Proteus mirabilis (DSM 788, ATCC 14153, IMET 11232)

Name: Proteus mirabilis (DSM 788, ATCC 14153, IMET 11232)
Creator: BacDive
License: http://creativecommons.org/licenses/by/4.0/

BacDive ID 5057

Type strain

Culture col. no. DSM 788 ATCC 14153 IMET 11232 CCUG 32232 PCI 765 3 more

NCBI tax ID(s) 584

Special Collections DSMZ CCUG CIP JMRC

History DSMZ <- ATCC; ATCC 14153 <- U.S. Food and Drug Administration (FDA), Washington, D.C., USA; PCI 765 CIP <- 1994, ATCC <- FDA: strain PCI 765

Links

Proteus mirabilis DSM 788 is an aerobe, Gram-negative, motile human pathogen of the family Morganellaceae.

Gram-negative motile rod-shaped aerobe human pathogen 16S sequence Bacteria

Name and taxonomic classification

SI-ID 92372

LMG 9077,ATCC 14153,NCIMB 12596,CIP 104032,CCUG 32232,IMET 11232,CECT 4101,VTT E-85229,NCAIM B.02038,CNCTC 6566,DSM 788

@ref 20215

Last LPSN update 2026-05-29 08:26:04

Domain Bacteria

Phylum Pseudomonadota

Class Gammaproteobacteria

Order Enterobacterales

Family Morganellaceae

Genus Proteus

Species Proteus mirabilis

Full scientific name Proteus mirabilis Hauser 1885 (Approved Lists 1980)

BacDive ID	Other strains from **Proteus mirabilis** (52)	Type strain
5058	P. mirabilis PR 14, DSM 4479, ATCC 29906, CIP 103181, ... (type strain)
5059	P. mirabilis LRA 080173, LRA 008 01 73, DSM 6674, ATCC ...
5060	P. mirabilis D1, DSM 18254, ATCC 12453, CCUG 34293
5061	P. mirabilis D 799, DSM 30115, ATCC 9240
5062	P. mirabilis WS 10039, DSM 30116
5063	P. mirabilis BL 47, DSM 46227, IMET 10762, SG 654
5064	P. mirabilis DSM 50903, ATCC 15363, ICPB 2575
130994	P. mirabilis CD1-T1542, DSM 28629
131878	P. mirabilis PGVI, DSM 102257
131879	P. mirabilis PG 400, DSM 102258
134505	P. mirabilis CF 09, CIP 105872
134641	P. mirabilis 89-Hb, CIP 107283
135785	P. mirabilis O, CIP A233
135941	P. mirabilis B-0087, CIP 107052
136530	P. mirabilis PM1, CIP 106474
138072	P. mirabilis CIP 104588, Ip R1
138172	P. mirabilis CF 1709, CIP 105104
138505	P. mirabilis SS, CIP 75.15
139060	P. mirabilis CIP A235
139103	P. mirabilis AP 3, CIP 103800
139220	P. mirabilis 74.87, CIP 102817
139221	P. mirabilis 73.87, CIP 102818
141192	P. mirabilis CCUG 138
141666	P. mirabilis CCUG 4637
141668	P. mirabilis CCUG 4640, CCUG 18993
141669	P. mirabilis CCUG 4641
141670	P. mirabilis CCUG 4642, CCUG 18994
141672	P. mirabilis CCUG 4644, CCUG 18996
141673	P. mirabilis CCUG 4645
141674	P. mirabilis CCUG 4646, CCUG 18999
141676	P. mirabilis CCUG 4648
141677	P. mirabilis CCUG 4649, CCUG 19005
143412	P. mirabilis CCUG 19004
143413	P. mirabilis CCUG 19011
143414	P. mirabilis CCUG 19016
144509	P. mirabilis CCUG 25418
145699	P. mirabilis CCUG 29299
147545	P. mirabilis CCUG 33773, ATCC 29245
147577	P. mirabilis CCUG 33828
147821	P. mirabilis CCUG 34294, NCDC 2059-70, ATCC 25933
149015	P. mirabilis CCUG 36728
149086	P. mirabilis CCUG 36839
150125	P. mirabilis CCUG 39049
150288	P. mirabilis CCUG 39506, ATCC 7002
151282	P. mirabilis CCUG 43605
153329	P. mirabilis CCUG 49244
156661	P. mirabilis CCUG 63961
173180	P. mirabilis CIMB 05-1153, CRBIP17.135
174547	P. mirabilis 115002, DSM 115002
179113	P. mirabilis IMET 10794, STI10794
179147	P. mirabilis IMET 11109, STI11109
177885	P. mirabilis 10762, SF002753

Morphology

Cell morphology

@ref	Gram stain	Cell shape	Motility
120969	negative	rod-shaped

Culture and growth conditions

Culture medium

@ref	Name	Medium link	Composition
446	NUTRIENT AGAR (DSMZ Medium 1)	Medium recipe at MediaDive	Name: NUTRIENT AGAR (DSMZ Medium 1) Composition: Agar 15.0 g/l Peptone 5.0 g/l Meat extract 3.0 g/l Distilled water
35612	MEDIUM 3 - Columbia agar		Columbia agar (39.000 g);distilled water (1000.000 ml)
446	COLUMBIA BLOOD MEDIUM (DSMZ Medium 693)	Medium recipe at MediaDive	Name: COLUMBIA BLOOD MEDIUM (DSMZ Medium 693) Composition: Defibrinated sheep blood 50.0 g/l Columbia agar base
120969	CIP Medium 3	Medium recipe at CIP

Culture temp

@ref	Growth	Type	Temperature (°C)
446	positive	growth	37
35612	positive	growth	30
50915	positive	growth	37
120969	positive	growth	10-41
120969	negative	growth	5

Physiology and metabolism

Oxygen tolerance

@ref	Oxygen tolerance
50915	aerobe
120969	facultative anaerobe

Metabolite utilization

@ref	Chebi-ID	Metabolite	Utilization activity	Kind of utilization tested
68371	27613 ChEBI	amygdalin	-	builds acid from	from API 50CH acid
68368	27613 ChEBI	amygdalin	-	fermentation	from API 20E
68371	18305 ChEBI	arbutin	-	builds acid from	from API 50CH acid
68374	29016 ChEBI	arginine	-	hydrolysis	from API ID32E
68368	29016 ChEBI	arginine	-	hydrolysis	from API 20E
68374	17057 ChEBI	cellobiose	-	builds acid from	from API ID32E
68371	17057 ChEBI	cellobiose	-	builds acid from	from API 50CH acid
120969	16947 ChEBI	citrate	+	carbon source
68368	16947 ChEBI	citrate	+	assimilation	from API 20E
68371	17108 ChEBI	D-arabinose	+	builds acid from	from API 50CH acid
68374	18333 ChEBI	D-arabitol	-	builds acid from	from API ID32E
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
68374	18024 ChEBI	D-galacturonic acid	-	builds acid from	from API ID32E
68374	17634 ChEBI	D-glucose	-	builds acid from	from API ID32E
68371	17634 ChEBI	D-glucose	+	builds acid from	from API 50CH acid
68368	17634 ChEBI	D-glucose	+	fermentation	from API 20E
68371	62318 ChEBI	D-lyxose	-	builds acid from	from API 50CH acid
68374	16899 ChEBI	D-mannitol	-	builds acid from	from API ID32E
68371	16899 ChEBI	D-mannitol	-	builds acid from	from API 50CH acid
68368	16899 ChEBI	D-mannitol	-	fermentation	from API 20E
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
68371	4853 ChEBI	esculin	-	builds acid from	from API 50CH acid
68371	16813 ChEBI	galactitol	-	builds acid from	from API 50CH acid
68368	5291 ChEBI	gelatin	-	hydrolysis	from API 20E
68371	28066 ChEBI	gentiobiose	-	builds acid from	from API 50CH acid
68371	24265 ChEBI	gluconate	+	builds acid from	from API 50CH acid
120969	17234 ChEBI	glucose	+	fermentation
120969	17234 ChEBI	glucose	+	degradation
68371	17754 ChEBI	glycerol	+	builds acid from	from API 50CH acid
68371	28087 ChEBI	glycogen	-	builds acid from	from API 50CH acid
68371	15443 ChEBI	inulin	-	builds acid from	from API 50CH acid
68374	30849 ChEBI	L-arabinose	-	builds acid from	from API ID32E
68371	30849 ChEBI	L-arabinose	-	builds acid from	from API 50CH acid
68368	30849 ChEBI	L-arabinose	-	fermentation	from API 20E
68374	18403 ChEBI	L-arabitol	-	builds acid from	from API ID32E
68371	18403 ChEBI	L-arabitol	-	builds acid from	from API 50CH acid
68371	18287 ChEBI	L-fucose	-	builds acid from	from API 50CH acid
68374	62345 ChEBI	L-rhamnose	-	builds acid from	from API ID32E
68371	62345 ChEBI	L-rhamnose	-	builds acid from	from API 50CH acid
68368	62345 ChEBI	L-rhamnose	-	fermentation	from API 20E
68371	17266 ChEBI	L-sorbose	-	builds acid from	from API 50CH acid
68371	65328 ChEBI	L-xylose	-	builds acid from	from API 50CH acid
120969	17716 ChEBI	lactose	-	fermentation
68371	17716 ChEBI	lactose	-	builds acid from	from API 50CH acid
68374	25094 ChEBI	lysine	-	degradation	from API ID32E
68368	25094 ChEBI	lysine	-	degradation	from API 20E
68374	15792 ChEBI	malonate	-	assimilation	from API ID32E
120969	15792 ChEBI	malonate	-	assimilation
68374	17306 ChEBI	maltose	-	builds acid from	from API ID32E
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
68368	28053 ChEBI	melibiose	-	fermentation	from API 20E
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
68374	17268 ChEBI	myo-inositol	-	builds acid from	from API ID32E
68371	17268 ChEBI	myo-inositol	-	builds acid from	from API 50CH acid
68368	17268 ChEBI	myo-inositol	-	fermentation	from API 20E
68371	59640 ChEBI	N-acetylglucosamine	+	builds acid from	from API 50CH acid
120969	17632 ChEBI	nitrate	+	reduction
120969	16301 ChEBI	nitrite	-	reduction
68374	18257 ChEBI	ornithine	+	degradation	from API ID32E
68368	18257 ChEBI	ornithine	+	degradation	from API 20E
68374	18394 ChEBI	palatinose	-	builds acid from	from API ID32E
68371	0 ChEBI	Potassium 2-ketogluconate	+	builds acid from	from API 50CH acid
68374	0 ChEBI	Potassium 5-ketogluconate	-	builds acid from	from API ID32E
68371	0 ChEBI	Potassium 5-ketogluconate	+	builds acid from	from API 50CH acid
68371	16634 ChEBI	raffinose	-	builds acid from	from API 50CH acid
68374	15963 ChEBI	ribitol	-	builds acid from	from API ID32E
68371	15963 ChEBI	ribitol	-	builds acid from	from API 50CH acid
68371	17814 ChEBI	salicin	-	builds acid from	from API 50CH acid
120969	132112 ChEBI	sodium thiosulfate	+	builds gas from
68374	30911 ChEBI	sorbitol	-	builds acid from	from API ID32E
68368	30911 ChEBI	sorbitol	-	fermentation	from API 20E
68371	28017 ChEBI	starch	-	builds acid from	from API 50CH acid
68374	17992 ChEBI	sucrose	-	builds acid from	from API ID32E
68371	17992 ChEBI	sucrose	+	builds acid from	from API 50CH acid
68368	17992 ChEBI	sucrose	-	fermentation	from API 20E
68371	27082 ChEBI	trehalose	+	builds acid from	from API 50CH acid
68374	27082 ChEBI	trehalose	+	builds acid from	from API ID32E
68374	27897 ChEBI	tryptophan	-	energy source	from API ID32E
68368	27897 ChEBI	tryptophan	-	energy source	from API 20E
68371	32528 ChEBI	turanose	-	builds acid from	from API 50CH acid
68374	16199 ChEBI	urea	+	hydrolysis	from API ID32E
68368	16199 ChEBI	urea	+	hydrolysis	from API 20E
68371	17151 ChEBI	xylitol	-	builds acid from	from API 50CH acid

Antibiotic resistance

@ref	Metabolite	Is sensitive	Is resistant
120969	0129 (2,4-Diamino-6,7-di-iso-propylpteridine phosphate)

Metabolite production

@ref	Chebi-ID	Metabolite
68368	16136 ChEBI	hydrogen sulfide	from API 20E
68374	35581 ChEBI	indole	from API ID32E
120969	35581 ChEBI	indole
68368	35581 ChEBI	indole	from API 20E

Metabolite tests

@ref	Chebi-ID	Metabolite	Indole test	Voges-proskauer-test	Methylred-test
120969	15688 ChEBI	acetoin		-
120969	17234 ChEBI	glucose			+
68374	35581 ChEBI	indole	-			from API ID32E
68368	35581 ChEBI	indole	-			from API 20E

Enzymes

@ref	Value	Activity	Ec
120969	alcohol dehydrogenase	-	1.1.1.1
68374	alpha-galactosidase	-	3.2.1.22	from API ID32E
68374	alpha-glucosidase	-	3.2.1.20	from API ID32E
68374	alpha-maltosidase	-		from API ID32E
68374	arginine dihydrolase	-	3.5.3.6	from API ID32E
68368	arginine dihydrolase	-	3.5.3.6	from API 20E
120969	beta-galactosidase	-	3.2.1.23
68374	beta-galactosidase	-	3.2.1.23	from API ID32E
68368	beta-galactosidase	-	3.2.1.23	from API 20E
68374	beta-glucosidase	-	3.2.1.21	from API ID32E
68374	beta-glucuronidase	-	3.2.1.31	from API ID32E
120969	catalase	+	1.11.1.6
68368	cytochrome oxidase	-	1.9.3.1	from API 20E
120969	gelatinase	-
68368	gelatinase	-		from API 20E
68374	L-aspartate arylamidase	+	3.4.11.21	from API ID32E
68374	lipase	-		from API ID32E
120969	lysine decarboxylase	-	4.1.1.18
68374	lysine decarboxylase	-	4.1.1.18	from API ID32E
68368	lysine decarboxylase	-	4.1.1.18	from API 20E
68374	N-acetyl-beta-glucosaminidase	-	3.2.1.52	from API ID32E
120969	ornithine decarboxylase	+	4.1.1.17
68374	ornithine decarboxylase	+	4.1.1.17	from API ID32E
68368	ornithine decarboxylase	+	4.1.1.17	from API 20E
120969	oxidase	-
120969	tryptophan deaminase	+
68368	tryptophan deaminase	+	4.1.99.1	from API 20E
120969	urease	+	3.5.1.5
68374	urease	+	3.5.1.5	from API ID32E
68368	urease	+	3.5.1.5	from API 20E

API 20E

@ref	ONPG	ADH (Arg)	LDC (Lys)	ODC	CIT	H2S productionH2S	URE	TDA (Trp)	IND	Acetoin production (Voges Proskauer test)VP	GEL	GLU	MAN	INO	Sor	RHA	SAC	MEL	AMY	ARA	OX	Nitrite productionNO2	Reduction to N2N2	MotilityMOB	Growth on MacConkey mediumMAC	OF-O	OF-F
446	-	-	-	+	+	-	+	+	-	-	-	+	-	-	-	-	-	-	-	-	-	not determinedn.d.	not determinedn.d.	not determinedn.d.	not determinedn.d.	not determinedn.d.	not determinedn.d.
446	-	-	-	+	+	-	+	+	-	+	-	+	-	-	-	-	-	-	-	-	-	not determinedn.d.	not determinedn.d.	not determinedn.d.	not determinedn.d.	not determinedn.d.	not determinedn.d.

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
120969	not determinedn.d.	+	-	+	-	+	+	-	-	-	+	+	+	+	-	-	-	-	-	-	-	-	+	-	-	-	-	-	-	-	-	+	+	-	-	-	-	-	-	-	-	-	-	-	-	-	-	+	+	+

API ID32E

@ref	ODC	ADH (Arg)	LDC (Lys)	URE	LARL	GAT	5KG	LipaseLIP	Phenol red (Acidification)RP	beta GLU	MAN	MAL	ADO	PLE	beta GUR	MNT	IND	N-Acetyl-beta-Glucosaminidasebeta NAG	beta GAL	GLU	SAC	LARA	DARL	alpha GLU	alpha GAL	TRE	RHA	INO	CEL	SOR	alpha-MaltosidasealphaMAL	L-aspartic acid arylamidaseAspA
50915	+	-	-	+	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	+	-	-	-	-	-	+

Isolation, sampling and environmental information

Interaction and safety

Risk assessment

@ref	Pathogenicity human	Pathogenicity animal	Biosafety level	Biosafety level comment
446			2	Risk group (German classification) According to TRBA 466
120969			2	Risk group (French classification) According to TRBA 466

Sequence information

16S sequences

@ref	Description	Accession	Length	Database	NCBI tax ID
20218	Proteus mirabilis strain ATCC 14153 16S ribosomal RNA gene, partial sequence	FJ971887	797		584

Genome-based predictions

Literature

Topic	Title	Authors	Journal	DOI	Year
	Cefsulodin and Vancomycin: A Supplement for Chromogenic Coliform Agar for Detection of Escherichia coli and Coliform Bacteria from Different Water Sources.	Schalli M, Inwinkl SM, Platzer S, Baumert R, Reinthaler FF, Ofner-Kopeinig P, Haas D.	Microorganisms	10.3390/microorganisms10122499	2022
	How Accurate Are Veterinary Clinicians Employing Flexicult Vet for Identification and Antimicrobial Susceptibility Testing of Urinary Bacteria?	Cugmas B, Avbersek M, Rosa T, Godec L, Struc E, Golob M, Zdovc I.	Antibiotics (Basel)	10.3390/antibiotics10101160	2021
	Chlorhexidine and octenidine susceptibility of bacterial isolates from clinical samples in a three-armed cluster randomised decolonisation trial.	Denkel LA, Kramer TS, Schwab F, Golembus J, Wolke S, Gastmeier P, Geffers C.	PLoS One	10.1371/journal.pone.0278569	2022
Enzymology	Large scale multiplex PCR improves pathogen detection by DNA microarrays.	Palka-Santini M, Cleven BE, Eichinger L, Kronke M, Krut O.	BMC Microbiol	10.1186/1471-2180-9-1	2009
Enzymology	Development of a LightCycler PCR assay for detection and quantification of Aspergillus fumigatus DNA in clinical samples from neutropenic patients.	Spiess B, Buchheidt D, Baust C, Skladny H, Seifarth W, Zeilfelder U, Leib-Mosch C, Morz H, Hehlmann R.	J Clin Microbiol	10.1128/jcm.41.5.1811-1818.2003	2003
	Strategy for sensitive and specific detection of Yersinia pestis in skeletons of the black death pandemic.	Seifert L, Harbeck M, Thomas A, Hoke N, Zoller L, Wiechmann I, Grupe G, Scholz HC, Riehm JM.	PLoS One	10.1371/journal.pone.0075742	2013
Enzymology	DNA microarray-based detection and identification of fungal pathogens in clinical samples from neutropenic patients.	Spiess B, Seifarth W, Hummel M, Frank O, Fabarius A, Zheng C, Morz H, Hehlmann R, Buchheidt D.	J Clin Microbiol	10.1128/jcm.00942-07	2007
Enzymology	Specific detection of Aspergillus species in blood and bronchoalveolar lavage samples of immunocompromised patients by two-step PCR.	Skladny H, Buchheidt D, Baust C, Krieg-Schneider F, Seifarth W, Leib-Mosch C, Hehlmann R.	J Clin Microbiol	10.1128/jcm.37.12.3865-3871.1999	1999
Phylogeny	DNA hybridization probe for the Pseudomonas fluorescens group.	Festl H, Ludwig W, Schleifer KH.	Appl Environ Microbiol	10.1128/aem.52.5.1190-1194.1986	1986
	Rapid direct disk diffusion testing for antibiotic resistance in urinary tract infections: a bacterial concentration-adjusted approach.	Sabersky-Mussigbrodt H, Russell S, Wantia N, Hayden O.	Microbiol Spectr	10.1128/spectrum.00888-25	2025
	Influence of the mowing and drying on the quality of the peppermint (Mentha x piperita L.) essential oil: Chemical profile, thermal properties, and biological activity	Durovic S, Micic D, Pezo L, Radic D, Bazarnova JG, Smyatskaya YA, Blagojevic S.	Industrial crops and products.		2022
	Ganoderma adspersum (Ganodermataceae): Investigation of Its Secondary Metabolites and the Antioxidant, Antimicrobial, and Cytotoxic Potential of Its Extracts.	Chafouz R, Karavergou S, Tsiftsoglou OS, Maskovic P, Lazari D.	Int J Mol Sci	10.3390/ijms25010516	2023
	Carbon Dots as Multifunctional Nanomaterials: A Review on Antimicrobial Activities and Fluorescence-Based Microbial Detection.	Romulo A, Suryoprabowo S, Setiarto RHB, Guo Y.	Molecules	10.3390/molecules30193969	2025
Phylogeny	Investigations on the Endemic Species Taraxacum mirabile Wagenitz: HPLC-MS and GC-MS Studies, Evaluation of Antioxidant, Anti-Inflammatory, and Antimicrobial Properties, and Isolation of Several Phenolic Compounds.	Karahuseyin S, Ozsoy N, Ozbek Celik B, Sari A.	Plants (Basel)	10.3390/plants13233304	2024
	In-vitro evaluation of the effect of okra (Abelmoschus esculentus L.) extract on periodontal cells: a comprehensive study of cellular and molecular impacts.	Tosun UU, Aydin ST, Tiryaki A, Baykara D, Yakut A, Rayaman E, Taskin T, Ekinci Dogan C, Gunduz O, Agrali OB.	BMC Complement Med Ther	10.1186/s12906-025-04828-8	2025
	Antibacterial and Antibiofouling Activities of Carbon Polymerized Dots/Polyurethane and C₆₀/Polyurethane Composite Films.	Markovic ZM, Budimir Filimonovic MD, Milivojevic DD, Kovac J, Todorovic Markovic BM.	J Funct Biomater	10.3390/jfb15030073	2024
	Antimicrobial activity of rhizomes of Ferulago trachycarpa Boiss. and bioguided isolation of active coumarin constituents	Dikpinar T, Suzgec-Selcuk S, Celik BO, Urusak EA.	Industrial crops and products.	10.1016/j.indcrop.2018.06.072	2018
	Hypericum empetrifolium subsp. empetrifolium: an assessment of its antifungal, antidiabetic, anti-aging, and neuroprotective potential.	Demirci Kayiran S, Tavli OF, Mataraci Kara E, Kaplan A, Sahin H, Boga M, Eroglu Ozkan E.	Front Pharmacol	10.3389/fphar.2025.1618761	2025
	Hydroxyapatite/TiO₂ Nanomaterial with Defined Microstructural and Good Antimicrobial Properties.	Mirkovic M, Filipovic S, Kalijadis A, Maskovic P, Maskovic J, Vlahovic B, Pavlovic V.	Antibiotics (Basel)	10.3390/antibiotics11050592	2022
	Unveiling Cytotoxic Bioactive Compounds from Erica carnea L.: Extraction Optimization, Kinetic Modeling, and Biological Activity Assessment.	Jevtovic V, Alabbosh KFS, Alyami RA, Alshammari MR, Alshammari B, Maskovic P, Maskovic J, Nikolic J, Mitic M.	Plants (Basel)	10.3390/plants14111679	2025
Pathogenicity	Decolonization potential of 0.02% polyhexanide irrigation solution in urethral catheters under practice-like in vitro conditions.	Brill FHH, Gabriel H, Brill H, Klock JH, Steinmann J, Arndt A.	BMC Urol	10.1186/s12894-018-0362-3	2018
	Natural-product-inspired design and synthesis of thiolated coenzyme Q analogs as promising agents against Gram-positive bacterial strains: insights into structure-activity relationship, activity profile, mode of action, and molecular docking.	Yildirim H, Yildiz M, Bayrak N, Mataraci-Kara E, Ozbek-Celik B, Otsuka M, Fujita M, Radwan MO, TuYuN AF.	RSC Adv	10.1039/d2ra02136f	2022
	Promising Antibacterial and Antifungal Agents Based on Thiolated Vitamin K3 Analogs: Synthesis, Bioevaluation, Molecular Docking.	Yildirim H, Yildiz M, Bayrak N, Mataraci-Kara E, Radwan MO, Jannuzzi AT, Otsuka M, Fujita M, TuYuN AF.	Pharmaceuticals (Basel)	10.3390/ph15050586	2022
	Papaver Plants: Current Insights on Phytochemical and Nutritional Composition Along with Biotechnological Applications.	Butnariu M, Quispe C, Herrera-Bravo J, Pentea M, Sarac I, Kusumler AS, Ozcelik B, Painuli S, Semwal P, Imran M, Gondal TA, Emamzadeh-Yazdi S, Lapava N, Yousaf Z, Kumar M, Eid AH, Al-Dhaheri Y, Suleria HAR, Del Mar Contreras M, Sharifi-Rad J, Cho WC.	Oxid Med Cell Longev	10.1155/2022/2041769	2022
	The Therapeutic Potential of Ethnomedicinally Important Anatolian Thyme Species: A Phytochemical and Biological Assessment.	Eroglu Ozkan E, Ersoy E, Yesil Canturk Y, Mataraci Kara E, Cinar E, Sahin H, Karahan S, Karaca Sancaktepe K, Yilmaz MA, Boga M.	Front Pharmacol	10.3389/fphar.2022.923063	2022
	Recovery of Biologically Active Compounds from Stinging Nettle Leaves Part II: Processing of Exhausted Plant Material after Supercritical Fluid Extraction.	Durovic S, Pezo L, Gasic U, Gorjanovic S, Pastor F, Bazarnova JG, Smyatskaya YA, Zekovic Z.	Foods	10.3390/foods12040809	2023
	Phytochemical, Cytotoxic, and Antimicrobial Evaluation of Tribulus terrestris L., Typha domingensis Pers., and Ricinus communis L.: Scientific Evidences for Folkloric Uses.	Khalid A, Algarni AS, Homeida HE, Sultana S, Javed SA, Rehman ZU, Abdalla H, Alhazmi HA, Albratty M, Abdalla AN.	Evid Based Complement Alternat Med	10.1155/2022/6519712	2022
	Shotgun Proteomics Analysis, Functional Networks, and Peptide Biomarkers for Seafood-Originating Biogenic-Amine-Producing Bacteria.	Abril AG, Calo-Mata P, Bohme K, Villa TG, Barros-Velazquez J, Pazos M, Carrera M.	Int J Mol Sci	10.3390/ijms24097704	2023
	Exploring the Relationships between Structure and Antimicrobial Potency of Quinolinequinones.	Mataraci-Kara E, Bayrak N, Yildiz M, Yildirim H, TuYuN AF.	Antibiotics (Basel)	10.3390/antibiotics11101397	2022
	Use of Supplemented or Human Material to Simulate PD Behavior of Antibiotics at the Target Site In Vitro.	Nussbaumer-Proll A, Zeitlinger M.	Pharmaceutics	10.3390/pharmaceutics12080773	2020
Pathogenicity	Investigation the potential use of silver nanoparticles synthesized by propolis extract as N-acyl-homoserine lactone-mediated quorum sensing systems inhibitor	Ilk S, Tan G, Emul E, Saglam N.	Turk J Med Sci	10.3906/sag-2004-148	2020
	Ecological Preferences and Diversity of Essential Oil Composition in Endangered Wild-Growing Populations of Sideritis sipylea Boiss. (Lamiaceae) of the East Aegean Islands (Greece): Evidencing Antioxidant Potential, Antimicrobial and Cytotoxic Activities.	Maskovic PZ, Stagiopoulou R, Miletic N, Krigas N, Lazari D.	Plants (Basel)	10.3390/plants12040836	2023
	Antibacterial activity of Centaurea pumilio L. root and aerial part extracts against some multidrug resistant bacteria.	Naeim H, El-Hawiet A, Abdel Rahman RA, Hussein A, El Demellawy MA, Embaby AM.	BMC Complement Med Ther	10.1186/s12906-020-2876-y	2020
	Design, synthesis, antitubercular and antiviral properties of new spirocyclic indole derivatives.	Cihan-Ustundag G, Naesens L, Satana D, Erkose-Genc G, Mataraci-Kara E, Capan G.	Monatsh Chem	10.1007/s00706-019-02457-9	2019
	Deverra tortuosa (Desf.) DC from Saudi Arabia as a new source of marmin and furanocoumarins derivatives with alpha-glucosidase, antibacterial and cytotoxic activities.	Oueslati MH, Guetat A, Bouajila J, Alzahrani AK, Basha J.	Heliyon	10.1016/j.heliyon.2021.e06656	2021
Pathogenicity	Variation of alkaloid contents and antimicrobial activities of Papaver rhoeas L. growing in Turkey and northern Cyprus.	Coban I, Toplan GG, Ozbek B, Gurer CU, Sariyar G.	Pharm Biol	10.1080/13880209.2017.1340964	2017
	Novel Naja atra cardiotoxin 1 (CTX-1) derived antimicrobial peptides with broad spectrum activity.	Sala A, Cabassi CS, Santospirito D, Polverini E, Flisi S, Cavirani S, Taddei S.	PLoS One	10.1371/journal.pone.0190778	2018
	Aminated Quinolinequinones as Privileged Scaffolds for Antibacterial Agents: Synthesis, In Vitro Evaluation, and Putative Mode of Action.	Yildirim H, Bayrak N, Yildiz M, Mataraci-Kara E, Korkmaz S, Shilkar D, Jayaprakash V, TuYuN AF.	ACS Omega	10.1021/acsomega.2c03193	2022
	Terpenoids in the Essential Oil and Concentrated Aromatic Products Obtained from Nicotiana glutinosa L. Leaves.	Popova V, Ivanova T, Stoyanova A, Nikolova V, Hristeva T, Gochev V, Yonchev Y, Nikolov N, Zheljazkov VD.	Molecules	10.3390/molecules25010030	2019
	High-Resolution Comparative and Quantitative Proteomics of Biogenic-Amine-Producing Bacteria and Virulence Factors Present in Seafood.	Abril AG, Calo-Mata P, Villa TG, Bohme K, Barros-Velazquez J, Sanchez-Perez A, Pazos M, Carrera M.	J Agric Food Chem	10.1021/acs.jafc.3c06607	2024
	Potential use of kraft and organosolv lignins as a natural additive for healthcare products.	Gordobil O, Herrera R, Yahyaoui M, Ilk S, Kaya M, Labidi J.	RSC Adv	10.1039/c8ra02255k	2018
Enzymology	A Tailspike with Exopolysaccharide Depolymerase Activity from a New Providencia stuartii Phage Makes Multidrug-Resistant Bacteria Susceptible to Serum-Mediated Killing.	Oliveira H, Pinto G, Mendes B, Dias O, Hendrix H, Akturk E, Noben JP, Gawor J, Lobocka M, Lavigne R, Azeredo J.	Appl Environ Microbiol	10.1128/aem.00073-20	2020
	Antibacterial activity of Aegle marmelos against leaf, bark and fruit extracts.	Poonkothai M, Saravanan M.	Anc Sci Life		2008
	A new family of azanaphthoquinones for antimicrobial evaluation.	Bayrak N.	Chem Cent J	10.1186/s13065-018-0388-3	2018
Enzymology	Solvent-Free Microwave-Assisted Extraction of Polyphenols from Olive Tree Leaves: Antioxidant and Antimicrobial Properties.	Sahin S, Samli R, Tan ASB, Barba FJ, Chemat F, Cravotto G, Lorenzo JM.	Molecules	10.3390/molecules22071056	2017
Pathogenicity	Synthesis and biological activity of new 1,3-dioxolanes as potential antibacterial and antifungal compounds.	Kucuk HB, Yusufoglu A, Mataraci E, Dosler S.	Molecules	10.3390/molecules16086806	2011
	Synthesis, Enzymatic Degradation, and Polymer-Miscibility Evaluation of Nonionic Antimicrobial Hyperbranched Polyesters with Indole or Isatin Functionalities.	Li X, Ilk S, Linares-Pasten JA, Liu Y, Raina DB, Demircan D, Zhang B.	Biomacromolecules	10.1021/acs.biomac.1c00343	2021
	Chemical Composition, Antioxidant, and Antimicrobial Activities of Lichen Umbilicaria cylindrica (L.) Delise (Umbilicariaceae).	Manojlovic NT, Vasiljevic PJ, Maskovic PZ, Juskovic M, Bogdanovic-Dusanovic G.	Evid Based Complement Alternat Med	10.1155/2012/452431	2012
	Self-Disinfecting Urethral Catheter to Overcome Urinary Infections: From Antimicrobial Photodynamic Action to Antibacterial Biochemical Entities.	Dias LD, Duarte LS, Naves PLF, Napolitano HB, Bagnato VS.	Microorganisms	10.3390/microorganisms10122484	2022
Pathogenicity	Anti-tuberculous activity of treponemycin produced by a streptomyces strain MS-6-6 isolated from Saudi Arabia.	Yassien MA, Abdallah HM, El-Halawany AM, Jiman-Fatani AA.	Molecules	10.3390/molecules20022576	2015
Metabolism	Rapid and economical method for biochemical screening of stool isolates for Salmonella and Shigella species.	Wilson G.	J Clin Microbiol	10.1128/jcm.42.10.4821-4823.2004	2004
	Antimicrobial and anticoagulant activities of N-chlorotaurine, N,N-dichloro-2,2-dimethyltaurine, and N-monochloro-2,2-dimethyltaurine in human blood.	Martini C, Hammerer-Lercher A, Zuck M, Jekle A, Debabov D, Anderson M, Nagl M.	Antimicrob Agents Chemother	10.1128/aac.05685-11	2012
Biotechnology	Medicinal properties and conservation of Pelargonium sidoides DC.	Moyo M, Van Staden J.	J Ethnopharmacol	10.1016/j.jep.2014.01.009	2014
Metabolism	Bactericidal activity of micromolar N-chlorotaurine: evidence for its antimicrobial function in the human defense system.	Nagl M, Hess MW, Pfaller K, Hengster P, Gottardi W.	Antimicrob Agents Chemother	10.1128/aac.44.9.2507-2513.2000	2000
Phylogeny	Rapid-cycle PCR and fluorimetry for detection of mycobacteria.	Lachnik J, Ackermann B, Bohrssen A, Maass S, Diephaus C, Puncken A, Stermann M, Bange FC.	J Clin Microbiol	10.1128/jcm.40.9.3364-3373.2002	2002
Phylogeny	Identification of human pathogens isolated from blood using microarray hybridisation and signal pattern recognition.	Wiesinger-Mayr H, Vierlinger K, Pichler R, Kriegner A, Hirschl AM, Presterl E, Bodrossy L, Noehammer C.	BMC Microbiol	10.1186/1471-2180-7-78	2007
Pathogenicity	Interspecific reconstitution of maltose transport and chemotaxis in Escherichia coli with maltose-binding protein from various enteric bacteria.	Dahl MK, Manson MD.	J Bacteriol	10.1128/jb.164.3.1057-1063.1985	1985
	Effect of blending Jersey and Holstein-Friesian milk on Cheddar cheese processing, composition, and quality.	Bland JH, Grandison AS, Fagan CC.	J Dairy Sci	10.3168/jds.2014-8433	2015
Pathogenicity	Impact of pH on activity of trimethoprim, fosfomycin, amikacin, colistin and ertapenem in human urine.	Burian A, Erdogan Z, Jandrisits C, Zeitlinger M	Pharmacology	10.1159/000342423	2012
Pathogenicity	Phenolic compounds and biological activity of Kitaibelia vitifolia.	Maskovic P, Solujic S, Mihailovic V, Mladenovic M, Cvijovic M, Mladenovic J, Acamovic-Dokovic G, Kurcubic V	J Med Food	10.1089/jmf.2011.0013	2011
Pathogenicity	Synthesis 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 M	Arzneimittelforschung		2006
Pathogenicity	Synthesis 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 G	Eur J Med Chem	10.1016/j.ejmech.2005.07.004	2005
Pathogenicity	Synthesis of some new 6-methylimidazo[2,1-b]thiazole-5-carbohydrazide derivatives and their antimicrobial activities.	Ur F, Cesur N, Birteksoz S, Otuk G	Arzneimittelforschung	10.1055/s-0031-1296947	2004
Pathogenicity	Synthesis 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 S	Arch Pharm (Weinheim)	10.1002/ardp.200390002	2003
Pathogenicity	An abietane diterpene and two phenolics from Salvia forskahlei.	Ulubelen A, Sonmez U, Topcu G, Bozok Johansson C	Phytochemistry	10.1016/0031-9422(95)00888-8	1996

References

#446	Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 788
#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 )
#20216	Curators of the JMRC: Jena Microbial Resource Collection (JMRC):
#20218	Verslyppe, B., De Smet, W., De Baets, B., De Vos, P., Dawyndt P.: StrainInfo introduces electronic passports for microorganisms.. Syst Appl Microbiol. 37: 42 - 50 2014 ( DOI 10.1016/j.syapm.2013.11.002 , PubMed 24321274 )
#35612	; Curators of the CIP;
#50915	Culture Collection University of Gothenburg (CCUG) ; Curators of the CCUG; CCUG 32232
#68368	Automatically annotated from API 20E .
#68371	Automatically annotated from API 50CH acid .
#68374	Automatically annotated from API ID32E .
#120969	Collection of Institut Pasteur ; Curators of the CIP; CIP 104032
#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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Proteus mirabilis (DSM 788, ATCC 14153, IMET 11232)

Name and taxonomic classification

Morphology

Cell morphology

Culture and growth conditions

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Physiology and metabolism

Oxygen tolerance

Metabolite utilization

Antibiotic resistance

Metabolite production

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Enzymes

API 20E

API 50CHac

API ID32E

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