ライフサイエンスコーパス: Serratia

1 reduced the abundance of the basal resource (Serratia).

2 strains of the opportunistic human pathogen, Serratia.

3 years; Nocardia, 0.81 per 100 patient-years; Serratia, 0.98 per 100 patient-years, and severe Staphyl

4 y transcriptional activator CarR(39006) from Serratia 39006 has no detectable affinity for cognate AH

5 toxin, showing a remarkable predominance of Serratia and Clostridium species, which switched from as

6 four plant-associated enterobacteria of the Serratia and Dickeya genera.

7 ytopathogenic strains of the enterobacteria, Serratia and Dickeya.

8 ers of two genera of Gram-negative bacteria, Serratia and Erwinia, produce a beta-lactam antibiotic,

9 convenient spectrophotometric assay, by the Serratia and Pseudomonas approximately 50-kDa extracellu

10 s such as the non-specific endonuclease from Serratia and the sequence-specific His-Cys box homing en

11 . subtilis colonies, swarming by Proteus and Serratia, and spatially organized interspecific metaboli

12 Using the bacterium Serratia as a model system, we have investigated two con

13 Serratia AS1 was genetically engineered for secretion of

14 g the production of secondary metabolites in Serratia ATCC 39006.

15 We describe a Serratia bacterium strain (AS1) isolated from Anopheles

16 However, estimated rates of encounter with Serratia based on these modifications were higher for in

17 pe I-E, I-F, and III-A CRISPR-Cas systems in Serratia cells in high-density populations.

18 cosmid containing approximately 35 kb of the Serratia chromosome encodes synthesis of the pigment in

19 We report the isolation of a third locus in Serratia, containing convergently transcribed genes, sma

20 Serratia endonuclease is an important member of a class

21 tom are conserved in nucleases homologous to Serratia endonuclease, suggesting that the water cluster

22 , to share a similar active site geometry to Serratia endonuclease.

23 The Serratia entomophila antifeeding prophage (Afp) is a bul

24 rom other insect-associated bacteria such as Serratia entomophila, an insect pathogen, and Yersinia p

25 ducreyi is the newest member of the Proteus/Serratia family of pore-forming toxins.

26 ures of the class A carbapenemase SFC-1 from Serratia fonticola and of complexes of its Ser70 Ala (Mi

27 comprised of (i) a bacterial basal resource (Serratia fonticola), (ii) an intermediate consumer (Para

28 monella, Escherichia, Bacillus, Pseudomonas, Serratia, Hafnia, Enterobacter, Citrobacter, and Lactoba

29 al ABC iron transporters that include Sfu of Serratia, Hit of Haemophilus, and Yfu of Yersinia entero

30 espite a poorly conserved sequence, which in Serratia includes a cysteine bridge thought to play a re

31 Molecular relatedness of available Serratia isolates was determined by pulsed-field gel ele

32 In a one month period, 10 Serratia liquefaciens bloodstream infections and 6 pyrog

33 ble protease Ser2 is secreted by the species Serratia liquefaciens, a psychrotrophic bacteria frequen

34 erine lactone-dependent swarming motility of Serratia liquefaciens.

35 % similarity to the phospholipase A found in Serratia liquefaciens.

36 r cloacae (9.1%), Acinetobacter spp. (6.2%), Serratia marcescens (5.5%), Enterobacter aerogenes (4.4%

37 Hemophores from Serratia marcescens (HasA(sm)) and Pseudomonas aeruginos

38 R-flagellins from Serratia marcescens (S. marcescens) and Salmonella muenc

39 east histone acetyltransferase 1) and SmAAT (Serratia marcescens aminoglycoside 3-N-acetyltransferase

40 luding yeast histone acetyltransferase 1 and Serratia marcescens aminoglycoside 3-N-acetyltransferase

41 cal GCN5-related N-acetyltransferase (GNAT), Serratia marcescens aminoglycoside 3-N-acetyltransferase

42 sequences of the cheA loci from isolates of Serratia marcescens and Enterobacter cloacae, demonstrat

43 the aspartate transcarbamoylases (ATCase) of Serratia marcescens and Escherichia coli differ in both

44 the aspartate transcarbamoylases (ATCase) of Serratia marcescens and Escherichia coli have distinct a

45 entical to the natural product isolated from Serratia marcescens and from overexpression of the biosy

46 sfu and hit operons previously reported for Serratia marcescens and Haemophilus influenzae, respecti

47 ence time of TLM on the ecFabB homologues in Serratia marcescens and Klebsiella pneumonia is an impor

48 Ds accumulate in midgut cells in response to Serratia marcescens and Sindbis virus or when the native

49 nces were noted among Acinetobacter spp. and Serratia marcescens and, to a lesser extent, with Strept

50 Using Serratia marcescens as a model organism, we identify her

51 l intensive care unit of a hospital acquired Serratia marcescens bacteremia.

52 ybrid microswimmer system driven by multiple Serratia marcescens bacteria, we quantify the chemotacti

53 In March 2011, Serratia marcescens bloodstream infections (BSIs) were i

54 idguts after they fed on the insect pathogen Serratia marcescens but not after feeding on the Leishma

55 functional antibiotic resistance enzyme from Serratia marcescens catalyzes adenylation and acetylatio

56 egative bacterium and opportunistic pathogen Serratia marcescens causes ocular infections in healthy

57 of an alpha + beta domain similar to that of Serratia marcescens chitinases A and B.

58 Serratia marcescens culture filtrates have been reported

59 , sensitive detection of Escherichia coli or Serratia marcescens cultures from 1 to 10(3) CFU mL(-1).

60 The hemophore protein HasA from Serratia marcescens cycles between two states as follows

61 The Serratia marcescens extracellular nuclease gene, nucA, i

62 A family of mutants overexpressing the Serratia marcescens extracellular nuclease has been know

63 The Serratia marcescens extracellular nuclease is a secreted

64 alf-site pairs of the trpEDCBA operator from Serratia marcescens indicated an obligate hierarchy of s

65 eudo-outbreaks of Pseudomonas aeruginosa and Serratia marcescens infections associated with bronchosc

66 a California hospital acquired postoperative Serratia marcescens infections, and 1 died.

67 Chitinase B (ChiB) from Serratia marcescens is a family 18 exo-chitinase whose c

68 Serratia marcescens is a gram-negative environmental bac

69 Serratia marcescens is a soil- and water-derived bacteri

70 Serratia marcescens is a well-known cause of nosocomial

71 Serratia marcescens is an extremely rare cause of necrot

72 The enteric bacterium Serratia marcescens is an opportunistic human pathogen.

73 Serratia marcescens is an opportunistic pathogen associa

74 Serratia marcescens is frequently isolated from lenses o

75 The extracellular nuclease of Serratia marcescens is one of a wide variety of enzymes

76 A Serratia marcescens isolate was particularly efficient i

77 olates, 6 Pseudomonas aeruginosa isolates, 1 Serratia marcescens isolate, 1 Aeromonas hydrophila isol

78 Three bla(SME)-carrying Serratia marcescens isolates and one bla(NDM-1) carrying

79 to 0.5 nM alpha-thrombin by only 10% whereas Serratia marcescens metalloprotease reduced the Ca2+ res

80 ion of extracellular nuclease (Nuc) from the Serratia marcescens nucA chromosomal locus is inhibited

81 The Serratia marcescens NucC protein is structurally and fun

82 Extracellular secretion of Serratia marcescens nuclease occurs as a two-step proces

83 immune priming during infections with either Serratia marcescens or with Escherichia coli.

84 e that is located upstream of NucC-dependent Serratia marcescens promoters and the late promoters of

85 sented here in complex with chitinase B from Serratia marcescens provide further insight into the mec

86 and hhdB, which, based on their homology to Serratia marcescens shlA and shlB genes, are believed to

87 ith exogenous bacteria (Enterobacter sp. and Serratia marcescens strain Db11) and parasitic African t

88 the RNA-binding protein, RsmA, in Ecc71 and Serratia marcescens strain SM274.

89 ed to the chromosome of carbapenem-resistant Serratia marcescens strains.

90 ing medium on prodigiosin (PG) production by Serratia marcescens TKU011 is examined.

91 We adsorbed swarmer cells of Serratia marcescens to polydimethylsiloxane or polystyre

92 lated data and experimental Tn-Seq data from Serratia marcescens transposon mutant library used to id

93 ce of infection with Burkholderia cepacia or Serratia marcescens was caused by a new strain in 9 of 1

94 ely 10,000 nM), and Enterobacter cloacae and Serratia marcescens were highly resistant (IC(50), >10,0

95 e, Proteus spp., Pseudomonas aeruginosa, and Serratia marcescens) and 6 antimicrobial resistance dete

96 that coevolution with a bacterial pathogen (Serratia marcescens) resulted in significantly more outc

97 roPhenoloxidase activity, resistance against Serratia marcescens), and for the life history traits, a

98 the clearance of a bacterial infection with Serratia marcescens, 3 Acps significantly reduced the ba

99 Secretomes from 95% of Serratia marcescens, 71% of Pseudomonas aeruginosa, 29%

100 Serratia marcescens, a member of the carbapenem-resistan

101 Serratia marcescens, a member of the Enterobacteriaceae

102 structure of anthranilate synthase (AS) from Serratia marcescens, a mesophilic bacterium, has been so

103 no known homologues, a homologue of OmpF of Serratia marcescens, and a locus (designated rscBAC) wit

104 revealed eradication of Pseudomonas species, Serratia marcescens, and Enterobacter aerogenes in most

105 trobacter freundii, Yersinia enterocolitica, Serratia marcescens, and Morganella morganii) and two no

106 (Neisseria gonorrhoeae and N. meningitidis), Serratia marcescens, and other gram-negative bacteria ut

107 ve gram-negative bacteria (Escherichia coli, Serratia marcescens, and Pseudomonas aeruginosa).

108 rium tumefaciens, Agrobacterium radiobacter, Serratia marcescens, and Pseudomonas aureofaciens) and f

109 st similar to biotin synthases from E. coli, Serratia marcescens, and Saccharomyces cerevisiae (about

110 inst Burkholderia cepacia, Escherichia coli, Serratia marcescens, and Stenotrophomonas maltophilia is

111 we identify a common fecal enterobacterium, Serratia marcescens, as the causal agent of white pox.

112 ngs were observed with another CGD pathogen, Serratia marcescens, but not with Escherichia coli.

113 of the enterobacteria Klebsiella pneumoniae, Serratia marcescens, Erwinia carotovora, and Proteus vul

114 the enteric bacteria Klebsiella pneumoniae, Serratia marcescens, Erwinia carotovora, and Proteus vul

115 nt algorithms, especially in differentiating Serratia marcescens, Escherichia coli, and Yersinia ente

116 phore secreted by the Gram-negative bacteria Serratia marcescens, extracts heme from host hemoprotein

117 film formation in the opportunistic pathogen Serratia marcescens, mutations in an oxyR homolog and pr

118 that contained group B Streptococcus (GBS), Serratia marcescens, or Escherichia coli before their se

119 is (20%, 3 of 15), and Enterobacter cloacae, Serratia marcescens, Pneumocystis carinii pneumonia, and

120 monas aeruginosa PAO1, Proteus mirabilis and Serratia marcescens, possibly by interfering with their

121 gens (Escherichia coli, Salmonella muenchen, Serratia marcescens, Proteus mirabilis, and Proteus vulg

122 li, Salmonella enterica serovar Typhimurium, Serratia marcescens, Shigella flexneri, Enterobacter aer

123 ebsiella pneumoniae, Pseudomonas aeruginosa, Serratia marcescens, Staphylococcus aureus, and Stenotro

124 caused by ingesting the pathogenic bacteria Serratia marcescens, suggesting that subdued has novel f

125 d the same set of D. melanogaster lines with Serratia marcescens, the bacterium used in the previous

126 coli, Pseudomonas spp., Salmonella enterica, Serratia marcescens, Vibrio vulnificus and Enterobacter

127 t the lipases produced by P. fluorescens and Serratia marcescens, which comprise a second sequence fa

128 e describe the structure of chitinase B from Serratia marcescens, which consists of a catalytic domai

129 FLP analysis except for Escherichia coli and Serratia marcescens, which could not be interdifferentia

130 ana, we isolated the Gram-negative bacterium Serratia marcescens, which is a potent entomopathogen th

131 nce to infection with the bacterial pathogen Serratia marcescens.

132 infection by a Gram-negative entomopathogen, Serratia marcescens.

133 acter freundii group, Enterobacter spp., and Serratia marcescens.

134 em receptors from Pseudomonas aeruginosa and Serratia marcescens.

135 study of the processive chitinase ChiA from Serratia marcescens.

136 ypocrea jecorina and the chitinase ChiA from Serratia marcescens.

137 One example is serratin, isolated from Serratia marcescens.

138 ost resistance test using the live bacterium Serratia marcescens.

139 controls, including Clostridium species and Serratia marcescens.

140 T6SS from the opportunistic human pathogen, Serratia marcescens.

141 y 18 nonprocessive endochitinase, ChiC, from Serratia marcescens.

142 display a TagJ homologue as shown here with Serratia marcescens.

143 restricted to Staphylococcus, Burkholderia, Serratia, Nocardia, and Aspergillus.

144 se structures suggests that the magnesium of Serratia nuclease participates in catalysis via an inner

145 analog for which structural data exist, the Serratia nuclease, indicates several interesting differe

146 On the genus level, FF mice had increased Serratia (P < 0.001) and Lactococcus (P < 0.05) whereas

147 The rhizobacterium Serratia plymuthica A153 produces several bioactive seco

148 irulent bacteriophage (PhiMAM1) that infects Serratia plymuthica was isolated from the natural enviro

149 hin a community dominated by a nearly clonal Serratia population and harboring a lower abundance Ente

150 Enterobacter and Serratia proliferation was impeded in tsetse that lacked

151 transglycosylation (TG) by chitinase D from Serratia proteamaculans (SpChiD).

152 At increasing elastase and Serratia protease concentrations, degradation of the STD

153 ble to protease degradation and suggest that Serratia protease is able to differentiate the GPIb-medi

154 Summary Serratia sp. ATCC 39006 (39006) uses a complex hierarchi

155 proteobacteria, such as the enterobacterium, Serratia sp. ATCC 39006 (S39006).

156 In Serratia sp. ATCC 39006 and the plant pathogen Erwinia c

157 a high-resolution crystal structure for the Serratia sp. ATCC 39006 carbapenem resistance protein Ca

158 Serratia sp. ATCC 39006 produces the carbapenem antibiot

159 Serratia sp. ATCC 39006 produces two secondary metabolit

160 The Gram-negative enterobacterium, Serratia sp. ATCC 39006 synthesizes several secondary me

161 enterobacterium Erwinia (Pectobacterium) and Serratia sp. ATCC 39006, intrinsic resistance to the car

162 every biosynthetic gene in the cluster from Serratia sp. ATCC 39006.

163 A Serratia sp. bacterium manufactures amorphous calcium ph

164 ponsible for prodigiosin biosynthesis in two Serratia sp. In this article we report the creation of i

165 gmented antibiotic, prodigiosin, produced by Serratia sp. is known to involve separate pathways for t

166 This taxonomically ill-defined Serratia sp. produces a carbapenem antibiotic (Car; a be

167 ic activity is essential for cytotoxicity in Serratia sp. SCBI and that its regulation appears to be

168 ion of predicted protease genes in wild-type Serratia sp. SCBI, the highest mRNA levels for the alkal

169 Serratia sp. strain ATCC 39006 produces the red-pigmente

170 ntial for extracellular protease activity in Serratia sp. strain SCBI and to determine what role prot

171 Serratia sp. strain SCBI displays high proteolytic activ

172 host-associated Gammaproteobacteria species (Serratia sp.) that was absent from soil yet observed in

173 living relatives, which include Yersinia and Serratia species (4.6-5.4 Mb).

174 A newly recognized Serratia species, termed South African Caenorhabditis br

175 ified in rates of BSI due to Enterobacter or Serratia species.

176 nal fluid cultures growing Enterobacter spp, Serratia spp, or Citrobacter spp were evaluated using th

177 uginosa (n = 14), Proteus mirabilis (n = 3), Serratia spp. (n = 10), Stenotrophomonas maltophilia (n

178 terococcus spp., Pseudomonas aeruginosa, and Serratia spp. were recovered from infected devices, whil

179 ingle patient isolates of Enterobacter spp., Serratia spp., Citrobacter spp., and Pseudomonas aerugin

180 differentiate Klebsiella, Enterobacter, and Serratia spp., enteric pathogens were identified only by

181 Homologues of the Serratia Ssp and Rap proteins are found encoded together

182 We report a new Serratia strain that produces serratiochelin and an anal

183 R-type regulator, AdmX, apparently unique to Serratia strains.

184 The second phylotype, 'Ca. Serratia symbiotica', resides in bacteriocytes of popula

185 catalytic residue corresponding to Arg57 in Serratia, the structure determined here indicates that A

186 Aspergillus and Serratia were somewhat more common in lower superoxide p