ライフサイエンスコーパス: Streptomyces

1 ested, with the most notable exception being Streptomyces.

2 been widely reported in bacteria but none in Streptomyces.

3 and B, indolosesquiterpenoids isolated from Streptomyces.

4 level for the proper cell differentiation in Streptomyces.

5 thesis is a requirement for morphogenesis in Streptomyces.

6 ted availability of the biochemical tools in Streptomyces.

7 influenced the contemporary biogeography of Streptomyces.

8 We showed previously that, in Streptomyces (a bacterium with a mycelial lifestyle simi

9 Here we show that in Streptomyces, a genus of Actinobacteria abundant in soil

10 oelicolor is a model system for the study of Streptomyces, a genus of bacteria responsible for the pr

11 draft genome sequence of the plant pathogen Streptomyces acidiscabies 84-104, an emergent plant path

12 me, hydroxyethylphosphonate dioxygenase from Streptomyces albus (SaHEPD), and find that it displays t

13 s isolated from the culture-broth extract of Streptomyces albus cultures cotransformed with an enviro

14 on, and fed it, along with synthetic MBC, to Streptomyces albus expressing redH and redG.

15 gene cluster was heterologously expressed in Streptomyces albus J1074 setting the stage for convenien

16 d HiTES to activate a silent gene cluster in Streptomyces albus J1074.

17 ologous expression of these gene clusters in Streptomyces albus led to the isolation of three new PPs

18 -membered metagenomic library constructed in Streptomyces albus, the species that exhibited the highe

19 When heterologously expressed in Streptomyces albus, this cluster produced an indolotrypt

20 in filamentous bacteria, including the genus Streptomyces, although here our mechanistic understandin

21 Here, we show interactions between Streptomyces and fungi trigger a previously unobserved m

22 dictions for testing this hypothesis both in Streptomyces and in other microorganisms.

23 roteins found only in actinomycetes, such as Streptomyces and Mycobacteria.

24 s in the prolific antibiotic-producing genus Streptomyces and provide strong evidence that antibiotic

25 biosynthetic genes in two "clean" strains of Streptomyces and showed the production of HSAF analogues

26 growth is found in the filamentous bacteria Streptomyces, and is directed by a polarisome-like compl

27 h that coats the aerial hyphae and spores in Streptomyces, and mutants lacking the chaplins are unabl

28 thetic gene cluster and its pathway-specific Streptomyces antibiotic regulatory protein (SARP) cloned

29 linone D8 (SD8) is an antibiotic produced by Streptomyces antibioticus that targets DNA gyrase.

30 is a potent DNA gyrase inhibitor produced by Streptomyces antibioticus Tu6040.

31 t only to bacterial PNPases from E. coli and Streptomyces antibioticus, but also PNPase from human mi

32 Streptomyces are best known for producing antimicrobial

33 Antibiotic-producing Streptomyces are complex bacteria that remodel global tr

34 in that patterns of genetic diversity within Streptomyces are consistent with genome surfing, and we

35 Members of the actinomycete genus Streptomyces are non-motile, filamentous bacteria that a

36 Streptomyces are of great biological and industrial sign

37 Streptomyces are spore forming filamentous bacteria whic

38 Streptomyces are ubiquitous soil bacteria that undergo a

39 In Streptomyces arenae this reaction is catalyzed by CYP161

40 ramycin is an antitumor compound produced by Streptomyces argillaceus that has been used for the trea

41 We demonstrate that upon exposure to Streptomyces at their head or tail, nematodes display an

42 is a potent antitumor antibiotic produced by Streptomyces atroolivaceus S-140, featuring an unusual 1

43 oned and sequenced the lnm gene cluster from Streptomyces atroolivaceus S-140.

44 ) annotated to perform housekeeping roles in Streptomyces avermitilis Biochemical experiments define

45 ed in the transcriptome of a pure culture of Streptomyces avermitilis, suggesting for the first time

46 stance to the avermectin-producing bacterium Streptomyces avermitilis.

47 The thiostrepton producer Streptomyces azureus prevents self-intoxication by expre

48 Streptomyces bacteria employ a newly-discovered cell typ

49 has long been thought that the life cycle of Streptomyces bacteria encompasses three developmental st

50 Philanthinus) cultivate a distinct clade of Streptomyces bacteria for protection against pathogenic

51 e that was first isolated from soil-dwelling Streptomyces bacteria.

52 s shown in the picture) produced by the same Streptomyces bacterium.

53 ning of an 11-gene berninamycin cluster from Streptomyces bernensis UC 5144, its heterologous express

54 Streptomyces cacaoi subsp. cacaoi, a Gram-positive, bran

55 mber of dps per genome among closely related Streptomyces can be explained by gene duplication or lat

56 new natural telomycin analogues produced by Streptomyces canus ATCC 12646 were identified.

57 elBE1sca and relBE2sca, on the chromosome of Streptomyces cattleya DSM 46488.

58 The organofluorine-producing microbe Streptomyces cattleya has evolved a fluoroacetyl-CoA thi

59 ine biosynthetic pathway first discovered in Streptomyces cattleya While fluoroacetate has long been

60 D, X2 and X0beta, produced by the bacterium Streptomyces CBR38; and the macrolides elaiophylin, efom

61 A and efomycin G, produced by the bacterium Streptomyces CBR53.These metabolites were found at the i

62 We term these Streptomyces cells 'explorers', for their ability to ado

63 red as a previously unreported metabolite of Streptomyces chromofuscus ATCC49982, and the gene cluste

64 gna unguiculata PLD, as well as the PLD from Streptomyces chromofuscus, cabbage, or peanuts, and no P

65 Bacillus subtilis and the phospholipase D of Streptomyces chromofuscus.

66 pentalenene synthase (Uniprot: B5GLM7) from Streptomyces clavuligerus was used in an automated compu

67 cin has been identified and characterized in Streptomyces clavuligerus.

68 NsrR from Streptomyces coelicolor (Sc) regulates the expression of

69 d 9 inhibited both Mtb GlgE and a variant of Streptomyces coelicolor (Sco) GlgEI with Ki = 237 +/- 27

70 produced from different microbes, including Streptomyces coelicolor , Bacillus subtilis , and Pseudo

71 member of the prodiginine group produced by Streptomyces coelicolor A3(2) and other actinobacteria.

72 oneidensis MR-1, Bacillus subtilis 3610, and Streptomyces coelicolor A3(2) as well as a mixed biofilm

73 e of 2-methylisoborneol synthase (MIBS) from Streptomyces coelicolor A3(2) has been determined in com

74 synthesis of this cofactor was discovered in Streptomyces coelicolor A3(2) in which chorismate is con

75 The whiE locus of Streptomyces coelicolor A3(2) is responsible for the bio

76 diphosphate C-methyltransferase (GPPMT) from Streptomyces coelicolor A3(2) is the first methyltransfe

77 We report here that the soil bacterium Streptomyces coelicolor also encodes a PecS homolog (SCO

78 ning RpfA function using the model bacterium Streptomyces coelicolor and have uncovered unprecedented

79 s transcription in actinobacteria, including Streptomyces coelicolor and Mycobacterium tuberculosis.

80 C-terminal HNH nuclease domain, Sco5333 from Streptomyces coelicolor and Tbis1 from Thermobispora bis

81 the copper centers of the small laccase from Streptomyces coelicolor at room temperature and pH 7.4,

82 netically refactored in a heterologous host, Streptomyces coelicolor CH999, to produce 3 mg/L A-74528

83 We have isolated an RNase J ortholog from Streptomyces coelicolor encoded by the gene sco5745.

84 The Streptomyces coelicolor genome encodes only a single put

85 ural studies have been with the very similar Streptomyces coelicolor GlgE isoform 1.

86 non-covalent inhibitors and GlgE, a variant Streptomyces coelicolor GlgEI (Sco GlgEI-V279S) was made

87 ucture resembles that of M. tuberculosis and Streptomyces coelicolor GlgEs, reported before, with eac

88 ructure, based on the cocrystal structure of Streptomyces coelicolor IHF duplex DNA, a bona fide rela

89 Streptomyces coelicolor is a model for studying bacteria

90 Streptomyces coelicolor is a model system for the study

91 Streptomyces coelicolor is a morphologically complex bac

92 Germicidin synthase (Gcs) from Streptomyces coelicolor is a type III polyketide synthas

93 e morphogenesis of the filamentous bacterium Streptomyces coelicolor is unknown.

94 on with RNA from an RNase III null mutant of Streptomyces coelicolor M145 and a primer complementary

95 nd native mass spectrometry demonstrate that Streptomyces coelicolor NsrR (ScNsrR), previously report

96 ulating the nitrosative stress response like Streptomyces coelicolor NsrR, Sven6563 binds to a conser

97 ggests that, following phosphate limitation, Streptomyces coelicolor PhoP functions as a 'master' reg

98 s in the genome-minimized model actinomycete Streptomyces coelicolor provided the 57.6 kb merochlorin

99 NsrR from Streptomyces coelicolor regulates its own expression and

100 his work, we show that the Rieske protein of Streptomyces coelicolor requires both the Sec and the Ta

101 e lipoprotein signal peptidase (lsp) gene in Streptomyces coelicolor results in growth and developmen

102 We present crystal structures of Streptomyces coelicolor RNase J with bound RNA in pre- a

103 d produced simocyclinone heterologously in a Streptomyces coelicolor strain engineered for improved a

104 a MarR family transcriptional regulator from Streptomyces coelicolor that is well represented in sequ

105 onally, the macrodomain protein SCO6735 from Streptomyces coelicolor This protein is a member of an u

106 m of the multicopper oxidase (MCO) SLAC from Streptomyces coelicolor was investigated by structural (

107 orthologues from Mycobacterium smegmatis and Streptomyces coelicolor were phosphorylated by the corre

108 The gene encoding Streptomyces coelicolor xanthine dehydrogenase regulator

109 we confirmed that both aerobic prokaryotic (Streptomyces coelicolor) and eukaryotic (Homo sapiens) F

110 he distantly related Pgl system described in Streptomyces coelicolor, are widely distributed in ~10%

111 escribe how PcaV, a MarR family regulator in Streptomyces coelicolor, controls transcription of genes

112 ransferase regulator), a MarR homologue from Streptomyces coelicolor, functions in oxidative stress r

113 entous high-GC Gram-positive actinobacterium Streptomyces coelicolor, involved in controlling colony

114 cterial genera, including Bacillus subtilis, Streptomyces coelicolor, Mycobacterium smegmatis, and Ps

115 On a large real network (Streptomyces coelicolor, phosphate depletion), we demons

116 tures were obtained for the enzyme pair from Streptomyces coelicolor, solved at 1.3 A (ScLPMO10B) and

117 -enteric bacteria Pseudomonas aeruginosa and Streptomyces coelicolor, SoxR is activated by endogenous

118 erine-based desferroxiamine E siderophore in Streptomyces coelicolor, the corresponding biosynthetic

119 ents of the transcriptome and translatome of Streptomyces coelicolor, the model antibiotic-producing

120 Here we report that in Streptomyces coelicolor, the protein stability of an ECF

121 ut transiently up-regulated by vancomycin in Streptomyces coelicolor.

122 tic taromycin A in the model expression host Streptomyces coelicolor.

123 ing sporulation in the filamentous bacterium Streptomyces coelicolor.

124 d a catalytic domain at its C terminus, from Streptomyces coelicolor.

125 otein assembly in the filamentous bacterium, Streptomyces coelicolor.

126 as found to induce prodiginine production by Streptomyces coelicolor.

127 ial hyphae formation in adjacent colonies of Streptomyces coelicolor.

128 global regulator of antibiotic production in Streptomyces coelicolor.

129 iosynthesis of the pacidamycin nucleoside in Streptomyces coeruleorubidus proceeds through three step

130 ne sequences identical to the type strain of Streptomyces cyaneofuscatus.

131 and confirm two of its main components: Scy (Streptomyces cytoskeletal element), a unique bacterial c

132 we show that new optimized derivatives from Streptomyces-derived griselimycin are highly active agai

133 The study of Streptomyces development has made significant advances i

134 ungi trigger a previously unobserved mode of Streptomyces development.

135 ll biological approach, we show that the two Streptomyces dynamins specifically localize to sporulati

136 ntalenolactone biosynthetic gene clusters of Streptomyces exfoliatus UC5319 and S. arenae TU469, resp

137 Fungi trigger Streptomyces exploratory growth in part by altering the

138 ng the composition of the growth medium, and Streptomyces explorer cells can communicate this explora

139 ptomyces sp. NRRL-F6652, a close relative of Streptomyces flavogriseus ATCC 33331.

140 E465-94 ATCC31158, and zorbamycin (ZBM) from Streptomyces flavoviridis SB9001.

141 sociated niches have selected some symbiotic Streptomyces for increased cellulose degrading activity

142 For instance, in the antibiotic producer Streptomyces fradiae, a layered network of TetRs regulat

143 Analysis of extracts derived from Streptomyces gandocaensis results in the discovery of th

144 omain searches for TA pairs in the sequenced Streptomyces genomes, we identified two putative relBE l

145 most probable evolutionary history of Dps in Streptomyces genomes.

146 and is not a conserved characteristic of the Streptomyces genus or host-associated strains.

147 f most steps of this biosynthetic pathway in Streptomyces ghanaensis (ATCC14672), except for the ulti

148 ), a clinically relevant antitumor agent, by Streptomyces globisporus that negative feedback can exte

149 nucleoside blasticidin S (BS) isolated from Streptomyces griseochromogenes was the first non-mercuri

150 TM biosynthetic gene cluster SGR810-815 from Streptomyces griseus and discover three new PTMs.

151 surprisingly, the eukaryote-like enzyme from Streptomyces griseus IleRS lacks this capacity; at the s

152 By contrast, in the closely related protease Streptomyces griseus Protease B (SGPB), the equivalent P

153 ense of NADPH, similar to its counterpart in Streptomyces griseus We obtained the crystal structure o

154 ia Escherichia coli, Lactococcus lactis, and Streptomyces griseus.

155 differentiation of the filamentous bacterium Streptomyces griseus.

156 modifications found in 16S and 23S rRNA from Streptomyces griseus.

157 valuated to stabilize polygalacturonase from Streptomyces halstedii ATCC 10897.

158 Over the last decades, the genus Streptomyces has stirred huge interest in the scientific

159 d the dimeric geometry from its hypothesized Streptomyces homologue CprB, which is a gamma-butyrolact

160 ity metagenomic cosmid libraries in the best Streptomyces host.

161 Enduracididine is produced in Streptomyces hygroscopicus by three enzymes, MppP, MppQ,

162 However, it is structurally more similar to Streptomyces hygroscopicus VldE, a GDP-valienol-dependen

163 amide synthase of the geldanamycin producer, Streptomyces hygroscopicus, shows a broader chemoselecti

164 litting mechanism that controls branching of Streptomyces hyphae.

165 Bacteria and Streptomyces, in particular, are known to utilize protei

166 s that drive plant biomass deconstruction in Streptomyces, including acquisition and selective retent

167 Pectobacterium, Pseudomonas, Ralstonia, and Streptomyces, involvement of prophage in disease symptom

168 understanding of the cellulolytic ability of Streptomyces is currently limited to a few soil-isolates

169 ass degrading genes (CAZy) are widespread in Streptomyces, key enzyme families are enriched in highly

170 a clinically useful antibiotic isolated from Streptomyces lincolnensis.

171 ressor protein (CsoR) has been identified in Streptomyces lividans (CsoR(Sl)) and found to regulate c

172 e use a structurally characterized CsoR from Streptomyces lividans (CsoR(Sl)) together with three spe

173 uxiliary activity family 10 (AA10) LPMO from Streptomyces lividans (SliLPMO10E).

174 The bacterial K(+) channel KcsA from Streptomyces lividans can be used to help elucidate ques

175 sed and manipulated in the heterologous host Streptomyces lividans K4-114.

176 nsis UC 5144, its heterologous expression in Streptomyces lividans TK24 and Streptomyces venezuelae A

177 nd PepN2, two neighboring PepN homologs from Streptomyces lividans were purified in E. coli but displ

178 Here we identify SlPatA, a GNAT in Streptomyces lividans with unique domain organization, a

179 griseochromogenes or a heterologous producer Streptomyces lividans WJ2.

180 o use KcsA (a K(+) channel from the bacteria Streptomyces lividans) as a surrogate because it lacks a

181 ent Actinobacteria (Mycobacterium smegmatis, Streptomyces lividans, and Rhodococcus jostii) each exhi

182 ion that induced prodiginine production from Streptomyces lividans, suggesting differential regulatio

183 The K(+) channel from Streptomyces lividians (KcsA) undergoes an inactivation

184 biotic, is a phosphonotripeptide produced by Streptomyces luridus, in which glycine and leucine are l

185 e desertomycin amidinohydrolase gene dstH in Streptomyces macronensis led to the accumulation of dese

186 tigation of another family member, EncP from Streptomyces maritimus, thereby expanding the biocatalyt

187 molecular basis of its action and impact on Streptomyces metabolism.

188 The Streptomyces metabolite XPO1 inhibitor leptomycin B (LMB

189 Transglutaminase from Streptomyces mobaraensis (MTG) is an important enzyme fo

190 ates were treated with transglutaminase from Streptomyces mobaraensis and tyrosinase from Trichoderma

191 tion of microbial transglutaminase (TG) from Streptomyces mobaraensis in different types of restructu

192 second step with the less specific MTG from Streptomyces mobaraensis, a successful bio-orthogonal la

193 tion of microbial transglutaminase (TG) from Streptomyces mobaraensis, and bovine and porcine fibrino

194 ation was compared to commonly used TG, from Streptomyces mobaraensis.

195 4-hydroxy-3-nitrosobenzamide biosynthesis in Streptomyces murayamaensis is performed by NspF, a mono-

196 for the nogalamycin monooxygenase (NMO) from Streptomyces nogalater As with flavin, dithranol oxidati

197 ical structures, was first demonstrated with Streptomyces parvulus in 1984.

198 The soil bacterium Streptomyces peucetius produces two widely used anticanc

199 re glycosylated anthracyclines isolated from Streptomyces peucetius.

200 cally abundant and geographically widespread Streptomyces phylogroups from our culture collection.

201 igate the key roles of type II TA systems in Streptomyces physiology and environmental stress respons

202 PtmT2 from Streptomyces platensis CB00739 was verified as an ent-co

203 tin (iso-MGS) biosynthetic gene cluster from Streptomyces platensis NRRL 18993 consists of 11 genes,

204 anipulation in the PTM-PTN dual overproducer Streptomyces platensis SB12029, revealing two genes, ptm

205 overed broad-spectrum antibiotic produced by Streptomyces platensis.

206 n FilP and DivIVA, the main component of the Streptomyces polarisome complex, leads to formation of a

207 Streptomyces population structure varied at regional spa

208 The discovery of Streptomyces-produced streptomycin founded the age of tu

209 The Streptomyces protein DivIVA is a critical determinant of

210 se-binding lectin (SL2-1) from the bacterium Streptomyces rapamycinicus was identified by analysis of

211 ory network that controls differentiation in Streptomyces, repressing a large regulon of developmenta

212 The extracellular protein HbpS from Streptomyces reticuli interacts with iron ions and heme.

213 consisting of orthogonal promoter sequences, Streptomyces ribosome binding sites, and yeast selectabl

214 inically approved antibiotic daptomycin from Streptomyces roseosporus, but has notable structural dif

215 Here we report the crystal structure of Streptomyces sahachiroi AlkZ (previously Orf1), a bacter

216 Streptomyces scabies is an economically important plant

217 zyme from the plant pathogen 87.22 strain of Streptomyces scabies Scabin shares nearly 40% sequence i

218 We establish that species of Streptomyces secrete dodecanoic acid, which is sensed by

219 oordinate phosphohistidine intermediate from Streptomyces sp .

220 74+/-0.019UmL(-1) of TG from a novel source; Streptomyces sp.

221 the marginolactone azalomycin F in mangrove Streptomyces sp. 211726 has shown that only nineteen ext

222 gates), were characterized as metabolites of Streptomyces sp. AD-23-14 isolated from the Rock Creek u

223 ), and tetranactin (3) in a crude extract of Streptomyces sp. AMC 23 in the precursor ion scan mode.

224 One bacterial strain (Streptomyces sp. CLI2509) from the bracket fungus Hymeno

225 inamide construction in the marine bacterium Streptomyces sp. CNB-091, which involves a novel intermo

226 biosynthetic logic of their construction in Streptomyces sp. CNH-287 based on the identification of

227 xplored its atropo-selective biosynthesis in Streptomyces sp. CNQ-418 in order to elucidate the N,C-b

228 The marine Streptomyces sp. CNQ-617 produces two diastereomers, mar

229 tinomycetes Salinispora pacifica CNS-143 and Streptomyces sp. CNT-179, highlighted by the unprecedent

230 to identify nigericin in a crude extract of Streptomyces sp. Eucal-26 by means of precursor ion scan

231 mily of anti-infective compounds produced by Streptomyces sp. K01-0509 with a novel mode of action.

232 ene cluster for herbicidin A biosynthesis in Streptomyces sp. L-9-10 as well as its verification by h

233 s units to surfactin in the agar proximal to Streptomyces sp. Mg1 but not other streptomycetes tested

234 ites exchanged between Bacillus subtilis and Streptomyces sp. Mg1 cultured together.

235 We observed that the aerial growth of Streptomyces sp. Mg1 was resistant to inhibition by surf

236 To identify possible enzymes from Streptomyces sp. Mg1 with surfactin hydrolase activity,

237 thway arising from an orphan gene cluster in Streptomyces sp. NRRL-F6652, a close relative of Strepto

238 been isolated from laboratory cultures of a Streptomyces sp. obtained from a tropical marine sedimen

239 ate the biomass-deconstructing capability of Streptomyces sp. SirexAA-E (ActE), an aerobic bacterium

240 Streptomyces sp. SirexAA-E is a highly cellulolytic bact

241 luding the anticancer agent cinerubin B from Streptomyces sp. SPB74 and an antibiotic, arenimycin B,

242 d the close relationship between CLI2509 and Streptomyces sp. SPB78, which was previously implicated

243 linispora tropica and a putative prophage in Streptomyces sp. strain C.

244 lorins A-D, produced by the marine bacterium Streptomyces sp. strain CNH-189, which possess novel che

245 ies and are produced by the marine bacterium Streptomyces sp. strain CNH-189.

246 been isolated from laboratory cultures of a Streptomyces sp. Svetamycins A-D, F, and G are cyclic de

247 Streptomyces species are generally non-pathogenic soil s

248 expression studies indicate that in several Streptomyces species at least one Dps is significantly o

249 s study, we examined a collection of diverse Streptomyces species for the best innate ability to hete

250 ted with primary metabolism in nonpathogenic Streptomyces species have been recruited as basic elemen

251 Individual Streptomyces species have the genetic potential to produ

252 Metabolic regulation in Streptomyces species is of interest due to the role of t

253 Phenotypic tests identified the isolate as a Streptomyces species, but 16S rRNA sequence analysis pro

254 a class of polyether ionophores produced by Streptomyces species, was investigated by accurate-mass

255 ence for a latitudinal diversity gradient in Streptomyces species.

256 cturally similar to polyketide cyclases from Streptomyces species.

257 none skeleton in the biosynthesis pathway of Streptomyces species.

258 n the proliferation of ftsZ mutants in other Streptomyces species.

259 put of the countless silent gene clusters in Streptomyces spp.

260 h-throughput transcriptional assay format in Streptomyces spp. by leveraging eGFP, inserted both at a

261 Our data suggest that loss of mce in Streptomyces spp. may have profound effects on survival

262 e antibiotic valanimycin was discovered in a Streptomyces strain.

263 l species, and that at least for the case of Streptomyces, strain de-replication based on SSU gene se

264 Although Streptomyces strains are good first options for heterolo

265 In Streptomyces strains in which another gene (tunB) is del

266 in (ACM) isolated from cultures of different Streptomyces strains is a potent mechanism-based inhibit

267 Streptomyces strains were isolated from perennial grass

268 iosynthetic pathways from cyanobacterial and Streptomyces strains.

269 those governing sporulation of Bacillus and Streptomyces, suggesting that Myxococcus evolved a highl

270 ng these genes may play an important role in Streptomyces survival in the environment.

271 Integrases, such as that of the Streptomyces temperate bacteriophage varphiC31, promote

272 Analysis of the NPE derived from Streptomyces tempisquensis led to the isolation of the n

273 rD3 genes from the apramycin gene cluster in Streptomyces tenebrarius were expressed in E. coli and t

274 Streptomyces thermoautotrophicus UBT1 has been described

275 In Streptomyces, they additionally regulate secondary metab

276 mental behaviours in bacteria, here, causing Streptomyces to deviate from its classically-defined lif

277 tected the same polyene tetramate as that in Streptomyces transformed with the PKS-NRPS alone.

278 During sporulation, the filamentous bacteria Streptomyces undergo a massive cell division event in wh

279 expression in Streptomyces lividans TK24 and Streptomyces venezuelae ATCC 10712, and detection of var

280 Streptomyces venezuelae CmlI catalyzes the six-electron

281 th PKS module from the pikromycin pathway of Streptomyces venezuelae creates a reaction chamber for t

282 Feeding of 34-36 to Streptomyces venezuelae expressing marG led to productio

283 e destruction of mycelial microcolonies of a Streptomyces venezuelae ftsZ mutant.

284 tion of this site, which is conserved in the Streptomyces venezuelae GlgE enzyme, did not affect the

285 We now confirm that OtsA from Streptomyces venezuelae has such a preference for GDP-gl

286 al S-adenosyl-L-methionine enzyme DesII from Streptomyces venezuelae is able to oxidize the C3 hydrox

287 Jadomycin Oct (1) was isolated from Streptomyces venezuelae ISP5230 and characterized as a s

288 n the jadomycin biosynthetic gene cluster of Streptomyces venezuelae ISP5230, affects both chloramphe

289 related compound methymycin are produced by Streptomyces venezuelae strain ATCC 15439.

290 Streptomyces venezuelae strains that expressed these PKS

291 a full-length PKS module from the bacterium Streptomyces venezuelae that revealed an unexpectedly di

292 n (MTM) and pikromycin (PKM), co-produced by Streptomyces venezuelae, represent minimalist macrolide

293 application of genome-wide approaches using Streptomyces venezuelae, which is capable of fairly sync

294 dl) genes by exploiting a new model species, Streptomyces venezuelae, which sporulates in liquid cult

295 to characterize a putative NsrR homologue in Streptomyces venezuelae.

296 the biosynthetic gene clusters for BLMs from Streptomyces verticillus ATCC15003, tallysomycins from S

297 The biogeography of Streptomyces was examined at regional spatial scales to

298 To investigate the role in Streptomyces we deleted the mce locus and studied its im

299 aenorhabditis elegans and the bacterial prey Streptomyces, which have evolved a powerful defense: the

300 ed the feasibility of these affinity tags in Streptomyces, which will be widely employed to explore t