ライフサイエンスコーパス: Caulobacter crescentus

1 dation by an EAL domain protein (CC3396 from Caulobacter crescentus).

2 plex in the absence of polar localization in Caulobacter crescentus.

3 we identify SocAB, an atypical TA system in Caulobacter crescentus.

4 rn is critical for cell cycle progression in Caulobacter crescentus.

5 cellular localization in the model bacterium Caulobacter crescentus.

6 ization of StpX, a stalk-specific protein in Caulobacter crescentus.

7 that spatially regulates Z ring formation in Caulobacter crescentus.

8 ion of an unrelated diguanylate cyclase from Caulobacter crescentus.

9 al and functional investigation of PerB from Caulobacter crescentus.

10 l activity against its phylogenetic relative Caulobacter crescentus.

11 f morphogenesis and cell cycle regulation in Caulobacter crescentus.

12 of the stringent response in the oligotroph, Caulobacter crescentus.

13 ion in the asymmetrically dividing bacterium Caulobacter crescentus.

14 ral gene is located between lpxA and lpxB in Caulobacter crescentus.

15 e hipBA modules in the alpha-proteobacterium Caulobacter crescentus.

16 signaling with cytokinesis in the bacterium Caulobacter crescentus.

17 ing proteins that influence FtsZ function in Caulobacter crescentus.

18 aracterize a member of this family (DipM) in Caulobacter crescentus.

19 n of about 100 cell cycle-regulated genes in Caulobacter crescentus.

20 necessary to drive cell cycle progression in Caulobacter crescentus.

21 ifferentiation are temporally coordinated in Caulobacter crescentus.

22 aracterization of a type III photolyase from Caulobacter crescentus.

23 etworks governing the cell division cycle of Caulobacter crescentus.

24 ell transition in the developmental cycle of Caulobacter crescentus.

25 nd asymmetric cell division in the bacterium Caulobacter crescentus.

26 available was the model freshwater organism Caulobacter crescentus.

27 ing up the correct polarity in the bacterium Caulobacter crescentus.

28 er-messenger RNA (tmRNA)-tagged proteins, in Caulobacter crescentus.

29 ant for control of cell cycle progression in Caulobacter crescentus.

30 tant for proper establishment of polarity in Caulobacter crescentus.

31 e MreC cell shape protein in this process in Caulobacter crescentus.

32 gression genes ftsA and ftsQ is prevented in Caulobacter crescentus.

33 ession and asymmetric polar morphogenesis in Caulobacter crescentus.

34 assay in Escherichia coli based on PopZ from Caulobacter crescentus.

35 CIR sequences) present in up to 21 copies in Caulobacter crescentus.

36 ogy in the dimorphic Gram-negative bacterium Caulobacter crescentus.

37 ere, we investigated the function of ZapA in Caulobacter crescentus.

38 as Escherichia coli, Bacillus subtilis, and Caulobacter crescentus.

39 es/follows an adder, as has been proposed in Caulobacter crescentus.

40 ous cargos, including chromosomal regions in Caulobacter crescentus.

41 ke phages, which infect freshwater bacterium Caulobacter crescentus.

42 hitectures in the asymmetric model bacterium Caulobacter crescentus.

43 atomic structure of a bactofilin domain from Caulobacter crescentus.

44 h as Escherichia coli, Bacillus subtilis, or Caulobacter crescentus.

45 Here we investigate CTL function in Caulobacter crescentus.

46 ives cell-cycle progression in the bacterium Caulobacter crescentus.

47 ng Aggregatibacter actinomycetemcomitans and Caulobacter crescentus.

48 bacterial cell division protein FtsZ in live Caulobacter crescentus.

49 cation of the ParB/parS partition complex in Caulobacter crescentus.

50 ll shape, we focused on the curved bacterium Caulobacter crescentus.

51 ms to divide asymmetrically is the bacterium Caulobacter crescentus.

52 ole of the asymmetrically dividing bacterium Caulobacter crescentus(4-8).

53 At the cell poles of Caulobacter crescentus, a 177-amino acid (aa) protein ca

54 In Caulobacter crescentus, a flagellum is built exclusively

55 ition in the polarized alpha-proteobacterium Caulobacter crescentus, a model for cell cycle regulatio

56 ve structural and one regulatory paralog, in Caulobacter crescentus, a monopolarly flagellated alpha-

57 ry information and apply it to the bacterium Caulobacter crescentus, a paradigm for cell-cycle contro

58 In this study, we focus on the behavior of Caulobacter crescentus, a singly flagellated bacterium,

59 s study, we observe the swimming patterns of Caulobacter crescentus, a uniflagellated bacterium, in a

60 narily distant bacteria Escherichia coli and Caulobacter crescentus achieve cell size homeostasis by

61 t the essential cell cycle regulator GcrA in Caulobacter crescentus activates the transcription of ta

62 eudomonas aeruginosa, Bacillus subtilis, and Caulobacter crescentus all provided various levels of, b

63 reB protein mediates global cell polarity in Caulobacter crescentus, although the intermediate filame

64 Here, we identify a small protein from Caulobacter crescentus, an assembly inhibitor of MreB (A

65 e from the free living alpha-proteobacterium Caulobacter crescentus and an orthologous system from an

66 this question, we worked with the bacterium Caulobacter crescentus and asked whether exposure to a m

67 the PhyR approximately P/NepR interaction in Caulobacter crescentus and characterized the effect of a

68 in situ hybridization, we show here that in Caulobacter crescentus and Escherichia coli, chromosomal

69 In Caulobacter crescentus and Escherichia coli, the protein

70 the motility of the uniflagellated bacterium Caulobacter crescentus and have found that each cell dis

71 protein, is required for the curved shape of Caulobacter crescentus and localizes to the inner cell c

72 TUs predicted on the Caulobacter crescentus and Mycobacterium tuberculosis (H

73 e time of cell division and polarization for Caulobacter crescentus and Pseudomonas aeruginosa.

74 The bacterium Caulobacter crescentus and related stalk bacterial speci

75 spreading event using purified proteins from Caulobacter crescentus and show that CTP is required for

76 s paper, we introduced site-specific DSBs in Caulobacter crescentus and then used time-lapse microsco

77 hogen -Escherichia coli, Myxococcus xanthus, Caulobacter crescentus, and Mycobacterium tuberculosis,

78 include Escherichia coli, Bacillus subtilis, Caulobacter crescentus, and Myxococcus xanthus.

79 ntify DipM, a putative LytM endopeptidase in Caulobacter crescentus, and show that it plays a critica

80 similar to those reported for the bacterium Caulobacter crescentus, and they are crucial for surviva

81 Polar development and cell division in Caulobacter crescentus are controlled and coordinated by

82 tributions of specific cell wall proteins in Caulobacter crescentus are sensitive to small external o

83 Here, using Caulobacter crescentus as a model, we exploit genome-wid

84 the polarly flagellated alphaproteobacterium Caulobacter crescentus as an experimental model system.

85 Caulobacter crescentus assembles many of its cellular ma

86 chromosomally encoded ParD-ParE complex from Caulobacter crescentus at 2.6 A resolution.

87 The aquatic bacterium Caulobacter crescentus attaches to solid surfaces throug

88 Caulobacter crescentus attachment is mediated by the hol

89 nm and 1 microm polystyrene microspheres and Caulobacter crescentus bacteria, to the trapping region.

90 eviously reported CtrA consensus sequence in Caulobacter crescentus Bacterial one-hybrid experiments

91 s the emergence of morphological patterns in Caulobacter crescentus biofilms.

92 with deep sequencing (Hi-C), we show that in Caulobacter crescentus, both transcription rate and tran

93 d investigation of bactofilin filaments from Caulobacter crescentus by high-resolution solid-state NM

94 (MESLO), the nonpathogenic aquatic bacterium Caulobacter crescentus (CAUCR), the plant pathogen Agrob

95 te determination in the asymmetric bacterium Caulobacter crescentus (Caulobacter) is triggered by the

96 The first protein, Cc0300, was from Caulobacter crescentus CB-15 (Cc0300), while the second

97 The substrate profiles for two proteins from Caulobacter crescentus CB15 (Cc2672 and Cc3125) and one

98 :H7) to that of GDP-perosamine synthase from Caulobacter crescentus CB15 suggested that only two muta

99 technique to assay the assembly of FtsZ from Caulobacter crescentus (CcFtsZ) and reported that assemb

100 entified by screening for inhibitors against Caulobacter crescentus CcrM, an essential DNA methyltran

101 DNA adenine methylation by Caulobacter crescentus Cell Cycle Regulated Methyltransf

102 The Caulobacter crescentus cell cycle-regulated DNA methyltr

103 .EcoGII and M.EcoP15I from Escherichia coli, Caulobacter crescentus cell cycle-regulated DNA methyltr

104 metry, and chromosome replication during the Caulobacter crescentus cell cycle.

105 calized protein complexes to orchestrate the Caulobacter crescentus cell cycle.

106 terize progression of the terminal stages of Caulobacter crescentus cell division.

107 (prosthecae), cylindrical extensions of the Caulobacter crescentus cell envelope, can take up and hy

108 In the Alphaproteobacterium Caulobacter crescentus, cell cycle progression is believ

109 In the alpha-proteobacterium Caulobacter crescentus, cell cycle-regulated transcripti

110 Caulobacter crescentus cells adhere to surfaces by using

111 odel we quantify the straightening of curved Caulobacter crescentus cells after disruption of the cel

112 d colonize sparse oligotrophic environments, Caulobacter crescentus cells divide asymmetrically, yiel

113 cision, we find that the sizes of individual Caulobacter crescentus cells increase exponentially in t

114 We found that reversible attachment of Caulobacter crescentus cells is mediated by motile cells

115 In Caulobacter crescentus cells lacking tmRNA activity ther

116 the restoration of rod shape in lemon-shaped Caulobacter crescentus cells pretreated with MP265 or A2

117 bility to isolate synchronous populations of Caulobacter crescentus cells to investigate assembly of

118 Caulobacter crescentus cells treated with amdinocillin,

119 cryotomographic reconstructions of dividing Caulobacter crescentus cells wherein individual arc-like

120 raging to visualize such interactions inside Caulobacter crescentus cells.

121 of the bacterial actin protein MreB in live Caulobacter crescentus cells.

122 moreceptor arrays in cryotomograms of intact Caulobacter crescentus cells.

123 t comprise chemoreceptor arrays in wild-type Caulobacter crescentus cells.

124 tional cell growth and shape data for single Caulobacter crescentus cells.

125 nt labeling of amines on the surface of live Caulobacter crescentus cells.

126 However, in Caulobacter crescentus, cells lacking the primary SOS-re

127 Here we provide direct evidence that the Caulobacter crescentus CgtA(C) protein is associated wit

128 lectron cryotomography, here we show that in Caulobacter crescentus, chemoreceptor arrays in cells gr

129 al loci that are dispersed over the circular Caulobacter crescentus chromosome and found that in livi

130 data and polymer modeling indicates that the Caulobacter crescentus chromosome consists of multiple,

131 tein, PopZ, required to anchor the separated Caulobacter crescentus chromosome origins at the cell po

132 GTP, as has recently been described for the Caulobacter crescentus composite GGDEF-EAL protein, CC33

133 is of an oxygen sensory/signaling network in Caulobacter crescentus consisting of the sensor histidin

134 The differentiating bacterium, Caulobacter crescentus, contains an operon encoding a tw

135 In Caulobacter crescentus, CpdR controls the polar localiza

136 tyrosine phosphatase homolog in a bacterium, Caulobacter crescentus CtpA.

137 In the oligotrophic freshwater bacterium Caulobacter crescentus, D-xylose induces expression of o

138 The cell-division cycle of Caulobacter crescentus depends on periodic activation an

139 te that the characteristic crescent shape of Caulobacter crescentus depends upon an inter-mediate fil

140 ree-dimensional structure of the enzyme from Caulobacter crescentus determined to a nominal resolutio

141 Caulobacter crescentus differentiates from a motile, for

142 The bacterium Caulobacter crescentus divides asymmetrically as part of

143 Caulobacter crescentus divides asymmetrically into a swa

144 The aquatic bacterium Caulobacter crescentus divides asymmetrically to a flage

145 The bacterium Caulobacter crescentus divides asymmetrically, producing

146 ymmetric (Bacillus subtilis) and asymmetric (Caulobacter crescentus) division and reconstruct their l

147 Here, we show that in Caulobacter crescentus, DnaX isoforms are unexpectedly g

148 that sigma32 from the alpha-proteobacterium Caulobacter crescentus does not need the extended -10 mo

149 ion in the freshwater oligotrophic bacterium Caulobacter crescentus during growth on three standard l

150 In Caulobacter crescentus, each cell cycle produces morphol

151 The bacterium Caulobacter crescentus employs a specialized dimorphic l

152 abel proteins in the Gram-negative bacterium Caulobacter crescentus, enabling long-time-scale protein

153 The bacterium Caulobacter crescentus encodes a soluble LOV-histidine k

154 The genome of Caulobacter crescentus encodes at least 31 sRNAs, and 27

155 For example, Caulobacter crescentus encodes six glycosyltransferase p

156 The chromosome of the alpha-proteobacterium, Caulobacter crescentus, encodes eight ParE/RelE-superfam

157 We report that the S-layer of Caulobacter crescentus exhibits calcium-mediated structu

158 The free-living aquatic bacterium, Caulobacter crescentus, exhibits two different morpholog

159 ermined the torque of the flagellar motor of Caulobacter crescentus for different motor rotation rate

160 genetically engineered the aerobic bacterium Caulobacter crescentus for REE adsorption through high-d

161 rane tether for FtsZ in bacteria, however in Caulobacter crescentus, FtsA arrives at midcell after st

162 We show here that the Caulobacter crescentus FtsK protein localizes to the div

163 Here, we describe a role for the CTL of Caulobacter crescentus FtsZ as an intrinsic regulator of

164 FtsZ, PC190723, had no stabilizing effect on Caulobacter crescentus FtsZ filaments in vitro, which co

165 Here, we show that in Caulobacter crescentus, FtsZ also plays a major role in

166 We show that in Caulobacter crescentus, FzlA must bind to FtsZ for divis

167 Here, we show that the bacterium Caulobacter crescentus generates a gradient of the activ

168 circuit recently described in the bacterium Caulobacter crescentus generates reciprocal oscillations

169 e three-dimensional (3D) architecture of the Caulobacter crescentus genome by combining genome-wide c

170 Caulobacter crescentus has a dimorphic life cycle compos

171 rphic and intrinsically asymmetric bacterium Caulobacter crescentus has become an important model org

172 The dimorphic bacterium Caulobacter crescentus has evolved marked phenotypic cha

173 The bacterium Caulobacter crescentus has morphologically and functiona

174 t finding of a U-specific stress response in Caulobacter crescentus has provided a foundation for stu

175 division proteins from Escherichia coli and Caulobacter crescentus have been shown to bind peptidogl

176 n and essential regulator of constriction in Caulobacter crescentus, helps link FtsZ to PG synthesis

177 t its properties are similar to those of the Caulobacter crescentus homolog CgtA(C).

178 We report a crystal structure of Caulobacter crescentus IbpA bound to myo-inositol at 1.4

179 ic screen for cell division cycle mutants of Caulobacter crescentus identified a temperature-sensitiv

180 ing, and mathematical modeling, our study in Caulobacter crescentus identifies a novel NAP (GapR) who

181 ked and swarmer cell cycles of the bacterium Caulobacter crescentus in a near-mechanical step-like fa

182 to image the widely studied model prokaryote Caulobacter crescentus in an intact, near-native state,

183 ators control the general stress response in Caulobacter crescentus, including sigma(T), its anti-sig

184 Caulobacter crescentus initiates a single round of DNA r

185 erial cells, including Proteus mirabilis and Caulobacter crescentus, initiates asymmetrically, accomp

186 In Caulobacter crescentus, intact cables of the actin homol

187 Caulobacter crescentus integrates phospho-signaling path

188 Cell division in Caulobacter crescentus involves constriction and fission

189 Chromosome segregation in the bacterium Caulobacter crescentus involves propulsion of the replic

190 Caulobacter crescentus is a model organism for studying

191 Caulobacter crescentus is a premier model organism for s

192 ports the hypothesis that stalk synthesis in Caulobacter crescentus is a specialized form of cell elo

193 Caulobacter crescentus is a species that has met this ne

194 Caulobacter crescentus is an oligotrophic alpha-proteoba

195 apsule of the synchronizable model bacterium Caulobacter crescentus is cell cycle regulated and we un

196 The cell cycle of Caulobacter crescentus is controlled by a complex signal

197 s by the gram-negative prothescate bacterium Caulobacter crescentus is mediated by a polar organelle

198 In aquatic environments, Caulobacter crescentus is one of the first colonizers of

199 - and repolarization in the model prokaryote Caulobacter crescentus is precisely orchestrated through

200 The expression of the flagellin proteins in Caulobacter crescentus is regulated by the progression o

201 ial transcription of late flagellar genes in Caulobacter crescentus is regulated by the sigma54 trans

202 have found that the abundance of SsrA RNA in Caulobacter crescentus is regulated with respect to the

203 Caulobacter crescentus lacks these systems, but recent w

204 subgroup of alpha-proteobacteria, including Caulobacter crescentus, lacks the critical G(-1) residue

205 Here, we show that in Caulobacter crescentus Lon controls deoxyribonucleoside

206 We show that Caulobacter crescentus makes use of and requires a dedic

207 that govern cell division and development in Caulobacter crescentus, many of which are also conserved

208 positions of three proteins in the bacterium Caulobacter crescentus: McpA, PopZ, and SpmX.

209 The UzcRS two-component system in Caulobacter crescentus mediates widespread transcription

210 t that the oligotrophic freshwater bacterium Caulobacter crescentus metabolizes D-xylose through a pa

211 vel datasets obtained with a custom-designed Caulobacter crescentus microarray chip, we identify tran

212 e perform molecular dynamics simulations for Caulobacter crescentus MreB to extract mechanical parame

213 In Caulobacter crescentus, MreC physically associates with

214 Caulobacter crescentus mutants that lack the trans trans

215 e (CCxylB) and a xylonolactonase (xylC) from Caulobacter crescentus, native E. coli xylonate dehydrat

216 ectories of the singly flagellated bacterium Caulobacter crescentus near a glass surface with total i

217 is hypothesis, we generated mutations in the Caulobacter crescentus obg gene (cgtAC) which, in Ras-li

218 "baby machine" to synchronize the bacterium Caulobacter crescentus on-chip and to move the synchroni

219 In the differentiating alphaproteobacterium Caulobacter crescentus, organelle synthesis at cell pole

220 We show that in Caulobacter crescentus, PBP3 accumulates at the new pole

221 adherence property of the aquatic bacterium Caulobacter crescentus permits visualization of single c

222 We present genetic evidence that Caulobacter crescentus PhyR is a phosphorylation-depende

223 We visualized Caulobacter crescentus pili undergoing dynamic cycles of

224 For Caulobacter crescentus, polar stalk synthesis is tied to

225 Two proteins in Caulobacter crescentus, PopZ and TipN, provide direction

226 In the Caulobacter crescentus predivisional cell, class III and

227 The alpha-proteobacterium Caulobacter crescentus produces a motile swarmer cell an

228 The differentiating bacterium Caulobacter crescentus produces two different cell types

229 In Caulobacter crescentus, progression through the cell cyc

230 In Caulobacter crescentus, protein degradation by the ClpXP

231 We identify nearly 300 localized Caulobacter crescentus proteins, up to 10-fold more than

232 netics assays of Cb13 and CbK phage-infected Caulobacter crescentus, provides insight into the mechan

233 mosomal homologues, including the ParAs from Caulobacter crescentus, Pseudomonas aeruginosa, Pseudomo

234 CckA, CtrA, FlbT, and FlaF, proteins that in Caulobacter crescentus regulate flagellum biosynthesis.

235 In the alpha-proteobacterium Caulobacter crescentus, regulated protein degradation is

236 cycle progression in the dimorphic bacterium Caulobacter crescentus requires spatiotemporal regulatio

237 -fate asymmetry in the predivisional cell of Caulobacter crescentus requires that the regulatory prot

238 The maintenance of cell shape in Caulobacter crescentus requires the essential gene mreB,

239 Here, we show that Caulobacter crescentus responds to DNA damage by coordin

240 The depletion of MreB in Caulobacter crescentus resulted in lemon-shaped cells th

241 In Caulobacter crescentus, RodZ is essential for viability

242 n unexpected finding was that when using the Caulobacter crescentus rrn leader sequence, there was li

243 cular dynamic simulations to clarify how the Caulobacter crescentus S-layer assembles on the lipopoly

244 an electron cryomicroscopy structure of the Caulobacter crescentus S-layer bound to the O-antigen of

245 haproteobacteria, Sinorhizobium meliloti and Caulobacter crescentus, serve as models for investigatin

246 of these species, Sinorhizobium meliloti and Caulobacter crescentus, simply lack any extra nucleotide

247 Here, we demonstrate that the Caulobacter crescentus SLP readily crystallizes into she

248 Here, using purified Caulobacter crescentus' sole S-layer protein RsaA, we ob

249 re we show that a developmental regulator of Caulobacter crescentus, SpmX, is co-opted in the genus A

250 We describe the identification of 27 novel Caulobacter crescentus sRNAs by analysis of RNA expressi

251 In Caulobacter crescentus, surface attachment and subsequen

252 loci of various interloci contour lengths in Caulobacter crescentus swarmer cells to determine the in

253 et al. identify a toxin-antitoxin system in Caulobacter crescentus that acts by a unique mechanism.

254 DivL is an essential tyrosine kinase in Caulobacter crescentus that controls an early step in th

255 utation in the morphogenetic protein MreB in Caulobacter crescentus that gives rise to cells with a v

256 ein bacteriocin in the alpha-proteobacterium Caulobacter crescentus that is retained on the surface o

257 Here, we demonstrate in Caulobacter crescentus that proteotoxic stress induces a

258 Here, we show in Caulobacter crescentus that the polarity factor TipN reg

259 In Caulobacter crescentus, the actin homologue MreB is crit

260 e first, called "ori-ter" and exemplified by Caulobacter crescentus, the chromosome arms lie side-by-

261 In Caulobacter crescentus, the ClpXP protease is essential

262 In Caulobacter crescentus, the G1-S transition involves the

263 In Caulobacter crescentus, the HHK ShkA is essential for ac

264 In the vibrioid bacterium Caulobacter crescentus, the intermediate filament-like p

265 In Caulobacter crescentus, the Lon protease degrades DnaA t

266 In Caulobacter crescentus, the origin of DNA replication is

267 In Caulobacter crescentus, the PopZ polar scaffold protein

268 ganelles featured by the dimorphic bacterium Caulobacter crescentus, the stalk, a cylindrical extensi

269 In Caulobacter crescentus, the temporal and spatial express

270 We rebuilt the essential genome of Caulobacter crescentus through the process of chemical s

271 In Caulobacter crescentus, timely degradation of the master

272 In Caulobacter crescentus, tmRNA was localized in a cell-cy

273 e protein Hfq from the alpha-proteobacterium Caulobacter crescentus to 2.15- angstrom resolution, res

274 le adhesion of single cells of the bacterium Caulobacter crescentus to a glass surface in a microflui

275 erse functions, from cell stalk formation in Caulobacter crescentus to chromosome segregation and mot

276 In Caulobacter crescentus, two-component signal transductio

277 The PG of Caulobacter crescentus, unlike that of many other Gram-n

278 Here, we provide evidence that Caulobacter crescentus uses a multimeric pole-organizing

279 A recent study suggests that Caulobacter crescentus uses a novel regulator, FzlA, to

280 The bacterium Caulobacter crescentus uses a ParA-based partitioning sy

281 Caulobacter crescentus uses the dynamic interactions bet

282 The bacterium Caulobacter crescentus uses two-component phospho-signal

283 ing stalk biogenesis, has been identified in Caulobacter crescentus using a bioinformatic screen, tar

284 dy, we investigate the distribution of HU in Caulobacter crescentus using a combination of super-reso

285 olocalized with the surface of the bacterium Caulobacter crescentus using a double-helix point spread

286 growing cells of the Gram-negative bacterium Caulobacter crescentus using cryo-electron tomography (C

287 We focus here on Caulobacter crescentus, Vibrio cholerae, Helicobacter py

288 face sensing drives cell-cycle initiation in Caulobacter crescentus We identify the type IV pilin pro

289 e not expressed during a life cycle stage of Caulobacter crescentus when the regulator is activated b

290 imensional microdomains at the cell poles in Caulobacter crescentus, where it functions as a hub prot

291 nvestigation is GDP-perosamine synthase from Caulobacter crescentus, which catalyzes the final step i

292 Here, we focus on Caulobacter crescentus, which encodes a ProRS with a tru

293 Focusing on the model bacterium Caulobacter crescentus, which generates two different ty

294 some assembly from the alpha-proteobacterium Caulobacter crescentus, which is a model organism for st

295 novel family of CheY-like (Cle) proteins in Caulobacter crescentus, which tune flagellar activity in

296 cell shape by studying the aquatic bacterium Caulobacter crescentus, whose cell cycle progression inv

297 lator CpdR couples phosphorylation events in Caulobacter crescentus with the AAA+ protease ClpXP to p

298 y of the alphaproteobacterial model organism Caulobacter crescentus, with a specific focus on LytM-li

299 been described in the alpha-proteobacterium Caulobacter crescentus, with the interacting partners of

300 Asymmetric cell division in Caulobacter crescentus yields daughter cells that have d