ライフサイエンスコーパス: Streptomyces

1 engineering of secondary metabolite BGCs in Streptomyces.

2 ested, with the most notable exception being Streptomyces.

3 ted availability of the biochemical tools in Streptomyces.

4 r ion balance and coordinated development in Streptomyces.

5 influenced the contemporary biogeography of Streptomyces.

6 been widely reported in bacteria but none in Streptomyces.

7 and B, indolosesquiterpenoids isolated from Streptomyces.

8 eterologous expression of gene clusters from Streptomyces.

9 by the actinobacterial members of the genus Streptomyces.

10 the Frankia and other actinobacteria such as Streptomyces.

11 d cell envelope stress response in the genus Streptomyces.

12 microbial-resistant pathogens more than soil Streptomyces.

13 bacteria, including the antibiotic-producing Streptomyces.

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

15 uction of the hydrophobic sheath that covers Streptomyces aerial hyphae and spores.

16 Thal, also known as ThdH, from the bacterium Streptomyces albogriseolus at 2.55 angstrom resolution.

17 tures of tryptophan 6-halogenase (Thal) from Streptomyces albogriseolus using stopped-flow, rapid-que

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

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

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

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

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

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

24 we characterize reciprocal inhibition among Streptomyces and Fusarium populations from prairie soil,

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

26 In this report, Streptomyces and Mycobacterium, belonging to the phylum

27 3 and 56 families were found to be unique to Streptomyces and Mycobacterium, respectively.

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

29 ,2-de]quinoline natural products produced by Streptomyces and Salinispora actinobacteria.

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

33 tagonistic interactions between Fusarium and Streptomyces are driven by resource competition, and sup

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

35 Streptomyces are of great biological and industrial sign

36 Streptomyces are our primary source of antibiotics, prod

37 Streptomyces are spore forming filamentous bacteria whic

38 Streptomyces are ubiquitous soil bacteria that undergo a

39 Natural products, particularly from Streptomyces, are the source of most antimicrobials, yet

40 In Streptomyces arenae this reaction is catalyzed by CYP161

41 metabolites, and provide global control over Streptomyces' arsenal of signaling and antagonistic comp

42 lase-mediated ICL unhooking was described in Streptomyces as a means of self-resistance to the genoto

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

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

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

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

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

48 tomyces venezuelae, Streptomyces rimosus and Streptomyces avermitilis.

49 nthesis genes among virtually all species of Streptomyces bacteria (and genes for the biosynthesis of

50 The pollinators can transfer the Streptomyces bacteria among flowers and plants, and Stre

51 Streptomyces bacteria are known for their prolific produ

52 Streptomyces bacteria employ a newly-discovered cell typ

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

54 rack the movement of an endophytic strain of Streptomyces bacteria throughout a managed strawberry ec

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

56 ness both explained significant variation in Streptomyces beta diversity.

57 from the chalcomycin biosynthetic pathway in Streptomyces bikiniensis These studies provided a basis

58 We evaluated Streptomyces biogeography in soils along a 1200 km latit

59 In rishirilide biosynthesis by Streptomyces bottropensis, (13)C-labeling studies previo

60 myces bacteria among flowers and plants, and Streptomyces can move into the plant vascular bundle fro

61 Herein, genome screening of Streptomyces candidus NRRL 3601 led to the discovery of

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

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

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

65 lkyne-containing amino acid in the bacterium Streptomyces cattleya.

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

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

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

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

70 red with nontarget lipase activities such as Streptomyces chromofuscus PLD or serum lipase.

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

72 sequence of beta-lactam antibiotic-producing Streptomyces clavuligerus ATCC 27 064 is completed, whic

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

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

75 interaction between vancomycin and VanS from Streptomyces coelicolor (VanS(SC)), a model Actinomycete

76 of a cellulose-active family AA10 LPMO from Streptomyces coelicolor A3(2) (ScLPMO10C, also known as

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

78 Streptomyces coelicolor A3(2) is amongst the best studie

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

80 We describe here mutant alleles of ftsZ in Streptomyces coelicolor and Streptomyces venezuelae that

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

82 The Streptomyces coelicolor genome encodes only a single put

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

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

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

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

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

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

89 Antibiotic production is coordinated in the Streptomyces coelicolor population through the use of di

90 NsrR from Streptomyces coelicolor regulates its own expression and

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

92 of this methodology to Bacillus subtilis and Streptomyces coelicolor revealed heterogeneity in chemic

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

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

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

96 rt dynamics at the TNC of small laccase from Streptomyces coelicolor using paramagnetic NMR and elect

97 The gene encoding Streptomyces coelicolor xanthine dehydrogenase regulator

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

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

100 In Streptomyces coelicolor, it is required for the late sta

101 allowed for rapid heterologous expression in Streptomyces coelicolor, leading to the identification a

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

103 n B, oxytetracycline and avermectin B(1a) in Streptomyces coelicolor, Streptomyces venezuelae, Strept

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

105 ator of the cell envelope stress response in Streptomyces coelicolor.

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

107 F. candida feeds on the Streptomyces colonies and disseminates spores both via f

108 ingtails were attracted to odours emitted by Streptomyces colonies.

109 Streptomyces communities exhibited both high dissimilari

110 cal for normal growth and differentiation in Streptomyces, connecting ionic stress to development.

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

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

113 The study of Streptomyces development has made significant advances i

114 ungi trigger a previously unobserved mode of Streptomyces development.

115 ablish c-di-GMP as the central integrator of Streptomyces development.

116 Streptomyces diversity was examined using high-throughpu

117 In Streptomyces, during sporulation, multiple Z rings are a

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

119 including formation of Bacillus endospores, Streptomyces exospores, and metabolically latent Mycobac

120 Fungi trigger Streptomyces exploratory growth in part by altering the

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

122 ovel antimicrobials, particularly the strain Streptomyces fildesensis So13.3, which first draft genom

123 train So13.3 was taxonomically affiliated as Streptomyces fildesensis.

124 tinobacteria predominantly belonged to genus Streptomyces, followed by Nocardia and Kribbella.

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

126 s the homologous P450 from tylosin-producing Streptomyces fradiae (TylHI) exhibits a high degree of s

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

128 eless, our knowledge on antibiotic-producing Streptomyces from Antarctic is very limited.

129 assess the distinct evolutionary lineages of Streptomyces from insect microbiomes as a source of new

130 of biosynthetic clusters by Lsr2 may protect Streptomyces from the inappropriate expression of specia

131 The evolutionary trajectories of Streptomyces from the insect microbiome influence their

132 robials, yet discovery campaigns focusing on Streptomyces from the soil largely rediscover known comp

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

134 Streptomyces genetics has revolutionised natural product

135 translational regulatory elements in GC-rich Streptomyces genomes is essential to elucidating the com

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

137 We then applied decRiPPter to mine 1,295 Streptomyces genomes, which led to the identification of

138 classes of BGCs in 1,110 publicly available Streptomyces genomes.

139 uch regulatory elements has been limited for Streptomyces genomes.

140 rce for antibiotics discovery and members of Streptomyces genus have historically been studied as nat

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

142 Application to Streptomyces ghanaensis identified amygdalin as an elici

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

144 the polyketide natural product Aurodox from Streptomyces goldiniensis is able to block the pathogene

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

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

147 tiviral mechanism developed in the bacterium Streptomyces griseus SgrAI is a type II restriction endo

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

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

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

151 valuated to stabilize polygalacturonase from Streptomyces halstedii ATCC 10897.

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

153 nus have been identified and most species of Streptomyces have yet to be described.

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

155 ity metagenomic cosmid libraries in the best Streptomyces host.

156 biosynthetic gene cluster in extremotolerant Streptomyces huasconensis HST28(T) from Salar de Huasco,

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

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

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

160 Insect-associated Streptomyces inhibit antimicrobial-resistant pathogens m

161 ine monophosphate (c-di-GMP) determines when Streptomyces initiate sporulation.

162 We show that a Streptomyces isolate found in the rhizosphere and on flo

163 Cultivated Streptomyces isolates represent a major source of clinic

164 Herein, a cosmid is identified from the Streptomyces kaniharaensis genome library that contains

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

166 al antibiotic produced by the soil bacterium Streptomyces lavendulae.

167 t of the sporulation process, completing the Streptomyces life cycle by facilitating dispersal of spo

168 a clinically useful antibiotic isolated from Streptomyces lincolnensis.

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

170 o it is not surprising that bacteria such as Streptomyces lividans can activate many of the available

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

172 griseochromogenes or a heterologous producer Streptomyces lividans WJ2.

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

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

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

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

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

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

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

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

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

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

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

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

185 Nogalamycin monooxygenase (NMO) from Streptomyces nogalater is a cofactor-independent enzyme

186 OlvS(A) encoded in the olv gene cluster from Streptomyces olivaceus NRRL B-3009 catalyzes the rearran

187 ally the same number of P450s in the genome, Streptomyces P450s are much more diverse than those of M

188 Streptomyces phage C31 integrase (Int)-a large serine si

189 Streptomyces phylogenetic diversity (Faith's PD) was cor

190 Cs and variable distribution patterns in the Streptomyces phylogeny, even among very closely related

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

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

193 sults present a tripartite mutualism between Streptomyces, plant and pollinator partners.

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

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

196 gase derived from a GH20 hexosaminidase from Streptomyces plicatus in which the catalytic acid/base g

197 Streptomyces population structure varied at regional spa

198 ce for local adaptation between Fusarium and Streptomyces populations as indicated by significantly g

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

200 migatus, which is activated by the bacterium Streptomyces rapamycinicus during the bacterial-fungal i

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

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

203 which depend on a type IV secretion system, Streptomyces requires only TraB protein to transfer the

204 rs-e.g., from Photorhabdus luminescens TT01, Streptomyces resistomycificus, Streptoccocus sp. GMD2S,

205 Genome mining of Streptomyces reveals high diversity of BGCs and variable

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

207 tomyces coelicolor, Streptomyces venezuelae, Streptomyces rimosus and Streptomyces avermitilis.

208 epsipeptide derived from the soil saprotroph Streptomyces roseosporus, and its antibiotic properties

209 Collectively, these results suggest that in Streptomyces, Rpfs have a structural rather than signali

210 We detected 1287 Streptomyces rpoB operational taxonomic units (OTUs) wit

211 oral microbiome signature (Pseudoxanthomonas-Streptomyces-Saccharopolyspora-Bacillus clausii) highly

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

213 Streptomyces scabies is an economically important plant

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

215 ce of a large and diverse number of P450s in Streptomyces secondary metabolism contributes to antibio

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

217 unexpectedly both abundant and widespread in Streptomyces Seven of 11 systematically selected T1PKS m

218 th domain 4 of the principal sigma factor of Streptomyces, sigma(HrdB) (sigma(HrdB) (4)).

219 rectly cloned the skt gene cluster using the Streptomyces site-specific integration vector pSET152.

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

227 Streptomyces sp. Kz-24 (GenBank accession no. KY000533;

228 9 (GenBank accession no. KU901725; 1313 bp), Streptomyces sp. Kz-28 (GenBank accession no. KY000534;

229 8 (GenBank accession no. KY000534; 1378 bp), Streptomyces sp. Kz-32 (GenBank accession no. KY000536;

230 GenBank accession no. KY000536; 1377 bp) and Streptomyces sp. Kz-67 (GenBank accession no. KY000540;

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

232 identification of the cytochrome P450, NzeB (Streptomyces sp. NRRL F-5053), which catalyzes both inte

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

234 Streptomyces sp. PB-79 (GenBank accession no. KU901725;

235 Therefore, the genome of Streptomyces sp. RKND-216 was sequenced to identify the

236 hybrid marine natural product isolated from Streptomyces sp. RKND-216.

237 The strain Streptomyces sp. So13.3 showed the greatest antibiotic a

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

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

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

241 cryptic type II PKS gene cluster (skt) from Streptomyces sp. Tu 6314.

242 as a natural product of ginseng-rhizospheric Streptomyces sp. WON17.

243 th MS-based molecular networking analysis of Streptomyces sp.QL37, elucidated 24 other rearranged and

244 Streptomyces species encode paralogous Lsr2 proteins (Ls

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

246 We also found that numerous Streptomyces species harbor BGCs known to encode antitum

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

248 Individual Streptomyces species have the genetic potential to produ

249 tes during the stationary phase of growth of Streptomyces species in fermenters.

250 angucycline-derived polyketide, produced by Streptomyces species QL37.

251 logous proteins are widely distributed among Streptomyces species, and their apparent substrate promi

252 nowledge about phylogenetic relationships of Streptomyces species, genome-wide diversity and distribu

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

254 moters identified in S. coelicolor across 19 Streptomyces species.

255 none skeleton in the biosynthesis pathway of Streptomyces species.

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

257 ence for a latitudinal diversity gradient in Streptomyces species.

258 of antibiotics, hitherto only isolated from Streptomyces species.

259 equencing of rpoB amplicons generated with a Streptomyces specific primer set.

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

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

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 lts highlight the potential of the Antarctic Streptomyces strains as a promising source of novel anti

265 activity of organic extracts from Antarctic Streptomyces strains was evaluated by disk diffusion ass

266 Streptomyces strains were isolated from perennial grass

267 iosynthetic pathways from cyanobacterial and Streptomyces strains.

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

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

270 Streptomyces thermoautotrophicus UBT1 has been described

271 In Streptomyces, they additionally regulate secondary metab

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

273 Streptomyces tsukubaensis harbours 42 ECFs to reprogram

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

275 for conjugative plasmid transfer in mycelial Streptomyces Unlike other conjugative systems, which dep

276 Antibiotic-producing Streptomyces use the diadenylate cyclase DisA to synthes

277 ted natural products, the thiovarsolins from Streptomyces varsoviensis.

278 vitro and in vivo experiments with WhiD from Streptomyces venezuelae (SvWhiD), which differs from S.

279 Streptomyces venezuelae CmlI catalyzes the six-electron

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

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

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

283 GT1 family glycosyltansferase, Sv0189, from Streptomyces venezuelae ISP5230 (ATCC 10721) was charact

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

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

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

287 Streptomyces venezuelae strains that expressed these PKS

288 leles of ftsZ in Streptomyces coelicolor and Streptomyces venezuelae that perturb cell division in su

289 es that c-di-GMP controls spore formation in Streptomyces venezuelae through sequestering the sporula

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

291 avermectin B(1a) in Streptomyces coelicolor, Streptomyces venezuelae, Streptomyces rimosus and Strept

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

293 to characterize a putative NsrR homologue in Streptomyces venezuelae.

294 3(2), this strain is more closely related to Streptomyces violaceoruber ISP5049 than to the type stra

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

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

297 he best studied representatives of the genus Streptomyces, which is the largest genus within the Acti

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

299 omycetes, which include members of the genus Streptomyces, with their bacterial cellular dimensions b

300 Vibrio cyclitrophicus, Escherichia coli and Streptomyces yokosukanensis, which has distinct genetic