ライフサイエンスコーパス: crescentus

1 EAL domain protein (CC3396 from Caulobacter crescentus).

2 imorphic Gram-negative bacterium Caulobacter crescentus.

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

4 SocAB, an atypical TA system in Caulobacter crescentus.

5 al for cell cycle progression in Caulobacter crescentus.

6 alization in the model bacterium Caulobacter crescentus.

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

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

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

10 ly regulates Z ring formation in Caulobacter crescentus.

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

12 related diguanylate cyclase from Caulobacter crescentus.

13 ional investigation of PerB from Caulobacter crescentus.

14 oordinately regulate stress physiology in C. crescentus.

15 gainst its phylogenetic relative Caulobacter crescentus.

16 Z curvature and efficient constriction in C. crescentus.

17 sis and cell cycle regulation in Caulobacter crescentus.

18 gent response in the oligotroph, Caulobacter crescentus.

19 symmetrically dividing bacterium Caulobacter crescentus.

20 located between lpxA and lpxB in Caulobacter crescentus.

21 ith cytokinesis in the bacterium Caulobacter crescentus.

22 that influence FtsZ function in Caulobacter crescentus.

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

24 00 cell cycle-regulated genes in Caulobacter crescentus.

25 drive cell cycle progression in Caulobacter crescentus.

26 including chromosomal regions in Caulobacter crescentus.

27 on are temporally coordinated in Caulobacter crescentus.

28 on of a type III photolyase from Caulobacter crescentus.

29 rning the cell division cycle of Caulobacter crescentus.

30 on in the developmental cycle of Caulobacter crescentus.

31 inducible heterologous gene expression in C. crescentus.

32 hich infect freshwater bacterium Caulobacter crescentus.

33 c cell division in the bacterium Caulobacter crescentus.

34 n the asymmetric model bacterium Caulobacter crescentus.

35 as the model freshwater organism Caulobacter crescentus.

36 ture of a bactofilin domain from Caulobacter crescentus.

37 chia coli, Bacillus subtilis, or Caulobacter crescentus.

38 stigated the function of ZapA in Caulobacter crescentus.

39 e we investigate CTL function in Caulobacter crescentus.

40 cle progression in the bacterium Caulobacter crescentus.

41 bacter actinomycetemcomitans and Caulobacter crescentus.

42 hia coli, Bacillus subtilis, and Caulobacter crescentus.

43 ll division protein FtsZ in live Caulobacter crescentus.

44 that control peptidoglycan remodeling in C. crescentus.

45 e ParB/parS partition complex in Caulobacter crescentus.

46 focused on the curved bacterium Caulobacter crescentus.

47 asymmetrically is the bacterium Caulobacter crescentus.

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

49 transcriptionally cell cycle-regulated in C. crescentus.

50 roteobacterial species closely related to C. crescentus.

51 absence of polar localization in Caulobacter crescentus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

67 In Caulobacter crescentus and Escherichia coli, the protein seems to pl

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

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

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

71 rk to understand regulated proteolysis in C. crescentus and show that RcdA is not an adaptor for CtrA

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

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

74 e chromosome I segregates like the one in C. crescentus and whose chromosome II like the one in E. co

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

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

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

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

79 regulated in a similar manner to that of C. crescentus, and that the outer membrane complements of H

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

81 membrane complements of H. neptunium and C. crescentus are remarkably similar.

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

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

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

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

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

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

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

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

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

97 hromosome replication during the Caulobacter crescentus cell cycle.

98 ein complexes to orchestrate the Caulobacter crescentus cell cycle.

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

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

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

102 Caulobacter crescentus cells adhere to surfaces by using an extremel

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

104 we measured the adhesion force of single C. crescentus cells attached to borosilicate substrates thr

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

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

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

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

109 In Caulobacter crescentus cells lacking tmRNA activity there is a delay

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

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

112 phic reconstructions of dividing Caulobacter crescentus cells wherein individual arc-like filaments w

113 growth and shape data for single Caulobacter crescentus cells.

114 erial actin protein MreB in live Caulobacter crescentus cells.

115 rrays in cryotomograms of intact Caulobacter crescentus cells.

116 hemoreceptor arrays in wild-type Caulobacter crescentus cells.

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

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

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

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

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

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

123 recently been described for the Caulobacter crescentus composite GGDEF-EAL protein, CC3396.

124 The differentiating bacterium, Caulobacter crescentus, contains an operon encoding a two-component

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 ligotrophic freshwater bacterium Caulobacter crescentus, D-xylose induces expression of over 50 genes

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

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

132 nal structure of the enzyme from Caulobacter crescentus determined to a nominal resolution of 1.8 A a

133 Caulobacter crescentus differentiates from a motile, foraging swarme

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

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

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

137 Caulobacter crescentus divides asymmetrically into a swarmer cell an

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

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

140 2 from the alpha-proteobacterium Caulobacter crescentus does not need the extended -10 motif for high

141 In Caulobacter crescentus, each cell cycle produces morphologically dis

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

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

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

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

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

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

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

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

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

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

152 torque of the flagellar motor of Caulobacter crescentus for different motor rotation rates by measuri

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

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

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

156 We show here that the Caulobacter crescentus FtsK protein localizes to the division plane,

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

158 23, had no stabilizing effect on Caulobacter crescentus FtsZ filaments in vitro, which complements pr

159 Here, we show that in Caulobacter crescentus, FtsZ also plays a major role in cell elongat

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

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

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

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

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

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

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

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

168 The bacterium Caulobacter crescentus has morphologically and functionally distinct

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

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

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

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

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

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

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

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

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

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

179 arine member of the DPB that differs from C. crescentus in that H. neptunium uses its stalk as a repr

180 Growing C. crescentus in the presence of blue light dramatically en

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

182 Caulobacter crescentus initiates a single round of DNA replication d

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

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

185 Caulobacter crescentus integrates phospho-signaling pathways and tra

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

187 ome segregation in the bacterium Caulobacter crescentus involves propulsion of the replication origin

188 Caulobacter crescentus is a premier model organism for studying the

189 pothesis that stalk synthesis in Caulobacter crescentus is a specialized form of cell elongation that

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

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

192 In aquatic environments, Caulobacter crescentus is one of the first colonizers of submerged s

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

194 Caulobacter crescentus lacks these systems, but recent work has unco

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

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

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

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

199 obtained with a custom-designed Caulobacter crescentus microarray chip, we identify transcriptional

200 In Caulobacter crescentus, MreC physically associates with penicillin-b

201 Caulobacter crescentus mutants that lack the trans translation pathw

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

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

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

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

206 Enzymes of the C. crescentus pathway, including an NAD(+)-dependent xylose

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

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

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

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

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

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

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

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

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

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

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

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

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

220 he molecular basis for this phenotype, 73 C. crescentus proteins were identified that are tagged by t

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

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

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

224 logues, including the ParAs from Caulobacter crescentus, Pseudomonas aeruginosa, Pseudomonas putida,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

239 the first histidine phosphotransferase in C. crescentus, ShpA, and show that it too is required for s

240 cies, Sinorhizobium meliloti and Caulobacter crescentus, simply lack any extra nucleotide on tRNA(His

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

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

243 e the identification of 27 novel Caulobacter crescentus sRNAs by analysis of RNA expression levels as

244 C. crescentus SspB shares limited sequence similarity with

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

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

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

248 In Caulobacter crescentus, surface attachment and subsequent biofilm gr

249 We derive from these results that the C. crescentus swarmer cells swim more efficiently than both

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

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

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

253 that this organism shares more genes with C. crescentus than it does with Silicibacter pomeroyi (a cl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

272 -limited, oligotrophic environments where C. crescentus thrives.

273 C. crescentus thus repurposes pilus retraction, typically u

274 In Caulobacter crescentus, timely degradation of the master regulator C

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

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

277 rity to the characterized motifs of other C. crescentus transcriptional regulators.

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

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

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

281 Here, we provide evidence that Caulobacter crescentus uses a multimeric pole-organizing factor (Pop

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

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

284 Caulobacter crescentus uses the dynamic interactions between ParA an

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

286 ogenesis, has been identified in Caulobacter crescentus using a bioinformatic screen, targeted disrup

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

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

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

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

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

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

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

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

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

296 y studying the aquatic bacterium Caulobacter crescentus, whose cell cycle progression involves the or

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.