ライフサイエンスコーパス: Gram-positive bacterium

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 0 mediates bactericidal activity against the Gram-positive bacterium Bacillus anthracis, the causativ

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

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

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

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

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

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

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

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

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

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

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

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

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

46 The Gram-positive bacterium Bacillus subtilis encodes three

47 The Gram-positive bacterium Bacillus subtilis forms biofilms

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 The Gram-positive bacterium Enterococcus faecalis and the fu

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

82 The Gram-positive bacterium Enterococcus faecalis is both a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

100 The Gram-positive bacterium Leuconostoc mesenteroides, ATCC

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

102 57BL/6 mouse infected with the intracellular gram-positive bacterium Listeria monocytogenes (LM) and

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

104 The Gram-positive bacterium Listeria monocytogenes adjusts c

105 The Gram-positive bacterium Listeria monocytogenes is a facu

106 The Gram-positive bacterium Listeria monocytogenes is a facu

107 The Gram-positive bacterium Listeria monocytogenes transitio

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

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

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

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

112 The Gram-positive bacterium Metabacterium polyspora is an un

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

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

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

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

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

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

119 The Gram-positive bacterium Propionibacterium acnes is a mem

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

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

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

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

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

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

126 The Gram-positive bacterium Staphylococcus aureus infects di

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 The gram-positive bacterium Streptococcus mutans is the prim

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

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

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

145 The Gram-positive bacterium Streptococcus pneumoniae is a ma

146 Gram-positive bacterium Streptococcus pneumoniae is an i

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

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

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

150 The Gram-positive bacterium Streptococcus pyogenes (also cal

151 The gram-positive bacterium Streptococcus pyogenes (group A

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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