ライフサイエンスコーパス: Pseudomonas putida

1 6S rRNA from whole human blood infected with Pseudomonas putida .

2 BPA) in the naphthalene catabolic pathway of Pseudomonas putida.

3 -component camphor-hydroxylating system from Pseudomonas putida.

4 e), an enzyme cancer therapeutic cloned from Pseudomonas putida.

5 r in the first step of camphor catabolism by Pseudomonas putida.

6 n Escherichia coli was the donor compared to Pseudomonas putida.

7 heme monooxygenase cytochrome P450(cam) from Pseudomonas putida.

8 sa were compared with planktonic cultures of Pseudomonas putida.

9 ine alpha,gamma-lyase (MET) gene cloned from Pseudomonas putida.

10 are similar to those of the same enzyme from Pseudomonas putida.

11 olite repression control has been studied in Pseudomonas putida.

12 to acid dehydrogenase multienzyme complex of Pseudomonas putida.

13 rom strain mt-2 of the purple soil bacterium Pseudomonas putida.

14 e biosynthesis in Pseudomonas aeruginosa and Pseudomonas putida.

15 t putidaredoxin/putidaredoxin reductase from Pseudomonas putida.

16 r to the 12-kDa FD of gamma-purple bacterium Pseudomonas putida.

17 nal activator of the inducible bkd operon of Pseudomonas putida.

18 cloned and expressed in Escherichia coli and Pseudomonas putida.

19 s bacterial members, primarily P-450cam from Pseudomonas putida.

20 nzyme have been obtained from rat kidney and Pseudomonas putida.

21 rved in various P. aeruginosa strains and in Pseudomonas putida.

22 ate auxotroph of the platform soil bacterium Pseudomonas putida.

23 l, a sustainable aviation fuel precursor, in Pseudomonas putida.

24 is are implemented in the platform bacterium Pseudomonas putida.

25 ly describe the dynamics of Cd(II) uptake by Pseudomonas putida.

26 the organism was initially misidentified as Pseudomonas putida.

27 swimming trajectories of the soil bacterium Pseudomonas putida.

28 ive analysis of the three CheR paralogues of Pseudomonas putida.

29 advantage in growth competition assays with Pseudomonas putida.

30 s 0.7%, p = 0.010), but a lower abundance of Pseudomonas putida (0.5% versus 0.8%, p = 0.020), compar

31 xy-4-oxoquinoline 2,4-dioxygenase (QDO) from Pseudomonas putida 33/1 are homologous cofactor-independ

32 Pseudomonas putida, a bacterium that colonizes plant roo

33 The muconate lactonizing enzyme (MLE) from Pseudomonas putida, a member of a family that catalyzes

34 (S)-Mandelate dehydrogenase (MDH) from Pseudomonas putida, a member of the flavin mononucleotid

35 (S)-Mandelate dehydrogenase from Pseudomonas putida, a member of the flavin mononucleotid

36 tiomics investigation of these mechanisms in Pseudomonas putida, a versatile soil bacterium of the Ga

37 hly conserved in diverse bacteria, including Pseudomonas putida, Acinetobacter calcoaceticus, Agrobac

38 In the presence of copper, Pseudomonas putida activates transcription of cinAQ via

39 in Escherichia coli, Pseudomonas aeruginosa, Pseudomonas putida, Agrobacterium tumefaciens, and Acine

40 r these reactions, alkane monooxygenase from Pseudomonas putida (alkB) is able to catalyze the diffic

41 (S)-Mandelate dehydrogenase from Pseudomonas putida, an FMN-dependent alpha-hydroxy acid

42 educed from crystal structures of PcaHG from Pseudomonas putida and Acinetobacter sp. as well as of r

43 egion encoding this protein can replicate in Pseudomonas putida and E. coli.

44 tudy, we cloned the L-methioninase gene from Pseudomonas putida and isolated pure and abundant recomb

45 We introduce a "sender device" in Pseudomonas putida and Klebsiella pneumoniae, that produ

46 avoenzyme mandelate dehydrogenase (MDH) from Pseudomonas putida and of the substrate-reduced enzyme h

47 tprinting) over the course of growth of both Pseudomonas putida and P. aeruginosa, and compared the w

48 eracts with the DnaB replicative helicase of Pseudomonas putida and Pseudomonas aeruginosa and initia

49 milar to head morphogenesis genes encoded by Pseudomonas putida and Pseudomonas aeruginosa bacterioph

50 encoding the replicative helicase, DnaB, of Pseudomonas putida and Pseudomonas aeruginosa were isola

51 similarity with two sequenced pseudomonads, Pseudomonas putida and Pseudomonas aeruginosa, yet revea

52 teins of similar size in crude extracts from Pseudomonas putida and Pseudomonas fluorescens, suggesti

53 spergillus pseudoterreus, Aspergillus niger, Pseudomonas putida and Rhodosporidium toruloides.

54 l beneficial interaction between a strain of Pseudomonas putida and the fungus Saccharomyces cerevisi

55 ylhomocysteine hydrolase (rSAHH) cloned from Pseudomonas putida and Trichomonas vaginalis, respective

56 hromosome, including Pseudomonas aeruginosa, Pseudomonas putida and Yersinia pestis, and in the prese

57 rated into chemical sensor circuits in soil (Pseudomonas putida) and aquatic (Rubrivivax gelatinosus)

58 Biofilms with protein-based (Pseudomonas putida) and polysaccharide based EPS (Pseudo

59 n soil bacteria, Pseudomonas fluorescens and Pseudomonas putida, and a mercury resistance (Hg(R)) pla

60 degradation such as Comamonas testosteroni, Pseudomonas putida, and Ochrobactrum anthropi were selec

61 hat the DnaA proteins from Escherichia coli, Pseudomonas putida, and Pseudomonas aeruginosa bind to t

62 s) has been generated from Escherichia coli, Pseudomonas putida, and Ralstonia eutropha.

63 gellar synthesis in Vibrio parahaemolyticus, Pseudomonas putida, and Shewanella putrefaciens, and it

64 pproaches were employed for EPS removal from Pseudomonas putida, and the measured sulfhydryl concentr

65 CjrB was homologous to the TonB protein from Pseudomonas putida; and CjrC was homologous to a putativ

66 myxobacterium, Cystobacter ferrugineus, with Pseudomonas putida as prey, we observed surviving phenot

67 es of the mandelate metabolic pathway permit Pseudomonas putida ATCC 12633 to utilize either or both

68 When Pseudomonas putida ATCC 39167 and plant-deleterious Pseu

69 Pseudomonas sp. 1A, Arthrobacter sp. JS443, Pseudomonas putida B2) in the pH range 6.1-8.6 with rest

70 and 4-chlorocatechol) was developed based on Pseudomonas putida bacteria harboring the plasmid pSMM50

71 a, Escherichia coli, Salmonella enterica and Pseudomonas putida, based on single nucleotide differenc

72 (S)-Mandelate dehydrogenase from Pseudomonas putida belongs to a FMN-dependent enzyme fam

73 In Pseudomonas putida, benzoate and 3-chlorobenzoate are co

74 In Pseudomonas putida biofilms, nutrient starvation trigger

75 Here, exoproteomic analysis of Pseudomonas putida BIRD-1 (BIRD-1), Pseudomonas fluoresc

76 Pseudomonas putida bloodstream infections were reported

77 The rhizobacterium Pseudomonas putida BTP1 stimulates induced systemic resi

78 was sufficient for autonomous replication in Pseudomonas putida but not in Escherichia coli.

79 ulation of roots with a biocontrol strain of Pseudomonas putida, but not with a siderophore-deficient

80 of the plant-associated terrestrial microbe Pseudomonas putida by Manuel Espinosa-Urgel's group that

81 Delta(5)-3-ketosteroid isomerase from Pseudomonas putida catalyzes a C-H bond cleavage and for

82 Glucarate dehydratase (GlucD) from Pseudomonas putida catalyzes the dehydration of both (D)

83 The caffeine degradation pathway of Pseudomonas putida CBB5 utilizes an unprecedented glutat

84 Pseudomonas putida CBB5 was isolated from soil by enrich

85 Some bacteria, such as Pseudomonas putida CBB5, utilize caffeine as a sole carb

86 Pseudomonas putida CBB5, which grows on several purine a

87 ned the crystal structure of the prokaryotic Pseudomonas putida CMLE (PpCMLE) at 2.6 A resolution.

88 The P450cam monooxygenase from Pseudomonas putida consists of three redox proteins: NAD

89 hrome p-cresol methylhydroxylase (PCMH) from Pseudomonas putida contains FAD covalently attached to T

90 Pseudomonas putida converts benzoate to catechol using t

91 the E. coli, Mycobacterium tuberculosis and Pseudomonas putida CRPs are considered in the context of

92 porters in Pseudomonas aeruginosa and six in Pseudomonas putida, different transporters were predicte

93 Here, we performed a transposon screen of Pseudomonas putida DSM 3601 to identify genes necessary

94 reading frames, three of them homologous to Pseudomonas putida, E. coli, and Haemophilus influenzae

95 Yarrowia lipolytica or indigoidine-producing Pseudomonas putida) encapsulated in calcium-alginate hyd

96 The catBCA operon of Pseudomonas putida encodes enzymes involved in the catab

97 a acetivorans, Sulfolobus acidocaldarius and Pseudomonas putida) enriched in (13) C, (15) N, (18) O,

98 monoaromatic hydrocarbons such as toluene in Pseudomonas putida F1 (PpF1) occurs via lateral diffusio

99 . coli K-12) in mixtures with soil bacteria (Pseudomonas putida F1 and Bacillus subtilis 168).

100 C 33694, Pantoea agglomerans ATCC 33243, and Pseudomonas putida F1 are collected and form a reference

101 addition to these two routes, we report that Pseudomonas putida F1 beta-ketoacyl-ACP synthase I (FabB

102 Toluene dioxygenase from Pseudomonas putida F1 has been studied extensively with

103 genase component of toluene dioxygenase from Pseudomonas putida F1 is an iron-sulfur protein (ISP(TOL

104 Exposure of Pseudomonas putida F1 to 0.1, 1.0, and 5.0 g/L of nZVI c

105 Pseudomonas putida F1 utilizes p-cumate (p-isopropylbenz

106 Pseudomonas putida F1 utilizes p-cymene (p-isopropyltolu

107 e toluene cis-dihydrodiol dehydrogenase from Pseudomonas putida F1 was used to produce enantiomerical

108 l structure of Pput2725 from the biodegrader Pseudomonas putida F1, a COG4313 channel of unknown func

109 al regulation in the solvent-tolerant strain Pseudomonas putida F1.

110 abolic pathway serve as chemoattractants for Pseudomonas putida F1.

111 ods on the aerobic degradation of toluene by Pseudomonas putida F1.

112 ay crystal structure of an OprB channel from Pseudomonas putida F1.

113 hysiological changes of the plant saprophyte Pseudomonas putida following 6 h of attachment to a sili

114 Here, we engineer Pseudomonas putida for high-yield production of the tric

115 driven, growth-coupled selection strategy in Pseudomonas putida for isoprenol, a potential aviation f

116 Naphthalene-degrading Pseudomonas putida G7 cells were exposed to glucose, sal

117 n-cell-size limit, in the presence of motile Pseudomonas putida G7 cells.

118 Pseudomonas putida G7 exhibits chemotaxis to naphthalene

119 achment, and transport of the soil bacterium Pseudomonas putida G7 in saturated porous media.

120 G7, which is chemotactic to naphthalene, and Pseudomonas putida G7 Y1, a nonchemotactic mutant strain

121 ding bacteria Mycobacterium gilvum VM552 and Pseudomonas putida G7, acting as representative nonflage

122 A 10 mL pulse of Pseudomonas putida G7, which is chemotactic to naphthale

123 r similar to that of NahR-regulated genes in Pseudomonas putida G7.

124 ator of the naphthalene degradation genes in Pseudomonas putida G7.

125 to Escherichia coli and to a PhaC- mutant of Pseudomonas putida gave a Pha+ phenotype in both strains

126 es produced by the biofilm-forming bacterium Pseudomonas putida GB-1 and the white-rot fungus Coprine

127 e extent and rate of Mn biomineralization by Pseudomonas putida GB-1 in an optically transparent two-

128 coding for MnxG and McoA, two Mn oxidases in Pseudomonas putida GB-1, in response to varying Mn(II) c

129 I) (Mn(II)), mediated by the obligate aerobe Pseudomonas putida GB-1, was tested in a column of quart

130 n and oxidation of the Mn-oxidizing bacteria Pseudomonas putida GB-1.

131 structure of (D)-glucarate dehydratase from Pseudomonas putida (GlucD) has been solved at 2.3 A reso

132 the structure of a domain-swapped dimer but Pseudomonas putida glyoxalase I has been reported to be

133 nes to the active sites of human, yeast, and Pseudomonas putida glyoxalase I, as the log K(i) values

134 cteria-Bacillus subtilis (Gram-positive) and Pseudomonas putida (Gram-negative)-to produce double-str

135 Here we show that Pseudomonas putida graTA-encoded antitoxin GraA and toxi

136 The Pseudomonas putida group in the Gammaproteobacteria has

137 wth rate predictions of Escherichia coli and Pseudomonas putida grown in different media and with phe

138 able in Stenotrophomonas maltophilia P21 and Pseudomonas putida H2.

139 (S)-mandelate dehydrogenase (MDH-GOX2) from Pseudomonas putida has been determined at 2.15 A resolut

140 combinant methioninase (rMETase) cloned from Pseudomonas putida has been found previously to be an ef

141 tochrome P450cam (CYP101) from the bacterium Pseudomonas putida has been investigated by high-resolut

142 T medium on catabolite repression control in Pseudomonas putida has been investigated using the bkd o

143 Pseudomonas putida has two chromosomally encoded arsH ge

144 of the cytochrome P450cam monooxygenase from Pseudomonas putida, has been determined to 1.90 A resolu

145 the third enzyme in the mandelate pathway of Pseudomonas putida, has been solved by multiple isomorph

146 ), from the camphor hydroxylation pathway of Pseudomonas putida have been investigated as a function

147 In contrast, Shewanella oneidensis and Pseudomonas putida have high iron but low intracellular

148 cytochrome P450cam monooxygenase system from Pseudomonas putida, have been studied.

149 identifications were Pseudomonas fluorescens-Pseudomonas putida (i.e., the strain was either P. fluor

150 Unsaturated biofilms of Pseudomonas putida, i.e., biofilms grown in humid air, w

151 ases, designated xenobiotic reductases, from Pseudomonas putida II-B and P. fluorescens I-C that remo

152 from NG-contaminated soil and identified as Pseudomonas putida II-B and P. fluorescens I-C.

153 , voltage (LOV) photoreceptor PpSB1-LOV from Pseudomonas putida in both the dark and light states.

154 ity, we solved crystal structures of MurU of Pseudomonas putida in native and ligand-bound states at

155 a missing step in the D-lysine catabolism of Pseudomonas putida in which 2OA is converted to D-2-hydr

156 cterial strains (Pseudomonas fluorescens and Pseudomonas putida) into laboratory microcosms inoculate

157 (S)-Mandelate dehydrogenase (MDH) from Pseudomonas putida is a flavin mononucleotide (FMN)-depe

158 (S)-Mandelate dehydrogenase from Pseudomonas putida is a member of a FMN-dependent enzyme

159 Benzaldehyde lyase (BAL) from Pseudomonas putida is a thiamin diphosphate (ThDP)-depen

160 Degradation of protocatechuate in Pseudomonas putida is accomplished by the products of th

161 (S)-Mandelate dehydrogenase from Pseudomonas putida is an FMN-dependent alpha-hydroxy aci

162 The soil bacterium Pseudomonas putida is capable of degrading many aromatic

163 hrome p-cresol methylhydroxylase (PCMH) from Pseudomonas putida is composed of a flavoprotein homodim

164 otocatechuate 3,4-dioxygenase (3,4-PCD) from Pseudomonas putida is ligated axially by Tyr447 and His4

165 e aromatic acid 4-hydroxybenzoate (4-HBA) by Pseudomonas putida is mediated by PcaK, a membrane-bound

166 ChrR of Pseudomonas putida is one such enzyme that has also been

167 P450cam from Pseudomonas putida is the best characterized member of t

168 Cytochrome P450cam (CYP101) from Pseudomonas putida is unusual among P450 enzymes in that

169 component of the beta-ketoadipate pathway of Pseudomonas putida, is a member of a family of related e

170 ing the only GGDEF/EAL response regulator in Pseudomonas putida, is transcriptionally regulated by Rp

171 temperature" X-ray crystallography data for Pseudomonas putida ketosteroid isomerase (KSI), and we o

172 fects on the deposition of bacterial strains Pseudomonas putida KT2440 and Pseudomonas fluorescens LP

173 The two As resistance arsRBC operons of Pseudomonas putida KT2440 are followed by a downstream g

174 Here, we investigate Pseudomonas putida KT2440 during processing of the sugar

175 this report we demonstrate that a strain of Pseudomonas putida KT2440 endowed with chromosomal expre

176 er II McpS chemotaxis receptor (McpS-LBR) of Pseudomonas putida KT2440 in complex with different chem

177 In this study, Pseudomonas putida KT2440 is engineered to convert gluco

178 The soil bacterium Pseudomonas putida KT2440 lacks a functional Embden-Meye

179 In the presence of copper, Pseudomonas putida KT2440 produces the CinA and CinQ pro

180 ,cis-muconic acid in an engineered strain of Pseudomonas putida KT2440 that conducts aromatic O-demet

181 of the biotechnologically relevant bacterium Pseudomonas putida KT2440 that greatly expands computabl

182 odel soil- and rhizosphere-dwelling organism Pseudomonas putida KT2440 to elaborate on the genomics a

183 , metabolomics, fluxomics, and proteomics in Pseudomonas putida KT2440 to investigate the constitutiv

184 y unidentified ability of the soil bacterium Pseudomonas putida KT2440 to synthesize nanoparticles of

185 Here, Pseudomonas putida KT2440 was engineered to convert mixe

186 mplete genome sequence of the soil bacterium Pseudomonas putida KT2440 was published in 2002 (Nelson

187 When non plasmid-harboring cells of Pseudomonas putida KT2440 were spiked with different dil

188 we demonstrate in vivo syringol turnover in Pseudomonas putida KT2440 with the GcoA-F169A variant.

189 of BXs on the interaction between maize and Pseudomonas putida KT2440, a competitive coloniser of th

190 oduct indigoidine, a sustainable pigment, in Pseudomonas putida KT2440, an emerging industrial microb

191 eudomonas syringae pv. tomato strain DC3000, Pseudomonas putida KT2440, and Agrobacterium tumefaciens

192 ures of various bacterial species, including Pseudomonas putida KT2440, Enterococcus faecalis ATCC 29

193 nd PP_3287) from a single bacterial species, Pseudomonas putida KT2440, have been analyzed.

194 GMP levels in the plant-beneficial bacterium Pseudomonas putida KT2440, identifying L-arginine as the

195 Across the three species investigated (Pseudomonas putida KT2440, Pseudomonas protegens Pf-5, a

196 oteome of three aromatic-catabolic bacteria: Pseudomonas putida KT2440, Rhodoccocus jostii RHA1, and

197 dhesion behaviors of five bacterial species, Pseudomonas putida KT2440, Salmonella Typhimurium ATCC 1

198 se a natural aromatic-catabolizing organism, Pseudomonas putida KT2440, to demonstrate that these aro

199 eudomonas strains, including E. coli K12 and Pseudomonas putida KT2440.

200 bolic basis of ethylene glycol metabolism in Pseudomonas putida KT2440.

201 en-gene operon that enables LA catabolism in Pseudomonas putida KT2440.

202 us irregularis and the rhizobacterial strain Pseudomonas putida KT2440.

203 ng LysR-type transcriptional regulators from Pseudomonas putida KT2440.

204 lysis of a promiscuous alanine racemase from Pseudomonas putida (KT2440) was coupled with that of PAM

205 n structures of mandelate racemase (MR) from Pseudomonas putida, Lys 166 and His 297 are positioned a

206 iscovered enzyme in the mandelate pathway of Pseudomonas putida, mandelamide hydrolase (MAH), catalyz

207 sferases yeast flavocytochrome b2 (FCB2) and Pseudomonas putida mandelate dehydrogenase (MDH).

208 ase (yjhG), a 2-keto acid decarboxylase from Pseudomonas putida (mdlC) and native E. coli aldehyde re

209 Immobilized dye-decolorizing peroxidase from Pseudomonas putida MET94 (PpDyP) and three variants gene

210 i harboring the pGFP plasmid and a strain of Pseudomonas putida modified with a Tn5 derivative, Tn5GF

211 Pseudomonas putida MPE exemplifies a novel clade of mang

212 Here, we report that the Pseudomonas putida MPE protein is a manganese-dependent

213 benzoate 1,2-dioxygenase system (BZDOS) from Pseudomonas putida mt-2 catalyzes the NADH-dependent oxi

214 al regulator XylR of the TOL plasmid pWW0 of Pseudomonas putida mt-2 for biodegradation of m-xylene w

215 4-OD) and vinylpyruvate hydratase (VPH) from Pseudomonas putida mt-2 form a complex that converts 2-o

216 4-OT, from Pseudomonas putida mt-2, catalyzes the conversion of 2-o

217 4-OT, a homohexamer from Pseudomonas putida mt-2, is the most extensively studied

218 luene-xylene TOL catabolic plasmid pWW0 from Pseudomonas putida mt-2.

219 homology with hypothetical polypeptides from Pseudomonas putida, Mycobacterium tuberculosis, Ricketts

220 on of naphthalene and 2-methylnaphthalene by Pseudomonas putida NCIB 9816 and Pseudomonas fluorescens

221 identity with the corresponding subunits in Pseudomonas putida NCIB 9816-4, for which the tertiary s

222 gn we offer a nicotine-degrading enzyme from Pseudomonas putida, NicA2, a flavin-containing protein.

223 Nitrile hydratase from Pseudomonas putida NRRL-18668 has been purified and char

224 d load the DnaB helicase of P. aeruginosa or Pseudomonas putida onto the RK2 origin in vitro and did

225 in the enzymes from Pseudomonas fluorescens, Pseudomonas putida or Azotobacter vinelandii.

226 oacetate and 2-phosphonopropionate by either Pseudomonas putida or Escherichia coli cells.

227 to detect the known TonB homologs of either Pseudomonas putida or Haemophilus influenzae but did ide

228 Two different binding sites for Pseudomonas putida PcaR differ from the consensus in onl

229 two different willow clones and a grass with Pseudomonas putida PD1 was found to promote root and sho

230 We report a novel Pseudomonas putida phage, MiCath, which is the first kno

231 tKSI) and approximately 10(3) M for KSI from Pseudomonas putida (pKSI).

232 The root-colonizing pseudomonad Pseudomonas putida (Pp) appears to produce two subunits,

233 Genes from Pseudomonas putida (Pp), sodA, encoding manganese-supero

234 he major CatA from a root-colonizing isolate Pseudomonas putida (Pp), was cloned by complementation i

235 Benzoylformate decarboxylase from Pseudomonas putida (PpBFDC) is a thiamin diphosphate-dep

236 describe a beta-ketoacyl-ACP reductase from Pseudomonas putida (PpFabG4) with an unusual selectivity

237 shells of the Co-type nitrile hydratase from Pseudomonas putida (ppNHase) that may be important for c

238 rystal structure of the anaerobic complex of Pseudomonas putida protocatechuate 3,4-dioxygenase (3,4-

239 P450cam-dependent monooxygenase system from Pseudomonas putida, putidaredoxin (Pdx) shuttles electro

240 ate (PHA) production in Escherichia coli and Pseudomonas putida, respectively.

241 an ABC transporter homologous to proteins in Pseudomonas putida responsible for the extrusion of orga

242 nscriptional start site of the bkd operon of Pseudomonas putida revealed that the transcriptional sta

243 ity) to the sigma(54) protein encoded by the Pseudomonas putida rpoN gene.

244 Previously, an efficient D-xylose utilizing Pseudomonas putida S12 strain was obtained by introducin

245 tida KT2440, Pseudomonas protegens Pf-5, and Pseudomonas putida S12), siderophore secretion is higher

246 rene catabolic and detoxification pathway of Pseudomonas putida S12.

247 The soil-dwelling bacterium Pseudomonas putida S16 can survive on nicotine as its so

248 N-independent activity of NicA2 to growth of Pseudomonas putida S16.

249 to Escherichia coli: Pseudomonas aeruginosa, Pseudomonas putida, Salmonella enterica serovar Typhimur

250 genetically distant hosts: Escherichia coli, Pseudomonas putida, Sphingobium japonicum, and Cupriavid

251 The environmental isolate Pseudomonas putida SQ1 is also able to use SQ for growth

252 nella enteritidis, Enterobacter agglomerans, Pseudomonas putida, Staphylococcus aureus, and Bacillus

253 uctase (MerA) extracted from an Hg-resistant Pseudomonas putida strain FB1.

254 Here we show that the plant root colonizer Pseudomonas putida strain IsoF is able to kill a wide ra

255 g the extent to which alginate production by Pseudomonas putida strain mt-2 and by other fluorescent

256 Pseudomonas putida strain mt-2 unsaturated biofilm forma

257 Pseudomonas putida strain PP3 produces two hydrolytic de

258 tative capillary assay and demonstrated that Pseudomonas putida strains F1 and PRS2000 were attracted

259 The consortium involves two Pseudomonas putida strains, specializing in terephthalic

260 nd three hosts, two Escherichia coli and one Pseudomonas putida strains.

261 lobacter crescentus, Pseudomonas aeruginosa, Pseudomonas putida, Streptomyces coelicolor, and chromos

262 Engineered strains of Pseudomonas putida support biological funneling of the o

263 Putidaredoxin of the CYP101A1 system from Pseudomonas putida supports substrate oxidation by CYP19

264 ensis TCA20, Pseudomonas palleroniana TCA16, Pseudomonas putida TCA23 and N7, and Pseudomonas stutzer

265 e use of mini-Tn5-'phoA to identify genes in Pseudomonas putida that are matric water stress controll

266 nabaena PCC 7120, Pseudomonas aeruginosa and Pseudomonas putida that bind multiple zinc ions with hig

267 rocatechol are central catabolic pathways of Pseudomonas putida that convert aromatic and chloroaroma

268 rocatechol are central catabolic pathways of Pseudomonas putida that convert aromatic and chloroaroma

269 a transporter and chemoreceptor protein from Pseudomonas putida that is encoded as part of the beta-k

270 ansmembrane portion of PcaK, a permease from Pseudomonas putida that transports 4-hydroxybenzoate (4-

271 In the camphor monooxygenase system from Pseudomonas putida, the [2Fe-2S]-containing putidaredoxi

272 Although cytochrome P450cam from Pseudomonas putida, the archetype for all heme monooxyge

273 In Pseudomonas putida, the plasmid-borne clcABD operon enco

274 olution of the model environmental bacterium Pseudomonas putida to ask whether bacteria respond diffe

275 port the directed evolution of the P450 from Pseudomonas putida to create mutants that hydroxylate na

276 uct was designed to allow the soil bacterium Pseudomonas putida to survive only in the presence of ar

277 Here, we used the soil bacterium Pseudomonas putida to uncover cell wall modulators from

278 expressed in the nonocular pathogenic host, Pseudomonas putida, to elucidate the molecular propertie

279 We engineer a robust soil bacterium, Pseudomonas putida, to funnel these oxygenated compounds

280 l structures of two outer membrane proteins, Pseudomonas putida TodX and Ralstonia pickettii TbuX, wh

281 , a vertebrate-type [2Fe-2S] ferredoxin from Pseudomonas putida, transfers electrons from NADH-putida

282 successfully transfer plasmid pBBR1MCS2 into Pseudomonas putida UWC1, Escherichia coli DH5alpha and P

283 s (Vibrio natriegens, Magnetococcus marinus, Pseudomonas putida, Vibrio fischeri, and Escherichia col

284 The swimming behavior of Pseudomonas putida was analyzed with a tracking microsco

285 mplexes of tartrate dehydrogenase (TDH) from Pseudomonas putida was carried out.

286 elope in the solvent tolerance mechanisms of Pseudomonas putida was investigated.

287 reductase (Pdr) and putidaredoxin (Pdx) from Pseudomonas putida was studied by molecular modeling, mu

288 Specifically, an engineered strain of Pseudomonas putida was used to produce mcl-PHAs containi

289 In this study, a genome-scale model of Pseudomonas putida was used to study the key issue of un

290 the electron donor to cytochrome P450cam in Pseudomonas putida, was improved by mutating non-ligatin

291 Using chemostat with cell retention (CCR) of Pseudomonas putida, we resolve this controversy and show

292 for the swimming behavior of soil bacterium Pseudomonas putida were based on literature values.

293 ite of Delta(5)-3-ketosteroid isomerase from Pseudomonas putida were found to exhibit substantial var

294 for Acinetobacter may also be applicable to Pseudomonas putida, where the PcaK permease has an addit

295 The flhF gene of Pseudomonas putida, which encodes a GTP-binding protein,

296 ranscription of TtgABC, a key efflux pump in Pseudomonas putida, which is highly resistant to antibio

297 om a verified minimal constrained cut-set in Pseudomonas putida, while providing additional high prio

298 work modeling the biosynthesis of mcl-PHA in Pseudomonas putida with respect to external C/N ratios,

299 oxygenase CYP101 (cytochrome P450(cam)) from Pseudomonas putida with the aim of generating novel syst