ライフサイエンスコーパス: Mycobacterium smegmatis

1 t form of M. leprae SodC (rSodC) produced in Mycobacterium smegmatis.

2 hogen Mycobacterium tuberculosis, but not in Mycobacterium smegmatis.

3 mation system in the fast-growing surrogate, Mycobacterium smegmatis.

4 e cell wall and the inner membrane lipids of Mycobacterium smegmatis.

5 RNA in M. tuberculosis, Escherichia coli and Mycobacterium smegmatis.

6 rium tuberculosis and its avirulent relative Mycobacterium smegmatis.

7 e degradation of lipids in the microorganism Mycobacterium smegmatis.

8 t in vitro models of rifampicin tolerance in Mycobacterium smegmatis.

9 nd Ms1712 lipoproteins of the model organism Mycobacterium smegmatis.

10 the poles in Mycobacterium tuberculosis and Mycobacterium smegmatis.

11 e the functional role of the CtpD protein of Mycobacterium smegmatis.

12 rium tuberculosis and its avirulent relative Mycobacterium smegmatis.

13 is of the mbt gene cluster ortholog found in Mycobacterium smegmatis.

14 membrane, midcell, and cell pole regions in Mycobacterium smegmatis.

15 but is important for proper cell division in Mycobacterium smegmatis.

16 conjugal DNA transfer process that occurs in Mycobacterium smegmatis.

17 longer restricts growth of the non-pathogen Mycobacterium smegmatis.

18 459c from M. tuberculosis and MSMEG3120 from Mycobacterium smegmatis.

19 of the ESX-3/type VII secretion system from Mycobacterium smegmatis.

20 ue of Rv3792 and a gene upstream of embC) in Mycobacterium smegmatis.

21 cidal activity in a whole-cell assay against Mycobacterium smegmatis.

22 ied an IS6110-related element in a strain of Mycobacterium smegmatis.

23 f genes involved in phosphate acquisition in Mycobacterium smegmatis.

24 and Omega, two related mycobacteriophages of Mycobacterium smegmatis.

25 thogenic, saprophytic mycobacterial species, Mycobacterium smegmatis.

26 eria, including the nonpathogenic saprophyte Mycobacterium smegmatis.

27 doglycan from Mycobacterium tuberculosis and Mycobacterium smegmatis.

28 ompared to cells infected with nonpathogenic Mycobacterium smegmatis.

29 carrier protein synthases, KasA and KasB, in Mycobacterium smegmatis.

30 cillus subtilis, Bacillus thuringiensis, and Mycobacterium smegmatis.

31 ects of a chromosomal DNA transfer system in Mycobacterium smegmatis.

32 ach of both Mycobacterium intracellulare and Mycobacterium smegmatis.

33 t occurs in the model mycobacterial organism Mycobacterium smegmatis.

34 m tuberculosis, Mycobacterium bovis BCG, and Mycobacterium smegmatis.

35 es for their ability to impair the growth of Mycobacterium smegmatis.

36 ng into the chromosome of the model organism Mycobacterium smegmatis.

37 ied and characterized the MceG orthologue of Mycobacterium smegmatis.

38 bility to suppress beta-lactam resistance in Mycobacterium smegmatis.

39 fied to be the second (p)ppGpp synthetase in Mycobacterium smegmatis.

40 erial species, including the closely related Mycobacterium smegmatis.

41 lated, sequenced, and compared 627 phages of Mycobacterium smegmatis.

42 not found in its ortholog from nonpathogenic Mycobacterium smegmatis.

43 selected and expressed in the surrogate host Mycobacterium smegmatis.

44 ies, which include the fast-growing organism Mycobacterium smegmatis.

45 expressing them in both Escherichia coli and Mycobacterium smegmatis.

46 terium glutamicum (5.20 +/- 0.20 kV/cm), and Mycobacterium smegmatis (5.56 +/- 0.08 kV/cm) have been

47 Expression of the lprI gene in Mycobacterium smegmatis (8-10-fold) protected its growth

48 this goal by creating a DeltamurI strain of Mycobacterium smegmatis, a close relative of Mycobacteri

49 e mechanism of protein pupylation by PafA in Mycobacterium smegmatis, a model mycobacterial organism.

50 with the observation that a mutant strain of Mycobacterium smegmatis, a nonpathogenic relative of M.

51 elE, relG, and relK induced growth arrest in Mycobacterium smegmatis; a phenotype that was completely

52 Disruption of the SucT-encoding gene in Mycobacterium smegmatis abolished AG and LAM succinylati

53 at an obligate aerobe, the soil actinomycete Mycobacterium smegmatis, adopts an anaerobe-type strateg

54 We show here that the Cpn60.2 homologue from Mycobacterium smegmatis also fails to oligomerize under

55 Overexpression of Rv3802 orthologs in Mycobacterium smegmatis and Corynebacterium glutamicum i

56 richia coli, or recombinant LprG produced in Mycobacterium smegmatis and digested by alpha-mannosidas

57 annosylation in the nonpathogenic saprophyte Mycobacterium smegmatis and in the human pathogen Mtb by

58 MspA is the major porin of Mycobacterium smegmatis and is important for diffusion o

59 ncentration of myo-[14C]inositol is rapid in Mycobacterium smegmatis and leads to production of radio

60 Deletion of pepD or mprAB in Mycobacterium smegmatis and M. tuberculosis alters the s

61 Here we show that Mycobacterium smegmatis and M. tuberculosis strains lack

62 stably integrated recombinant genes in both Mycobacterium smegmatis and M. tuberculosis, with maxima

63 ten called persisters, within populations of Mycobacterium smegmatis and M. tuberculosis.

64 e regulation over two orders of magnitude in Mycobacterium smegmatis and M.tuberculosis.

65 MspA is the major porin of Mycobacterium smegmatis and mediates diffusion of small

66 Analysis of Mycobacterium smegmatis and Mycobacterium bovis bacille

67 er repression of reporter gene activities in Mycobacterium smegmatis and Mycobacterium bovis BCG.

68 Mycobacterium smegmatis and Mycobacterium kansasii were

69 ections with the fast-growing, nonpathogenic Mycobacterium smegmatis and Mycobacterium phlei.

70 In contrast, Mycobacterium smegmatis and Mycobacterium tuberculosis a

71 igated primarily with the readily cultivable Mycobacterium smegmatis and Mycobacterium tuberculosis a

72 ave reported that overexpression of NAT from Mycobacterium smegmatis and Mycobacterium tuberculosis m

73 les and Ms6 attB sites in the chromosomes of Mycobacterium smegmatis and Mycobacterium tuberculosis y

74 e used as a counterselectable marker in both Mycobacterium smegmatis and Mycobacterium tuberculosis.

75 Ac is acetyl) is the major thiol produced by Mycobacterium smegmatis and other actinomycetes.

76 IC 47 microM) but showed growth promotion of Mycobacterium smegmatis and other bacteria.

77 We report here that the genomes of Mycobacterium smegmatis and other soil mycobacteria cont

78 Further assays using membranes from Mycobacterium smegmatis and purified PimA and PimB' indi

79 ive integral membrane proteins, MSMEG4250 in Mycobacterium smegmatis and Rv2181 in M. tuberculosis, w

80 The GlgE orthologues from Mycobacterium smegmatis and Streptomyces coelicolor were

81 rent mycobacterial species, the fast-growing Mycobacterium smegmatis and the slow-growing M. bovis M.

82 We previously showed that nonpathogenic Mycobacterium smegmatis and to a lesser extent pathogeni

83 les were unable to mediate LAM production in Mycobacterium smegmatis and were unable to complement an

84 ifferent stop codon usage (Escherichia coli, Mycobacterium smegmatis, and Bacillus subtilis), we show

85 DnaK is essential in Mycobacterium smegmatis, and ClpB is involved in asymmet

86 e suborder, namely, Mycobacterium bovis BCG, Mycobacterium smegmatis, and Corynebacterium glutamicum,

87 E-glnA2 cluster, was expressed separately in Mycobacterium smegmatis, and its gene product was charac

88 lmark of all TA toxins, in Escherichia coli, Mycobacterium smegmatis, and M. tuberculosis.

89 Bacillus subtilis, Streptomyces coelicolor, Mycobacterium smegmatis, and Pseudomonas aeruginosa.

90 1), C16:0 (sn-2) in the natural product from Mycobacterium smegmatis, and the structural assignment o

91 product lost its antibiotic activity against Mycobacterium smegmatis, and this loss in bioactivity is

92 GPLs from Mycobacterium smegmatis are composed of a lipopeptide co

93 hia coli; recombinant DesA3 was expressed in Mycobacterium smegmatis as a catalytically active membra

94 tration (MIC) by broth microdilution against Mycobacterium smegmatis as a function of the initial cel

95 d study bacterial cell wall structures using Mycobacterium smegmatis as a model organism.

96 Using Mycobacterium smegmatis as an expression host, we purifi

97 identified the cellular function of HspX in Mycobacterium smegmatis as both a pro-aggregase and pola

98 ftsEX and ripC caused similar phenotypes in Mycobacterium smegmatis, as expected for genes in a sing

99 We report the first apo-MbtA structure from Mycobacterium smegmatis at 2.3 A.

100 d protein EspB from both M. tuberculosis and Mycobacterium smegmatis at a homologous cut site in vitr

101 th the rapidly growing mycobacterial species Mycobacterium smegmatis bearing an intact esx-3 locus we

102 Here we show that the FM in Mycobacterium smegmatis biofilms is produced through the

103 Full development of Mycobacterium smegmatis biofilms requires addition of su

104 Growth of Mycobacterium smegmatis biofilms requires multiple facto

105 e in phagosomes of macrophages infected with Mycobacterium smegmatis but increased in those infected

106 ding enzyme from the closely related species Mycobacterium smegmatis but not by the enzyme from Esche

107 functional for this purpose in fast-growing Mycobacterium smegmatis but not in slow-growing mycobact

108 that repression of pyr operon expression in Mycobacterium smegmatis by exogenous uracil requires the

109 ported that a genetically modified strain of Mycobacterium smegmatis called IKEPLUS is a promising TB

110 We describe here a mutant strain of Mycobacterium smegmatis, called DL1215, which demonstrat

111 arate or oxygen become available, suggesting Mycobacterium smegmatis can switch between fermentation,

112 not phosphorylation-defective PknK(Mtb), in Mycobacterium smegmatis cause significant retardation of

113 Conversely, expression of ppgS in Mycobacterium smegmatis conferred upon this species othe

114 Their expression in Mycobacterium smegmatis confirmed that these PE/PPE prot

115 Here we report that cydAB and cydDC in Mycobacterium smegmatis constitute two separate operons

116 active membrane and cell wall fractions from Mycobacterium smegmatis containing the overexpressed Rv3

117 Mycobacterium smegmatis contains 6 homologous mce (mamma

118 a TAT signal sequence, we demonstrated that Mycobacterium smegmatis contains a TAT system.

119 The outer membrane of the saprophytic Mycobacterium smegmatis contains the Msp family of porin

120 Mycobacterium smegmatis contains three hemerythrin-like

121 Mycobacterium smegmatis contains three putative TA syste

122 Deletion of M. tuberculosis or Mycobacterium smegmatis ctpC leads to cytosolic Mn(2+) a

123 homeostasis of Co(2+) and Fe(2+) Mutation of Mycobacterium smegmatis ctpJ affects the homeostasis of

124 rved a 40-fold increase in light output from Mycobacterium smegmatis cultures 2 h after adding 20 ng

125 For single-cell Raman microscopy, Mycobacterium smegmatis cultures were fixed using a new

126 of a mutant strain (designated MSMEG4245) of Mycobacterium smegmatis, defective in a broadly conserve

127 compounds identified as lipid I and II from Mycobacterium smegmatis demonstrated that the lipid moie

128 the comparable C-terminal sequence from the Mycobacterium smegmatis DesA3 homolog Msmeg_1886 also co

129 Notably, nonpathogenic Mycobacterium smegmatis did not increase MDR1 expression

130 on with lipopolysachharide or infection with Mycobacterium smegmatis diminished expression of both en

131 This study unveils Mycobacterium smegmatis DinB2 as the founder of a clade

132 Mycobacterium smegmatis DinB2 is the founder of a clade

133 The mshA::Tn5 mutant of Mycobacterium smegmatis does not produce mycothiol (MSH)

134 tate cluster at the pore interface unique to Mycobacterium smegmatis Dps protein, MsDps2.

135 In contrast to E. coli, Bacillus brevis and Mycobacterium smegmatis Dps:DNA complexes, in which DNA

136 ulties associated with the overexpression of Mycobacterium smegmatis EgtE protein, the proposed EgtE

137 rticle cryo-electron microscopy structure of Mycobacterium smegmatis EmbB, providing insights on subs

138 Mycobacterium smegmatis encodes four RNase H enzymes: Rn

139 sts including Mycobacterium tuberculosis and Mycobacterium smegmatis, encompass substantial genetic d

140 yrA-G81C variant of Escherichia coli and its Mycobacterium smegmatis equivalent (GyrA-G89C).

141 oteins from M. tuberculosis (EsxG and EsxH), Mycobacterium smegmatis (EsxA and EsxB), and Corynebacte

142 The model mycobacterium Mycobacterium smegmatis executes homologous recombinatio

143 say of phosphoribosyltransferase activity in Mycobacterium smegmatis expressing recombinant Rv3242c (

144 and purified highly active Mtb NDH-2 using a Mycobacterium smegmatis expression system, and the stead

145 ycobacteria, we executed a genetic screen in Mycobacterium smegmatis for biotin auxotrophs and identi

146 ulatory modules of Rv1747 and its homolog in Mycobacterium smegmatis form liquid-like condensates as

147 itecture of the enzyme (MsAcT) isolated from Mycobacterium smegmatis forms the mechanistic basis for

148 We report that the Mycobacterium smegmatis gene annotated as encoding Tam,

149 The Mycobacterium tuberculosis and Mycobacterium smegmatis genomes contain open reading fra

150 Pseudomonas fluorescens, gi 70731221 ; anti, Mycobacterium smegmatis, gi 118470554 ) document that th

151 Inactivation of the Mycobacterium smegmatis groEL1 gene by phage Bxb1 integr

152 Glu(83) of the (75)DPSDVARVE(83) element of Mycobacterium smegmatis GTP-dependent phosphoenolpyruvat

153 hydroxylation reaction and demonstrated that Mycobacterium smegmatis has an enzyme activity that can

154 We show that Mycobacterium smegmatis has an enzyme catalyzing transfe

155 The porin MspA of Mycobacterium smegmatis has remarkable stability against

156 Here we demonstrate that Mycobacterium smegmatis has three DSB repair pathway opt

157 The soil saprophyte Mycobacterium smegmatis has two such [NiFe] hydrogenases

158 ve recombinant HBHA vaccines in fast-growing Mycobacterium smegmatis have been unsuccessful so far, w

159 sents the structure of MsAcg (MSMEG_5246), a Mycobacterium smegmatis homologue of Mycobacterium tuber

160 whmD, the Mycobacterium smegmatis homologue of Streptomyces coelic

161 ersely, episomal expression of LprE (Mtb) in Mycobacterium smegmatis improved bacterial survival.

162 tional derepression in the heterologous host Mycobacterium smegmatis in a way that requires metal sit

163 s efficient repression of lacZ expression in Mycobacterium smegmatis in the presence but not the abse

164 ort here the crystal structures of PatA from Mycobacterium smegmatis in the presence of its naturally

165 Phage RedRock forms stable lysogens in Mycobacterium smegmatis in which the prophage replicates

166 cies, specifically Staphylococcus aureus and Mycobacterium smegmatis, in a MscL-dependent manner.

167 o be potentially expressed on the surface of Mycobacterium smegmatis incubated with HEp-2 cells and,

168 pE gene is lethal to Helicobacter pylori and Mycobacterium smegmatis, indicating that DapE's are esse

169 e show that nonvirulent mycobacteria such as Mycobacterium smegmatis induce AIM2 inflammasome activat

170 The fast-growing bacterium Mycobacterium smegmatis is a model mycobacterial system,

171 The MS of Mycobacterium smegmatis is cytoplasmic but the M. tb MS

172 teomic approaches, we established that PE of Mycobacterium smegmatis is exported to the cell envelope

173 A deletion of the homologous operon in Mycobacterium smegmatis is more susceptible to ethidium

174 an ABC transporter encoded by the genome of Mycobacterium smegmatis is stabilized by d-threitol.

175 octameric transmembrane channel protein from Mycobacterium smegmatis, is one of the most stable prote

176 EG_5243 (fsq), a gene of unknown function in Mycobacterium smegmatis, is up-regulated in response to

177 These lysine acyltransferases from Mycobacterium smegmatis (KATms) and Mycobacterium tuberc

178 ncentrations (10 uM) are required to observe Mycobacterium smegmatis killing.

179 o long chain fatty acids synthesized using a Mycobacterium smegmatis lysate.

180 hromosome dynamics at a single-cell level in Mycobacterium smegmatis (M. smegmatis) and Mycobacterium

181 microbial activities were determined against Mycobacterium smegmatis (M. smegmatis).

182 The high G6P level in Mycobacterium smegmatis may result from 10-25-fold highe

183 When expressed in noninvasive Mycobacterium smegmatis, MBP-1 increased the ability of

184 In our present work, Mycobacterium smegmatis mc(2) 155 (WTMsm) was used as a

185 namely, Mycobacterium bovis BCG Pasteur and Mycobacterium smegmatis mc(2) 155.

186 phages known to infect a single common host, Mycobacterium smegmatis mc(2) 155.

187 vidually expressed in the heterologous host, Mycobacterium smegmatis mc(2)-155.

188 GC measurements, that the soil actinomycete Mycobacterium smegmatis mc(2)155 constitutively oxidizes

189 arge set of phages infecting the common host Mycobacterium smegmatis mc(2)155 shows that they span co

190 Temperature-sensitive mutant 2-20/32 of Mycobacterium smegmatis mc(2)155 was isolated and geneti

191 ince an ortholog of MT1671 is not present in Mycobacterium smegmatis mc(2)155, a recombinant strain w

192 pulation of phages that can infect the host, Mycobacterium smegmatis mc(2)155.

193 ent of mft genes for ethanol assimilation in Mycobacterium smegmatis mc(2)155.

194 cetylation of Cys-GlcN-Ins to produce MSH in Mycobacterium smegmatis mc2155, and Cys-GlcN-Ins is main

195 We report the characterization of Mycobacterium smegmatis MmpL11.

196 Here, we report a crystal structure of Mycobacterium smegmatis MmpL3 at a resolution of 2.59 an

197 the functionally related ESX-1 apparatus of Mycobacterium smegmatis (Ms) to show that fluorescently

198 , the orthologous ESAT-6 from non-pathogenic Mycobacterium smegmatis (MsESAT-6) was essentially inact

199 Recombinant Mycobacterium smegmatis MshC catalyzes the ATP-dependent

200 Mycobacterium smegmatis MshC catalyzes the ATP-dependent

201 -steady-state approaches, of the recombinant Mycobacterium smegmatis MshC.

202 vival (Eis) protein improves the survival of Mycobacterium smegmatis (Msm) in macrophages and functio

203 rt a 3.2 A-resolution crystal structure of a Mycobacterium smegmatis (Msm) open promoter complex (RPo

204 iratory polyketide quinones (PkQs) from both Mycobacterium smegmatis (Msmeg) and Mtb.

205 e, we show that exposure to an esterase from Mycobacterium smegmatis (Msmeg_1529), hydrolyzing the es

206 acteria, we deleted the Rv3574 orthologue in Mycobacterium smegmatis (MSMEG_6042) and used real-time

207 When overexpressed in Escherichia coli or Mycobacterium smegmatis, MtbFHb remained associated with

208 ivity to ampicillin and chloramphenicol of a Mycobacterium smegmatis mutant lacking the main porin Ms

209 We identified a Mycobacterium smegmatis mutant, named FUEL (which stands

210 We isolated 27 Mycobacterium smegmatis mutants that were hypersusceptib

211 The four Ub2-resistant Mycobacterium smegmatis mutants were also resistant to t

212 occus gordonii, Streptococcus parasanguinis, Mycobacterium smegmatis, Mycobacterium tuberculosis and

213 Here we report that Mycobacterium smegmatis NucS/EndoMS, a putative endonucl

214 Conjugal DNA transfer in Mycobacterium smegmatis occurs by a mechanism distinct f

215 ansfer of chromosomal DNA between strains of Mycobacterium smegmatis occurs by a novel mechanism.

216 igated, using a GFP reporter system, whether Mycobacterium smegmatis OhrR has the ability to sense an

217 f phagocytic and nonphagocytic cell lines by Mycobacterium smegmatis or M. bovis BCG harboring a plas

218 ffect several reporter proteins in wild-type Mycobacterium smegmatis or Mycobacterium tuberculosis.

219 s strategy in Corynebacterium glutamicum and Mycobacterium smegmatis, organisms that serve as models

220 pare the RNA and DNA modifying activities of Mycobacterium smegmatis PNPase.

221 ngle DNA template strands through a modified Mycobacterium smegmatis porin A (M2MspA) nanopore under

222 otein nanopores such as alpha-haemolysin and Mycobacterium smegmatis porin A (MspA) can be used to se

223 200 mV, with a frequency of 200 Hz, across a Mycobacterium smegmatis porin A (MspA) nanopore, thus ch

224 e use the engineered biological protein pore Mycobacterium smegmatis porin A (MspA) to detect and map

225 tivity of a mutated form of the protein pore Mycobacterium smegmatis porin A (MspA) with phi29 DNA po

226 single-stranded DNA-NeutrAvidin complex in a Mycobacterium smegmatis porin A nanopore.

227 force and diffusion constant of DNA inside a Mycobacterium smegmatis porin A pore were determined to

228 hat the ionic current through the engineered Mycobacterium smegmatis porin A, MspA, has the ability t

229 not complement the permeability defects of a Mycobacterium smegmatis porin mutant to glucose, serine

230 Mycobacterium smegmatis possesses two such transporters,

231 overexpression of the Rv2629 191C allele in Mycobacterium smegmatis produced an eightfold increase i

232 Here we show that a Mycobacterium smegmatis protein homologous to eubacteria

233 enetic diversity of phages of a common host, Mycobacterium smegmatis, provides a higher resolution of

234 ed mechanisms of RMPs in both reactions with Mycobacterium smegmatis RecO (MsRecO) and demonstrated t

235 Disruption of the ortholog of Rv3789 in Mycobacterium smegmatis resulted in a reduction of the a

236 trated that deletion of MSMEG_6281 (Ami1) in Mycobacterium smegmatis resulted in the formation of cel

237 rium abscessus, as well as the nonpathogenic Mycobacterium smegmatis, results in hypersensitivity to

238 proteins, expression in a Deltatat mutant of Mycobacterium smegmatis revealed a defect in precursor p

239 Studies with a model Mycobacterium (Mycobacterium smegmatis) revealed that by removing salts

240 ative HBHA with recombinant HBHA produced in Mycobacterium smegmatis (rHBHA-Ms), we could link antige

241 a cryo-EM structure of a complex between the Mycobacterium smegmatis RNAP and HelD.

242 ive integral membrane proteins, MSMEG2785 in Mycobacterium smegmatis, Rv2673 in Mycobacterium tubercu

243 trom cryo-electron microscopy structure of a Mycobacterium smegmatis Sdh, which forms a trimer.

244 is and the nonpathogenic model mycobacterium Mycobacterium smegmatis, SecA1 is essential for protein

245 lectively access mycolates on the surface of Mycobacterium smegmatis spheroplasts, allowing us to mon

246 bacterial activity against Escherichia coli, Mycobacterium smegmatis, Staphylococcus aureus and Staph

247 Deletion of polD1, polD2, or both from a Mycobacterium smegmatis strain carrying an inactivating

248 ow that priming with a prototype recombinant Mycobacterium smegmatis strain expressing human immunode

249 plasmid-based NHEJ assay and a collection of Mycobacterium smegmatis strains bearing deletions or mut

250 and homologous recombination (HR)-deficient Mycobacterium smegmatis strains to probe the importance

251 showed that three different Actinobacteria (Mycobacterium smegmatis, Streptomyces lividans, and Rhod

252 Analysis of Mycobacterium smegmatis subcellular fractions and sphero

253 but not kasA mutants, could be generated in Mycobacterium smegmatis, suggesting that unlike kasB, ka

254 source dependent in Mtb and did not occur in Mycobacterium smegmatis, suggesting that V-58-mediated g

255 aneous mutants of DAP-auxotrophic strains of Mycobacterium smegmatis that can grow in the absence of

256 t strain was constructed in ManLAM-deficient Mycobacterium smegmatis that coexpressed Rv2181 and Rv16

257 ns in genes encoding ribosomal components in Mycobacterium smegmatis that confer resistance to severa

258 polymerase in Mycobacterium tuberculosis and Mycobacterium smegmatis that has evolved independently f

259 We have previously identified a USP in Mycobacterium smegmatis that is a product of the msmeg_4

260 ne a LigD ligase-independent NHEJ pathway in Mycobacterium smegmatis that requires the ATP-dependent

261 In the nonpathogen Mycobacterium smegmatis, the ESX-1 T7SS plays a role in

262 noxia upregulates a homologue of HU (Hlp) in Mycobacterium smegmatis, the nonpathogenic model of Myco

263 However, when expressed in Mycobacterium smegmatis, the Rv0348 transcripts were sig

264 Here, we show that in Mycobacterium smegmatis, the small heat shock protein Hs

265 s lack activity against Escherichia coli and Mycobacterium smegmatis, they proved to be highly potent

266 , MSMEG_5437, in the intrinsic resistance of Mycobacterium smegmatis to a variety of stresses includi

267 ant (secA2 K129R) of the model mycobacterium Mycobacterium smegmatis to better understand the pathway

268 in determining the spectrum of responses of Mycobacterium smegmatis to challenge with rifampicin.

269 umor activity required coadministration with Mycobacterium smegmatis to induce IL-1beta production an

270 Ablation of UvrD1 sensitizes Mycobacterium smegmatis to killing by ultraviolet and io

271 Escherichia coli, Staphylococcus aureus, and Mycobacterium smegmatis to quinolone antibiotics.

272 Titration of small ssDNA oligonucleotides to Mycobacterium smegmatis topoisomerase I with progressive

273 essential for conjugal recipient activity in Mycobacterium smegmatis Transcription of esx4 genes in t

274 ate of reactive oxygen species production in Mycobacterium smegmatis treated with CFZ and a CFZ analo

275 Here, we report the crystal structure of the Mycobacterium smegmatis TreS:Pep2 complex, containing tr

276 ned the global protein turnover profiles for Mycobacterium smegmatis under acid shock and iron starva

277 tions and their impact on gene expression in Mycobacterium smegmatis under hypochlorite stress.

278 The biological sample model included two Mycobacterium smegmatis unlabeled cell cultures grown at

279 Q TLR2 polymorphism on macrophage sensing of Mycobacterium smegmatis Upon infection with M. smegmatis

280 roteomic responses to cysteine limitation in Mycobacterium smegmatis using mass spectrometry.

281 By characterizing truncated versions of Mycobacterium smegmatis UvrD2, we show that whereas the

282 erminal domain, the embC knock-out mutant of Mycobacterium smegmatis was complemented with plasmids e

283 combination of monosodium urate crystals and Mycobacterium smegmatis was effective at delaying the gr

284 nonpathogenic, rapidly growing mycobacterium Mycobacterium smegmatis was engineered as a vector expre

285 Sulfite reduction in Mycobacterium smegmatis was investigated using a combina

286 Phosphatase activity in whole cells of Mycobacterium smegmatis was significantly lower than tha

287 The enzyme Msd from Mycobacterium smegmatis was taken as a representative ca

288 repair pattern and genome-wide repair map of Mycobacterium smegmatis We find that M. smegmatis, which

289 screening of an M. avium genomic library in Mycobacterium smegmatis, we have identified a number of

290 en for antibiotic resistance determinants in Mycobacterium smegmatis, we identified a multidrug-sensi

291 actions from wild-type and DeltasecA2 mutant Mycobacterium smegmatis, we identified the Msmeg1712 and

292 e dynamics of 379 extracellular compounds of Mycobacterium smegmatis were deconvoluted with a genome-

293 ttempts to delete the NCgl2760 orthologue in Mycobacterium smegmatis were unsuccessful, consistent wi

294 ree different glycosyltransferase mutants of Mycobacterium smegmatis were used here to investigate th

295 exhibited impaired cell wall localization in Mycobacterium smegmatis, whereas mPDE-4A behaved similar

296 hate (ATP) synthase has been determined from Mycobacterium smegmatis which hydrolyzes ATP very poorly

297 suite of compounds, inhibited the growth of Mycobacterium smegmatis with an MIC80 value of 2 mug/mL.

298 ed mutants of Mycobacterium tuberculosis and Mycobacterium smegmatis with deletions in the genes for

299 d to the NMOs from Aspergillus fumigatus and Mycobacterium smegmatis with K(d) values of 2.1 +/- 0.2

300 When deployed in Mycobacterium smegmatis with quantitative proteomics, th