Name: Bacillus subtilis DSM 2109
Creator: BacDive
License: https://creativecommons.org/licenses/by/4.0/

Strain identifier

BacDive ID: 967

Type strain:

Species: Bacillus subtilis

Culture col. no.: DSM 2109, ATCC 11774, NCTC 8236, CCUG 50054, NCIMB 8739, ICI 2/4, CIP 1.83

Strain history: CIP <- 1982, ATCC <- NCTC <- 1952, J.H. Humphrey

NCBI tax ID(s): 1423 (species)

SI-ID 35425

ATCC 11774, NCTC 8236, DSM 2109, NCIB 8739, NCIMB 8739, CCM2217, IMET10899, NCIMB9269, NCIB 8565, CIP 1.83, LMD 80.10, CECT 35, NCCB 80010, BCRC 16068, CCRC 16068, CCUG 50054, NBIMCC 1711, NCIM 2717, NCIM 2718, NCIB 9269, ACM 2789, CNCTC 6217, CGMCC 1.3382

Special Collections

Other strains from Bacillus subtilis

Section

Bacillus subtilis DSM 2109 is an obligate aerobe, spore-forming, Gram-positive human pathogen that produces antibiotic compounds.

antibiotic compound production
Gram-positive
motile
rod-shaped
spore-forming
human pathogen
obligate 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	*Bacillota*
	Class	*Bacilli*
	Order	*Caryophanales*
	Family	*Bacillaceae*
	Genus	*Bacillus*
	Species	**Bacillus subtilis**
	Full Scientific Name (LPSN)	Bacillus subtilis (Ehrenberg 1835) Cohn 1872 (Approved Lists 1980)

Synonym

"Vibrio subtilis"

Information on morphological and physiological properties Morphology

[Ref.: #123356]	Gram stain	positive

[Ref.: #123356]	Cell shape	rod-shaped

[Ref.: #123356]	Motility	yes

[Ref.: #123356]

Hemolysis ability

Information on culture and growth conditions Culture and growth conditions

[Ref.: #964]

Culture medium

NUTRIENT AGAR (DSMZ Medium 1)

[Ref.: #964]

Culture medium growth

[Ref.: #964]

Culture medium link

Medium recipe at MediaDive

[Ref.: #964]

Culture medium composition

expand / minimize

[Ref.: #35250]

Culture medium

MEDIUM 72- for trypto casein soja agar

[Ref.: #35250]

Culture medium growth

[Ref.: #35250]

Culture medium composition

expand / minimize

[Ref.: #123356]

Culture medium

CIP Medium 72

[Ref.: #123356]

Culture medium growth

[Ref.: #123356]

Culture medium link

Medium recipe provided by DSMZ

	Kind of temperature		Temperature
[Ref.: #964]		growth	30 °C
[Ref.: #35250]		growth	30 °C
[Ref.: #123356]		growth	22-45 °C
[Ref.: #123356]	no	growth	10 °C
[Ref.: #123356]	no	growth	55 °C

	pH	Kind of pH		pH
[Ref.: #123356]			growth	6

Information on physiology and metabolism Physiology and metabolism

[Ref.: #123356]

Oxygen tolerance

obligate aerobe

[Ref.: #123356]	Ability of spore formation	yes
[Ref.: #69480]	Ability of spore formation	yes Confidence in %95.33
[Ref.: #69481]	Ability of spore formation	yes Confidence in %100

[Ref.: #964]

Name of produced compound

streptomycin

	Halophily	Salt	Tested relation		Salt conc.
[Ref.: #123356]		NaCl		growth	0-10	%

	Metabolite	Utilization activity	Kind of utilization tested
[Ref.: #68371]	arbutin ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	cellobiose ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #123356]	citrate ChEBI	-	carbon source
[Ref.: #68371]	D-arabinose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	D-arabitol ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	D-fructose ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	D-fucose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	D-galactose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	D-glucose ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	D-lyxose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	D-mannitol ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	D-mannose ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	D-tagatose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	erythritol ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #123356]	esculin ChEBI	+	hydrolysis
[Ref.: #68371]	esculin ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	galactitol ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	glycerol ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	glycogen ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #123356]	hippurate ChEBI	-	hydrolysis
[Ref.: #68371]	L-arabinose ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	L-arabitol ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	L-fucose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	L-rhamnose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	L-sorbose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	L-xylose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	lactose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	maltose ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	melezitose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	melibiose ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	methyl alpha-D-glucopyranoside ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	methyl alpha-D-mannoside ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	methyl beta-D-xylopyranoside ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #123356]	nitrate ChEBI	+	reduction
[Ref.: #123356]	nitrate ChEBI	-	respiration
[Ref.: #123356]	nitrite ChEBI	-	reduction
[Ref.: #68371]	Potassium 2-ketogluconate ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	Potassium 5-ketogluconate ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	ribitol ChEBI	-	builds acid from	* from API 50CH acid
[Ref.: #68371]	salicin ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	starch ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	sucrose ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	trehalose ChEBI	+	builds acid from	* from API 50CH acid
[Ref.: #68371]	xylitol ChEBI	-	builds acid from	* from API 50CH acid
	Only first 10 entries are displayed. Click here to see all.

	Metabolite production	Metabolite	Production
[Ref.: #123356]		indole ChEBI	no

	Physiological tests	Metabolite	Methylred-test
[Ref.: #123356]		glucose ChEBI	-

	Enzyme	Enzyme activity	EC number
[Ref.: #68382]	acid phosphatase	+	3.1.3.2	* from API zym
[Ref.: #123356]	alcohol dehydrogenase	-	1.1.1.1
[Ref.: #68382]	alkaline phosphatase	+	3.1.3.1	* from API zym
[Ref.: #68382]	alpha-chymotrypsin	-	3.4.21.1	* from API zym
[Ref.: #68382]	alpha-fucosidase	-	3.2.1.51	* from API zym
[Ref.: #68382]	alpha-galactosidase	-	3.2.1.22	* from API zym
[Ref.: #68382]	alpha-glucosidase	+	3.2.1.20	* from API zym
[Ref.: #68382]	alpha-mannosidase	-	3.2.1.24	* from API zym
[Ref.: #123356]	amylase	+
[Ref.: #123356]	beta-galactosidase	+	3.2.1.23
[Ref.: #68382]	beta-galactosidase	-	3.2.1.23	* from API zym
[Ref.: #68382]	beta-glucosidase	-	3.2.1.21	* from API zym
[Ref.: #68382]	beta-glucuronidase	-	3.2.1.31	* from API zym
[Ref.: #123356]	caseinase	+	3.4.21.50
[Ref.: #123356]	catalase	+	1.11.1.6
[Ref.: #68382]	cystine arylamidase	-	3.4.11.3	* from API zym
[Ref.: #123356]	DNase	+
[Ref.: #68382]	esterase (C 4)	+		* from API zym
[Ref.: #68382]	esterase lipase (C 8)	+		* from API zym
[Ref.: #123356]	gamma-glutamyltransferase	+	2.3.2.2
[Ref.: #123356]	gelatinase	+/-
[Ref.: #123356]	lecithinase	+
[Ref.: #68382]	leucine arylamidase	-	3.4.11.1	* from API zym
[Ref.: #123356]	lipase	+
[Ref.: #68382]	lipase (C 14)	-		* from API zym
[Ref.: #123356]	lysine decarboxylase	-	4.1.1.18
[Ref.: #68382]	N-acetyl-beta-glucosaminidase	-	3.2.1.52	* from API zym
[Ref.: #68382]	naphthol-AS-BI-phosphohydrolase	+		* from API zym
[Ref.: #123356]	ornithine decarboxylase	-	4.1.1.17
[Ref.: #123356]	oxidase	-
[Ref.: #123356]	phenylalanine ammonia-lyase	-	4.3.1.24
[Ref.: #123356]	protease	+
[Ref.: #68382]	trypsin	-	3.4.21.4	* from API zym
[Ref.: #123356]	tryptophan deaminase	-
[Ref.: #123356]	tween esterase	-
[Ref.: #123356]	urease	-	3.5.1.5
[Ref.: #68382]	valine arylamidase	-		* from API zym
	Only first 10 entries are displayed. Click here to see all.

API® 50CH acid:

Note that the displayed test results represent raw data and therefore may deviate!

	API ID	ControlQ	Acid from glycerolGLY	Acid from erythritolERY	Acid from D-arabinoseDARA	Acid from L-arabinoseLARA	Acid from D-riboseRIB	Acid from D-xyloseDXYL	Acid from L-xyloseLXYL	Acid from D-adonitolADO	Acid from methyl beta-D-xylopyranosideMDX	Acid from D-galactoseGAL	Acid from D-glucoseGLU	Acid from D-fructoseFRU	Acid from D-mannoseMNE	Acid from L-sorboseSBE	Acid from L-rhamnoseRHA	Acid from dulcitolDUL	Acid from inositolINO	Acid from D-mannitolMAN	Acid from D-sorbitolSOR	Acid from methyl alpha-D-mannopyranosideMDM	Acid from methyl alpha-D-glucopyranosideMDG	Acid from N-acetyl-glucosamineNAG	Acid from amygdalinAMY	Acid from arbutinARB	Acid from esculinESC	Acid from salicinSAL	Acid from cellobioseCEL	Acid from maltoseMAL	Acid from lactoseLAC	Acid from melibioseMEL	Acid from sucroseSAC	Acid from trehaloseTRE	Acid from inulinINU	Acid from melezitoseMLZ	Acid from raffinoseRAF	Acid from starchAMD	Acid from glycogenGLYG	Acid from xylitolXLT	Acid from gentiobioseGEN	Acid from turanoseTUR	Acid from D-lyxoseLYX	Acid from D-tagatoseTAG	Acid from D-fucoseDFUC	Acid from L-fucoseLFUC	Acid from D-arabitolDARL	Acid from L-arabitolLARL	Acid from gluconateGNT	Acid from 2-Ketogluconate2KG	Acid from 5-Ketogluconate5KG
[Ref.: #123356]	8633	not determinedn.d.	-	-	-	+	+/-	+/-	-	-	-	-	+	+	+	-	-	-	+/-	+	+/-	-	+	+/-	+/-	+	+	+	+	+	-	-	+	+	+/-	-	+/-	+	+	-	+/-	+/-	-	-	-	-	-	-	+/-	-	-

API® Biotype100:

Note that the displayed test results represent raw data and therefore may deviate!

	API ID	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
[Ref.: #123356]	1	not determinedn.d.	+	+	-	+	+	-	+	+	+	+	+	-	-	-	+	+	+	+	+	+	+	+	+	-	-	-	-	-	-	-	-	+	+	+	+	+	+	-	-	-	-	+	-	+	+	-	-	-	-	+	+	+	-	+	-	+	-	-	-	+	+	-	-	-	-	-	-	-	-	-	-	-	-	-	-	+	-	-	-	+	+	-	-	-	-	-	+	-	-	+	+	+	+	+	-	-	-	-	-

API® zym:

Note that the displayed test results represent raw data and therefore may deviate!

	API ID	Control	2-naphthyl phosphateAlkaline phosphatase	2-naphthyl butyrateEsterase (C 4)	2-naphtyl caprylateEsterase Lipase (C 8)	2-naphthyl myristateLipase (C 14)	L-leucyl-2-naphthylamideLeucine arylamidase	L-valyl-2-naphthylamideValine arylamidase	L-cystyl-2-naphthylamideCystine arylamidase	N-benzoyl-DL-arginine-2-naphthylamideTrypsin	N-glutaryl-phenylalanine-2-naphthylamidealpha- Chymotrypsin	2-naphthyl phosphateAcid phosphatase	Naphthol-AS-BI-phosphateNaphthol-AS-BI-phosphohydrolase	6-Br-2-naphthyl-alphaD-galactpyranosidealpha- Galactosidase	2-naphthyl-betaD-galactpyranosidebeta- Galactosidase	Naphthol-AS-BI-betaD-glucuronidebeta- Glucuronidase	2-naphthyl-alphaD-glucopyranosidealpha- Glucosidase	6-Br-2-naphthyl-betaD-glucopyranosidebeta- Glucosidase	1-naphthyl-N-acetyl-betaD-glucosaminideN-acetyl-beta- glucosaminidase	6-Br-2-naphthyl-alphaD-mannopyranosidealpha- Mannosidase	2-naphthyl-alphaL-fucopyranosidealpha- Fucosidase
[Ref.: #123356]	6534	-	+	+	+	-	-	-	-	-	-	+	+	-	-	-	+	-	-	-	-

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

[Ref.: #964]	Pathogenicity (human)	yes, in single cases
[Ref.: #964]	Biosafety level	1	Risk group (German classification) According to TRBA 466
[Ref.: #123356]	Biosafety level	1	Risk group (French classification)

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.: #20218]	Bacillus subtilis strain ATCC 11774 16S ribosomal RNA gene, partial sequence	JF749285	804	GenBank ENA	1423 tax ID	*

Genome sequence information:

	Sequence accession description	Seq. accession number	Assembly level	Sequence database	Associated NCBI tax ID
[Ref.: #66792]	Bacillus subtilis strain ATCC 11774	1423.741	complete	PATRIC	1423 tax ID	*
[Ref.: #66792]	Bacillus subtilis ATCC 11774	2925634727	complete	JGI IMG/M	1423 tax ID	*
[Ref.: #66792]	Bacillus subtilis ATCC 11774	GCA_004101945	complete	GenBank ENA	1423 tax ID	*

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

	Trait	Model	Prediction	Confidence in %	In training data
	Predictions from GenomeNet Sporulation v. 1 based on: Bacillus subtilis ATCC 11774 NCBI: GCA_004101945.1
[Ref.: #69481]	spore-forming	spore-formingⓘ	yes	100	no

	Trait	Model	Prediction	Confidence in %	In training data
	Predictions from Diaspora project based on: Bacillus subtilis ATCC 11774 NCBI: GCA_004101945.1
[Ref.: #69480]	gram-positive	gram-positiveⓘ	yes	81.79	no
[Ref.: #69480]	anaerobic	anaerobicⓘ	no	88.953	no
[Ref.: #69480]	aerobic	aerobicⓘ	yes	71.323	yes
[Ref.: #69480]	spore-forming	spore-formingⓘ	yes	95.33	no
[Ref.: #69480]	thermophilic	thermophileⓘ	no	95.271	yes
[Ref.: #69480]	flagellated	motile2+ⓘ	yes	87.527	no

Availability in culture collections External links

[Ref.: #964]

Culture collection no.

DSM 2109, ATCC 11774, NCTC 8236, CCUG 50054, NCIMB 8739, ICI 2/4, CIP 1.83

[Ref.: #70640]

SI-ID 35425

Literature:

Only first 10 entries are displayed. Click here to see all.

	Title	Authors	Journal	DOI	Year
Metabolism	Enhancement of beta-Mannanase Production by Bacillus subtilis ATCC11774 through Optimization of Medium Composition.	Norizan NABM, Halim M, Tan JS, Abbasiliasi S, Mat Sahri M, Othman F, Ariff AB	Molecules	10.3390/molecules25153516	2020	*
Phylogeny	Antituberculotic activity of actinobacteria isolated from the rare habitats.	Hussain A, Rather MA, Shah AM, Bhat ZS, Shah A, Ahmad Z, Parvaiz Hassan Q	Lett Appl Microbiol	10.1111/lam.12773	2017	*
Enzymology	Purification of beta-mannanase derived from Bacillus subtilis ATCC 11774 using ionic liquid as adjuvant in aqueous two-phase system.	Aziz NFHA, Abbasiliasi S, Ng HS, Phapugrangkul P, Bakar MHA, Tam YJ, Tan JS	J Chromatogr B Analyt Technol Biomed Life Sci	10.1016/j.jchromb.2017.04.029	2017	*
Biotechnology	Chitinase production by Bacillus subtilis ATCC 11774 and its effect on biocontrol of Rhizoctonia diseases of potato.	Saber WI, Ghoneem KM, Al-Askar AA, Rashad YM, Ali AA, Rashad EM	Acta Biol Hung	10.1556/018.66.2015.4.8	2015	*
Phylogeny	Pseudomonas putida Strain FStm2 Isolated from Shark Skin: A Potential Source of Bacteriocin.	Ahmad A, Hamid R, Dada AC, Usup G	Probiotics Antimicrob Proteins	10.1007/s12602-013-9140-4	2013	*
Enzymology	Antibacterial, antifungal and antioxidant activities of the ethanol extract of the stem bark of Clausena heptaphylla.	Fakruddin M, Mannan KS, Mazumdar RM, Afroz H	BMC Complement Altern Med	10.1186/1472-6882-12-232	2012	*
Pathogenicity	Flavonols and an oxychromonol from Piliostigma reticulatum.	Babajide OJ, Babajide OO, Daramola AO, Mabusela WT	Phytochemistry	10.1016/j.phytochem.2008.05.003	2008	*
Pathogenicity	Flavonoid analysis and antimicrobial activity of commercially available propolis products.	Kosalec I, Pepeljnjak S, Bakmaz M, Vladimir-Knezevic S	Acta Pharm		2005	*
Metabolism	Mycotoxigenicity of clinical and environmental Aspergillus fumigatus and A. flavus isolates.	Kosalec I, Pepeljnjak S	Acta Pharm		2005	*
Pathogenicity	Anti-bacterial activity of synthetic N-heterocyclic oxidizing compounds.	Babalola GO	Lett Appl Microbiol	10.1046/j.1472-765x.1998.00266.x	1998	*
Metabolism	Non-variable sources of pure water and the germination and outgrowth of Bacillus subtilis spores.	Knott AG, Dancer BN, Hann AC, Russell AD	J Appl Microbiol	10.1111/j.1365-2672.1997.tb03583.x	1997	*
Pathogenicity	Revival of Bacillus subtilis spores from biocide-induced injury in the germination process.	Williams ND, Russell AD	J Appl Bacteriol	10.1111/j.1365-2672.1993.tb03411.x	1993	*
Metabolism	Revival of biocide-treated spores of Bacillus subtilis.	Williams ND, Russell AD	J Appl Bacteriol	10.1111/j.1365-2672.1993.tb03410.x	1993	*
Pathogenicity	Injury and repair in biocide-treated spores of Bacillus subtilis.	Williams ND, Russell AD	FEMS Microbiol Lett	10.1111/j.1574-6968.1993.tb05956.x	1993	*
Pathogenicity	The nature and site of biocide-induced sublethal injury in Bacillus subtilis spores.	Williams ND, Russell AD	FEMS Microbiol Lett	10.1016/0378-1097(92)90040-u	1992	*
Pathogenicity	Uptake of L-[14C]-alanine by glutaraldehyde-treated and untreated spores of Bacillus subtilis.	Power EG, Russell AD	FEMS Microbiol Lett	10.1016/0378-1097(90)90295-2	1990	*
Metabolism	Glutaraldehyde: its uptake by sporing and non-sporing bacteria, rubber, plastic and an endoscope.	Power EG, Russell AD	J Appl Bacteriol	10.1111/j.1365-2672.1989.tb02502.x	1989	*
Pathogenicity	Possible mechanisms for the revival of glutaraldehyde-treated spores of Bacillus subtilis NCTC 8236.	Power EG, Dancer BN, Russell AD	J Appl Bacteriol	10.1111/j.1365-2672.1989.tb04959.x	1989	*
Pathogenicity	Mechanism of resistance of Bacillus subtilis spores to chlorhexidine.	Shaker LA, Furr JR, Russell AD	J Appl Bacteriol	10.1111/j.1365-2672.1988.tb02444.x	1988	*
Metabolism	Thermal injury and recovery of Bacillus subtilis.	Miller LL, Ordal ZJ	Appl Microbiol	10.1128/am.24.6.878-884.1972	1972	*
Pathogenicity	Resistance of Bacillus subtilis spores to inactivation by gamma irradiation and heating in the presence of a bactericide. 3. Factors affecting rates of inactivation by phenylmercuric nitrate.	Deasy PB, Kuster E, Timoney RF	Appl Microbiol	10.1128/am.22.4.567-570.1971	1971	*
Stress	Resistance of Bacillus subtilis spores to inactivation by gamma irradiation and heating in the presence of a bactericide. II. Factors affecting rates of inactivation by phenolic bactericides.	Deasy PB, Kuster E, Timoney RF	Appl Microbiol	10.1128/am.20.3.461-464.1970	1970	*
Cultivation	Resistance of Bacillus subtilis spores to inactivation by gamma irradiation and heating in the presence of a bactericide. I. Suitability of viable count procedures.	Deasy PB, Kuster E, Timoney RF	Appl Microbiol	10.1128/am.20.3.455-460.1970	1970	*
	Ecofriendly Synthesis of Silver Nanoparticles Using Ananas comosus Fruit Peels: Anticancer and Antimicrobial Activities.	Baran A, Keskin C, Baran MF, Huseynova I, Khalilov R, Eftekhari A, Irtegun-Kandemir S, Kavak DE	Bioinorg Chem Appl	10.1155/2021/2058149	2021	*
	Antibacterial Activity of Free Fatty Acids from Hydrolyzed Virgin Coconut Oil Using Lipase from Candida rugosa.	Nguyen VTA, Le TD, Phan HN, Tran LB	J Lipids	10.1155/2017/7170162	2017	*
	Silver-embedded modified hyperbranched epoxy/clay nanocomposites as antibacterial materials.	Roy B, Bharali P, Konwar BK, Karak N	Bioresour Technol	10.1016/j.biortech.2012.09.129	2012	*

References

#964	Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 2109

#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 )

#35250 ; 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) .

#68371

Automatically annotated from API 50CH acid .

#68382

Automatically annotated from API zym .

#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 )

#70640

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-ID35425.1 )

#123356 Collection of Institut Pasteur ; Curators of the CIP; CIP 1.83
* These data were automatically processed and therefore are not curated

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Bacillus subtilis ATCC 11774

Bacillus subtilis ATCC 11774

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