ライフサイエンスコーパス: crescentus

1 EAL domain protein (CC3396 from Caulobacter crescentus).

2 bacter actinomycetemcomitans and Caulobacter crescentus.

3 ll division protein FtsZ in live Caulobacter crescentus.

4 e ParB/parS partition complex in Caulobacter crescentus.

5 focused on the curved bacterium Caulobacter crescentus.

6 asymmetrically is the bacterium Caulobacter crescentus.

7 ulons of CtrA and DnaA in S. meliloti and C. crescentus.

8 transcriptionally cell cycle-regulated in C. crescentus.

9 roteobacterial species closely related to C. crescentus.

10 absence of polar localization in Caulobacter crescentus.

11 efaciens are vertically-integrated, as in C. crescentus.

12 SocAB, an atypical TA system in Caulobacter crescentus.

13 al for cell cycle progression in Caulobacter crescentus.

14 alization in the model bacterium Caulobacter crescentus.

15 rates of the ClpP associated proteases in C. crescentus.

16 kinases called pdhS1 and pdhS2, absent in C. crescentus.

17 tpX, a stalk-specific protein in Caulobacter crescentus.

18 ly regulates Z ring formation in Caulobacter crescentus.

19 ght temporal control of the cell cycle in C. crescentus.

20 related diguanylate cyclase from Caulobacter crescentus.

21 ional investigation of PerB from Caulobacter crescentus.

22 oordinately regulate stress physiology in C. crescentus.

23 gainst its phylogenetic relative Caulobacter crescentus.

24 sis and cell cycle regulation in Caulobacter crescentus.

25 gent response in the oligotroph, Caulobacter crescentus.

26 symmetrically dividing bacterium Caulobacter crescentus.

27 located between lpxA and lpxB in Caulobacter crescentus.

28 ith cytokinesis in the bacterium Caulobacter crescentus.

29 that influence FtsZ function in Caulobacter crescentus.

30 les in the alpha-proteobacterium Caulobacter crescentus.

31 member of this family (DipM) in Caulobacter crescentus.

32 00 cell cycle-regulated genes in Caulobacter crescentus.

33 drive cell cycle progression in Caulobacter crescentus.

34 herichia coli based on PopZ from Caulobacter crescentus.

35 imorphic Gram-negative bacterium Caulobacter crescentus.

36 AimB with MreB conformational dynamics in C. crescentus.

37 stigated the function of ZapA in Caulobacter crescentus.

38 hia coli, Bacillus subtilis, and Caulobacter crescentus.

39 that control peptidoglycan remodeling in C. crescentus.

40 n adder, as has been proposed in Caulobacter crescentus.

41 Z curvature and efficient constriction in C. crescentus.

42 including chromosomal regions in Caulobacter crescentus.

43 hich infect freshwater bacterium Caulobacter crescentus.

44 n the asymmetric model bacterium Caulobacter crescentus.

45 hways lead to persister cell formation in C. crescentus.

46 ture of a bactofilin domain from Caulobacter crescentus.

47 chia coli, Bacillus subtilis, or Caulobacter crescentus.

48 develop a model of nutrient signaling in C. crescentus.

49 e we investigate CTL function in Caulobacter crescentus.

50 cle progression in the bacterium Caulobacter crescentus.

51 symmetrically dividing bacterium Caulobacter crescentus(4-8).

52 At the cell poles of Caulobacter crescentus, a 177-amino acid (aa) protein called PopZ se

53 tiple flagella and no prosthecae, whereas C. crescentus, a freshwater bacterium, has a single polar f

54 polarized alpha-proteobacterium Caulobacter crescentus, a model for cell cycle regulation and asymme

55 l and one regulatory paralog, in Caulobacter crescentus, a monopolarly flagellated alpha-proteobacter

56 on and apply it to the bacterium Caulobacter crescentus, a paradigm for cell-cycle control.

57 udy, we focus on the behavior of Caulobacter crescentus, a singly flagellated bacterium, at the air/w

58 observe the swimming patterns of Caulobacter crescentus, a uniflagellated bacterium, in a linear oxyg

59 nt bacteria Escherichia coli and Caulobacter crescentus achieve cell size homeostasis by growing, on

60 ial cell cycle regulator GcrA in Caulobacter crescentus activates the transcription of target genes i

61 ruginosa, Bacillus subtilis, and Caulobacter crescentus all provided various levels of, but functiona

62 we identify a small protein from Caulobacter crescentus, an assembly inhibitor of MreB (AimB).

63 ree living alpha-proteobacterium Caulobacter crescentus and an orthologous system from an obligate in

64 the dynamics of c-di-GMP and (p)ppGpp in C. crescentus and analyze how the guanine nucleotide-based

65 on, we worked with the bacterium Caulobacter crescentus and asked whether exposure to a moderate conc

66 roximately P/NepR interaction in Caulobacter crescentus and characterized the effect of aspartyl phos

67 lymorphic locus, zwf, between lab-adapted C. crescentus and clinical isolates of Pseudomonas aerugino

68 rrangements of FtsZ and FtsA filaments in C. crescentus and E. coli cells and inside constricting lip

69 ridization, we show here that in Caulobacter crescentus and Escherichia coli, chromosomally expressed

70 of the uniflagellated bacterium Caulobacter crescentus and have found that each cell displays two di

71 required for the curved shape of Caulobacter crescentus and localizes to the inner cell curvature.

72 ll division and polarization for Caulobacter crescentus and Pseudomonas aeruginosa.

73 ent using purified proteins from Caulobacter crescentus and show that CTP is required for spreading.

74 similarity between the division cycle of C. crescentus and that of A. tumefaciens, the functional co

75 introduced site-specific DSBs in Caulobacter crescentus and then used time-lapse microscopy to visual

76 y network that controls the cell cycle of C. crescentus and, presumably, of many other Alphaproteobac

77 richia coli, Myxococcus xanthus, Caulobacter crescentus, and Mycobacterium tuberculosis, respectively

78 erichia coli, Bacillus subtilis, Caulobacter crescentus, and Myxococcus xanthus.

79 a putative LytM endopeptidase in Caulobacter crescentus, and show that it plays a critical role in ma

80 those reported for the bacterium Caulobacter crescentus, and they are crucial for survival in the hos

81 f specific cell wall proteins in Caulobacter crescentus are sensitive to small external osmotic upshi

82 tended to provide a taste of the power of C. crescentus as a model system to explore a diverse range

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

84 flagellated alphaproteobacterium Caulobacter crescentus as an experimental model system.

85 y encoded ParD-ParE complex from Caulobacter crescentus at 2.6 A resolution.

86 Caulobacter crescentus attachment is mediated by the holdfast, a com

87 rom polystyrene microspheres and Caulobacter crescentus bacteria, to the trapping region.

88 orted CtrA consensus sequence in Caulobacter crescentus Bacterial one-hybrid experiments showed that

89 nce of morphological patterns in Caulobacter crescentus biofilms.

90 quencing (Hi-C), we show that in Caulobacter crescentus, both transcription rate and transcript lengt

91 ion of bactofilin filaments from Caulobacter crescentus by high-resolution solid-state NMR spectrosco

92 cal functionality of the genome design in C. crescentus by transposon mutagenesis.

93 In C. crescentus, c-di-GMP works as a major regulator of pole

94 tion in the asymmetric bacterium Caulobacter crescentus (Caulobacter) is triggered by the localizatio

95 first protein, Cc0300, was from Caulobacter crescentus CB-15 (Cc0300), while the second one (Sgx9355

96 e profiles for two proteins from Caulobacter crescentus CB15 (Cc2672 and Cc3125) and one protein (Sgx

97 of GDP-perosamine synthase from Caulobacter crescentus CB15 suggested that only two mutations would

98 assay the assembly of FtsZ from Caulobacter crescentus (CcFtsZ) and reported that assembly required

99 Genome sequencing has revealed many C. crescentus cell cycle genes are conserved in other Alpha

100 DNA adenine methylation by Caulobacter crescentus Cell Cycle Regulated Methyltransferase (CcrM)

101 M.EcoP15I from Escherichia coli, Caulobacter crescentus cell cycle-regulated DNA methyltransferase (C

102 The Caulobacter crescentus cell cycle-regulated DNA methyltransferase (C

103 hromosome replication during the Caulobacter crescentus cell cycle.

104 ce of power-law statistics in the tail of C. crescentus cell-size distribution, although there is a d

105 In the Alphaproteobacterium Caulobacter crescentus, cell cycle progression is believed to be con

106 In the alpha-proteobacterium Caulobacter crescentus, cell cycle-regulated transcription plays an

107 tify the straightening of curved Caulobacter crescentus cells after disruption of the cell-curving cr

108 parse oligotrophic environments, Caulobacter crescentus cells divide asymmetrically, yielding a motil

109 e peptide side chains of PG isolated from C. crescentus cells grown in the complex laboratory medium

110 ind that the sizes of individual Caulobacter crescentus cells increase exponentially in time.

111 nd that reversible attachment of Caulobacter crescentus cells is mediated by motile cells bearing pil

112 ion of rod shape in lemon-shaped Caulobacter crescentus cells pretreated with MP265 or A22 under nont

113 olate synchronous populations of Caulobacter crescentus cells to investigate assembly of the divisome

114 of amines on the surface of live Caulobacter crescentus cells.

115 erial actin protein MreB in live Caulobacter crescentus cells.

116 rrays in cryotomograms of intact Caulobacter crescentus cells.

117 sualize such interactions inside Caulobacter crescentus cells.

118 hemoreceptor arrays in wild-type Caulobacter crescentus cells.

119 growth and shape data for single Caulobacter crescentus cells.

120 ern is due to the low ParA copy number in C. crescentus cells.

121 However, in Caulobacter crescentus, cells lacking the primary SOS-regulated inhi

122 tomography, here we show that in Caulobacter crescentus, chemoreceptor arrays in cells grown in diffe

123 ymer modeling indicates that the Caulobacter crescentus chromosome consists of multiple, largely inde

124 required to anchor the separated Caulobacter crescentus chromosome origins at the cell poles, a funct

125 and a role in ClpX positioning similar to C. crescentus CpdR, suggesting a conserved function of CpdR

126 In Caulobacter crescentus, CpdR controls the polar localization of the

127 sphatase homolog in a bacterium, Caulobacter crescentus CtpA.

128 Paradoxically, C. crescentus curvature is robustly maintained in the wild

129 The principal components of the C. crescentus degradosome are the endoribonuclease RNase E,

130 The cell-division cycle of Caulobacter crescentus depends on periodic activation and deactivati

131 Caulobacter crescentus differentiates from a motile, foraging swarme

132 he logic of stringent response control in C. crescentus differs from E. coli, the global transcriptio

133 sistent with its ecological distribution, C. crescentus displays a narrow range of osmotolerance, wit

134 Using these data, we show that C. crescentus displays aerotactic behavior by extending the

135 Caulobacter crescentus divides asymmetrically into a swarmer cell an

136 cillus subtilis) and asymmetric (Caulobacter crescentus) division and reconstruct their lineages to c

137 Here, we show that in Caulobacter crescentus, DnaX isoforms are unexpectedly generated thr

138 2 from the alpha-proteobacterium Caulobacter crescentus does not need the extended -10 motif for high

139 The bacterium Caulobacter crescentus employs a specialized dimorphic life cycle co

140 s in the Gram-negative bacterium Caulobacter crescentus, enabling long-time-scale protein tracking an

141 The bacterium Caulobacter crescentus encodes a soluble LOV-histidine kinase, LovK,

142 The genome of Caulobacter crescentus encodes at least 31 sRNAs, and 27 of these sR

143 For example, Caulobacter crescentus encodes six glycosyltransferase paralogs of l

144 me of the alpha-proteobacterium, Caulobacter crescentus, encodes eight ParE/RelE-superfamily toxins t

145 We report that the S-layer of Caulobacter crescentus exhibits calcium-mediated structural plastici

146 e free-living aquatic bacterium, Caulobacter crescentus, exhibits two different morphologies during i

147 We used fluorescence microscopy of C. crescentus expressing green fluorescent protein to track

148 We show here that C. crescentus extracellular DNA (eDNA) inhibits the ability

149 ays a role in the surface modification of C. crescentus, facilitating the uptake of nutrients during

150 The podJ gene, originally identified in C. crescentus for its role in polar organelle development,

151 engineered the aerobic bacterium Caulobacter crescentus for REE adsorption through high-density cell

152 for FtsZ in bacteria, however in Caulobacter crescentus, FtsA arrives at midcell after stable Z-ring

153 e describe a role for the CTL of Caulobacter crescentus FtsZ as an intrinsic regulator of lateral int

154 23, had no stabilizing effect on Caulobacter crescentus FtsZ filaments in vitro, which complements pr

155 We show that in Caulobacter crescentus, FzlA must bind to FtsZ for division to occur

156 Z to the membrane and demonstrate that in C. crescentus, FzlC is one such membrane anchor.

157 e regulator LovR also function within the C. crescentus general stress pathway.

158 Here, we show that the bacterium Caulobacter crescentus generates a gradient of the active, phosphory

159 nsional (3D) architecture of the Caulobacter crescentus genome by combining genome-wide chromatin int

160 les unable to bind myo-inositol abolishes C. crescentus growth in medium containing myo-inositol as t

161 h-affinity ribose binding allele affected C. crescentus growth on D-ribose as a carbon source, provid

162 The dimorphic bacterium Caulobacter crescentus has evolved marked phenotypic changes during

163 The bacterium Caulobacter crescentus has morphologically and functionally distinct

164 a U-specific stress response in Caulobacter crescentus has provided a foundation for studying the me

165 Studying C. crescentus has reformed our understanding of bacterial i

166 Studies in C. crescentus have also deepened our knowledge of other top

167 oteins from Escherichia coli and Caulobacter crescentus have been shown to bind peptidoglycan.

168 ial regulator of constriction in Caulobacter crescentus, helps link FtsZ to PG synthesis to promote d

169 We also show that C. crescentus Hfq has sRNA binding and RNA annealing activi

170 enesis at the predicted catalytic site of C. crescentus HfsH phenocopied the DeltahfsH mutant and abo

171 Here we show that recombinant C. crescentus HisRS allowed complete histidylation of a C.

172 e U20a, created a competent substrate for C. crescentus HisRS.

173 f G(-1) did not improve aminoacylation by C. crescentus HisRS.

174 divergent (based on sequence similarity) C. crescentus HisRS.

175 We report a crystal structure of Caulobacter crescentus IbpA bound to myo-inositol at 1.45 A resoluti

176 hematical modeling, our study in Caulobacter crescentus identifies a novel NAP (GapR) whose activity

177 mer cell cycles of the bacterium Caulobacter crescentus in a near-mechanical step-like fashion.

178 l the general stress response in Caulobacter crescentus, including sigma(T), its anti-sigma factor Ne

179 Caulobacter crescentus initiates a single round of DNA replication d

180 including Proteus mirabilis and Caulobacter crescentus, initiates asymmetrically, accompanied by asy

181 In Caulobacter crescentus, intact cables of the actin homologue, MreB,

182 Caulobacter crescentus integrates phospho-signaling pathways and tra

183 Cell division in Caulobacter crescentus involves constriction and fission of the inne

184 Caulobacter crescentus is a premier model organism for studying the

185 Caulobacter crescentus is a species that has met this need effective

186 e synchronizable model bacterium Caulobacter crescentus is cell cycle regulated and we unearth a bact

187 The cell cycle of Caulobacter crescentus is controlled by a complex signalling network

188 rization in the model prokaryote Caulobacter crescentus is precisely orchestrated through at least th

189 alpha-proteobacteria, including Caulobacter crescentus, lacks the critical G(-1) residue.

190 Here, we show that in Caulobacter crescentus Lon controls deoxyribonucleoside triphosphate

191 Lysates of E. coli in which C. crescentus LpxI (CcLpxI) is overexpressed display high l

192 We show that Caulobacter crescentus makes use of and requires a dedicated mechani

193 cell division and development in Caulobacter crescentus, many of which are also conserved among diver

194 three proteins in the bacterium Caulobacter crescentus: McpA, PopZ, and SpmX.

195 he UzcRS two-component system in Caulobacter crescentus mediates widespread transcriptional activatio

196 and that this interaction is favored for C. crescentus MreB over Escherichia coli MreB because of a

197 lecular dynamics simulations for Caulobacter crescentus MreB to extract mechanical parameters for inp

198 Caulobacter crescentus mutants that lack the trans translation pathw

199 nd a xylonolactonase (xylC) from Caulobacter crescentus, native E. coli xylonate dehydratase (yjhG),

200 the singly flagellated bacterium Caulobacter crescentus near a glass surface with total internal refl

201 ne" to synchronize the bacterium Caulobacter crescentus on-chip and to move the synchronized populati

202 erentiating alphaproteobacterium Caulobacter crescentus, organelle synthesis at cell poles is critica

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

204 oroughly characterized the composition of C. crescentus peptidoglycan by high-performance liquid chro

205 Remarkably, glycine incorporation into C. crescentus peptidoglycan occurred even in the presence o

206 roperty of the aquatic bacterium Caulobacter crescentus permits visualization of single cells in a li

207 litative and quantitative analysis of the C. crescentus PG by high-performance liquid chromatography

208 here that glycine incorporation into the C. crescentus PG depends on the presence of exogenous glyci

209 Hence, the C. crescentus PG is able to retain its physiological functi

210 We present genetic evidence that Caulobacter crescentus PhyR is a phosphorylation-dependent stress re

211 We visualized Caulobacter crescentus pili undergoing dynamic cycles of extension a

212 For Caulobacter crescentus, polar stalk synthesis is tied to its dimorph

213 Two proteins in Caulobacter crescentus, PopZ and TipN, provide directional cues at t

214 The alpha-proteobacterium Caulobacter crescentus produces a motile swarmer cell and a sessile

215 In Caulobacter crescentus, progression through the cell cycle is govern

216 We show that C. crescentus ProRS can readily form Cys- and Ala-tRNA(Pro)

217 In Caulobacter crescentus, protein degradation by the ClpXP protease is

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

219 s of Cb13 and CbK phage-infected Caulobacter crescentus, provides insight into the mechanisms of infe

220 Substrate specificity of C. crescentus ProXp-ala is determined, in part, by elements

221 FlbT, and FlaF, proteins that in Caulobacter crescentus regulate flagellum biosynthesis.

222 In the alpha-proteobacterium Caulobacter crescentus, regulated protein degradation is required fo

223 ssion in the dimorphic bacterium Caulobacter crescentus requires spatiotemporal regulation of gene ex

224 try in the predivisional cell of Caulobacter crescentus requires that the regulatory protein DivL loc

225 The maintenance of cell shape in Caulobacter crescentus requires the essential gene mreB, which encod

226 Here, we show that Caulobacter crescentus responds to DNA damage by coordinately induci

227 Loss of PflI function in C. crescentus results in an abnormally high frequency of ce

228 xamination of the hfsH deletion mutant in C. crescentus revealed that this strain synthesizes holdfas

229 how that, unlike its E. coli counterpart, C. crescentus RhlB interacts directly with a segment of the

230 Furthermore, C. crescentus RNase E appears associated with the DNA indep

231 The crystal structure of a portion of C. crescentus RNase E encompassing the helicase-binding reg

232 In Caulobacter crescentus, RodZ is essential for viability and is invol

233 finding was that when using the Caulobacter crescentus rrn leader sequence, there was little effect

234 c simulations to clarify how the Caulobacter crescentus S-layer assembles on the lipopolysaccharides

235 cryomicroscopy structure of the Caulobacter crescentus S-layer bound to the O-antigen of lipopolysac

236 eria, Sinorhizobium meliloti and Caulobacter crescentus, serve as models for investigating the geneti

237 In C. crescentus, several CheY homologs regulate motor functio

238 Here, we demonstrate that the Caulobacter crescentus SLP readily crystallizes into sheets in vitro

239 Here, using purified Caulobacter crescentus' sole S-layer protein RsaA, we obtained a 2.7

240 hat a developmental regulator of Caulobacter crescentus, SpmX, is co-opted in the genus Asticcacaulis

241 We also used modified E. coli and C. crescentus ssrA tags to independently control the degrad

242 Based on the previous observation that C. crescentus stalks are lysozyme-resistant, we compared th

243 ty, and stationary-phase survival between C. crescentus strain CB15 and its derivative NA1000 is dete

244 demonstrate that cell curvature enhances C. crescentus surface colonization in flow.

245 In Caulobacter crescentus, surface attachment and subsequent biofilm gr

246 Forward swimming C. crescentus swarmer cells tend to get physically trapped

247 We analyzed the adaptive response of C. crescentus swarmer cells to carbon starvation and found

248 ous interloci contour lengths in Caulobacter crescentus swarmer cells to determine the in vivo config

249 tify a toxin-antitoxin system in Caulobacter crescentus that acts by a unique mechanism.

250 he morphogenetic protein MreB in Caulobacter crescentus that gives rise to cells with a variable-widt

251 cin in the alpha-proteobacterium Caulobacter crescentus that is retained on the surface of producer c

252 Here, we demonstrate in Caulobacter crescentus that proteotoxic stress induces a cell-cycle

253 Here, we show in Caulobacter crescentus that the polarity factor TipN regulates the d

254 y diffusing mRNA, and provide evidence in C. crescentus that this mRNA localization restricts ribosom

255 In C. crescentus the CtrA response regulator serves as the mas

256 In Caulobacter crescentus, the actin homologue MreB is critical for cel

257 led "ori-ter" and exemplified by Caulobacter crescentus, the chromosome arms lie side-by-side, with t

258 In Caulobacter crescentus, the ClpXP protease is essential and drives c

259 LD-crosslinking or lysozyme resistance in C. crescentus, the correlation between these two properties

260 In C. crescentus, the directionality of the transport is set u

261 l cycle regulatory genes are essential in C. crescentus, the essential genes of two Alphaproteobacter

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

263 In Caulobacter crescentus, the HHK ShkA is essential for accurate timin

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

265 In Caulobacter crescentus, the Lon protease degrades DnaA to coordinate

266 In Caulobacter crescentus, the PopZ polar scaffold protein supports asy

267 As in C. crescentus, the S. meliloti PodJ1 protein appears to act

268 tured by the dimorphic bacterium Caulobacter crescentus, the stalk, a cylindrical extension of all ce

269 A. tumefaciens pathway resembles that of C. crescentus there are specific differences including addi

270 rebuilt the essential genome of Caulobacter crescentus through the process of chemical synthesis rew

271 C. crescentus thus repurposes pilus retraction, typically u

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

273 q from the alpha-proteobacterium Caulobacter crescentus to 2.15- angstrom resolution, resolving the c

274 of single cells of the bacterium Caulobacter crescentus to a glass surface in a microfluidic device.

275 y alterations in pilus activity stimulate C. crescentus to bypass its developmentally programmed temp

276 ns, from cell stalk formation in Caulobacter crescentus to chromosome segregation and motility in Myx

277 Thus, the major recognition elements in C. crescentus tRNA(His) are the anticodon, the discriminato

278 HisRS allowed complete histidylation of a C. crescentus tRNA(His) transcript (lacking G(-1)).

279 The PG of Caulobacter crescentus, unlike that of many other Gram-negative bact

280 A recent study suggests that Caulobacter crescentus uses a novel regulator, FzlA, to activate rin

281 The bacterium Caulobacter crescentus uses a ParA-based partitioning system to segr

282 Caulobacter crescentus uses the dynamic interactions between ParA an

283 The bacterium Caulobacter crescentus uses two-component phospho-signalling to regu

284 tigate the distribution of HU in Caulobacter crescentus using a combination of super-resolution fluor

285 ith the surface of the bacterium Caulobacter crescentus using a double-helix point spread function mi

286 s of the Gram-negative bacterium Caulobacter crescentus using cryo-electron tomography (CET) and stat

287 We focus here on Caulobacter crescentus, Vibrio cholerae, Helicobacter pylori, and Ca

288 drives cell-cycle initiation in Caulobacter crescentus We identify the type IV pilin protein PilA as

289 d tracking the S-layer protein (SLP) from C. crescentus, we show that 2D protein self-assembly is suf

290 sed during a life cycle stage of Caulobacter crescentus when the regulator is activated by phosphoryl

291 icrodomains at the cell poles in Caulobacter crescentus, where it functions as a hub protein that rec

292 is GDP-perosamine synthase from Caulobacter crescentus, which catalyzes the final step in GDP-perosa

293 Here, we focus on Caulobacter crescentus, which encodes a ProRS with a truncated INS d

294 Focusing on the model bacterium Caulobacter crescentus, which generates two different types of daugh

295 y from the alpha-proteobacterium Caulobacter crescentus, which is a model organism for studying morph

296 y of CheY-like (Cle) proteins in Caulobacter crescentus, which tune flagellar activity in response to

297 ouples phosphorylation events in Caulobacter crescentus with the AAA+ protease ClpXP to provide punct

298 haproteobacterial model organism Caulobacter crescentus, with a specific focus on LytM-like endopepti

299 bed in the alpha-proteobacterium Caulobacter crescentus, with the interacting partners of RNase E ide

300 nfirmed that these species are cleared by C. crescentus YbaK and ProXp-ala, respectively.