ライフサイエンスコーパス: Gram-positive bacterium

1 poprotein biogenesis could be essential in a Gram-positive bacterium.

2 ted with the periplasm and cell surface in a Gram-positive bacterium.

3 d structure of a tyrosine phosphatase from a Gram-positive bacterium.

4 hyaluronan lyase is a surface enzyme of this Gram-positive bacterium.

5 yaluronate lyase is a surface enzyme of this Gram-positive bacterium.

6 Homologs of pylS and pylT are found in a Gram-positive bacterium.

7 t these genes may have been recruited from a gram-positive bacterium.

8 haemin and haemoglobin as iron sources by a Gram-positive bacterium.

9 pe pol III is essential for replication in a Gram-positive bacterium.

10 py and the first 3D-structure of MreB from a Gram-positive bacterium.

11 f Hfq in posttranscriptional regulation in a gram-positive bacterium.

12 he first confirmed RNA sponge described in a Gram-positive bacterium.

13 ailed molecular characterisation of Tfp in a Gram-positive bacterium.

14 ide reduction in an environmentally relevant Gram-positive bacterium.

15 of Bacillus subtilis, a non-U(VI)-reducing, Gram-positive bacterium.

16 SdbA, that affects multiple phenotypes in a Gram-positive bacterium.

17 ted by the Tat pathway to the cell wall of a Gram-positive bacterium.

18 for the first time, c-di-GMP production in a gram-positive bacterium.

19 ting electrons across the cell envelope of a Gram-positive bacterium.

20 e c-type cytochromes (MHCs) is unusual for a Gram-positive bacterium.

21 e causative agent, Tropheryma whipplei, is a Gram-positive bacterium about which little is known.

22 The gram-positive bacterium Alloiococcus otitis (A. otitidis

23 rize the first sialyltransferase gene from a Gram- positive bacterium and provide compelling evidence

24 ogical agent of anthrax, is a spore-forming, Gram-positive bacterium and a category A biothreat agent

25 The model represents the first ME-model of a Gram-positive bacterium and captures all major central m

26 the effect of c-di-GMP on the motility of a gram-positive bacterium and on aggregation of C. diffici

27 Enterococcus faecalis, a Gram-positive bacterium, and Candida albicans, a fungus,

28 ogeneity, completely inhibited growth of the Gram-positive bacterium at 4.5 microm while a mixture of

29 WMG1 shows dark toxicity to the Gram positive bacterium B. subtilis and good phototherma

30 ns drive metabolic reprograming in the model Gram-positive bacterium B. subtilis.

31 microscopy showing that a wild strain of the Gram positive bacterium Bacillus subtilis builds such a

32 hese spectral variants of GFP for use in the Gram positive bacterium Bacillus subtilis.

33 In the environment, the gram-positive bacterium Bacillus anthracis persists as a

34 The ability of the endospore-forming, gram-positive bacterium Bacillus anthracis to survive in

35 0 mediates bactericidal activity against the Gram-positive bacterium Bacillus anthracis, the causativ

36 Here, we discover that the gram-positive bacterium Bacillus anthracis, the causativ

37 The spore-forming, gram-positive bacterium Bacillus anthracis, the causativ

38 Anthrax is caused by the spore-forming, gram-positive bacterium Bacillus anthracis.

39 -negative bacterium Serratia marcescens, the gram-positive bacterium Bacillus cereus and the fungus M

40 in Escherichia coli from genomic DNA of the Gram-positive bacterium Bacillus cereus.

41 obacterium salinarum (HemAT-Hs) and from the Gram-positive bacterium Bacillus subtilis (HemAT-Bs) con

42 Predict Web server to infer TRN in the model Gram-positive bacterium Bacillus subtilis and 10 related

43 zed a mobile genetic element, ICEBs1, in the Gram-positive bacterium Bacillus subtilis and found that

44 pp, all directly interact with XPRT from the Gram-positive bacterium Bacillus subtilis and inhibit XP

45 emonstrate that FlgM is also secreted in the Gram-positive bacterium Bacillus subtilis and is degrade

46 uptake during natural transformation in the Gram-positive bacterium Bacillus subtilis and the Gram-n

47 ids as a positive determinant of size in the Gram-positive bacterium Bacillus subtilis and the single

48 led Hag) is homeostatically regulated in the Gram-positive bacterium Bacillus subtilis by a partner-s

49 e, we investigated c-di-GMP signaling in the Gram-positive bacterium Bacillus subtilis by constructin

50 Here, we show that the Gram-positive bacterium Bacillus subtilis can be program

51 The Gram-positive bacterium Bacillus subtilis can divide via

52 The Gram-positive bacterium Bacillus subtilis can utilize se

53 Similarly, the gram-positive bacterium Bacillus subtilis class-II fumar

54 Biofilms formed by the Gram-positive bacterium Bacillus subtilis depend on the

55 n precursor, Lipid II, produced in the model Gram-positive bacterium Bacillus subtilis differs from L

56 The Gram-positive bacterium Bacillus subtilis encodes three

57 The Gram-positive bacterium Bacillus subtilis exhibits compl

58 The Gram-positive bacterium Bacillus subtilis forms biofilms

59 When starved, the Gram-positive bacterium Bacillus subtilis forms durable

60 The gram-positive bacterium Bacillus subtilis has become a m

61 ar basis of endospore formation in the model gram-positive bacterium Bacillus subtilis has been inves

62 The model gram-positive bacterium Bacillus subtilis has recently b

63 pendent proteins and enzymes produced by the Gram-positive bacterium Bacillus subtilis have been char

64 The Gram-positive bacterium Bacillus subtilis initiates the

65 rmination and outgrowth of endospores of the Gram-positive bacterium Bacillus subtilis involves the d

66 Entry into sporulation by the Gram-positive bacterium Bacillus subtilis is governed by

67 The Gram-positive bacterium Bacillus subtilis maintains appr

68 z protein modified during sporulation in the gram-positive bacterium Bacillus subtilis support the hy

69 For the Gram-positive bacterium Bacillus subtilis the process in

70 troduce an isotopic labeling strategy in the gram-positive bacterium Bacillus subtilis to investigate

71 The Gram-positive bacterium Bacillus subtilis uses serine no

72 the solution structure of sigma1.1 from the Gram-positive bacterium Bacillus subtilis We found that

73 Herein, we modify the peptide stems of the Gram-positive bacterium Bacillus subtilis with noncanoni

74 the cyt c biogenesis gene ccdA, found in the gram-positive bacterium Bacillus subtilis, and to the ce

75 In the Gram-positive bacterium Bacillus subtilis, genetic compe

76 sure to heat-killed Salmonella enterica, the Gram-positive bacterium Bacillus subtilis, or Mycobacter

77 In Gram-positive bacterium Bacillus subtilis, Rho is involv

78 In the Gram-positive bacterium Bacillus subtilis, the starvatio

79 l sporulation, with an emphasis on the model gram-positive bacterium Bacillus subtilis, to highlight

80 gulation of wall thickness in the rod-shaped Gram-positive bacterium Bacillus subtilis, we analyzed e

81 stable antimicrobial peptide secreted by the Gram-positive bacterium Bacillus subtilis.

82 e intracellular concentration of FtsZ in the gram-positive bacterium Bacillus subtilis.

83 (stationary-phase) mutagenesis occurs in the gram-positive bacterium Bacillus subtilis.

84 lular localization of the SMC protein in the gram-positive bacterium Bacillus subtilis.

85 proteobacteria (purple bacteria) and in the Gram-positive bacterium Bacillus subtilis.

86 natural sample, peptidoglycan isolated from Gram-positive bacterium Bacillus subtilis.

87 oduced an atlas of terminators for the model Gram-positive bacterium Bacillus subtilis.

88 igate the TLS polymerase Pol Y1 in the model gram-positive bacterium Bacillus subtilis.

89 of an exclusion mechanism in ICEBs1 from the Gram-positive bacterium Bacillus subtilis.

90 eplication upon amino acid starvation in the Gram-positive bacterium Bacillus subtilis.

91 ment of oriC during spore development in the Gram-positive bacterium Bacillus subtilis.

92 ial replicative DNA polymerases found in the Gram-positive bacterium Bacillus subtilis.

93 distantly related and genetically tractable Gram-positive bacterium Bacillus subtilis.

94 de (p)ppGpp inhibits GTP biosynthesis in the Gram-positive bacterium Bacillus subtilis.

95 the interaction of daptomycin with the model Gram-positive bacterium Bacillus subtilis.

96 ifferentiation that is known to occur in the gram-positive bacterium Bacillus subtilis: we investigat

97 ass II transposable element derived from the gram-positive bacterium Bacillus thuringiensis.

98 The RecA protein from the Gram-positive bacterium, Bacillus subtilis, has been rep

99 tablishment of a medial division site in the Gram-positive bacterium, Bacillus subtilis.

100 o damage caused by Listeria monocytogenes, a Gram-positive bacterium, BCV rupture by Gram-negative pa

101 ibe the characterization of a MINPP from the Gram-positive bacterium Bifidobacterium longum (BlMINPP)

102 The enzyme has been purified from the Gram-positive bacterium Brevibacterium fuscum and charac

103 The disease is caused by a gram-positive bacterium called Tropheryma whipplei.

104 Bacillus anthracis, a spore-forming gram-positive bacterium, causes anthrax.

105 The Gram-positive bacterium Clostridioides difficile is the

106 yringe-like molecular machine that kills the Gram-positive bacterium Clostridioides difficile.

107 Staphylococcus aureus, a Gram-positive bacterium colonizing nares, skin, and the

108 Clostridium difficile is a Gram-positive bacterium commonly found in health care an

109 Bacillus subtilis is a model gram-positive bacterium, commonly used to explore questi

110 or Rho from Micrococcus luteus, a high G + C Gram-positive bacterium, contains an unusual extra seque

111 This Gram-positive bacterium displays a set of virulence-asso

112 of bacterial genomes, since B.subtilis is a Gram-positive bacterium, E.coli is a Gram-negative bacte

113 tact heat-killed Streptococcus pneumoniae, a gram-positive bacterium, elicited a rapid primary pneumo

114 The Gram-positive bacterium Enterococcus faecalis and the fu

115 We report that the Gram-positive bacterium Enterococcus faecalis encodes a

116 The Gram-positive bacterium Enterococcus faecalis is both a

117 The fungus Candida albicans and the Gram-positive bacterium Enterococcus faecalis share muco

118 encoding a protective protein antigen of the gram-positive bacterium Erysipelothrix rhusiopathiae, an

119 galactiae (group B streptococcus [GBS]) is a Gram-positive bacterium found in the female rectovaginal

120 the B. subtilis rho is the only gene from a Gram-positive bacterium found to be regulated by Rho.

121 otogenic yeast, and a Bacillus sp. strain, a Gram-positive bacterium, generated approximately one and

122 enic Archaea but also in a distantly related Gram-positive Bacterium, indicating past horizontal gene

123 dopted a top-down approach of transforming a Gram-positive bacterium into a lipid-vesicle-like state.

124 Micrococcus luteus , a Gram-positive bacterium, is incapable of translating at

125 enibacterium salmoninarum, a slowly growing, Gram-positive bacterium, is responsible for bacterial ki

126 Staphylococcus aureus, a gram-positive bacterium, is the leading cause of death f

127 A1-JK(T) is a metabolically versatile Gram-positive bacterium isolated from the oxic-anoxic in

128 th Streptococcus pneumoniae, an encapsulated Gram-positive bacterium known to require Ab-mediated ops

129 acterization of a new group II intron in the Gram-positive bacterium L. lactis and demonstrate for th

130 We found that the probiotic Gram-positive bacterium Lactobacillus acidophilus NCFM i

131 ponse is not restricted to pathogens, as the Gram-positive bacterium Lactobacillus acidophilus, a nat

132 expression of Sav1866 in the drug-sensitive, Gram-positive bacterium Lactococcus lactis Delta lmrA De

133 Our previous studies in the Gram-positive bacterium Lactococcus lactis showed that h

134 The small genome of the Gram-positive bacterium Lactococcus lactis ssp. lactis I

135 ng KAS III, a fabH mutant constructed in the Gram-positive bacterium Lactococcus lactis subspecies la

136 es from the P335 and 936 families infect the Gram-positive bacterium Lactococcus lactis using recepto

137 AM714), were compared with the nonpathogenic gram-positive bacterium, Lactococcus lactis K1, for the

138 The Gram-positive bacterium Leuconostoc mesenteroides, ATCC

139 lethanolamine halve during elongation of the Gram-positive bacterium Listeria innocua.

140 57BL/6 mouse infected with the intracellular gram-positive bacterium Listeria monocytogenes (LM) and

141 IFN pathway through TLR4, the intracellular Gram-positive bacterium Listeria monocytogenes (LM) can

142 The Gram-positive bacterium Listeria monocytogenes adjusts c

143 The Gram-positive bacterium Listeria monocytogenes is a facu

144 The Gram-positive bacterium Listeria monocytogenes is a facu

145 The Gram-positive bacterium Listeria monocytogenes transitio

146 al stress transcription factor sigmaB in the gram-positive bacterium Listeria monocytogenes was isola

147 LO) is an essential virulence factor for the gram-positive bacterium Listeria monocytogenes.

148 e Gram-negative bacterium Salmonella and the Gram-positive bacterium Listeria.

149 terminus was not observed in another low-G+C gram-positive bacterium, Listeria monocytogenes, althoug

150 aphylococcus epidermidis (S. epidermidis), a Gram-positive bacterium, live inside the human nasal cav

151 The Gram-positive bacterium Metabacterium polyspora is an un

152 , promising antimicrobial activity against a Gram-positive bacterium (methicillin-resistant Staphyloc

153 nt with LPS, CpG oligodeoxynucleotides, or a gram-positive bacterium (Micococcus luteus).

154 rmination factor (Rho) was purified from the Gram-positive bacterium Micrococcus luteus, and the comp

155 ects survival to infection by the pathogenic Gram-positive bacterium Micrococcus luteus.

156 leCellKB-MG, a comprehensive database of the Gram-positive bacterium Mycoplasma genitalium using over

157 The dextransucrase DSR-OK from the Gram-positive bacterium Oenococcus kitaharae DSM17330 pr

158 hat QS is a cooperative social behavior in a Gram-positive bacterium, our results suggest convergent,

159 acterial GH161 gene sequence (PapP) from the Gram-positive bacterium Paenibacillus polymyxa ATCC 842

160 owing endarterectomy for the presence of the Gram-positive bacterium Propionibacterium acnes and its

161 The Gram-positive bacterium Propionibacterium acnes is a mem

162 Deinococcus radiodurans is a gram-positive bacterium resistant to extreme levels of i

163 Staphylococcus aureus is a Gram-positive bacterium responsible for a number of dise

164 Staphylococcus aureus is a gram-positive bacterium responsible for a wide range of

165 Bacillus anthracis is a spore-forming, Gram-positive bacterium responsible for anthrax, an acut

166 Bacillus anthracis is a spore-forming gram-positive bacterium responsible for anthrax, an infe

167 The fungus Candida albicans and the Gram-positive bacterium S. aureus can form polymicrobial

168 e gram-negative bacterium Salmonella and the gram-positive bacterium S. aureus to induce expression o

169 e polymers that are potent inhibitors of the Gram-positive bacterium S. aureus, with potential applic

170 ort the 2,038,615-bp genomic sequence of the gram-positive bacterium S. pneumoniae R6.

171 To understand how Hfq from the Gram-positive bacterium Staphylococcus aureus (Sa) binds

172 epithelial cells (HCECs) to infection by the Gram-positive bacterium Staphylococcus aureus and to det

173 tance in the preeminent etiologic agent, the Gram-positive bacterium Staphylococcus aureus Bacterial

174 this technology for selective killing of the Gram-positive bacterium Staphylococcus aureus by targeti

175 The Gram-positive bacterium Staphylococcus aureus infects di

176 The Gram-positive bacterium Staphylococcus aureus produces v

177 The gram-positive bacterium Staphylococcus aureus secretes a

178 hat microglial activation in response to the Gram-positive bacterium Staphylococcus aureus was not co

179 or the stringent response nucleotides in the Gram-positive bacterium Staphylococcus aureus We demonst

180 HslV, and FtsH, have been identified in the Gram-positive bacterium Staphylococcus aureus, a pathoge

181 synthesis and exhibit activities against the Gram-positive bacterium Staphylococcus aureus, including

182 R2 agonist, peptidoglycan (PGN) derived from Gram-positive bacterium Staphylococcus aureus, induced c

183 y lipoteichoic acid and peptidoglycan of the Gram-positive bacterium Staphylococcus aureus, synergize

184 ntial growth-inhibitory activity towards the Gram-positive bacterium Staphylococcus aureus, the Gram-

185 hes are needed to control infection with the Gram-positive bacterium Staphylococcus aureus, which is

186 hesis of cell wall material in the spherical Gram-positive bacterium Staphylococcus aureus.

187 lso prevent biofilm formation by the related Gram-positive bacterium Staphylococcus aureus.

188 The Gram-positive bacterium, Staphylococcus aureus, is a ver

189 c acid (LTA) and peptidoglycan (PepG) of the gram-positive bacterium, Staphylococcus aureus, synergiz

190 ine), the numbers of viable cells of another Gram-positive bacterium, Staphylococcus epidermidis, as

191 and micromolide, against S. marcescens and a Gram-positive bacterium, Staphylococcus hyicus, in broth

192 into these events during infection with the Gram positive bacterium Streptococcus pneumoniae.

193 The gram-positive bacterium Streptococcus mutans is the prim

194 ntaining antibiotics) and is produced by the Gram-positive bacterium Streptococcus mutans.

195 enicillin-binding protein 1b (PBP 1b) of the gram-positive bacterium Streptococcus pneumoniae catalyz

196 The naturally transformable Gram-positive bacterium Streptococcus pneumoniae has two

197 The Gram-positive bacterium Streptococcus pneumoniae is a ma

198 The Gram-positive bacterium Streptococcus pneumoniae is a ma

199 Gram-positive bacterium Streptococcus pneumoniae is an i

200 etic means that CL targets DNA gyrase in the gram-positive bacterium Streptococcus pneumoniae, and pr

201 In the Gram-positive bacterium Streptococcus pneumoniae, the Cp

202 A (PsaA) is a surface-exposed protein of the gram-positive bacterium Streptococcus pneumoniae.

203 The Gram-positive bacterium Streptococcus pyogenes (also cal

204 The gram-positive bacterium Streptococcus pyogenes (group A

205 An understanding of how the heme-deficient gram-positive bacterium Streptococcus pyogenes establish

206 terial immunotherapeutic protein against the Gram-positive bacterium Streptococcus pyogenes This prot

207 n of the cysteine protease of the pathogenic gram-positive bacterium Streptococcus pyogenes.

208 cysteine proteinase (SCP) of the pathogenic Gram-positive bacterium Streptococcus pyogenes.

209 The first structure of an ASADH from a Gram-positive bacterium, Streptococcus pneumoniae, has n

210 Under iron limitation, the Gram-positive bacterium Streptomyces coelicolor A3(2) ex

211 systematically mutagenise the genome of the Gram-positive bacterium Streptomyces coelicolor A3(2), w

212 Here we identify lipoproteins in the model Gram-positive bacterium Streptomyces coelicolor using bi

213 ps-like orthologues within the genome of the Gram-positive bacterium Streptomyces coelicolor.

214 ed for the late stages of sporulation in the Gram-positive bacterium Streptomyces coelicolor.

215 sL, a cytochrome P450 monooxygenase from the Gram-positive bacterium Streptomyces noursei, catalyzes

216 In the Gram-positive bacterium, Streptomyces coelicolor A3(2),

217 cus pyogenes, or Group A Streptococcus, is a Gram-positive bacterium that can be both a human commens

218 Enterococcus faecalis is a gram-positive bacterium that can cause a variety of noso

219 Staphylococcus aureus is a Gram-positive bacterium that can cause both superficial

220 Listeria monocytogenes is a Gram-positive bacterium that can cause septicemia and me

221 Staphylococcus aureus is a ubiquitous gram-positive bacterium that can cause superficial to se

222 Listeria monocytogenes is a ubiquitous gram-positive bacterium that can cause systemic and ofte

223 ii is a spore-forming, obligately anaerobic, Gram-positive bacterium that can cause toxic shock syndr

224 Clostridium perfringens is an anaerobic, Gram-positive bacterium that causes a range of diseases

225 Clostridium difficile is an anaerobic Gram-positive bacterium that causes intestinal infection

226 Listeria monocytogenes is a Gram-positive bacterium that causes listeriosis.

227 Listeria monocytogenes is a Gram-positive bacterium that causes severe opportunistic

228 Clostridioides difficile is an anaerobic Gram-positive bacterium that colonizes the gut of patien

229 up B streptococcus (GBS) is a beta-hemolytic gram-positive bacterium that colonizes the lower genital

230 Listeria monocytogenes is an intracellular Gram-positive bacterium that induces expression of type

231 lum is a thermophilic, obligately anaerobic, gram-positive bacterium that is a candidate microorganis

232 treptococcus agalactiae is a beta-hemolytic, Gram-positive bacterium that is a leading cause of neona

233 Staphylococcus aureus is a Gram-positive bacterium that is responsible for severe n

234 Bacillus anthracis is a sporulating Gram-positive bacterium that is the causative agent of a

235 Bacillus subtilis is a Gram-positive bacterium that is used to dissect the mech

236 he biofilm-forming Streptococcus mutans is a gram-positive bacterium that resides in the human oral c

237 te the properties of an ion channel from the Gram-positive bacterium Tsukamurella paurometabola with

238 Spx in the control of sulfur metabolism in a gram-positive bacterium under nonstressful growth condit

239 iphoviridae and infect Lactococcus lactis, a gram-positive bacterium used in commercial dairy ferment

240 ococcus suis, an important emerging zoonotic Gram-positive bacterium, while only RelA is functional u

241 Bacillus subtilis is a plant-beneficial Gram-positive bacterium widely used as a biofertilizer.

242 Bacillus subtilis is a prototypical Gram-positive bacterium with a lipoteichoic acid structu

243 Clostridium difficile is a Gram-positive bacterium with an S-layer covering its pep

244 hermophilic, dissimilatory Fe(III)-reducing, Gram-positive bacterium with capability to generate elec