Name: Rhodohalobacter barkolensis 15182
Creator: BacDive
License: http://creativecommons.org/licenses/by-nc/4.0/

Strain identifier

BacDive ID: 158667

Type strain:

Species: Rhodohalobacter barkolensis

Strain Designation: 15182

Culture col. no.: KCTC 62172, MCCC 1K03442

NCBI tax ID(s): 2053187 (species)

Section

Rhodohalobacter barkolensis 15182 is an aerobe, Gram-negative, rod-shaped bacterium that forms circular colonies and was isolated from water sample ).

colony-forming
Gram-negative
rod-shaped
aerobe
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	*Balneolota*
	Class	*Balneolia*
	Order	*Balneolales*
	Family	*Balneolaceae*
	Genus	*Rhodohalobacter*
	Species	**Rhodohalobacter barkolensis**
	Full Scientific Name (LPSN)	Rhodohalobacter barkolensis Han et al. 2018

Information on morphological and physiological properties Morphology

[Ref.: #65395]	Gram stain	negative

[Ref.: #65395]	Cell length	2.5-20.6 µm

[Ref.: #65395]	Cell width	0.3-0.7 µm

[Ref.: #65395]	Cell shape	rod-shaped

[Ref.: #65395]	Motility	no

[Ref.: #65395]	Colony size	1-2 mm
[Ref.: #65395]	Colony color	reddish
[Ref.: #65395]	Colony shape	circular
[Ref.: #65395]	Incubation period	5 days
[Ref.: #65395]	Cultivation medium used	marine agar

Information on culture and growth conditions Culture and growth conditions

[Ref.: #65395]

Culture medium

Marine agar (MA)

[Ref.: #65395]

Culture medium growth

	Temperatures	Kind of temperature		Temperature
[Ref.: #65395]			growth	10-40 °C
[Ref.: #65395]			optimum	37 °C

[Ref.: #65395]

Temperature range

mesophilic

	pH	Kind of pH		pH
[Ref.: #65395]			optimum	7.5
[Ref.: #65395]			growth	7-8

Information on physiology and metabolism Physiology and metabolism

[Ref.: #65395]

Oxygen tolerance

aerobe

	Halophily	Salt	Tested relation		Salt conc.
[Ref.: #65395]		NaCl		growth	0.5-4	%(w/v)
[Ref.: #65395]		NaCl		optimum	2-3	%(w/v)

[Ref.: #65395]

Observation

No growth is observed in anaerobic conditions by anaerobic respiration with S2O32-, SO32-, SO42-, NO2 or NO3-as electron acceptors.

	Metabolite	Utilization activity	Kind of utilization tested
[Ref.: #65395]	2,3-butanediol ChEBI	+	carbon source
[Ref.: #65395]	2-oxoglutarate ChEBI	+	carbon source
[Ref.: #65395]	2-oxopentanoate ChEBI	+	carbon source
[Ref.: #65395]	alginate ChEBI	+	hydrolysis
[Ref.: #65395]	amygdalin ChEBI	-	builds acid from
[Ref.: #65395]	arbutin ChEBI	-	builds acid from
[Ref.: #65395]	carboxymethylcellulose ChEBI	-	hydrolysis
[Ref.: #65395]	casein	-	hydrolysis
[Ref.: #65395]	cellobiose ChEBI	-	builds acid from
[Ref.: #65395]	D-alanine ChEBI	+	carbon source
[Ref.: #65395]	D-arabinose ChEBI	-	builds acid from
[Ref.: #65395]	D-arabitol ChEBI	-	builds acid from
[Ref.: #65395]	D-fructose ChEBI	-	builds acid from
[Ref.: #65395]	D-fucose ChEBI	-	builds acid from
[Ref.: #65395]	D-galactose ChEBI	-	builds acid from
[Ref.: #65395]	D-glucose ChEBI	+	builds acid from
[Ref.: #65395]	D-lyxose ChEBI	-	builds acid from
[Ref.: #65395]	D-mannitol ChEBI	+	builds acid from
[Ref.: #65395]	D-mannose ChEBI	-	builds acid from
[Ref.: #65395]	D-ribose ChEBI	-	builds acid from
[Ref.: #65395]	D-saccharate ChEBI	+	carbon source
[Ref.: #65395]	D-serine ChEBI	+	carbon source
[Ref.: #65395]	D-sorbitol ChEBI	-	builds acid from
[Ref.: #65395]	D-sorbitol ChEBI	+	carbon source
[Ref.: #65395]	D-tagatose ChEBI	-	builds acid from
[Ref.: #65395]	D-xylose ChEBI	-	builds acid from
[Ref.: #65395]	dextrin ChEBI	+	carbon source
[Ref.: #65395]	erythritol ChEBI	-	builds acid from
[Ref.: #65395]	esculin ChEBI	+	hydrolysis
[Ref.: #65395]	esculin ferric citrate	+	builds acid from
[Ref.: #65395]	ethanolamine ChEBI	+	carbon source
[Ref.: #65395]	galactitol ChEBI	-	builds acid from
[Ref.: #65395]	gelatin ChEBI	-	hydrolysis
[Ref.: #65395]	gentiobiose ChEBI	-	builds acid from
[Ref.: #65395]	glycerol ChEBI	-	builds acid from
[Ref.: #65395]	glycerol ChEBI	+	carbon source
[Ref.: #65395]	glycerol 1-phosphate ChEBI	+	carbon source
[Ref.: #65395]	glycogen ChEBI	+	builds acid from
[Ref.: #65395]	glycyl L-aspartic acid ChEBI	+	carbon source
[Ref.: #65395]	inulin ChEBI	-	builds acid from
[Ref.: #65395]	L-alanine ChEBI	+	carbon source
[Ref.: #65395]	L-alanylglycine ChEBI	+	carbon source
[Ref.: #65395]	L-arabinose ChEBI	-	builds acid from
[Ref.: #65395]	L-arabitol ChEBI	-	builds acid from
[Ref.: #65395]	L-aspartate ChEBI	+	carbon source
[Ref.: #65395]	L-fucose ChEBI	-	builds acid from
[Ref.: #65395]	L-glutamate ChEBI	+	carbon source
[Ref.: #65395]	L-proline ChEBI	+	carbon source
[Ref.: #65395]	L-pyroglutamic acid ChEBI	+	carbon source
[Ref.: #65395]	L-rhamnose ChEBI	-	builds acid from
[Ref.: #65395]	L-serine ChEBI	+	carbon source
[Ref.: #65395]	L-sorbose ChEBI	-	builds acid from
[Ref.: #65395]	L-threonine ChEBI	+	carbon source
[Ref.: #65395]	L-xylose ChEBI	-	builds acid from
[Ref.: #65395]	lactate ChEBI	+	carbon source
[Ref.: #65395]	lactose ChEBI	-	builds acid from
[Ref.: #65395]	lactose ChEBI	+	carbon source
[Ref.: #65395]	maltose ChEBI	+	builds acid from
[Ref.: #65395]	melezitose ChEBI	-	builds acid from
[Ref.: #65395]	melibiose ChEBI	-	builds acid from
[Ref.: #65395]	methyl alpha-D-glucopyranoside ChEBI	-	builds acid from
[Ref.: #65395]	methyl alpha-D-mannoside ChEBI	-	builds acid from
[Ref.: #65395]	methyl beta-D-xylopyranoside ChEBI	-	builds acid from
[Ref.: #65395]	myo-inositol ChEBI	-	builds acid from
[Ref.: #65395]	myo-inositol ChEBI	+	carbon source
[Ref.: #65395]	N-acetylgalactosamine ChEBI	+	carbon source
[Ref.: #65395]	N-acetylglucosamine ChEBI	-	builds acid from
[Ref.: #65395]	N-acetylglucosamine ChEBI	+	carbon source
[Ref.: #65395]	nitrate ChEBI	-	reduction
[Ref.: #65395]	potassium 2-dehydro-D-gluconate	+	builds acid from
[Ref.: #65395]	potassium 5-dehydro-D-gluconate	+	builds acid from
[Ref.: #65395]	potassium gluconate ChEBI	-	builds acid from
[Ref.: #65395]	raffinose ChEBI	-	builds acid from
[Ref.: #65395]	raffinose ChEBI	+	carbon source
[Ref.: #65395]	ribitol ChEBI	+	carbon source
[Ref.: #65395]	ribitol ChEBI	-	builds acid from
[Ref.: #65395]	salicin ChEBI	-	builds acid from
[Ref.: #65395]	starch ChEBI	+	builds acid from
[Ref.: #65395]	starch ChEBI	+	hydrolysis
[Ref.: #65395]	sucrose ChEBI	-	builds acid from
[Ref.: #65395]	sucrose ChEBI	+	carbon source
[Ref.: #65395]	trehalose ChEBI	-	builds acid from
[Ref.: #65395]	trehalose ChEBI	+	carbon source
[Ref.: #65395]	turanose ChEBI	-	builds acid from
[Ref.: #65395]	turanose ChEBI	+	carbon source
[Ref.: #65395]	tween 20 ChEBI	-	hydrolysis
[Ref.: #65395]	tween 40 ChEBI	-	hydrolysis
[Ref.: #65395]	tween 80 ChEBI	-	hydrolysis
[Ref.: #65395]	tween 80 ChEBI	+	carbon source
[Ref.: #65395]	tyrosine ChEBI	-	hydrolysis
[Ref.: #65395]	xylitol ChEBI	-	builds acid from
[Ref.: #65395]	xylitol ChEBI	+	carbon source
	Only first 10 entries are displayed. Click here to see all.

	Metabolite	Antibiotic sensitivity	Concentration		Antibiotic resistance	Concentration
[Ref.: #65395]	amikacin ChEBI				yes	30	µg (disc)
[Ref.: #65395]	amoxicillin ChEBI	yes	10	µg (disc)
[Ref.: #65395]	bacitracin ChEBI				yes	0.04	Unit (disc)
[Ref.: #65395]	cefoxitin ChEBI	yes	30	µg (disc)
[Ref.: #65395]	cephalothin ChEBI	yes	30	µg (disc)
[Ref.: #65395]	chloramphenicol ChEBI	yes	30	µg (disc)
[Ref.: #65395]	clindamycin ChEBI	yes	2	µg (disc)
[Ref.: #65395]	doxycycline ChEBI				yes	30	µg (disc)
[Ref.: #65395]	erythromycin ChEBI	yes	15	µg (disc)
[Ref.: #65395]	gentamicin ChEBI				yes	2	µg (disc)
[Ref.: #65395]	gentamicin ChEBI				yes	10	µg (disc)
[Ref.: #65395]	kanamycin ChEBI				yes	30	µg (disc)
[Ref.: #65395]	nalidixic acid ChEBI				yes	30	µg (disc)
[Ref.: #65395]	norfloxacin ChEBI	yes	10	µg (disc)
[Ref.: #65395]	novobiocin ChEBI	yes	30	µg (disc)
[Ref.: #65395]	nystatin ChEBI				yes	100	µg (disc)
[Ref.: #65395]	ofloxacin ChEBI				yes	5	µg (disc)
[Ref.: #65395]	penicillin g ChEBI	yes	10	Unit (disc)
[Ref.: #65395]	rifampicin ChEBI	yes	5	µg (disc)
[Ref.: #65395]	streptomycin ChEBI	yes	10	µg (disc)
[Ref.: #65395]	tetracycline ChEBI				yes	30	µg (disc)
[Ref.: #65395]	vancomycin ChEBI	yes	30	µg (disc)
	Only first 10 entries are displayed. Click here to see all.

	Metabolite production	Metabolite	Production
[Ref.: #65395]		hydrogen sulfide ChEBI	no
[Ref.: #65395]		indole ChEBI	no

	Enzyme	Enzyme activity	EC number
[Ref.: #65395]	acid phosphatase	+	3.1.3.2
[Ref.: #65395]	alkaline phosphatase	+	3.1.3.1
[Ref.: #65395]	catalase	+	1.11.1.6
[Ref.: #65395]	chymotrypsin	+	3.4.4.5
[Ref.: #65395]	cystine arylamidase	+	3.4.11.3
[Ref.: #65395]	cytochrome oxidase	-	1.9.3.1
[Ref.: #65395]	esterase (C 4)	+
[Ref.: #65395]	esterase Lipase (C 8)	+
[Ref.: #65395]	leucine arylamidase	+	3.4.11.1
[Ref.: #65395]	naphthol-AS-BI-phosphohydrolase	+
[Ref.: #65395]	trypsin	+	3.4.21.4
[Ref.: #65395]	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]	C4 and CAM-carbon fixation	100	8 of 8
[Ref.: #66794]	glycogen metabolism	100	5 of 5
[Ref.: #66794]	methylglyoxal degradation	100	5 of 5
[Ref.: #66794]	lipoate biosynthesis	100	5 of 5
[Ref.: #66794]	ppGpp biosynthesis	100	4 of 4
[Ref.: #66794]	palmitate biosynthesis	100	22 of 22
[Ref.: #66794]	adipate degradation	100	2 of 2
[Ref.: #66794]	cis-vaccenate biosynthesis	100	2 of 2
[Ref.: #66794]	phenylacetate degradation (aerobic)	100	5 of 5
[Ref.: #66794]	vitamin K metabolism	100	5 of 5
[Ref.: #66794]	coenzyme A metabolism	100	4 of 4
[Ref.: #66794]	sulfopterin metabolism	100	4 of 4
[Ref.: #66794]	denitrification	100	2 of 2
[Ref.: #66794]	CDP-diacylglycerol biosynthesis	100	2 of 2
[Ref.: #66794]	anapleurotic synthesis of oxalacetate	100	1 of 1
[Ref.: #66794]	folate polyglutamylation	100	1 of 1
[Ref.: #66794]	suberin monomers biosynthesis	100	2 of 2
[Ref.: #66794]	UDP-GlcNAc biosynthesis	100	3 of 3
[Ref.: #66794]	starch degradation	90	9 of 10
[Ref.: #66794]	CO2 fixation in Crenarchaeota	88.89	8 of 9
[Ref.: #66794]	gluconeogenesis	87.5	7 of 8
[Ref.: #66794]	photosynthesis	85.71	12 of 14
[Ref.: #66794]	cellulose degradation	80	4 of 5
[Ref.: #66794]	metabolism of amino sugars and derivatives	80	4 of 5
[Ref.: #66794]	threonine metabolism	80	8 of 10
[Ref.: #66794]	propionate fermentation	80	8 of 10
[Ref.: #66794]	d-mannose degradation	77.78	7 of 9
[Ref.: #66794]	chorismate metabolism	77.78	7 of 9
[Ref.: #66794]	pyrimidine metabolism	77.78	35 of 45
[Ref.: #66794]	serine metabolism	77.78	7 of 9
[Ref.: #66794]	phenylalanine metabolism	76.92	10 of 13
[Ref.: #66794]	alanine metabolism	75.86	22 of 29
[Ref.: #66794]	acetate fermentation	75	3 of 4
[Ref.: #66794]	CMP-KDO biosynthesis	75	3 of 4
[Ref.: #66794]	glycogen biosynthesis	75	3 of 4
[Ref.: #66794]	purine metabolism	73.4	69 of 94
[Ref.: #66794]	flavin biosynthesis	73.33	11 of 15
[Ref.: #66794]	NAD metabolism	72.22	13 of 18
[Ref.: #66794]	tetrahydrofolate metabolism	71.43	10 of 14
[Ref.: #66794]	glutamate and glutamine metabolism	71.43	20 of 28
[Ref.: #66794]	glycolysis	70.59	12 of 17
[Ref.: #66794]	histidine metabolism	68.97	20 of 29
[Ref.: #66794]	valine metabolism	66.67	6 of 9
[Ref.: #66794]	aspartate and asparagine metabolism	66.67	6 of 9
[Ref.: #66794]	formaldehyde oxidation	66.67	2 of 3
[Ref.: #66794]	acetoin degradation	66.67	2 of 3
[Ref.: #66794]	peptidoglycan biosynthesis	66.67	10 of 15
[Ref.: #66794]	acetyl CoA biosynthesis	66.67	2 of 3
[Ref.: #66794]	L-lactaldehyde degradation	66.67	2 of 3
[Ref.: #66794]	isoprenoid biosynthesis	65.38	17 of 26
[Ref.: #66794]	methionine metabolism	65.38	17 of 26
[Ref.: #66794]	lipid metabolism	64.52	20 of 31
[Ref.: #66794]	heme metabolism	64.29	9 of 14
[Ref.: #66794]	ketogluconate metabolism	62.5	5 of 8
[Ref.: #66794]	isoleucine metabolism	62.5	5 of 8
[Ref.: #66794]	dTDPLrhamnose biosynthesis	62.5	5 of 8
[Ref.: #66794]	6-hydroxymethyl-dihydropterin diphosphate biosynthesis	62.5	5 of 8
[Ref.: #66794]	lysine metabolism	61.9	26 of 42
[Ref.: #66794]	cysteine metabolism	61.11	11 of 18
[Ref.: #66794]	Entner Doudoroff pathway	60	6 of 10
[Ref.: #66794]	degradation of aromatic, nitrogen containing compounds	58.33	7 of 12
[Ref.: #66794]	citric acid cycle	57.14	8 of 14
[Ref.: #66794]	propanol degradation	57.14	4 of 7
[Ref.: #66794]	ubiquinone biosynthesis	57.14	4 of 7
[Ref.: #66794]	degradation of sugar alcohols	56.25	9 of 16
[Ref.: #66794]	tryptophan metabolism	55.26	21 of 38
[Ref.: #66794]	non-pathway related	55.26	21 of 38
[Ref.: #66794]	vitamin B6 metabolism	54.55	6 of 11
[Ref.: #66794]	pentose phosphate pathway	54.55	6 of 11
[Ref.: #66794]	leucine metabolism	53.85	7 of 13
[Ref.: #66794]	urea cycle	53.85	7 of 13
[Ref.: #66794]	quinate degradation	50	1 of 2
[Ref.: #66794]	phenylmercury acetate degradation	50	1 of 2
[Ref.: #66794]	ethanol fermentation	50	1 of 2
[Ref.: #66794]	myo-inositol biosynthesis	50	5 of 10
[Ref.: #66794]	kanosamine biosynthesis II	50	1 of 2
[Ref.: #66794]	coenzyme M biosynthesis	50	5 of 10
[Ref.: #66794]	glycolate and glyoxylate degradation	50	3 of 6
[Ref.: #66794]	biotin biosynthesis	50	2 of 4
[Ref.: #66794]	tyrosine metabolism	50	7 of 14
[Ref.: #66794]	butanoate fermentation	50	2 of 4
[Ref.: #66794]	glutathione metabolism	50	7 of 14
[Ref.: #66794]	arginine metabolism	45.83	11 of 24
[Ref.: #66794]	ascorbate metabolism	45.45	10 of 22
[Ref.: #66794]	lipid A biosynthesis	44.44	4 of 9
[Ref.: #66794]	polyamine pathway	43.48	10 of 23
[Ref.: #66794]	cardiolipin biosynthesis	42.86	3 of 7
[Ref.: #66794]	reductive acetyl coenzyme A pathway	42.86	3 of 7
[Ref.: #66794]	carotenoid biosynthesis	40.91	9 of 22
[Ref.: #66794]	arachidonate biosynthesis	40	2 of 5
[Ref.: #66794]	ethylmalonyl-CoA pathway	40	2 of 5
[Ref.: #66794]	3-chlorocatechol degradation	40	2 of 5
[Ref.: #66794]	arachidonic acid metabolism	38.89	7 of 18
[Ref.: #66794]	vitamin B1 metabolism	38.46	5 of 13
[Ref.: #66794]	oxidative phosphorylation	38.46	35 of 91
[Ref.: #66794]	carnitine metabolism	37.5	3 of 8
[Ref.: #66794]	d-xylose degradation	36.36	4 of 11
[Ref.: #66794]	proline metabolism	36.36	4 of 11
[Ref.: #66794]	degradation of hexoses	33.33	6 of 18
[Ref.: #66794]	cyanate degradation	33.33	1 of 3
[Ref.: #66794]	4-hydroxymandelate degradation	33.33	3 of 9
[Ref.: #66794]	selenocysteine biosynthesis	33.33	2 of 6
[Ref.: #66794]	pantothenate biosynthesis	33.33	2 of 6
[Ref.: #66794]	molybdenum cofactor biosynthesis	33.33	3 of 9
[Ref.: #66794]	octane oxidation	33.33	1 of 3
[Ref.: #66794]	enterobactin biosynthesis	33.33	1 of 3
[Ref.: #66794]	IAA biosynthesis	33.33	1 of 3
[Ref.: #66794]	(5R)-carbapenem carboxylate biosynthesis	33.33	1 of 3
[Ref.: #66794]	degradation of pentoses	32.14	9 of 28
[Ref.: #66794]	androgen and estrogen metabolism	31.25	5 of 16
[Ref.: #66794]	sulfate reduction	30.77	4 of 13
[Ref.: #66794]	phenylpropanoid biosynthesis	30.77	4 of 13
[Ref.: #66794]	glycine metabolism	30	3 of 10
[Ref.: #66794]	mevalonate metabolism	28.57	2 of 7
[Ref.: #66794]	degradation of sugar acids	28	7 of 25
[Ref.: #66794]	dolichyl-diphosphooligosaccharide biosynthesis	27.27	3 of 11
[Ref.: #66794]	metabolism of disaccharids	27.27	3 of 11
[Ref.: #66794]	3-phenylpropionate degradation	26.67	4 of 15
[Ref.: #66794]	cyclohexanol degradation	25	1 of 4
[Ref.: #66794]	lactate fermentation	25	1 of 4
[Ref.: #66794]	catecholamine biosynthesis	25	1 of 4
[Ref.: #66794]	toluene degradation	25	1 of 4
[Ref.: #66794]	phosphatidylethanolamine bioynthesis	23.08	3 of 13
[Ref.: #66794]	nitrate assimilation	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.: #65395]	Sample type/isolated from	water sample (pH of the lake water is 7.0 and the salinity is 22.6 % (w/v))
[Ref.: #65395]	Geographic location (country and/or sea, region)	lake Barkol, Xinjiang province
[Ref.: #65395]	Country	China
[Ref.: #65395]	Country ISO 3 Code	CHN
[Ref.: #65395]	Continent	Asia
[Ref.: #65395]	Geographic location	43.6193°/92.7724°
[Ref.: #65395]	Enrichment culture	marine agar 2216
[Ref.: #65395]	Enrichment culture duration	7 days
[Ref.: #65395]	Enrichment culture temperature	30 ̊C
[Ref.: #65395]	Isolation/enrichment procedure	tenfold dilution series method
* marker position based on {}

Isolation sources categories

#Environmental

#Aquatic

#Lake (large)

What are isolation sources categories?

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.: #65395]	16S rRNA gene sequence	MF618255		GenBank

Genome sequence information:

	Sequence accession description	Seq. accession number	Assembly level	Sequence database	Associated NCBI tax ID
[Ref.: #66792]	Rhodohalobacter barkolensis 15182	GCA_002834295	contig	GenBank	2053187 tax ID	*
[Ref.: #66792]	Rhodohalobacter barkolensis 15182	2882395943	draft	JGI IMG/M	2053187 tax ID	*

[Ref.: #65395]

GC-content

42.4 mol%

genome sequence analysis

Availability in culture collections External links

[Ref.: #65395]

Culture collection no.

KCTC 62172, MCCC 1K03442

Literature:

Topic	Title	Authors	Journal	DOI	Year
Phylogeny	Rhodohalobacter barkolensis sp. nov., isolated from a saline lake and emended description of the genus Rhodohalobacter.	Han SB, Yu YH, Ju Z, Li Y, Zhang R, Hou XJ, Ma XY, Yu XY, Sun C, Wu M	Int J Syst Evol Microbiol	10.1099/ijsem.0.002775	2018	*
Phylogeny	Rhodohalobacter sulfatireducens sp. nov., isolated from a marine solar saltern.	Wang YS, Yue YY, Bai YL, Zhang XY, Wang S, Du ZJ	Arch Microbiol	10.1007/s00203-022-03078-3	2022	*

References

#20215

Parte, A.C., Sardà Carbasse, J., Meier-Kolthoff, J.P., Reimer, L.C. and Göker, M.: List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ. IJSEM ( DOI 10.1099/ijsem.0.004332 )

#65395

Shuai-Bo Han, Yang-Huan Yu, Zhao Ju, Yu Li, Ran Zhang, Xin-Jun Hou, Xin-Yuan Ma, Xiao-Yun Yu, Cong Sun, Min Wu: Rhodohalobacter barkolensis sp. nov., isolated from a saline lake and emended description of the genus Rhodohalobacter. IJSEM 68: 1949 - 1954 2018 ( DOI 10.1099/ijsem.0.002775 , PubMed 29676726 )

#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 )

* These data were automatically processed and therefore are not curated

Change proposal

You found an error in BacDive? Please tell us about it!

Note that changes will be reviewed and judged. If your changes are legitimate, changes will occur within the next BacDive update. Only proposed changes supported by the according reference will be reviewed. The BacDive team reserves the right to reject proposed changes.

Search for species Rhodohalobacter barkolensis in external resources:
SILVA
BRENDA
PANGAEA
StrainInfo
GBIF