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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.

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