Rossellomorea aquimaris (DSM 16205, JCM 11545, KCCM 41589)

Name: Rossellomorea aquimaris (DSM 16205, JCM 11545, KCCM 41589)
Creator: BacDive
License: http://creativecommons.org/licenses/by/4.0/

BacDive ID 1225

Type strain

Strain Designation TF-12

Culture col. no. DSM 16205 JCM 11545 KCCM 41589 TF-12 CIP 108136

NCBI tax ID(s) 189382

Special Collections DSMZ JCM CIP Literature strains

Links

Rossellomorea aquimaris TF-12 is an aerobe, spore-forming, mesophilic prokaryote that forms circular colonies and was isolated from sea water of a tidal flat.

spore-forming Gram-variable motile rod-shaped colony-forming aerobe mesophilic genome sequence 16S sequence

Name and taxonomic classification

SI-ID 81585

JCM 11545,DSM 16205,CIP 108136,KCTC 3903,LMG 23073

@ref 20215

Last LPSN update 2025-12-16 09:47:03

Domain Bacillati

Phylum Bacillota

Class Bacilli

Order Caryophanales

Family Bacillaceae

Genus Rossellomorea

Species Rossellomorea aquimaris

Full scientific name Rossellomorea aquimaris (Yoon et al. 2003) Gupta et al. 2020

Synonyms (1)

Bacillus aquimaris

Morphology

Cell morphology

@ref	Gram stain	Cell length	Cell width	Cell shape	Motility	Flagellum arrangement
23314	variable	1.2-3.5 µm	0.5-0.7 µm	rod-shaped		peritrichous
116458	positive			rod-shaped

Colony morphology

@ref	Colony size	Colony color	Colony shape	Incubation period	Medium used	Hemolysis ability
23314	2-4 mm	pale orange-yellow	circular	3-4 days	MA
116458						1

Culture and growth conditions

Culture medium

@ref	Name	Medium link	Composition
6324	BACTO MARINE BROTH (DIFCO 2216) (DSMZ Medium 514)	Medium recipe at MediaDive	Name: BACTO MARINE BROTH (DIFCO 2216) (DSMZ Medium 514) Composition: NaCl 19.45 g/l MgCl2 5.9 g/l Bacto peptone 5.0 g/l Na2SO4 3.24 g/l CaCl2 1.8 g/l Yeast extract 1.0 g/l KCl 0.55 g/l NaHCO3 0.16 g/l Fe(III) citrate 0.1 g/l KBr 0.08 g/l SrCl2 0.034 g/l H3BO3 0.022 g/l Na2HPO4 0.008 g/l Na-silicate 0.004 g/l NaF 0.0024 g/l (NH4)NO3 0.0016 g/l Distilled water
23314	Marine agar (MA)
32894	Marine agar (MA)		Distilled water make up to (1000.000 ml);Marine agar (55.100 g)
116458	CIP Medium 13	Medium recipe at CIP
116458	CIP Medium 72	Medium recipe at CIP

Culture temp

@ref	Growth	Type	Temperature (°C)	Range
6324	positive	growth	30	mesophilic
23314	positive	growth	10-44
23314	negative	growth	4
23314	negative	growth	>45
23314	positive	optimum	30-37	mesophilic
32894	positive	growth	30	mesophilic
67770	positive	growth	30	mesophilic
116458	positive	growth	10-45
116458	negative	growth	55

Culture pH

@ref	Ability	Type	PH
23314	positive	optimum	6.0-7.0
23314		growth	9.0
23314		growth	4.5
116458		growth	6

Physiology and metabolism

Oxygen tolerance

@ref	Oxygen tolerance	Confidence
23314	aerobe
116458	obligate aerobe
125439	obligate aerobe	96.2

Spore formation

@ref	Spore description	Type of spore	Confidence
23314	ellipsoidal, central, large swollen sporangia	endospore
116458
125439			94.4
125438			93.653

Halophily

@ref	Salt	Growth	Tested relation	Concentration	Halophily level
23314	NaCl	positive	optimum	2-5 %
23314	NaCl	inconsistent	growth	0 %
23314	NaCl	positive	maximum	18 %
23314					moderately halophilic
116458	NaCl		growth	0 %
116458	NaCl		growth	2 %
116458	NaCl		growth	4 %
116458	NaCl		growth	6 %
116458	NaCl		growth	8 %
116458	NaCl		growth	10 %

Observation

67770

Observationquinones: MK-7

Metabolite utilization

@ref	Chebi-ID	Metabolite	Utilization activity	Kind of utilization tested
23314	16808 ChEBI	2-dehydro-D-gluconate	-	builds acid from
23314	17426 ChEBI	5-dehydro-D-gluconate	-	builds acid from
23314	17426 ChEBI	5-dehydro-D-gluconate	+	builds acid from
23314	27613 ChEBI	amygdalin	-	builds acid from
68371	27613 ChEBI	amygdalin	-	builds acid from	from API 50CH acid
23314	18305 ChEBI	arbutin	-	builds acid from
23314	18305 ChEBI	arbutin	+	builds acid from
68371	18305 ChEBI	arbutin	-	builds acid from	from API 50CH acid
23314		casein	+	hydrolysis
23314	17057 ChEBI	cellobiose	-	builds acid from
23314	17057 ChEBI	cellobiose	+	builds acid from
68371	17057 ChEBI	cellobiose	-	builds acid from	from API 50CH acid
116458	16947 ChEBI	citrate	-	carbon source
23314	17108 ChEBI	D-arabinose	-	builds acid from
68371	17108 ChEBI	D-arabinose	-	builds acid from	from API 50CH acid
23314	18333 ChEBI	D-arabitol	-	builds acid from
68371	18333 ChEBI	D-arabitol	-	builds acid from	from API 50CH acid
23314	15824 ChEBI	D-fructose	+	builds acid from
68371	15824 ChEBI	D-fructose	+	builds acid from	from API 50CH acid
23314	28847 ChEBI	D-fucose	-	builds acid from
68371	28847 ChEBI	D-fucose	-	builds acid from	from API 50CH acid
23314	12936 ChEBI	D-galactose	-	builds acid from
23314	12936 ChEBI	D-galactose	+/-	builds acid from
68371	12936 ChEBI	D-galactose	-	builds acid from	from API 50CH acid
23314	17634 ChEBI	D-glucose	+	builds acid from
68371	17634 ChEBI	D-glucose	+	builds acid from	from API 50CH acid
23314	62318 ChEBI	D-lyxose	-	builds acid from
68371	62318 ChEBI	D-lyxose	-	builds acid from	from API 50CH acid
23314	16899 ChEBI	D-mannitol	-	builds acid from
23314	16899 ChEBI	D-mannitol	+	builds acid from
68371	16899 ChEBI	D-mannitol	-	builds acid from	from API 50CH acid
23314	16024 ChEBI	D-mannose	-	builds acid from
23314	16024 ChEBI	D-mannose	+	builds acid from
68371	16024 ChEBI	D-mannose	-	builds acid from	from API 50CH acid
23314	16988 ChEBI	D-ribose	+	builds acid from
68371	16988 ChEBI	D-ribose	+	builds acid from	from API 50CH acid
23314	17924 ChEBI	D-sorbitol	-	builds acid from
68371	17924 ChEBI	D-sorbitol	-	builds acid from	from API 50CH acid
23314	16443 ChEBI	D-tagatose	-	builds acid from
68371	16443 ChEBI	D-tagatose	-	builds acid from	from API 50CH acid
23314	16551 ChEBI	D-trehalose	+	builds acid from
23314	65327 ChEBI	D-xylose	-	builds acid from
23314	65327 ChEBI	D-xylose	+	builds acid from
68371	65327 ChEBI	D-xylose	-	builds acid from	from API 50CH acid
23314	17113 ChEBI	erythritol	-	builds acid from
68371	17113 ChEBI	erythritol	-	builds acid from	from API 50CH acid
23314	4853 ChEBI	esculin	-	builds acid from
23314	4853 ChEBI	esculin	-	hydrolysis
23314	4853 ChEBI	esculin	+	builds acid from
23314	4853 ChEBI	esculin	+	hydrolysis
116458	4853 ChEBI	esculin	-	hydrolysis
68371	4853 ChEBI	esculin	+	builds acid from	from API 50CH acid
23314	16813 ChEBI	galactitol	-	builds acid from
68371	16813 ChEBI	galactitol	-	builds acid from	from API 50CH acid
23314	28066 ChEBI	gentiobiose	+	builds acid from
68371	28066 ChEBI	gentiobiose	-	builds acid from	from API 50CH acid
23314	24265 ChEBI	gluconate	-	builds acid from
68371	24265 ChEBI	gluconate	-	builds acid from	from API 50CH acid
23314	17754 ChEBI	glycerol	+	builds acid from
23314	28087 ChEBI	glycogen	-	builds acid from
23314	28087 ChEBI	glycogen	+	builds acid from
68371	28087 ChEBI	glycogen	+	builds acid from	from API 50CH acid
116458	606565 ChEBI	hippurate	-	hydrolysis
23314	17368 ChEBI	hypoxanthine	-	hydrolysis
23314	15443 ChEBI	inulin	-	builds acid from
68371	15443 ChEBI	inulin	-	builds acid from	from API 50CH acid
23314	30849 ChEBI	L-arabinose	-	builds acid from
68371	30849 ChEBI	L-arabinose	-	builds acid from	from API 50CH acid
23314	18403 ChEBI	L-arabitol	-	builds acid from
68371	18403 ChEBI	L-arabitol	-	builds acid from	from API 50CH acid
23314	18287 ChEBI	L-fucose	-	builds acid from
68371	18287 ChEBI	L-fucose	-	builds acid from	from API 50CH acid
23314	62345 ChEBI	L-rhamnose	-	builds acid from
68371	62345 ChEBI	L-rhamnose	-	builds acid from	from API 50CH acid
23314	17266 ChEBI	L-sorbose	-	builds acid from
68371	17266 ChEBI	L-sorbose	-	builds acid from	from API 50CH acid
23314	65328 ChEBI	L-xylose	-	builds acid from
68371	65328 ChEBI	L-xylose	-	builds acid from	from API 50CH acid
23314	17716 ChEBI	lactose	-	builds acid from
68371	17716 ChEBI	lactose	-	builds acid from	from API 50CH acid
23314	17306 ChEBI	maltose	+	builds acid from
68371	17306 ChEBI	maltose	+	builds acid from	from API 50CH acid
23314	6731 ChEBI	melezitose	-	builds acid from
68371	6731 ChEBI	melezitose	-	builds acid from	from API 50CH acid
23314	28053 ChEBI	melibiose	-	builds acid from
23314	28053 ChEBI	melibiose	+	builds acid from
68371	28053 ChEBI	melibiose	-	builds acid from	from API 50CH acid
23314	320061 ChEBI	methyl alpha-D-glucopyranoside	-	builds acid from
68371	320061 ChEBI	methyl alpha-D-glucopyranoside	-	builds acid from	from API 50CH acid
23314	43943 ChEBI	methyl alpha-D-mannoside	-	builds acid from
23314	43943 ChEBI	methyl alpha-D-mannoside	+	builds acid from
68371	43943 ChEBI	methyl alpha-D-mannoside	-	builds acid from	from API 50CH acid
23314	74863 ChEBI	methyl beta-D-xylopyranoside	-	builds acid from
68371	74863 ChEBI	methyl beta-D-xylopyranoside	-	builds acid from	from API 50CH acid
23314	17268 ChEBI	myo-inositol	-	builds acid from
68371	17268 ChEBI	myo-inositol	-	builds acid from	from API 50CH acid
23314	506227 ChEBI	N-acetylglucosamine	-	builds acid from
68371	59640 ChEBI	N-acetylglucosamine	-	builds acid from	from API 50CH acid
116458	17632 ChEBI	nitrate	-	reduction
116458	17632 ChEBI	nitrate	-	respiration
116458	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
23314	16634 ChEBI	raffinose	-	builds acid from
23314	16634 ChEBI	raffinose	+/-	builds acid from
68371	16634 ChEBI	raffinose	-	builds acid from	from API 50CH acid
23314	15963 ChEBI	ribitol	-	builds acid from
68371	15963 ChEBI	ribitol	-	builds acid from	from API 50CH acid
23314	17814 ChEBI	salicin	-	builds acid from
23314	17814 ChEBI	salicin	+	builds acid from
68371	17814 ChEBI	salicin	-	builds acid from	from API 50CH acid
23314	17164 ChEBI	stachyose	-	builds acid from
23314	17164 ChEBI	stachyose	+	builds acid from
23314	28017 ChEBI	starch	-	builds acid from
23314	28017 ChEBI	starch	-	hydrolysis
23314	28017 ChEBI	starch	+	builds acid from
23314	28017 ChEBI	starch	+	hydrolysis
68371	28017 ChEBI	starch	+	builds acid from	from API 50CH acid
23314	17992 ChEBI	sucrose	+	builds acid from
68371	27082 ChEBI	trehalose	+	builds acid from	from API 50CH acid
23314	32528 ChEBI	turanose	-	builds acid from
68371	32528 ChEBI	turanose	-	builds acid from	from API 50CH acid
23314	53426 ChEBI	tween 80	-	hydrolysis
23314	53426 ChEBI	tween 80	+	hydrolysis
23314	18186 ChEBI	tyrosine	-	hydrolysis
23314	15318 ChEBI	xanthine	-	hydrolysis
23314	17151 ChEBI	xylitol	-	builds acid from
68371	17151 ChEBI	xylitol	-	builds acid from	from API 50CH acid

Metabolite production

@ref	Chebi-ID	Metabolite	Production
116458	35581 ChEBI	indole

Metabolite tests

@ref	Chebi-ID	Metabolite	Voges-proskauer-test	Methylred-test
116458	15688 ChEBI	acetoin	-
116458	17234 ChEBI	glucose		+

Enzymes

@ref	Value	Activity	Ec
68382	acid phosphatase	-	3.1.3.2	from API zym
116458	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
116458	amylase	+
68382	beta-galactosidase	-	3.2.1.23	from API zym
116458	beta-galactosidase	+	3.2.1.23
68382	beta-glucosidase	-	3.2.1.21	from API zym
68382	beta-glucuronidase	-	3.2.1.31	from API zym
116458	caseinase	+	3.4.21.50
23314	catalase	+	1.11.1.6
116458	catalase	+	1.11.1.6
68382	cystine arylamidase	-	3.4.11.3	from API zym
23314	cytochrome oxidase	-	1.9.3.1
116458	DNase	+
68382	esterase (C 4)	-		from API zym
68382	esterase lipase (C 8)	+		from API zym
116458	gamma-glutamyltransferase	+	2.3.2.2
116458	gelatinase	+/-
116458	lecithinase	-
68382	leucine arylamidase	-	3.4.11.1	from API zym
116458	lipase	+
68382	lipase (C 14)	-		from API zym
116458	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
116458	ornithine decarboxylase	-	4.1.1.17
116458	oxidase	-
116458	protease	+
68382	trypsin	-	3.4.21.4	from API zym
116458	tween esterase	-
23314	urease	-	3.5.1.5
116458	urease	-	3.5.1.5
68382	valine arylamidase	-		from API zym

Pathway annotation

Computationally determined by

@ref	pathway	enzyme coverage	annotated reactions
66794	cellulose degradation	100	5 of 5
66794	acetoin degradation	100	3 of 3
66794	butanoate fermentation	100	4 of 4
66794	vitamin K metabolism	100	5 of 5
66794	ribulose monophosphate pathway	100	2 of 2
66794	methylglyoxal degradation	100	5 of 5
66794	starch degradation	100	10 of 10
66794	pentose phosphate pathway	100	11 of 11
66794	enterobactin biosynthesis	100	3 of 3
66794	aspartate and asparagine metabolism	100	9 of 9
66794	adipate degradation	100	2 of 2
66794	lipoate biosynthesis	100	5 of 5
66794	gluconeogenesis	100	8 of 8
66794	formaldehyde oxidation	100	3 of 3
66794	anapleurotic synthesis of oxalacetate	100	1 of 1
66794	aerobactin biosynthesis	100	1 of 1
66794	acetate fermentation	100	4 of 4
66794	folate polyglutamylation	100	1 of 1
66794	coenzyme A metabolism	100	4 of 4
66794	suberin monomers biosynthesis	100	2 of 2
66794	UDP-GlcNAc biosynthesis	100	3 of 3
66794	CDP-diacylglycerol biosynthesis	100	2 of 2
66794	teichoic acid biosynthesis	100	1 of 1
66794	biotin biosynthesis	100	4 of 4
66794	threonine metabolism	100	10 of 10
66794	palmitate biosynthesis	95.45	21 of 22
66794	vitamin B1 metabolism	92.31	12 of 13
66794	serine metabolism	88.89	8 of 9
66794	valine metabolism	88.89	8 of 9
66794	pyrimidine metabolism	88.89	40 of 45
66794	chorismate metabolism	88.89	8 of 9
66794	C4 and CAM-carbon fixation	87.5	7 of 8
66794	flavin biosynthesis	86.67	13 of 15
66794	peptidoglycan biosynthesis	86.67	13 of 15
66794	glutamate and glutamine metabolism	85.71	24 of 28
66794	tetrahydrofolate metabolism	85.71	12 of 14
66794	reductive acetyl coenzyme A pathway	85.71	6 of 7
66794	leucine metabolism	84.62	11 of 13
66794	glycolate and glyoxylate degradation	83.33	5 of 6
66794	alanine metabolism	82.76	24 of 29
66794	purine metabolism	80.85	76 of 94
66794	methionine metabolism	80.77	21 of 26
66794	glycine betaine biosynthesis	80	4 of 5
66794	Entner Doudoroff pathway	80	8 of 10
66794	metabolism of amino sugars and derivatives	80	4 of 5
66794	glycogen metabolism	80	4 of 5
66794	propionate fermentation	80	8 of 10
66794	photosynthesis	78.57	11 of 14
66794	citric acid cycle	78.57	11 of 14
66794	d-mannose degradation	77.78	7 of 9
66794	molybdenum cofactor biosynthesis	77.78	7 of 9
66794	CO2 fixation in Crenarchaeota	77.78	7 of 9
66794	NAD metabolism	77.78	14 of 18
66794	phenylalanine metabolism	76.92	10 of 13
66794	glycolysis	76.47	13 of 17
66794	sulfopterin metabolism	75	3 of 4
66794	glycogen biosynthesis	75	3 of 4
66794	ppGpp biosynthesis	75	3 of 4
66794	isoleucine metabolism	75	6 of 8
66794	6-hydroxymethyl-dihydropterin diphosphate biosynthesis	75	6 of 8
66794	proline metabolism	72.73	8 of 11
66794	propanol degradation	71.43	5 of 7
66794	heme metabolism	71.43	10 of 14
66794	cardiolipin biosynthesis	71.43	5 of 7
66794	histidine metabolism	68.97	20 of 29
66794	tryptophan metabolism	68.42	26 of 38
66794	non-pathway related	68.42	26 of 38
66794	cyanate degradation	66.67	2 of 3
66794	arginine metabolism	66.67	16 of 24
66794	acetyl CoA biosynthesis	66.67	2 of 3
66794	L-lactaldehyde degradation	66.67	2 of 3
66794	selenocysteine biosynthesis	66.67	4 of 6
66794	degradation of sugar alcohols	62.5	10 of 16
66794	dTDPLrhamnose biosynthesis	62.5	5 of 8
66794	ketogluconate metabolism	62.5	5 of 8
66794	urea cycle	61.54	8 of 13
66794	phosphatidylethanolamine bioynthesis	61.54	8 of 13
66794	isoprenoid biosynthesis	61.54	16 of 26
66794	oxidative phosphorylation	60.44	55 of 91
66794	phenylacetate degradation (aerobic)	60	3 of 5
66794	3-chlorocatechol degradation	60	3 of 5
66794	lipid metabolism	58.06	18 of 31
66794	glutathione metabolism	57.14	8 of 14
66794	tyrosine metabolism	57.14	8 of 14
66794	cysteine metabolism	55.56	10 of 18
66794	d-xylose degradation	54.55	6 of 11
66794	pantothenate biosynthesis	50	3 of 6
66794	dolichol and dolichyl phosphate biosynthesis	50	1 of 2
66794	kanosamine biosynthesis II	50	1 of 2
66794	degradation of hexoses	50	9 of 18
66794	CMP-KDO biosynthesis	50	2 of 4
66794	cis-vaccenate biosynthesis	50	1 of 2
66794	glycine metabolism	50	5 of 10
66794	lysine metabolism	50	21 of 42
66794	ethanol fermentation	50	1 of 2
66794	degradation of pentoses	46.43	13 of 28
66794	vitamin B6 metabolism	45.45	5 of 11
66794	metabolism of disaccharids	45.45	5 of 11
66794	ubiquinone biosynthesis	42.86	3 of 7
66794	degradation of aromatic, nitrogen containing compounds	41.67	5 of 12
66794	gallate degradation	40	2 of 5
66794	bacilysin biosynthesis	40	2 of 5
66794	hydrogen production	40	2 of 5
66794	4-hydroxyphenylacetate degradation	40	4 of 10
66794	myo-inositol biosynthesis	40	4 of 10
66794	polyamine pathway	39.13	9 of 23
66794	phenylpropanoid biosynthesis	38.46	5 of 13
66794	ascorbate metabolism	36.36	8 of 22
66794	octane oxidation	33.33	1 of 3
66794	lipid A biosynthesis	33.33	3 of 9
66794	nitrate assimilation	33.33	3 of 9
66794	IAA biosynthesis	33.33	1 of 3
66794	(5R)-carbapenem carboxylate biosynthesis	33.33	1 of 3
66794	4-hydroxymandelate degradation	33.33	3 of 9
66794	degradation of sugar acids	32	8 of 25
66794	sulfate reduction	30.77	4 of 13
66794	coenzyme M biosynthesis	30	3 of 10
66794	arachidonic acid metabolism	27.78	5 of 18
66794	cholesterol biosynthesis	27.27	3 of 11
66794	phenol degradation	25	5 of 20
66794	lactate fermentation	25	1 of 4
66794	cyclohexanol degradation	25	1 of 4
66794	toluene degradation	25	1 of 4
66794	androgen and estrogen metabolism	25	4 of 16
66794	allantoin degradation	22.22	2 of 9

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
116458	-	+	-	+	-	-	-	-	-	+	-	-	-	-	-	-	-	-	+	-

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
116458	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
116458	not determinedn.d.	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	+	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-

Isolation, sampling and environmental information

Isolation source categories

Cat1	Cat2	Cat3
#Environmental	#Aquatic	#Marine
#Environmental	#Terrestrial	#Tidal flat

Isolation

@ref	Sample type	Geographic location	Country	Country ISO 3 Code	Continent
6324	sea water of a tidal flat	Yellow Sea	Republic of Korea	KOR	Asia
67770	Seawater of a tidal flat of the Yellow Sea		Republic of Korea	KOR	Asia
116458	Environment, Tidal flat	Yellow sea	Republic of Korea	KOR	Asia

Taxonmaps

69479

Global distribution of 16S sequence AF483625 (>99% sequence identity) for Bacillus from Microbeatlas

Aquatic Samples	996
Soil Samples	945
Animal Samples	294
Plant Samples	97
Total Samples	2332

Interaction and safety

Risk assessment

@ref	Biosafety level	Biosafety level comment
6324	1	Risk group (German classification) According to TRBA 466
116458	1	Risk group (French classification) According to TRBA 466

Sequence information

Genome sequences

@ref	Description	Assembly level	INSDC accession	IMG accession	NCBI tax ID	Score
67770	ASM164855v1 assembly for Rossellomorea aquimaris TF-12 TF12	contig	GCA_001648555	2731957964	1073842	62.54

16S sequences

@ref	Description	Accession	Length	Database	NCBI tax ID
6324	Bacillus aquaemaris strain TF-12 16S ribosomal RNA gene, partial sequence	AF483625	1507		1073842

GC content

@ref	GC-content (mol%)	Method
6324	38	high performance liquid chromatography (HPLC)
23314	38.00	high performance liquid chromatography (HPLC)

Genome-based predictions

Predictions

Predictions from Deep Learning for Genome Sequence Data. R package version 0.3.1 based on: Rossellomorea aquimaris TF-12 TF12
NCBI: GCA_001648555

@ref	Trait	Model	Prediction	Confidence in %	In training data
125439	spore_formation	BacteriaNetⓘ	yes	94.40	no
125439	motility	BacteriaNetⓘ	yes	87.10	no
125439	gram_stain	BacteriaNetⓘ	variable	78.70	no
125439	oxygen_tolerance	BacteriaNetⓘ	obligate aerobe	96.20	no

Predictions from bacterial phenotypic traits through improved machine learning using high-quality, curated datasets based on: Rossellomorea aquimaris TF-12 TF12
NCBI: GCA_001648555.1

@ref	Trait	Model	Prediction	Confidence in %	In training data
125438	gram-positive	gram-positiveⓘ	yes	78.90	no
125438	anaerobic	anaerobicⓘ	no	90.10	no
125438	aerobic	aerobicⓘ	yes	82.08	yes
125438	spore-forming	spore-formingⓘ	yes	93.65	yes
125438	thermophilic	thermophileⓘ	no	88.79	no
125438	flagellated	motile2+ⓘ	yes	86.40	yes

Literature

Topic	Title	Authors	Journal	DOI	Year
Phylogeny	Bacillus salacetis sp. nov., a slightly halophilic bacterium from Thai shrimp paste (Ka-pi).	Daroonpunt R, Yiamsombut S, Sitdhipol J, Tanasupawat S	Int J Syst Evol Microbiol	10.1099/ijsem.0.003286	2019
Phylogeny	Bacillus haikouensis sp. nov., a facultatively anaerobic halotolerant bacterium isolated from a paddy soil.	Li J, Yang G, Lu Q, Zhao Y, Zhou S	Antonie Van Leeuwenhoek	10.1007/s10482-014-0248-7	2014
Phylogeny	Bacillus oryzaecorticis sp. nov., a moderately halophilic bacterium isolated from rice husks.	Hong SW, Kwon SW, Kim SJ, Kim SY, Kim JJ, Lee JS, Oh MH, Kim AJ, Chung KS	Int J Syst Evol Microbiol	10.1099/ijs.0.058768-0	2014
Phylogeny	Bacillus seohaeanensis sp. nov., a halotolerant bacterium that contains L-lysine in its cell wall.	Lee JC, Lim JM, Park DJ, Jeon CO, Li WJ, Kim CJ	Int J Syst Evol Microbiol	10.1099/ijs.0.64237-0	2006
Phylogeny	Bacillus marisflavi sp. nov. and Bacillus aquimaris sp. nov., isolated from sea water of a tidal flat of the Yellow Sea in Korea.	Yoon JH, Kim IG, Kang KH, Oh TK, Park YH	Int J Syst Evol Microbiol	10.1099/ijs.0.02365-0	2003

References

#6324	Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 16205
#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 )
#23314	Jung-Hoon Yoon, In-Gi Kim, Kook Hee Kang, Tae-Kwang Oh, Yong-Ha Park: Bacillus marisflavi sp. nov. and Bacillus aquimaris sp. nov., isolated from sea water of a tidal flat of the Yellow Sea in Korea. IJSEM 53: 1297 - 1303 2003 ( DOI 10.1099/ijs.0.02365-0 , PubMed 13130010 )
#32894	; Curators of the CIP;
#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 )
#67770	Japan Collection of Microorganism (JCM) ; Curators of the JCM;
#68371	Automatically annotated from API 50CH acid .
#68382	Automatically annotated from API zym .
#69479	João F Matias Rodrigues, Janko Tackmann,Gregor Rot, Thomas SB Schmidt, Lukas Malfertheiner, Mihai Danaila,Marija Dmitrijeva, Daniela Gaio, Nicolas Näpflin and Christian von Mering. University of Zurich.: MicrobeAtlas 1.0 beta .
#116458	Collection of Institut Pasteur ; Curators of the CIP; CIP 108136
#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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Rossellomorea aquimaris (DSM 16205, JCM 11545, KCCM 41589)

Name and taxonomic classification

Morphology

Cell morphology

Colony morphology

Culture and growth conditions

Culture medium

Culture temp

Culture pH

Physiology and metabolism

Oxygen tolerance

Spore formation

Halophily

Observation

Metabolite utilization

Metabolite production

Metabolite tests

Enzymes

Pathway annotation

API zym

API 50CHac

API biotype100

Isolation, sampling and environmental information

Isolation source categories

Isolation

Taxonmaps

Interaction and safety

Risk assessment

Sequence information

Genome sequences

Genome browser: GCA_001648555

16S sequences

GC content

Genome-based predictions

Predictions

Literature

Literature

References

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