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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

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