ライフサイエンスコーパス: periplasmic

1 opting bipartite topologies, whereas TprF is periplasmic.

2 e, although BoMan26A and BoGal36A are likely periplasmic.

3 CsgE is a periplasmic accessory protein that plays a crucial role

4 AcrB located in the inner membrane, and the periplasmic AcrA, which bridges these two integral membr

5 Unexpectedly, the periplasmic adaptor protein CusB is a key metal-sensing

6 mplex machinery comprised of outer membrane, periplasmic adaptor, and inner membrane protein componen

7 -ATPase proton pump efflux that dissociates periplasmic AGP-Ca(2+) resulting in a Ca(2+) influx that

8 coli, encode several functionally redundant periplasmic amidases.

9 s metabolic arrangement, the distribution of periplasmic and cytoplasmic carbon fluxes was studied in

10 Interestingly, the periplasmic and cytoplasmic domains were somewhat dispen

11 opening and closing of deep cavities on the periplasmic and cytoplasmic sides.

12 ta indicated that, in the periplasm, various periplasmic and peripheral membrane enzymes transform ch

13 y which OprM is activated via opening of its periplasmic aperture through a concerted interaction wit

14 novel Hechtian oscillator that integrates a periplasmic arabinogalactan glycoprotein-calcium (AGP-Ca

15 Using the novel phenotype of periplasmic beta-galactosidase activity, we show that th

16 rface endo-1,6-beta-glucanase, BT3312, and a periplasmic beta-glucosidase that targets primarily 1,6-

17 o results show that MtrE can be regulated by periplasmic binding events and that the interaction betw

18 As an alternative, we demonstrate use of a periplasmic binding protein (PBP) to provide high affini

19 h-throughput method relies upon the thiamine periplasmic binding protein (TBP) from Escherichia coli

20 Here, we show that the periplasmic binding protein CeuE of Campylobacter jejuni

21 In Campylobacter jejuni the periplasmic binding protein CeuE, an integral part of th

22 Here we present how a gene duplication of a periplasmic binding protein in a mannose ATP-binding cas

23 the TonB-dependent transporter MbnT and the periplasmic binding protein MbnE.

24 e pathogenicity and are mediated through the periplasmic binding protein NspS and the transmembrane b

25 ed using three biological examples, namely a periplasmic binding protein, aspartate carbamoyltransfer

26 structures and ligand binding affinities of periplasmic binding proteins from bacterial phosphite an

27 cholerae, and other bacteria with homologous periplasmic binding proteins.

28 after activation of DcuS by fumarate at the periplasmic binding site.

29 nts and imported into the bacterial cell via periplasmic-binding proteins (PBPs) and ABC-transporters

30 d adaptive advantage for the presence of two periplasmic-binding proteins in ATP-binding cassette tra

31 N-terminal domain on the cell surface and a periplasmic C-terminal domain.

32 Our results identify CccA, the most abundant periplasmic c-type cytochrome in C. jejuni, as a novel a

33 bouring TatC molecules from positions in the periplasmic cap but abolished a substrate-induced disulp

34 negative TatC activity were localised to the periplasmic cap region.

35 ght-transmembrane helix fold that supports a periplasmic carbon-nitrogen hydrolase domain containing

36 tein with a cytoplasmic amino terminus and a periplasmic carboxyl terminus.

37 esent crystal structures revealing the MCR-1 periplasmic, catalytic domain to be a zinc metalloprotei

38 With LacY in proteoliposomes, the periplasmic cavity is tightly sealed and the substrate-b

39 Therefore, opening of the periplasmic cavity not only limits access of sugar to th

40 of periplasmic probes due to opening of the periplasmic cavity.

41 (SilP), an effluxer complex (SilCFBA) and a periplasmic chaperon of Ag(+) (SilE).

42 RND) system) and of a putative Cu(+)-binding periplasmic chaperone and the unusual presence of two cy

43 eta-galactosidase activity, we show that the periplasmic chaperone FkpA contributes to LacZ folding i

44 ome-binding bacterial chaperone, and SurA, a periplasmic chaperone in Gram-negative bacteria.

45 s thought to explain the essentiality of the periplasmic chaperone LolA and its OM receptor LolB that

46 g of proteins from the Sec translocon to the periplasmic chaperone network that contains SurA, Skp, D

47 We identified the PCuA C-like periplasmic chaperone PccA and analyzed its contribution

48 irected cross-linking, we show here that the periplasmic chaperone PpiD is located in front of the la

49 mitochondria-targeted form of the bacterial periplasmic chaperone Skp, but not with SurA or SecB, re

50 HdeA is a periplasmic chaperone that is rapidly activated upon shi

51 direct Cu(+) transfer from the ATPase to the periplasmic chaperone was observed.

52 Other factors, including periplasmic chaperones and inner membrane proteins, have

53 se that TraR increases the concentrations of periplasmic chaperones and proteases by directly activat

54 In bacteria, soluble cytoplasmic and periplasmic chaperones bind and deliver Cu(+) to target

55 We find that some periplasmic chaperones function primarily as quality-con

56 damage, bacteria contain the acid-activated periplasmic chaperones HdeA and HdeB.

57 of membrane thickness, the Escherichia coli periplasmic chaperones Skp and SurA, and BamA, the centr

58 iological role in the cell overlaps with the periplasmic chaperones SurA and Skp.

59 gram-negative bacteria involves delivery by periplasmic chaperones to the beta-barrel assembly machi

60 brane efflux protein TolC and with PstS, the periplasmic component of the ABC transporter complex (Ps

61 ass ZipA, indicating that linkage of FtsA to periplasmic components of the divisome through FtsN was

62 ux kinetics through the determination of its periplasmic concentrations by quantitation of the first

63 cal BAM pathway, while formation of a stable periplasmic conformer involves an export-related, foldin

64 The periplasmic conversion of ferribactin to pyoverdine is e

65 Finally I suggest that the periplasmic conversion of nutrients acquired across the

66 al envelope-restricts the expression of this periplasmic copper resistance protein solely to cells en

67 site is well preserved and the hydrolysis of periplasmic CSS anti-sigma factors is widely observed, w

68 ane transporters, whereas CopR/S responds to periplasmic Cu(+) Analysis of DeltacopR and DeltacueR mu

69 CusF is a periplasmic Cu(+) chaperone that supplies Cu(+) to the C

70 a CopR regulon composed of genes involved in periplasmic Cu(+) homeostasis and its putative DNA recog

71 Periplasmic CueO was readily activated by the addition o

72 is consistent with MbnE's proposed role as a periplasmic CuMbn transporter.

73 both cytochrome bd-type quinol oxidases and periplasmic cytochromes requires the ATP-binding cassett

74 Expression of the chimeric periplasmic-cytoplasmic MalE-LacZ72-47 protein is an his

75 um vinosum, the reaction is catalyzed by the periplasmic diheme c-type cytochrome thiosulfate dehydro

76 ively with the strength of the much stronger periplasmic dimerization of CadC.

77 y, nickel import ATP-binding protein (NikE), periplasmic dipeptide transport protein (DppA), and oute

78 lasm upon activation is complementary to the periplasmic displacement of 3-4 A of the C-terminal part

79 Z misfolding and that, in the absence of the periplasmic disulfide bond catalyst DsbA, LacZ folds in

80 DddY is the only known periplasmic DMSP lyase and is present in beta-, gamma-,

81 velocity depends on the concentration of the periplasmic DNA-binding protein ComE, indicating that Co

82 and produced a soluble version of AcrB [AcrB periplasmic domain (AcrBper)], which is highly congruent

83 bitopic inner membrane proteins with a large periplasmic domain (denoted FtsQp, FtsBp, and FtsLp) tha

84 d LptG are composed of a beta-jellyroll-like periplasmic domain and six alpha-helical segments in the

85 In addition, a small region of FtsN's periplasmic domain appears to interact with the FtsQLB c

86 Because the RodZ periplasmic domain cannot dimerize, the chimera cannot a

87 ified-PbgA oligomers are tetrameric, and the periplasmic domain contains a globular region that binds

88 ructure thus far reported for TolR is of the periplasmic domain from Haemophilus influenzae in which

89 onent analysis, we study the dynamics of the periplasmic domain of aspartate chemoreceptor Tar dimer

90 The periplasmic domain of BamA was in a closed state that pr

91 nt the 1.7-A crystal structure of the intact periplasmic domain of E. coli TolR (TolR(36-142)).

92 A deletion in the periplasmic domain of EvgS abolished the response to low

93 on of this protein, the apo-structure of the periplasmic domain of PslG (PslG(31-442)) and its comple

94 We prove this using a chimera in which the periplasmic domain of RodZ-a type II membrane protein in

95 Thirteen protomers form a large periplasmic domain of six stacked rings and a secretin d

96 Cleavage by Tsp occurs in the periplasmic domain of TcpP and requires residues TcpPA17

97 PelB, a membrane-embedded porin with a large periplasmic domain predicted to contain 19 tetratricopep

98 rithms predict to possess a large N-terminal periplasmic domain that is absent from FliO of Escherich

99 sts of a membrane-embedded beta-barrel and a periplasmic domain with five polypeptide translocation-a

100 inner membrane-anchored protein with a large periplasmic domain Y3729 (HmsC) inhibits HmsD DGC activi

101 almonella Typhimurium, we identified PbgA, a periplasmic domain-containing transmembrane protein, whi

102 intermolecular disulphide bonds in the TcpP periplasmic domain.

103 f a membrane domain on which sits a globular periplasmic domain.

104 nscription factors with relatively undefined periplasmic domains and transcription activator cytoplas

105 The crystal structure of the periplasmic domains of the VtrA/VtrC heterodimer reveals

106 The periplasmic domains of YidC and SecD are poised at the p

107 occurred with high efficiency for all TM and periplasmic domains tested, thus eliminating the need fo

108 nd a pair of hydrophobic patches keeping the periplasmic domains together in the native dimer.

109 mains drives opening and closing of the MacB periplasmic domains via concerted movements of the secon

110 thought to interact through their respective periplasmic domains, ToxRp and ToxSp.

111 hydrophobic cavity toward the transporter's periplasmic domains.Lipopolysaccharides (LPS) are synthe

112 , the rod substructure of the flagellum is a periplasmic driveshaft that couples the torque generated

113 is cytoplasmic motif had to be linked to the periplasmic E domain of FtsN to bypass ZipA, indicating

114 correlated with the reduction levels of the periplasmic electron transfer proteins; the limiting fir

115 terestingly, a spontaneous suppressor, D35E (periplasmic end of helix I), was isolated from the R363Q

116 an SPase I cleavage site (AAA or AQA) at the periplasmic end of the TM helix.

117 Out of five periplasmic enzymes, PvdM, PvdN, PvdO, PvdP, and PvdQ, f

118 ly depolymerized to mannose by the action of periplasmic enzymes.

119 , with its catalytic cavity connected to the periplasmic exit of the TM domain.

120 embedded cavity with a lateral opening and a periplasmic exit.

121 This study focuses on the periplasmic ExoR regulator, which was identified based o

122 ansfer of l-Ara4N to the LPS molecule at the periplasmic face of the inner membrane, but its topology

123 americ adaptor that binds and closes off the periplasmic face of the secretion channel, creating a 24

124 adD21, and Pks3/4; that of PAT occurs on the periplasmic face via transesterification reactions betwe

125 ncharacterized helical membrane domain and a periplasmic facing soluble domain.

126 The periplasmic five-POTRA domain of BamA is flexible in sol

127 gy with hook-shaped ends and the presence of periplasmic flagella (PF) with pronounced spontaneous su

128 investigated the role played by T. denticola periplasmic flagella (PF), unique motility organelles of

129 for spirochetal morphology and motility, the periplasmic flagella display no additional properties re

130 th one or two flat curves, and have 10 to 14 periplasmic flagella inserted at each cell end.

131 rted that a nonmotile flaB mutant that lacks periplasmic flagella is rod shaped and unable to infect

132 tor rotation or merely the possession of the periplasmic flagella was crucial for cellular morphology

133 pathogenicity; indeed, spirochaete flagella (periplasmic flagella) reside and rotate within the perip

134 hete, and motility, which is provided by its periplasmic flagella, is critical for every part of the

135 otB mutant that is nonmotile but retains its periplasmic flagella.

136 lated bacteria, spirochetes possess a unique periplasmic flagellar structure called the collar.

137 ve generated bacterial strains with enhanced periplasmic folding capacity.

138 pathogen, Campylobacter jejuni, possesses a periplasmic formate dehydrogenase and two terminal oxida

139 equent electron transfer could proceed via a periplasmic formate dehydrogenase and/or hydrogenase, al

140 Introduction of mutations in the periplasmic gate lead to the formation of a channel that

141 entral secretin PilQ shift by ~30 A, and two periplasmic gates open to make way for pilus extrusion.

142 In this study, we reveal that a putative periplasmic GH115 from the human gut symbiont Bacteroide

143 the first two crystal structures of soluble periplasmic globular domain of PbgA from S. typhimurium

144 e production of type I LTA and osmoregulated periplasmic glucans in gram-negative bacteria are highli

145 ween the ppgL gene (PA4204), which encodes a periplasmic gluconolactonase, and, in the opposite orien

146 first high resolution crystal structures of periplasmic glucose-binding protein fromPseudomonas puti

147 hat FoxR undergoes self-cleavage between the periplasmic Gly-191 and Thr-192 residues independent of

148 are consistent with the conclusion that the periplasmic half-channel is more easily protonated in a

149 phenomenon of production of both surface and periplasmic immunogenic lipoprotein isoforms has possibl

150 ToxR requires its operon partner ToxS, a periplasmic integral membrane protein, for full activity

151 dhesion proteins of the outer membrane via a periplasmic interaction platform, which presumably invol

152 The binding of a TonB fragment to the periplasmic interface alters the configuration of the se

153 of at least two VirB substrates that have a periplasmic intermediate and that it directly interacts

154 Furthermore, the mutant does not accumulate periplasmic L-amino acid oxidase during N deprivation.

155 flet of the inner membrane is flipped to the periplasmic leaflet by MsbA, an ATP-binding cassette tra

156 binds deep inside MsbA at the height of the periplasmic leaflet, establishing extensive hydrophilic

157 ement of 3-4 A of the C-terminal part of the periplasmic ligand-binding domain upon ligand occupancy

158 are long helical proteins that consist of a periplasmic ligand-binding domain; a transmembrane regio

159 ms, assembles into an oligomeric ring in the periplasmic-like space between the two membranes.

160 from the nitrilase domain interacts with the periplasmic lipid leaflet, forming an interfacial entran

161 a gene, virJ, that codes for a protein with periplasmic localization that is involved in the intrace

162 s a broad impact on gene expression from its periplasmic location, a genetic screen was performed to

163 rane segments and reveals a newly identified periplasmic loop between the third and fourth transmembr

164 Two helices located in a periplasmic loop between two transmembrane helices conta

165 icularly a single residue located at the TM1/periplasmic loop interface, F47 of Staphylococcus aureus

166 ng binds and the other located in the second periplasmic loop of DsbB, which interacts with DsbA.

167 chor sequence promoting translocation of the periplasmic loop via a hairpin mechanism.

168 ransmembrane helices (TMHs), a large central periplasmic loop, and a C-terminal domain containing the

169 er contains 12 transmembrane helices and two periplasmic loops that suggest a plausible pathway for s

170 alF-MalG; a homodimeric ATPase, MalK2; and a periplasmic maltose receptor, MalE.

171 A periplasmic maltose-binding protein (MBP) delivers malto

172 in modifications are well characterized, the periplasmic maturation steps are far from understood.

173 flux transporters function in complexes with periplasmic membrane fusion proteins (MFPs) that enable

174 o communicate conformational changes between periplasmic, membrane, and cytoplasmic regions.

175 ructural model of CnrX where a cradle-shaped periplasmic metal sensor domain is anchored into the inn

176 de two routes for methylamine oxidation: the periplasmic methylamine dehydrogenase (MaDH) and the cyt

177 M1, the best-studied aerobic methylotroph, a periplasmic methylamine dehydrogenase that catalyzes the

178 icotinate and related modulators on the BvgS periplasmic moiety by using site-directed mutagenesis an

179 The periplasmic moiety of the homodimeric sensor kinase BvgS

180 affects the conformation and dynamics of the periplasmic moiety.

181 MS also identified candidate partners for periplasmic MOSP, including TDE1658, a spirochete-specif

182 se, and unassembled lipopolysaccharides bind periplasmic MucB, releasing MucA and facilitating its pr

183 This result suggests that the periplasmic nitrate reductase (Nap) of S. gotlandica str

184 Classified into three distinct types--periplasmic nitrate reductase (Nap), respiratory nitrate

185 In contrast, a strain lacking a functional periplasmic nitrate reductase (napA mutant) exhibited a

186 results suggest that S. Typhimurium uses the periplasmic nitrate reductase to support its growth on t

187 he second section focuses on the features of periplasmic nitrate reductase where the catalytic subuni

188 iated growth inhibition, whereas all but the periplasmic nitrite reductase NrfA provide protection ag

189 e Escherichia coli K-12 nrf operon encodes a periplasmic nitrite reductase, the expression of which i

190 It involves two proteins: a periplasmic one, MsrP, previously named YedY, carrying o

191 nst a LacY mutant immobilized in an outward (periplasmic)-open conformation bind to the flexible WT p

192 s (Nbs) against a LacY mutant in an outward (periplasmic)-open conformation to stabilize this state o

193 Recently, a structure with a narrow periplasmic opening and an occluded galactoside was obta

194 itrosoglutathione (GSNO) in vitro However, a periplasmic or extracellular denitrosylase has not been

195 binding proteins, and degradation is largely periplasmic or intracellular.

196 actin, and their fluorophore is generated by periplasmic oxidation and cyclization reactions of d-tyr

197 NOX family and involved in the reduction of periplasmic oxidized proteins.

198 Here we report that the putative periplasmic oxidoreductase PvdO of Pseudomonas fluoresce

199 Although only the soluble, periplasmic part of AcrB binds and exports the ligands,

200 ch is highly congruent in structure with the periplasmic part of the full-length protein, and is capa

201 ia coli, a proteolytic system comprising the periplasmic PDZ-protease Prc and the lipoprotein adaptor

202 hey operate efficiently without compromising periplasmic plasticity.

203 upon cellular demand while still maintaining periplasmic plasticity; this could be broadly relevant t

204 nquenching of fluorescence in three pairs of periplasmic probes due to opening of the periplasmic cav

205 -competent, they were slowly degraded by the periplasmic protease DegP.

206 ies have established the essentiality of the periplasmic protease MarP for Mtb to survive in acidifie

207 e receptor for c-di-GMP, LapD, and a cognate periplasmic protease, LapG.

208 lipoprotein of unknown function, NlpI, and a periplasmic protease, Prc (or Tsp).

209 e stalled autotransporter is not degraded by periplasmic proteases; and (v) inverse autotransporter p

210 We discovered that the periplasmic protein CsgC was a highly effective inhibito

211 a coli disulfide bond formation pathway, the periplasmic protein DsbA introduces disulfide bonds into

212 The periplasmic protein FlhE is a member of the flhBAE opero

213 es and chaperones exhibit important roles in periplasmic protein quality control and stress responses

214 xin MqsR degrades YgiS mRNA, which encodes a periplasmic protein that promotes deoxycholate uptake an

215 ty to the N-terminal domain of the prevalent periplasmic protein TolB.

216 -GMP production by YfiN was repressed by the periplasmic protein YfiR, and deletion of yfiR promoted

217 Fvs was confirmed by competitive ELISA using periplasmic protein.

218 NAs encoding outer-membrane, cytoplasmic and periplasmic proteins are distributed throughout the cyto

219 olated were found to overexpress one or more periplasmic proteins including OsmY, Ivy, DppA, OppA, an

220 compassing 90% inner- and outer-membrane and periplasmic proteins of Escherichia coli.

221 to be specifically involved in the repair of periplasmic proteins oxidized by hypochlorous acid.

222 tect against the acid-induced aggregation of periplasmic proteins.

223 TAA autotransport is assisted by additional periplasmic proteins.

224 electron acceptors for oxidative folding of periplasmic proteins.

225 To protect their periplasmic proteome against rapid acid-mediated damage,

226 ant predators can replicate unusually in the periplasmic region between the peptidoglycan wall and th

227 uorimetry showed interaction of the isolated periplasmic region of McpX (McpX(PR) and McpX34-306 ) wi

228 olves association of the plug helices in the periplasmic region of the MotB dimer into a parallel coi

229 We previously showed that the periplasmic region of the protein, particularly a single

230 that link the outer membrane to the aqueous periplasmic region.

231 s with most of the transmembrane helices and periplasmic regions of SecY, with a clustering of intera

232 Four highly conserved periplasmic residues in B. cenocepacia ArnT, tyrosine-43

233 sought to determine whether PelB serves as a periplasmic scaffold that recruits other components of t

234 s direct interactions with transmembrane and periplasmic segments, as well as peripheral interactions

235 The absence of a periplasmic sensing domain suggested that PilS may sense

236 Salmonella PhoQ is a histidine kinase with a periplasmic sensor domain (PD) that promotes virulence b

237 tion of osmotic upshift does not require its periplasmic sensor domain.

238 SagS harbours a periplasmic sensory HmsP, and phosphorelay HisKA and Rec

239 The Escherichia coli Tsr protein contains a periplasmic serine-binding domain that transmits ligand

240 ight unique Nbs that bind exclusively to the periplasmic side and block transport, but increase the a

241 el with a large pore that is occluded on the periplasmic side by the N-terminal 15 residues of the pr

242 Surprisingly, the opening on the periplasmic side is sufficiently narrow that sugar canno

243 of bacterial cytochrome c oxidase lie on the periplasmic side of the cytoplasmic membrane.

244 polysaccharides (LPS) are synthesized at the periplasmic side of the inner membrane of Gram-negative

245 The nitrilase domain is located on the periplasmic side of the membrane, with its catalytic cav

246 showed that the protein is localized at the periplasmic side of the outer membrane.

247 ble-Trp mutant, which is already open on the periplasmic side, the Nbs have little effect.

248 almost occluded and is partially open to the periplasmic side; the cytoplasmic side is tightly sealed

249 However, its periplasmic signal sensor domain is unique and is found

250 are transported by chaperones, including the periplasmic Skp.

251 main determinant of NccX dimerization is the periplasmic soluble domain and that the interaction betw

252 cific and high-affinity binding of zinc by a periplasmic solute-binding protein (SBP).

253 -electron tomograms show that tubes span the periplasmic space and are present while the genome is be

254 The rod subunits self-assemble, spanning the periplasmic space and stopping at the outer membrane whe

255 esis and translocation of DAT and PAT to the periplasmic space are coupled and topologically split ac

256 at rod length is limited by the width of the periplasmic space between the inner and outer membranes.

257 eria have two lipid membranes separated by a periplasmic space containing peptidoglycan.

258 combinant chimeras that were produced in the periplasmic space of E. coli as soluble pentamers, as co

259 involved in the release of agmatine into the periplasmic space of E. coli.

260 cetes, including a defined outer membrane, a periplasmic space that can be greatly enlarged and convo

261 ecules can be taken up and accumulate in the periplasmic space through unclear mechanisms.

262 rA and PEB3, depends on translocation to the periplasmic space via the general secretory pathway.

263 The concentrations of proteins in the periplasmic space were estimated to be 350 and 25 mg/ml

264 asmic flagella) reside and rotate within the periplasmic space(2-11).

265 0 nm) formed either in the cytoplasm, in the periplasmic space, or extracellularly.

266 anslocation across the two membranes and the periplasmic space.

267 te channels of sufficient length to span the periplasmic space.

268 e channel, followed by diffusion towards the periplasmic space.

269 oth inner and outer membranes separated by a periplasmic space.

270 The periplasmic SPOR domain of FtsN was previously shown to

271 ytoplasm, a cytoplasmic disc and dome, and a periplasmic stem.

272 city may prepare the bacterium to endure the periplasmic stress of sex pilus biosynthesis during mati

273 tense transition state that involves a large periplasmic structural block.

274 ut the bulk of the protein exists as a large periplasmic structure enclosing an extensive lumen.

275 A small periplasmic subdomain ((E) FtsN) is required and suffici

276 Using a mutant with a periplasmic substitution in ToxS, we found that the prot

277 transmembrane domain homodimer, RbsC2; and a periplasmic substrate binding protein, RbsB.

278 Periplasmic substrate-binding proteins (SBPs) bind to th

279 e transported into the cytoplasm, or via the periplasmic sugar binding protein, ChvE, play a critical

280 , which is able to bind both Hep and HS, and periplasmic sulfatases reveal the major specificity dete

281 toplasmic Cu(+) can be precisely directed to periplasmic targets via specific transporter-chaperone i

282 During this process, the periplasmic thiol-disulfide oxidoreductase DsbA is thoug

283 We show here that a periplasmic thioredoxin (TlpA) acts as a specific reduct

284 on of holocytochromes c by CcmFH and CcmG, a periplasmic thioredoxin, independent of CcmABCDE (we ter

285 onstrate that signaling also occurs from the periplasmic to the extracellular surface in BtuB.

286 Moreover, mutants in the periplasmic Ton box that are transport-defective alter t

287 ther proteobacteria that we termed PtaA for "periplasmic transaminase A" An in-frame-deleted ptaA mut

288 In silico analyses indicated a periplasmic transaminase in fluorescent pseudomonads and

289 verdine-producing bacteria, its catalysis of periplasmic transaminations is most likely a general too

290 gaB associates with PNAG continuously during periplasmic transport.

291 proteins, including overwhelmingly abundant periplasmic transporters for nutrient acquisition and pr

292 as applied to the tripartite ATP-independent periplasmic transporters.

293 The tripartite ATP-independent periplasmic (TRAP) transporters are a widespread class o

294 Tripartite ATP-independent periplasmic (TRAP) transporters are secondary transporte

295 OSP in TDE exists as outer membrane (OM) and periplasmic trimeric conformers; PelB-MOSP, in contrast,

296 the fluorophore is known to be driven by the periplasmic tyrosinase PvdP.

297 that this discrepancy can be resolved if the periplasmic volume decreases as the cell wall becomes so

298 ow alterations of cell wall stiffness affect periplasmic volume regulation.

299 The length of Braun's lipoprotein determines periplasmic width by tethering the outer membrane to the

300 This work extends our understanding of periplasmic zinc trafficking and the function of chapero