Actinoplanes utahensis (DSM 43147, ATCC 14539, CBS 367.66)

Name: Actinoplanes utahensis (DSM 43147, ATCC 14539, CBS 367.66)
Creator: BacDive
License: http://creativecommons.org/licenses/by/4.0/

BacDive ID 7815

Type strain

Strain Designation UNCC 260

Culture col. no. DSM 43147 ATCC 14539 CBS 367.66 IFO 13244 JCM 3122 19 more

NCBI tax ID(s) 1869

Special Collections DSMZ JCM KCTC JMRC

History DSMZ <- KCC <- A. Domnas, UNCC, 260 JCM <-- KCC A-0122 <-- A. Domnas UNCC 260.

Links

Actinoplanes utahensis UNCC 260 is a bacterium that was isolated from soil.

genome sequence 16S sequence Bacteria

Name and taxonomic classification

SI-ID 88620

ATCC 14539,DSM 43147,IFO 13244,JCM 3122,CCRC 13336,IMET 9252,NCIMB 12886,NRRL B-16727,VKM Ac-674,CBS 367.66,KCTC 9545,NBRC 13244,BCRC 13336,CGMCC 4.1543,CGMCC 4.1489

@ref 20215

Last LPSN update 2026-05-29 08:26:44

Domain Bacteria

Phylum Actinomycetota

Class Actinomycetes

Order Micromonosporales

Family Micromonosporaceae

Genus Actinoplanes

Species Actinoplanes utahensis

Full scientific name Actinoplanes utahensis Couch 1963 (Approved Lists 1980)

BacDive ID	Other strains from **Actinoplanes utahensis** (9)	Type strain
100083	A. utahensis STI09058(IMET), 1031-003,
100084	A. utahensis STI09061(IMET), 1110-002,
100085	A. utahensis STI09081(IMET), 1136-035,
100086	A. utahensis STI09082(IMET), 1141-033,
100087	A. utahensis STI09063(IMET), 1110-006,
100088	A. utahensis STI09203or(IMET), 486-3,
100089	A. utahensis STI09083(IMET), 1141-035,
100090	A. utahensis STI09214(IMET), 485-12,
128604	A. utahensis SF001199,

Morphology

Cell morphology

@ref	Motility	Confidence	Gram stain
125439		93.516
125439		99.819	positive

Multimedia

@ref:	10817
multimedia content:	DSM_43147.jpg
multimedia.multimedia content:	https://www.dsmz.de/microorganisms/photos/DSM_43147.jpg
caption:	Medium 65 28°C
intellectual property rights:	© Leibniz-Institut DSMZ
manual_annotation:	1

Culture and growth conditions

Culture medium

@ref	Name	Growth	Medium link	Composition
10817	GYM STREPTOMYCES MEDIUM (DSMZ Medium 65)		Medium recipe at MediaDive	Name: GYM STREPTOMYCES MEDIUM (DSMZ Medium 65) Composition: Agar 18.0 g/l Malt extract 10.0 g/l Yeast extract 4.0 g/l Glucose 4.0 g/l CaCO3 2.0 g/l Distilled water
10817	CZAPEK PEPTONE AGAR (DSMZ Medium 83)		Medium recipe at MediaDive	Name: CZAPEK PEPTONE AGAR (DSMZ Medium 83) Composition: Sucrose 30.0 g/l Agar 20.0 g/l Peptone 5.0 g/l NaNO3 3.0 g/l Yeast extract 2.0 g/l K2HPO4 1.0 g/l MgSO4 x 7 H2O 0.5 g/l KCl 0.5 g/l FeSO4 x 7 H2O 0.01 g/l Distilled water

Culture temp

@ref	Growth	Type	Temperature (°C)
10817	positive	growth	28
67770	positive	growth	28

Physiology and metabolism

Oxygen tolerance

@ref	Oxygen tolerance	Confidence
125439	obligate aerobe	99.355

Spore formation

@ref	Spore formation	Confidence
125439		96.339

Observation

67770

Observationquinones: MK-9(H₄), MK-10(H₄), MK-9(H₄), MK-9(H₆)

Pathway annotation

Computationally determined by

@ref	pathway	enzyme coverage	annotated reactions
66794	cellulose degradation	100	5 of 5
66794	butanoate fermentation	100	4 of 4
66794	taurine degradation	100	1 of 1
66794	suberin monomers biosynthesis	100	2 of 2
66794	valine metabolism	100	9 of 9
66794	UDP-GlcNAc biosynthesis	100	3 of 3
66794	CDP-diacylglycerol biosynthesis	100	2 of 2
66794	glycogen metabolism	100	5 of 5
66794	phenylacetate degradation (aerobic)	100	5 of 5
66794	sulfopterin metabolism	100	4 of 4
66794	coenzyme A metabolism	100	4 of 4
66794	glycolate and glyoxylate degradation	100	6 of 6
66794	enterobactin biosynthesis	100	3 of 3
66794	formaldehyde oxidation	100	3 of 3
66794	adipate degradation	100	2 of 2
66794	starch degradation	100	10 of 10
66794	reductive acetyl coenzyme A pathway	100	7 of 7
66794	biotin biosynthesis	100	4 of 4
66794	methylglyoxal degradation	100	5 of 5
66794	ribulose monophosphate pathway	100	2 of 2
66794	cardiolipin biosynthesis	100	7 of 7
66794	threonine metabolism	100	10 of 10
66794	folate polyglutamylation	100	1 of 1
66794	ethanol fermentation	100	2 of 2
66794	cis-vaccenate biosynthesis	100	2 of 2
66794	acetate fermentation	100	4 of 4
66794	palmitate biosynthesis	100	22 of 22
66794	anapleurotic synthesis of oxalacetate	100	1 of 1
66794	1,4-dihydroxy-6-naphthoate biosynthesis	100	6 of 6
66794	pentose phosphate pathway	100	11 of 11
66794	ppGpp biosynthesis	100	4 of 4
66794	kanosamine biosynthesis II	100	2 of 2
66794	NAD metabolism	94.44	17 of 18
66794	phenylalanine metabolism	92.31	12 of 13
66794	urea cycle	92.31	12 of 13
66794	myo-inositol biosynthesis	90	9 of 10
66794	molybdenum cofactor biosynthesis	88.89	8 of 9
66794	4-hydroxymandelate degradation	88.89	8 of 9
66794	aspartate and asparagine metabolism	88.89	8 of 9
66794	serine metabolism	88.89	8 of 9
66794	CO2 fixation in Crenarchaeota	88.89	8 of 9
66794	dTDPLrhamnose biosynthesis	87.5	7 of 8
66794	C4 and CAM-carbon fixation	87.5	7 of 8
66794	isoleucine metabolism	87.5	7 of 8
66794	gluconeogenesis	87.5	7 of 8
66794	glutathione metabolism	85.71	12 of 14
66794	glutamate and glutamine metabolism	85.71	24 of 28
66794	photosynthesis	85.71	12 of 14
66794	propanol degradation	85.71	6 of 7
66794	heme metabolism	85.71	12 of 14
66794	ubiquinone biosynthesis	85.71	6 of 7
66794	aclacinomycin biosynthesis	85.71	6 of 7
66794	leucine metabolism	84.62	11 of 13
66794	alanine metabolism	82.76	24 of 29
66794	glycolysis	82.35	14 of 17
66794	proline metabolism	81.82	9 of 11
66794	methionine metabolism	80.77	21 of 26
66794	3-chlorocatechol degradation	80	4 of 5
66794	Entner Doudoroff pathway	80	8 of 10
66794	peptidoglycan biosynthesis	80	12 of 15
66794	vitamin K metabolism	80	4 of 5
66794	glycine betaine biosynthesis	80	4 of 5
66794	flavin biosynthesis	80	12 of 15
66794	gallate degradation	80	4 of 5
66794	factor 420 biosynthesis	80	4 of 5
66794	degradation of sugar acids	80	20 of 25
66794	purine metabolism	79.79	75 of 94
66794	tetrahydrofolate metabolism	78.57	11 of 14
66794	citric acid cycle	78.57	11 of 14
66794	chorismate metabolism	77.78	7 of 9
66794	allantoin degradation	77.78	7 of 9
66794	pyrimidine metabolism	77.78	35 of 45
66794	phosphatidylethanolamine bioynthesis	76.92	10 of 13
66794	vitamin B1 metabolism	76.92	10 of 13
66794	tryptophan metabolism	76.32	29 of 38
66794	glycogen biosynthesis	75	3 of 4
66794	CMP-KDO biosynthesis	75	3 of 4
66794	6-hydroxymethyl-dihydropterin diphosphate biosynthesis	75	6 of 8
66794	non-pathway related	73.68	28 of 38
66794	oxidative phosphorylation	73.63	67 of 91
66794	metabolism of disaccharids	72.73	8 of 11
66794	degradation of hexoses	72.22	13 of 18
66794	lipid metabolism	70.97	22 of 31
66794	vitamin B12 metabolism	70.59	24 of 34
66794	propionate fermentation	70	7 of 10
66794	histidine metabolism	68.97	20 of 29
66794	cyanate degradation	66.67	2 of 3
66794	acetoin degradation	66.67	2 of 3
66794	acetyl CoA biosynthesis	66.67	2 of 3
66794	L-lactaldehyde degradation	66.67	2 of 3
66794	lysine metabolism	66.67	28 of 42
66794	sulfoquinovose degradation	66.67	2 of 3
66794	arginine metabolism	66.67	16 of 24
66794	d-mannose degradation	66.67	6 of 9
66794	octane oxidation	66.67	2 of 3
66794	isoprenoid biosynthesis	65.38	17 of 26
66794	phenol degradation	65	13 of 20
66794	degradation of pentoses	64.29	18 of 28
66794	tyrosine metabolism	64.29	9 of 14
66794	d-xylose degradation	63.64	7 of 11
66794	degradation of sugar alcohols	62.5	10 of 16
66794	carnitine metabolism	62.5	5 of 8
66794	ketogluconate metabolism	62.5	5 of 8
66794	androgen and estrogen metabolism	62.5	10 of 16
66794	cysteine metabolism	61.11	11 of 18
66794	3-phenylpropionate degradation	60	9 of 15
66794	lipoate biosynthesis	60	3 of 5
66794	metabolism of amino sugars and derivatives	60	3 of 5
66794	degradation of aromatic, nitrogen containing compounds	58.33	7 of 12
66794	chlorophyll metabolism	55.56	10 of 18
66794	nitrate assimilation	55.56	5 of 9
66794	vitamin B6 metabolism	54.55	6 of 11
66794	carotenoid biosynthesis	54.55	12 of 22
66794	sulfate reduction	53.85	7 of 13
66794	quinate degradation	50	1 of 2
66794	pantothenate biosynthesis	50	3 of 6
66794	phenylmercury acetate degradation	50	1 of 2
66794	selenocysteine biosynthesis	50	3 of 6
66794	glycine metabolism	50	5 of 10
66794	aminopropanol phosphate biosynthesis	50	1 of 2
66794	4-hydroxyphenylacetate degradation	50	5 of 10
66794	toluene degradation	50	2 of 4
66794	grixazone biosynthesis	50	1 of 2
66794	mannosylglycerate biosynthesis	50	1 of 2
66794	polyamine pathway	47.83	11 of 23
66794	bile acid biosynthesis, neutral pathway	47.06	8 of 17
66794	arachidonic acid metabolism	44.44	8 of 18
66794	benzoyl-CoA degradation	42.86	3 of 7
66794	ascorbate metabolism	40.91	9 of 22
66794	coenzyme M biosynthesis	40	4 of 10
66794	ethylmalonyl-CoA pathway	40	2 of 5
66794	arachidonate biosynthesis	40	2 of 5
66794	D-cycloserine biosynthesis	40	2 of 5
66794	phenylpropanoid biosynthesis	38.46	5 of 13
66794	cholesterol biosynthesis	36.36	4 of 11
66794	methane metabolism	33.33	1 of 3
66794	IAA biosynthesis	33.33	1 of 3
66794	lipid A biosynthesis	33.33	3 of 9
66794	(5R)-carbapenem carboxylate biosynthesis	33.33	1 of 3
66794	sphingosine metabolism	33.33	2 of 6
66794	mevalonate metabolism	28.57	2 of 7
66794	dolichyl-diphosphooligosaccharide biosynthesis	27.27	3 of 11
66794	cyclohexanol degradation	25	1 of 4
66794	vitamin E metabolism	25	1 of 4
66794	lactate fermentation	25	1 of 4
66794	alginate biosynthesis	25	1 of 4
66794	catecholamine biosynthesis	25	1 of 4
66794	daunorubicin biosynthesis	22.22	2 of 9

Isolation, sampling and environmental information

Isolation source categories

Cat1	Cat2	Cat3
#Environmental	#Terrestrial	#Soil

Isolation

@ref	Sample type	Geographic location	Country	Country ISO 3 Code	Continent
10817	soil
67770	Soil, Liberty Park	Salt Lake City, UT	USA	USA	North America

Interaction and safety

Risk assessment

@ref	Biosafety level	Biosafety level comment
10817	1	Risk group (German classification) According to TRBA 466

Sequence information

Genome sequences

@ref	Description	Assembly level	INSDC accession	BV-BRC accession	IMG accession	NCBI tax ID	Score
124043	ASM4266090v1 assembly for Actinoplanes utahensis JCM 3122	contig	GCA_042660905			1869	63.06
66792	ASM1686245v1 assembly for Actinoplanes utahensis NBRC 13244	contig	GCA_016862455	1869.6	8110488615	1869	41.33
124043	ASM3954398v1 assembly for Actinoplanes utahensis JCM 3122	scaffold	GCA_039543985			1869	29.71

16S sequences

@ref	Description	Accession	Length	Database	NCBI tax ID
20218	Actinoplanes utahensis gene for 16S rRNA, partial sequence	AB037012	1471		1869
10817	Actinoplanes utahensis partial 16S rRNA gene, strain IMSNU 20044T	AJ277574	1508		1869

GC content

67770

GC-content (mol%)72.6

Genome-based predictions

Predictions

Predictions from Deep Learning for Genome Sequence Data. R package version 0.3.1 based on: ASM4266090v1 assembly for Actinoplanes utahensis JCM 3122
NCBI: GCA_042660905

@ref	Trait	Model	Prediction	Confidence in %	In training data
125439	oxygen_tolerance	BacteriaNetⓘ	obligate aerobe	99.36	no
125439	gram_stain	BacteriaNetⓘ	positive	99.82	no
125439	motility	BacteriaNetⓘ	no	93.52	no
125439	spore_formation	BacteriaNetⓘ	yes	96.34	no

Predictions from bacterial phenotypic traits through improved machine learning using high-quality, curated datasets based on: Actinoplanes utahensis strain NBRC 13244
PATRIC: 1869.6

@ref	Trait	Model	Prediction	Confidence in %	In training data
125438	gram-positive	gram-positiveⓘ	yes	89.71	no
125438	anaerobic	anaerobicⓘ	no	94.55	no
125438	spore-forming	spore-formingⓘ	yes	84.74	no
125438	aerobic	aerobicⓘ	yes	85.96	no
125438	thermophilic	thermophileⓘ	no	95.75	yes
125438	flagellated	motile2+ⓘ	no	61.33	no

Literature

Topic	Title	Authors	Journal	DOI	Year
Metabolism	Effects of intracellular trehalose content on Streptomyces griseus spores.	McBride MJ, Ensign JC.	J Bacteriol	10.1128/jb.169.11.4995-5001.1987	1987
	Statistical optimization and sequential scale-up of alpha-galactosidase production by Actinoplanes utahensis B1 from shake flask to pilot scale.	John Babu D, Balumahendra K, Venkateswarulu TC, Sathish T.	Prep Biochem Biotechnol	10.1080/10826068.2024.2344500	2024
	Hydrophobic substrate binding pocket remodeling of echinocandin B deacylase based on multi-dimensional rational design.	Tang H, Zhu HY, Huang YF, Wu ZY, Zou SP, Liu ZQ, Zheng YG.	Int J Biol Macromol	10.1016/j.ijbiomac.2024.131473	2024
Metabolism	Functional expression of an echinocandin B deacylase from Actinoplanes utahensis in Escherichia coli.	Zou SP, Han X, Zhu HY, Sheng Q, Tang H, Liu ZQ, Zheng YG.	Int J Biol Macromol	10.1016/j.ijbiomac.2021.07.146	2021
Pathogenicity	Efficient side-chain deacylation of polymyxin B1 in recombinant Streptomyces strains.	Wang X, Wu K, Zhang H, Liu J, Yang Z, Bai J, Liu H, Shao L.	Biotechnol Lett	10.1007/s10529-022-03290-7	2022
	Comparative proteome analysis of Actinoplanes utahensis grown on various saccharides based on 2D-DIGE and MALDI-TOF/TOF-MS.	Weng CY, Wang CE, Xie WB, Xu SY, Wang YJ, Zheng YG.	J Proteomics	10.1016/j.jprot.2021.104193	2021
	Screening of Protein Tyrosine Phosphatase 1B Inhibitors from Actinomycete Extracts Using Recombinant Saccharomyces cerevisiae.	Lee HY, Kwun SY, Park EH, Yoon JA, Kim MD.	J Microbiol Biotechnol	10.4014/jmb.2502.02001	2025
Enzymology	Acylase enzymes disrupting quorum sensing alter the transcriptome and phenotype of Pseudomonas aeruginosa, and the composition of bacterial biofilms from wastewater treatment plants.	de Celis M, Serrano-Aguirre L, Belda I, Liebana-Garcia R, Arroyo M, Marquina D, de la Mata I, Santos A.	Sci Total Environ	10.1016/j.scitotenv.2021.149401	2021
Enzymology	Enhancing Catalytic Efficiency of an Actinoplanes utahensis Echinocandin B Deacylase through Random Mutagenesis and Site-Directed Mutagenesis.	Cheng YN, Qiu S, Cheng F, Weng CY, Wang YJ, Zheng YG.	Appl Biochem Biotechnol	10.1007/s12010-019-03170-3	2020
	Evaluating the toxicity and efficacy of the endophytic bacterium Kosakonia sp. ZO-Rh4 on antidiabetes and associated complications in a mouse model.	Xuan Dai TT, Linh TC, Tai TL.	Biochem Biophys Rep	10.1016/j.bbrep.2025.102319	2025
Transcriptome	Transcriptome analysis of Actinoplanes utahensis reveals molecular signature of saccharide impact on acarbose biosynthesis.	Weng CY, Shi LZ, Wang YJ, Zheng YG.	3 Biotech	10.1007/s13205-020-02466-0	2020
	Novel Bifunctional Acylase from Actinoplanes utahensis: A Versatile Enzyme to Synthesize Antimicrobial Compounds and Use in Quorum Quenching Processes.	Serrano-Aguirre L, Velasco-Bucheli R, Garcia-Alvarez B, Saborido A, Arroyo M, de la Mata I.	Antibiotics (Basel)	10.3390/antibiotics10080922	2021
	Real-time pH and temperature monitoring in solid-state fermentation reveals culture physiology and optimizes enzyme harvesting for tailored applications.	Kabir MF, Ovi AQ, Ju LK.	Microb Cell Fact	10.1186/s12934-025-02820-y	2025
	Deacylation of Echinocandin B by Streptomyces species: a novel method for the production of Echinocandin B nucleus.	Shivakumar MC, Manohar S, Ishwar B, Raghu P, Savitha J.	3 Biotech	10.1007/s13205-019-1946-7	2019
	A Hadal Streptomyces-Derived Echinocandin Acylase Discovered through the Prioritization of Protein Families.	Jiang X, Shu H, Feng S, Wang P, Zhang Z, Wang N.	Mar Drugs	10.3390/md22050212	2024
	Optimization of media composition and culture conditions for acarbose production by Actinoplanes utahensis ZJB-08196	Wang YJ, Liu L, Feng ZH, Liu ZQ, Zheng YG.	World J Microbiol Biotechnol	10.1007/s11274-011-0751-1	2011
	Enzymatic hydrolysis of capsaicins for the production of vanillylamine using ECB deacylase from Actinoplanes utahensis	Romano D, Gandolfi R, Guglielmetti S, Molinari F.	Food Chem	10.1016/j.foodchem.2010.06.070	2011
Metabolism	Actinoplanes utahensis ZJB-08196 fed-batch fermentation at elevated osmolality for enhancing acarbose production.	Wang YJ, Liu LL, Wang YS, Xue YP, Zheng YG, Shen YC.	Bioresour Technol	10.1016/j.biortech.2011.09.121	2012
Metabolism	Significantly enhanced production of acarbose in fed-batch fermentation with the addition of S-adenosylmethionine.	Sun LH, Li MG, Wang YS, Zheng YG.	J Microbiol Biotechnol	10.4014/jmb.1111.11047	2012
Metabolism	Immobilized aculeacin A acylase from Actinoplanes utahensis: characterization of a novel biocatalyst.	Hormigo D, de la Mata I, Acebal C, Arroyo M.	Bioresour Technol	10.1016/j.biortech.2010.01.117	2010
	Acarbose May Function as a Competitive Exclusion Agent for the Producing Bacteria.	Tanoeyadi S, Tsunoda T, Ito T, Philmus B, Mahmud T.	ACS Chem Biol	10.1021/acschembio.2c00795	2023
Metabolism	Cloning and expression of the FR901379 acylase gene from Streptomyces sp. no. 6907.	Ueda S, Shibata T, Ito K, Oohata N, Yamashita M, Hino M, Yamada M, Isogai Y, Hashimoto S.	J Antibiot (Tokyo)	10.1038/ja.2010.151	2011
Metabolism	Semisynthetic approaches to laspartomycin analogues.	Curran WV, Leese RA, Jarolmen H, Borders DB, Dugourd D, Chen Y, Cameron DR.	J Nat Prod	10.1021/np068062b	2007
	A Novel Lipase from Streptomyces exfoliatus DSMZ 41693 for Biotechnological Applications.	Rodriguez-Alonso G, Toledo-Marcos J, Serrano-Aguirre L, Rumayor C, Pasero B, Flores A, Saborido A, Hoyos P, Hernaiz MJ, de la Mata I, Arroyo M.	Int J Mol Sci	10.3390/ijms242317071	2023
Enzymology	Cloning and characterization of penicillin V acylase from Streptomyces mobaraensis.	Zhang D, Koreishi M, Imanaka H, Imamura K, Nakanishi K.	J Biotechnol	10.1016/j.jbiotec.2006.12.017	2007
Pathogenicity	Association between antidiabetic agents use and leukocyte telomere shortening rates in patients with type 2 diabetes.	Liu J, Ge Y, Wu S, Ma D, Xu W, Zhang Y, Yang Y.	Aging (Albany NY)	10.18632/aging.101781	2019
Metabolism	Enhanced production of acarbose and concurrently reduced formation of impurity c by addition of validamine in fermentation of Actinoplanes utahensis ZJB-08196.	Xue YP, Qin JW, Wang YJ, Wang YS, Zheng YG.	Biomed Res Int	10.1155/2013/705418	2013
Metabolism	Newly discovered penicillin acylase activity of aculeacin A acylase from Actinoplanes utahensis.	Torres-Bacete J, Hormigo D, Stuart M, Arroyo M, Torres P, Castillon MP, Acebal C, Garcia JL, de la Mata I.	Appl Environ Microbiol	10.1128/aem.00452-07	2007
	Investigations on rhizoplane Actinobacteria communities of papyrus (Cyperus papyrus) from an Egyptian wetland.	Rifaat HM, Marialigeti K, Kovacs G.	Acta Microbiol Immunol Hung	10.1556/amicr.49.2002.4.1	2002
Metabolism	Acyl-homoserine lactone acylase from Ralstonia strain XJ12B represents a novel and potent class of quorum-quenching enzymes.	Lin YH, Xu JL, Hu J, Wang LH, Ong SL, Leadbetter JR, Zhang LH.	Mol Microbiol	10.1046/j.1365-2958.2003.03351.x	2003
	Quorum sensing interference by phenolic compounds - A matter of bacterial misunderstanding.	Lima EMF, Winans SC, Pinto UM.	Heliyon	10.1016/j.heliyon.2023.e17657	2023
	In silico docking studies of alpha-amylase inhibitors from the anti-diabetic plant Leucas ciliata Benth. and an endophyte, Streptomyces longisporoflavus.	Akshatha JV, SantoshKumar HS, Prakash HS, Nalini MS.	3 Biotech	10.1007/s13205-020-02547-0	2021
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	Cloning and sequencing of the aculeacin A acylase-encoding gene from Actinoplanes utahensis and expression in Streptomyces lividans.	Inokoshi J, Takeshima H, Ikeda H, Omura S.	Gene	10.1016/0378-1119(92)90063-u	1992
	Physicochemical and Functional Characterization of Blue-Shelled Eggs in Korea.	Sujiwo J, Kim D, Yoon JY, Kim H, Kim JS, Lee SK, Jang A.	Korean J Food Sci Anim Resour	10.5851/kosfa.2017.37.2.181	2017
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Enzymology	Overexpression of penicillin V acylase from Streptomyces lavendulae and elucidation of its catalytic residues.	Torres-Bacete J, Hormigo D, Torres-Guzman R, Arroyo M, Castillon MP, Garcia L, Acebal C, de la Mata I.	Appl Environ Microbiol	10.1128/aem.02352-14	2015
Genetics	Reconstruction and in silico analysis of an Actinoplanes sp. SE50/110 genome-scale metabolic model for acarbose production.	Wang Y, Xu N, Ye C, Liu L, Shi Z, Wu J.	Front Microbiol	10.3389/fmicb.2015.00632	2015
Metabolism	A deacylation enzyme for aculeacin A, a neutral lipopeptide antibiotic, from Actinoplanes utahensis: purification and characterization.	Takeshima H, Inokoshi J, Takada Y, Tanaka H, Omura S.	J Biochem	10.1093/oxfordjournals.jbchem.a122712	1989
Metabolism	Deacylation of echinocandin B by Actinoplanes utahensis.	Boeck LD, Fukuda DS, Abbott BJ, Debono M.	J Antibiot (Tokyo)	10.7164/antibiotics.42.382	1989
	Quorum Sensing versus Quenching Bacterial Isolates Obtained from MBR Plants Treating Leachates from Municipal Solid Waste.	Soler A, Arregui L, Arroyo M, Mendoza JA, Muras A, Alvarez C, Garcia-Vera C, Marquina D, Santos A, Serrano S.	Int J Environ Res Public Health	10.3390/ijerph15051019	2018
Metabolism	Deacylation of A21978C, an acidic lipopeptide antibiotic complex, by Actinoplanes utahensis.	Boeck LD, Fukuda DS, Abbott BJ, Debono M.	J Antibiot (Tokyo)	10.7164/antibiotics.41.1085	1988
	Membrane Binding and Oligomerization of the Lipopeptide A54145 Studied by Pyrene Fluorescence.	Zhang T, Taylor SD, Palmer M, Duhamel J.	Biophys J	10.1016/j.bpj.2016.07.018	2016
Enzymology	Functional expression of a penicillin acylase from the extreme thermophile Thermus thermophilus HB27 in Escherichia coli.	Torres LL, Ferreras ER, Cantero A, Hidalgo A, Berenguer J.	Microb Cell Fact	10.1186/1475-2859-11-105	2012
Metabolism	A54145, a new lipopeptide antibiotic complex: microbial and chemical modification.	Fukuda DS, Debono M, Molloy RM, Mynderse JS.	J Antibiot (Tokyo)	10.7164/antibiotics.43.601	1990
Metabolism	A54145, a new lipopeptide antibiotic complex: factor control through precursor directed biosynthesis.	Boeck LD, Wetzel RW.	J Antibiot (Tokyo)	10.7164/antibiotics.43.607	1990
Metabolism	A probable aculeacin A acylase from the Ralstonia solanacearum GMI1000 is N-acyl-homoserine lactone acylase with quorum-quenching activity.	Chen CN, Chen CJ, Liao CT, Lee CY.	BMC Microbiol	10.1186/1471-2180-9-89	2009
Metabolism	The complete genome sequence of the acarbose producer Actinoplanes sp. SE50/110.	Schwientek P, Szczepanowski R, Ruckert C, Kalinowski J, Klein A, Selber K, Wehmeier UF, Stoye J, Puhler A.	BMC Genomics	10.1186/1471-2164-13-112	2012
	Synthesis of new analogs of echinocandin B by enzymatic deacylation and chemical reacylation of the echinocandin B peptide: synthesis of the antifungal agent cilofungin (LY121019).	Debono M, Abbott BJ, Fukuda DS, Barnhart M, Willard KE, Molloy RM, Michel KH, Turner JR, Butler TF, Hunt AH.	J Antibiot (Tokyo)	10.7164/antibiotics.42.389	1989
Enzymology	The quorum-quenching N-acyl homoserine lactone acylase PvdQ is an Ntn-hydrolase with an unusual substrate-binding pocket.	Bokhove M, Nadal Jimenez P, Quax WJ, Dijkstra BW.	Proc Natl Acad Sci U S A	10.1073/pnas.0911839107	2010
	Enzymatic and chemical modifications of lipopeptide antibiotic A21978C: the synthesis and evaluation of daptomycin (LY146032).	Debono M, Abbott BJ, Molloy RM, Fukuda DS, Hunt AH, Daupert VM, Counter FT, Ott JL, Carrell CB, Howard LC.	J Antibiot (Tokyo)	10.7164/antibiotics.41.1093	1988
Metabolism	A21978C, a complex of new acidic peptide antibiotics: isolation, chemistry, and mass spectral structure elucidation.	Debono M, Barnhart M, Carrell CB, Hoffmann JA, Occolowitz JL, Abbott BJ, Fukuda DS, Hamill RL, Biemann K, Herlihy WC.	J Antibiot (Tokyo)	10.7164/antibiotics.40.761	1987
Metabolism	Microbial conversion of steffimycin and steffimycin B to 10-dihydrosteffimycin and 10-dihydrosteffimycin B.	Wiley PF, Elrod DW, Slavicek JM, Marshall VP.	J Antibiot (Tokyo)	10.7164/antibiotics.33.819	1980
Enzymology	A Rhodococcus qsdA-encoded enzyme defines a novel class of large-spectrum quorum-quenching lactonases.	Uroz S, Oger PM, Chapelle E, Adeline MT, Faure D, Dessaux Y.	Appl Environ Microbiol	10.1128/aem.02014-07	2008
Metabolism	Inactivation of the lipopeptide antibiotic daptomycin by hydrolytic mechanisms.	D'Costa VM, Mukhtar TA, Patel T, Koteva K, Waglechner N, Hughes DW, Wright GD, De Pascale G.	Antimicrob Agents Chemother	10.1128/aac.05441-11	2012
Enzymology	Engineering the substrate specificity of a thermophilic penicillin acylase from thermus thermophilus.	Torres LL, Cantero A, del Valle M, Marina A, Lopez-Gallego F, Guisan JM, Berenguer J, Berenguer J, Hidalgo A.	Appl Environ Microbiol	10.1128/aem.03215-12	2013
Metabolism	Characterization of S-triazine herbicide metabolism by a Nocardioides sp. isolated from agricultural soils.	Topp E, Mulbry WM, Zhu H, Nour SM, Cuppels D.	Appl Environ Microbiol	10.1128/aem.66.8.3134-3141.2000	2000
	alpha-Glucosidase inhibitors and their use in clinical practice.	Derosa G, Maffioli P.	Arch Med Sci	10.5114/aoms.2012.31621	2012
	Fermentation, Isolation, Structure, and antidiabetic activity of NFAT-133 produced by Streptomyces strain PM0324667.	Kulkarni-Almeida AA, Brahma MK, Padmanabhan P, Mishra PD, Parab RR, Gaikwad NV, Thakkar CS, Tokdar P, Ranadive PV, Nair AS, Damre AA, Bahirat UA, Deshmukh NJ, Doshi LS, Dixit AV, George SD, Vishwakarma RA, Nemmani KV, Mahajan GB.	AMB Express	10.1186/2191-0855-1-42	2011
	Interference of bacterial cell-to-cell communication: a new concept of antimicrobial chemotherapy breaks antibiotic resistance.	Hirakawa H, Tomita H.	Front Microbiol	10.3389/fmicb.2013.00114	2013
Enzymology	Identification of extracellular N-acylhomoserine lactone acylase from a Streptomyces sp. and its application to quorum quenching.	Park SY, Kang HO, Jang HS, Lee JK, Koo BT, Yum DY.	Appl Environ Microbiol	10.1128/aem.71.5.2632-2641.2005	2005
	Analysis of dofA, a fruA-dependent developmental gene, and its homologue, dofB, in Myxococcus xanthus.	Horiuchi T, Akiyama T, Inouye S, Komano T.	J Bacteriol	10.1128/jb.184.24.6803-6810.2002	2002
	Teichulosonic acid, an anionic polymer of a new class from the cell wall of Actinoplanes utahensis VKM Ac-674(T).	Shashkov AS, Streshinskaya GM, Kozlova YI, Tul'skaya EM, Senchenkova SN, Arbatskii NP, Bueva OV, Evtushenko LI	Biochemistry (Mosc)	10.1134/S0006297912050112	2012

References

#10817	Leibniz Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH ; Curators of the DSMZ; DSM 43147
#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 )
#20216	Curators of the JMRC: Jena Microbial Resource Collection (JMRC):
#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 )
#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 )
#67770	Japan Collection of Microorganism (JCM) ; Curators of the JCM;
#124043	Isabel Schober, Julia Koblitz: Data extracted from sequence databases, automatically matched based on designation and taxonomy .
#125438	Julia Koblitz, Lorenz Christian Reimer, Rüdiger Pukall, Jörg Overmann: Predicting bacterial phenotypic traits through improved machine learning using high-quality, curated datasets. 2024 ( DOI 10.1101/2024.08.12.607695 )
#125439	Philipp Münch, René Mreches, Martin Binder, Hüseyin Anil Gündüz, Xiao-Yin To, Alice McHardy: deepG: Deep Learning for Genome Sequence Data. R package version 0.3.1 .
#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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Actinoplanes utahensis (DSM 43147, ATCC 14539, CBS 367.66)

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