Name: Chelatococcus asaccharovorans TE2
Creator: BacDive
License: http://creativecommons.org/licenses/by-nc/4.0/

Strain identifier

BacDive ID: 1652

Type strain:

Species: Chelatococcus asaccharovorans

Strain Designation: TE2

Culture col. no.: DSM 6462, ATCC 51531

Strain history: <- T. Egli; TE2

NCBI tax ID(s): 28210 (species)

SI-ID 43036

ATCC 51531, DSM 6462, KACC 10923, NCIMB 13984, VTT E-072692, LMG 25503

Other strains from Chelatococcus asaccharovorans

C. asaccharovorans TE1, DSM 6461

Section

Chelatococcus asaccharovorans TE2 is a mesophilic, coccus-shaped bacterium that was isolated from waste water and soil.

coccus-shaped
mesophilic
16S sequence
Bacteria
genome sequence

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

	Last LPSN update	14-12-2023 (DD-MM-YYYY)
	Domain	"Bacteria"
	Phylum	*Pseudomonadota*
	Class	*Alphaproteobacteria*
	Order	*Hyphomicrobiales*
	Family	*Chelatococcaceae*
	Genus	*Chelatococcus*
	Species	**Chelatococcus asaccharovorans**
	Full Scientific Name (LPSN)	Chelatococcus asaccharovorans Auling et al. 1993

Information on morphological and physiological properties Morphology

[Ref.: #69480]	Gram stain	negative Confidence in %99.875

[Ref.: #23363]	Cell shape	coccus-shaped

[Ref.: #23363]	Motility	no

Information on culture and growth conditions Culture and growth conditions

[Ref.: #2685]

Culture medium

PLATE COUNT AGAR (DSMZ Medium 464)

[Ref.: #2685]

Culture medium growth

[Ref.: #2685]

Culture medium link

Medium recipe at MediaDive

[Ref.: #2685]

Culture medium composition

expand / minimize

[Ref.: #2685]

Culture medium

NITRILOTRIACETATE MEDIUM (DSMZ Medium 463)

[Ref.: #2685]

Culture medium growth

[Ref.: #2685]

Culture medium link

Medium recipe at MediaDive

[Ref.: #2685]

Culture medium composition

expand / minimize

	Temperatures	Kind of temperature		Temperature
[Ref.: #2685]			growth	30 °C

[Ref.: #2685]

Temperature range

mesophilic

		pH
[Ref.: #23363]	maximum	9.5
[Ref.: #23363]	minimum	5.5
[Ref.: #23363]	optimum	7.0-8.0

Information on physiology and metabolism Physiology and metabolism

[Ref.: #69481]	Ability of spore formation	no Confidence in %100
[Ref.: #69480]	Ability of spore formation	no Confidence in %99.989

[Ref.: #2685]	Name of produced compound	iminodiacetate dehydrogenase
[Ref.: #2685]	Name of produced compound	nitrilotriacetate monooxygenase

	Halophily	Salt	Tested relation		Salt conc.
[Ref.: #23363]		NaCl		growth	0-2.5	%(w/v)

	Metabolite	Utilization activity	Kind of utilization tested
[Ref.: #23146]	2-dehydro-D-gluconate ChEBI	+	carbon source
[Ref.: #23146]	5-dehydro-D-gluconate ChEBI	+	carbon source
[Ref.: #23146]	adipate ChEBI	+	carbon source
[Ref.: #23146]	amygdalin ChEBI	-	builds acid from
[Ref.: #23146]	amygdalin ChEBI	-	carbon source
[Ref.: #23146]	arabinose ChEBI	-	builds acid from
[Ref.: #23363]	arabinose ChEBI	+	builds acid from
[Ref.: #23146]	arbutin ChEBI	-	carbon source
[Ref.: #23146]	casein	-	hydrolysis
[Ref.: #23363]	cellobiose ChEBI	-	carbon source
[Ref.: #23146]	cellobiose ChEBI	-	carbon source
[Ref.: #23146]	citrate ChEBI	-	carbon source
[Ref.: #23363]	cysteine ChEBI	+	carbon source
[Ref.: #23363]	D-arabinose ChEBI	+	carbon source
[Ref.: #23146]	D-arabinose ChEBI	+	carbon source
[Ref.: #23146]	D-arabitol ChEBI	-	carbon source
[Ref.: #23146]	D-lyxose ChEBI	+	carbon source
[Ref.: #23146]	D-tagatose ChEBI	-	carbon source
[Ref.: #23146]	D-xylose ChEBI	+	carbon source
[Ref.: #23146]	erythritol ChEBI	-	carbon source
[Ref.: #23363]	esculin ChEBI	-	carbon source
[Ref.: #23146]	esculin ChEBI	-	carbon source
[Ref.: #23146]	esculin ChEBI	+	hydrolysis
[Ref.: #23146]	fructose ChEBI	-	carbon source
[Ref.: #23146]	galactitol ChEBI	-	carbon source
[Ref.: #23363]	galactose ChEBI	-	carbon source
[Ref.: #23146]	galactose ChEBI	-	carbon source
[Ref.: #23146]	gelatin ChEBI	-	hydrolysis
[Ref.: #23363]	gelatin ChEBI	+	hydrolysis
[Ref.: #23146]	gentiobiose ChEBI	-	carbon source
[Ref.: #23363]	gluconate ChEBI	+	carbon source
[Ref.: #23146]	gluconate ChEBI	+	carbon source
[Ref.: #23146]	glucose ChEBI	-	builds acid from
[Ref.: #23363]	glucose ChEBI	+	builds acid from
[Ref.: #23146]	glucose ChEBI	+	carbon source
[Ref.: #23363]	glycerol ChEBI	-	carbon source
[Ref.: #23146]	glycerol ChEBI	-	carbon source
[Ref.: #23363]	glycine ChEBI	+	carbon source
[Ref.: #23146]	glycogen ChEBI	-	carbon source
[Ref.: #23146]	hydrogen sulfide ChEBI	-	other
[Ref.: #23146]	hypoxanthine ChEBI	-	hydrolysis
[Ref.: #23146]	inulin ChEBI	-	carbon source
[Ref.: #23146]	L-arabinose ChEBI	+	carbon source
[Ref.: #23146]	L-arabitol ChEBI	-	carbon source
[Ref.: #23146]	L-fucose ChEBI	+	carbon source
[Ref.: #23146]	L-tyrosine ChEBI	-	hydrolysis
[Ref.: #23146]	L-xylose ChEBI	+/-	carbon source
[Ref.: #23146]	lactose ChEBI	-	carbon source
[Ref.: #23363]	lysine ChEBI	-	carbon source
[Ref.: #23146]	malate ChEBI	+	carbon source
[Ref.: #23146]	maltose ChEBI	-	carbon source
[Ref.: #23146]	mannitol ChEBI	-	builds acid from
[Ref.: #23146]	mannitol ChEBI	-	carbon source
[Ref.: #23363]	mannose ChEBI	+	carbon source
[Ref.: #23146]	mannose ChEBI	+	carbon source
[Ref.: #23146]	melezitose ChEBI	-	carbon source
[Ref.: #23146]	melibiose ChEBI	-	builds acid from
[Ref.: #23146]	melibiose ChEBI	-	carbon source
[Ref.: #23363]	methionine ChEBI	-	carbon source
[Ref.: #23146]	methyl alpha-D-glucopyranoside ChEBI	-	carbon source
[Ref.: #23146]	methyl alpha-D-mannoside ChEBI	-	carbon source
[Ref.: #23146]	methyl beta-D-xylopyranoside ChEBI	-	carbon source
[Ref.: #23146]	myo-inositol ChEBI	-	builds acid from
[Ref.: #23363]	myo-inositol ChEBI	-	carbon source
[Ref.: #23146]	myo-inositol ChEBI	-	carbon source
[Ref.: #23363]	myo-inositol ChEBI	+	builds acid from
[Ref.: #23146]	N-acetylglucosamine ChEBI	-	carbon source
[Ref.: #23146]	phenylacetate ChEBI	+	carbon source
[Ref.: #23146]	raffinose ChEBI	-	carbon source
[Ref.: #23146]	rhamnose ChEBI	-	builds acid from
[Ref.: #23363]	rhamnose ChEBI	-	carbon source
[Ref.: #23363]	rhamnose ChEBI	+	builds acid from
[Ref.: #23146]	rhamnose ChEBI	+	carbon source
[Ref.: #23363]	ribitol ChEBI	-	carbon source
[Ref.: #23146]	ribitol ChEBI	-	carbon source
[Ref.: #23146]	ribose ChEBI	+	carbon source
[Ref.: #23363]	salicin ChEBI	-	carbon source
[Ref.: #23146]	salicin ChEBI	-	carbon source
[Ref.: #23146]	sorbitol ChEBI	-	builds acid from
[Ref.: #23146]	sorbitol ChEBI	-	carbon source
[Ref.: #23146]	sorbose ChEBI	-	carbon source
[Ref.: #23146]	starch ChEBI	-	carbon source
[Ref.: #23146]	starch ChEBI	-	hydrolysis
[Ref.: #23146]	sucrose ChEBI	-	builds acid from
[Ref.: #23146]	sucrose ChEBI	-	carbon source
[Ref.: #23363]	threonine ChEBI	-	carbon source
[Ref.: #23146]	trehalose ChEBI	-	carbon source
[Ref.: #23146]	turanose ChEBI	-	carbon source
[Ref.: #23146]	tween 20 ChEBI	-	hydrolysis
[Ref.: #23146]	tween 40 ChEBI	-	hydrolysis
[Ref.: #23146]	tween 60 ChEBI	-	hydrolysis
[Ref.: #23146]	tween 80 ChEBI	-	hydrolysis
[Ref.: #23363]	tyrosine ChEBI	-	carbon source
[Ref.: #23146]	xanthine ChEBI	-	hydrolysis
[Ref.: #23363]	xylitol ChEBI	-	carbon source
[Ref.: #23146]	xylitol ChEBI	-	carbon source
[Ref.: #23363]	xylose ChEBI	+	carbon source
	Only first 10 entries are displayed. Click here to see all.

	Metabolite	Antibiotic sensitivity
[Ref.: #23146]	ampicillin ChEBI	yes
[Ref.: #23146]	carbenicillin ChEBI	yes
[Ref.: #23146]	cephalothin ChEBI	yes
[Ref.: #23146]	chloramphenicol ChEBI	no
[Ref.: #23146]	gentamicin ChEBI	yes
[Ref.: #23146]	kanamycin ChEBI	yes
[Ref.: #23146]	lincomycin ChEBI	yes
[Ref.: #23146]	neomycin ChEBI	yes
[Ref.: #23146]	novobiocin ChEBI	yes
[Ref.: #23146]	oleandomycin ChEBI	yes
[Ref.: #23146]	penicillin g ChEBI	yes
[Ref.: #23146]	polymyxin b ChEBI	yes
[Ref.: #23146]	streptomycin ChEBI	no
[Ref.: #23146]	tetracycline ChEBI	yes
	Only first 10 entries are displayed. Click here to see all.

	Enzyme	Enzyme activity	EC number
[Ref.: #23146]	acid phosphatase	+	3.1.3.2
[Ref.: #23146]	alkaline phosphatase	+	3.1.3.1
[Ref.: #23146]	alpha-chymotrypsin	-	3.4.21.1
[Ref.: #23146]	alpha-fucosidase	-	3.2.1.51
[Ref.: #23146]	alpha-galactosidase	-	3.2.1.22
[Ref.: #23146]	alpha-glucosidase	-	3.2.1.20
[Ref.: #23146]	alpha-mannosidase	-	3.2.1.24
[Ref.: #23146]	arginine dihydrolase	+	3.5.3.6
[Ref.: #23146]	beta-galactosidase	-	3.2.1.23
[Ref.: #23146]	beta-glucosidase	-	3.2.1.21
[Ref.: #23146]	beta-glucuronidase	-	3.2.1.31
[Ref.: #23146]	cystine arylamidase	-	3.4.11.3
[Ref.: #23146]	cytochrome oxidase	+	1.9.3.1
[Ref.: #23146]	esterase (C 4)	+
[Ref.: #23146]	esterase lipase (C 8)	+
[Ref.: #23146]	leucine arylamidase	+	3.4.11.1
[Ref.: #23146]	lipase (C 14)	-
[Ref.: #23146]	lysine decarboxylase	-	4.1.1.18
[Ref.: #23146]	N-acetyl-beta-glucosaminidase	-	3.2.1.52
[Ref.: #23146]	naphthol-AS-BI-phosphohydrolase	+
[Ref.: #23146]	nitrate reductase	+	1.7.99.4
[Ref.: #23146]	ornithine decarboxylase	-	4.1.1.17
[Ref.: #23146]	trypsin	-	3.4.21.4
[Ref.: #23146]	tryptophan deaminase	-	4.1.99.1
[Ref.: #23146]	urease	+	3.5.1.5
[Ref.: #23146]	valine arylamidase	-
	Only first 10 entries are displayed. Click here to see all.

	Pathway	Enzyme coverage	Annotated reactions
	Pathway annotation	Computationally determined by
[Ref.: #66794]	L-lactaldehyde degradation	100	3 of 3
[Ref.: #66794]	CMP-KDO biosynthesis	100	4 of 4
[Ref.: #66794]	butanoate fermentation	100	4 of 4
[Ref.: #66794]	resorcinol degradation	100	2 of 2
[Ref.: #66794]	valine metabolism	100	9 of 9
[Ref.: #66794]	UDP-GlcNAc biosynthesis	100	3 of 3
[Ref.: #66794]	ketogluconate metabolism	100	8 of 8
[Ref.: #66794]	cardiolipin biosynthesis	100	7 of 7
[Ref.: #66794]	gallate degradation	100	5 of 5
[Ref.: #66794]	denitrification	100	2 of 2
[Ref.: #66794]	teichoic acid biosynthesis	100	1 of 1
[Ref.: #66794]	ribulose monophosphate pathway	100	2 of 2
[Ref.: #66794]	cis-vaccenate biosynthesis	100	2 of 2
[Ref.: #66794]	phenylacetate degradation (aerobic)	100	5 of 5
[Ref.: #66794]	starch degradation	100	10 of 10
[Ref.: #66794]	formaldehyde oxidation	100	3 of 3
[Ref.: #66794]	CDP-diacylglycerol biosynthesis	100	2 of 2
[Ref.: #66794]	methylglyoxal degradation	100	5 of 5
[Ref.: #66794]	C4 and CAM-carbon fixation	100	8 of 8
[Ref.: #66794]	adipate degradation	100	2 of 2
[Ref.: #66794]	4-hydroxymandelate degradation	100	9 of 9
[Ref.: #66794]	palmitate biosynthesis	100	22 of 22
[Ref.: #66794]	folate polyglutamylation	100	1 of 1
[Ref.: #66794]	anapleurotic synthesis of oxalacetate	100	1 of 1
[Ref.: #66794]	ethanol fermentation	100	2 of 2
[Ref.: #66794]	threonine metabolism	100	10 of 10
[Ref.: #66794]	ppGpp biosynthesis	100	4 of 4
[Ref.: #66794]	suberin monomers biosynthesis	100	2 of 2
[Ref.: #66794]	gluconeogenesis	100	8 of 8
[Ref.: #66794]	aerobactin biosynthesis	100	1 of 1
[Ref.: #66794]	phenol degradation	95	19 of 20
[Ref.: #66794]	citric acid cycle	92.86	13 of 14
[Ref.: #66794]	leucine metabolism	92.31	12 of 13
[Ref.: #66794]	phenylalanine metabolism	92.31	12 of 13
[Ref.: #66794]	degradation of sugar acids	92	23 of 25
[Ref.: #66794]	pentose phosphate pathway	90.91	10 of 11
[Ref.: #66794]	propionate fermentation	90	9 of 10
[Ref.: #66794]	Entner Doudoroff pathway	90	9 of 10
[Ref.: #66794]	lipid A biosynthesis	88.89	8 of 9
[Ref.: #66794]	chorismate metabolism	88.89	8 of 9
[Ref.: #66794]	molybdenum cofactor biosynthesis	88.89	8 of 9
[Ref.: #66794]	CO2 fixation in Crenarchaeota	88.89	8 of 9
[Ref.: #66794]	NAD metabolism	88.89	16 of 18
[Ref.: #66794]	reductive acetyl coenzyme A pathway	85.71	6 of 7
[Ref.: #66794]	tyrosine metabolism	85.71	12 of 14
[Ref.: #66794]	ubiquinone biosynthesis	85.71	6 of 7
[Ref.: #66794]	propanol degradation	85.71	6 of 7
[Ref.: #66794]	glutamate and glutamine metabolism	85.71	24 of 28
[Ref.: #66794]	vitamin B12 metabolism	85.29	29 of 34
[Ref.: #66794]	tryptophan metabolism	84.21	32 of 38
[Ref.: #66794]	purine metabolism	84.04	79 of 94
[Ref.: #66794]	alanine metabolism	82.76	24 of 29
[Ref.: #66794]	methionine metabolism	80.77	21 of 26
[Ref.: #66794]	3-chlorocatechol degradation	80	4 of 5
[Ref.: #66794]	glycogen metabolism	80	4 of 5
[Ref.: #66794]	flavin biosynthesis	80	12 of 15
[Ref.: #66794]	4-hydroxyphenylacetate degradation	80	8 of 10
[Ref.: #66794]	creatinine degradation	80	4 of 5
[Ref.: #66794]	ethylmalonyl-CoA pathway	80	4 of 5
[Ref.: #66794]	metabolism of amino sugars and derivatives	80	4 of 5
[Ref.: #66794]	peptidoglycan biosynthesis	80	12 of 15
[Ref.: #66794]	photosynthesis	78.57	11 of 14
[Ref.: #66794]	serine metabolism	77.78	7 of 9
[Ref.: #66794]	aspartate and asparagine metabolism	77.78	7 of 9
[Ref.: #66794]	cysteine metabolism	77.78	14 of 18
[Ref.: #66794]	d-mannose degradation	77.78	7 of 9
[Ref.: #66794]	lysine metabolism	76.19	32 of 42
[Ref.: #66794]	histidine metabolism	75.86	22 of 29
[Ref.: #66794]	glycogen biosynthesis	75	3 of 4
[Ref.: #66794]	sulfopterin metabolism	75	3 of 4
[Ref.: #66794]	isoleucine metabolism	75	6 of 8
[Ref.: #66794]	acetate fermentation	75	3 of 4
[Ref.: #66794]	degradation of sugar alcohols	75	12 of 16
[Ref.: #66794]	biotin biosynthesis	75	3 of 4
[Ref.: #66794]	6-hydroxymethyl-dihydropterin diphosphate biosynthesis	75	6 of 8
[Ref.: #66794]	toluene degradation	75	3 of 4
[Ref.: #66794]	lipid metabolism	74.19	23 of 31
[Ref.: #66794]	non-pathway related	73.68	28 of 38
[Ref.: #66794]	oxidative phosphorylation	73.63	67 of 91
[Ref.: #66794]	pyrimidine metabolism	73.33	33 of 45
[Ref.: #66794]	3-phenylpropionate degradation	73.33	11 of 15
[Ref.: #66794]	metabolism of disaccharids	72.73	8 of 11
[Ref.: #66794]	proline metabolism	72.73	8 of 11
[Ref.: #66794]	tetrahydrofolate metabolism	71.43	10 of 14
[Ref.: #66794]	glutathione metabolism	71.43	10 of 14
[Ref.: #66794]	arginine metabolism	70.83	17 of 24
[Ref.: #66794]	glycolysis	70.59	12 of 17
[Ref.: #66794]	vitamin B1 metabolism	69.23	9 of 13
[Ref.: #66794]	glycolate and glyoxylate degradation	66.67	4 of 6
[Ref.: #66794]	methane metabolism	66.67	2 of 3
[Ref.: #66794]	octane oxidation	66.67	2 of 3
[Ref.: #66794]	acetyl CoA biosynthesis	66.67	2 of 3
[Ref.: #66794]	enterobactin biosynthesis	66.67	2 of 3
[Ref.: #66794]	acetoin degradation	66.67	2 of 3
[Ref.: #66794]	selenocysteine biosynthesis	66.67	4 of 6
[Ref.: #66794]	cyanate degradation	66.67	2 of 3
[Ref.: #66794]	degradation of pentoses	64.29	18 of 28
[Ref.: #66794]	heme metabolism	64.29	9 of 14
[Ref.: #66794]	d-xylose degradation	63.64	7 of 11
[Ref.: #66794]	vitamin B6 metabolism	63.64	7 of 11
[Ref.: #66794]	androgen and estrogen metabolism	62.5	10 of 16
[Ref.: #66794]	sulfate reduction	61.54	8 of 13
[Ref.: #66794]	urea cycle	61.54	8 of 13
[Ref.: #66794]	myo-inositol biosynthesis	60	6 of 10
[Ref.: #66794]	hydrogen production	60	3 of 5
[Ref.: #66794]	cellulose degradation	60	3 of 5
[Ref.: #66794]	vitamin K metabolism	60	3 of 5
[Ref.: #66794]	lipoate biosynthesis	60	3 of 5
[Ref.: #66794]	degradation of aromatic, nitrogen containing compounds	58.33	7 of 12
[Ref.: #66794]	nitrate assimilation	55.56	5 of 9
[Ref.: #66794]	isoprenoid biosynthesis	53.85	14 of 26
[Ref.: #66794]	phosphatidylethanolamine bioynthesis	53.85	7 of 13
[Ref.: #66794]	bile acid biosynthesis, neutral pathway	52.94	9 of 17
[Ref.: #66794]	coenzyme A metabolism	50	2 of 4
[Ref.: #66794]	coenzyme M biosynthesis	50	5 of 10
[Ref.: #66794]	lactate fermentation	50	2 of 4
[Ref.: #66794]	ascorbate metabolism	50	11 of 22
[Ref.: #66794]	sphingosine metabolism	50	3 of 6
[Ref.: #66794]	glycine metabolism	50	5 of 10
[Ref.: #66794]	degradation of hexoses	50	9 of 18
[Ref.: #66794]	aminopropanol phosphate biosynthesis	50	1 of 2
[Ref.: #66794]	quinate degradation	50	1 of 2
[Ref.: #66794]	cyclohexanol degradation	50	2 of 4
[Ref.: #66794]	pantothenate biosynthesis	50	3 of 6
[Ref.: #66794]	phenylmercury acetate degradation	50	1 of 2
[Ref.: #66794]	kanosamine biosynthesis II	50	1 of 2
[Ref.: #66794]	dTDPLrhamnose biosynthesis	50	4 of 8
[Ref.: #66794]	polyamine pathway	47.83	11 of 23
[Ref.: #66794]	allantoin degradation	44.44	4 of 9
[Ref.: #66794]	benzoyl-CoA degradation	42.86	3 of 7
[Ref.: #66794]	carotenoid biosynthesis	40.91	9 of 22
[Ref.: #66794]	O-antigen biosynthesis	40	2 of 5
[Ref.: #66794]	factor 420 biosynthesis	40	2 of 5
[Ref.: #66794]	bacilysin biosynthesis	40	2 of 5
[Ref.: #66794]	arachidonate biosynthesis	40	2 of 5
[Ref.: #66794]	arachidonic acid metabolism	38.89	7 of 18
[Ref.: #66794]	carnitine metabolism	37.5	3 of 8
[Ref.: #66794]	sulfoquinovose degradation	33.33	1 of 3
[Ref.: #66794]	IAA biosynthesis	33.33	1 of 3
[Ref.: #66794]	phenylpropanoid biosynthesis	30.77	4 of 13
[Ref.: #66794]	alginate biosynthesis	25	1 of 4
[Ref.: #66794]	catecholamine biosynthesis	25	1 of 4
[Ref.: #66794]	daunorubicin biosynthesis	22.22	2 of 9
		Only first 10 entries are displayed. Click here to see all.

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

[Ref.: #2685]	Sample type/isolated from	waste water and soil
[Ref.: #2685]	Geographic location (country and/or sea, region)	Dübendorf
[Ref.: #2685]	Country	Switzerland
[Ref.: #2685]	Country ISO 3 Code	CHE
[Ref.: #2685]	Continent	Europe
* marker position based on {}

Isolation sources categories

#Engineered	#Waste	#Wastewater
#Environmental	#Terrestrial	#Soil

What are isolation sources categories?

[Ref.: #69479]

Global distribution of 16S sequence AJ294349 (>99% sequence identity) for Chelatococcus asaccharovorans subclade from Microbeatlas

Aquatic Samples	343
Soil Samples	246
Animal Samples	85
Plant Samples	168
Total Samples	842

Information on possible application of the strain and its possible interaction with e.g. potential hosts Safety information

[Ref.: #2685]

Biosafety level

Risk group (German classification)
According to TRBA 466

Information on genomic background e.g. entries in nucleic sequence databass Sequence information

16S Sequence information:

	Sequence accession description	Seq. accession number	Sequence length (bp)	Sequence database	Associated NCBI tax ID
[Ref.: #2685]	Chelatococcus asaccharovorans partial 16S rRNA gene, strain TE2	AJ294349	1366	ENA	28210 tax ID
[Ref.: #20218]	C.asaccharovorans 16S rRNA fragment	X64551	157	ENA	28210 tax ID	*

Genome sequence information:

Only first 5 entries are displayed. Click here to see all.

	Sequence accession description	Seq. accession number	Assembly level	Sequence database	Associated NCBI tax ID
[Ref.: #66792]	Chelatococcus asaccharovorans DSM 6462	GCA_018398275	contig	GenBank	28210 tax ID	*
[Ref.: #66792]	Chelatococcus asaccharovorans DSM 6462	GCA_003201475	scaffold	GenBank	28210 tax ID	*
[Ref.: #66792]	Chelatococcus asaccharovorans strain DSM 6462	28210.14	wgs	PATRIC	28210 tax ID	*
[Ref.: #66792]	Chelatococcus asaccharovorans strain DSM 6462	28210.3	wgs	PATRIC	28210 tax ID	*
[Ref.: #66792]	Chelatococcus asaccharovorans DSM 6462	2756170239	draft	JGI IMG/M	28210 tax ID	*
[Ref.: #66792]	Chelatococcus asaccharovorans DSM 6462	2928729937	draft	JGI IMG/M	28210 tax ID	*

Data predicted using genome information as a basis Genome-based predictions

	Trait	Prediction	Confidence in %	In training data
	Predictions from GenomeNet Sporulation v. 1 based on: Chelatococcus asaccharovorans DSM 6462 NCBI: GCA_003201475.1
[Ref.: #69481]	spore-forming	no	100	no

	Trait	Prediction	Confidence in %	In training data
	Predictions from Diaspora project based on: Chelatococcus asaccharovorans DSM 6462 NCBI: GCA_003201475.1
[Ref.: #69480]	flagellated	no	93.996	no
[Ref.: #69480]	gram-positive	no	98.47	no
[Ref.: #69480]	anaerobic	no	98.919	no
[Ref.: #69480]	halophile	no	94.503	no
[Ref.: #69480]	spore-forming	no	95.716	no
[Ref.: #69480]	glucose-util	yes	88.949	yes
[Ref.: #69480]	aerobic	yes	91.739	no
[Ref.: #69480]	thermophile	no	98.221	yes
[Ref.: #69480]	motile	no	85.165	yes
[Ref.: #69480]	glucose-ferment	no	90.457	no

Availability in culture collections External links

[Ref.: #2685]

Culture collection no.

DSM 6462, ATCC 51531

[Ref.: #71299]

SI-ID 43036

Literature:

Topic	Title	Authors	Journal	DOI	Year
Enzymology	Acesulfame aerobic biodegradation by enriched consortia and Chelatococcus spp.: Kinetics, transformation products, and genomic characterization.	Huang Y, Deng Y, Law JC, Yang Y, Ding J, Leung KS, Zhang T	Water Res	10.1016/j.watres.2021.117454	2021	*
Phylogeny	Chelatococcus caeni sp. nov., isolated from a biofilm reactor sludge sample.	Jin L, Ko SR, Lee HG, Kim BH, Kim HS, Ahn CY, Oh HM	Int J Syst Evol Microbiol	10.1099/ijs.0.000032	2014	*
Phylogeny	Chelatococcus sambhunathii sp. nov., a moderately thermophilic alphaproteobacterium isolated from hot spring sediment.	Panday D, Das SK	Int J Syst Evol Microbiol	10.1099/ijs.0.013466-0	2009	*
Phylogeny	Chelatococcus daeguensis sp. nov., isolated from wastewater of a textile dye works, and emended description of the genus Chelatococcus.	Yoon JH, Kang SJ, Im WT, Lee ST, Oh TK	Int J Syst Evol Microbiol	10.1099/ijs.0.65291-0	2008	*

References

#2685

Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 6462

#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 )

#23146

Jung-Hoon Yoon, So-Jung Kang, Wan-Taek Im, Sung-Taik Lee, Tae-Kwang Oh: Chelatococcus daeguensis sp. nov., isolated from wastewater of a textile dye works, and emended description of the genus Chelatococcus. IJSEM 58: 2224 - 2228 2008 ( DOI 10.1099/ijs.0.65291-0 , PubMed 18768633 )

#23363

Digvijay Panday, Subrata K. Das: Chelatococcus sambhunathii sp. nov., a moderately thermophilic alphaproteobacterium isolated from hot spring sediment. IJSEM 60: 861 - 865 2010 ( DOI 10.1099/ijs.0.013466-0 , PubMed 19661510 )

#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 )

#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 .

#69480

Julia Koblitz, Joaquim Sardà, Lorenz Christian Reimer, Boyke Bunk, Jörg Overmann: Predictions based on genome sequence made in the Diaspora project (Digital Approaches for the Synthesis of Poorly Accessible Biodiversity Information) .

#69481

Xiao-Yin To, René Mreches, Martin Binder, Alice C. McHardy, Philipp C. Münch: Predictions based on the model GenomeNet Sporulation v. 1 . ( DOI 10.21203/rs.3.rs-2527258/v1 )

#71299

Reimer, L.C., Lissin, A.,Schober, I., Witte,J.F., Podstawka, A., Lüken, H., Bunk, B.,Overmann, J.: StrainInfo: A central database for resolving microbial strain identifiers . ( DOI 10.60712/SI-ID43036.1 )

* These data were automatically processed and therefore are not curated

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Chelatococcus asaccharovorans DSM 6462

Chelatococcus asaccharovorans DSM 6462

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