Name: Proteus vulgaris CIP 54.160
Creator: BacDive
License: http://creativecommons.org/licenses/by-nc/4.0/

Strain identifier

BacDive ID: 134601

Type strain:

Species: Proteus vulgaris

Culture col. no.: CIP 54.160, NCTC 8313, NCIMB 8261, CCUG 55607, CECT 174, ATCC 6380, CCTM La 2326, CNCTC Pro 2/35

Strain history: 1954, A. Felix, PHLS, London, UK: strain OX19

NCBI tax ID(s): 585 (species)

Other strains from Proteus vulgaris

Section

Proteus vulgaris CIP 54.160 is a mesophilic bacterium of the family Morganellaceae.

mesophilic
Bacteria

Information on the name and the taxonomic classification. Name and taxonomic classification

	Last LPSN update	07-12-2022 (DD-MM-YYYY)
	Domain	"Bacteria"
	Phylum	*Pseudomonadota*
	Class	*Gammaproteobacteria*
	Order	*Enterobacterales*
	Family	*Morganellaceae*
	Genus	*Proteus*
	Species	**Proteus vulgaris**
	Full Scientific Name (PNU)	Proteus vulgaris Hauser 1885 (Approved Lists 1980)

Information on culture and growth conditions Culture and growth conditions

[Ref.: #33026]

Culture medium

MEDIUM 3 - Columbia agar

[Ref.: #33026]

Culture medium growth

[Ref.: #33026]

Culture medium composition

expand / minimize

	Temperatures	Kind of temperature		Temperature
[Ref.: #33026]			growth	30 °C

[Ref.: #33026]

Temperature range

mesophilic

Information on physiology and metabolism Physiology and metabolism

	Metabolite	Utilization activity	Kind of utilization tested
[Ref.: #68374]	arginine ChEBI	-	hydrolysis	* from API ID32E
[Ref.: #68374]	cellobiose ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	D-arabitol ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	D-galacturonic acid ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	D-glucose ChEBI	+	builds acid from	* from API ID32E
[Ref.: #68374]	D-mannitol ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	L-arabinose ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	L-arabitol ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	L-rhamnose ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	lysine ChEBI	-	degradation	* from API ID32E
[Ref.: #68374]	malonate ChEBI	-	assimilation	* from API ID32E
[Ref.: #68374]	maltose ChEBI	+	builds acid from	* from API ID32E
[Ref.: #68374]	myo-inositol ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	ornithine ChEBI	-	degradation	* from API ID32E
[Ref.: #68374]	palatinose ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	Potassium 5-ketogluconate	-	builds acid from	* from API ID32E
[Ref.: #68374]	ribitol ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	sorbitol ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	sucrose ChEBI	+	builds acid from	* from API ID32E
[Ref.: #68374]	trehalose ChEBI	-	builds acid from	* from API ID32E
[Ref.: #68374]	tryptophan ChEBI	+	energy source	* from API ID32E
[Ref.: #68374]	urea ChEBI	+	hydrolysis	* from API ID32E
	Only first 10 entries are displayed. Click here to see all.

	Metabolite production	Metabolite
[Ref.: #68374]		indole ChEBI	* from API ID32E

	Physiological tests	Metabolite	Indole test
[Ref.: #68374]		indole ChEBI	+	* from API ID32E

	Enzyme	Enzyme activity	EC number
[Ref.: #68374]	alpha-galactosidase	-	3.2.1.22	* from API ID32E
[Ref.: #68374]	alpha-glucosidase	+	3.2.1.20	* from API ID32E
[Ref.: #68374]	alpha-maltosidase	+		* from API ID32E
[Ref.: #68374]	arginine dihydrolase	-	3.5.3.6	* from API ID32E
[Ref.: #68374]	beta-galactosidase	-	3.2.1.23	* from API ID32E
[Ref.: #68374]	beta-glucosidase	+	3.2.1.21	* from API ID32E
[Ref.: #68374]	beta-glucuronidase	-	3.2.1.31	* from API ID32E
[Ref.: #68374]	L-aspartate arylamidase	-	3.4.11.21	* from API ID32E
[Ref.: #68374]	lipase	-		* from API ID32E
[Ref.: #68374]	lysine decarboxylase	-	4.1.1.18	* from API ID32E
[Ref.: #68374]	N-acetyl-beta-glucosaminidase	-	3.2.1.52	* from API ID32E
[Ref.: #68374]	ornithine decarboxylase	-	4.1.1.17	* from API ID32E
[Ref.: #68374]	urease	+	3.5.1.5	* from API ID32E
	Only first 10 entries are displayed. Click here to see all.

Fatty acid profile

Metadata FA analysis

Reference

[Ref.: #60668]

Fatty acid	Percentage	ECL
C16:1 ω7c	33.9	15.819
C16:0	29.3	16
C14:0	12.7	14
C18:1 ω7c /12t/9t	7.6	17.824
C14:0 3OH/C16:1 ISO I	5.3	15.485
C15:0	5	15
C17:0 CYCLO	3.5	16.888
C17:0	0.6	17
C17:1 ω8c	0.6	16.792
unknown 14.503	0.6	14.503
C12:0 ALDE ?	0.4	10.915
C18:2 ω6,9c/C18:0 ANTE	0.4	17.724

API® ID32E:

Note that the displayed test results represent raw data and therefore may deviate!

	API ID	Ornithine decarboxylaseODC	Arginine dihydrolaseADH (Arg)	Lysine decarboxylaseLDC (Lys)	Urease/urea hydrolysisURE	Acid from L-arabitolLARL	Acid from D-galacturonic acidGAT	Acid from 5-Ketogluconate5KG	LipaseLIP	Phenol red (Acidification)RP	beta-Glucosidasebeta GLU	Acid from D-mannitolMAN	Acid from maltoseMAL	Acid from D-adonitolADO	Acid from palatinosePLE	beta-Glucuronidasebeta GUR	MalonateMNT	Indole productionIND	N-Acetyl-beta-Glucosaminidasebeta NAG	beta-Galactosidasebeta GAL	Acid from D-glucoseGLU	Acid from sucroseSAC	Acid from L-arabinoseLARA	Acid from D-arabitolDARL	alpha-Glucosidasealpha GLU	alpha-Galactosidasealpha GAL	Acid from trehaloseTRE	Acid from L-rhamnoseRHA	Acid from inositolINO	Acid from cellobioseCEL	Acid from sorbitolSOR	alpha-MaltosidasealphaMAL	L-aspartic acid arylamidaseAspA
[Ref.: #60668]	1846	-	-	-	+	-	-	-	-	+	+	-	+	-	-	-	-	+	-	-	+	+	-	-	+	-	-	-	-	-	-	+	-

Information on isolation source, the sampling and environmental conditions Isolation, sampling and environmental information

[Ref.: #33026]	Country	United Kingdom
[Ref.: #33026]	Country ISO 3 Code	GBR
[Ref.: #33026]	Continent	Europe
* marker position based on {}

Availability in culture collections External links

[Ref.: #33026]

Culture collection no.

CIP 54.160, NCTC 8313, NCIMB 8261, CCUG 55607, CECT 174, ATCC 6380, CCTM La 2326, CNCTC Pro 2/35

[Ref.: #20218]

Associated Passport(s) in StrainInfo

234474, 153980, 206898

Literature:

Topic	Title	Authors	Journal	DOI	Year
Pathogenicity	In vitro antimicrobial effects of a novel Pentaherbs concoction for atopic dermatitis.	Hon KL, Ip M, Wong CK, Chan BCL, Leung PC, Leung TF	J Dermatolog Treat	10.1080/09546634.2017.1395804	2017	*
	Synthesis, Antibacterial, and Cytotoxicity Evaluation of Oleanolic Acid-4-aminoquinoline Based Hybrid Compounds.	Khwaza V, Oyedeji OO, Aderibigbe BA, Morifi E, Fonkui TY, Ndinteh DT, Steenkamp V	Recent Adv Antiinfect Drug Discov	10.2174/1574891X16666210210165547	2021	*
	Chemical Compounds, Antitumor and Antimicrobial Activities of Dry Ethanol Extracts from Koelreuteria paniculata Laxm.	Andonova T, Muhovski Y, Fidan H, Slavov I, Stoyanova A, Dimitrova-Dyulgerova I	Plants (Basel)	10.3390/plants10122715	2021	*
	Synthesis, Structural Characterization, Hirshfeld Surface Analysis, and Antibacterial Study of Pd(II) and Ni(II) Schiff Base Complexes Derived from Aliphatic Diamine.	Nasaruddin NH, Ahmad SN, Sirat SS, Tan KW, Zakaria NA, Mohamad Nazam SS, Rahman NMMA, Mohd Yusof NS, Bahron H	ACS Omega	10.1021/acsomega.2c04688	2022	*

References

#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 )

#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 )

#33026 Collection of Institut Pasteur ; Curators of the CIP; CIP 54.160
#60668 Culture Collection University of Gothenburg (CCUG) ; Curators of the CCUG; CCUG 55607

#68374

Automatically annotated from API ID32E .

* These data were automatically processed and therefore are not curated

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