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 ogy in the dimorphic Gram-negative bacterium Caulobacter crescentus.

3 that spatially regulates Z ring formation in Caulobacter crescentus.

4 ion of an unrelated diguanylate cyclase from Caulobacter crescentus.

5 al and functional investigation of PerB from Caulobacter crescentus.

6 l activity against its phylogenetic relative Caulobacter crescentus.

7 f morphogenesis and cell cycle regulation in Caulobacter crescentus.

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

9 ion in the asymmetrically dividing bacterium Caulobacter crescentus.

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

11 signaling with cytokinesis in the bacterium Caulobacter crescentus.

12 ing proteins that influence FtsZ function in Caulobacter crescentus.

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

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

15 necessary to drive cell cycle progression in Caulobacter crescentus.

16 ifferentiation are temporally coordinated in Caulobacter crescentus.

17 aracterization of a type III photolyase from Caulobacter crescentus.

18 etworks governing the cell division cycle of Caulobacter crescentus.

19 ell transition in the developmental cycle of Caulobacter crescentus.

20 ous cargos, including chromosomal regions in Caulobacter crescentus.

21 nd asymmetric cell division in the bacterium Caulobacter crescentus.

22 available was the model freshwater organism Caulobacter crescentus.

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

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

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

26 tant for proper establishment of polarity in Caulobacter crescentus.

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

28 ke phages, which infect freshwater bacterium Caulobacter crescentus.

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

30 hitectures in the asymmetric model bacterium Caulobacter crescentus.

31 ession and asymmetric polar morphogenesis in Caulobacter crescentus.

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

33 normal timing of the G(1)-to-S transition in Caulobacter crescentus.

34 uired for the vibrioid and helical shapes of Caulobacter crescentus.

35 A, is critical for cell cycle progression in Caulobacter crescentus.

36 ation cycle in the differentiating bacterium Caulobacter crescentus.

37 cription of flagellar genes in the bacterium Caulobacter crescentus.

38 to study chemoreceptor polar localization in Caulobacter crescentus.

39 la putrefaciens, Sinorhizobium meliloti, and Caulobacter crescentus.

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

41 atomic structure of a bactofilin domain from Caulobacter crescentus.

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

43 Here we investigate CTL function in Caulobacter crescentus.

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

45 ng Aggregatibacter actinomycetemcomitans and Caulobacter crescentus.

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

47 bacterial cell division protein FtsZ in live Caulobacter crescentus.

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

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

50 ms to divide asymmetrically is the bacterium Caulobacter crescentus.

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

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

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

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

55 cellular localization in the model bacterium Caulobacter crescentus.

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

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

58 In Caulobacter crescentus, a flagellum is built exclusively

59 Caulobacter crescentus, a Gram-negative alpha-purple pro

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

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

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

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

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

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

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

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

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

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

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

71 In Caulobacter crescentus and Escherichia coli, the protein

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

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

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

75 dence that ferrochelatases from the bacteria Caulobacter crescentus and Mycobacterium tuberculosis po

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

77 The bacterium Caulobacter crescentus and related stalk bacterial speci

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

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

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

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

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

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

84 Swarmer cells of Caulobacter crescentus are devoid of the cell division i

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

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

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

88 Caulobacter crescentus assembles many of its cellular ma

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

90 The aquatic bacterium Caulobacter crescentus attaches to solid surfaces throug

91 Caulobacter crescentus attachment is mediated by the hol

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

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

94 ParA and ParB of Caulobacter crescentus belong to a conserved family of b

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

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

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

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

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

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

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

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

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

104 e step and the gain of motility later in the Caulobacter crescentus cell cycle, respectively.

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

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

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

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

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

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

111 Caulobacter crescentus cells adhere to surfaces by using

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

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

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

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

116 In Caulobacter crescentus cells lacking tmRNA activity ther

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

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

119 Caulobacter crescentus cells treated with amdinocillin,

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

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

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

123 moreceptor arrays in cryotomograms of intact Caulobacter crescentus cells.

124 t comprise chemoreceptor arrays in wild-type 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 The Caulobacter crescentus CgtA protein is a member of the O

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

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

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

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

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

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

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

135 Caulobacter crescentus contains one of the two known pro

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

137 The first flagellar assembly checkpoint of Caulobacter crescentus couples assembly of the early cla

138 In Caulobacter crescentus, CpdR controls the polar localiza

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

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

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

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

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

144 Caulobacter crescentus differentiates from a motile, for

145 The bacterium Caulobacter crescentus divides asymmetrically as part of

146 Caulobacter crescentus divides asymmetrically into a swa

147 The aquatic bacterium Caulobacter crescentus divides asymmetrically to a flage

148 The bacterium Caulobacter crescentus divides asymmetrically, producing

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

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

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

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

153 In Caulobacter crescentus, each cell cycle produces morphol

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

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

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

157 For example, Caulobacter crescentus encodes six glycosyltransferase p

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

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

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

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

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

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

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

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

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

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

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

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

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

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

172 Caulobacter crescentus has a dimorphic life cycle compos

173 The gram-negative bacterium Caulobacter crescentus has a life cycle that includes tw

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

175 The dimorphic bacterium Caulobacter crescentus has evolved marked phenotypic cha

176 The bacterium Caulobacter crescentus has morphologically and functiona

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

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

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

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

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

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

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

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

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

186 Caulobacter crescentus initiates a single round of DNA r

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

188 In Caulobacter crescentus, intact cables of the actin homol

189 Caulobacter crescentus integrates phospho-signaling path

190 quarter of the cell-cycle-regulated genes in Caulobacter crescentus, integrating DNA replication, mor

191 Cell division in Caulobacter crescentus involves constriction and fission

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

193 Caulobacter crescentus is a model organism for studying

194 Caulobacter crescentus is a premier model organism for s

195 Caulobacter crescentus is a small, single-celled bacteri

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

197 Caulobacter crescentus is an oligotrophic alpha-proteoba

198 Each cell division in Caulobacter crescentus is asymmetric, yielding a swarmer

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

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

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

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

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

204 Biogenesis of the single polar flagellum of Caulobacter crescentus is regulated by a complex interpl

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

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

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

208 Caulobacter crescentus lacks these systems, but recent w

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

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

211 In the bacterium Caulobacter crescentus, many cellular processes are temp

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

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

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

215 In Caulobacter crescentus, MreC physically associates with

216 Caulobacter crescentus mutants that lack the trans trans

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

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

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

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

221 trA, the master regulator regulating FlbD in Caulobacter crescentus) or are expressed from a sigma70-

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

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

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

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

226 We visualized Caulobacter crescentus pili undergoing dynamic cycles of

227 ted elements from both the sigma54-dependent Caulobacter crescentus polar flagellar hierarchy and the

228 Caulobacter crescentus possesses a single SMC homolog th

229 In the Caulobacter crescentus predivisional cell, class III and

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

231 The differentiating bacterium Caulobacter crescentus produces two different cell types

232 In Caulobacter crescentus, progression through the cell cyc

233 In Caulobacter crescentus, protein degradation by the ClpXP

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

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

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

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

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

239 on of polar development and cell division in Caulobacter crescentus relies on the dynamic localizatio

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

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

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

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

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

245 In Caulobacter crescentus, RodZ is essential for viability

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

247 The Caulobacter crescentus sensor kinase DivJ is required fo

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

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

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

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

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

253 In Caulobacter crescentus, surface attachment and subsequen

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

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

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

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

258 a systematic approach to genetic mapping in Caulobacter crescentus that is based on bacteriophage-me

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

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

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

262 In Caulobacter crescentus the partitioning proteins ParA an

263 In Caulobacter crescentus, the actin homologue MreB is crit

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

265 In Caulobacter crescentus, the ClpXP protease is essential

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

267 In Caulobacter crescentus, the genes encoding the chromosom

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

269 In Caulobacter crescentus, the origin of DNA replication is

270 In Caulobacter crescentus, the PopZ polar scaffold protein

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

272 In Caulobacter crescentus, the temporal and spatial express

273 In Caulobacter crescentus, timely degradation of the master

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

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

276 e modified a stalk-shedding mutant strain of Caulobacter crescentus to increase the yield of stalk ma

277 In both Salmonella and Caulobacter crescentus, translational regulation influen

278 In Caulobacter crescentus, two-component signal transductio

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

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

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

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

283 Caulobacter crescentus uses the dynamic interactions bet

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

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

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

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

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

289 The complete genome sequence of Caulobacter crescentus was determined to be 4,016,942 ba

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

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