ライフサイエンスコーパス: Streptomyces coelicolor

1 systems (TPA-stimulated mammalian cells and Streptomyces coelicolor).

2 pically regulates antibiotic biosynthesis in Streptomyces coelicolor.

3 SCO5883 (redU) and SCO6673 were disrupted in Streptomyces coelicolor.

4 g of BldD, a key regulator of development in Streptomyces coelicolor.

5 'more complex', pharmaceutically important, Streptomyces coelicolor.

6 ctants, with emphasis on the SapB protein of Streptomyces coelicolor.

7 forming soil bacteria, Bacillus subtilis and Streptomyces coelicolor.

8 e stress-response sigma factor, sigma(R), in Streptomyces coelicolor.

9 degree of similarity to the single SerRS of Streptomyces coelicolor.

10 h morphogenesis and antibiotic production in Streptomyces coelicolor.

11 thway for initiation of BCFA biosynthesis in Streptomyces coelicolor.

12 n N-terminal polyhistidine-tagged protein in Streptomyces coelicolor.

13 elium formation by the filamentous bacterium Streptomyces coelicolor.

14 f sporulation in the Gram-positive bacterium Streptomyces coelicolor.

15 teins called chaplins has been identified in Streptomyces coelicolor.

16 es has been proposed to polyadenylate RNA in Streptomyces coelicolor.

17 ory systems and the developmental program in Streptomyces coelicolor.

18 one of the Ku homologs from the Actinomycete Streptomyces coelicolor.

19 vestigated in Amycolatopsis mediterranei and Streptomyces coelicolor.

20 s required for normal cell wall integrity in Streptomyces coelicolor.

21 ity to the CCRs of Streptomyces collinus and Streptomyces coelicolor.

22 identical to the corresponding protein from Streptomyces coelicolor.

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

24 d repeat in the IS110 insertion element from Streptomyces coelicolor.

25 he actinorhodin biosynthetic gene cluster of Streptomyces coelicolor.

26 hat is 80% identical to the proposed oriC of Streptomyces coelicolor.

27 ing sporulation in the filamentous bacterium Streptomyces coelicolor.

28 s and mammals, was cloned and sequenced from Streptomyces coelicolor.

29 ired for sporulation in the aerial hyphae of Streptomyces coelicolor.

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

31 otein assembly in the filamentous bacterium, Streptomyces coelicolor.

32 as found to induce prodiginine production by Streptomyces coelicolor.

33 ial hyphae formation in adjacent colonies of Streptomyces coelicolor.

34 global regulator of antibiotic production in Streptomyces coelicolor.

35 O-pnp operon in an RNase III (rnc) mutant of Streptomyces coelicolor.

36 chia coli, and the small laccase (SLAC) from Streptomyces coelicolor.

37 l antibiotic-producing filamentous bacterium Streptomyces coelicolor.

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

39 cal development and antibiotic production in Streptomyces coelicolor.

40 as overexpression causes hyphal branching in Streptomyces coelicolor.

41 are dispensable for growth and viability of Streptomyces coelicolor.

42 om a fully sequenced microbe is Sco3058 from Streptomyces coelicolor.

43 in the genome of the Gram-positive bacterium Streptomyces coelicolor.

44 quired for the late stages of sporulation in Streptomyces coelicolor.

45 ample, the genome of the model streptomycete Streptomyces coelicolor.

46 cherichia coli, Saccharomyces cerevisiae, or Streptomyces coelicolor.

47 with the distribution of two antibiotics in Streptomyces coelicolor (a mycelial bacterium).

48 regulated cell division are of interest for Streptomyces coelicolor, a sporulating, filamentous bact

49 le sporulation septation of aerial hyphae of Streptomyces coelicolor A3(2) and for the expression of

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

51 Transformation of tryptophan auxotrophs of Streptomyces coelicolor A3(2) and subsequent analysis ha

52 linear chromosomes of the model actinomycete Streptomyces coelicolor A3(2) and the closely related St

53 An afsA homologue, scbA, was identified in Streptomyces coelicolor A3(2) and was found to lie adjac

54 f the Gram-positive, soil-dwelling bacterium Streptomyces coelicolor A3(2) as part of a two-gene clus

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

56 For a bacterium, Streptomyces coelicolor A3(2) contains a relatively larg

57 malR of Streptomyces coelicolor A3(2) encodes a homologue of the

58 The sigE gene of Streptomyces coelicolor A3(2) encodes an RNA polymerase

59 iron limitation, the Gram-positive bacterium Streptomyces coelicolor A3(2) excretes three siderophore

60 Streptomyces coelicolor A3(2) ftsI- and ftsW-null mutant

61 quencing of the entire genetic complement of Streptomyces coelicolor A3(2) has been completed with th

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

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

64 We show that the cell division gene ftsQ of Streptomyces coelicolor A3(2) is dispensable for growth

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

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

67 Mutants of Streptomyces coelicolor A3(2) J1929 (Delta pglY) were is

68 The mycelial prokaryote Streptomyces coelicolor A3(2) possesses a large linear c

69 Streptomyces coelicolor A3(2) produces at least four che

70 n and characterization of a gene (ptpA) from Streptomyces coelicolor A3(2) that codes for a protein w

71 from Bacillus subtilis, Bacillus cereus, and Streptomyces coelicolor A3(2) that shared low overall id

72 Production of ppGpp in Streptomyces coelicolor A3(2) was achieved independently

73 nt of the (p)ppGpp synthetase gene, relA, of Streptomyces coelicolor A3(2) was amplified from genomic

74 iotics, the x-ray structure of CYP154C1 from Streptomyces coelicolor A3(2) was determined (Protein Da

75 everal widely used laboratory derivatives of Streptomyces coelicolor A3(2) were found to have 1.06 Mb

76 mers of biflaviolin and one triflaviolin) in Streptomyces coelicolor A3(2) which protect the soil bac

77 Here we report that SCO1815 from Streptomyces coelicolor A3(2), an uncharacterized homolo

78 By complementing developmental mutants of Streptomyces coelicolor A3(2), at least 15 regulatory ge

79 e growth limitation (Pgl) system, encoded by Streptomyces coelicolor A3(2), confers protection agains

80 has been used to amplify a 2,181-bp ORF from Streptomyces coelicolor A3(2), designated SC9B1.20 (= SC

81 In the Gram-positive bacterium, Streptomyces coelicolor A3(2), expression of the thiored

82 ynthase (EIZS), a sesquiterpene cyclase from Streptomyces coelicolor A3(2), has been determined at 1.

83 ulatory protein for antibiotic production in Streptomyces coelicolor A3(2), is homologous to RedD and

84 One of the 18 P450s in Streptomyces coelicolor A3(2), P450 105D5, was found to

85 ram-positive, antibiotic-producing bacterium Streptomyces coelicolor A3(2), the thiol-disulphide stat

86 se the genome of the Gram-positive bacterium Streptomyces coelicolor A3(2), we have employed high-thr

87 technique and applied it to actII-orf4 from Streptomyces coelicolor A3(2), which encodes the pathway

88 located on the 356-kb linear plasmid SCP1 of Streptomyces coelicolor A3(2).

89 phiC31, in the antibiotic producing bacteria Streptomyces coelicolor A3(2).

90 ivIC in the gram-positive mycelial bacterium Streptomyces coelicolor A3(2).

91 06-sco1208) in the prototypic soil bacterium Streptomyces coelicolor A3(2).

92 of undecylprodigiosin by the Red cluster in Streptomyces coelicolor A3(2).

93 ted site specifically into the chromosome of Streptomyces coelicolor A3(2).

94 ly described as essential for sporulation in Streptomyces coelicolor A3(2).

95 ram-positive, antibiotic-producing bacterium Streptomyces coelicolor A3(2).

96 at specifies the polyketide spore pigment in Streptomyces coelicolor A3(2).

97 involved in the synthesis of fatty acids in Streptomyces coelicolor A3(2).

98 is of this antibiotic in the soil bacterium, Streptomyces coelicolor A3(2).

99 uence on the biosynthesis of actinorhodin in Streptomyces coelicolor A3(2).

100 The Streptomyces coelicolor absA two-component system was in

101 The Streptomyces coelicolor absB gene encodes an RNase III f

102 A three-dimensional model of the Streptomyces coelicolor actinorhodin beta-ketoacyl synth

103 which is required for the differentiation of Streptomyces coelicolor aerial hyphae into mature spore

104 This reporter system is based on the Streptomyces coelicolor agarase protein, which is secret

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

106 us, calcium-dependent antibiotic produced by Streptomyces coelicolor and A54145 produced by Streptomy

107 arity to SigF sporulation sigma factors from Streptomyces coelicolor and Bacillus subtilis and to Sig

108 ons of the nickel-dependent SOD (NiSOD) from Streptomyces coelicolor and for a series of mutants that

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

110 important bacterial genus, the model species Streptomyces coelicolor and its relatives have been the

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

112 ults from analysis of the recently sequenced Streptomyces coelicolor and Streptomyces avermitilis gen

113 r open reading frame, orfX, also observed in Streptomyces coelicolor and Streptomyces avermitilis, ma

114 from S. turgidiscabies to the non-pathogens Streptomyces coelicolor and Streptomyces diastatochromog

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

116 cetes, including the soil dwelling bacterium Streptomyces coelicolor and the human pathogen Mycobacte

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

118 Pseudomonas aeruginosa, Pseudomonas putida, Streptomyces coelicolor, and chromosome I of Vibrio chol

119 oire of Escherichia coli, Bacillus subtilis, Streptomyces coelicolor, and cyanobacteria to illustrate

120 ch an antibiotically inactive precursor of a Streptomyces coelicolor antibiotic induces resistance --

121 Sporulation mutants of Streptomyces coelicolor appear white because they are de

122 The four antibiotics produced by Streptomyces coelicolor are all affected by mutations in

123 from Gluconobacter oxidans, and Sco4986 from Streptomyces coelicolor are currently annotated as d-ami

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

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

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

127 nalysis to be essential for the viability of Streptomyces coelicolor, Bentley et al. have suggested t

128 Mutants of Streptomyces coelicolor blocked at the earliest visible

129 In Streptomyces coelicolor, both overexpression and deletio

130 nic, non-glycopeptide-producing actinomycete Streptomyces coelicolor carries a cluster of seven genes

131 Epi-isozizaene synthase from Streptomyces coelicolor catalyzes the multistep cyclizat

132 e gene encoding this enzyme was expressed in Streptomyces coelicolor CH999 together with the actinorh

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

134 Streptomyces coelicolor CH999/pJRJ2 harbors a plasmid en

135 th factor (KS/CLF) complex was purified from Streptomyces coelicolor CH999/pSEK38, and assayed with p

136 observed a spontaneous amplification of the Streptomyces coelicolor chromosome, including genes enco

137 Hybrids of the Streptomyces coelicolor conjugative plasmid SCP2* and th

138 (act) minimal polyketide synthase (PKS) from Streptomyces coelicolor consists of three proteins: an a

139 Streptomyces coelicolor contained an innate Tc-controlla

140 Streptomyces coelicolor contains paralogous versions of

141 The genome sequence of Streptomyces coelicolor contains three open reading fram

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

143 hemical study on the catalytic properties of Streptomyces coelicolor cytochrome P450 (P450) 154A1, kn

144 t different alleles of this locus can arrest Streptomyces coelicolor development at very distinct sta

145 The filamentous bacterium Streptomyces coelicolor differentiates by forming specia

146 The Streptomyces coelicolor dnaE gene, encoding the catalyti

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

148 The absB locus of Streptomyces coelicolor encodes a homolog of bacterial R

149 The dnaK operon of Streptomyces coelicolor encodes the DnaK chaperone machi

150 The dnaK operon of Streptomyces coelicolor encodes the DnaK chaperone machi

151 age of the vancomycin-dependent phenotype of Streptomyces coelicolor femX null mutants to isolate a c

152 tion, we solved the crystal structure of the Streptomyces coelicolor FGE homolog to 2.1 A resolution.

153 The filamentous bacterium Streptomyces coelicolor forms an aerial mycelium as a pr

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

155 e under the control of the ermE* promoter in Streptomyces coelicolor furthermore led to the productio

156 A Streptomyces coelicolor gene, called spaA, homologous to

157 Here, we identify a Streptomyces coelicolor gene, rns, encoding a 140 kDa pr

158 The Streptomyces coelicolor genome encodes only a single put

159 hree GTP cyclohydrolase II homologues in the Streptomyces coelicolor genome have been shown to cataly

160 The Streptomyces coelicolor genome sequence was searched for

161 The 8.7-Mb Streptomyces coelicolor genome was previously sequenced

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

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

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

165 Activity of the Streptomyces coelicolor Group IV family member, sigma(R)

166 The extracellular proteome of Streptomyces coelicolor grown in a liquid medium was ana

167 erved movies of replisome trafficking during Streptomyces coelicolor growth.

168 The gram-positive filamentous bacterium Streptomyces coelicolor has a complex developmental cycl

169 The transport of metal-citrate complexes in Streptomyces coelicolor has been investigated.

170 Streptomyces coelicolor has nine SigB-like RNA polymeras

171 Streptomyces coelicolor has two genes encoding tryptopha

172 tives of the actinorhodin (act) PKS ACP from Streptomyces coelicolor have been prepared and structura

173 ecent studies on prodiginine biosynthesis in Streptomyces coelicolor have elucidated the function of

174 talyzed by a GCH II ortholog (SCO 6655) from Streptomyces coelicolor; however, SCO 6655, like other G

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

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

177 Morphogenesis in the bacterium Streptomyces coelicolor involves the formation of a lawn

178 Streptomyces coelicolor is a model for studying bacteria

179 Streptomyces coelicolor is a model system for the study

180 Streptomyces coelicolor is a morphologically complex bac

181 Streptomyces coelicolor is a representative of the group

182 The ActVA-ActVB system from Streptomyces coelicolor is a two-component flavin-depend

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

184 differentiation in the filamentous bacterium Streptomyces coelicolor is believed to involve a mechani

185 tamine synthetase I (GSI) enzyme activity in Streptomyces coelicolor is controlled post-translational

186 The newly sequenced genome of Streptomyces coelicolor is estimated to encode 7825 theo

187 The best cofactor for citrate uptake in Streptomyces coelicolor is Fe(3+), but uptake was also n

188 f disulphide stress in actinomycetes such as Streptomyces coelicolor is known to involve the zinc-con

189 The chromosome of the filamentous bacterium Streptomyces coelicolor is linear, but the genetic map i

190 Streptomyces coelicolor is more amenable to strain impro

191 ryptophanyl-tRNA synthetase gene (trpRS1) in Streptomyces coelicolor is regulated by a ribosome-media

192 Here, we show that one of these clusters in Streptomyces coelicolor is regulated, at least in part,

193 Streptomyces coelicolor is the model organism for the ac

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

195 bacterial species, Streptomyces lividans and Streptomyces coelicolor, it normally is expressed only i

196 gh similarity to the primary sigma factor in Streptomyces coelicolor, it was postulated that sigmaA h

197 ies lgt mutant but restored by expression of Streptomyces coelicolor lgt1 or lgt2 confirming that bot

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

199 described the X-ray crystal structure of the Streptomyces coelicolor MAT and suggested active site re

200 The single recombinant expressing the Streptomyces coelicolor minimal whiE (spore pigment) pol

201 We report herein the generation of a Streptomyces coelicolor mutant (YL/ecFabH) in which the

202 Streptomyces coelicolor mutants lacking the zinc-respons

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

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

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

206 terium plasmid pAL5000 were transferred from Streptomyces coelicolor or Streptomyces lividans to Myco

207 ochrome P450 (CYP) genes in the actinomycete Streptomyces coelicolor, ordered active site water molec

208 In Streptomyces coelicolor ParB is required for accurate ch

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

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

211 In contrast, a Streptomyces coelicolor polynucleotide phosphorylase hom

212 The eubacterial species Streptomyces coelicolor proceeds through a complex growt

213 xpression of these genes in the actinomycete Streptomyces coelicolor produced epothilones A and B.

214 Streptomyces coelicolor produces four genetically and st

215 Streptomyces coelicolor produces several structurally an

216 ect to the carboxyltransferase domain of the Streptomyces coelicolor propionyl-CoA carboxylase.

217 D gene, which encodes a homologue of WhiB, a Streptomyces coelicolor protein required for sporulation

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

219 NsrR from Streptomyces coelicolor regulates its own expression and

220 lysis and adventitious overexpression of key Streptomyces coelicolor regulators to investigate functi

221 on and sporulation in the mycelial bacterium Streptomyces coelicolor rely on establishing distinct pa

222 The model organism Streptomyces coelicolor represents a genus that produces

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

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

225 gene expression studies in P. aeruginosa and Streptomyces coelicolor revealed that the majority of So

226 In Streptomyces coelicolor Rex binds to operator (ROP) site

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

228 The Streptomyces coelicolor rpoC gene, that encodes the beta

229 Streptomyces coelicolor RppA (Sc-RppA), a bacterial type

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

231 ) was cloned by hybridization with bldA from Streptomyces coelicolor (Sc).

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

233 y described a transposon-generated mutant in Streptomyces coelicolor, SE293, that resulted in a bld s

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

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

236 Sporulation-specific cell division of Streptomyces coelicolor ssgB mutants is restored by intr

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

238 ryptophan was fed to the Trp-His auxotrophic Streptomyces coelicolor strain WH101.

239 f polynucleotide phosphorylase (PNPase) from Streptomyces coelicolor, Streptomyces antibioticus, and

240 and phosphorolysis activities of PNPase from Streptomyces coelicolor, Streptomyces antibioticus, and

241 the recently discovered epsilon-subunits of Streptomyces coelicolor, suggesting that it might be an

242 e apo-ACP from the actinorhodin (act) PKS of Streptomyces coelicolor (synthetic apo-ACP) has therefor

243 ial characterization of three new mutants of Streptomyces coelicolor that are defective in morphogene

244 zed a cluster of seven genes (vanSRJKHAX) in Streptomyces coelicolor that confers inducible, high-lev

245 lopmental events, we screened for mutants of Streptomyces coelicolor that exhibit aberrant morphologi

246 res aerial mycelium formation to a mutant of Streptomyces coelicolor that is defective in morphologic

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

248 n this issue by Park and Roe showing that in Streptomyces coelicolor the redox controlled anti-sigma

249 In Streptomyces coelicolor, the AbsA1-AbsA2 two-component s

250 In the filamentous bacterium Streptomyces coelicolor, the cell division protein FtsZ

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

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

253 l markers or plasmids between derivatives of Streptomyces coelicolor, the principal genetic model sys

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

255 These results suggest that, in Streptomyces coelicolor, the reductase component ActVB c

256 y unobserved form of genetic instability for Streptomyces coelicolor, the replacement of one chromoso

257 In Streptomyces coelicolor, the sco7700 and sco7701 genes a

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

259 rial type III PKS crystal structure, that of Streptomyces coelicolor THNS, and identify by mutagenesi

260 signal transduction system proposed to allow Streptomyces coelicolor to sense and respond to changes

261 FasR is a Streptomyces coelicolor transcriptional activator of gen

262 l transcriptome data for the model organism, Streptomyces coelicolor, under different environmental a

263 The filamentous soil bacterium Streptomyces coelicolor undergoes a complex cycle of mor

264 The filamentous bacterium Streptomyces coelicolor undergoes a complex process of m

265 The filamentous bacterium Streptomyces coelicolor undergoes a complicated process

266 roteins in the model Gram-positive bacterium Streptomyces coelicolor using bioinformatics coupled wit

267 val of a marker flanked by two loxP sites in Streptomyces coelicolor, using a derivative of the tempe

268 for the metal-citrate transport observed in Streptomyces coelicolor was cloned and overexpressed in

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

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

271 n altered pattern of genetic instability for Streptomyces coelicolor when the bacterium harbored a fo

272 mD, the Mycobacterium smegmatis homologue of Streptomyces coelicolor whiB, is essential in M. smegmat

273 construct and the pccB and accA1 genes from Streptomyces coelicolor, which enable methylmalonyl-CoA

274 best characterized ZAS proteins is RsrA from Streptomyces coelicolor, which responds to disulfide str

275 The RNase III gene of Streptomyces coelicolor, which was discovered initially

276 stasis in the antibiotic-producing bacterium Streptomyces coelicolor, with a similar role in other ac

277 The gene encoding Streptomyces coelicolor xanthine dehydrogenase regulator