Name: Mesobacillus zeae JJ-247
Creator: BacDive
License: http://creativecommons.org/licenses/by-nc/4.0/

Strain identifier

BacDive ID: 140266

Type strain:

Species: Mesobacillus zeae

Strain Designation: JJ-247

Culture col. no.: DSM 103964, CCM 8726, LMG 29876

Strain history: <- P. Kämpfer, Justus-Liebig-Universität, Giessen, Germany <- J. A. McInroy; JJ-247

NCBI tax ID(s): 1917180 (species)

Section

Mesobacillus zeae JJ-247 is an aerobe, thermophilic, Gram-positive bacterium that forms circular colonies and was isolated from rhizosphere of field-grown Zea mays plants.

colony-forming
Gram-positive
rod-shaped
aerobe
thermophilic
16S sequence
Bacteria
genome sequence

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

	Last LPSN update	15-12-2021 (DD-MM-YYYY)
	Domain	Bacteria
	Phylum	Firmicutes
	Class	Bacilli
	Order	Caryophanales
	Family	Bacillaceae
	Genus	Mesobacillus
	Species	Mesobacillus zeae
	Full Scientific Name (PNU)	Mesobacillus zeae (Kämpfer et al. 2017) Patel and Gupta 2020

Synonym

Bacillus zeae

Information on morphological and physiological properties Morphology

[Ref.: #43173]	Gram stain	positive
[Ref.: #43173]	Cell length	3.5 µm
[Ref.: #43173]	Cell width	1 µm
[Ref.: #43173]	Cell shape	rod-shaped
[Ref.: #43173]	Motility	no

[Ref.: #43173]	Colony color	beige
[Ref.: #43173]	Colony shape	circular
[Ref.: #43173]	Cultivation medium used	nutritient agar (NA)

Information on culture and growth conditions Culture and growth conditions

[Ref.: #43173]

Culture medium

nutritient agar (NA)

[Ref.: #43173]

Culture medium growth

[Ref.: #43173]

Culture medium

brain heart infusion agar

[Ref.: #43173]

Culture medium growth

[Ref.: #43173]

Culture medium

tryptic soy agar (TSA)

[Ref.: #43173]

Culture medium growth

[Ref.: #43173]

Culture medium

Reasoner's 2A agar (R2A)

[Ref.: #43173]

Culture medium growth

[Ref.: #42873]

Culture medium

CASO AGAR (MERCK 105458) (DSMZ Medium 220)

[Ref.: #42873]

Culture medium growth

[Ref.: #42873]

Culture medium link

Medium recipe at BacMedia

[Ref.: #42873]

Culture medium composition

expand / minimize

[Ref.: #42873]

Culture medium

PLATE COUNT AGAR (DSMZ Medium 464)

[Ref.: #42873]

Culture medium growth

[Ref.: #42873]

Culture medium link

Medium recipe at BacMedia

[Ref.: #42873]

Culture medium composition

expand / minimize

		Temperature
[Ref.: #42873]	growth	30 °C
[Ref.: #43173]	maximum	50 °C
[Ref.: #43173]	minimum	10 °C
[Ref.: #43173]	optimum	28-30 °C
[Ref.: #43173]	growth	20-30 °C

[Ref.: #42873]	Temperature range	mesophilic
[Ref.: #43173]	Temperature range	thermophilic
[Ref.: #43173]	Temperature range	psychrophilic
[Ref.: #43173]	Temperature range	mesophilic

	pH	Kind of pH		pH
[Ref.: #43173]			optimum	7
[Ref.: #43173]			growth	6.0-10.0

Information on physiology and metabolism Physiology and metabolism

[Ref.: #43173]

Oxygen tolerance

aerobe

[Ref.: #43173]

Ability of spore formation

	Halophily	Salt	Tested relation		Salt conc.
[Ref.: #43173]		NaCl		growth	0-8.0	%(w/v)
[Ref.: #43173]		NaCl		optimum	3-5	%(w/v)

	Metabolite	Utilization activity	Kind of utilization tested
[Ref.: #43173]	2-deoxythymidine-5'-4-nitrophenyl phosphate	-	hydrolysis
[Ref.: #43173]	2-oxoglutarate ChEBI	-	carbon source
[Ref.: #43173]	3-hydroxybenzoate ChEBI	-	carbon source
[Ref.: #43173]	3-hydroxybutyrate ChEBI	-	carbon source
[Ref.: #43173]	3-O-methyl alpha-D-glucopyranoside	-	builds acid from
[Ref.: #43173]	4-hydroxybenzoate ChEBI	-	carbon source
[Ref.: #43173]	4-nitrophenyl alpha-D-glucopyranoside ChEBI	+	hydrolysis
[Ref.: #43173]	4-nitrophenyl beta-D-galactopyranoside ChEBI	-	hydrolysis
[Ref.: #43173]	4-nitrophenyl beta-D-glucopyranoside ChEBI	-	hydrolysis
[Ref.: #43173]	4-nitrophenyl beta-D-glucuronide ChEBI	-	hydrolysis
[Ref.: #43173]	4-nitrophenyl beta-D-xylopyranoside ChEBI	-	hydrolysis
[Ref.: #43173]	acetate ChEBI	+	carbon source
[Ref.: #43173]	adipate ChEBI	-	carbon source
[Ref.: #43173]	azelaate ChEBI	-	carbon source
[Ref.: #43173]	beta-alanine ChEBI	-	carbon source
[Ref.: #43173]	bis-4-nitrophenyl phosphate ChEBI	+	hydrolysis
[Ref.: #43173]	bis-4-nitrophenyl-phosphorylcholine ChEBI	-	hydrolysis
[Ref.: #43173]	casein	-	hydrolysis
[Ref.: #43173]	cellobiose ChEBI	-	carbon source
[Ref.: #43173]	cis-aconitate ChEBI	-	carbon source
[Ref.: #43173]	citrate ChEBI	-	carbon source
[Ref.: #43173]	D-arabitol ChEBI	-	builds acid from
[Ref.: #43173]	D-fructose ChEBI	-	carbon source
[Ref.: #43173]	D-galactose ChEBI	-	carbon source
[Ref.: #43173]	D-glucose ChEBI	+	builds acid from
[Ref.: #43173]	D-glucose ChEBI	+	carbon source
[Ref.: #43173]	D-mannitol ChEBI	-	builds acid from
[Ref.: #43173]	D-mannitol ChEBI	-	carbon source
[Ref.: #43173]	D-mannose ChEBI	-	carbon source
[Ref.: #43173]	D-ribose ChEBI	-	carbon source
[Ref.: #43173]	D-sorbitol ChEBI	-	builds acid from
[Ref.: #43173]	D-sorbitol ChEBI	-	carbon source
[Ref.: #43173]	D-xylose ChEBI	-	builds acid from
[Ref.: #43173]	D-xylose ChEBI	-	carbon source
[Ref.: #43173]	dna ChEBI	-	hydrolysis
[Ref.: #43173]	erythritol ChEBI	-	builds acid from
[Ref.: #43173]	fumarate ChEBI	-	carbon source
[Ref.: #43173]	galactitol ChEBI	-	builds acid from
[Ref.: #43173]	gamma-aminobutyric acid ChEBI	-	carbon source
[Ref.: #43173]	gamma-L-glutamate-4-nitroanilide	-	hydrolysis
[Ref.: #43173]	gelatin ChEBI	-	hydrolysis
[Ref.: #43173]	gluconate ChEBI	-	carbon source
[Ref.: #43173]	glutarate ChEBI	-	carbon source
[Ref.: #43173]	glycerol ChEBI	-	carbon source
[Ref.: #43173]	itaconate ChEBI	-	carbon source
[Ref.: #43173]	L-alanine ChEBI	-	carbon source
[Ref.: #43173]	L-alanine 4-nitroanilide	-	hydrolysis
[Ref.: #43173]	L-arabinose ChEBI	-	builds acid from
[Ref.: #43173]	L-arabinose ChEBI	-	carbon source
[Ref.: #43173]	L-aspartate ChEBI	-	carbon source
[Ref.: #43173]	L-histidine ChEBI	-	carbon source
[Ref.: #43173]	L-leucine ChEBI	-	carbon source
[Ref.: #43173]	L-ornithine ChEBI	-	carbon source
[Ref.: #43173]	L-phenylalanine ChEBI	-	carbon source
[Ref.: #43173]	L-proline ChEBI	-	carbon source
[Ref.: #43173]	L-proline-4-nitroanilide	-	hydrolysis
[Ref.: #43173]	L-rhamnose ChEBI	-	builds acid from
[Ref.: #43173]	L-rhamnose ChEBI	-	carbon source
[Ref.: #43173]	L-serine ChEBI	-	carbon source
[Ref.: #43173]	L-tryptophan ChEBI	-	carbon source
[Ref.: #43173]	lactate ChEBI	-	carbon source
[Ref.: #43173]	lactose ChEBI	-	builds acid from
[Ref.: #43173]	maltitol ChEBI	-	carbon source
[Ref.: #43173]	maltose ChEBI	-	builds acid from
[Ref.: #43173]	maltose ChEBI	-	carbon source
[Ref.: #43173]	melibiose ChEBI	-	builds acid from
[Ref.: #43173]	melibiose ChEBI	-	carbon source
[Ref.: #43173]	mesaconate ChEBI	-	carbon source
[Ref.: #43173]	myo-inositol ChEBI	-	builds acid from
[Ref.: #43173]	myo-inositol ChEBI	-	carbon source
[Ref.: #43173]	N-acetylgalactosamine ChEBI	-	carbon source
[Ref.: #43173]	N-acetylglucosamine ChEBI	-	carbon source
[Ref.: #43173]	phenylacetate ChEBI	-	carbon source
[Ref.: #43173]	propionate ChEBI	+	carbon source
[Ref.: #43173]	putrescine ChEBI	-	carbon source
[Ref.: #43173]	pyruvate ChEBI	-	carbon source
[Ref.: #43173]	raffinose ChEBI	-	builds acid from
[Ref.: #43173]	ribitol ChEBI	-	builds acid from
[Ref.: #43173]	ribitol ChEBI	-	carbon source
[Ref.: #43173]	salicin ChEBI	-	builds acid from
[Ref.: #43173]	salicin ChEBI	-	carbon source
[Ref.: #43173]	starch ChEBI	-	hydrolysis
[Ref.: #43173]	suberic acid ChEBI	-	carbon source
[Ref.: #43173]	sucrose ChEBI	+	builds acid from
[Ref.: #43173]	sucrose ChEBI	-	carbon source
[Ref.: #43173]	trans-aconitate ChEBI	-	carbon source
[Ref.: #43173]	trehalose ChEBI	-	builds acid from
[Ref.: #43173]	tyrosine ChEBI	-	hydrolysis
	Only first 10 entries are displayed. Click here to see all.

	Metabolite production	Metabolite	Production
[Ref.: #43173]		hydrogen sulfide ChEBI	no
[Ref.: #43173]		indole ChEBI	no

	Enzyme	Enzyme activity	EC number
[Ref.: #43173]	arginine dihydrolase	-	3.5.3.6
[Ref.: #43173]	beta-galactosidase	-	3.2.1.23
[Ref.: #43173]	catalase	+	1.11.1.6
[Ref.: #43173]	cytochrome oxidase	+	1.9.3.1
[Ref.: #43173]	lysine decarboxylase	-	4.1.1.18
[Ref.: #43173]	ornithine decarboxylase	-	4.1.1.17
[Ref.: #43173]	urease	-	3.5.1.5

Fatty acid profile

Metadata FA analysis

Reference

[Ref.: #43173]

Fatty acid	Percentage
C15:0 iso	41.9
C17:1 iso ω10c	9.3
C17:0 iso	9.1
C16:0 iso	7.7
C16:1ω7c OH	4.9
C15:0 anteiso	4.8
C17:0 anteiso	4.5
iso-C17:1 l / anteiso-C17:1 B	4.3
C16:1ω11c	3.6
C16:0	3.1
C15:0	2.7
C14:0 iso	2.5
C15:1 iso F	1.5

	Pathway	Enzyme coverage	Annotated reactions
	Pathway annotation	Computationally determined by
[Ref.: #66794]	adipate degradation	100	2 of 2
[Ref.: #66794]	vitamin K metabolism	100	5 of 5
[Ref.: #66794]	cis-vaccenate biosynthesis	100	2 of 2
[Ref.: #66794]	aspartate and asparagine metabolism	100	9 of 9
[Ref.: #66794]	palmitate biosynthesis	100	22 of 22
[Ref.: #66794]	methylglyoxal degradation	100	5 of 5
[Ref.: #66794]	butanoate fermentation	100	4 of 4
[Ref.: #66794]	valine metabolism	100	9 of 9
[Ref.: #66794]	lipoate biosynthesis	100	5 of 5
[Ref.: #66794]	molybdenum cofactor biosynthesis	100	9 of 9
[Ref.: #66794]	biotin biosynthesis	100	4 of 4
[Ref.: #66794]	C4 and CAM-carbon fixation	100	8 of 8
[Ref.: #66794]	reductive acetyl coenzyme A pathway	100	7 of 7
[Ref.: #66794]	sulfopterin metabolism	100	4 of 4
[Ref.: #66794]	CDP-diacylglycerol biosynthesis	100	2 of 2
[Ref.: #66794]	UDP-GlcNAc biosynthesis	100	3 of 3
[Ref.: #66794]	folate polyglutamylation	100	1 of 1
[Ref.: #66794]	teichoic acid biosynthesis	100	1 of 1
[Ref.: #66794]	coenzyme A metabolism	100	4 of 4
[Ref.: #66794]	suberin monomers biosynthesis	100	2 of 2
[Ref.: #66794]	anapleurotic synthesis of oxalacetate	100	1 of 1
[Ref.: #66794]	tetrahydrofolate metabolism	92.86	13 of 14
[Ref.: #66794]	glutamate and glutamine metabolism	92.86	26 of 28
[Ref.: #66794]	vitamin B1 metabolism	92.31	12 of 13
[Ref.: #66794]	propionate fermentation	90	9 of 10
[Ref.: #66794]	threonine metabolism	90	9 of 10
[Ref.: #66794]	serine metabolism	88.89	8 of 9
[Ref.: #66794]	CO2 fixation in Crenarchaeota	88.89	8 of 9
[Ref.: #66794]	chorismate metabolism	88.89	8 of 9
[Ref.: #66794]	gluconeogenesis	87.5	7 of 8
[Ref.: #66794]	photosynthesis	85.71	12 of 14
[Ref.: #66794]	heme metabolism	85.71	12 of 14
[Ref.: #66794]	propanol degradation	85.71	6 of 7
[Ref.: #66794]	leucine metabolism	84.62	11 of 13
[Ref.: #66794]	alanine metabolism	82.76	24 of 29
[Ref.: #66794]	cellulose degradation	80	4 of 5
[Ref.: #66794]	flavin biosynthesis	80	12 of 15
[Ref.: #66794]	glycine betaine biosynthesis	80	4 of 5
[Ref.: #66794]	peptidoglycan biosynthesis	80	12 of 15
[Ref.: #66794]	glycogen metabolism	80	4 of 5
[Ref.: #66794]	vitamin B12 metabolism	79.41	27 of 34
[Ref.: #66794]	citric acid cycle	78.57	11 of 14
[Ref.: #66794]	pyrimidine metabolism	77.78	35 of 45
[Ref.: #66794]	phenylalanine metabolism	76.92	10 of 13
[Ref.: #66794]	glycolysis	76.47	13 of 17
[Ref.: #66794]	tryptophan metabolism	76.32	29 of 38
[Ref.: #66794]	ppGpp biosynthesis	75	3 of 4
[Ref.: #66794]	isoleucine metabolism	75	6 of 8
[Ref.: #66794]	glycogen biosynthesis	75	3 of 4
[Ref.: #66794]	acetate fermentation	75	3 of 4
[Ref.: #66794]	6-hydroxymethyl-dihydropterin diphosphate biosynthesis	75	6 of 8
[Ref.: #66794]	phenol degradation	75	15 of 20
[Ref.: #66794]	methionine metabolism	73.08	19 of 26
[Ref.: #66794]	proline metabolism	72.73	8 of 11
[Ref.: #66794]	pentose phosphate pathway	72.73	8 of 11
[Ref.: #66794]	purine metabolism	72.34	68 of 94
[Ref.: #66794]	NAD metabolism	72.22	13 of 18
[Ref.: #66794]	cardiolipin biosynthesis	71.43	5 of 7
[Ref.: #66794]	starch degradation	70	7 of 10
[Ref.: #66794]	urea cycle	69.23	9 of 13
[Ref.: #66794]	arginine metabolism	66.67	16 of 24
[Ref.: #66794]	L-lactaldehyde degradation	66.67	2 of 3
[Ref.: #66794]	selenocysteine biosynthesis	66.67	4 of 6
[Ref.: #66794]	glycolate and glyoxylate degradation	66.67	4 of 6
[Ref.: #66794]	acetyl CoA biosynthesis	66.67	2 of 3
[Ref.: #66794]	cyanate degradation	66.67	2 of 3
[Ref.: #66794]	formaldehyde oxidation	66.67	2 of 3
[Ref.: #66794]	acetoin degradation	66.67	2 of 3
[Ref.: #66794]	enterobactin biosynthesis	66.67	2 of 3
[Ref.: #66794]	non-pathway related	65.79	25 of 38
[Ref.: #66794]	histidine metabolism	65.52	19 of 29
[Ref.: #66794]	glutathione metabolism	64.29	9 of 14
[Ref.: #66794]	oxidative phosphorylation	62.64	57 of 91
[Ref.: #66794]	cysteine metabolism	61.11	11 of 18
[Ref.: #66794]	coenzyme M biosynthesis	60	6 of 10
[Ref.: #66794]	phenylacetate degradation (aerobic)	60	3 of 5
[Ref.: #66794]	lipid metabolism	58.06	18 of 31
[Ref.: #66794]	isoprenoid biosynthesis	57.69	15 of 26
[Ref.: #66794]	tyrosine metabolism	57.14	8 of 14
[Ref.: #66794]	d-mannose degradation	55.56	5 of 9
[Ref.: #66794]	Entner Doudoroff pathway	50	5 of 10
[Ref.: #66794]	CMP-KDO biosynthesis	50	2 of 4
[Ref.: #66794]	pantothenate biosynthesis	50	3 of 6
[Ref.: #66794]	aminopropanol phosphate biosynthesis	50	1 of 2
[Ref.: #66794]	4-hydroxyphenylacetate degradation	50	5 of 10
[Ref.: #66794]	lysine metabolism	50	21 of 42
[Ref.: #66794]	ethanol fermentation	50	1 of 2
[Ref.: #66794]	degradation of aromatic, nitrogen containing compounds	50	6 of 12
[Ref.: #66794]	ketogluconate metabolism	50	4 of 8
[Ref.: #66794]	glycine metabolism	50	5 of 10
[Ref.: #66794]	phenylpropanoid biosynthesis	46.15	6 of 13
[Ref.: #66794]	sulfate reduction	46.15	6 of 13
[Ref.: #66794]	vitamin B6 metabolism	45.45	5 of 11
[Ref.: #66794]	degradation of hexoses	44.44	8 of 18
[Ref.: #66794]	4-hydroxymandelate degradation	44.44	4 of 9
[Ref.: #66794]	nitrate assimilation	44.44	4 of 9
[Ref.: #66794]	androgen and estrogen metabolism	43.75	7 of 16
[Ref.: #66794]	ubiquinone biosynthesis	42.86	3 of 7
[Ref.: #66794]	ascorbate metabolism	40.91	9 of 22
[Ref.: #66794]	3-phenylpropionate degradation	40	6 of 15
[Ref.: #66794]	gallate degradation	40	2 of 5
[Ref.: #66794]	metabolism of amino sugars and derivatives	40	2 of 5
[Ref.: #66794]	arachidonate biosynthesis	40	2 of 5
[Ref.: #66794]	hydrogen production	40	2 of 5
[Ref.: #66794]	phosphatidylethanolamine bioynthesis	38.46	5 of 13
[Ref.: #66794]	polyamine pathway	34.78	8 of 23
[Ref.: #66794]	IAA biosynthesis	33.33	1 of 3
[Ref.: #66794]	(5R)-carbapenem carboxylate biosynthesis	33.33	1 of 3
[Ref.: #66794]	lipid A biosynthesis	33.33	3 of 9
[Ref.: #66794]	octane oxidation	33.33	1 of 3
[Ref.: #66794]	allantoin degradation	33.33	3 of 9
[Ref.: #66794]	degradation of pentoses	32.14	9 of 28
[Ref.: #66794]	cholesterol biosynthesis	27.27	3 of 11
[Ref.: #66794]	metabolism of disaccharids	27.27	3 of 11
[Ref.: #66794]	alginate biosynthesis	25	1 of 4
[Ref.: #66794]	methanogenesis from CO2	25	3 of 12
[Ref.: #66794]	cyclohexanol degradation	25	1 of 4
[Ref.: #66794]	lactate fermentation	25	1 of 4
[Ref.: #66794]	degradation of sugar alcohols	25	4 of 16
[Ref.: #66794]	dTDPLrhamnose biosynthesis	25	2 of 8
[Ref.: #66794]	toluene degradation	25	1 of 4
[Ref.: #66794]	bile acid biosynthesis, neutral pathway	23.53	4 of 17
[Ref.: #66794]	arachidonic acid metabolism	22.22	4 of 18
		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.: #42873]	Sample type/isolated from	rhizosphere of field-grown Zea mays plants
[Ref.: #42873]	Host species	Zea mays
[Ref.: #42873]	Geographic location (country and/or sea, region)	Nebraska, Dunbar
[Ref.: #42873]	Country	USA
[Ref.: #42873]	Country ISO 3 Code	USA
[Ref.: #42873]	Continent	North America

[Ref.: #43173]	Sample type/isolated from	rhizosphere of maize plants
[Ref.: #43173]	Geographic location (country and/or sea, region)	field in Dunbar, Nebraska
[Ref.: #43173]	Country	USA
[Ref.: #43173]	Country ISO 3 Code	USA
[Ref.: #43173]	Continent	North America
[Ref.: #43173]	Enrichment culture	nutrient agar (NA; Sigma-Aldrich)
[Ref.: #43173]	Enrichment culture duration	2 days
[Ref.: #43173]	Enrichment culture temperature	30 ̊C
[Ref.: #43173]	Isolation/enrichment procedure	serial dilution plating technique

Isolation sources categories

#Engineered	#Agriculture	#Field
#Host	#Plants	#Herbaceous plants (Grass,Crops)
#Host Body-Site	#Plant	#Rhizosphere

What are isolation sources categories?

* marker position based on {}

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

[Ref.: #42873]

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.: #42873]	Bacillus zeae strain JJ-247 16S ribosomal RNA gene, partial sequence	KY114944	1473	ENA	1917180 tax ID

Genome sequence information:

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

	Sequence accession description	Seq. accession number	Assembly level (bp)	Sequence database	Associated NCBI tax ID
[Ref.: #66792]	Mesobacillus zeae JJ-247	GCA_013618945	contig	GenBank	1917180 tax ID	*
[Ref.: #66792]	Mesobacillus zeae JJ-247	GCA_003570705	contig	GenBank	1917180 tax ID	*
[Ref.: #66792]	Bacillus zeae strain JJ-247	1917180.3	wgs	PATRIC	1917180 tax ID	*
[Ref.: #66792]	Mesobacillus zeae strain DSM 103964	1917180.7	wgs	PATRIC	1917180 tax ID	*
[Ref.: #66792]	Mesobacillus zeae strain JJ-247	1917180.5	wgs	PATRIC	1917180 tax ID	*
[Ref.: #66792]	Mesobacillus zeae DSM 103964	2913584337	draft	JGI IMG/M	1917180 tax ID	*

[Ref.: #43173]	GC-content	44.5 mol%	Thermal denaturation, fluorometry
[Ref.: #42873]	GC-content	44.5 mol%	fluorimetric

Availability in culture collections External links

[Ref.: #42873]

Culture collection no.

DSM 103964, CCM 8726, LMG 29876

References

#20215

Leibniz Institute DSMZ D.Gleim, M.Kracht, N.Weiss et. al.: Prokaryotic Nomenclature Up-to-date - compilation of all names of Bacteria and Archaea, validly published according to the Bacteriological Code since 1. Jan. 1980, and validly published nomenclatural changes since .

#42873

Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 103964

#43173

Peter Kämpfer, Hans-Jürgen Busse, John A. McInroy, Chia-Hui Hu, Joseph W. Kloepper, Stefanie P. Glaeser: Bacillus zeae sp. nov., isolated from the rhizosphere of Zea mays. IJSEM 67: 1241 - 1246 2017 ( DOI 10.1099/ijsem.0.001791 , PubMed 28086067 )

#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 References are textmined

Change proposal

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