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1 S. coelicolor A3(2), M600 and J1501 possess L-TIRs, wher
2 S. coelicolor membranes were also able to catalyse the t
3 S. coelicolor mutants globally deficient in antibiotic p
4 S. coelicolor PecS, which exists as a homodimer, binds t
5 S. coelicolor PNPase was more effective than its E. coli
6 S. coelicolor produces SapB, an amphipathic peptide that
7 S. coelicolor shows a bias toward one type of genetic in
9 her characterize the Amycolatopsis sp. AA4 - S. coelicolor interaction by examining expression of dev
11 d near the RNase ES termini interact with an S. coelicolor homologue of polynucleotide phosphorylase
12 minal region of RbpA and sigma domain 2, and S. coelicolor RbpA mutants that are defective in binding
14 x range of -450 to +80 mV, P. aeruginosa and S. coelicolor SoxR are less sensitive to viologens, whic
16 of colony biofilms in both P. aeruginosa and S. coelicolor, which shows that "secondary metabolites"
17 s possible to predict operons in E. coli and S. coelicolor with 83% and 93% accuracy respectively, us
19 hat the Streptomyces species S. lividans and S. coelicolor, morphologically complex gram-positive soi
21 n both the S. coelicolor parental strain and S. coelicolor YL/sgFabH (a deltafabH mutant carrying a p
22 t, we screened FGEs from M. tuberculosis and S. coelicolor against synthetic peptide libraries and id
24 surfactin acts antagonistically by arresting S. coelicolor aerial development and causing altered exp
28 o-ACP was phosphopantetheinylated to 100% by S. coelicolor holo-acyl carrier protein synthase (ACPS),
31 s to find that deferrioxamine E, produced by S. coelicolor, could be readily utilized by Amycolatopsi
34 e development of aerial hyphae and spores by S. coelicolor is inhibited by surfactin, a lipopeptide s
36 nd show that, in contrast to most other CIS, S. coelicolor CIS (CIS(Sc)) mediate cell death in respon
38 removed or duplicated hundreds of contiguous S. coelicolor genes, altering up to 33% of the chromosom
39 C3 were shown to restore to a SapB-deficient S. coelicolor mutant the capacity to undergo complete mo
40 xtracellular signalling cascade proposed for S. coelicolor and is a member of the bldD extracellular
42 Our data suggests a comprehensive role for S. coelicolor AfsS as a master regulator of both antibio
46 r structural zinc, the RbpA orthologues from S. coelicolor and M. tuberculosis share a common structu
51 active precursor, modulates SoxR activity in S. coelicolor to stimulate the production of a membrane
53 first time the presence of albaflavenone in S. coelicolor and clearly demonstrate that the biosynthe
56 vious studies of prodiginine biosynthesis in S. coelicolor support a novel role for RedJ in facilitat
57 al activator of actinorhodin biosynthesis in S. coelicolor, is inhibited by the binding of heptaene,
62 agent 5'-aza-2'-deoxycytidine (5-aza-dC) in S. coelicolor cultures, demonstrating that m5C affects b
63 metabolism and morphological development in S. coelicolor and the identification of host-encoded lea
64 n production or morphological development in S. coelicolor, although their mutation could influence t
67 onCI, encoding a flavin-linked epoxidase, in S. coelicolor was shown to significantly increase the ab
69 ed were substrates, including those found in S. coelicolor extracts, and all yielded several products
72 x reductase (FDR) proteins coded by genes in S. coelicolor were expressed in Escherichia coli, purifi
73 lly, coexpressing the rifG-N and -J genes in S. coelicolor YU105 under the control of the act promote
76 n M. tuberculosis and critical for growth in S. coelicolor, these data support a model in which RbpA
78 dence that many of the targets identified in S. coelicolor are also under the control of the sigmaR h
79 th 76% amino acid identity was identified in S. coelicolor, and insertional mutagenesis indicated tha
80 is the third ACP to have been identified in S. coelicolor; the two previously characterized ACPs are
81 are consistent with duplication of GCH II in S. coelicolor promoting evolution of a new function.
83 ferring rifampin-resistance, was isolated in S. coelicolor to provide a genetic marker to follow tran
85 tibiotics and other secondary metabolites in S. coelicolor, suggest that revision of the currently pr
86 rated by the absence of RamS modification in S. coelicolor hyphae treated with the Bacillus subtilis
87 coelicolor, it normally is expressed only in S. coelicolor-generating the deep-blue colonies responsi
88 ly increase the database of known operons in S. coelicolor and provide valuable information for explo
90 RNA increases during the stationary phase in S. coelicolor and that induction of a plasmid-borne copy
93 under the control of its native promoter in S. coelicolor M512, a host lacking the SCP1 plasmid, and
97 w that a representative of these proteins in S. coelicolor possesses a dodecameric quaternary structu
101 [3H]-adenosine were used to label the RNA in S. coelicolor cultures of different ages, and total RNA
103 re color, showing that disruption of sigF in S. coelicolor changes the nature of the spore pigment ra
110 tionally mutated library was introduced into S. coelicolor, and transposon insertions were recovered
113 d that a 4.9 Mb central region of the linear S. coelicolor chromosome encodes 'core' functions expres
117 ore genes were downregulated when grown near S. coelicolor, leading us to find that deferrioxamine E,
118 report the genome sequence of PhiCAM, a new S. coelicolor generalized transducing bacteriophage, iso
119 own to significantly increase the ability of S. coelicolor to epoxidize linalool, a model substrate f
120 oarrays to measure globally the abundance of S. coelicolor transcripts in cells growing in liquid med
121 ift assays revealed an increased affinity of S. coelicolor PNPase for the substrate possessing a 3' s
122 chromatography/mass spectrometry analysis of S. coelicolor culture extracts established the presence
124 as also capable of restoring the capacity of S. coelicolor and S. tendae bald mutants to erect aerial
126 During stationary phase, the composition of S. coelicolor transcripts appears to shift from large qu
127 chain elongation intermediate to cultures of S. coelicolor CH999/pJRJ2 results in formation of a 16-m
129 rbpA expression is induced upon exposure of S. coelicolor to rifampicin and that this, in part, invo
134 with our previous demonstration that ftsZ of S. coelicolor is not needed for viability, these finding
136 omoters changed over the course of growth of S. coelicolor and studies in three sigma factor mutant s
137 genes expressed during vegetative growth of S. coelicolor cultures, we used DNA microarrays to measu
138 tively constant over the course of growth of S. coelicolor M145, but that on a molar basis, the level
139 alin A (ConA) inhibited phi C31 infection of S. coelicolor J1929, and this could be partially reverse
143 study that reports the cytosine methylome of S. coelicolor M145, supporting the crucial role ascribed
144 tions, construction of a sigF null mutant of S. coelicolor M145 caused the same change in spore color
145 that all of the characterized bld mutants of S. coelicolor are defective in the regulation of galP1,
147 cedure for generating insertional mutants of S. coelicolor based on in vitro transposition of a plasm
154 t Streptomyces lividans, a close relative of S. coelicolor and naturally Pgl-, does not contain homol
155 Addition of the gamma-butyrolactone SCB1 of S. coelicolor resulted in loss of the DNA-binding abilit
156 al and essential sigma factor (sigmaHrdB) of S. coelicolor restored Act and Red production in the afs
158 -Seq, we have examined the transcriptomes of S. coelicolor M145 and an RNase III (rnc)-null mutant of
160 ing to the approximate mass of the predicted S. coelicolor msdA product (52.6 kDa), and specific MSDH
162 ion of a pentapeptide (HCDLP) to recombinant S. coelicolor NiSOD lacking these N-terminal residues, N
165 two phylogenetically distant streptomycetes, S. coelicolor A3(2) and S. griseus: (1) gamma -butyrolac
166 perature and osmotic upshifts, we found that S. coelicolor transiently induces a set of several hundr
170 in vitro and in vivo experiments showed that S. coelicolor ParB protein interacts specifically with t
175 predominate (approximately 70%) in both the S. coelicolor parental strain and S. coelicolor YL/sgFab
176 tion of differentiation-related mRNAs by the S. coelicolor AbsB/RNase III enzyme occurs largely by ri
177 lated globally and differentially during the S. coelicolor growth cycle by the RNaseIII homologue Abs
181 rth protein was sought and purified from the S. coelicolor CH999 host on the basis of its ability to
182 isolated SigT-interactive proteins from the S. coelicolor lysate based on the tandem affinity purifi
183 st other members of this class, however, the S. coelicolor bkdR gene product serves to repress transc
184 ese results suggest the cells arising in the S. coelicolor division of labor are analogous to altruis
186 re 57 putative GntR family regulators in the S. coelicolor genome) that respond to nutritional and/or
187 for an uridylyltransferase) are found in the S. coelicolor genome, the regulation of the GSI activity
193 d to be glycosylated with a trihexose in the S. coelicolor parent strain, J1929, but not in the pmt(-
195 Unlike the E. coli soxR deletion mutant, the S. coelicolor equivalent is not hypersensitive to oxidan
196 of the predicted amino acid sequence of the S. coelicolor beta' subunit to those characterized from
197 ted mutagenesis, the carboxy terminus of the S. coelicolor beta' subunit was modified to contain six
199 kinetics, and protein crystallography of the S. coelicolor enzyme, we have now identified the +1 to +
201 gene (fabD) encoding another subunit of the S. coelicolor FAS, malonyl coenzyme A:ACP acyl-transfera
203 rresponding to the 4.9 Mb core region of the S. coelicolor M145 chromosome were more highly expressed
206 beta' subunits, one of which consists of the S. coelicolor subunit and those from Mycobacterium lepra
207 f the cleavage sites in the stem-loop of the S. coelicolor transcript are more akin to those identifi
208 those obtained by microarray analysis of the S. coelicolor transcriptome and with studies describing
209 acin and ramoplanin were not inducers of the S. coelicolor VanRS system, in contrast to results obtai
210 s of genes immediately adjacent to it on the S. coelicolor chromosome that likely encode an ATP-bindi
211 We exploited this distinction to replace the S. coelicolor vanRS genes with the vanRS genes from S. t
212 ination, indicating the possibility that the S. coelicolor promoter/activator functions appropriately
213 lmL), which exhibits a low similarity to the S. coelicolor SerRS, is hypothesized to play a role in v
216 ted interchange of this residue in the three S. coelicolor intragenomic homologues is necessary and s
218 levels changed by >/= 2-fold between the two S. coelicolor strains and organized those transcripts in
221 wapping experiments, support a model whereby S. coelicolor umbrella toxin diversification at the leve
222 triketide 6, compounds 18, 31, and 32, with S. coelicolor CH999/pJRJ2, resulting in the formation of