Neisseria weaveri (CIP 103942, CCUG 9689, CNPM 8)

Name: Neisseria weaveri (CIP 103942, CCUG 9689, CNPM 8)
Creator: BacDive
License: http://creativecommons.org/licenses/by/4.0/

BacDive ID 135338

Type strain

Strain Designation CNPM 8

Culture col. no. CIP 103942 CCUG 9689 CNPM 8

NCBI tax ID(s) 28091

Special Collections CCUG CIP

History CIP <- 1994, F. Escande, Inst. Pasteur, Paris, France: strain CNPM 8 <- 1994, CCUG <- K. Boevre, Oslo, Norway <- R.E. Weaver, CDC: strain D1674, Neisseria parelongata

Links

Neisseria weaveri CNPM 8 is an obligate aerobe, mesophilic, Gram-negative prokaryote of the family Neisseriaceae.

Gram-negative oval-shaped obligate aerobe mesophilic

Name and taxonomic classification

SI-ID 55906

CCUG 9689,CIP 103942

@ref 20215

Last LPSN update 2025-12-16 10:02:17

Domain Pseudomonadati

Phylum Pseudomonadota

Class Betaproteobacteria

Order Neisseriales

Family Neisseriaceae

Genus Neisseria

Species Neisseria weaveri

Full scientific name Neisseria weaveri Holmes et al. 1993

Synonyms (1)

Neisseria weaveri

BacDive ID	Other strains from **Neisseria weaveri** (56)	Type strain
10481	N. weaveri ISL775/91, DSM 17688, ATCC 51410, CCM 4587, ... (type strain)
135115	N. weaveri CNPM 11, CIP 103941, CCUG 4130 B
135339	N. weaveri CNPM 6, CIP 103943, CCUG 9690
135340	N. weaveri CNPM 7, CIP 103944, CCUG 9693
138902	N. weaveri CNPM 9, CIP 103945, CCUG 22467
142003	N. weaveri CCUG 9688
142684	N. weaveri CCUG 13906
142687	N. weaveri CCUG 13910 B
143530	N. weaveri CCUG 19865
143596	N. weaveri CCUG 20520
144463	N. weaveri CCUG 25017
145409	N. weaveri CCUG 28384
145432	N. weaveri CCUG 28485
145448	N. weaveri CCUG 28573
145526	N. weaveri CCUG 28753
146101	N. weaveri CCUG 30381
146284	N. weaveri CCUG 30799, ATCC 51223, CCM 4588
146737	N. weaveri CCUG 32043
146831	N. weaveri CCUG 32194
147026	N. weaveri CCUG 32667
147082	N. weaveri CCUG 32819
147142	N. weaveri CCUG 32933
147302	N. weaveri CCUG 33337
147527	N. weaveri CCUG 33743
147534	N. weaveri CCUG 33757
147570	N. weaveri CCUG 33819
147714	N. weaveri CCUG 34064
147969	N. weaveri CCUG 34597
148006	N. weaveri CCUG 34658
148007	N. weaveri CCUG 34659
148008	N. weaveri CCUG 34660
148034	N. weaveri CCUG 34714
148174	N. weaveri CCUG 34972
148858	N. weaveri CCUG 36508
148894	N. weaveri CCUG 36560
149134	N. weaveri CCUG 36908
149141	N. weaveri CCUG 36923
149366	N. weaveri CCUG 37598
149885	N. weaveri CCUG 38612
150023	N. weaveri CCUG 38857
150255	N. weaveri CCUG 39397
150277	N. weaveri CCUG 39472
150313	N. weaveri CCUG 39614
151017	N. weaveri CCUG 43048
151121	N. weaveri CCUG 43321
151195	N. weaveri CCUG 43441
151355	N. weaveri CCUG 43831
151584	N. weaveri CCUG 44385
151788	N. weaveri CCUG 44880
154109	N. weaveri CCUG 52390
154262	N. weaveri CCUG 52919
154556	N. weaveri CCUG 54397
154641	N. weaveri CCUG 54715
155424	N. weaveri CCUG 57703
156747	N. weaveri CCUG 64766
174301	N. weaveri CIMB 04-6129, CRBIP17.113

Morphology

Cell morphology

@ref	Gram stain	Cell shape	Motility
34434	negative	oval-shaped

Culture and growth conditions

Culture medium

@ref	Name	Growth	Composition	Medium link
34434	MEDIUM 3 - Columbia agar		Columbia agar (39.000 g);distilled water (1000.000 ml)
34434	CIP Medium 3			Medium recipe at CIP

Culture temp

@ref	Growth	Type	Temperature (°C)	Range
34434	positive	growth	30	mesophilic
34434	positive	growth	22-30
34434	negative	growth	5
34434	negative	growth	45

Physiology and metabolism

Oxygen tolerance

34434

Oxygen toleranceobligate aerobe

Metabolite utilization

@ref	Chebi-ID	Metabolite	Utilization activity	Kind of utilization tested
34434	17632 ChEBI	nitrate	-	reduction
34434	16301 ChEBI	nitrite	-	reduction
34434	35020 ChEBI	tributyrin	-	hydrolysis

Antibiotic resistance

@ref	Metabolite	Is sensitive	Is resistant
34434	0129 (2,4-Diamino-6,7-di-iso-propylpteridine phosphate)

Metabolite production

@ref	Chebi-ID	Metabolite	Production
34434	35581 ChEBI	indole
34434		polysaccharides

Enzymes

@ref	Value	Activity	Ec
34434	alcohol dehydrogenase	-	1.1.1.1
34434	beta-galactosidase	+	3.2.1.23
34434	catalase	+	1.11.1.6
34434	DNase	+
34434	gamma-glutamyltransferase	-	2.3.2.2
34434	lysine decarboxylase	-	4.1.1.18
34434	ornithine decarboxylase	-	4.1.1.17
34434	oxidase	-
34434	urease	-	3.5.1.5

Pathway annotation

Computationally determined by

@ref	pathway	enzyme coverage	annotated reactions
66794	ubiquinone biosynthesis	100	7 of 7
66794	CDP-diacylglycerol biosynthesis	100	2 of 2
66794	UDP-GlcNAc biosynthesis	100	3 of 3
66794	coenzyme A metabolism	100	4 of 4
66794	formaldehyde oxidation	100	3 of 3
66794	suberin monomers biosynthesis	100	2 of 2
66794	L-lactaldehyde degradation	100	3 of 3
66794	anapleurotic synthesis of oxalacetate	100	1 of 1
66794	denitrification	100	2 of 2
66794	ppGpp biosynthesis	100	4 of 4
66794	biotin biosynthesis	100	4 of 4
66794	folate polyglutamylation	100	1 of 1
66794	palmitate biosynthesis	95.45	21 of 22
66794	pentose phosphate pathway	90.91	10 of 11
66794	valine metabolism	88.89	8 of 9
66794	lipid A biosynthesis	88.89	8 of 9
66794	chorismate metabolism	88.89	8 of 9
66794	isoleucine metabolism	87.5	7 of 8
66794	photosynthesis	85.71	12 of 14
66794	phenylalanine metabolism	84.62	11 of 13
66794	threonine metabolism	80	8 of 10
66794	peptidoglycan biosynthesis	80	12 of 15
66794	methylglyoxal degradation	80	4 of 5
66794	citric acid cycle	78.57	11 of 14
66794	tetrahydrofolate metabolism	78.57	11 of 14
66794	serine metabolism	77.78	7 of 9
66794	aspartate and asparagine metabolism	77.78	7 of 9
66794	NAD metabolism	77.78	14 of 18
66794	vitamin B1 metabolism	76.92	10 of 13
66794	CMP-KDO biosynthesis	75	3 of 4
66794	C4 and CAM-carbon fixation	75	6 of 8
66794	gluconeogenesis	75	6 of 8
66794	lactate fermentation	75	3 of 4
66794	6-hydroxymethyl-dihydropterin diphosphate biosynthesis	75	6 of 8
66794	butanoate fermentation	75	3 of 4
66794	vitamin B6 metabolism	72.73	8 of 11
66794	propanol degradation	71.43	5 of 7
66794	glutamate and glutamine metabolism	71.43	20 of 28
66794	cardiolipin biosynthesis	71.43	5 of 7
66794	reductive acetyl coenzyme A pathway	71.43	5 of 7
66794	purine metabolism	70.21	66 of 94
66794	acetoin degradation	66.67	2 of 3
66794	d-mannose degradation	66.67	6 of 9
66794	flavin biosynthesis	66.67	10 of 15
66794	heme metabolism	64.29	9 of 14
66794	proline metabolism	63.64	7 of 11
66794	isoprenoid biosynthesis	61.54	16 of 26
66794	methionine metabolism	61.54	16 of 26
66794	Entner Doudoroff pathway	60	6 of 10
66794	propionate fermentation	60	6 of 10
66794	glycolysis	58.82	10 of 17
66794	non-pathway related	57.89	22 of 38
66794	pyrimidine metabolism	57.78	26 of 45
66794	tyrosine metabolism	57.14	8 of 14
66794	CO2 fixation in Crenarchaeota	55.56	5 of 9
66794	arginine metabolism	54.17	13 of 24
66794	leucine metabolism	53.85	7 of 13
66794	histidine metabolism	51.72	15 of 29
66794	alanine metabolism	51.72	15 of 29
66794	cis-vaccenate biosynthesis	50	1 of 2
66794	cyclohexanol degradation	50	2 of 4
66794	ethanol fermentation	50	1 of 2
66794	sulfopterin metabolism	50	2 of 4
66794	glycolate and glyoxylate degradation	50	3 of 6
66794	dTDPLrhamnose biosynthesis	50	4 of 8
66794	acetate fermentation	50	2 of 4
66794	glycogen biosynthesis	50	2 of 4
66794	glutathione metabolism	50	7 of 14
66794	glycine metabolism	50	5 of 10
66794	degradation of aromatic, nitrogen containing compounds	50	6 of 12
66794	adipate degradation	50	1 of 2
66794	quinate degradation	50	1 of 2
66794	ketogluconate metabolism	50	4 of 8
66794	degradation of sugar alcohols	50	8 of 16
66794	ribulose monophosphate pathway	50	1 of 2
66794	cysteine metabolism	50	9 of 18
66794	oxidative phosphorylation	48.35	44 of 91
66794	lysine metabolism	47.62	20 of 42
66794	tryptophan metabolism	47.37	18 of 38
66794	phosphatidylethanolamine bioynthesis	46.15	6 of 13
66794	urea cycle	46.15	6 of 13
66794	lipid metabolism	45.16	14 of 31
66794	factor 420 biosynthesis	40	2 of 5
66794	D-cycloserine biosynthesis	40	2 of 5
66794	glycogen metabolism	40	2 of 5
66794	metabolism of amino sugars and derivatives	40	2 of 5
66794	lipoate biosynthesis	40	2 of 5
66794	hydrogen production	40	2 of 5
66794	cyanate degradation	33.33	1 of 3
66794	selenocysteine biosynthesis	33.33	2 of 6
66794	enterobactin biosynthesis	33.33	1 of 3
66794	molybdenum cofactor biosynthesis	33.33	3 of 9
66794	acetyl CoA biosynthesis	33.33	1 of 3
66794	pantothenate biosynthesis	33.33	2 of 6
66794	(5R)-carbapenem carboxylate biosynthesis	33.33	1 of 3
66794	octane oxidation	33.33	1 of 3
66794	IAA biosynthesis	33.33	1 of 3
66794	sulfate reduction	30.77	4 of 13
66794	polyamine pathway	30.43	7 of 23
66794	coenzyme M biosynthesis	30	3 of 10
66794	4-hydroxyphenylacetate degradation	30	3 of 10
66794	metabolism of disaccharids	27.27	3 of 11
66794	cholesterol biosynthesis	27.27	3 of 11
66794	3-phenylpropionate degradation	26.67	4 of 15
66794	degradation of pentoses	25	7 of 28
66794	toluene degradation	25	1 of 4
66794	catecholamine biosynthesis	25	1 of 4
66794	alginate biosynthesis	25	1 of 4
66794	phenylpropanoid biosynthesis	23.08	3 of 13
66794	carotenoid biosynthesis	22.73	5 of 22
66794	degradation of hexoses	22.22	4 of 18
66794	nitrate assimilation	22.22	2 of 9
66794	4-hydroxymandelate degradation	22.22	2 of 9

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
34434	not determinedn.d.	+	+	+	+	+	-	-	+	+	+	+	+	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	+	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	+	-	-	-	-	-	-	-	-	-	+	-	-	-	-	-	-	-	-	+	-	-	-	-	-	-	+	-	-	-	+	+	-	-	-	-	-	-	-	-	-	-	-	+	+	-	-	-	-	+

Isolation, sampling and environmental information

Isolation source categories

Cat1	Cat2	Cat3
#Host	#Mammals	#Canidae (Dog)
#Host Body-Site	#Oral cavity and airways	#Mouth

Isolation

@ref	Sample type	Sampling date	Country	Country ISO 3 Code	Continent	Isolation date
34434			USA	USA	North America
45214	Dog mouth	1978	USA	USA	North America
34434	Animal, Dog, mouth		United States of America	USA	North America	1978

Interaction and safety

Risk assessment

@ref	Biosafety level	Biosafety level comment
34434	1	Risk group (French classification)

Sequence information

Genome-based predictions

Literature

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 )
#34434	Collection of Institut Pasteur ; Curators of the CIP; CIP 103942
#45214	Culture Collection University of Gothenburg (CCUG) ; Curators of the CCUG; CCUG 9689
#66794	Antje Chang, Lisa Jeske, Sandra Ulbrich, Julia Hofmann, Julia Koblitz, Ida Schomburg, Meina Neumann-Schaal, Dieter Jahn, Dietmar Schomburg: BRENDA, the ELIXIR core data resource in 2021: new developments and updates. Nucleic Acids Res. 49: D498 - D508 2020 ( DOI 10.1093/nar/gkaa1025 , PubMed 33211880 )
#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 )

Rate our new design

Content

About us