ライフサイエンスコーパス: Shewanella

1 exclusively in marine bacteria of the genus Shewanella.

2 rts have examined EET from marine strains of Shewanella.

3 sual periplasmic fumarate reductase found in Shewanella.

4 st that this strategy is a common feature of Shewanella.

5 ansporting proteins to the outer membrane in Shewanella.

6 In Shewanella algae ACDC, genes encoding these enzymes resi

7 alginolyticus B522, a vigorous swarmer, and Shewanella algae B516, which inhibits V. alginolyticus s

8 The work with recombinant shewasin A from Shewanella amazonensis provided the first documentation

9 The crystal structure of Hda from Shewanella amazonensis SB2B at 1.75 A resolution reveals

10 Phylotypes most closely related to Shewanella and a Chloroflexi strain dominated the Lake C

11 by the dissimilatory iron-reducing bacterium Shewanella and can function as endogenous electron trans

12 ram-negative bacteria including Pseudomonas, Shewanella and Enterobacter.

13 imilatory metal-reducing bacteria, including Shewanella and Geobacter species, can reduce a wide rang

14 tate oxidation coupled to metal reduction in Shewanella and other Gammaproteobacteria.

15 tified the response for different strains of Shewanella and shown that the response correlates with c

16 ed by genome-wide regulon reconstructions in Shewanella and Streptococcus genera and a large-scale pr

17 signal transduction pathway is conserved in Shewanella, and histidine kinase and flagella-mediated m

18 studied in model genera such as Escherichia, Shewanella, and Rhodobacter, although TMAO reductases ar

19 ur genera, including Aeromonas, Pseudomonas, Shewanella, and Sphingopyxis.

20 Here we describe five Shewanella baltica genomes recovered from the same sampl

21 ion and temporal dynamics of a collection of Shewanella baltica strains from the redox transition zon

22 ediction of ArcA-P binding sites not only in Shewanella but also in related bacterial genomes.

23 could support the anaerobic respiration of a Shewanella cell.

24 We propose the use of Shewanella CPS conjugates as a component of an anthrax v

25 ugates induced antibodies that bound to both Shewanella CPS variants by ELISA and to B. anthracis spo

26 Here, we report that both Shewanella CPS variants react with anti-B. anthracis spo

27 to protein conjugates of the two variants of Shewanella CPS.

28 Contrary to anthrose, neither of the Shewanella CPSs is 2-O methylated.

29 AQS), during microbial goethite reduction by Shewanella decolorationis S12, a dissimilatory iron redu

30 udies to shewasin D, the pepsin homolog from Shewanella denitrificans, to gain further insight into t

31 -like protein from the marine proteobactrium Shewanella denitrificans, which exhibits an innate dimer

32 e genes involved in the proposed pathway for Shewanella extracellular electron transfer (EET) are hig

33 Conversely, studies using the Shewanella exudate only, containing biogenic Fe(II), dis

34 appears to be the same as that reported for Shewanella flavocytochrome c treated with fumarate.

35 The electrode also allows coculturing with Shewanella for syntrophic electrogenesis, which grants t

36 Thus, Shewanella frigidimarina (an isolate from Antarctic Sea

37 ction by the soluble fumarate reductase from Shewanella frigidimarina involves hydride transfer from

38 n applied a new comparative approach on five Shewanella genomes that allowed us to systematically ide

39 We performed a bioinformatic analysis of Shewanella genomes to identify S. oneidensis chemotaxis

40 seven newly sequenced and distantly related Shewanella genomes.

41 ybridized to the same array, or by employing Shewanella genomic DNA as a standard reference.

42 mutational hotspots in clades of Vibrio and Shewanella intI genes.

43 The respiratory versatility of Shewanella is attributed in part to a set of c-type cyto

44 hat extracellular respiration of minerals by Shewanella is more complex than originally conceived.

45 ctionation during U(VI) reduction by a novel Shewanella isolate, Shewanella sp. (NR), in batch incuba

46 Approximately 1/3 of Shewanella isolates harbour a prophage at the tmRNA (ssr

47 Using the Pfa PUFA synthase from Shewanella japonica as a model system, we report here th

48 ith which they have the greatest similarity: Shewanella-like (SLP), Rhizobiales-like (RLPH), and ApaH

49 rate that Arabidopsis (Arabidopsis thaliana) Shewanella-like protein phosphatase 2 (AtSLP2) is a bona

50 compared to the homologous Npsr enzyme from Shewanella loihica PV-4 and homologous enzymes known to

51 ive studies involving EET from a fresh water Shewanella microbe (S. oneidensis MR-1) to soluble and i

52 The Shewanella nanowires display a surprising nonlinear elec

53 te that the molecular constituents along the Shewanella nanowires possess an intricate electronic str

54 acteria such as Geobacter sulfurreducens and Shewanella onedensis produce electrical current during t

55 nditions in order to evaluate the ability of Shewanella oneidenisis MR-1 to reduce the former in the

56 and even the strongly electrogenic organism, Shewanella oneidensis (25 muW/cm(2)).

57 Bioelectricity generation, by Shewanella oneidensis (S. oneidensis) MR-1, has become p

58 he ferrous-oxy complexes of human (hIDO) and Shewanella oneidensis (sIDO) indoleamine 2,3-dioxygenase

59 act of dimerization upon the activity of the Shewanella oneidensis (So) bCcP by the preparation of si

60 ases in the versatile respiratory network of Shewanella oneidensis .

61 Previous claims that Shewanella oneidensis also produce conductive pili have

62 uter-membrane deca-heme cytochrome MtrC from Shewanella oneidensis and flavin mononucleotide (FMN in

63 In PIPES buffer at pH 7 with excess H(2), Shewanella oneidensis and Geobacter sulfurreducens both

64 e availability of whole genome sequences for Shewanella oneidensis and Geobacter sulfurreducens has p

65 Microbial (Shewanella oneidensis and Geobacter sulfurreducens) and

66 in Vibrio cholerae, Pseudomonas aeruginosa, Shewanella oneidensis and Methylomicrobium alcaliphilum,

67 In contrast, Shewanella oneidensis and Pseudomonas putida have high i

68 ergy in DNA-protein interactions between the Shewanella oneidensis ArcA two-component transcription f

69 urface power density of 89.4 muW/cm(2) using Shewanella oneidensis as a model biocatalyst without any

70 we applied QENS to study water transport in Shewanella oneidensis at ambient (0.1 MPa) and high (200

71 diffusion and rotational relaxation in live Shewanella oneidensis bacteria at pressures up to 500 MP

72 Shewanella oneidensis bacteria use an abiotic reaction t

73 Here we show that the facultative electrogen Shewanella oneidensis can control metal-catalysed living

74 The facultative anaerobe Shewanella oneidensis can reduce a number of insoluble e

75 ctropotentiometry showed that nitrite-loaded Shewanella oneidensis ccNiR is reduced in a concerted tw

76 genomic expression patterns were examined in Shewanella oneidensis cells exposed to elevated sodium c

77 lla pneumophila, Pseudomonas aeruginosa, and Shewanella oneidensis cells, we study flagellar motor di

78 f energy by Fe(III)-reducing species such as Shewanella oneidensis could potentially control the redo

79 Shewanella oneidensis cytochrome c nitrite reductase (so

80 we show that an H-NOX protein (SO2144) from Shewanella oneidensis directly interacts with the sensor

81 Both standard proteins and a complex Shewanella oneidensis global protein extract were digest

82 ics of the respiratorily versatile bacterium Shewanella oneidensis grown under aerobic, lactate-limit

83 The bacterium Shewanella oneidensis has evolved a sophisticated electr

84 representative multiheme cytochrome STC from Shewanella oneidensis in aqueous solution.

85 crystal structures of the H-NOX protein from Shewanella oneidensis in the unligated, intermediate six

86 Fe(II)-NO complex of the H-NOX protein from Shewanella oneidensis inhibits the autophosphorylation o

87 Shewanella oneidensis interacts with electrodes primaril

88 ulation of sigma(S) in the aquatic bacterium Shewanella oneidensis involves the CrsR-CrsA partner-swi

89 Shewanella oneidensis is a dissimilatory metal reducing

90 Shewanella oneidensis is a metal reducer that uses the c

91 Shewanella oneidensis is known for its ability to respir

92 Shewanella oneidensis is used as a model organism.

93 of the Fe(III)-reducing facultative anaerobe Shewanella oneidensis manipulated under controlled labor

94 alysis of the HexR regulatory network in the Shewanella oneidensis model system.

95 fied a conserved chromosomal gene cluster in Shewanella oneidensis MR-1 (locus tag: SO_1522-SO_1518)

96 nt chromium (Cr(VI)) were investigated using Shewanella oneidensis MR-1 (MR-1) as a biocatalyst and p

97 coli (E. coli) and an electrogenic bacterium Shewanella oneidensis MR-1 (S. oneidensis).

98 ional analysis of the cold shock response of Shewanella oneidensis MR-1 after a temperature downshift

99 physical barrier, the Gram-negative bacteria Shewanella oneidensis MR-1 and Geobacter sulfurreducens

100 AuNP samples was evaluated for the bacterium Shewanella oneidensis MR-1 and is quantitatively correla

101 mical techniques to probe intact biofilms of Shewanella oneidensis MR-1 and Shewanella sp. MR-4 grown

102 r to characterize electron transport between Shewanella oneidensis MR-1 and the metal oxide birnessit

103 mutagenesis in the metal-reducing bacterium Shewanella oneidensis MR-1 and the pathogenic yeast Cand

104 the presence of the iron reducing bacterium Shewanella oneidensis MR-1 are investigated under contro

105 ed the reduction of six-line ferrihydrite by Shewanella oneidensis MR-1 as a model system to demonstr

106 metabolic responses of metabolically active Shewanella oneidensis MR-1 biofilms to U(VI) (uranyl, UO

107 We found that in 12-hour-old Shewanella oneidensis MR-1 biofilms, a reduction in cell

108 ed that detachment of cells from biofilms of Shewanella oneidensis MR-1 can be induced by arresting t

109 In this paper, population-level taxis of Shewanella oneidensis MR-1 cells in the presence of a ra

110 enous method to increase power output from a Shewanella oneidensis MR-1 containing MFC by adding calc

111 kout collection of the electroactive microbe Shewanella oneidensis MR-1 containing representatives fo

112 Shewanella oneidensis MR-1 contains a gene encoding a pu

113 Shewanella oneidensis MR-1 exhibits diverse metal ion-re

114 Shewanella oneidensis MR-1 expresses two distinct types

115 echniques to investigate binding between the Shewanella oneidensis MR-1 extracellular electron transf

116 Anaerobic cultures of Shewanella oneidensis MR-1 grown with nitrate as the sol

117 The decaheme cytochrome MtrC from Shewanella oneidensis MR-1 immobilized on an ITO electro

118 lectron transport chain of the DIR bacterium Shewanella oneidensis MR-1 in Escherichia coli, we showe

119 the extracellular electron transfer chain of Shewanella oneidensis MR-1 into the model microbe Escher

120 Shewanella oneidensis MR-1 is a facultative Fe(III)- and

121 Shewanella oneidensis MR-1 is a facultatively anaerobic

122 Shewanella oneidensis MR-1 is an invaluable host for the

123 We previously reported that Shewanella oneidensis MR-1 is highly sensitive to UVC (2

124 (IR) dose that yields 20% survival (D20) of Shewanella oneidensis MR-1 is lower by factors of 20 and

125 Shewanella oneidensis MR-1 is purported to express outer

126 Shewanella oneidensis MR-1 is quickly becoming a synthet

127 t the dissimilatory metal-reducing bacterium Shewanella oneidensis MR-1 lacks chemotactic responses t

128 Expression from the Shewanella oneidensis MR-1 nnrS gene promoter, cloned in

129 Shewanella oneidensis MR-1 possesses two different stato

130 Shewanella oneidensis MR-1 produced electrically conduct

131 determined that graphene oxide reduction by Shewanella oneidensis MR-1 requires the Mtr respiratory

132 Shewanella oneidensis MR-1 sequentially utilizes lactate

133 cally connect a three-dimensional network of Shewanella oneidensis MR-1 to a gold electrode, thereby

134 whole-genome analyses of DNA methylation in Shewanella oneidensis MR-1 to examine its possible role

135 The molecular response of Shewanella oneidensis MR-1 to variations in extracellula

136 iron) and the common metal-reducing microbe Shewanella oneidensis MR-1 under several endmember condi

137 t use FNR to regulate anaerobic respiration, Shewanella oneidensis MR-1 uses the cyclic AMP receptor

138 nder anaerobic or oxygen-limited conditions, Shewanella oneidensis MR-1 uses the serine-isocitrate ly

139 The gammaproteobacterium Shewanella oneidensis MR-1 utilizes a complex electron t

140 Shewanella oneidensis MR-1 was used as a model bacterial

141 s extracted from the periplasmic fraction of Shewanella oneidensis MR-1 were further identified using

142 the toxicity of AgNPs to a bacterial model (Shewanella oneidensis MR-1) decreases most significantly

143 Shewanella oneidensis MR-1, a gammaproteobacterium with

144 Using Shewanella oneidensis MR-1, an environmentally versatile

145 trometry (MS/MS) to annotate the proteome of Shewanella oneidensis MR-1, an important microbe for bio

146 his study, we used a model organism in MFCs, Shewanella oneidensis MR-1, and (13)C pathway analysis t

147 ssimilatory metal-reducing bacteria, such as Shewanella oneidensis MR-1, as model organisms.

148 echnique, we investigated single colonies of Shewanella oneidensis MR-1, Bacillus subtilis 3610, and

149 networks in the dissimilatory metal reducer Shewanella oneidensis MR-1, global mRNA patterns were ex

150 F and OmcA from the metal-reducing bacterium Shewanella oneidensis MR-1, we show that electron transp

151 507, originally annotated as hypothetical in Shewanella oneidensis MR-1, were suggested to encode nov

152 vestigate extracellular electron transfer in Shewanella oneidensis MR-1, where an array of nanoholes

153 the dissimilatory metal-reducing bacterium, Shewanella oneidensis MR-1, whose electron transport sys

154 an existing genome-scale metabolic model of Shewanella oneidensis MR-1.

155 d biogenic and abiogenic Fe(III) minerals by Shewanella oneidensis MR-1.

156 f the dissimilatory metal-reducing bacterium Shewanella oneidensis MR-1.

157 f the dissimilatory metal-reducing bacterium Shewanella oneidensis MR-1.

158 ectrodes by expressing the cytochrome c from Shewanella oneidensis MR-1.

159 y the dissimilatory metal-reducing bacterium Shewanella oneidensis MR-1.

160 c foundation for carbon source metabolism in Shewanella oneidensis MR-1.

161 with MtrA, a decaheme c-type cytochrome from Shewanella oneidensis MR-1.

162 variations impact biocurrent generation from Shewanella oneidensis MR-1.

163 al membranes and the Gram-negative bacterium Shewanella oneidensis MR-1.

164 anowires in the model metal-reducing microbe Shewanella oneidensis MR-1.

165 l modeling with bioreactor experiments using Shewanella oneidensis MR-1.

166 Two well-known exoelectrogens, Shewanella oneidensis MR1 and Pseudomonas aeruginosa PA0

167 alyze the metabolite composition of streaked Shewanella oneidensis MR1 and Pseudomonas stutzeri RCH2

168 similar resources and manual annotations on Shewanella oneidensis MR1 genome.

169 VI) by the model Fe(III)-reducing bacterium, Shewanella oneidensis MR1, proceeds via a single electro

170 t Crp and Fnr sites, and expression from the Shewanella oneidensis nrfA control region cloned in E. c

171 nipulating the lipopolysaccharide content in Shewanella oneidensis outer membranes, we observed the e

172 tion of this method to the identification of Shewanella oneidensis peptides/proteins exhibiting diffe

173 fferent tryptic peptides from >2000 distinct Shewanella oneidensis proteins ( approximately 40% of th

174 0 unique peptides that covered 1443 distinct Shewanella oneidensis proteins from a 300-ng tryptic dig

175 When applied to a global tryptic digest of Shewanella oneidensis proteins, an order-of-magnitude in

176 tching system of the aquatic Proteobacterium Shewanella oneidensis regulates post-translationally sig

177 ent the first crystal structure of YcjX from Shewanella oneidensis solved at 1.9- angstrom resolution

178 , we measured the rate of U(VI) reduction by Shewanella oneidensis strain MR-1 as function of NaHCO3

179 Shewanella oneidensis strain MR-1 can respire using carb

180 FF (Fl FFF) methodology to separate cells of Shewanella oneidensis strain MR-1 from exopolymers prese

181 The gamma-proteobacterium Shewanella oneidensis strain MR-1 is a metabolically ver

182 The Mtr respiratory pathway of Shewanella oneidensis strain MR-1 is required to effecti

183 Shewanella oneidensis strain MR-1 is well known for its

184 Here, we identify two gene clusters in Shewanella oneidensis strain MR-1 that each contain homo

185 Shewanella oneidensis strain MR-1 utilizes soluble and i

186 of hydrogenotrophic iron-reducing bacteria (Shewanella oneidensis strain MR-1) on the corrosion rate

187 Here, we show that Shewanella oneidensis strain MR-1, a nonfermentative, fa

188 he non-arsenate-respiring Shewanella species Shewanella oneidensis strain MR-1, has pleiotropic effec

189 Compared to a previous whole-cell study with Shewanella oneidensis strain MR-1, our findings suggest

190 n in the Gram negative gamma-proteobacterium Shewanella oneidensis strain MR-1.

191 ated substrates are encoded in the genome of Shewanella oneidensis strain MR-1.

192 ry metal reducing bacteria which include the Shewanella oneidensis strain MR-1.

193 by fibers derived from a distant homolog in Shewanella oneidensis that shares less than 30% identity

194 Performance was evaluated using a Shewanella oneidensis tryptic digest, and approximately

195 a tagged alpha-subunit of RNA polymerase in Shewanella oneidensis under controlled growth conditions

196 nent of the metal reduction (Mtr) pathway of Shewanella oneidensis under the control of an arsenic-se

197 The mineral-respiring bacterium Shewanella oneidensis uses a protein complex, MtrCAB, co

198 The crystal structure of SO1698 protein from Shewanella oneidensis was determined by a SAD method and

199 ransformation experiments in the presence of Shewanella oneidensis were modeled with this exercise re

200 resolution structure of a YiiP homolog from Shewanella oneidensis within a lipid bilayer in the abse

201 Shewanella oneidensis, a metal reducer and facultative a

202 species-specific function, were monitored in Shewanella oneidensis, a metal reducing bacterium, follo

203 e cloned and expressed the MsrBA enzyme from Shewanella oneidensis, a metal-reducing bacterium and fi

204 enomic analysis of the cis-regulatory map of Shewanella oneidensis, an important model organism for b

205 a global proteome extract from the bacteria Shewanella oneidensis, and mouse plasma, as well as (18)

206 -host-range plasmid was poorly maintained in Shewanella oneidensis, but rapidly adapted through mutat

207 In Shewanella oneidensis, H-NOX-mediated NO sensing increas

208 g bioenergy and bioremediation applications, Shewanella oneidensis, in minimal and rich media.

209 estris TDO and a related protein SO4414 from Shewanella oneidensis, including the structure at 1.6-A

210 lla pneumophila, Pseudomonas aeruginosa, and Shewanella oneidensis, providing the first views of inta

211 g three independently derived AMT databases (Shewanella oneidensis, Salmonella typhimurium, Yersinia

212 s, including those from Nostoc sp. PCC 7120, Shewanella oneidensis, Shewanella woodyi, and Clostridiu

213 the growth of the metal-respiring bacterium Shewanella oneidensis, specifically through the reductio

214 ke in the nonmethylating facultative aerobe, Shewanella oneidensis, under both anaerobic and aerobic

215 ranscriptomic studies to characterize Fur in Shewanella oneidensis, with regard to its roles in iron

216 ter for Kdo8N biosynthesis was identified in Shewanella oneidensis.

217 cerevisiae and TyrR-LiuR network in bacteria Shewanella oneidensis.

218 for Escherichia coli, Bacillus subtilis, and Shewanella oneidensis.

219 e a molecular pathway for H-NOX signaling in Shewanella oneidensis.

220 e of the mammalian peptide transporters from Shewanella oneidensis.

221 residue next to the RNase domain of HepT in Shewanella oneidensis.

222 microbes such as Desulfovibrio vulgaris and Shewanella oneidensis.

223 ts were performed in a gamma-proteobacterium Shewanella oneidensis.

224 cherichia coli, Saccharomyces cerevisiae and Shewanella oneidensis.

225 yses of global tryptic digest of the microbe Shewanella oneidensis.

226 Sera produced by immunization with Shewanella or P. syringae cells bound to B. anthracis sp

227 ophile Escherichia coli and the extremophile Shewanella piezotolerans both expanded their growth rang

228 -fermenting Gram-negative species, including Shewanella, Pseudomonas and Acinetobacter.

229 Isolates belonged to five genera, including Shewanella, Pseudomonas, Psychromonas (Gammaproteobacter

230 As numerous bacterial species, Shewanella putrefaciens CN-32 possesses a complete secon

231 emotaxis response toward arsenate (As(V)) by Shewanella putrefaciens CN-32, a model dissimilatory met

232 In experiments with Shewanella putrefaciens CN32 and excess electron donor,

233 oreduction of both U(VI) and clay-Fe(III) by Shewanella putrefaciens CN32 can occur.

234 e(2.74)(SO(4))(2)(OH)(5.22)(H(2)O)(0.78), by Shewanella putrefaciens CN32 using batch experiments und

235 ocrocite was rapidly reduced to magnetite by Shewanella putrefaciens CN32, and over time the magnetit

236 Here we described a novel ArsR from Shewanella putrefaciens selective for MAs(III).

237 Shewanella putrefaciens strain 200 respires a wide range

238 Analysis of the genome sequence of Shewanella putrefaciens strain CN-32 showed that it also

239 Attachment of live cells of Shewanella putrefaciens strain CN-32 to the surface of h

240 K, Geobacter sulfurreducens strain PCA, and Shewanella putrefaciens strain CN-32, and compared it to

241 The biogenic mackinawite produced by Shewanella putrefaciens strain CN32 was characterized by

242 the dissimilatory Fe(III)-reducing bacterium Shewanella putrefaciens strain CN32.

243 arosite (PbFe(3)(SO(4),AsO(4))(2)(OH)(6)) by Shewanella putrefaciens using batch experiments under an

244 avior of the monopolarly flagellated species Shewanella putrefaciens with fluorescently labeled flage

245 gelloides, Vibrio cholerae, Vibrio fischeri, Shewanella putrefaciens, and Pseudomonas aeruginosa.

246 Using the model species Shewanella putrefaciens, we show that FlhG links assembl

247 mes of several Shewanella species, including Shewanella putrefaciens, which is hypothesized to direct

248 o confirm the anti-bacterial activity versus Shewanella putrefaciens.

249 the metabolically versatile marine bacterium Shewanella putrefaciens.

250 transformations in the environmental microbe Shewanella putrefaciens.

251 lis and the Gram-negative, polar-flagellated Shewanella putrefaciens.

252 However, the mechanism of flavin release by Shewanella remains unknown.

253 To obtain a system-level understanding of Shewanella's robustness and versatility, the complex int

254 mily and central to anaerobic respiration in Shewanella sp.

255 VI) reduction by a novel Shewanella isolate, Shewanella sp. (NR), in batch incubations.

256 rite (molar As/Fe: 0.05; Fe tot: 32.1 mM) by Shewanella sp. ANA-3 (10(8) cells/mL) in the presence of

257 and the GalN-6-phosphate deaminase AgaS from Shewanella sp. ANA-3 were validated in vitro using indiv

258 an algicidal exudate (IRI-160AA) produced by Shewanella sp. IRI-160 that is effective against dinofla

259 t biofilms of Shewanella oneidensis MR-1 and Shewanella sp. MR-4 grown by using a poised electrode as

260 and detoxifying (ars) reduction pathways in Shewanella sp. strain ANA-3 are induced by arsenite and

261 acterized the expression and activity of the Shewanella sp. strain ANA-3 arsenate respiratory reducta

262 pression and extracellular respiration using Shewanella sp. strain ANA-3 as a model organism.

263 In Shewanella sp. strain ANA-3, the arsenate respiration ge

264 In Shewanella sp. strain ANA-3, utilization of arsenate as

265 ependent regulator of arr and ars operons in Shewanella sp. strain ANA-3.

266 regulating arsenate respiratory reduction in Shewanella sp. strain ANA-3.

267 der which these two systems are expressed in Shewanella sp. strain ANA-3.

268 ypic characterization of an ackA deletion in Shewanella sp. strain MR-4 and genomic analysis of other

269 system using a lambda Red Beta homolog from Shewanella sp. W3-18-1.

270 is evident from Fe-reducibility assays using Shewanella sp., however was undetectable by chemical ext

271 r of Pediococcus, Halomonas, Escherichia and Shewanella species (P < 0.01).

272 Shewanella species are renowned for their respiratory ve

273 It has been suggested that in Shewanella species electrons cross the outer membrane to

274 Shewanella species grow in widely disparate environments

275 We overexpressed pubC from Shewanella species MR-4 and MR-7 in E. coli.

276 ochrome, which in the non-arsenate-respiring Shewanella species Shewanella oneidensis strain MR-1, ha

277 Other Shewanella species tested accumulated flavins in superna

278 cluster in the sequenced genomes of several Shewanella species, including Shewanella putrefaciens, w

279 In Shewanella species, MtrA, an ~35-kDa periplasmic decahem

280 luble electron transfer mediator produced by Shewanella species.

281 d lldD) in any of the 13 analyzed genomes of Shewanella spp.

282 oducing isolates, Sulfitobacter spp. 376 and Shewanella spp. 79, were transformed with plasmids expre

283 he napD and nrfA operon control regions from Shewanella spp. also have apparent Crp and Fnr sites, an

284 eliable method used for introducing DNA into Shewanella spp. at high efficiency was bacterial conjuga

285 hain of the capsular polysaccharide (CPS) of Shewanella spp. MR-4.

286 the AHLs produced by Sulfitobacter spp. and Shewanella spp. or the bacterial products they regulate

287 n clinical isolates of the emergent pathogen Shewanella spp., to compare their transfer efficiency an

288 s the range of carbon substrates utilized by Shewanella spp., unambiguously identifies several genes

289 We isolated a Shewanella strain capable of oxidizing acetate anaerobic

290 physiological studies of 10 closely related Shewanella strains and species to provide quantitative i

291 Consistent with genomic data, all tested Shewanella strains except S. frigidimarina, which lacked

292 trC copurified with tagged OmcA in wild-type Shewanella, suggesting a direct association.

293 porting extracellular mineral respiration in Shewanella that may extend into other genera of Gram-neg

294 obes by revealing the positive chemotaxis of Shewanella to As(V).

295 mediated energy taxis, is proposed by which Shewanella use riboflavin as both an electron shuttle an

296 egrees C demonstrated that all genera except Shewanella were psychrophiles with optimal growth below

297 All isolates were denitrifiers, except Shewanella, which exhibited the capacity for dissimilato

298 most proteobacteria, including 11 species of Shewanella with completely sequenced genomes.

299 Nostoc sp. PCC 7120, Shewanella oneidensis, Shewanella woodyi, and Clostridium botulinum, indicating

300 diguanylate cyclase functional partners from Shewanella woodyi, we demonstrate that mutation of the c