Bacillus subtilis (CIP 53.159, ATCC 9466, IAM 1026)

Name: Bacillus subtilis (CIP 53.159, ATCC 9466, IAM 1026)
Creator: BacDive
License: http://creativecommons.org/licenses/by/4.0/

BacDive ID 136375

Type strain

Strain Designation B-558

Culture col. no. CIP 53.159 ATCC 9466 IAM 1026 NCDO 737 NCIMB 8159 9 more

NCBI tax ID(s) 1423

Special Collections JCM CIP

Links

Bacillus subtilis B-558 is an obligate aerobe, spore-forming, mesophilic prokaryote of the family Bacillaceae.

spore-forming Gram-positive motile obligate aerobe mesophilic

Name and taxonomic classification

SI-ID 79523

ATCC 9466,NCIB 8159,IAM 1026,NCDO 737,NCIMB 8159,CCM1997,VKM B-436,NRRL 558,VKM B-915,NRRL B-558,CIP 53.159,BCRC 11224,CCRC 11224,NCIM 2117,JCM 20014

@ref 20215

Last LPSN update 2025-12-16 10:02:33

Domain Bacillati

Phylum Bacillota

Class Bacilli

Order Caryophanales

Family Bacillaceae

Genus Bacillus

Species Bacillus subtilis

Full scientific name Bacillus subtilis (Ehrenberg 1835) Cohn 1872 (Approved Lists 1980)

Synonyms (1)

"Vibrio subtilis"

BacDive ID	Other strains from **Bacillus subtilis** (270)	Type strain
1172	B. subtilis Marburg, 744, DSM 10, ATCC 6051, CCM 2216, ... (type strain)
962	B. subtilis DSM 1088, IFO 13169, NBRC 13169, OUT 8353
963	B. subtilis RCTI 140, DSM 1089, IFO 3026, NBRC 3026, ...
964	B. subtilis DSM 1092, IFO 3009, NBRC 3009, OUT 8235
965	B. subtilis DSM 1970, ATCC 21228, SC 8584 (SO-4)
966	B. subtilis 4-3 Ky, DSM 1971, ATCC 21394
967	B. subtilis DSM 2109, ATCC 11774, NCTC 8236, CCUG 50054, ...
969	B. subtilis SA 22, DSM 4181, NCA 72-52
970	B. subtilis natto 3335 UM4, 3335 UM4, pLS20, DSM 4449
971	B. subtilis natto 3335 UM8, pLS20, 3335 UM8, DSM 4450, ...
972	B. subtilis DSM 4451
973	B. subtilis DB163, pGR71, DSM 4515
974	B. subtilis pMW1, DSM 4608, BR 157
975	B. subtilis DSM 5552, NRS 254
976	B. subtilis DSM 5611, NRRL B-360, NRS 230
977	B. subtilis SB 491, DSM 6397, BGSC 1A2
978	B. subtilis DSM 13019, SSI MK1
979	B. subtilis DSM 21393
980	B. subtilis ES2-W11c1, DSM 30651
981	B. subtilis ES2-W11c2, DSM 30652
982	B. subtilis ES1-131, DSM 30512
983	B. subtilis ES1-179-1, DSM 30529
984	B. subtilis ES1-181-2, DSM 30533
985	B. subtilis ES1-182-1, DSM 30534
986	B. subtilis ES1-188-2, DSM 30540
987	B. subtilis ES1-188-3, DSM 30541
988	B. subtilis ES1-227, DSM 30551
989	B. subtilis ES1-257-2, DSM 30558
990	B. subtilis ES1-272, DSM 30562
991	B. subtilis ES1-306a, DSM 30570
992	B. subtilis ES1-311-1, DSM 30581
993	B. subtilis ES2-8b1, DSM 30597
994	B. subtilis FR2-W7Bb, DSM 30711
995	B. subtilis ES2-W7c1, DSM 30642
996	B. subtilis FR2-S1Ab, DSM 30671
997	B. subtilis FR2-S6Ba, DSM 30676
998	B. subtilis FR2-S7Aa, DSM 30677
999	B. subtilis FR2-S11Ca, DSM 30682
1000	B. subtilis FR1-49con, DSM 30723
1001	B. subtilis TW17/1, DSM 30801
1002	B. subtilis 1E9(pBC16), DSM 23521
1003	B. subtilis strain 168, DSM 23778
1004	B. subtilis YB886, DSM 25152
1156	B. subtilis 168, DSM 402, NBRC 111470, NCIB 10106, JCM ...
1157	B. subtilis S 237, DSM 1090, OUT 8424
1158	B. subtilis S 239, DSM 1091, OUT 8425
1159	B. subtilis DSM 3256, IAM 1213
1160	B. subtilis DSM 3257, IAM 1259, JCM 20132
1170	B. subtilis DSM 5213, BGSC 1A40, BR 151
1171	B. subtilis BD 393, DSM 5214, BGSC 1A511
1173	B. subtilis CU 1050, DSM 5545, BGSC 1A459/SU+III, HER ...
1174	B. subtilis DSM 5660, NRRL B-362, NRS 624
1175	B. subtilis 110NA, DSM 5547, HER 1243
1176	B. subtilis DSM 6198, ATCC 39090, BGSC 1S53
1177	B. subtilis RUB 331, DSM 6223, ATCC 31578
1179	B. subtilis NP40, 1A309, DSM 6887, BGSC 1A309
1180	B. subtilis 1A658, DA 65, DSM 6889, BGSC 1A658
1186	B. subtilis DSM 9565, ATCC 33677, BR 151
130881	B. subtilis T3_6, DSM 31033
130880	B. subtilis D13-1, DSM 100614
130877	B. subtilis FS3-1, DSM 100605
130878	B. subtilis D6-1, DSM 100612
130879	B. subtilis D8-1, DSM 100613
130876	B. subtilis Amp-T18, DSM 28592
22915	B. subtilis P5/4_1, DSM 30924
22916	B. subtilis P8/5_1, DSM 30927
22917	B. subtilis P8/15_1, DSM 30928
22918	B. subtilis P10/7_1, DSM 30929
22919	B. subtilis P10/14_1, DSM 30925
23667	B. subtilis D1, DSM 30941
23668	B. subtilis D-FC1, DSM 30942
130185	B. subtilis G20, DSM 31020
130186	B. subtilis G23, DSM 31021
130187	B. subtilis b9_4, DSM 31008
130188	B. subtilis b9_5, DSM 31009
130189	B. subtilis b9_6, DSM 31010
131652	B. subtilis Stev2, DSM 103044
131653	B. subtilis Stev9, DSM 103047
131654	B. subtilis Stev18, DSM 103051
131655	B. subtilis D36_1, DSM 103758
134612	B. subtilis PM 15, CIP 76.53
134701	B. subtilis AA 56, CIP 76.87
134853	B. subtilis FS 437, CIP 76.34
134854	B. subtilis PM 43, CIP 76.63
134856	B. subtilis FS 32, CIP 76.81
134857	B. subtilis AA 77, CIP 76.91
134858	B. subtilis AA 79, CIP 76.92
134859	B. subtilis AA 92, CIP 76.93
135155	B. subtilis FA 10, CIP 76.72
135173	B. subtilis FF 25, CIP 76.80
135255	B. subtilis CIP 51.55
135269	B. subtilis FD 10, CIP 76.29
135270	B. subtilis FE 9, CIP 76.30
135280	B. subtilis CIP 61.6, ATCC 4529, NRRL NRS-1004, NRRL: ...
135297	B. subtilis PM 16, CIP 76.54
135365	B. subtilis NRS-230, CIP 52.66
135516	B. subtilis 1576, CIP 51.15
135545	B. subtilis CIP 51.51
135547	B. subtilis PM 14, CIP 76.52
135577	B. subtilis PM 44, CIP 76.64
135581	B. subtilis PM 26, CIP 76.56
135590	B. subtilis PM 32, CIP 76.57
135620	B. subtilis 5a, CIP 61.7, NCTC 2590
135643	B. subtilis PM 36, CIP 76.58
135676	B. subtilis PM 39, CIP 76.60
135695	B. subtilis AB 93-8-1, CIP 76.44
135696	B. subtilis AB 53, CIP 76.103
135697	B. subtilis AB 72, CIP 76.104
135698	B. subtilis AB 73, CIP 76.105
135699	B. subtilis AD 8, CIP 76.106
135700	B. subtilis AD 19, CIP 76.107
135701	B. subtilis AA 48, CIP 76.108
135783	B. subtilis PM 42, CIP 76.62
135784	B. subtilis EV 15, CIP 76.70
135900	B. subtilis CIP 104473, ATCC 19659, IFO 13722, PRD 66
135909	B. subtilis 3R9675, CIP 54.10, ATCC 9524
136058	B. subtilis CIP A33
136391	B. subtilis CIP 53.173, NCTC 2121
136392	B. subtilis CIP 53.174, ATCC 8190, NCTC 2118
136394	B. subtilis CIP 53.176, NCTC 2116
136395	B. subtilis CIP 53.178, NCTC 2123
136501	B. subtilis 168 CA, CIP 106309
136948	B. subtilis AA 4, CIP 76.83
136959	B. subtilis AA 16, CIP 76.85
136969	B. subtilis AA 5, CIP 76.84
136972	B. subtilis AA 51, CIP 76.86
136975	B. subtilis AA 57, CIP 76.88
136991	B. subtilis AA 62, CIP 76.89
136992	B. subtilis AA 64, CIP 76.90
137036	B. subtilis B2, CIP 55.96
137087	B. subtilis FE 6, CIP 76.75
137100	B. subtilis PM 25, CIP 76.55
137129	B. subtilis AA 2, CIP 76.82
137272	B. subtilis 796, CIP 104611, ATCC 82, ATCC 8037
137292	B. subtilis CIP 53.179, ATCC 8188, NCTC 2122
137348	B. subtilis FS 381, CIP 76.32
137349	B. subtilis FS 436, CIP 76.33
137416	B. subtilis PM 13, CIP 76.51
137419	B. subtilis AC 27, CIP 76.96
137433	B. subtilis AC 28, CIP 76.97
137537	B. subtilis CIP A4
137923	B. subtilis 99-86, CIP 102199
138447	B. subtilis CIP 51.48
138480	B. subtilis CIP 51.54
138711	B. subtilis PM 37, CIP 76.48
138730	B. subtilis PM 40, CIP 76.49
138739	B. subtilis PM 7, CIP 76.50
138763	B. subtilis AC 32, CIP 76.99
138773	B. subtilis AC 33, CIP 76.100
138777	B. subtilis AC 34, CIP 76.101
138779	B. subtilis AC 35, CIP 76.102
138875	B. subtilis FE 19, CIP 76.79
138909	B. subtilis Caron, CIP A155
138915	B. subtilis PM 38, CIP 76.59
138956	B. subtilis AB 12, CIP 76.35
138957	B. subtilis 168, CIP 76.45
138958	B. subtilis PM 6, CIP 76.46
138959	B. subtilis CB 22, CIP 76.26
138964	B. subtilis DB 16, CIP 76.27
138965	B. subtilis FA 10, CIP 76.28
138967	B. subtilis FS 336, CIP 76.31
138968	B. subtilis FS 223, CIP 76.38
138970	B. subtilis FS 319, CIP 76.36
138971	B. subtilis AB 35, CIP 76.37
138972	B. subtilis FS 382, CIP 76.39
138973	B. subtilis AB 34, CIP 76.40
138974	B. subtilis AA 32, CIP 76.41
138975	B. subtilis AB 91-2-2, CIP 76.43
138976	B. subtilis PM 9, CIP 76.47
138979	B. subtilis PM 41, CIP 76.61
138980	B. subtilis PM 47, CIP 76.65
138981	B. subtilis PM 49, CIP 76.66
138982	B. subtilis SB 5-2, CIP 76.67
138983	B. subtilis BD 68, CIP 76.68
138984	B. subtilis EC 21, CIP 76.69
138985	B. subtilis EV 16, CIP 76.71
138986	B. subtilis FA 20-1, CIP 76.73
138987	B. subtilis FC 10, CIP 76.74
138988	B. subtilis FE 10, CIP 76.76
138989	B. subtilis FE 20, CIP 76.77
138990	B. subtilis FF 15, CIP 76.78
138992	B. subtilis AA 94, CIP 76.94
138993	B. subtilis AB 8, CIP 76.95
138994	B. subtilis AC 31, CIP 76.98
138995	B. subtilis AB 34-1, CIP 76.42
139174	B. subtilis 543, CIP 51.49
139209	B. subtilis CIP 102517
139407	B. subtilis CIP 53.175, NCTC 2119
139411	B. subtilis CIP 53.177, NCTC 2117
139520	B. subtilis Parry1, CIP 110271, NCIMB 13061, NCTC 5398, ...
139538	B. subtilis RS2008, CIP 109935
139539	B. subtilis CIP 63.8
141283	B. subtilis CCUG 625
141686	B. subtilis CCUG 4783
142101	B. subtilis CCUG 10780, ATCC 12432, NCTC 10315, ATCC ...
142397	B. subtilis CCUG 12316
145153	B. subtilis CCUG 27765, NRRL NRS-356, NRRL NRS-238, NRRL ...
146436	B. subtilis CCUG 31131
146685	B. subtilis CCUG 31949
146735	B. subtilis CCUG 32040
147533	B. subtilis CCUG 33755
147568	B. subtilis CCUG 33816
148233	B. subtilis CCUG 35081
148234	B. subtilis CCUG 35082
148235	B. subtilis CCUG 35083
148236	B. subtilis CCUG 35084
148237	B. subtilis CCUG 35085
148238	B. subtilis CCUG 35086
148239	B. subtilis CCUG 35087
148240	B. subtilis CCUG 35088
148241	B. subtilis CCUG 35089
148242	B. subtilis CCUG 35090
148243	B. subtilis CCUG 35091
148244	B. subtilis CCUG 35092
148245	B. subtilis CCUG 35093
148436	B. subtilis CCUG 35445
149160	B. subtilis CCUG 36967
149203	B. subtilis CCUG 37263
149428	B. subtilis CCUG 37730
149469	B. subtilis CCUG 37799
149478	B. subtilis CCUG 37815 A
149479	B. subtilis CCUG 37815 B
149600	B. subtilis CCUG 38041
149872	B. subtilis CCUG 38587
150261	B. subtilis CCUG 39418
150473	B. subtilis CCUG 41392
150474	B. subtilis CCUG 41393
151897	B. subtilis CCUG 45145
153228	B. subtilis CCUG 48815 A
157307	B. subtilis IMI 347329
157622	B. subtilis 2dA_C27, DSM 103912
157623	B. subtilis SB-14, DSM 109343
158869	B. subtilis Fh040319_C2, DSM 109511
158870	B. subtilis Fh040319_C10, DSM 109512
158871	B. subtilis Fh040319_C12, DSM 109513
158872	B. subtilis Fh040319_C14, DSM 109514
158873	B. subtilis FH4_1, DSM 110116
161119	B. subtilis JCM 11003
162225	B. subtilis JCM 18293
162706	B. subtilis JCM 20036, IAM 1071
162708	B. subtilis JCM 20038, IAM 1076
162718	B. subtilis JCM 20057, IAM 1114
162729	B. subtilis JCM 20073, ATCC 14593, IAM 1145
162736	B. subtilis JCM 20083, IAM 1163
162738	B. subtilis JCM 20085, IAM 1168
162739	B. subtilis JCM 20086, IAM 1169
162746	B. subtilis JCM 20094, IAM 1191
162747	B. subtilis JCM 20095, IAM 1192
162748	B. subtilis JCM 20096, IAM 1193, IFO 3033, NBRC 3033
162755	B. subtilis JCM 20105, IAM 1207
162758	B. subtilis JCM 20108, IAM 1212
162767	B. subtilis JCM 20118, IAM 1231
162773	B. subtilis JCM 20127, IAM 1247
162882	B. subtilis JCM 20333, ATCC 4925, IAM 11060
162883	B. subtilis JCM 20336, ATCC 6460, IAM 11063
162890	B. subtilis JCM 20352, IAM 12019
162891	B. subtilis JCM 20353, IAM 12020
162952	B. subtilis JCM 20520, IAM 12366
163112	B. subtilis JCM 21228, IAM 14446
163798	B. subtilis JCM 30446
164104	B. subtilis JCM 31626
164106	B. subtilis JCM 31628
164275	B. subtilis JCM 32485
174177	B. subtilis CIMB 05-2416, CRBIP17.22
174358	B. subtilis P7, DSM 115556
174359	B. subtilis ZH1, DSM 115557
176404	B. subtilis SZB3, DSM 115815
176405	B. subtilis BEST7003, Bacillus subtilis BEST7003, DSM ...
176406	B. subtilis BP20.15, DSM 119457
176407	B. subtilis BB10.1, DSM 119458

Morphology

Cell morphology

@ref	Gram stain	Motility
35770	positive

Colony morphology

Culture and growth conditions

Culture medium

@ref	Name	Growth	Composition	Medium link
35770	MEDIUM 72- for trypto casein soja agar		Distilled water make up to (1000.000 ml);Trypto casein soy agar (40.000 g)
35770	CIP Medium 72			Medium recipe at CIP

Culture temp

@ref	Growth	Type	Temperature (°C)	Range
35770	positive	growth	30	mesophilic
35770	positive	growth	22-45
35770	negative	growth	10
35770	negative	growth	55
67770	positive	growth	30	mesophilic

Culture pH

@ref	Ability	Type	PH
35770	positive	growth	6

Physiology and metabolism

Oxygen tolerance

35770

Oxygen toleranceobligate aerobe

Spore formation

35770

Spore formationyes

Halophily

@ref	Salt	Growth	Tested relation	Concentration
35770	NaCl	positive	growth	0-10 %

Metabolite utilization

@ref	Chebi-ID	Metabolite	Utilization activity	Kind of utilization tested
68371	27613 ChEBI	amygdalin	+	builds acid from	from API 50CH acid
68371	18305 ChEBI	arbutin	+	builds acid from	from API 50CH acid
68371	17057 ChEBI	cellobiose	+	builds acid from	from API 50CH acid
35770	16947 ChEBI	citrate	+	carbon source
68371	17108 ChEBI	D-arabinose	-	builds acid from	from API 50CH acid
68371	18333 ChEBI	D-arabitol	-	builds acid from	from API 50CH acid
68371	15824 ChEBI	D-fructose	+	builds acid from	from API 50CH acid
68371	28847 ChEBI	D-fucose	-	builds acid from	from API 50CH acid
68371	12936 ChEBI	D-galactose	-	builds acid from	from API 50CH acid
68371	17634 ChEBI	D-glucose	+	builds acid from	from API 50CH acid
68371	62318 ChEBI	D-lyxose	-	builds acid from	from API 50CH acid
68371	16899 ChEBI	D-mannitol	+	builds acid from	from API 50CH acid
68371	16024 ChEBI	D-mannose	+	builds acid from	from API 50CH acid
68371	16988 ChEBI	D-ribose	+	builds acid from	from API 50CH acid
68371	17924 ChEBI	D-sorbitol	+	builds acid from	from API 50CH acid
68371	16443 ChEBI	D-tagatose	-	builds acid from	from API 50CH acid
68371	65327 ChEBI	D-xylose	+	builds acid from	from API 50CH acid
68371	17113 ChEBI	erythritol	-	builds acid from	from API 50CH acid
35770	4853 ChEBI	esculin	+	hydrolysis
68371	4853 ChEBI	esculin	+	builds acid from	from API 50CH acid
68371	16813 ChEBI	galactitol	-	builds acid from	from API 50CH acid
68371	28066 ChEBI	gentiobiose	+	builds acid from	from API 50CH acid
68371	24265 ChEBI	gluconate	+	builds acid from	from API 50CH acid
68371	17754 ChEBI	glycerol	+	builds acid from	from API 50CH acid
68371	28087 ChEBI	glycogen	+	builds acid from	from API 50CH acid
35770	606565 ChEBI	hippurate	+	hydrolysis
68371	15443 ChEBI	inulin	+	builds acid from	from API 50CH acid
68371	30849 ChEBI	L-arabinose	+	builds acid from	from API 50CH acid
68371	18403 ChEBI	L-arabitol	-	builds acid from	from API 50CH acid
68371	18287 ChEBI	L-fucose	-	builds acid from	from API 50CH acid
68371	62345 ChEBI	L-rhamnose	-	builds acid from	from API 50CH acid
68371	17266 ChEBI	L-sorbose	-	builds acid from	from API 50CH acid
68371	65328 ChEBI	L-xylose	-	builds acid from	from API 50CH acid
68371	17716 ChEBI	lactose	-	builds acid from	from API 50CH acid
68371	17306 ChEBI	maltose	+	builds acid from	from API 50CH acid
68371	6731 ChEBI	melezitose	-	builds acid from	from API 50CH acid
68371	28053 ChEBI	melibiose	-	builds acid from	from API 50CH acid
68371	320061 ChEBI	methyl alpha-D-glucopyranoside	+	builds acid from	from API 50CH acid
68371	43943 ChEBI	methyl alpha-D-mannoside	-	builds acid from	from API 50CH acid
68371	74863 ChEBI	methyl beta-D-xylopyranoside	-	builds acid from	from API 50CH acid
68371	17268 ChEBI	myo-inositol	-	builds acid from	from API 50CH acid
68371	59640 ChEBI	N-acetylglucosamine	+	builds acid from	from API 50CH acid
35770	17632 ChEBI	nitrate	+	reduction
35770	17632 ChEBI	nitrate	-	respiration
35770	16301 ChEBI	nitrite	-	reduction
68371		Potassium 2-ketogluconate	-	builds acid from	from API 50CH acid
68371		Potassium 5-ketogluconate	-	builds acid from	from API 50CH acid
68371	16634 ChEBI	raffinose	-	builds acid from	from API 50CH acid
68371	15963 ChEBI	ribitol	-	builds acid from	from API 50CH acid
68371	17814 ChEBI	salicin	+	builds acid from	from API 50CH acid
68371	28017 ChEBI	starch	+	builds acid from	from API 50CH acid
68371	17992 ChEBI	sucrose	+	builds acid from	from API 50CH acid
68371	27082 ChEBI	trehalose	+	builds acid from	from API 50CH acid
68371	32528 ChEBI	turanose	+	builds acid from	from API 50CH acid
68371	17151 ChEBI	xylitol	-	builds acid from	from API 50CH acid

Metabolite production

@ref	Chebi-ID	Metabolite	Production
35770	35581 ChEBI	indole

Metabolite tests

@ref	Chebi-ID	Metabolite	Voges-proskauer-test	Methylred-test
35770	15688 ChEBI	acetoin	+
35770	17234 ChEBI	glucose		-

Enzymes

@ref	Value	Activity	Ec
68382	acid phosphatase	+	3.1.3.2	from API zym
35770	alcohol dehydrogenase	-	1.1.1.1
68382	alkaline phosphatase	+	3.1.3.1	from API zym
68382	alpha-chymotrypsin	-	3.4.21.1	from API zym
68382	alpha-fucosidase	-	3.2.1.51	from API zym
68382	alpha-galactosidase	-	3.2.1.22	from API zym
68382	alpha-glucosidase	+	3.2.1.20	from API zym
68382	alpha-mannosidase	-	3.2.1.24	from API zym
35770	amylase	+
35770	beta-galactosidase	+	3.2.1.23
68382	beta-galactosidase	-	3.2.1.23	from API zym
68382	beta-glucosidase	+	3.2.1.21	from API zym
68382	beta-glucuronidase	-	3.2.1.31	from API zym
35770	caseinase	+	3.4.21.50
35770	catalase	+	1.11.1.6
68382	cystine arylamidase	-	3.4.11.3	from API zym
35770	DNase	+
68382	esterase (C 4)	+		from API zym
68382	esterase lipase (C 8)	+		from API zym
35770	gamma-glutamyltransferase	+	2.3.2.2
35770	gelatinase	+
35770	lecithinase	-
68382	leucine arylamidase	-	3.4.11.1	from API zym
35770	lipase	-
68382	lipase (C 14)	-		from API zym
35770	lysine decarboxylase	-	4.1.1.18
68382	N-acetyl-beta-glucosaminidase	-	3.2.1.52	from API zym
68382	naphthol-AS-BI-phosphohydrolase	+		from API zym
35770	ornithine decarboxylase	-	4.1.1.17
35770	oxidase	-
35770	protease	+
68382	trypsin	-	3.4.21.4	from API zym
35770	tween esterase	-
35770	urease	-	3.5.1.5
68382	valine arylamidase	-		from API zym

API zym

@ref	Control	Alkaline phosphatase	Esterase (C 4)	2-naphtyl caprylateEsterase Lipase (C 8)	Lipase (C 14)	L-leucyl-2-naphthylamideLeucine arylamidase	L-valyl-2-naphthylamideValine arylamidase	L-cystyl-2-naphthylamideCystine arylamidase	Trypsin	alpha- Chymotrypsin	Acid phosphatase	Naphthol-AS-BI-phosphateNaphthol-AS-BI-phosphohydrolase	alpha- Galactosidase	beta- Galactosidase	beta- Glucuronidase	alpha- Glucosidase	beta- Glucosidase	N-acetyl-beta- glucosaminidase	alpha- Mannosidase	alpha- Fucosidase
35770	-	+	+	+	-	-	-	-	-	-	+	+	-	-	-	+	+	-	-	-

API 50CHac

@ref	ControlQ	GLY	ERY	DARA	LARA	RIB	DXYL	LXYL	ADO	MDX	GAL	GLU	FRU	MNE	SBE	RHA	DUL	INO	MAN	SOR	MDM	MDG	NAG	AMY	ARB	ESC	SAL	CEL	MAL	LAC	MEL	SAC	TRE	INU	MLZ	RAF	AMD	GLYG	XLT	GEN	TUR	LYX	TAG	DFUC	LFUC	DARL	LARL	GNT	2KG	5KG
35770	not determinedn.d.	+	-	-	+	+	+	-	-	-	-	+	+	+	-	-	-	-	+	+	-	+	+	+	+	+	+	+	+	-	-	+	+	+	-	-	+	+	-	+	+	-	-	-	-	-	-	+	-	-

API biotype100

@ref	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
35770	not determinedn.d.	+	+	-	+	+	-	+	+	+	+	+	-	-	-	+	+	+	+	+	+	+	+	+	-	-	-	-	-	-	-	-	+	+	+	+	+	+	-	-	-	-	+	-	+	-	-	-	-	-	+	+	-	-	+	-	+	-	-	-	+	+	-	-	-	-	-	-	-	-	-	-	-	-	-	-	+	-	-	-	+	+	-	-	-	-	-	+	-	-	+	+	+	+	+	-	-	-	-	-

Isolation, sampling and environmental information

Interaction and safety

Risk assessment

@ref	Biosafety level	Biosafety level comment
35770	1	Risk group (French classification)

Sequence information

Genome-based predictions

Literature

Topic	Title	Authors	Journal	DOI	Year
	In ovo probiotic supplementation supports hatchability and improves hatchling quality in broilers.	Gao M, Ren Y, Lu S, Reddyvari R, Venkitanarayanan K, Amalaradjou MA.	Poult Sci	10.1016/j.psj.2024.103624	2024
	In ovo Feeding as a Tool for Improving Performance and Gut Health of Poultry: A Review.	Das R, Mishra P, Jha R.	Front Vet Sci	10.3389/fvets.2021.754246	2021
	Non-Antibiotics Strategies to Control Salmonella Infection in Poultry.	Ruvalcaba-Gomez JM, Villagran Z, Valdez-Alarcon JJ, Martinez-Nunez M, Gomez-Godinez LJ, Ruesga-Gutierrez E, Anaya-Esparza LM, Arteaga-Garibay RI, Villarruel-Lopez A.	Animals (Basel)	10.3390/ani12010102	2022
Phylogeny	Buckyballs conjugated with nucleic acid sequences identifies microorganisms in live cell assays.	Cheng Q, Parvin B.	J Nanobiotechnology	10.1186/s12951-017-0315-0	2017
Enzymology	Purification and characterization of a cephalosporin esterase from Rhodosporidium toruloides.	Politino M, Tonzi SM, Burnett WV, Romancik G, Usher JJ.	Appl Environ Microbiol	10.1128/aem.63.12.4807-4811.1997	1997
	Genetic Factors in Radiation Resistance of Bacillus subtilis.	Zamenhof S, Bursztyn H, Reddy TK, Zamenhof PJ.	J Bacteriol	10.1128/jb.90.1.108-115.1965	1965
Phylogeny	Unrelatedness of Bacillus amyloliquefaciens and Bacillus subtilis.	Welker NE, Campbell LL.	J Bacteriol	10.1128/jb.94.4.1124-1130.1967	1967
Phylogeny	Agar diffusion method for the differentiation of Bacillus anthracis.	Angelety LH, Wright GG.	Appl Microbiol	10.1128/am.21.1.157-159.1971	1971
Metabolism	Identification of an antibiotic-producing bacterium from the human intestinal tract and characterization of its antimicrobial product.	Iglewski WJ, Gerhardt NB.	Antimicrob Agents Chemother	10.1128/aac.13.1.81	1978
Pathogenicity	Studies on the antibacterial and antifungal properties of 1, 4-naphthoquinones.	Ambrogi V, Artini D, De Carneri I, Castellino S, Dradi E, Logemann W, Meinardi G, Di Somma M, Tosolini G, Vecchi E.	Br J Pharmacol	10.1111/j.1476-5381.1970.tb10662.x	1970
	Reexamination of the association between melting point, buoyant density, and chemical base composition of deoxyribonucleic acid.	De Ley J.	J Bacteriol	10.1128/jb.101.3.738-754.1970	1970
	H⁺-capacitor and ATP production in obligate alkaliphilic Bacillaceae: insights into cytochrome c and H⁺ transport mechanisms.	Yumoto I.	Front Microbiol	10.3389/fmicb.2025.1637315	2025
	Differences in Bioenergetic Metabolism of Obligately Alkaliphilic Bacillaceae Under High pH Depend on the Aeration Conditions.	Goto T, Ogami S, Yoshimume K, Yumoto I.	Front Microbiol	10.3389/fmicb.2022.842785	2022
	The oxazolomycin family: a review of current knowledge.	Oleksak P, Gonda J, Nepovimova E, Kuca K, Musilek K.	RSC Adv	10.1039/d0ra08396h	2020
Pathogenicity	Bioenergetics and the role of soluble cytochromes C for alkaline adaptation in gram-negative alkaliphilic Pseudomonas.	Matsuno T, Yumoto I.	Biomed Res Int	10.1155/2015/847945	2015
Metabolism	Intracellular biosynthesis and removal of copper nanoparticles by dead biomass of yeast isolated from the wastewater of a mine in the Brazilian Amazonia.	Salvadori MR, Ando RA, Oller do Nascimento CA, Correa B.	PLoS One	10.1371/journal.pone.0087968	2014
Metabolism	Mycocerein, a novel antifungal peptide antibiotic produced by Bacillus cereus.	Wakayama S, Ishikawa F, Oishi K.	Antimicrob Agents Chemother	10.1128/aac.26.6.939	1984
Pathogenicity	A mechanism of resistance to hydrogen peroxide in Vibrio rumoiensis S-1.	Ichise N, Morita N, Hoshino T, Kawasaki K, Yumoto I, Okuyama H.	Appl Environ Microbiol	10.1128/aem.65.1.73-79.1999	1999
Enzymology	Bacilysocin, a novel phospholipid antibiotic produced by Bacillus subtilis 168.	Tamehiro N, Okamoto-Hosoya Y, Okamoto S, Ubukata M, Hamada M, Naganawa H, Ochi K.	Antimicrob Agents Chemother	10.1128/aac.46.2.315-320.2002	2002
Pathogenicity	Development of an antivirulence drug against Streptococcus mutans: repression of biofilm formation, acid tolerance, and competence by a histidine kinase inhibitor, walkmycin C.	Eguchi Y, Kubo N, Matsunaga H, Igarashi M, Utsumi R.	Antimicrob Agents Chemother	10.1128/aac.01646-10	2011
	Synthesis of new macrocyclic polyamides as antimicrobial agent candidates.	El-Salam OI, Al-Omar MA, Fayed AA, Flefel EM, Amr Ael-G.	Molecules	10.3390/molecules171214510	2012
	Occurrence of phosphorylserine in the spore coat of Bacillus subtilis NRRL B558.	Sano K, Ichikawa T, Kondo M.	Microbios		1975
	Penicillin Assay Techniques: A Comparative Study.	Dolkart RE, Dey FL, Schwemlein GX.	J Bacteriol	10.1128/jb.53.1.17-24.1947	1947
	Penicillin: VI. Effect of Dissociation Phases of Bacillus subtilis on Penicillin Assay.	Schmidt WH, Ward GE, Coghill RD.	J Bacteriol	10.1128/jb.49.4.411-412.1945	1945
	A Note on Detergent Interference in the Serial Dilution Assay of Penicillin Using Bacillus subtilis.	Hickey RJ.	J Bacteriol		1948
	Penicillin: X. The Effect of Phenylacetic Acid on Penicillin Production.	Moyer AJ, Coghill RD.	J Bacteriol		1947
	Cytochemical Mechanisms of Penicillin Action: VII. Effects on Activity of Alkaline Phosphatase.	Dufrenoy J, Pratt R.	J Bacteriol		1948
Metabolism	The Production of Penicillin X in Submerged Culture.	Raper KB, Fennell DI.	J Bacteriol	10.1128/jb.51.6.761-777.1946	1946
	Cytochemical Mechanisms of Penicillin Action: VI. The Influence of Cobalt on the Optimal Bacteriostatic Concentration of Penicillin.	Pratt R, Dufrenoy J.	J Bacteriol		1948
	Cytochemical Mechanisms of Penicillin Action: IV. Comparative Responses of Gram-positive and Gram-negative Bacteria to Penicillin.	Pratt R, Dufrenoy J.	J Bacteriol		1947
	Novel antimicrobial activities of a peptide derived from a Japanese soybean fermented food, Natto, against Streptococcus pneumoniae and Bacillus subtilis group strains.	Kitagawa M, Shiraishi T, Yamamoto S, Kutomi R, Ohkoshi Y, Sato T, Wakui H, Itoh H, Miyamoto A, Yokota SI.	AMB Express	10.1186/s13568-017-0430-1	2017
Metabolism	Biosynthesis of linkage units for teichoic acids in gram-positive bacteria: distribution of related enzymes and their specificities for UDP-sugars and lipid-linked intermediates.	Yokoyama K, Mizuguchi H, Araki Y, Kaya S, Ito E.	J Bacteriol	10.1128/jb.171.2.940-946.1989	1989
	Comparative studies of lipoteichoic acids from several Bacillus strains.	Iwasaki H, Shimada A, Ito E.	J Bacteriol	10.1128/jb.167.2.508-516.1986	1986
	Occurrence of glucosamine residues with free amino groups in cell wall peptidoglycan from bacilli as a factor responsible for resistance to lysozyme.	Hayashi H, Araki Y, Ito E.	J Bacteriol	10.1128/jb.113.2.592-598.1973	1973
Metabolism	Function of alpha-D-glucosyl monophosphorylpolyprenol in biosynthesis of cell wall teichoic acids in Bacillus coagulans.	Shimada A, Tamatukuri J, Ito E.	J Bacteriol	10.1128/jb.171.5.2835-2841.1989	1989
Metabolism	Structure and glycosylation of lipoteichoic acids in Bacillus strains.	Iwasaki H, Shimada A, Yokoyama K, Ito E.	J Bacteriol	10.1128/jb.171.1.424-429.1989	1989
Metabolism	Contribution of intracellular negative ion capacity to Donnan effect across the membrane in alkaliphilic Bacillus spp.	Goto T, Hirabayashi T, Morimoto H, Yamazaki K, Inoue N, Matsuyama H, Yumoto I	J Bioenerg Biomembr	10.1007/s10863-015-9641-9	2016
	Relationship between rates of respiratory proton extrusion and ATP synthesis in obligately alkaliphilic Bacillus clarkii DSM 8720(T).	Hirabayashi T, Goto T, Morimoto H, Yoshimune K, Matsuyama H, Yumoto I	J Bioenerg Biomembr	10.1007/s10863-012-9430-7	2012
Metabolism	The obligate alkaliphile Bacillus clarkii K24-1U retains extruded protons at the beginning of respiration.	Yoshimune K, Morimoto H, Hirano Y, Sakamoto J, Matsuyama H, Yumoto I	J Bioenerg Biomembr	10.1007/s10863-010-9278-7	2010
Biotechnology	Growth inhibitory effect of shelf life extending agents on Bacillus subtilis IAM 1026.	Mitsuboshi S, Obitsu R, Muramatsu K, Furube K, Yoshitake S, Kiuchi K	Biocontrol Sci	10.4265/bio.12.71	2007
Enzymology	MJ347-81F4 A & B, novel antibiotics from Amycolatopsis sp.: taxonomic characteristics, fermentation, and antimicrobial activity.	Sasaki T, Otani T, Matsumoto H, Unemi N, Hamada M, Takeuchi T, Hori M	J Antibiot (Tokyo)	10.7164/antibiotics.51.715	1998
Phylogeny	N-acetylmannosaminyl(1----4)N-acetylglucosamine, a linkage unit between glycerol teichoic acid and peptidoglycan in cell walls of several Bacillus strains.	Kaya S, Yokoyama K, Araki Y, Ito E	J Bacteriol	10.1128/jb.158.3.990-996.1984	1984
	In ovo administration of Bacillus subtilis serotypes effect hatchability, 21-day performance, and intestinal microflora.	Castaneda CD, Gamble JN, Wamsley KGS, McDaniel CD, Kiess AS	Poult Sci	10.1016/j.psj.2021.101125	2021
	Characterization of a facultatively psychrophilic bacterium, vibrio rumoiensis sp. nov., that exhibits high catalase activity	Yumoto I, Iwata H, Sawabe T, Ueno K, Ichise N, Matsuyama H, Okuyama H, Kawasaki K.	Appl Environ Microbiol	10.1128/aem.65.1.67-72.1999	1999

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 )
#35770	Collection of Institut Pasteur ; Curators of the CIP; CIP 53.159
#67770	Japan Collection of Microorganism (JCM) ; Curators of the JCM;
#68371	Automatically annotated from API 50CH acid .
#68382	Automatically annotated from API zym .
#126262	A. Lissin, I. Schober, J. F. Witte, H. Lüken, A. Podstawka, J. Koblitz, B. Bunk, P. Dawyndt, P. Vandamme, P. de Vos, J. Overmann, L. C. Reimer: StrainInfo—the central database for linked microbial strain identifiers. ( DOI 10.1093/database/baaf059 )

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Bacillus subtilis (CIP 53.159, ATCC 9466, IAM 1026)

Name and taxonomic classification

Morphology

Cell morphology

Colony morphology

Culture and growth conditions

Culture medium

Culture temp

Culture pH

Physiology and metabolism

Oxygen tolerance

Spore formation

Halophily

Metabolite utilization

Metabolite production

Metabolite tests

Enzymes

API zym

API 50CHac

API biotype100

Isolation, sampling and environmental information

Interaction and safety

Risk assessment

Sequence information

Genome-based predictions

Literature

Literature

References

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