Name: Planococcus salinus LCB217
Creator: BacDive
License: http://creativecommons.org/licenses/by-nc/4.0/

Strain identifier

BacDive ID: 158688

Type strain:

Species: Planococcus salinus

Strain Designation: LCB217

Culture col. no.: CGMCC 1.15685, KCTC 33861

Strain history: <- Longzhan GAN, Sichuan Univ.

NCBI tax ID(s): 1848460 (species)

Section

Planococcus salinus LCB217 is an aerobe, moderately halophilic, Gram-positive bacterium that forms circular colonies and was isolated from a saline-alkali soil of Jade Gate Pass.

coccus-shaped
colony-forming
Gram-positive
motile
aerobe
moderately halophilic
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	*Bacillota*
	Class	*Bacilli*
	Order	*Caryophanales*
	Family	*Caryophanaceae*
	Genus	*Planococcus*
	Species	**Planococcus salinus**
	Full Scientific Name (LPSN)	Planococcus salinus Gan et al. 2018

Information on morphological and physiological properties Morphology

[Ref.: #65424]	Gram stain	positive
[Ref.: #67771]	Gram stain	positive

[Ref.: #65424]	Cell width	0.6-1.0 µm

[Ref.: #65424]	Cell shape	coccus-shaped
[Ref.: #67771]	Cell shape	coccus-shaped

[Ref.: #65424]	Motility	yes
[Ref.: #67771]	Motility	yes

[Ref.: #65424]	Colony size	1-2 mm
[Ref.: #65424]	Colony color	reddish-orange
[Ref.: #65424]	Colony shape	circular
[Ref.: #65424]	Incubation period	3 days
[Ref.: #65424]	Cultivation medium used	LB

Information on culture and growth conditions Culture and growth conditions

[Ref.: #65424]

Culture medium

LB (Luria-Bertani) MEDIUM

[Ref.: #65424]

Culture medium growth

		Temperature
[Ref.: #65424]	growth	10-45 °C
[Ref.: #65424]	optimum	30 °C
[Ref.: #67771]	growth	30 °C

[Ref.: #65424]	Temperature range	mesophilic
[Ref.: #67771]	Temperature range	mesophilic

	pH	Kind of pH		pH
[Ref.: #65424]			optimum	9
[Ref.: #65424]			growth	7-9

Information on physiology and metabolism Physiology and metabolism

[Ref.: #65424]	Oxygen tolerance	aerobe
[Ref.: #67771]	Oxygen tolerance	aerobe

[Ref.: #65424]

Halophily / tolerance level

moderately halophilic

	Halophily	Salt	Tested relation		Salt conc.
[Ref.: #65424]		NaCl		growth	3-15	%
[Ref.: #65424]		NaCl		optimum	3-5	%

[Ref.: #65424]	Observation	the peptidoglycan type is A4a (L-Lys-D-Glu)
[Ref.: #65424]	Observation	the predominant menaquinones are MK-7 and MK-8
[Ref.: #65424]	Observation	the polar lipids are diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine, phosphatidylcholine, one unidentified phospholipid, one unidentified aminophospholipid and one unidentified lipid
[Ref.: #67771]	Observation	quinones: MK-7, MK-8

	Metabolite	Utilization activity	Kind of utilization tested
[Ref.: #65424]	(R)-lactate ChEBI	+	carbon source
[Ref.: #65424]	(S)-lactate ChEBI	-	carbon source
[Ref.: #65424]	2-hydroxybutyrate ChEBI	-	carbon source
[Ref.: #65424]	3-O-methyl-D-glucose ChEBI	+	carbon source
[Ref.: #65424]	4-hydroxyphenylacetic acid ChEBI	-	carbon source
[Ref.: #65424]	acetate ChEBI	+	carbon source
[Ref.: #65424]	alpha-D-glucose ChEBI	+	carbon source
[Ref.: #65424]	alpha-hydroxyglutarate-gamma-lactone ChEBI	-	carbon source
[Ref.: #65424]	beta-hydroxybutyrate ChEBI	+	carbon source
[Ref.: #65424]	bromosuccinate ChEBI	-	carbon source
[Ref.: #65424]	cellobiose ChEBI	-	builds acid from
[Ref.: #65424]	cellobiose ChEBI	+	carbon source
[Ref.: #65424]	cellulose ChEBI	-	hydrolysis
[Ref.: #65424]	citrate ChEBI	-	carbon source
[Ref.: #65424]	D-arabitol ChEBI	+	carbon source
[Ref.: #65424]	D-aspartate ChEBI	-	carbon source
[Ref.: #65424]	D-fructose ChEBI	+	carbon source
[Ref.: #65424]	D-fructose 6-phosphate ChEBI	+	carbon source
[Ref.: #65424]	D-fucose ChEBI	+	carbon source
[Ref.: #65424]	D-galactose ChEBI	-	builds acid from
[Ref.: #65424]	D-galactose ChEBI	+	carbon source
[Ref.: #65424]	D-galacturonic acid ChEBI	-	carbon source
[Ref.: #65424]	D-gluconate ChEBI	-	carbon source
[Ref.: #65424]	D-glucose 6-phosphate ChEBI	-	carbon source
[Ref.: #65424]	D-glucuronate ChEBI	-	carbon source
[Ref.: #65424]	D-malate ChEBI	+	carbon source
[Ref.: #65424]	D-mannitol ChEBI	-	builds acid from
[Ref.: #65424]	D-mannitol ChEBI	+	carbon source
[Ref.: #65424]	D-mannose ChEBI	+	carbon source
[Ref.: #65424]	D-saccharate ChEBI	-	carbon source
[Ref.: #65424]	D-serine ChEBI	-	carbon source
[Ref.: #65424]	D-sorbitol ChEBI	-	builds acid from
[Ref.: #65424]	D-sorbitol ChEBI	+	carbon source
[Ref.: #65424]	formate ChEBI	+	carbon source
[Ref.: #65424]	fructose ChEBI	-	builds acid from
[Ref.: #65424]	gamma-aminobutyric acid ChEBI	-	carbon source
[Ref.: #65424]	gamma-cyclodextrin ChEBI	+	carbon source
[Ref.: #65424]	gelatin ChEBI	-	carbon source
[Ref.: #65424]	gelatin ChEBI	-	hydrolysis
[Ref.: #65424]	gentiobiose ChEBI	+	carbon source
[Ref.: #65424]	glucose ChEBI	-	builds acid from
[Ref.: #65424]	glucuronamide ChEBI	+	carbon source
[Ref.: #65424]	glycerol ChEBI	+	carbon source
[Ref.: #65424]	glycine-proline ChEBI	-	carbon source
[Ref.: #65424]	inosine ChEBI	+	carbon source
[Ref.: #65424]	L-alanine 4-nitroanilide	-	carbon source
[Ref.: #65424]	L-arginine ChEBI	-	carbon source
[Ref.: #65424]	L-aspartate ChEBI	-	carbon source
[Ref.: #65424]	L-fucose ChEBI	+	carbon source
[Ref.: #65424]	L-galactonic acid gamma-lactone ChEBI	+	carbon source
[Ref.: #65424]	L-glutamate ChEBI	-	carbon source
[Ref.: #65424]	L-histidine ChEBI	+	carbon source
[Ref.: #65424]	L-malate ChEBI	-	carbon source
[Ref.: #65424]	L-pyroglutamic acid ChEBI	-	carbon source
[Ref.: #65424]	L-rhamnose ChEBI	+	carbon source
[Ref.: #65424]	L-serine ChEBI	-	carbon source
[Ref.: #65424]	lactose ChEBI	+	carbon source
[Ref.: #65424]	maltose ChEBI	-	builds acid from
[Ref.: #65424]	maltose ChEBI	+	carbon source
[Ref.: #65424]	melibiose ChEBI	+	carbon source
[Ref.: #65424]	methyl D-glucoside ChEBI	+	carbon source
[Ref.: #65424]	methyl pyruvate ChEBI	-	carbon source
[Ref.: #65424]	myo-inositol ChEBI	+	carbon source
[Ref.: #65424]	N-acetyl-beta-D-mannosamine ChEBI	+	carbon source
[Ref.: #65424]	N-acetylgalactosamine ChEBI	+	carbon source
[Ref.: #65424]	N-acetylglucosamine ChEBI	+	carbon source
[Ref.: #65424]	n-acetylneuraminate ChEBI	-	carbon source
[Ref.: #65424]	nitrate ChEBI	+	reduction
[Ref.: #65424]	pectin ChEBI	-	carbon source
[Ref.: #65424]	propionate ChEBI	+	carbon source
[Ref.: #65424]	quinate ChEBI	-	carbon source
[Ref.: #65424]	raffinose ChEBI	+	carbon source
[Ref.: #65424]	salicin ChEBI	+	carbon source
[Ref.: #65424]	stachyose ChEBI	+	carbon source
[Ref.: #65424]	starch ChEBI	-	hydrolysis
[Ref.: #65424]	sucrose ChEBI	-	builds acid from
[Ref.: #65424]	sucrose ChEBI	+	carbon source
[Ref.: #65424]	trehalose ChEBI	-	builds acid from
[Ref.: #65424]	trehalose ChEBI	+	carbon source
[Ref.: #65424]	turanose ChEBI	+	carbon source
[Ref.: #65424]	tween 20 ChEBI	+	hydrolysis
[Ref.: #65424]	tween 40 ChEBI	+	carbon source
[Ref.: #65424]	tween 40 ChEBI	+	hydrolysis
[Ref.: #65424]	tween 60 ChEBI	+	hydrolysis
[Ref.: #65424]	tween 80 ChEBI	-	hydrolysis
[Ref.: #65424]	urea ChEBI	-	hydrolysis
	Only first 10 entries are displayed. Click here to see all.

	Metabolite production	Metabolite	Production
[Ref.: #65424]		indole ChEBI	yes
[Ref.: #65424]		sulfide ChEBI	no

	Physiological tests	Metabolite	Voges-Proskauer-test	Methylred-test
[Ref.: #65424]		acetoin ChEBI	-
[Ref.: #65424]		glucose ChEBI		-

	Enzyme	Enzyme activity	EC number
[Ref.: #65424]	acid phosphatase	+	3.1.3.2
[Ref.: #65424]	alkaline phosphatase	+	3.1.3.1
[Ref.: #65424]	alpha-chymotrypsin	+	3.4.21.1
[Ref.: #65424]	alpha-fucosidase	-	3.2.1.51
[Ref.: #65424]	alpha-galactosidase	-	3.2.1.22
[Ref.: #65424]	alpha-glucosidase	-	3.2.1.20
[Ref.: #65424]	alpha-mannosidase	-	3.2.1.24
[Ref.: #65424]	beta-galactosidase	-	3.2.1.23
[Ref.: #65424]	beta-glucosidase	-	3.2.1.21
[Ref.: #65424]	beta-glucuronidase	-	3.2.1.31
[Ref.: #65424]	cystine arylamidase	+	3.4.11.3
[Ref.: #65424]	cytochrome oxidase	+	1.9.3.1
[Ref.: #65424]	esterase (C 4)	+
[Ref.: #65424]	esterase Lipase (C 8)	+
[Ref.: #65424]	leucine arylamidase	+	3.4.11.1
[Ref.: #65424]	lipase (C 14)	+
[Ref.: #65424]	N-acetyl-beta-glucosaminidase	-	3.2.1.52
[Ref.: #65424]	naphthol-AS-BI-phosphohydrolase	+
[Ref.: #65424]	trypsin	+	3.4.21.4
[Ref.: #65424]	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]	adipate degradation	100	2 of 2
[Ref.: #66794]	propionate fermentation	100	10 of 10
[Ref.: #66794]	threonine metabolism	100	10 of 10
[Ref.: #66794]	acetate fermentation	100	4 of 4
[Ref.: #66794]	C4 and CAM-carbon fixation	100	8 of 8
[Ref.: #66794]	vitamin K metabolism	100	5 of 5
[Ref.: #66794]	palmitate biosynthesis	100	22 of 22
[Ref.: #66794]	lipoate biosynthesis	100	5 of 5
[Ref.: #66794]	ppGpp biosynthesis	100	4 of 4
[Ref.: #66794]	valine metabolism	100	9 of 9
[Ref.: #66794]	cis-vaccenate biosynthesis	100	2 of 2
[Ref.: #66794]	propanol degradation	100	7 of 7
[Ref.: #66794]	anapleurotic synthesis of oxalacetate	100	1 of 1
[Ref.: #66794]	suberin monomers biosynthesis	100	2 of 2
[Ref.: #66794]	UDP-GlcNAc biosynthesis	100	3 of 3
[Ref.: #66794]	folate polyglutamylation	100	1 of 1
[Ref.: #66794]	CDP-diacylglycerol biosynthesis	100	2 of 2
[Ref.: #66794]	teichoic acid biosynthesis	100	1 of 1
[Ref.: #66794]	sulfopterin metabolism	100	4 of 4
[Ref.: #66794]	coenzyme A metabolism	100	4 of 4
[Ref.: #66794]	formaldehyde oxidation	100	3 of 3
[Ref.: #66794]	methylglyoxal degradation	100	5 of 5
[Ref.: #66794]	citric acid cycle	92.86	13 of 14
[Ref.: #66794]	glutamate and glutamine metabolism	89.29	25 of 28
[Ref.: #66794]	chorismate metabolism	88.89	8 of 9
[Ref.: #66794]	gluconeogenesis	87.5	7 of 8
[Ref.: #66794]	peptidoglycan biosynthesis	86.67	13 of 15
[Ref.: #66794]	leucine metabolism	84.62	11 of 13
[Ref.: #66794]	selenocysteine biosynthesis	83.33	5 of 6
[Ref.: #66794]	NAD metabolism	83.33	15 of 18
[Ref.: #66794]	pentose phosphate pathway	81.82	9 of 11
[Ref.: #66794]	glycogen metabolism	80	4 of 5
[Ref.: #66794]	flavin biosynthesis	80	12 of 15
[Ref.: #66794]	cellulose degradation	80	4 of 5
[Ref.: #66794]	photosynthesis	78.57	11 of 14
[Ref.: #66794]	serine metabolism	77.78	7 of 9
[Ref.: #66794]	d-mannose degradation	77.78	7 of 9
[Ref.: #66794]	aspartate and asparagine metabolism	77.78	7 of 9
[Ref.: #66794]	molybdenum cofactor biosynthesis	77.78	7 of 9
[Ref.: #66794]	CO2 fixation in Crenarchaeota	77.78	7 of 9
[Ref.: #66794]	phenylalanine metabolism	76.92	10 of 13
[Ref.: #66794]	vitamin B1 metabolism	76.92	10 of 13
[Ref.: #66794]	glycolysis	76.47	13 of 17
[Ref.: #66794]	alanine metabolism	75.86	22 of 29
[Ref.: #66794]	isoleucine metabolism	75	6 of 8
[Ref.: #66794]	butanoate fermentation	75	3 of 4
[Ref.: #66794]	ketogluconate metabolism	75	6 of 8
[Ref.: #66794]	glycogen biosynthesis	75	3 of 4
[Ref.: #66794]	biotin biosynthesis	75	3 of 4
[Ref.: #66794]	lysine metabolism	73.81	31 of 42
[Ref.: #66794]	proline metabolism	72.73	8 of 11
[Ref.: #66794]	purine metabolism	72.34	68 of 94
[Ref.: #66794]	tetrahydrofolate metabolism	71.43	10 of 14
[Ref.: #66794]	cardiolipin biosynthesis	71.43	5 of 7
[Ref.: #66794]	heme metabolism	71.43	10 of 14
[Ref.: #66794]	pyrimidine metabolism	71.11	32 of 45
[Ref.: #66794]	tryptophan metabolism	68.42	26 of 38
[Ref.: #66794]	non-pathway related	68.42	26 of 38
[Ref.: #66794]	acetyl CoA biosynthesis	66.67	2 of 3
[Ref.: #66794]	L-lactaldehyde degradation	66.67	2 of 3
[Ref.: #66794]	acetoin degradation	66.67	2 of 3
[Ref.: #66794]	octane oxidation	66.67	2 of 3
[Ref.: #66794]	glycolate and glyoxylate degradation	66.67	4 of 6
[Ref.: #66794]	6-hydroxymethyl-dihydropterin diphosphate biosynthesis	62.5	5 of 8
[Ref.: #66794]	degradation of sugar alcohols	62.5	10 of 16
[Ref.: #66794]	arginine metabolism	62.5	15 of 24
[Ref.: #66794]	urea cycle	61.54	8 of 13
[Ref.: #66794]	oxidative phosphorylation	61.54	56 of 91
[Ref.: #66794]	methionine metabolism	61.54	16 of 26
[Ref.: #66794]	isoprenoid biosynthesis	61.54	16 of 26
[Ref.: #66794]	cysteine metabolism	61.11	11 of 18
[Ref.: #66794]	3-chlorocatechol degradation	60	3 of 5
[Ref.: #66794]	factor 420 biosynthesis	60	3 of 5
[Ref.: #66794]	starch degradation	60	6 of 10
[Ref.: #66794]	glutathione metabolism	57.14	8 of 14
[Ref.: #66794]	reductive acetyl coenzyme A pathway	57.14	4 of 7
[Ref.: #66794]	histidine metabolism	55.17	16 of 29
[Ref.: #66794]	lipid metabolism	54.84	17 of 31
[Ref.: #66794]	phosphatidylethanolamine bioynthesis	53.85	7 of 13
[Ref.: #66794]	bile acid biosynthesis, neutral pathway	52.94	9 of 17
[Ref.: #66794]	degradation of aromatic, nitrogen containing compounds	50	6 of 12
[Ref.: #66794]	Entner Doudoroff pathway	50	5 of 10
[Ref.: #66794]	dTDPLrhamnose biosynthesis	50	4 of 8
[Ref.: #66794]	glycine metabolism	50	5 of 10
[Ref.: #66794]	dolichol and dolichyl phosphate biosynthesis	50	1 of 2
[Ref.: #66794]	ethanol fermentation	50	1 of 2
[Ref.: #66794]	CMP-KDO biosynthesis	50	2 of 4
[Ref.: #66794]	toluene degradation	50	2 of 4
[Ref.: #66794]	androgen and estrogen metabolism	50	8 of 16
[Ref.: #66794]	aminopropanol phosphate biosynthesis	50	1 of 2
[Ref.: #66794]	pantothenate biosynthesis	50	3 of 6
[Ref.: #66794]	resorcinol degradation	50	1 of 2
[Ref.: #66794]	phenylpropanoid biosynthesis	46.15	6 of 13
[Ref.: #66794]	4-hydroxymandelate degradation	44.44	4 of 9
[Ref.: #66794]	degradation of sugar acids	44	11 of 25
[Ref.: #66794]	polyamine pathway	43.48	10 of 23
[Ref.: #66794]	ubiquinone biosynthesis	42.86	3 of 7
[Ref.: #66794]	phenylacetate degradation (aerobic)	40	2 of 5
[Ref.: #66794]	arachidonate biosynthesis	40	2 of 5
[Ref.: #66794]	gallate degradation	40	2 of 5
[Ref.: #66794]	creatinine degradation	40	2 of 5
[Ref.: #66794]	sulfate reduction	38.46	5 of 13
[Ref.: #66794]	carnitine metabolism	37.5	3 of 8
[Ref.: #66794]	vitamin B6 metabolism	36.36	4 of 11
[Ref.: #66794]	cholesterol biosynthesis	36.36	4 of 11
[Ref.: #66794]	tyrosine metabolism	35.71	5 of 14
[Ref.: #66794]	vitamin B12 metabolism	35.29	12 of 34
[Ref.: #66794]	phenol degradation	35	7 of 20
[Ref.: #66794]	arachidonic acid metabolism	33.33	6 of 18
[Ref.: #66794]	lipid A biosynthesis	33.33	3 of 9
[Ref.: #66794]	nitrate assimilation	33.33	3 of 9
[Ref.: #66794]	IAA biosynthesis	33.33	1 of 3
[Ref.: #66794]	cyanate degradation	33.33	1 of 3
[Ref.: #66794]	3-phenylpropionate degradation	33.33	5 of 15
[Ref.: #66794]	enterobactin biosynthesis	33.33	1 of 3
[Ref.: #66794]	(5R)-carbapenem carboxylate biosynthesis	33.33	1 of 3
[Ref.: #66794]	allantoin degradation	33.33	3 of 9
[Ref.: #66794]	degradation of hexoses	33.33	6 of 18
[Ref.: #66794]	sulfoquinovose degradation	33.33	1 of 3
[Ref.: #66794]	degradation of pentoses	32.14	9 of 28
[Ref.: #66794]	ascorbate metabolism	31.82	7 of 22
[Ref.: #66794]	myo-inositol biosynthesis	30	3 of 10
[Ref.: #66794]	4-hydroxyphenylacetate degradation	30	3 of 10
[Ref.: #66794]	coenzyme M biosynthesis	30	3 of 10
[Ref.: #66794]	benzoyl-CoA degradation	28.57	2 of 7
[Ref.: #66794]	metabolism of disaccharids	27.27	3 of 11
[Ref.: #66794]	dolichyl-diphosphooligosaccharide biosynthesis	27.27	3 of 11
[Ref.: #66794]	cyclohexanol degradation	25	1 of 4
[Ref.: #66794]	lactate fermentation	25	1 of 4
[Ref.: #66794]	alginate biosynthesis	25	1 of 4
		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.: #65424]	Sample type/isolated from	a saline-alkali soil of Jade Gate Pass
[Ref.: #65424]	Geographic location (country and/or sea, region)	Gansu Province
[Ref.: #65424]	Country	China
[Ref.: #65424]	Country ISO 3 Code	CHN
[Ref.: #65424]	Continent	Asia
[Ref.: #65424]	Enrichment culture	saline agar medium
[Ref.: #65424]	Enrichment culture composition	per litre, 7.5 g casein peptone, 100 g NaCl, 10 g yeast extract, 1.5 ml MS mixture (0.05 g each of betaine, proline, glycine, D-sorbitol and glutamate, added to 1000 ml H 2 O), 20 g agar (adjusted to pH 8.0 with HCl/NaOH)
[Ref.: #65424]	Enrichment culture duration	3 days
[Ref.: #65424]	Enrichment culture temperature	37 ̊C

[Ref.: #67771]	Sample type/isolated from	From saline-alkali soil of Jade Gate Pass
[Ref.: #67771]	Geographic location (country and/or sea, region)	Gansu Province
[Ref.: #67771]	Country	China
[Ref.: #67771]	Country ISO 3 Code	CHN
[Ref.: #67771]	Continent	Asia
* marker position based on {}

Isolation sources categories

#Environmental	#Terrestrial	#Soil
#Condition	#Alkaline	-
#Condition	#Saline	-

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.: #65424]	16S rRNA gene sequence	KX008965		GenBank

Genome sequence information:

	Sequence accession description	Seq. accession number	Assembly level	Sequence database	Associated NCBI tax ID
[Ref.: #66792]	Planococcus salinus LCB217	GCA_003719725	contig	GenBank	1848460 tax ID	*
[Ref.: #66792]	Planococcus salinus LCB217	2843378535	draft	JGI IMG/M	1848460 tax ID	*

[Ref.: #65424]	GC-content	49.4 mol%	thermal denaturation, midpoint method (Tm)
[Ref.: #67771]	GC-content	49.4 mol%

Availability in culture collections External links

[Ref.: #65424]

Culture collection no.

CGMCC 1.15685, KCTC 33861

Literature:

Topic	Title	Authors	Journal	DOI	Year
Phylogeny	Indiicoccus explosivorum gen. nov., sp. nov., isolated from an explosives waste contaminated site.	Pal Y, Mayilraj S, Paul M, Schumann P, Krishnamurthi S	Int J Syst Evol Microbiol	10.1099/ijsem.0.003541	2019	*
Phylogeny	Planococcus salinus sp. nov., a moderately halophilic bacterium isolated from a saline-alkali soil.	Gan L, Zhang H, Tian J, Li X, Long X, Zhang Y, Dai Y, Tian Y	Int J Syst Evol Microbiol	10.1099/ijsem.0.002548	2018	*

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 )

#65424

Longzhan Gan, Heming Zhang, Jiewei Tian, Xiaoguang Li, Xiufeng Long, Yuqin Zhang, Yumei Dai, Yongqiang Tian: Planococcus salinus sp. nov., a moderately halophilic bacterium isolated from a saline-alkali soil. IJSEM 68: 589 - 595 2018 ( DOI 10.1099/ijsem.0.002548 , PubMed 29300160 )

#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 )

#67771 Korean Collection for Type Cultures (KCTC) ; Curators of the KCTC;
* These data were automatically processed and therefore are not curated

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