ライフサイエンスコーパス: Streptomyces coelicolor

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

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

3 cherichia coli, Saccharomyces cerevisiae, or Streptomyces coelicolor.

4 pically regulates antibiotic biosynthesis in Streptomyces coelicolor.

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

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

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

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

9 forming soil bacteria, Bacillus subtilis and Streptomyces coelicolor.

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

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

12 h morphogenesis and antibiotic production in Streptomyces coelicolor.

13 thway for initiation of BCFA biosynthesis in Streptomyces coelicolor.

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

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

16 elium formation by the filamentous bacterium Streptomyces coelicolor.

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

18 teins called chaplins has been identified in Streptomyces coelicolor.

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

20 ory systems and the developmental program in Streptomyces coelicolor.

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

22 vestigated in Amycolatopsis mediterranei and Streptomyces coelicolor.

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

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

25 identical to the corresponding protein from Streptomyces coelicolor.

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

27 he actinorhodin biosynthetic gene cluster of Streptomyces coelicolor.

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

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

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

31 ron overload drug desferrioxamine (DFO) B in Streptomyces coelicolor.

32 ve plasmid SCP2 in the filamentous bacterium Streptomyces coelicolor.

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

34 ing sporulation in the filamentous bacterium Streptomyces coelicolor.

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

36 otein assembly in the filamentous bacterium, Streptomyces coelicolor.

37 as found to induce prodiginine production by Streptomyces coelicolor.

38 ial hyphae formation in adjacent colonies of Streptomyces coelicolor.

39 global regulator of antibiotic production in Streptomyces coelicolor.

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

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

42 l antibiotic-producing filamentous bacterium Streptomyces coelicolor.

43 cal development and antibiotic production in Streptomyces coelicolor.

44 as overexpression causes hyphal branching in Streptomyces coelicolor.

45 are dispensable for growth and viability of Streptomyces coelicolor.

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

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

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

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

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

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

52 s of the filamentous multicellular bacterium Streptomyces coelicolor, a subpopulation of cells arises

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

98 06-sco1208) in the prototypic soil bacterium Streptomyces coelicolor A3(2).

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

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

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

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

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

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

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

106 The Streptomyces coelicolor absA two-component system was in

107 The Streptomyces coelicolor absB gene encodes an RNase III f

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

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

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

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

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

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

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

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

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

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

118 e Gram-positive multicellular model organism Streptomyces coelicolor and show that, in contrast to mo

119 sa, and two bacterial AA10 LPMOs, ScAA10C of Streptomyces coelicolor and SmAA10A of Serratia marcesce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

137 Mutants of Streptomyces coelicolor blocked at the earliest visible

138 In Streptomyces coelicolor, both overexpression and deletio

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

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

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

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

143 Streptomyces coelicolor CH999/pJRJ2 harbors a plasmid en

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

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

146 CIS from Streptomyces coelicolor (CIS(Sc)) are localized in the c

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

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

149 Streptomyces coelicolor contained an innate Tc-controlla

150 Streptomyces coelicolor contains paralogous versions of

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

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

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

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

155 The filamentous bacterium Streptomyces coelicolor differentiates by forming specia

156 The Streptomyces coelicolor dnaE gene, encoding the catalyti

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

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

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

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

161 Streptomyces coelicolor encodes three umbrella particles

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

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

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

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

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

167 A Streptomyces coelicolor gene, called spaA, homologous to

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

169 The Streptomyces coelicolor genome encodes only a single put

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

171 The Streptomyces coelicolor genome sequence was searched for

172 The 8.7-Mb Streptomyces coelicolor genome was previously sequenced

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

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

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

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

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

178 erved movies of replisome trafficking during Streptomyces coelicolor growth.

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

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

181 Streptomyces coelicolor has nine SigB-like RNA polymeras

182 Streptomyces coelicolor has two genes encoding tryptopha

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

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

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

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

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

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

189 Streptomyces coelicolor is a model for studying bacteria

190 Streptomyces coelicolor is a model system for the study

191 Streptomyces coelicolor is a morphologically complex bac

192 Streptomyces coelicolor is a representative of the group

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

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

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

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

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

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

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

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

201 Streptomyces coelicolor is more amenable to strain impro

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

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

204 Streptomyces coelicolor is the model organism for the ac

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

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

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

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

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

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

211 was confirmed by heterologous expression in Streptomyces coelicolor M1152.

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

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

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

215 Here, we present crystal structures of Streptomyces coelicolor MqnA and its active site mutants

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

217 can restore the ability to form hyphae in a Streptomyces coelicolor mutant that carries a deletion i

218 Streptomyces coelicolor mutants lacking the zinc-respons

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

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

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

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

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

224 In Streptomyces coelicolor ParB is required for accurate ch

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

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

227 In contrast, a Streptomyces coelicolor polynucleotide phosphorylase hom

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

229 The eubacterial species Streptomyces coelicolor proceeds through a complex growt

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

231 Streptomyces coelicolor produces four genetically and st

232 Streptomyces coelicolor produces several structurally an

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

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

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

236 NsrR from Streptomyces coelicolor regulates its own expression and

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

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

239 The model organism Streptomyces coelicolor represents a genus that produces

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

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

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

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

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

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

246 The Streptomyces coelicolor rpoC gene, that encodes the beta

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

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

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

250 coside of valienamine (8) as an inhibitor of Streptomyces coelicolor (Sco) GlgE1-V279S which belongs

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

268 Analysis of another gene cluster in Streptomyces coelicolor that is widespread in actinobact

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

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

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

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

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

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

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

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

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

278 In Streptomyces coelicolor, the sco7700 and sco7701 genes a

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

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

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

282 FasR is a Streptomyces coelicolor transcriptional activator of gen

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

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

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

286 The filamentous bacterium Streptomyces coelicolor undergoes a complicated process

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

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

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

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

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

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

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

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

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

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

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

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

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

300 The gene encoding Streptomyces coelicolor xanthine dehydrogenase regulator