ライフサイエンスコーパス: Bacillus cereus

1 reated based on the known structure of BcNr (Bacillus cereus).

2 tructure of BcpA, the major pilin subunit of Bacillus cereus.

3 semble BcpA pilin subunits on the surface of Bacillus cereus.

4 e sphingomyelinases of Listeria ivanovii and Bacillus cereus.

5 ene expression of the phage in a model host, Bacillus cereus.

6 he pathogenic species Bacillus anthracis and Bacillus cereus.

7 t is closely related to the highly hemolytic Bacillus cereus.

8 dentity to the type I beta-lactamase gene of Bacillus cereus.

9 spectrum, aminopolyol antibiotic produced by Bacillus cereus.

10 m genomic DNA of the Gram-positive bacterium Bacillus cereus.

11 tructed a promoter-trap plasmid, pAD123, for Bacillus cereus.

12 ese as the low-G+C Gram-positive eubacterium Bacillus cereus.

13 food poisoning syndrome caused by strains of Bacillus cereus.

14 pidly progressing, fatal pneumonia caused by Bacillus cereus.

15 regulator of most known virulence factors in Bacillus cereus.

16 RT toxin from the pathogenic G9241 strain of Bacillus cereus.

17 s subtilis, as well as the spore surfaces of Bacillus cereus 569 and the Sterne strain of Bacillus an

18 the 16/23S rDNA interspace region (ISR) from Bacillus cereus 6464 produced a mixture of products.

19 In addition to multiple virulence factors, Bacillus cereus a pathogen that causes food poisoning an

20 t crystal structures of the NaK channel from Bacillus cereus, a non-selective tetrameric cation chann

21 The p K a of the Bacillus cereus ADI (BcADI) was determined by UV-pH titr

22 formed in the reaction of L-canavanine with Bacillus cereus ADI partitions between the product formi

23 valuate the efficacy of the biocontrol agent Bacillus cereus against the seed pathogen Pythium torulo

24 rystal structures of the recently discovered Bacillus cereus AlkD glycosylase in complex with DNAs co

25 Bacillus cereus AlkD is the only DNA glycosylase known t

26 The crystal structure of Bacillus cereus AlkD presented here shows that the prote

27 It was thought to differ from Bacillus cereus, an opportunistic pathogen and cause of

28 During growth under iron limitation, Bacillus cereus and Bacillus anthracis, two human pathog

29 sely related to, if not the same species as, Bacillus cereus and Bacillus anthracis.

30 as well as the two closely related species, Bacillus cereus and Bacillus mycoides, has made a sequen

31 Superdormant spores of Bacillus cereus and Bacillus subtilis germinated just as

32 PA) during nutrient germination of spores of Bacillus cereus and Bacillus subtilis showed that heat a

33 dye SYTO 16 during germination of individual Bacillus cereus and Bacillus subtilis spores.

34 considering that the closely related species Bacillus cereus and Bacillus thuringiensis typically pro

35 Isogenic plcR-deficient mutants of Bacillus cereus and Bacillus thuringiensis were construc

36 ease secreted by the closely related species Bacillus cereus and Bacillus thuringiensis, but the patt

37 tte, and Basilisk, which infect the pathogen Bacillus cereus and carry genes that may contribute to i

38 ylococcus aureus, Leuconostoc mesenteroides, Bacillus cereus and Enterococcus faecalis proving its an

39 s study, the genes encoding phosphonatase in Bacillus cereus and in Salmonella typhimurium were clone

40 In Bacillus cereus and its close relative Bacillus anthraci

41 Bacillus cereus and other Gram-positive bacteria elabora

42 phages, like GIL16 or Bam35, whose hosts are Bacillus cereus and related Gram-positive bacteria.

43 foodborne pathogens (Listeria monocytogenes, Bacillus cereus and Staphylococcus aureus) at low concen

44 d found in RIF-sensitive bacteria, including Bacillus cereus and the pathogen Listeria monocytogenes.

45 lococcus aureus, Listeria monocytogenes, and Bacillus cereus) and Gram-negative microbes (Salmonella

46 am positive (Staphylococcus aureus, MRSA and Bacillus cereus) and two Gram negative (Escherichia coli

47 th 42 strains of B. anthracis, 36 strains of Bacillus cereus, and 12 strains of Bacillus thuringiensi

48 coli and shown to replicate in B. anthracis, Bacillus cereus, and Bacillus subtilis.

49 Bacillus anthracis, Bacillus cereus, and Bacillus thuringiensis are closely

50 omosomal homology exists among B. anthracis, Bacillus cereus, and Bacillus thuringiensis.

51 s Bacillus megaterium, one was identified as Bacillus cereus, and one was an unidentifiable Bacillus

52 ans) and bacterial species (Esherichia coli, Bacillus cereus, and Pseudomonas aeruginosa) compared to

53 tal of four proteins from Bacillus subtilis, Bacillus cereus, and Streptomyces coelicolor A3(2) that

54 ools for identifying regulatory sequences in Bacillus cereus, and that flow cytometry and cell sortin

55 e full-length protein, except in the case of Bacillus cereus, and using GFP-tagged cell wall-binding

56 s PcrA helicases from Bacillus anthracis and Bacillus cereus are capable of unwinding Staphylococcus

57 Vegetative forms of Bacillus cereus are reported to form pili, thin protein

58 ed genomes of Methanocaldococcus jannaschii, Bacillus cereus ATCC 10987 and Methylococcus capsulatus.

59 Bacillus cereus ATCC 10987 contains a single large plasm

60 were also isolated from the closely related Bacillus cereus ATCC 10987 strain, and from the B. cereu

61 We sequenced the complete genome of Bacillus cereus ATCC 10987, a non-lethal dairy isolate i

62 the secondary cell wall polysaccharide from Bacillus cereus ATCC 10987, a strain that is closely rel

63 lobacter salexigens, Vibrio breoganii 1C-10, Bacillus cereus ATCC 10987, Campylobacter jejuni subsp.

64 se structure were linked to spore glycans in Bacillus cereus ATCC 14579 and ATCC 10876.

65 Thiocillins from Bacillus cereus ATCC 14579 are members of the well-known

66 The thiocillins from Bacillus cereus ATCC 14579 are natural products from the

67 Bacillus cereus ATCC 14579 converts the C-terminal 14 re

68 nts for TclM from thiocillin biosynthesis in Bacillus cereus ATCC 14579.

69 erprints for Bacillus atrophaeus ATCC 49337, Bacillus cereus ATCC 14579T, Escherichia coli ATCC 33694

70 We report that the native form of Bacillus cereus ATCC10987 BioC functionally replaced E.

71 Purified superdormant spores of Bacillus cereus, B. megaterium, and B. subtilis isolated

72 crystalline fragments from the exosporium of Bacillus cereus, B. thuringiensis and B. anthracis strai

73 triad Glu residue was recently identified in Bacillus cereus ((BACCR)NAT3) but has not yet been chara

74 n-like proteases and is distantly related to Bacillus cereus bacillolysin.

75 ered and purified from the culture medium of Bacillus cereus, Bacillus anthracis, and Bacillus thurin

76 ods to belong to Bacillus amyloliquefaciens, Bacillus cereus, Bacillus licheniformis, Bacillus megate

77 llus cereus group, i.e., Bacillus anthracis, Bacillus cereus, Bacillus mycoides, and Bacillus thuring

78 t different ions are desorbed from spores of Bacillus cereus, Bacillus thuringiensis, Bacillus subtil

79 d in this unique process, we imaged purified Bacillus cereus, Bacillus thuringiensis, Bacillus subtil

80 seudomonas aeruginosa (PA) and Gram-positive Bacillus cereus (BC) biofilm-laden glass beads were sele

81 e amounts of Bacillus thuringiensis (BT) and Bacillus cereus (BC) is presented based on a novel PZT-a

82 , within a phage integrated in the bacterium Bacillus cereus (Bc).

83 ed by cobalt substituted beta-lactamase from Bacillus cereus (BcII) are biphasic.

84 sis of the native zinc and metal substituted Bacillus cereus (BcII) metallo-beta-lactamase have been

85 ealed by V/K) for the TEM beta-lactamase and Bacillus cereus beta-lactamase I.

86 xamined the conformational properties of the Bacillus cereus beta-lactamase II in the presence of che

87 at the dynamics of an anthrax-causing agent, Bacillus cereus biovar anthracis, in a tropical rainfore

88 II resembles the ADP-ribosylating toxin from Bacillus cereus, but the active site has been mutated an

89 oacetaldehyde hydrolase (phosphonatase) from Bacillus cereus catalyzes hydrolytic P-C bond cleavage o

90 A Nudix enzyme from Bacillus cereus catalyzes the hydrolysis of CDP-choline

91 e electrode (PGE) biosensor for detection of Bacillus cereus, causative agent of two types of food-bo

92 Bacillus cereus causes a highly fulminant endophthalmiti

93 Bacillus cereus causes one of the most rapidly blinding

94 Bacillus cereus causes the most virulent and refractory

95 ls can be trapped by the beta-lactamase from Bacillus cereus, causing inhibition of the enzyme.

96 to 2008, 1229 foodborne outbreaks caused by Bacillus cereus, Clostridium perfringens, and Staphyloco

97 (HBL) is a unique membrane-lytic toxin from Bacillus cereus composed of three distinct proteins, des

98 The genome of Bacillus cereus contains 26 Nudix hydrolase genes, secon

99 Three isolates, Bacillus cereus D-17, B. cereus 43881, and Bacillus thur

100 In the case of Bacillus cereus detection, the device was able to specif

101 Endophthalmitis caused by Bacillus cereus develops as acute inflammation with infi

102 The enzyme from Bacillus cereus differs from the Bacteroides fragilis en

103 asmid-cured B. anthracis tester strain and a Bacillus cereus driver was used to find a unique chromos

104 We present the first case of native valve Bacillus cereus endocarditis with no apparent risk facto

105 B) permeability occurred during experimental Bacillus cereus endophthalmitis and whether tight juncti

106 virulence for three common ocular pathogens (Bacillus cereus, Enterococcus faecalis, and Staphylococc

107 lococcus epidermidis, Staphylococcus aureus, Bacillus cereus, Enterococcus faecalis, Enterococcus fae

108 amase: TEM-1 (class A), p99 (class C), and a Bacillus cereus enzyme sold by Genzyme (class B).

109 effectiveness against Staphylococcus aureus, Bacillus cereus, Escherichia coli O157:H7, Pseudomonas a

110 than THC (1) against Staphylococcus aureus, Bacillus cereus, Escherichia coli, and Yersinia enteroco

111 Antimicrobial properties on tester strains (Bacillus cereus, Escherichia coli, Staphylococcus aureus

112 tion rate, and recombination tract length of Bacillus cereus from a whole genome alignment.

113 Bacillus cereus G9241 causes an anthrax-like respiratory

114 Bacillus cereus G9241 was isolated from a welder sufferi

115 Bacillus cereus G9241 was isolated from a welder with a

116 Bacillus cereus G9241, the causative agent of anthrax-li

117 Bacillus cereus G9241, which caused an anthrax-like infe

118 The Bacillus cereus genome possesses three type IA topoisome

119 s model provides a good fit to a data set of Bacillus cereus genomes and estimate several recombinati

120 plifications of 700- and 305-bp fragments of Bacillus cereus genomic DNA have been demonstrated.

121 hods in an attempt to identify variants of a Bacillus cereus glmS ribozyme that expand the range of c

122 The spores of the Bacillus cereus group (B. cereus, Bacillus anthracis, an

123 mplified from the genome of three members of Bacillus cereus group and a 114 nucleotide region from t

124 variety of bacterial species, members of the Bacillus cereus group are unique in that they have a tot

125 Members of the Bacillus cereus group contain cell wall carbohydrates th

126 array to investigate the genome diversity of Bacillus cereus group members and elucidate the events a

127 Importance: The Bacillus cereus group of bacteria contains several human

128 Representative strains of the Bacillus cereus group of bacteria, including Bacillus an

129 onstitute a major cell wall structure in the Bacillus cereus group of bacteria.

130 several megaplasmids found in members of the Bacillus cereus group of bacteria.

131 llus anthracis, two human pathogens from the Bacillus cereus group of Gram-positive bacteria, secrete

132 nt to the sinIR locus that are unique to the Bacillus cereus group species.

133 purpose, we used a set of well characterized Bacillus cereus group strains isolated from poisoned foo

134 sis of 16S rRNA genes from 50 strains of the Bacillus cereus group, i.e., Bacillus anthracis, Bacillu

135 The exosporium of the Bacillus cereus group, including the anthrax pathogen, c

136 sed for discrimination of the members of the Bacillus cereus group, we analyzed 183 16S rRNA and 74 2

137 ost isolates were motile and not even in the Bacillus cereus group.

138 designated Cot alpha, was found only in the Bacillus cereus group.

139 rentiation of them from other species in the Bacillus cereus group.

140 to an alignment of 13 whole genomes from the Bacillus cereus group.

141 Bacillus cereus grown in a biofilm-inducing medium has b

142 ence and surface proteins have homologues in Bacillus cereus, highlighting the similarity of B. anthr

143 bacter pylori, Burkholderia pseudomallei and Bacillus cereus), illustrating that bacterial species va

144 we demonstrate the quantitative detection of Bacillus cereus in buffer medium and Escherichia coli in

145 lus, tissue factor, or a bacterial stimulus, Bacillus cereus, initiated coagulation of human platelet

146 Bacillus cereus is a rare cause of endocarditis, typical

147 Bacillus cereus is a rare cause of serious human infecti

148 The nonspecific phospholipase C from Bacillus cereus is a zinc metalloenzyme that catalyzes t

149 Bacillus cereus is an opportunistic pathogen causing foo

150 Bacillus cereus is an uncommon but potentially serious b

151 sitol-specific phospholipase C (PI-PLC) from Bacillus cereus is inhibited by myo-inositol-1-O-dodecyl

152 Bacillus cereus is often associated with mild to moderat

153 Bacillus cereus is ubiquitous in nature, and while most

154 A resolution x-ray crystal structure of the Bacillus cereus metA protein in complex with homoserine,

155 The variants of the non-selective Bacillus cereus NaK cation channel we examine are all se

156 or rupture of dormant spores of B. subtilis, Bacillus cereus or Bacillus megaterium, although germina

157 Anthrose was not found in spores of either Bacillus cereus or Bacillus thuringiensis, two species t

158 ine the kinetics and subsite interactions of Bacillus cereus phosphatidylinositol-specific phospholip

159 Substrate analog inhibitors of Bacillus cereus phosphatidylinositol-specific phospholip

160 is study, the X-ray crystal structure of the Bacillus cereus phosphonatase homodimer complexed with t

161 nding was carried out using Mg(II)-activated Bacillus cereus phosphonoacetaldehyde hydrolase (phospho

162 that a small beta-strand (Vb) is present in Bacillus cereus PI-PLC and is absent in the enzyme from

163 A catalytic diad at the active site of Bacillus cereus PI-PLC composed of aspartate-274 and his

164 the crystal structure of the closely related Bacillus cereus PI-PLC, the rim of the active site is fl

165 cate that G418 is an allosteric activator of Bacillus cereus PI-PLC.

166 ogs, Clostridium perfringens alpha-toxin and Bacillus cereus PLC (PLCBc), we generated PC-PLC mutants

167 a widely used, competitive inhibitor of the Bacillus cereus PLC.

168 tidylcholine-preferring phospholipase C from Bacillus cereus (PLC(Bc)) follows the order phosphatidyl

169 tidylcholine-preferring phospholipase C from Bacillus cereus (PLC(Bc)) is a 28.5 kDa enzyme with thre

170 tidylcholine-preferring phospholipase C from Bacillus cereus (PLCBc) have been evaluated for phosphat

171 tidylcholine-preferring phospholipase C from Bacillus cereus (PLCBc) is a 28.5 kDa enzyme with three

172 hatidylcholine-preferring phospholipase C of Bacillus cereus (PLCBc) might play in binding and cataly

173 tidylcholine-preferring phospholipase C from Bacillus cereus (PLCBc) was prepared in which the glutam

174 the phosphatidylcholine preferring PLC from Bacillus cereus (PLCBc).

175 plasmid pUTE29-plcR-papR carrying the native Bacillus cereus plcR-papR gene cluster did not activate

176 We investigated the reaction mechanism of Bacillus cereus PPM using a combination of structural an

177 spot syndrome virus, Streptococcus equi, and Bacillus cereus predicts that the collagen-like sequence

178 Mixing BCTP or BCTP 401 with Bacillus cereus prior to subcutaneous injection in mice

179 , relying on the gamma phage derivative of a Bacillus cereus prophage called W.

180 hromosomal mercury resistance determinant of Bacillus cereus RC607 confers resistance to inorganic me

181 oss of the cytochrome c maturation system in Bacillus cereus results in increased transcription of th

182 Bacillus cereus secretes molecules that activate express

183 ndancy genome sequences of 45 strains of the Bacillus cereus sensu lato (s.l.) species that were chos

184 The plasmids of the members of the Bacillus cereus sensu lato group of organisms are essent

185 racis, the anthrax agent, is a member of the Bacillus cereus sensu lato group, which includes invasiv

186 r has been identified only in members of the Bacillus cereus sensu lato group.

187 related (97% identity) wild-type PI-PLC from Bacillus cereus, significant conformational differences

188 , we report a two-component lantibiotic from Bacillus cereus SJ1 with unusual structural features tha

189 Purified mature Bacillus cereus SleB without its signal sequence (SleB(M

190 We found that like the full-length Bacillus cereus SleB, the catalytic C-terminal domain (S

191 Treatment of cells with Bacillus cereus sphingomyelinase (bSMase) increases the

192 We cloned the Bacillus cereus sphingomyelinase gene by polymerase chai

193 cillus anthracis, 10 Bacillus subtilis and 1 Bacillus cereus spore.

194 Bacillus cereus spores are assembled with a series of co

195 ells bound to B. anthracis spores but not to Bacillus cereus spores in a fluorescent microscopy assay

196 of changes during the germination of single Bacillus cereus spores in both nutrient (l-alanine) and

197 distribution, and movement in single dormant Bacillus cereus spores using confocal Raman microspectro

198 s an example, intact Bacillus atrophaeus and Bacillus cereus spores, either pure or in mixtures, were

199 th Escherichia coli, Listeria monocytogenes, Bacillus cereus, Staphylococcus aureus and Salmonella en

200 al action against four food-borne pathogens--Bacillus cereus, Staphylococcus aureus, Escherichia coli

201 ent anti-microbial activity than THC against Bacillus cereus, Staphylococcus aureus, Escherichia coli

202 racts inhibited the growth of gram-positive (Bacillus cereus, Staphylococcus aureus, Listeria monocyt

203 ities were tested on selected Gram-positive (Bacillus cereus, Staphylococcus aureus, Staphylococcus s

204 frameshifted in the pathogenic pXO1-bearing Bacillus cereus strain G9241.

205 cum, ColT from C. tetani, and ColQ1 from the Bacillus cereus strain Q1, while showing negligible acti

206 The genomes of two Bacillus cereus strains (ATCC 10987 and ATCC 14579) have

207 MR was approximately 10(3) CFU/microg, while Bacillus cereus strains 569 and ATCC 10987 were transfor

208 Bacillus cereus strains elaborate pili on their surface

209 Bacillus cereus strains harboring a pXO1-like virulence

210 Most Bacillus cereus strains produced positive cytotoxicity r

211 nce analysis of the complete ORFs from three Bacillus cereus strains shows maintenance of the ORF acr

212 We identified three encapsulated Bacillus cereus strains, isolated from patients with sev

213 es from the severe food-poisoning bacterium, Bacillus cereus subsp. cytotoxis NVH 391-98, that are in

214 Intact protein biomarkers from Bacillus cereus T spores have been analyzed by high-reso

215 coccus aureus, Staphylococcus epidermis, and Bacillus cereus taken over a span of three days in the p

216 from the gram-positive pathogenic bacterium Bacillus cereus that binds multinuclear ferric citrate c

217 s a novel aminopolyol antibiotic produced by Bacillus cereus that is active against diverse bacteria

218 resent the crystal structure of an EIIC from Bacillus cereus that transports diacetylchitobiose.

219 In SspC from Bacillus subtilis and Bce1 from Bacillus cereus the acidic residues involved in cross-li

220 The method utilizes sphingomyelinase from Bacillus cereus to completely hydrolyze the sphingomyeli

221 Bacillus cereus topoisomerase IIIbeta (bcTopo IIIbeta) h

222 Most Bacillus cereus toxin production is controlled by the qu

223 Here we report crystal structures for Bacillus cereus TSPO (BcTSPO) down to 1.7 A resolution,

224 Among the tested bacteria, Bacillus cereus was the most sensitive and Yersinia ente

225 Escherichia coli, Listeria monocytogenes and Bacillus cereus) was evaluated.

226 A pairs into a thiocillin producer strain of Bacillus cereus .We demonstrate that thiopeptide variant

227 Using the DNA glycosylase AlkD from Bacillus cereus, we crystallographically monitored excis

228 In the spore-forming Bacillus cereus, we have identified three principal enzy

229 Here, we report on a six-gene cassette in Bacillus cereus which, when integrated into the Bacillus

230 s found in mononuclear B1 enzymes (BcII from Bacillus cereus) while providing a more efficient single

231 Here we report that Bacillus cereus YxeB facilitates iron-exchange from Fe-s