 g/l Distilled water
41345	MEDIUM 72- for trypto casein soja agar		Distilled water make up to (1000.000 ml);Trypto casein soy agar (40.000 g)
123740	CIP Medium 72	Medium recipe at CIP

Culture temp

@ref	Growth	Type	Temperature (°C)	Range
2987	positive	growth	37	mesophilic
41345	positive	growth	37	mesophilic
123740	positive	growth	25-41
123740	negative	growth	10
123740	negative	growth	15
123740	negative	growth	45

Physiology and metabolism

Oxygen tolerance

@ref	Oxygen tolerance
123740	obligate aerobe
125439	microaerophile

Halophily

@ref	Salt	Growth	Tested relation	Concentration
123740	NaCl	positive	growth	0-4 %
123740	NaCl		growth	6 %
123740	NaCl		growth	8 %
123740	NaCl		growth	10 %

Murein

@ref	Murein short key	Type
2987	A31	A1gamma m-Dpm-direct

Metabolite utilization

@ref	Chebi-ID	Metabolite	Utilization activity	Kind of utilization tested
68371	27613 ChEBI	amygdalin	-	builds acid from	from API 50CH acid
68371	18305 ChEBI	arbutin	-	builds acid from	from API 50CH acid
68371	17057 ChEBI	cellobiose	-	builds acid from	from API 50CH acid
123740	16947 ChEBI	citrate	-	carbon source
68371	17108 ChEBI	D-arabinose	-	builds acid from	from API 50CH acid
68371	18333 ChEBI	D-arabitol	-	builds acid from	from API 50CH acid
68371	15824 ChEBI	D-fructose	-	builds acid from	from API 50CH acid
68371	28847 ChEBI	D-fucose	-	builds acid from	from API 50CH acid
68371	12936 ChEBI	D-galactose	-	builds acid from	from API 50CH acid
68371	17634 ChEBI	D-glucose	-	builds acid from	from API 50CH acid
68371	62318 ChEBI	D-lyxose	-	builds acid from	from API 50CH acid
68371	16899 ChEBI	D-mannitol	-	builds acid from	from API 50CH acid
68371	16024 ChEBI	D-mannose	-	builds acid from	from API 50CH acid
68371	16988 ChEBI	D-ribose	-	builds acid from	from API 50CH acid
68371	17924 ChEBI	D-sorbitol	-	builds acid from	from API 50CH acid
68371	16443 ChEBI	D-tagatose	-	builds acid from	from API 50CH acid
68371	65327 ChEBI	D-xylose	-	builds acid from	from API 50CH acid
68371	17113 ChEBI	erythritol	-	builds acid from	from API 50CH acid
123740	4853 ChEBI	esculin	-	hydrolysis
68371	4853 ChEBI	esculin	-	builds acid from	from API 50CH acid
68371	16813 ChEBI	galactitol	-	builds acid from	from API 50CH acid
68371	28066 ChEBI	gentiobiose	-	builds acid from	from API 50CH acid
68371	24265 ChEBI	gluconate	-	builds acid from	from API 50CH acid
68371	17754 ChEBI	glycerol	-	builds acid from	from API 50CH acid
68371	28087 ChEBI	glycogen	-	builds acid from	from API 50CH acid
123740	606565 ChEBI	hippurate	+	hydrolysis
68371	15443 ChEBI	inulin	-	builds acid from	from API 50CH acid
68371	30849 ChEBI	L-arabinose	-	builds acid from	from API 50CH acid
68371	18403 ChEBI	L-arabitol	-	builds acid from	from API 50CH acid
68371	18287 ChEBI	L-fucose	-	builds acid from	from API 50CH acid
68371	62345 ChEBI	L-rhamnose	-	builds acid from	from API 50CH acid
68371	17266 ChEBI	L-sorbose	-	builds acid from	from API 50CH acid
68371	65328 ChEBI	L-xylose	-	builds acid from	from API 50CH acid
68371	17716 ChEBI	lactose	-	builds acid from	from API 50CH acid
68371	17306 ChEBI	maltose	-	builds acid from	from API 50CH acid
68371	6731 ChEBI	melezitose	-	builds acid from	from API 50CH acid
68371	28053 ChEBI	melibiose	-	builds acid from	from API 50CH acid
68371	320061 ChEBI	methyl alpha-D-glucopyranoside	-	builds acid from	from API 50CH acid
68371	43943 ChEBI	methyl alpha-D-mannoside	-	builds acid from	from API 50CH acid
68371	74863 ChEBI	methyl beta-D-xylopyranoside	-	builds acid from	from API 50CH acid
68371	17268 ChEBI	myo-inositol	-	builds acid from	from API 50CH acid
68371	59640 ChEBI	N-acetylglucosamine	-	builds acid from	from API 50CH acid
123740	17632 ChEBI	nitrate	-	reduction
123740	17632 ChEBI	nitrate	-	respiration
123740	16301 ChEBI	nitrite	-	reduction
68371		Potassium 2-ketogluconate	-	builds acid from	from API 50CH acid
68371		Potassium 5-ketogluconate	-	builds acid from	from API 50CH acid
68371	16634 ChEBI	raffinose	-	builds acid from	from API 50CH acid
68371	15963 ChEBI	ribitol	-	builds acid from	from API 50CH acid
68371	17814 ChEBI	salicin	-	builds acid from	from API 50CH acid
68371	28017 ChEBI	starch	-	builds acid from	from API 50CH acid
68371	17992 ChEBI	sucrose	-	builds acid from	from API 50CH acid
68371	27082 ChEBI	trehalose	-	builds acid from	from API 50CH acid
68371	32528 ChEBI	turanose	-	builds acid from	from API 50CH acid
68371	17151 ChEBI	xylitol	-	builds acid from	from API 50CH acid

Antibiotic resistance

@ref	Metabolite	Is antibiotic	Is sensitive	Is resistant
123740	0129 (2,4-Diamino-6,7-di-iso-propylpteridine phosphate)

Metabolite production

@ref	Chebi-ID	Metabolite	Production
123740	35581 ChEBI	indole

Metabolite tests

@ref	Chebi-ID	Metabolite	Voges-proskauer-test
123740	15688 ChEBI	acetoin	-
123740	17234 ChEBI	glucose

Enzymes

@ref	Value	Activity	Ec
68382	acid phosphatase	-	3.1.3.2	from API zym
123740	alcohol dehydrogenase	-	1.1.1.1
68382	alkaline phosphatase	-	3.1.3.1	from API zym
68382	alpha-chymotrypsin	-	3.4.21.1	from API zym
68382	alpha-fucosidase	-	3.2.1.51	from API zym
68382	alpha-galactosidase	-	3.2.1.22	from API zym
68382	alpha-glucosidase	-	3.2.1.20	from API zym
68382	alpha-mannosidase	-	3.2.1.24	from API zym
123740	amylase	-
123740	beta-galactosidase	-	3.2.1.23
68382	beta-galactosidase	-	3.2.1.23	from API zym
68382	beta-glucosidase	-	3.2.1.21	from API zym
68382	beta-glucuronidase	-	3.2.1.31	from API zym
123740	caseinase	-	3.4.21.50
123740	catalase	+	1.11.1.6
68382	cystine arylamidase	-	3.4.11.3	from API zym
123740	DNase	-
68382	esterase (C 4)	+		from API zym
68382	esterase lipase (C 8)	+		from API zym
123740	gamma-glutamyltransferase	-	2.3.2.2
123740	gelatinase	-
123740	lecithinase	-
68382	leucine arylamidase	-	3.4.11.1	from API zym
123740	lipase	-
68382	lipase (C 14)	+		from API zym
123740	lysine decarboxylase	-	4.1.1.18
68382	N-acetyl-beta-glucosaminidase	-	3.2.1.52	from API zym
68382	naphthol-AS-BI-phosphohydrolase	+		from API zym
123740	ornithine decarboxylase	-	4.1.1.17
123740	oxidase	-
123740	phenylalanine ammonia-lyase	-	4.3.1.24
123740	protease	-
68382	trypsin	-	3.4.21.4	from API zym
123740	tryptophan deaminase	-
123740	tween esterase	+
123740	urease	+	3.5.1.5
68382	valine arylamidase	-		from API zym

API zym

@ref	Control	Alkaline phosphatase	Esterase (C 4)	2-naphtyl caprylateEsterase Lipase (C 8)	Lipase (C 14)	L-leucyl-2-naphthylamideLeucine arylamidase	L-valyl-2-naphthylamideValine arylamidase	L-cystyl-2-naphthylamideCystine arylamidase	Trypsin	alpha- Chymotrypsin	Acid phosphatase	Naphthol-AS-BI-phosphateNaphthol-AS-BI-phosphohydrolase	alpha- Galactosidase	beta- Galactosidase	beta- Glucuronidase	alpha- Glucosidase	beta- Glucosidase	N-acetyl-beta- glucosaminidase	alpha- Mannosidase	alpha- Fucosidase
123740	-	-	+	+	+	-	-	-	-	-	-	+	-	-	-	-	-	-	-	-

API 50CHac

@ref	ControlQ	GLY	ERY	DARA	LARA	RIB	DXYL	LXYL	ADO	MDX	GAL	GLU	FRU	MNE	SBE	RHA	DUL	INO	MAN	SOR	MDM	MDG	NAG	AMY	ARB	ESC	SAL	CEL	MAL	LAC	MEL	SAC	TRE	INU	MLZ	RAF	AMD	GLYG	XLT	GEN	TUR	LYX	TAG	DFUC	LFUC	DARL	LARL	GNT	2KG	5KG
123740	not determinedn.d.	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-

API biotype100

@ref	ControlQ	D-glucose as carbon sourceGLU	D-fructose as carbon sourceFRU	D-galactose as carbon sourceGAL	D-trehalose as carbon sourceTRE	D-mannose as carbon sourceMNE	L-sorbose as carbon sourceSBE	D-melibiose as carbon sourceMEL	sucrose as carbon sourceSAC	D-raffinose as carbon sourceRAF	maltotriose as carbon sourceMTE	maltose as carbon sourceMAL	lactose as carbon sourceLAC	lactulose as carbon sourceLTE	1-O-methyl-beta-galactopyranoside as carbon sourceMbGa	1-O-methyl-alpha-galactopyranoside as carbon sourceMaGa	D-cellobiose as carbon sourceCEL	gentiobiose as carbon sourceGEN	1-O-methyl-beta-D-glucopyranoside as carbon sourceMbGu	esculin as carbon sourceESC	D-ribose as carbon sourceRIB	L-arabinose as carbon sourceARA	D-xylose as carbon sourceXYL	palatinose as carbon sourcePLE	L-rhamnose as carbon sourceRHA	L-fucose as carbon sourceFUC	D-melezitose as carbon sourceMLZ	D-arabitol as carbon sourceDARL	L-arabitol as carbon sourceLARL	xylitol as carbon sourceXLT	dulcitol as carbon sourceDUL	D-tagatose as carbon sourceTAG	glycerol as carbon sourceGLY	myo-inositol as carbon sourceINO	D-mannitol as carbon sourceMAN	maltitol as carbon sourceMTL	D-turanose as carbon sourceTUR	D-sorbitol as carbon sourceSOR	adonitol as carbon sourceADO	hydroxyquinoline-beta-glucuronide as carbon sourceHBG	D-lyxose as carbon sourceLYX	i-erythritol as carbon sourceERY	1-O-methyl-alpha-D-glucoside as carbon sourceMDG	3-O-methyl-D-glucose as carbon source3MDG	D-saccharate as carbon sourceSAT	mucate as carbon sourceMUC	L-tartrate as carbon sourceLTAT	D-tartrate as carbon sourceDTAT	meso-tartrate as carbon sourceMTAT	D-malate as carbon sourceDMLT	L-malate as carbon sourceLMLT	cis-aconitate as carbon sourceCATE	trans-aconitate as carbon sourceTATE	tricarballylate as carbon sourceTTE	citrate as carbon sourceCIT	D-glucuronate as carbon sourceGRT	D-galacturonate as carbon sourceGAT	2-ketogluconate as carbon source2KG	5-ketogluconate as carbon source5KG	tryptophan as carbon sourceTRY	N-acetyl-D-glucosamine as carbon sourceNAG	D-gluconate as carbon sourceGNT	phenylacetate as carbon sourcePAC	protocatechuate as carbon sourcePAT	4-hydroxybenzoate as carbon sourcepOBE	quinate as carbon sourceQAT	gentisate as carbon sourceGTE	3-hydroxybenzoate as carbon sourcemOBE	benzoate as carbon sourceBAT	3-phenylpropionate as carbon sourcePPAT	m-coumarate as carbon sourceCMT	trigonelline as carbon sourceTGE	betaine as carbon sourceBET	putrescine as carbon sourcePCE	4-aminobutyrate as carbon sourceABT	histamine as carbon sourceHIN	DL-lactate as carbon sourceLAT	caprate as carbon sourceCAP	caprylate as carbon sourceCYT	L-histidine as carbon sourceHIS	succinate as carbon sourceSUC	fumarate as carbon sourceFUM	glutarate as carbon sourceGRE	DL-glycerate as carbon sourceGYT	5-aminovalerate as carbon sourceAVT	ethanolamine as carbon sourceETN	tryptamine as carbon sourceTTN	D-glucosamine as carbon sourceGLN	itaconate as carbon sourceITA	3-hydroxybutyrate as carbon source3OBU	L-aspartate as carbon sourceAPT	L-glutamate as carbon sourceGTT	L-proline as carbon sourcePRO	D-alanine as carbon sourceDALA	L-alanine as carbon sourceLALA	L-serine as carbon sourceSER	malonate as carbon sourceMNT	propionate as carbon sourcePROP	L-tyrosine as carbon sourceTYR	2-ketoglutarate as carbon source2KT
123740	not determinedn.d.	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-

Isolation, sampling and environmental information

Isolation source categories

Cat1	Cat2	Cat3
#Host Body Product	#Fluids	#Urine

Isolation

@ref	Sample type
2987	urine
123740	Human, Urine

Interaction and safety

Risk assessment

@ref	Pathogenicity human	Pathogenicity animal	Biosafety level	Biosafety level comment
2987			2	Risk group (German classification) According to TRBA 466
123740			2	Risk group (French classification) According to TRBA 466

Sequence information

Genome sequences

@ref	Description	Assembly level	INSDC accession	BV-BRC accession	NCBI tax ID	Score
124043	ASM1640326v1 assembly for Corynebacterium urealyticum FDAARGOS_995	chromosome	GCA_016403265	43771.88	43771	86.11

Genome browser: GCA_016403265

Genome-based predictions

Predictions

Predictions from Deep Learning for Genome Sequence Data. R package version 0.3.1 based on: Corynebacterium urealyticum strain FDAARGOS_995
PATRIC: 43771.88

@ref	Trait	Model	Prediction	Confidence in %	In training data
125439	spore_formation	BacteriaNetⓘ	no	84.10	no
125439	motility	BacteriaNetⓘ	no	95.50	no
125439	gram_stain	BacteriaNetⓘ	positive	95.30	no
125439	oxygen_tolerance	BacteriaNetⓘ	microaerophile	90.60	no

Predictions from bacterial phenotypic traits through improved machine learning using high-quality, curated datasets based on: Corynebacterium urealyticum strain FDAARGOS_995 strain Not applicable
PATRIC: 43771.88

@ref	Trait	Model	Prediction	Confidence in %	In training data
125438	gram-positive	gram-positiveⓘ	yes	91.13	no
125438	anaerobic	anaerobicⓘ	no	94.00	yes
125438	spore-forming	spore-formingⓘ	no	80.79	no
125438	aerobic	aerobicⓘ	yes	59.78	yes
125438	thermophilic	thermophileⓘ	no	94.50	yes
125438	flagellated	motile2+ⓘ	no	92.00	no

Literature

Title	Authors	Journal	DOI	Year
Is the sequence-specific binding of aminoacyl-tRNAs by EF-Tu universal among bacteria?	Schrader JM, Uhlenbeck OC.	Nucleic Acids Res	10.1093/nar/gkr641	2011
Preliminary in Vitro Studies on Corynebacterium urealyticum Pathogenetic Mechanisms, a Possible Candidate for Chronic Idiopathic Prostatitis?	Nicolosi D, Genovese C, Cutuli MA, D'Angeli F, Pietrangelo L, Davinelli S, Petronio Petronio G, Di Marco R.	Microorganisms	10.3390/microorganisms8040463	2020
Exploration of the role of the penicillin binding protein 2c (Pbp2c) in inducible beta-lactam resistance in Corynebacteriaceae.	Lavollay M, Buon C, Le Moigne V, Compain F, Guyonvarch A, Fonvielle M.	Front Microbiol	10.3389/fmicb.2024.1327723	2024
Expression of Genes for a Flavin Adenine Dinucleotide-Binding Oxidoreductase and a Methyltransferase from Mycobacterium chlorophenolicum Is Necessary for Biosynthesis of 10-Methyl Stearic Acid from Oleic Acid in Escherichia coli.	Machida S, Bakku RK, Suzuki I.	Front Microbiol	10.3389/fmicb.2017.02061	2017
Influence of external factors in resistance of Corynebacterium urealyticum to antimicrobial agents.	Garcia-Bravo M, Aguado JM, Morales JM, Noriega AR.	Antimicrob Agents Chemother	10.1128/aac.40.2.497	1996
Molecular Assay for Detection of Genetic Markers Associated with Decreased Susceptibility to Cephalosporins in Neisseria gonorrhoeae.	Peterson SW, Martin I, Demczuk W, Bharat A, Hoang L, Wylie J, Allen V, Lefebvre B, Tyrrell G, Horsman G, Haldane D, Garceau R, Wong T, Mulvey MR.	J Clin Microbiol	10.1128/jcm.00493-15	2015
Identification of clinical coryneform bacterial isolates: comparison of biochemical methods and sequence analysis of 16S rRNA and rpoB genes.	Adderson EE, Boudreaux JW, Cummings JR, Pounds S, Wilson DA, Procop GW, Hayden RT.	J Clin Microbiol	10.1128/jcm.01849-07	2008
Comparative in vitro activities of new quinolones against coryneform bacteria.	Martinez-Martinez L, Suarez AI, Ortega MC, Perea EJ.	Antimicrob Agents Chemother	10.1128/aac.38.6.1439	1994
Comparison of E-test with broth microdilution and disk diffusion for susceptibility testing of coryneform bacteria.	Martinez-Martinez L, Ortega MC, Suarez AI.	J Clin Microbiol	10.1128/jcm.33.5.1318-1321.1995	1995
In vitro activity of 79 antimicrobial agents against Corynebacterium group D2.	Garcia-Rodriguez JA, Garcia Sanchez JE, Munoz Bellido JL, Nebreda Mayoral T, Garcia Sanchez E, Garcia Garcia I.	Antimicrob Agents Chemother	10.1128/aac.35.10.2140	1991
Evaluation of API Coryne system for identifying coryneform bacteria.	Soto A, Zapardiel J, Soriano F.	J Clin Pathol	10.1136/jcp.47.8.756	1994
High-performance liquid chromatography of corynomycolic acids as a tool in identification of Corynebacterium species and related organisms.	De Briel D, Couderc F, Riegel P, Jehl F, Minck R.	J Clin Microbiol	10.1128/jcm.30.6.1407-1417.1992	1992

References

#2987	Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 7110
#20215	Parte, A.C., Sardà Carbasse, J., Meier-Kolthoff, J.P., Reimer, L.C. and Göker, M.: List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ. IJSEM ( DOI 10.1099/ijsem.0.004332 )
#41345	; Curators of the CIP;
#68371	Automatically annotated from API 50CH acid .
#68382	Automatically annotated from API zym .
#123740	Collection of Institut Pasteur ; Curators of the CIP; CIP 103425
#124043	Isabel Schober, Julia Koblitz: Data extracted from sequence databases, automatically matched based on designation and taxonomy .
#125438	Julia Koblitz, Lorenz Christian Reimer, Rüdiger Pukall, Jörg Overmann: Predicting bacterial phenotypic traits through improved machine learning using high-quality, curated datasets. 2024 ( DOI 10.1101/2024.08.12.607695 )
#125439	Philipp Münch, René Mreches, Martin Binder, Hüseyin Anil Gündüz, Xiao-Yin To, Alice McHardy: deepG: Deep Learning for Genome Sequence Data. R package version 0.3.1 .
#126262	A. Lissin, I. Schober, J. F. Witte, H. Lüken, A. Podstawka, J. Koblitz, B. Bunk, P. Dawyndt, P. Vandamme, P. de Vos, J. Overmann, L. C. Reimer: StrainInfo—the central database for linked microbial strain identifiers. ( DOI 10.1093/database/baaf059 )

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Corynebacterium urealyticum (DSM 7110, ATCC 43043, Bajo)

Name and taxonomic classification

Morphology

Cell morphology

Colony morphology

Culture and growth conditions

Culture medium

Culture temp

Physiology and metabolism

Oxygen tolerance

Halophily

Murein

Metabolite utilization

Antibiotic resistance

Metabolite production

Metabolite tests

Enzymes

API zym

API 50CHac

API biotype100

Isolation, sampling and environmental information

Isolation source categories

Isolation

Interaction and safety

Risk assessment

Sequence information

Genome sequences

Genome browser: GCA_016403265

Genome-based predictions

Predictions

Literature

Literature

References

BacDive

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