ライフサイエンスコーパス: Shewanella

1 sual periplasmic fumarate reductase found in Shewanella.

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

3 ansporting proteins to the outer membrane in Shewanella.

4 five different electron transfer pathways in Shewanella.

5 exclusively in marine bacteria of the genus Shewanella.

6 rts have examined EET from marine strains of Shewanella.

7 y mixed with one species not in the library (Shewanella alga BrY), is performed by comparison to the

8 In Shewanella algae ACDC, genes encoding these enzymes resi

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

10 similatory Fe-reducing bacteria of the genus Shewanella algae grown on a ferrihydrite substrate indic

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

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

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

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

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

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

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

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

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

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

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

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

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

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 R402A, R402K, and R402Y mutant forms of the Shewanella enzyme.

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

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

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

36 Thus, Shewanella frigidimarina (an isolate from Antarctic Sea

37 Recent work on the enzyme from Shewanella frigidimarina has strengthened the assignment

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

39 n-induced flavocytochrome c(3), Ifc(3), from Shewanella frigidimarina NCIMB400, derivatized with a 2-

40 cture of the soluble fumarate reductase from Shewanella frigidimarina shows the presence of four, bis

41 ion of the H61M and H61A mutant forms of the Shewanella fumarate reductase.

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

43 seven newly sequenced and distantly related Shewanella genomes.

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

45 Fe(III)-reducing microorganisms in the genus Shewanella have resolved this problem by releasing solub

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

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

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

49 Shewanella isolates produced much less acetone.

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

51 We identified the first Shewanella lambda-like phage, providing a potential tool

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

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

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

55 capsulatus dimethyl sulfoxide reductase, and Shewanella massilia trimethylamine N-oxide reductase as

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

57 The Shewanella nanowires display a surprising nonlinear elec

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

59 orces that characterize interactions between Shewanella oneidensis (a dissimilatory metal-reducing ba

60 found in the unannotated genome sequence of Shewanella oneidensis (formerly S. putrefaciens) MR-1.

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

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

63 ases in the versatile respiratory network of Shewanella oneidensis .

64 Previous claims that Shewanella oneidensis also produce conductive pili have

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

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

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

68 Microbial (Shewanella oneidensis and Geobacter sulfurreducens) and

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

70 the acnD and prpF genes from two organisms, Shewanella oneidensis and Vibrio cholerae, and found tha

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

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

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

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

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

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

77 Shewanella oneidensis cytochrome c nitrite reductase (so

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

79 the effect of an insertional mutation in the Shewanella oneidensis etrA (electron transport regulator

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

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

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

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

84 Shewanella oneidensis interacts with electrodes primaril

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

86 Shewanella oneidensis is a metal reducer that can use se

87 Shewanella oneidensis is a metal reducer that uses the c

88 Shewanella oneidensis is an important model organism for

89 Shewanella oneidensis is an important model organism for

90 Shewanella oneidensis is known for its ability to respir

91 Shewanella oneidensis is used as a model organism.

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

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

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

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

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

97 PCR primers specific to individual ORFs from Shewanella oneidensis MR-1 and Deinococcus radiodurans R

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

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

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

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

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

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

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

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

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

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

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

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

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

111 Shewanella oneidensis MR-1 expresses two distinct types

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

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

114 lability of the complete genome sequence for Shewanella oneidensis MR-1 has permitted a comprehensive

115 The tetraheme c-type cytochrome, CymA, from Shewanella oneidensis MR-1 has previously been shown to

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

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

118 ure of the small tetraheme cytochrome c from Shewanella oneidensis MR-1 in two crystal forms and two

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

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

124 Shewanella oneidensis MR-1 is purported to express outer

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

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

127 Shewanella oneidensis MR-1 possesses two different stato

128 Shewanella oneidensis MR-1 produced electrically conduct

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

130 Shewanella oneidensis MR-1 sequentially utilizes lactate

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

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

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

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

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

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

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

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

139 Shewanella oneidensis MR-1, a gammaproteobacterium with

140 Using Shewanella oneidensis MR-1, an environmentally versatile

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

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

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

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

145 507, originally annotated as hypothetical in Shewanella oneidensis MR-1, were suggested to encode nov

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

165 0 unique peptides that covered 1443 distinct Shewanella oneidensis proteins from a 300-ng tryptic dig

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

167 platform is demonstrated for the analysis of Shewanella oneidensis proteome, which has considerable i

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

169 we provide genetic evidence that AQDS enters Shewanella oneidensis strain MR-1 and causes cell death

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

171 Shewanella oneidensis strain MR-1 can respire using carb

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

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

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

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

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

177 Shewanella oneidensis strain MR-1 utilizes soluble and i

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

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

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

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

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

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

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

185 rved physiological and metabolic activity of Shewanella oneidensis strain MR1 and Escherichia coli st

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

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

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

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

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

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

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

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

194 ied by MS/MS from a different microorganism (Shewanella oneidensis).

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

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

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

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

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

200 hanococcus jannaschii, Pyro coccus furiosus, Shewanella oneidensis, Escherichia coli and Deinococcus

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

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

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

204 rrays constructed with full length ORFs from Shewanella oneidensis, MR-1, were hybridized with genomi

205 ntly supports 10 organisms (Vibrio cholerae, Shewanella oneidensis, Saccharomyces cerevisiae, Schizos

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

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

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

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

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

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

212 e of the mammalian peptide transporters from Shewanella oneidensis.

213 microbes such as Desulfovibrio vulgaris and Shewanella oneidensis.

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

215 cherichia coli, Saccharomyces cerevisiae and Shewanella oneidensis.

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

217 ter for Kdo8N biosynthesis was identified in Shewanella oneidensis.

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

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

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

221 The genus Shewanella produces a unique small tetraheme cytochrome

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

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

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

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

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

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

228 Shewanella putrefaciens is a facultative anaerobe that c

229 Shewanella putrefaciens is a facultative anaerobe that u

230 Shewanella putrefaciens MR-1 has emerged as a good model

231 Shewanella putrefaciens MR-1 possesses a complex electro

232 In contrast, Shewanella putrefaciens organisms (Gilardi biovars 1 and

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

234 Shewanella putrefaciens strain 200 respires a wide range

235 Shewanella putrefaciens strain 200 respires anaerobicall

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

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

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

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

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

241 plore this process, we identified mutants in Shewanella putrefaciens that are unable to respire on hu

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

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

244 Two Tn5-generated mutants of Shewanella putrefaciens with insertions in menD and menB

245 were found in genomes of Xylella fastidiosa, Shewanella putrefaciens, and P. gingivalis.

246 g poorly, in contrast to hybridizations with Shewanella putrefaciens, formerly considered to be the s

247 ii, Legionella pneumophila, Vibrio cholerae, Shewanella putrefaciens, Sinorhizobium meliloti, and Cau

248 ycoplasma genitalium, Mycoplasma pneumoniae, Shewanella putrefaciens, Synechocystis sp., Deinococcus

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

250 the metabolically versatile marine bacterium Shewanella putrefaciens.

251 transformations in the environmental microbe Shewanella putrefaciens.

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

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

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

255 c domain of soluble fumarate reductases from Shewanella sp.

256 mily and central to anaerobic respiration in Shewanella sp.

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

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

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

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

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

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

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

264 nate respiratory reduction) in the bacterium Shewanella sp. strain ANA-3 specifically confers respira

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

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

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

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

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

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

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

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

273 hybridized with genomic DNA from nine other Shewanella species and Escherichia coli K-12.

274 Shewanella species are renowned for their respiratory ve

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

276 Shewanella species grow in widely disparate environments

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

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

279 Other Shewanella species tested accumulated flavins in superna

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

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

282 y conserved among other known metal-reducing Shewanella species.

283 luble electron transfer mediator produced by Shewanella species.

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

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

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

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

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

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

290 We isolated a Shewanella strain capable of oxidizing acetate anaerobic

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

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

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

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

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