Microbacterium esteraromaticum (DSM 8609, ATCC 8091, CCM 4371)

Name: Microbacterium esteraromaticum (DSM 8609, ATCC 8091, CCM 4371)
Creator: BacDive
License: http://creativecommons.org/licenses/by/4.0/

BacDive ID 7399

Type strain

Culture col. no. DSM 8609 ATCC 8091 CCM 4371 IFO 3751 NBRC 3751 12 more

NCBI tax ID(s) 57043

Special Collections DSMZ JCM CIP Wink compendium

History <- IFO <- ATCC <- C.P. Hegarty IFO 3751 <-- ATCC 8091 <-- C. P. Hegarty. CIP <- 1993ATCC, Aureobacterium sp. <- C.P. Hegarty, Georgetown Univ., Flavobacterium esteraromaticum

Links

Microbacterium esteraromaticum DSM 8609 is an obligate aerobe, mesophilic, Gram-positive prokaryote that was isolated from Environment, Soil.

Gram-positive motile rod-shaped obligate aerobe mesophilic genome sequence 16S sequence

Name and taxonomic classification

SI-ID 2822

LMG 4020,ATCC 8091,IFO 3751,NCDO 2277,NCIB 8186,CIP 103916,CCM 4371,DSM 8609,JCM 9172,CCRC 15447,NCFB 2277,NCIMB 8186,VKM Ac-1942,NBRC 3751,BCRC 15447,NRRL B-24213,IAM 15198,VTT E-991287

@ref 20215

Last LPSN update 2026-02-09 11:19:28

Domain Bacteria

Phylum Actinomycetota

Class Actinomycetes

Order Micrococcales

Family Microbacteriaceae

Genus Microbacterium

Species Microbacterium esteraromaticum

Full scientific name Microbacterium esteraromaticum (Omelianski 1923) Takeuchi and Hatano 1998

Synonyms (3)

"Bacterium esteraromaticum"
Aureobacterium esteraromaticum
Flavobacterium esteraromaticum

BacDive ID	Other strains from **Microbacterium esteraromaticum** (4)	Type strain
100775	M. esteraromaticum ST033247(HKI),
136950	M. esteraromaticum CIP 55.80, ATCC 8375, CCM 1948, NCIMB 8535, ...
153129	M. esteraromaticum CCUG 48543
157193	M. esteraromaticum CCUG 70367

Morphology

Cell morphology

@ref	Gram stain	Cell shape	Motility	Confidence
119134	positive	rod-shaped
125439	positive			95.8

Colony morphology

@ref	Colony color	Incubation period	Medium used
20208	Colorless	10-14 days	ISP 2
20208	Beige (1001)	10-14 days	ISP 3
20208	Colorless	10-14 days	ISP 4
20208	Beige (1001)	10-14 days	ISP 5
20208	Colorless	10-14 days	ISP 6
20208	Beige (1001)	10-14 days	ISP 7
119134

Multicellular morphology

@ref	Forms multicellular complex	Medium name
20208		ISP 2
20208		ISP 3
20208		ISP 4
20208		ISP 5
20208		ISP 6
20208		ISP 7

Culture and growth conditions

Culture medium

@ref	Name	Medium link	Composition
3331	TRYPTICASE SOY YEAST EXTRACT MEDIUM (DSMZ Medium 92)	Medium recipe at MediaDive	Name: TRYPTICASE SOY YEAST EXTRACT MEDIUM (DSMZ Medium 92) Composition: Trypticase soy broth 30.0 g/l Agar 15.0 g/l Yeast extract 3.0 g/l Distilled water
20208	ISP 2		Name: ISP 2 / Yeast Malt Agar (5265); 5265 Composition Malt extract 10.0 g/l Yeast extract 4.0 g/l Glucose 4.0 g/l Agar 15.0 g/l Preparation: Sterilisation: 20 minutes at 121°C pH before sterilisation: 7.0 Usage: Maintenance and Taxonomy Organisms: All Actinomycetes
20208	ISP 3		Name: ISP 3; 5315 Composition Dog oat flakes 20.0 g/l Trace element solution (5314) 2.5 ml/l Agar 18.0 g/l Preparation: Oat flakes are cooked for 20 minutes, trace element solution and agar are added (in the case of non rolled oat flakes the suspension has to bee filtrated). Sterilisation: 20 minutes at 121°C pH before sterilisation: 7.8 Usage: Maintenance and taxonomy (e.g. SEM As liquid medium for metabolite production) Organisms: All Actinomycetes Trace element solution 5314 Name: Trace element solution 5314; 5314 Composition CaCl2 x H2O 3.0 g/l Fe-III-citrate 1.0 g/l MnSO4 0.2 g/l ZnCl2 0.1 g/l CuSO4 x 5 H2O 0.025 g/l Sodium tetra borate 0.2 g/l CoCl2 x 6 H2O 0.004 g/l Sodium molybdate 0.01 g/l Preparation: Use double destillated water. Sterilisation: 20 minutes at 121°C pH before sterilisation: Usage: Trace element solution for different media Organisms:
20208	ISP 4		Name: ISP 4; DSM 547 Solution I: Difco soluble starch, 10.0 g. Make a paste of the starch with a small amount of cold distilled water and bring to a volume of 500 ml. Solution II: CaCO3 2.0 g K2HPO4 (anhydrous) 1.0 g MgSO4 x 7 H2O 1.0 g NaCl 1.0 g (NH4)2SO4 2.0 g Distilled water 500.0 ml Trace salt solution (see below) 1.0 ml The pH should be between 7.0 and 7.4. Do not adjust if it is within this range. Mix solutions I and II together. Add 20.0 g agar. Liquify agar by steaming at 100°C for 10 to 20 min. Trace element solution: FeSO4 x 7 H2O 0.1 g MnCl2 x 4 H2O 0.1 g ZnSO4 x 7 H2O 0.1 g Distilled water 100.0 ml
20208	ISP 5		Name: ISP 5 (5323) Composition L-Asparagine 1.0 g/l Glycerol 10.0 g/l K2HPO4 1.0 g/l Salt solution (see preparation) 1.0 ml/l Agar 20.0 g/l Preparation: Salt solution 1.0 g FeSO4 x 7 H2O 1.0 g MnCl2 x 4 H2O 1.0 g ZNSO4 x 7 H2O in 100 ml water Sterilisation: 20 minutes at 121°C pH before sterilisation: 7.2 Usage: Maintenance and taxonomy Organisms: All Actinomycetes
20208	ISP 6		Name: ISP 6 (5318) Composition Peptone 15.0 g/l Proteose peptose 5.0 g/l Ferric ammonium citrate 0.5 g/l Sodium glycerophosphate 1.0 g/l Sodium thiosulfate 0.08 g/l Yeast extract 1.0 g/l Agar 15.0 g/l Sterilisation: 20 minutes at 121°C pH before sterilisation: Usage: Production of melanoid pigments Organisms: All Actinomycetes
20208	ISP 7		Name: ISP 7 (5322) Composition Glycerol 15.0 g/l L-Tyrosine 0.5 g/l L-Asparagine 1.0 g/l K2HPO4 0.5 g/l NaCl 0.5 g/l FeSO4 x 7 H2O 0.01 g/l Trace element solution 5343 1.0 ml/l Agar 20.0 Sterilisation: 20 minutes at 121°C pH before sterilisation: 7.3 Usage: Production of melanoid pigments Organisms: All Actinomycetes
38155	MEDIUM 3 - Columbia agar		Columbia agar (39.000 g);distilled water (1000.000 ml)
119134	CIP Medium 3	Medium recipe at CIP

Culture temp

@ref	Growth	Type	Temperature (°C)	Range
3331	positive	growth	30	mesophilic
20208	positive	optimum	28	mesophilic
38155	positive	growth	30	mesophilic
67770	positive	growth	30	mesophilic
119134	positive	growth	15-37
119134	negative	growth	10
119134	negative	growth	41
119134	negative	growth	45

Physiology and metabolism

Oxygen tolerance

@ref	Oxygen tolerance	Confidence
119134	obligate aerobe
125439	obligate aerobe	99.7

Spore formation

@ref	Spore formation	Confidence
125439		91.9

Halophily

@ref	Salt	Growth	Tested relation	Concentration
119134	NaCl	positive	growth	0-4 %
119134	NaCl		growth	6 %
119134	NaCl		growth	8 %
119134	NaCl		growth	10 %

Murein

@ref	Murein short key	Type
3331	B06	B2ß {Gly} [L-Hsr] D-Glu(Hyg)-Gly-D-Orn

Observation

67770

Observationquinones: MK-12, MK-13

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
119134	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
68379	17634 ChEBI	D-glucose	-	fermentation	from API Coryne
68371	17634 ChEBI	D-glucose	-	builds acid from	from API 50CH acid
68371	62318 ChEBI	D-lyxose	-	builds acid from	from API 50CH acid
68379	16899 ChEBI	D-mannitol	-	fermentation	from API Coryne
68371	16899 ChEBI	D-mannitol	-	builds acid from	from API 50CH acid
68371	16024 ChEBI	D-mannose	-	builds acid from	from API 50CH acid
68379	16988 ChEBI	D-ribose	-	fermentation	from API Coryne
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
68379	65327 ChEBI	D-xylose	-	fermentation	from API Coryne
68371	65327 ChEBI	D-xylose	-	builds acid from	from API 50CH acid
68371	17113 ChEBI	erythritol	-	builds acid from	from API 50CH acid
68379	4853 ChEBI	esculin	+	hydrolysis	from API Coryne
119134	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
68379	5291 ChEBI	gelatin	-	hydrolysis	from API Coryne
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
68379	28087 ChEBI	glycogen	-	fermentation	from API Coryne
68371	28087 ChEBI	glycogen	-	builds acid from	from API 50CH acid
119134	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
68379	17716 ChEBI	lactose	-	fermentation	from API Coryne
68371	17716 ChEBI	lactose	-	builds acid from	from API 50CH acid
68379	17306 ChEBI	maltose	-	fermentation	from API Coryne
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
68379	17632 ChEBI	nitrate	-	reduction	from API Coryne
119134	17632 ChEBI	nitrate	-	reduction
119134	17632 ChEBI	nitrate	-	respiration
119134	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
119134	132112 ChEBI	sodium thiosulfate	+	builds gas from
68371	28017 ChEBI	starch	-	builds acid from	from API 50CH acid
68379	17992 ChEBI	sucrose	-	fermentation	from API Coryne
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
68379	16199 ChEBI	urea	-	hydrolysis	from API Coryne
68371	17151 ChEBI	xylitol	-	builds acid from	from API 50CH acid

Antibiotic resistance

@ref	Metabolite	Is sensitive	Is resistant
119134	0129 (2,4-Diamino-6,7-di-iso-propylpteridine phosphate)

Metabolite production

@ref	Chebi-ID	Metabolite	Production
119134	35581 ChEBI	indole

Metabolite tests

@ref	Chebi-ID	Metabolite	Voges-proskauer-test	Methylred-test
119134	15688 ChEBI	acetoin	-
119134	17234 ChEBI	glucose		-

Enzymes

@ref	Value	Activity	Ec
119134	alcohol dehydrogenase	-	1.1.1.1
68379	alkaline phosphatase	-	3.1.3.1	from API Coryne
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
68379	alpha-glucosidase	+	3.2.1.20	from API Coryne
68382	alpha-mannosidase	+	3.2.1.24	from API zym
119134	amylase	+
119134	beta-galactosidase	+	3.2.1.23
68379	beta-galactosidase	-	3.2.1.23	from API Coryne
68382	beta-glucosidase	+	3.2.1.21	from API zym
68379	beta-glucosidase	+	3.2.1.21	from API Coryne
68379	beta-glucuronidase	-	3.2.1.31	from API Coryne
119134	caseinase	-	3.4.21.50
119134	catalase	+	1.11.1.6
119134	DNase	+
68382	esterase (C 4)	+		from API zym
68382	esterase lipase (C 8)	+		from API zym
119134	gamma-glutamyltransferase	-	2.3.2.2
119134	gelatinase	-
68379	gelatinase	-		from API Coryne
119134	lecithinase	-
68382	leucine arylamidase	+	3.4.11.1	from API zym
119134	lipase	-
119134	lysine decarboxylase	-	4.1.1.18
68379	N-acetyl-beta-glucosaminidase	-	3.2.1.52	from API Coryne
119134	ornithine decarboxylase	-	4.1.1.17
119134	oxidase	+
119134	phenylalanine ammonia-lyase	-	4.3.1.24
119134	protease	+
68379	pyrazinamidase	-	3.5.1.B15	from API Coryne
68379	pyrrolidonyl arylamidase	-	3.4.19.3	from API Coryne
68382	trypsin	+	3.4.21.4	from API zym
119134	tryptophan deaminase	-
119134	tween esterase	+
119134	urease	-	3.5.1.5
68379	urease	-	3.5.1.5	from API Coryne
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	cis-vaccenate biosynthesis	100	2 of 2
66794	phenylacetate degradation (aerobic)	100	5 of 5
66794	threonine metabolism	100	10 of 10
66794	coenzyme A metabolism	100	4 of 4
66794	palmitate biosynthesis	100	22 of 22
66794	denitrification	100	2 of 2
66794	CDP-diacylglycerol biosynthesis	100	2 of 2
66794	UDP-GlcNAc biosynthesis	100	3 of 3
66794	vitamin K metabolism	100	5 of 5
66794	lactate fermentation	100	4 of 4
66794	folate polyglutamylation	100	1 of 1
66794	suberin monomers biosynthesis	100	2 of 2
66794	anapleurotic synthesis of oxalacetate	100	1 of 1
66794	adipate degradation	100	2 of 2
66794	pentose phosphate pathway	90.91	10 of 11
66794	molybdenum cofactor biosynthesis	88.89	8 of 9
66794	NAD metabolism	88.89	16 of 18
66794	chorismate metabolism	88.89	8 of 9
66794	valine metabolism	88.89	8 of 9
66794	gluconeogenesis	87.5	7 of 8
66794	photosynthesis	85.71	12 of 14
66794	glutamate and glutamine metabolism	82.14	23 of 28
66794	starch degradation	80	8 of 10
66794	Entner Doudoroff pathway	80	8 of 10
66794	flavin biosynthesis	80	12 of 15
66794	peptidoglycan biosynthesis	80	12 of 15
66794	methylglyoxal degradation	80	4 of 5
66794	glycogen metabolism	80	4 of 5
66794	gallate degradation	80	4 of 5
66794	citric acid cycle	78.57	11 of 14
66794	serine metabolism	77.78	7 of 9
66794	CO2 fixation in Crenarchaeota	77.78	7 of 9
66794	d-mannose degradation	77.78	7 of 9
66794	purine metabolism	77.66	73 of 94
66794	phenylalanine metabolism	76.92	10 of 13
66794	leucine metabolism	76.92	10 of 13
66794	methionine metabolism	76.92	20 of 26
66794	vitamin B1 metabolism	76.92	10 of 13
66794	glycolysis	76.47	13 of 17
66794	pyrimidine metabolism	75.56	34 of 45
66794	ppGpp biosynthesis	75	3 of 4
66794	acetate fermentation	75	3 of 4
66794	6-hydroxymethyl-dihydropterin diphosphate biosynthesis	75	6 of 8
66794	butanoate fermentation	75	3 of 4
66794	sulfopterin metabolism	75	3 of 4
66794	ketogluconate metabolism	75	6 of 8
66794	glycogen biosynthesis	75	3 of 4
66794	C4 and CAM-carbon fixation	75	6 of 8
66794	isoleucine metabolism	75	6 of 8
66794	proline metabolism	72.73	8 of 11
66794	alanine metabolism	72.41	21 of 29
66794	cardiolipin biosynthesis	71.43	5 of 7
66794	myo-inositol biosynthesis	70	7 of 10
66794	histidine metabolism	68.97	20 of 29
66794	degradation of sugar alcohols	68.75	11 of 16
66794	formaldehyde oxidation	66.67	2 of 3
66794	cyanate degradation	66.67	2 of 3
66794	acetyl CoA biosynthesis	66.67	2 of 3
66794	acetoin degradation	66.67	2 of 3
66794	octane oxidation	66.67	2 of 3
66794	L-lactaldehyde degradation	66.67	2 of 3
66794	tryptophan metabolism	65.79	25 of 38
66794	tetrahydrofolate metabolism	64.29	9 of 14
66794	heme metabolism	64.29	9 of 14
66794	degradation of sugar acids	64	16 of 25
66794	d-xylose degradation	63.64	7 of 11
66794	non-pathway related	63.16	24 of 38
66794	oxidative phosphorylation	62.64	57 of 91
66794	isoprenoid biosynthesis	61.54	16 of 26
66794	urea cycle	61.54	8 of 13
66794	cysteine metabolism	61.11	11 of 18
66794	metabolism of amino sugars and derivatives	60	3 of 5
66794	propionate fermentation	60	6 of 10
66794	lipoate biosynthesis	60	3 of 5
66794	4-hydroxyphenylacetate degradation	60	6 of 10
66794	D-cycloserine biosynthesis	60	3 of 5
66794	phenol degradation	60	12 of 20
66794	arginine metabolism	58.33	14 of 24
66794	ubiquinone biosynthesis	57.14	4 of 7
66794	degradation of pentoses	57.14	16 of 28
66794	propanol degradation	57.14	4 of 7
66794	aspartate and asparagine metabolism	55.56	5 of 9
66794	lipid metabolism	54.84	17 of 31
66794	lysine metabolism	54.76	23 of 42
66794	metabolism of disaccharids	54.55	6 of 11
66794	phenylmercury acetate degradation	50	1 of 2
66794	glycolate and glyoxylate degradation	50	3 of 6
66794	quinate degradation	50	1 of 2
66794	ribulose monophosphate pathway	50	1 of 2
66794	kanosamine biosynthesis II	50	1 of 2
66794	degradation of hexoses	50	9 of 18
66794	ethanol fermentation	50	1 of 2
66794	dTDPLrhamnose biosynthesis	50	4 of 8
66794	vitamin B6 metabolism	45.45	5 of 11
66794	glutathione metabolism	42.86	6 of 14
66794	degradation of aromatic, nitrogen containing compounds	41.67	5 of 12
66794	glycine metabolism	40	4 of 10
66794	3-phenylpropionate degradation	40	6 of 15
66794	arachidonate biosynthesis	40	2 of 5
66794	ethylmalonyl-CoA pathway	40	2 of 5
66794	tyrosine metabolism	35.71	5 of 14
66794	selenocysteine biosynthesis	33.33	2 of 6
66794	enterobactin biosynthesis	33.33	1 of 3
66794	IAA biosynthesis	33.33	1 of 3
66794	lipid A biosynthesis	33.33	3 of 9
66794	sphingosine metabolism	33.33	2 of 6
66794	(5R)-carbapenem carboxylate biosynthesis	33.33	1 of 3
66794	4-hydroxymandelate degradation	33.33	3 of 9
66794	chlorophyll metabolism	33.33	6 of 18
66794	ascorbate metabolism	31.82	7 of 22
66794	androgen and estrogen metabolism	31.25	5 of 16
66794	bile acid biosynthesis, neutral pathway	29.41	5 of 17
66794	mevalonate metabolism	28.57	2 of 7
66794	benzoyl-CoA degradation	28.57	2 of 7
66794	reductive acetyl coenzyme A pathway	28.57	2 of 7
66794	carotenoid biosynthesis	27.27	6 of 22
66794	carnitine metabolism	25	2 of 8
66794	cyclohexanol degradation	25	1 of 4
66794	vitamin E metabolism	25	1 of 4
66794	CMP-KDO biosynthesis	25	1 of 4
66794	toluene degradation	25	1 of 4
66794	phenylpropanoid biosynthesis	23.08	3 of 13
66794	nitrate assimilation	22.22	2 of 9
66794	arachidonic acid metabolism	22.22	4 of 18

API coryne

@ref	Reduction of nitrateNIT	PYZ	PYRA	PAL	beta GUR	beta GAL	alpha GLU	beta NAG	ESC	URE	GEL	Control fermentationControl	GLU	RIB	XYL	MAN	MAL	LAC	SAC	GLYG	CAT
20208	-	-	-	-	-	-	+	-	+	-	-	not determinedn.d.	-	-	-	-	-	-	-	-	not determinedn.d.

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
20208	not determinedn.d.	-	+	+	+	+	+	-	+	-	-	-	-	-	+	+	+	-	+	+
119134	-	+	+	+	-	+	+	+	+	-	+	+	-	+	-	+	+	+	+	+

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
119134	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
119134	not determinedn.d.	+	+	+	+	+	-	-	+	-	+	+	-	-	-	-	+	-	-	+	-	+	-	+	-	-	-	-	-	-	-	-	+	-	-	-	+	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	-	+	+	-	-	-	-	-	-	-	-	-	-	-	+	+	-	+	-	-	+	-	-	-	-	-	-	-	+	-	-	-	+	+	-	+	+	-	-	+	-

Isolation, sampling and environmental information

Isolation

119134

Sample typeEnvironment, Soil

Interaction and safety

Risk assessment

@ref	Biosafety level	Biosafety level comment
3331	1	Risk group (German classification) According to TRBA 466
20208	1	German classification According to TRBA 466
119134	1	Risk group (French classification) According to TRBA 466

Sequence information

Genome sequences

@ref	Description	Assembly level	INSDC accession	BV-BRC accession	IMG accession	NCBI tax ID	Score
66792	ASM1690731v1 assembly for Microbacterium esteraromaticum DSM 8609	contig	GCA_016907315	57043.11	2893536966	57043	78.25
124043	ASM3953392v1 assembly for Microbacterium esteraromaticum JCM 9172	scaffold	GCA_039533925			57043	67.31

16S sequences

@ref	Description	Accession	Length	NCBI tax ID
20218	Microbacterium esteraromaticum 16S rRNA gene	Y17231	1463	57043
124043	Microbacterium esteraromaticum strain DSM 8609 16S ribosomal RNA gene, partial sequence.	MW198114	601	57043
124043	Microbacterium esteraromaticum strain DSM 8609 16S ribosomal RNA gene, partial sequence.	MZ276284	1425	57043
124043	Microbacterium esteraromaticum strain DSM 8609(T) 16S ribosomal RNA gene, partial sequence.	MW111244	609	57043

GC content

@ref	GC-content (mol%)	Method
3331	69	high performance liquid chromatography (HPLC)
67770	68.8	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: Microbacterium esteraromaticum DSM 8609
NCBI: GCA_016907315

@ref	Trait	Model	Prediction	Confidence in %	In training data
125439	spore_formation	BacteriaNetⓘ	no	91.90	no
125439	motility	BacteriaNetⓘ	no	57.90	no
125439	gram_stain	BacteriaNetⓘ	positive	95.80	no
125439	oxygen_tolerance	BacteriaNetⓘ	obligate aerobe	99.70	no

Predictions from bacterial phenotypic traits through improved machine learning using high-quality, curated datasets based on: Microbacterium esteraromaticum strain DSM 8609
PATRIC: 57043.11

@ref	Trait	Model	Prediction	Confidence in %	In training data
125438	gram-positive	gram-positiveⓘ	yes	86.65	no
125438	anaerobic	anaerobicⓘ	no	97.71	yes
125438	spore-forming	spore-formingⓘ	no	80.61	no
125438	aerobic	aerobicⓘ	yes	86.97	no
125438	thermophilic	thermophileⓘ	no	98.46	yes
125438	flagellated	motile2+ⓘ	no	74.75	no

Literature

Topic	Title	Authors	Journal	DOI	Year
Phylogeny	Hydrolytic Exoenzymes Produced by Bacteria Isolated and Identified From the Gastrointestinal Tract of Bombay Duck.	Hossain TJ, Chowdhury SI, Mozumder HA, Chowdhury MNA, Ali F, Rahman N, Dey S.	Front Microbiol	10.3389/fmicb.2020.02097	2020
Phylogeny	Isolation and characterization of endophytic colonizing bacteria from agronomic crops and prairie plants.	Zinniel DK, Lambrecht P, Harris NB, Feng Z, Kuczmarski D, Higley P, Ishimaru CA, Arunakumari A, Barletta RG, Vidaver AK.	Appl Environ Microbiol	10.1128/aem.68.5.2198-2208.2002	2002
Metabolism	Gene cloning and characterization of two NADH-dependent 3-quinuclidinone reductases from Microbacterium luteolum JCM 9174.	Isotani K, Kurokawa J, Suzuki F, Nomoto S, Negishi T, Matsuda M, Itoh N.	Appl Environ Microbiol	10.1128/aem.03099-12	2013
	Isolation and characterization of multi-drug-resistant Microbacterium esteraromaticum bacteriophage: assessment of antibacterial efficacy and genomic insights.	Cheng S, Wang H, Zhang K, Liu F, Gao X, Du L.	Int Microbiol	10.1007/s10123-025-00703-1	2025
Pathogenicity	Enzymatic degradation of Ochratoxin A by a novel bacterium, Microbacterium esteraromaticum ASAG1016.	Jia R, Zhao J, Tian S, Sadiq FA, Lu S, Gao P, Zhang G.	Int J Food Microbiol	10.1016/j.ijfoodmicro.2025.111155	2025
	Bioremediation of polyaromatic hydrocarbon polluted sewage sludge soil employing a bacterial consortium and phytotoxicity evaluation.	Khan G, Tiwari A, Patel DK, Anbumani S, Manickam N.	Lett Appl Microbiol	10.1093/lambio/ovae130	2024
	Exploring the potential of a new marine bacterium associated with plastisphere to metabolize dibutyl phthalate and bis(2-ethylhexyl) phthalate by enrichment cultures combined with multi-omics analysis.	Sun Y, Zhang Y, Ma Y, Xin R, Li X, Niu Z.	Environ Pollut	10.1016/j.envpol.2023.123146	2024
Phylogeny	Novel BTEX-degrading strains from subsurface soil: Isolation, identification and growth evaluation.	Kaur G, Lecka J, Krol M, Brar SK.	Environ Pollut	10.1016/j.envpol.2023.122303	2023
	Enzymatic modification of native chitin and chitin oligosaccharides by an alkaline chitin deacetylase from Microbacterium esteraromaticum MCDA02.	Yang G, Hou X, Lu J, Wang M, Wang Y, Huang Y, Liu Q, Liu S, Fang Y.	Int J Biol Macromol	10.1016/j.ijbiomac.2022.01.167	2022
	Microbially Derived P=S and P=Se Bond Formation.	Trotter CL, Era Y, Gordon R, Law S, Switzer CH, Wallace S.	JACS Au	10.1021/jacsau.5c00262	2025
	Enhancing hexahydro-1, 3, 5-trinitro-1, 3, 5-triazine (RDX) remediation through water-dispersible Microbacterium esteraromaticum granules.	Yadav S, Sharma A, Khan MA, Sharma R, Celin M, Malik A, Sharma S.	J Environ Manage	10.1016/j.jenvman.2020.110446	2020
	Characterization of novel cold-active chitin deacetylase for green production of bioactive chitosan.	Abd El-Ghany MN, Hamdi SA, Zahran AK, Abou-Taleb MA, Heikel AM, Abou El-Kheir MT, Farahat MG.	AMB Express	10.1186/s13568-024-01804-2	2025
	Microbial degradation and community structure analysis of hydroxyl-terminated polybutadiene (HTPB).	Zhang Y, Zou M, Lodhi AF, Deng YL.	AMB Express	10.1186/s13568-021-01334-1	2021
	Characterization and properties of the biosurfactant produced by PAH-degrading bacteria isolated from contaminated oily sludge environment.	Tripathi V, Gaur VK, Dhiman N, Gautam K, Manickam N.	Environ Sci Pollut Res Int	10.1007/s11356-019-05591-3	2020
	Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model.	Kim WH, Choi WJ, Kim JE, Choi J, Hong YD, Nam J, Park WS, Shim SM.	Curr Res Pharmacol Drug Discov	10.1016/j.crphar.2023.100165	2023
	Improved polycyclic aromatic hydrocarbon degradation in a crude oil by individual and a consortium of bacteria.	Kumari S, Regar RK, Manickam N.	Bioresour Technol	10.1016/j.biortech.2018.01.075	2018
	Transformation of Ginsenosides by Lactiplantibacillus plantarum MB11 Fermentation: Minor Ginsenosides Conversion and Enhancement of Anti-Colorectal Cancer Activity.	Shen Y, Gao Y, Yang G, Zhao Z, Zhao Y, Gao L, Zhao L, Li S.	Molecules	10.3390/molecules29010027	2023
	Biotransformation of High Concentrations of Ginsenoside Substrate into Compound K by beta-glycosidase from Sulfolobus solfataricus.	Wang P, Tang C, Liu Y, Yang J, Fan D.	Genes (Basel)	10.3390/genes14040897	2023
	Deep learning for HGT insertion sites recognition.	Li C, Chen J, Li SC.	BMC Genomics	10.1186/s12864-020-07296-1	2020
Phylogeny	Phenanthrene Degradation by Photosynthetic Bacterial Consortium Dominated by Fischerella sp.	Marquez-Villa JM, Rodriguez-Sierra JC, Amtanus Chequer N, Cob-Calan NN, Garcia-Maldonado JQ, Cadena S, Hernandez-Nunez E.	Life (Basel)	10.3390/life13051108	2023
	Bioconversion of BIOGF1K, a compound-K-rich fraction from ginseng root and its effect on epidermal barrier function.	Kim WH, Kim JE, Kim S, Na Y, Hong YD, Choi J, Park WS, Shim SM.	Heliyon	10.1016/j.heliyon.2023.e14803	2023
Enzymology	Isolation and characterization of novel ginsenoside-hydrolyzing glycosidase from Microbacterium esteraromaticum that transforms ginsenoside Rb2 to rare ginsenoside 20(S)-Rg3.	Quan LH, Wang C, Jin Y, Wang TR, Kim YJ, Yang DC.	Antonie Van Leeuwenhoek	10.1007/s10482-013-9933-1	2013
Metabolism	Enzymatic transformation of the major ginsenoside Rb2 to minor compound Y and compound K by a ginsenoside-hydrolyzing beta-glycosidase from Microbacterium esteraromaticum.	Quan LH, Jin Y, Wang C, Min JW, Kim YJ, Yang DC.	J Ind Microbiol Biotechnol	10.1007/s10295-012-1158-1	2012
Metabolism	Enzymatic biotransformation of ginsenoside Rb1 to compound K by recombinant beta-glucosidase from Microbacterium esteraromaticum.	Quan LH, Min JW, Jin Y, Wang C, Kim YJ, Yang DC.	J Agric Food Chem	10.1021/jf300186a	2012
Metabolism	Enzymatic biotransformation of ginsenoside Rb1 to 20(S)-Rg3 by recombinant beta-glucosidase from Microbacterium esteraromaticum.	Quan LH, Min JW, Yang DU, Kim YJ, Yang DC.	Appl Microbiol Biotechnol	10.1007/s00253-011-3861-7	2012
	Enhanced Bioremediation of Aged Polycyclic Aromatic Hydrocarbons in Soil Using Immobilized Microbial Consortia Combined with Strengthening Remediation Strategies.	Zhou H, Gao X, Wang S, Zhang Y, Coulon F, Cai C.	Int J Environ Res Public Health	10.3390/ijerph20031766	2023
	Expression and Molecular Modification of Chitin Deacetylase from Streptomyces bacillaris.	Yin L, Wang Q, Sun J, Mao X.	Molecules	10.3390/molecules28010113	2022
	Airborne bacteria in show caves from Southern Spain.	Dominguez-Monino I, Jurado V, Rogerio-Candelera MA, Hermosin B, Saiz-Jimenez C.	Microb Cell	10.15698/mic2021.10.762	2021
	Bioprospecting from plant waste composting: Actinobacteria against phytopathogens producing damping-off.	Jurado MM, Suarez-Estrella F, Lopez MJ, Lopez-Gonzalez JA, Moreno J.	Biotechnol Rep (Amst)	10.1016/j.btre.2019.e00354	2019
	Degradation of a mixture of 13 polycyclic aromatic hydrocarbons by commercial effective microorganisms.	Ksiazek-Trela P, Figura D, Wezka D, Szpyrka E.	Open Life Sci	10.1515/biol-2022-0831	2024
	Ecology and resistance to UV light and antibiotics of microbial communities on UV cabins in the dermatology service of a Spanish hospital.	Molina-Menor E, Carlotto N, Vidal-Verdu A, Perez-Ferriols A, Perez-Pastor G, Porcar M.	Sci Rep	10.1038/s41598-023-40996-8	2023
	Optimization and Chemical Characterization of Biosurfactant Produced from a Novel Pseudomonas guguanensis Strain Iraqi ZG.K.M.	Ghazi Faisal Z, Sallal Mahdi M, Alobaidi KH.	Int J Microbiol	10.1155/2023/1571991	2023
Enzymology	Production of Minor Ginsenosides C-K and C-Y from Naturally Occurring Major Ginsenosides Using Crude beta-Glucosidase Preparation from Submerged Culture of Fomitella fraxinea.	Kim DW, Lee WJ, Gebru YA, Upadhyaya J, Ko SR, Kim YH, Kim MK.	Molecules	10.3390/molecules26164820	2021
	Study on the Biochemical Characterization and Selectivity of Three beta-Glucosidases From Bifidobacterium adolescentis ATCC15703.	Hu Y, Zhai L, Hong H, Shi Z, Zhao J, Liu D.	Front Microbiol	10.3389/fmicb.2022.860014	2022
Metabolism	Hydrolysis of fenamiphos and its toxic oxidation products by Microbacterium sp. in pure culture and groundwater.	Caceres TP, Megharaj M, Malik S, Beer M, Naidu R.	Bioresour Technol	10.1016/j.biortech.2008.12.043	2009
Enzymology	Novel enzymatic elimination method for the chromatographic purification of ginsenoside Rb₃ in an isomeric mixture.	Cui CH, Fu Y, Jeon BM, Kim SC, Im WT.	J Ginseng Res	10.1016/j.jgr.2019.08.003	2020
Enzymology	Isolation and diversity analysis of arsenite-resistant bacteria in communities enriched from deep-sea sediments of the Southwest Indian Ocean Ridge.	Chen S, Shao Z.	Extremophiles	10.1007/s00792-008-0195-1	2009
	Molecular Cloning and Functional Characterization of a beta-Glucosidase Gene to Produce Platycodin D in Platycodon grandiflorus.	Su X, Meng F, Liu Y, Jiang W, Wang Z, Wu L, Guo X, Yao X, Wu J, Sun Z, Zha L, Gui S, Peng D, Xing S.	Front Plant Sci	10.3389/fpls.2022.955628	2022
Phylogeny	Isolation, characterization, and genome sequencing of a novel chitin deacetylase producing Bacillus aryabhattai TCI-16.	Liang YY, Yan LQ, Tan MH, Li GH, Fang JH, Peng JY, Li KT.	Front Microbiol	10.3389/fmicb.2022.999639	2022
Metabolism	Isolation and characterization of biosurfactant-producing Alcanivorax strains: hydrocarbon accession strategies and alkane hydroxylase gene analysis.	Olivera NL, Nievas ML, Lozada M, Del Prado G, Dionisi HM, Sineriz F.	Res Microbiol	10.1016/j.resmic.2008.09.011	2009
Enzymology	Identification and characterization of a ginsenoside-transforming beta-glucosidase from Pseudonocardia sp. Gsoil 1536 and its application for enhanced production of minor ginsenoside Rg2(S).	Du J, Cui CH, Park SC, Kim JK, Yu HS, Jin FX, Sun C, Kim SC, Im WT.	PLoS One	10.1371/journal.pone.0096914	2014
	Coaggregation between Acinetobacter johnsonii S35 and Microbacterium esteraromaticum strains isolated from sewage activated sludge.	Malik A, Sakamoto M, Ono T, Kakii K.	J Biosci Bioeng	10.1016/s1389-1723(03)90090-9	2003
Enzymology	MALDI-TOF mass spectrometry and identification of new bacteria species in air samples from Makkah, Saudi Arabia.	Angelakis E, Yasir M, Azhar EI, Papadioti A, Bibi F, Aburizaiza AS, Metidji S, Memish ZA, Ashshi AM, Hassan AM, Harakeh S, Gautret P, Raoult D.	BMC Res Notes	10.1186/1756-0500-7-892	2014
Genetics	Cytobacts: Abundant and Diverse Vertically Seed-Transmitted Cultivation-Recalcitrant Intracellular Bacteria Ubiquitous to Vascular Plants.	Thomas P, Rajendran TP, Franco CMM.	Front Microbiol	10.3389/fmicb.2022.806222	2022
	Microbiome Structure of the Aphid Myzus persicae (Sulzer) Is Shaped by Different Solanaceae Plant Diets.	He B, Chen X, Yang H, Cernava T.	Front Microbiol	10.3389/fmicb.2021.667257	2021
Metabolism	Effects of pH amendment on metal working fluid wastewater biological treatment using a defined bacterial consortium.	van der Gast CJ, Thompson IP.	Biotechnol Bioeng	10.1002/bit.20351	2005
	Pair-dependent co-aggregation behavior of non-flocculating sludge bacteria.	Malik A, Kakii K.	Biotechnol Lett	10.1023/a:1024009511113	2003
Metabolism	Identification and characterization of a Mucilaginibacter sp. strain QM49 beta-glucosidase and its use in the production of the pharmaceutically active minor ginsenosides (S)-Rh1 and (S)-Rg2.	Cui CH, Liu QM, Kim JK, Sung BH, Kim SG, Kim SC, Im WT.	Appl Environ Microbiol	10.1128/aem.01150-13	2013
Genetics	Genome sequencing of strain Cellulosimicrobium sp. TH-20 with ginseng biotransformation ability.	Zheng F, Zhang W, Chu X, Dai Y, Li J, Zhao H, Wen L, Yue H, Yu S.	3 Biotech	10.1007/s13205-017-0850-2	2017
Phylogeny	Response of Tomato Rhizosphere Bacteria to Root-Knot Nematodes, Fenamiphos and Sampling Time Shows Differential Effects on Low Level Taxa.	Colagiero M, Rosso LC, Catalano D, Schena L, Ciancio A.	Front Microbiol	10.3389/fmicb.2020.00390	2020
	Microbial communities in the native habitats of Agaricus sinodeliciosus from Xinjiang Province revealed by amplicon sequencing.	Zhou J, Bai X, Zhao R.	Sci Rep	10.1038/s41598-017-16082-1	2017
Biotechnology	Optimization of single plate-serial dilution spotting (SP-SDS) with sample anchoring as an assured method for bacterial and yeast cfu enumeration and single colony isolation from diverse samples.	Thomas P, Sekhar AC, Upreti R, Mujawar MM, Pasha SS.	Biotechnol Rep (Amst)	10.1016/j.btre.2015.08.003	2015
Phylogeny	Union of the genera Microbacterium Orla-Jensen and Aureobacterium Collins et al. in a redefined genus Microbacterium.	Takeuchi M, Hatano K.	Int J Syst Bacteriol	10.1099/00207713-48-3-739	1998
Pathogenicity	Effect of Fermented Red Ginseng Extract Enriched in Ginsenoside Rg3 on the Differentiation and Mineralization of Preosteoblastic MC3T3-E1 Cells.	Siddiqi MZ, Siddiqi MH, Kim YJ, Jin Y, Huq MA, Yang DC.	J Med Food	10.1089/jmf.2014.3251	2015
	Enzymatic Biotransformation of Ginsenoside Rb1 and Gypenoside XVII into Ginsenosides Rd and F2 by Recombinant beta-glucosidase from Flavobacterium johnsoniae.	Hong H, Cui CH, Kim JK, Jin FX, Kim SC, Im WT.	J Ginseng Res	10.5142/jgr.2012.36.4.418	2012
	Microbial biocatalysis of quercetin-3-glucoside and isorhamnetin-3-glucoside in Salicornia herbacea and their contribution to improved anti-inflammatory activity.	Ahn HJ, You HJ, Park MS, Li Z, Choe D, Johnston TV, Ku S, Ji GE.	RSC Adv	10.1039/c9ra08059g	2020
	Improved conversion of ginsenoside Rb₁ to compound K by semi-rational design of Sulfolobus solfataricus beta-glycosidase.	Shin KC, Choi HY, Seo MJ, Oh DK.	AMB Express	10.1186/s13568-017-0487-x	2017
Metabolism	Enhanced Production of Gypenoside LXXV Using a Novel Ginsenoside-Transforming beta-Glucosidase from Ginseng-Cultivating Soil Bacteria and Its Anti-Cancer Property.	Cui CH, Kim DJ, Jung SC, Kim SC, Im WT.	Molecules	10.3390/molecules22050844	2017
	Dalangtan Playa (Qaidam Basin, NW China): Its microbial life and physicochemical characteristics and their astrobiological implications.	Huang T, Wang R, Xiao L, Wang H, Martinez JM, Escudero C, Amils R, Cheng Z, Xu Y.	PLoS One	10.1371/journal.pone.0200949	2018
	Compound K Production from Red Ginseng Extract by beta-Glycosidase from Sulfolobus solfataricus Supplemented with alpha-L-Arabinofuranosidase from Caldicellulosiruptor saccharolyticus.	Shin KC, Choi HY, Seo MJ, Oh DK.	PLoS One	10.1371/journal.pone.0145876	2015
Enzymology	Coaggregation among nonflocculating bacteria isolated from activated sludge.	Malik A, Sakamoto M, Hanazaki S, Osawa M, Suzuki T, Tochigi M, Kakii K.	Appl Environ Microbiol	10.1128/aem.69.10.6056-6063.2003	2003
	Rhizosphere Microbiome Recruited from a Suppressive Compost Improves Plant Fitness and Increases Protection against Vascular Wilt Pathogens of Tomato.	Antoniou A, Tsolakidou MD, Stringlis IA, Pantelides IS.	Front Plant Sci	10.3389/fpls.2017.02022	2017
	Proteomics and Transcriptomics Uncover Key Processes for Elasnin Tolerance in Methicillin-Resistant Staphylococcus aureus.	Sulaiman JE, Long L, Qian PY, Lam H.	mSystems	10.1128/msystems.01393-21	2022
Enzymology	Catheter-related Microbacterium bacteremia identified by 16S rRNA gene sequencing.	Lau SK, Woo PC, Woo GK, Yuen KY.	J Clin Microbiol	10.1128/jcm.40.7.2681-2685.2002	2002
Phylogeny	Proposal of six new species in the genus Aureobacterium and transfer of Flavobacterium esteraromaticum Omelianski to the genus Aureobacterium as Aureobacterium esteraromaticum comb. nov.	Yokota A, Takeuchi M, Sakane T, Weiss N	Int J Syst Bacteriol	10.1099/00207713-43-3-555	1993
Phylogeny	Microbacterium aerolatum sp. nov., isolated from the air in the 'Virgilkapelle' in Vienna.	Zlamala C, Schumann P, Kampfer P, Valens M, Rossello-Mora R, Lubitz W, Busse HJ.	Int J Syst Evol Microbiol	10.1099/00207713-52-4-1229	2002
Phylogeny	Microbacterium suwonense sp. nov., isolated from cow dung.	Anandham R, Tamura T, Hamada M, Weon HY, Kim SJ, Kim YS, Suzuki K, Kwon SW	J Microbiol	10.1007/s12275-011-1036-y	2011
Phylogeny	Microbacterium soli sp. nov., an alpha-glucosidase-producing bacterium isolated from soil of a ginseng field.	Srinivasan S, Kim MK, Sathiyaraj G, Kim YJ, Jung SK, In JG, Yang DC	Int J Syst Evol Microbiol	10.1099/ijs.0.012526-0	2009

References

#3331	Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 8609
#20208	Wink, J.: Compendium of Actinobacteria. HZI-Helmholtz-Centre for Infection Research, Braunschweig .
#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 )
#38155	; Curators of the CIP;
#66792	Julia Koblitz, Joaquim Sardà, Lorenz Christian Reimer, Boyke Bunk, Jörg Overmann: Automatically annotated for the DiASPora project (Digital Approaches for the Synthesis of Poorly Accessible Biodiversity Information) .
#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 .
#68379	Automatically annotated from API Coryne .
#68382	Automatically annotated from API zym .
#119134	Collection of Institut Pasteur ; Curators of the CIP; CIP 103916
#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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Microbacterium esteraromaticum (DSM 8609, ATCC 8091, CCM 4371)

Name and taxonomic classification

Morphology

Cell morphology

Colony morphology

Multicellular morphology

Culture and growth conditions

Culture medium

Culture temp

Physiology and metabolism

Oxygen tolerance

Spore formation

Halophily

Murein

Observation

Metabolite utilization

Antibiotic resistance

Metabolite production

Metabolite tests

Enzymes

Pathway annotation

API coryne

API zym

API 50CHac

API biotype100

Isolation, sampling and environmental information

Isolation

Interaction and safety

Risk assessment

Sequence information

Genome sequences

Genome browser: GCA_016907315

16S sequences

GC content

Genome-based predictions

Predictions

Literature

Literature

References

BacDive

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