ライフサイエンスコーパス: planta

1 enhanced BPM1 stability and accumulation in planta.

2 midgut surface of insect vectors, but not in planta.

3 s impact, little is known about Al action in planta.

4 tive sites to support carboxylation rates in planta.

5 tein complexes in monolignol biosynthesis in planta.

6 ectic domain rhamnogalacturonan II (RGII) in planta.

7 sed protein stability of the PSR1 mutants in planta.

8 heat (Triticum aestivum) Actin1 (TaACT1), in planta.

9 d by both Leptosphaeria spp. in vitro and in planta.

10 s that they are found in very low amounts in planta.

11 ulated genes not detectably bound by NLP7 in planta.

12 OsSQE2 is the preferred partner of OsONS1 in planta.

13 TP-binding protein that formed homodimers in planta.

14 ly been investigated after overexpression in planta.

15 turation into an active form in vitro and in planta.

16 athway (ABI3, ABI4 and ABI5) was observed in planta.

17 adly used to investigate effector biology in planta.

18 AMT1;1 and AMT1;2 in yeast, oocytes, and in planta.

19 Rx1 binds to NbGlk1 in vitro and in planta.

20 or difference in sensitivity in vitro and in planta.

21 ching of ROS by carnosic acid takes place in planta.

22 aining proteins able to induce cell death in-planta.

23 a novel processing mechanism is occurring in planta.

24 e, indicative of increased TCE metabolism in planta.

25 C glucuronosylation could not be analyzed in planta.

26 en ER bodies and glucosinolate metabolism in planta.

27 fectors enabled direct effector detection in planta.

28 minearum is reorganized both in vitro and in planta.

29 emain incompletely understood, especially in planta.

30 e formation of mature and bioactive CLE40 in planta.

31 t SOT1 is responsible for their formation in planta.

32 easy platform for assessing gene function in planta.

33 "gatekeeper" Tyr both in vitro as well as in planta.

34 d to investigate the RNA binding proteome in planta.

35 s integrated into the complex HSR network in planta.

36 ake and sunlight-triggered release of T6P in planta.

37 OW transcriptional cascade were validated in planta.

38 ic fruiting bodies and GFP was detectable in planta.

39 ave a higher probability of being present in planta.

40 on strategy directly modulates T6P levels in planta.

41 he Bradi5g03300 UGT converts DON into D3G in planta.

42 of self-regulated auxin-based patterning in planta.

43 state and explaining its weaker activity in planta.

44 ssue-specific expression of BAS1 and SOB7 in planta.

45 an absolute requirement for all cysteines in planta.

46 iding with strongly reduced fungal growth in planta.

47 ect and analyze PCD processes in vivo and in planta.

48 rting a role for PSKR1 signaling via cGMP in planta.

49 in reorganization of the COP1/SPA complex in planta.

50 nd over-expression lines of CGR2 and CGR3 in planta.

51 FUL) and ARF proteins directly associate in planta.

52 ectopic expression of specific antibodies in planta.

53 s colonization when transiently expressed in planta.

54 3 confirmed the regulatory role of CIPK23 in planta.

55 directly interacts with RACB in yeast and in planta.

56 nfirm the N and C terminus of the peptide in planta.

57 ating lignin composition and/or structure in planta.

58 ole of a phenylpropanoid coupling product in planta.

59 PP2A constitutively associates with BAK1 in planta.

60 LS1 protein facilitates the movement of B in planta.

61 Specific interactions were verified in planta.

62 he nematode and insect molecules secreted in planta.

63 which interacts with AvrPtoB in yeast and in planta.

64 nfers transcriptional activation activity in planta.

65 evelopment by affecting auxin homeostasis in planta.

66 stably fine-tuning residual gene function in planta.

67 yping data from synthetic peptide screens in planta.

68 the accumulation of sulfated salicinoids in planta.

69 ifunctionality and the structure of cutin in planta.

70 ting that they interact to form a complex in planta.

71 precursor, strictosidine, to various TIAs in planta.

72 with other bacterial species in vitro and in planta.

73 unannotated ORFs generate stable proteins in planta.

74 analysis of protein-protein interactions in planta.

75 heterologous experimental system and also in planta.

76 eracts with herbivory-induced CALMODULIN2 in planta.

77 Aphis gossypii, Ag10k, interact with TFT7 in planta.

78 V, and traces of CO V, both ex planta and in planta.

79 y the functional status of xylem networks in planta.

80 with components of the decapping complex in planta.

81 tion of chemical specificity on autophagy in planta.

82 To check this mechanism in planta, a benzyl etherification of nonesterified hydroxy

83 the legal scheduling of Cannabis, the low in planta abundances of nearly all of the dozens of known c

84 a role in the regulation of HPR1 activity in planta, although it was not required for growth under am

85 In planta analyses revealed that AVR1 and Sec5 are in close

86 However, detailed in planta analyses suggest that the biosynthesis of 2,3-DP

87 its inception, the available options for in planta analysis are still subject to very low signal-to-

88 In planta analysis of IAA, PAA, SA, and BA and their respec

89 Using in planta ancestral protein reconstruction, we demonstrate

90 e investigated the role of the ACT domain in planta and confirmed its involvement in chloroplast diff

91 FDH is ubiquitinated in planta and degraded by the 26S proteasome.

92 vrBs2 and xopX both showed reduced growth in planta and delayed spread through the vasculature system

93 no relationship was seen between fitness in planta and either the magnitude of their expression in p

94 disease and its pathogen was investigated in planta and fungal growth and sporulation production was

95 evidence obtained through gene silencing in planta and heterologous expression in bacteria supports

96 O III and CO IV, and traces of CO V, both ex planta and in planta.

97 tes, complementing and extending previous in planta and in vitro investigations.

98 Functional studies (in planta and in vitro) show that Vv3AT has a broad anthocy

99 We evaluated, both in planta and in vitro, how whitefly infestation affects cr

100 eir roles have been difficult to decipher in planta and in vitro.

101 pathway and interact physically in vitro, in planta and in wheat cells.

102 immunity and protein-protein interactions in planta and in yeast (Saccharomyces cerevisiae).

103 triggers Sr50-dependent defense responses in planta and interacts directly with the Sr50 protein.

104 its antioxidative features, this compound in planta and its antioxidant mechanism have received littl

105 Excess Mn also increased the interaction in planta and led to greater accumulation of the complex at

106 how the levels of tyrosine are controlled in planta and linked to overall growth and development.

107 -related Accelerated Cell Death11 (ACD11) in planta and promotes the proteasome-dependent turnover of

108 defined toolkit for H(2) O(2) monitoring in planta and showed that intracellular H(2) O(2) measureme

109 roid vectors is significantly affected by in planta and soil concentration gradients and when concent

110 o a dissolution of the low soluble CeO(2) in planta and subsequent precipitation.

111 show that HsGCPII cannot substitute AMP1 in planta and that an HsGCPII-specific inhibitor does not e

112 vides fitness and colonization advantages in planta and that the role of the T6SS is not restricted t

113 e genes can determine anthocyanin content in planta and, hence, fitness under UV-B irradiation stress

114 -ol and germacrene-d-4-ol were detectable in planta, and gene expression analysis of the biosynthetic

115 etome of X. fastidiosa, both in vitro and in planta, and identified LesA as one of the pathogenicity

116 ndent interbacterial competition activity in planta, and the C-terminal variable region of VgrG2 gove

117 structure, the function of these glycans in planta, and the mechanisms by which they are depolymeriz

118 LA10 can self-associate both in vitro and in planta, and this self-association correlates with their

119 ormed to validate one of the interactions in planta, and virus-induced gene silencing was used for fu

120 nctional roles of individual NCR peptides in planta are not known.

121 In planta as in the moss Physcomitrella patens protoplasts,

122 relationship appears to be very specific in planta, as other fatty acids (FA) desaturases do not req

123 read conidia infect ash and may sporulate in planta, as well as in forest debris.

124 site and tested these by mutagenesis and in planta assays of necrosis induction by expression in N.

125 In vitro and in planta assays showed that unlike SrCPS and SrKS1, SrCPS2

126 of Jas9-VENUS to analyse responses to JA in planta at a cellular scale, both quantitatively and dyna

127 ation and quantification of fungal growth in planta at early infection stages surpassing visualizatio

128 l group of endogenous molecules affecting in planta auxin concentrations.

129 In planta, auxin is the first hormone group that was discov

130 PYL6 and MYC2 interact in planta based on bimolecular fluorescence complementation

131 PGIPs are predominantly studied in planta because their heterologous expression in microbia

132 red, many of which have not been reported in planta before.

133 In planta bimolecular fluorescence complementation assays c

134 S8 based on a yeast two-hybrid screen and in planta bimolecular fluorescence complementation.

135 roader DNA structural features may define in planta binding.

136 oil microbiome analysis with in vitro and in planta bioassays to show that competition for iron via s

137 an integrated approach to understand the in planta biotransformation of KAuCl4 into AuNPs.

138 knockout mutant background revealed that, in planta, both forms are negative regulators of abscisic a

139 d plant callose biosynthesis in vitro and in planta but also partially restored virulence to the Delt

140 necessary for natural rubber biosynthesis in planta, but yeast-expressed CPTL2 and CPT3 alone could n

141 ere, we show that induction of cell death in planta by a secreted plant protein GRIM REAPER (GRI) is

142 tent-specifically, RNAs 3 and 4-assembled in planta by agrobacterium-mediated transient expression.

143 y suggesting that the antibiome expressed in planta by B. amyloliquefaciens does not reflect the vast

144 Gbetagamma dimers at the plasma membrane in planta by bimolecular fluorescence complementation.

145 These interactions were confirmed in planta by FLIM-FRET and BiFC and the roles of SR34 domai

146 est the hypothesis that OGs are generated in planta by partial inhibition of pathogen-encoded polygal

147 verified that a similar trimer is formed in planta by the common bean (Phaseolus vulgaris) NF-Y subu

148 east or Xenopus laevis oocytes, and their in planta cellular and subcellular localization.

149 By in planta co-expression of tyrosyl protein sulfotransferase

150 However, in an in planta coinfection assay, A. tumefaciens used Tde effect

151 t are transcriptionally regulated by LEC1 in planta Collectively, our results show that LEC1 controls

152 pression in planta or degree of induction in planta compared to in vitro conditions measured in other

153 Results indicate that in planta concentrations are significantly and positively r

154 In planta concentrations of these compounds strongly inhibi

155 The biofilms formed by the exDNase mutant in planta contained more and thicker fibres.

156 Therefore, in planta, CUS1 can catalyze the esterification of both pri

157 rtain types of cells at defined stages of in planta development for in-depth analysis.

158 The altered Ce in planta distribution was partially associated with the fo

159 e have recently provided the first direct in planta evidence for polyspermy induced polyploidization.

160 induced programmed cell death, providing in planta evidence of allosteric CNGC regulation by CaM.

161 s to assemble each virion type separately in planta Experimental approaches analyzing the morphology,

162 Some in planta experiments designed to test the validity of PB1

163 In planta expression identified an effector, with an N term

164 In planta expression of a thermophilic endoglucanase (AcCel

165 Elevated in planta expression of resistance-type Rhg1 alpha-SNAPs de

166 In planta expression of SAUR-immune pp2c.d2 or pp2c.d5 deri

167 Here, we show that in planta expression of the RXLR effector Pi04314 enhances

168 nsient Agrobacterium tumefaciens-mediated in planta expression, transformation of P. infestans with f

169 In planta feeding of C(14) or C(13)-labelled tZ suggests th

170 ualist services to hosts and had superior in planta fitness during clonal infections, consistent with

171 Here, we assessed in planta flg22-signaling competency in the context of liga

172 We used in planta fluorescence lifetime imaging microscopy and fluo

173 ncluding yeast two-hybrid, pull-down, and in planta fluorescence resonance energy transfer assays, we

174 ve broad application as it determines the in planta flux control that a single component has upon acc

175 , we scrutinized the requirement of Rad54 in planta for two distinct fully infectious geminiviruses w

176 alysis of E. lathyris L. mature seeds and in planta functional characterization, we identified three

177 haracterized at biochemical levels, their in planta functions remain uncertain.

178 of ligands and discriminate between their in planta functions.

179 enzyme variant can produce bioactive GAs in planta Furthermore, a genetically modified GA3ox5 varian

180 on of acetolactate synthase1 gene through in planta gene editing.

181 The in planta generation of one of the most complex human prote

182 AtBRCA1 physically interact in vitro and in planta Genetic interaction between the RBR-silenced amiR

183 t had not been previously associated with in planta growth were also required for maximum epiphytic o

184 l of plant-pathogenic fungi during on and in planta growth, following the elucidation of infection st

185 rge aggregates without the cognate Se SSU in planta, harboring active Rubisco that enables plant grow

186 ants; however, their antioxidant activity in planta has been debated.

187 ism of heme-dependent inhibition of GluTR in planta has remained elusive.

188 In this study we determined that the in planta heterologous expressed OeGLU, an oleuropein-speci

189 Such high specialization of class II CPRs in planta highlights the evolutionary strategy that ensures

190 utin influences many biological processes in planta; however, due to its complexity and highly branch

191 tein interaction resource, obtained using in planta immunoprecipitation (IP) followed by mass spectro

192 the nucleus and interact with each other in planta in bimolecular fluorescence complementation and c

193 gth Sr33 and Sr50 proteins self-associate in planta In contrast, truncated CC domains equivalent in s

194 l and biophysical techniques in vitro and in planta, including kinase assays, microscale thermophores

195 rect effects of BAR-containing transgenes in planta, including modified amino acid levels, have been

196 In planta, increasing NEDD8 gene dosage is sufficient to su

197 Subcellular localization in planta indicated that AtPyrP2 was localized in plastids

198 In planta-induced mobilization of HAI2 was regulated by quo

199 In planta interactions between UVR8 and PIF5 are not observ

200 ansporters, root exudate composition, and ex planta interactions with agriculturally and economically

201 profiling revealed that MDCA is converted in planta into piperonylic acid (PA), an inhibitor of CINNA

202 In planta, IPK acts in parallel with the MVA pathway and pl

203 metabolism for colonization and survival in planta Kiwellin (KWL) proteins are a widespread family o

204 a dysfunctional protein that accumulates in planta like wild-type PEN3.

205 s spectrometry analysis, we show that the in planta mature form of proGrCLE1, a multidomain CLE effec

206 rties of the sensor that are critical for in planta measurements, including specificity, pH stability

207 Here we present an efficient in planta method for Agrobacterium-mediated genetic transfo

208 of genetic factors associated solely with in planta mobilization of an ICE demonstrates that this pro

209 mutants, were performed to elucidate the in planta molecular mechanisms involved in induced resistan

210 with COP1 in yeast two-hybrid assays and in planta Mutations in the VP motif of CRY2 abolished the C

211 n summary, we established a technique for in planta NAD redox monitoring to deliver important insight

212 In planta, NatB complex formation was essential for enzymat

213 Both antibodies were efficiently sulfated in planta on coexpression of an engineered human tyrosylpro

214 ions on protein function and localization in planta, on metal-binding properties in vitro and on prot

215 ctors that participate in gene expression in planta or are suspected to be involved in that process b

216 either the magnitude of their expression in planta or degree of induction in planta compared to in v

217 s and the improvement of MIA availability in planta or in vitro.

218 useful in the engineering of anthocyanins in planta or in vitro.

219 Unlike previous in planta or intra-genomic homologous recombination reports

220 the duration of photoreceptor activation in planta Our findings show that slowing the phototropin ph

221 We have developed an in planta packaging assay based on the transient expression

222 ecent progress in understanding SL action in planta, particularly in the context of the regulation of

223 itation at a force of 5 N was applied to the planta pedis of the transplanted limb for 10 days, 4 tim

224 ion of recombinantly produced enzymes and in planta peptide cyclization assays, we define the molecul

225 es enhanced leaf colonization mediated by in planta Pi04314 expression.

226 nteraction between cryptochromes and Cop1 in planta, pointing to a common ancestor in which the crypt

227 e kinases in vitro but are phosphorylated in planta, possibly by an unknown kinase.

228 or pathogen cues triggers pathogen growth in-planta post penetration.

229 Genetic analysis shows that both in planta PR gene expression and release of elicitors are t

230 in profiling analyses documented that the in planta presence of 4E02 does not impede enzymatic activi

231 contribution SiMPull is poised to make to in planta protein interaction studies.

232 dge validated here for the first time for in planta quantitation of biopharmaceuticals, is especially

233 The functional roles of XIP in planta remain poorly identified.

234 r the regulation of nuclear-encoded genes in planta remains to be explored.

235 ndependent ABA-signaling branches and the in planta requirement of simultaneous phosphorylation at tw

236 ate 76% and 87% of TF(1) indirect targets in planta, respectively.

237 Our in planta results show that OPT3 is important for leaf phlo

238 This is the first study to employ in planta RNAi approach to target the Rs-cps gene for the c

239 To evaluate the effect of in planta RNAi on the control of this nematode, a specific

240 III peroxidases (PRXs) in plants, but the in planta role of most members of this family still remains

241 Next we showed that in planta sgRNAs bound to Cas9 are devoid of the expected 5

242 RNA sequencing analysis in planta showed that SnTox1 was differentially expressed b

243 Here, we perform in planta silencing efficacy assays on seven Arabidopsis MY

244 on than wild-type plants, and vice versa, in planta silencing of MjTTL5 substantially increased plant

245 family of GPCRs, with many of them having in planta-specific upregulation and a common promoter eleme

246 Knowledge of thapsigargin in planta storage and biosynthesis has been limited.

247 In vitro and in planta studies demonstrate that P2K2 and P2K1 interact a

248 In planta, such monolignol-pCA conjugates become incorporat

249 d when co-expressed with a functional KEG in planta, suggesting that KEG contributes to FDH degradati

250 Nevertheless, bioassays using an in Planta System showed that the Asian citrus psyllid was v

251 uantitative proteomics, we established an in planta system that enables rapid study of MPK4 signaling

252 bioenergy crops to accumulate bioproducts in planta that can be fractionated and recovered at biorefi

253 hree proteins may be present in a complex in planta that is required to coordinate a correct photoper

254 We found that, in planta, the constitutively active, GTP-bound AtGPA1(Q222

255 pression analyses in mutants reveal that, in planta, the majority of these regulators repress the tra

256 intact when AvrRpt2 is directly expressed in planta These observations led us to discovery of a netwo

257 made in yeast, Lr67res reduced Glc uptake in planta These results confirm that the pathway by which L

258 retention of ATG8CL binding in vitro and in planta This study offers new insights into structure/fun

259 our toolbox can be used to deploy the FBP in planta to build auto-luminescent reporters for the study

260 emical assays and heterologous expression in planta to demonstrate that TcADH2 encodes an enzyme that

261 PCBER is to reduce phenylpropanoid dimers in planta to form antioxidants that protect the plant again

262 s revealed that SPT known to be activated in planta to SPT-enol acts as a developmental inhibitor of

263 s the auxin-responsive PIN3 transcription in planta to steer the early steps of lateral root formatio

264 it Regulatory Particle AAA-ATPase6 (RPT6) in planta to suppress proteasome activity, resulting in the

265 We developed a novel in planta transcriptional activation/repression assay and s

266 y, particularly rhizosphere interactions, in planta transformations, and physicochemical properties b

267 ng mechanisms of uptake and accumulation, in planta transformations, the effects of PPCPs on plants,

268 Tobacco rattle virus-derived plasmid for in planta transient expression of double stranded RNA (dsRN

269 In planta transient expression of NnCYP76B6 showed a signif

270 Furthermore, the in planta transient expression of these three selected nano

271 In planta transient over-expression of WsMYC2 showed signif

272 In planta transport assays demonstrate that PIC30 specifica

273 h NbGlk1 and prevents its assembly on DNA in planta unless activated by PVX.

274 ossible co-evolution with host plants and in-planta up-regulation in particular, aided identification

275 these sites is substantially more stable in planta upon photoconversion to Pfr and is hyperactive in

276 Here we describe the in planta use of carbon-based nanoparticles produced by low

277 te a fungal bioluminescence pathway (FBP) in planta using a composable toolbox of parts.

278 ve hyphae was required for optimal growth in planta Using a multicell model of fungal hyphae, we show

279 s of three PLRV-interacting host proteins in planta using a reverse-genetics approach revealed a comp

280 ; (2) confirmation of the identified hits in planta using Arabidopsis (Arabidopsis thaliana); (3) fur

281 ever, the genetic determinants underlying in planta variation of cannabinoid alkyl side-chain length

282 pHapo was monitored in planta via microscopy-based ratio imaging, and the leaf-

283 cells to indirect targets responding only in planta via Network Walking.

284 length, motility, biofilm formation, and in planta virulence.

285 rabidopsis and rice transiently expressed in planta, we demonstrate that a urease-UreD-UreF-UreG comp

286 In yeast (Saccharomyces cerevisiae) and in planta, we further demonstrated by both coimmunoprecipit

287 Here, through a forward genetic screen in planta, we identify a conserved amino acid residue that

288 osition of developing embryos match those in planta were used to quantify substrate uptake and respir

289 BAK1 and SOBIR1 associate with each other in planta when the function of BIR1 is compromised.

290 cal relevance of the CaM-based regulation in planta, where stomatal closure, induced by exogenous Ca(

291 and 2-phenylethyl-beta-d-glucopyranoside in planta, whereas PtAAS1 likely contributes to the herbivo

292 nction, but not for localization, of HMA4 in planta, whereas the Glu residue is important but not ess

293 nfection structures and was nonpathogenic in planta, which was partially recovered by addition of exo

294 PRR5 can be O-fucosylated by SPY in planta, while point mutation in the catalytic domain of

295 Likewise, ACHT4 reacted in planta with 2-Cys Prx, indicating that it is oxidized by

296 Pi04089 interacts in yeast and in planta with a putative potato K-homology (KH) RNA-bindin

297 t cell periphery, interacted in yeast and in planta with multiple receptor-like kinases, including th

298 urthermore, DKM can interact in yeast and in planta with proteins involved in shoot apical meristem m

299 e host nucleus and interacts in yeast and in planta with StUBK.

300 lation occurs at multiple serine residues in planta, with S258 phosphorylation significantly reduced