ライフサイエンスコーパス: in planta

1 h wheat (Triticum aestivum) Actin1 (TaACT1), in planta.

2 genic fruiting bodies and GFP was detectable in planta.

3 t have a higher probability of being present in planta.

4 ntion strategy directly modulates T6P levels in planta.

5 t the Bradi5g03300 UGT converts DON into D3G in planta.

6 ies of self-regulated auxin-based patterning in planta.

7 und state and explaining its weaker activity in planta.

8 tissue-specific expression of BAS1 and SOB7 in planta.

9 ng an absolute requirement for all cysteines in planta.

10 at OsSQE2 is the preferred partner of OsONS1 in planta.

11 inciding with strongly reduced fungal growth in planta.

12 detect and analyze PCD processes in vivo and in planta.

13 pporting a role for PSKR1 signaling via cGMP in planta.

14 ng in reorganization of the COP1/SPA complex in planta.

15 s and over-expression lines of CGR2 and CGR3 in planta.

16 as FUL) and ARF proteins directly associate in planta.

17 n ATP-binding protein that formed homodimers in planta.

18 he ectopic expression of specific antibodies in planta.

19 nces colonization when transiently expressed in planta.

20 pk23 confirmed the regulatory role of CIPK23 in planta.

21 confirm the N and C terminus of the peptide in planta.

22 dulating lignin composition and/or structure in planta.

23 t role of a phenylpropanoid coupling product in planta.

24 PP2A constitutively associates with BAK1 in planta.

25 arily been investigated after overexpression in planta.

26 e TLS1 protein facilitates the movement of B in planta.

27 Specific interactions were verified in planta.

28 he long-distance translocation of cytokinins in planta.

29 maturation into an active form in vitro and in planta.

30 to the production of further glycoconjugates in planta.

31 he endoplasmic reticulum and Golgi membranes in planta.

32 the mutation reduced this enzymatic activity in planta.

33 broadly used to investigate effector biology in planta.

34 nthesis of hundreds of different TAG species in planta.

35 e conjugates that are used for lignification in planta.

36 cetylation but not H3K23 acetylation of IDM1 in planta.

37 matically diverge in transcript distribution in planta.

38 by bimolecular fluorescence complementation in planta.

39 vesicle induction to the BMV infection cycle in planta.

40 viral control elements for genetic variation in planta.

41 s and reveal novel aspects of K(+) transport in planta.

42 of genes that regulate stomatal development in planta.

43 monstrated that proteins interacted pairwise in planta.

44 LPs are present in a complex with SOBIR1/EVR in planta.

45 for normal BRI1 signaling and tomato growth in planta.

46 tated HopQ1 protein showed reduced stability in planta.

47 In addition, XB25 associates with XA21 in planta.

48 in the sealing function of lipidic polymers in planta.

49 utive and inducible over-expression of MYB46 in planta.

50 ation and is required for starch degradation in planta.

51 ensitivity, and limit sphingolipid synthesis in planta.

52 ial for cell cycle release and proliferation in planta.

53 on and amplification of transgene expression in planta.

54 efficiency of these custom-designed proteins in planta.

55 to be engineered and assembled successfully in planta.

56 alization and virulence-promoting activities in planta.

57 n, and the two proteins physically associate in planta.

58 confirm FaEGSs as genuine eugenol synthases in planta.

59 n the accumulation of glycosylated stilbenes in planta.

60 R in comparison to the terpenes accumulating in planta.

61 c approach was used to study the role of SN1 in planta.

62 in culture, and it fails to inject effectors in planta.

63 (2+)-ATPase (ACA8) forms a complex with FLS2 in planta.

64 erved in tobacco leaves, which was confirmed in planta.

65 ith AMT1;1 and AMT1;2 in yeast, oocytes, and in planta.

66 C3000, KatE can also provide some protection in planta.

67 otein VirE2 in a yeast two-hybrid system and in planta.

68 Rx1 binds to NbGlk1 in vitro and in planta.

69 t recapitulated the trichome chemistry found in planta.

70 minor difference in sensitivity in vitro and in planta.

71 uenching of ROS by carnosic acid takes place in planta.

72 ng a novel processing mechanism is occurring in planta.

73 here, indicative of increased TCE metabolism in planta.

74 GIPC glucuronosylation could not be analyzed in planta.

75 tween ER bodies and glucosinolate metabolism in planta.

76 effectors enabled direct effector detection in planta.

77 graminearum is reorganized both in vitro and in planta.

78 n remain incompletely understood, especially in planta.

79 ited by both Leptosphaeria spp. in vitro and in planta.

80 nd easy platform for assessing gene function in planta.

81 on "gatekeeper" Tyr both in vitro as well as in planta.

82 thod to investigate the RNA binding proteome in planta.

83 y is integrated into the complex HSR network in planta.

84 s is that they are found in very low amounts in planta.

85 uptake and sunlight-triggered release of T6P in planta.

86 ECROW transcriptional cascade were validated in planta.

87 ontaining proteins able to induce cell death in-planta.

88 To check this mechanism in planta, a benzyl etherification of nonesterified hydr

89 ensor mediating the signal that triggers the in planta activation of the saprotrophic program.

90 TaALMT1, is physiologically associated with in planta aluminum (Al) resistance.

91 Subsequent in planta analyses revealed SOC1 repression by several f

92 In planta analyses revealed that AVR1 and Sec5 are in cl

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

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

95 In planta analysis of IAA, PAA, SA, and BA and their res

96 me these problems, we performed an extensive in planta analysis of published BiFC fragments used in m

97 horylated forms of AtCPK5 were detected both in planta and after expression of AtCPK5 in a cell-free

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

99 m avrBs2 and xopX both showed reduced growth in planta and delayed spread through the vasculature sys

100 infestans infection on potato plants, using in planta and detached leaf assays.

101 ng disease and its pathogen was investigated in planta and fungal growth and sporulation production w

102 ary evidence obtained through gene silencing in planta and heterologous expression in bacteria suppor

103 These results were observed both in planta and in detached leaf assays.

104 diates, complementing and extending previous in planta and in vitro investigations.

105 Functional studies (in planta and in vitro) show that Vv3AT has a broad anth

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

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

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

109 of its antioxidative features, this compound in planta and its antioxidant mechanism have received li

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

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

112 ased effectiveness of NAA and BTOA as auxins in planta and provides a tool for designing new and effe

113 role for IAA in the regulation of abscission in planta and reveal, to our knowledge for the first tim

114 entroid vectors is significantly affected by in planta and soil concentration gradients and when conc

115 We show that HsGCPII cannot substitute AMP1 in planta and that an HsGCPII-specific inhibitor does no

116 provides fitness and colonization advantages in planta and that the role of the T6SS is not restricte

117 bolism consistent with reduced PXA1 activity in planta and that, based on the double mutant cgi-58 px

118 ecretome of X. fastidiosa, both in vitro and in planta, and identified LesA as one of the pathogenici

119 severely compromised in its ability to grow in planta, and its growth can be partially rescued by th

120 free ubiquitin and a CEP12 peptide (GrCEP12) in planta, and that GrCEP12 suppresses resistance gene-m

121 AGB1 each physically interact with PLDalpha1 in planta, and that mutation of the so-called PLDalpha1

122 ependent interbacterial competition activity in planta, and the C-terminal variable region of VgrG2 g

123 led structure, the function of these glycans in planta, and the mechanisms by which they are depolyme

124 d MLA10 can self-associate both in vitro and in planta, and this self-association correlates with the

125 onstrate the potential of SRS for a range of in planta applications by presenting in situ chemical an

126 maize (Zea mays; ZmNRH), using in vitro and in planta approaches.

127 functional roles of individual NCR peptides in planta are not known.

128 in phosphatase type 2C (PAPP2C) in yeast and in planta as evidenced by co-immunoprecipitation and bim

129 In planta as in the moss Physcomitrella patens protoplas

130 -spread conidia infect ash and may sporulate in planta, as well as in forest debris.

131 In vitro and in planta assays showed that unlike SrCPS and SrKS1, SrC

132 terization of four CfTPSs using in vitro and in planta assays.

133 abidopsis thaliana leads to dwarfism, making in planta assessment of SA effects difficult in this mod

134 ity of Jas9-VENUS to analyse responses to JA in planta at a cellular scale, both quantitatively and d

135 provide evidence that phyB is phosphorylated in planta at Ser-86 located in the N-terminal domain of

136 HopK1 is processed in planta at the same processing site found in AvrRps4.

137 mall group of endogenous molecules affecting in planta auxin concentrations.

138 PYL6 and MYC2 interact in planta based on bimolecular fluorescence complementat

139 overed, many of which have not been reported in planta before.

140 In planta bimolecular fluorescence complementation assay

141 SIS8 based on a yeast two-hybrid screen and in planta bimolecular fluorescence complementation.

142 amily in a yeast two-hybrid system and by an in planta bimolecular fluorescent complementation assay.

143 In planta binding assays show that GmRIN4a can associate

144 t broader DNA structural features may define in planta binding.

145 In planta bioluminescence resonance energy transfer anal

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

147 ited plant callose biosynthesis in vitro and in planta but also partially restored virulence to the D

148 is necessary for natural rubber biosynthesis in planta, but yeast-expressed CPTL2 and CPT3 alone coul

149 ungal or plant genomes, or by RNAi generated in planta by a plant virus infection.

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

151 ngly suggesting that the antibiome expressed in planta by B. amyloliquefaciens does not reflect the v

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

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

154 se two subunits contribute to K(+) transport in planta by forming heteromeric channels with other Sha

155 tion between mitochondrial SAT3 and OAS-TL C in planta by FRET and establish the role of the mitochon

156 ovel components of the BRL3 receptor complex in planta by immunoprecipitation and mass spectrometry a

157 nctions as an important structural regulator in planta by modulating the precise status of pectin ace

158 o test the hypothesis that OGs are generated in planta by partial inhibition of pathogen-encoded poly

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

160 In this study, we analyzed their interaction in planta by using site-directed mutagenesis of NdhS.

161 A comparison of the transcriptomes from in planta cells and from cells exposed to osmotic stress

162 n yeast or Xenopus laevis oocytes, and their in planta cellular and subcellular localization.

163 rase pull-down, in vitro ubiquitination, and in planta coimmunoprecipitation experiments.

164 However, in an in planta coinfection assay, A. tumefaciens used Tde eff

165 that are transcriptionally regulated by LEC1 in planta Collectively, our results show that LEC1 contr

166 Results indicate that in planta concentrations are significantly and positivel

167 In planta concentrations of these compounds strongly inh

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

169 Therefore, in planta, CUS1 can catalyze the esterification of both

170 fy TNT, properties that could be applied for in planta detoxification of TNT in the field.

171 certain types of cells at defined stages of in planta development for in-depth analysis.

172 The altered Ce in planta distribution was partially associated with the

173 Unexpectedly, in planta, E. coli CPS acts primarily on the sn-1 positi

174 s are uniquely relevant to rapid N signaling in planta, enriched in dynamic N-responsive genes, and r

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

176 We report that in planta excision of a plastid aurea bar gene (bar(au)

177 Some in planta experiments designed to test the validity of P

178 und, avoiding the complexity inherent in the in planta experiments.

179 Here, we report that in planta expressed HopM1 suppresses two early PAMP-trig

180 In planta expression of a thermophilic endoglucanase (Ac

181 Elevated in planta expression of resistance-type Rhg1 alpha-SNAPs

182 Here, we show that in planta expression of the RXLR effector Pi04314 enhanc

183 Enzyme kinetics, in planta expression, lignin structural analysis, and im

184 transient Agrobacterium tumefaciens-mediated in planta expression, transformation of P. infestans wit

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

186 Here, we assessed in planta flg22-signaling competency in the context of l

187 We used in planta fluorescence lifetime imaging microscopy and f

188 s including yeast two-hybrid, pull-down, and in planta fluorescence resonance energy transfer assays,

189 ort, we scrutinized the requirement of Rad54 in planta for two distinct fully infectious geminiviruse

190 The in planta function of PpORS, therefore, is probably rela

191 In planta functional characterization of these TPS enzym

192 analysis of E. lathyris L. mature seeds and in planta functional characterization, we identified thr

193 ation of acetolactate synthase1 gene through in planta gene editing.

194 This study demonstrates that BSMV-mediated in planta-generated RNAi is an effective strategy for fu

195 agments in this system can be used to obtain in planta-generated silencing of corresponding genes ins

196 The in planta generation of one of the most complex human pr

197 Here we report the in planta generation of the functionally active monoclon

198 and AtBRCA1 physically interact in vitro and in planta Genetic interaction between the RBR-silenced a

199 0-fold), enzyme activity level (7-fold), and in planta geranyl diphosphate and geranylgeranyl diphosp

200 Moreover, extensive in planta glycoengineering allowed the generation of SM6

201 Differences between in vitro- versus in planta-grown embryos suggest that metabolic heterogen

202 sive hyphae from primary hyphae, but further in planta growth was aborted.

203 wall of plant-pathogenic fungi during on and in planta growth, following the elucidation of infection

204 Efficient in planta GT was achieved in Arabidopsis thaliana by exp

205 xidants; however, their antioxidant activity in planta has been debated.

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

207 Such high specialization of class II CPRs in planta highlights the evolutionary strategy that ensu

208 Following transient expression in planta, HopQ1 was shown to copurify with host 14-3-3

209 to the nucleus and interact with each other in planta in bimolecular fluorescence complementation an

210 length Sr33 and Sr50 proteins self-associate in planta In contrast, truncated CC domains equivalent i

211 Overexpression of OST1 in planta in the absence of ABA application does not aff

212 ndirect effects of BAR-containing transgenes in planta, including modified amino acid levels, have be

213 In planta, increasing NEDD8 gene dosage is sufficient to

214 Subcellular localization in planta indicated that AtPyrP2 was localized in plasti

215 In planta-induced mobilization of HAI2 was regulated by

216 ic profiling revealed that MDCA is converted in planta into piperonylic acid (PA), an inhibitor of CI

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

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

219 mass spectrometry analysis, we show that the in planta mature form of proGrCLE1, a multidomain CLE ef

220 Here we present an efficient in planta method for Agrobacterium-mediated genetic tran

221 ing chromatin immunoprecipitation (ChIP) and in planta microarrays.

222 on of genetic factors associated solely with in planta mobilization of an ICE demonstrates that this

223 Both antibodies were efficiently sulfated in planta on coexpression of an engineered human tyrosyl

224 tations on protein function and localization in planta, on metal-binding properties in vitro and on p

225 factors that participate in gene expression in planta or are suspected to be involved in that proces

226 be useful in the engineering of anthocyanins in planta or in vitro.

227 ymes and the improvement of MIA availability in planta or in vitro.

228 s recent progress in understanding SL action in planta, particularly in the context of the regulation

229 ishes enhanced leaf colonization mediated by in planta Pi04314 expression.

230 Extension of the protocol to in planta plastid transformation depends on the developm

231 and mediates the interaction of BSL1 with R2 in planta, possibly through the formation of a ternary c

232 trometric and NMR analysis revealed that the in planta produced peptide differs from the synthetic ve

233 inhibition of fungal growth correlated with in planta production of siRNAs corresponding to the targ

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

235 wledge validated here for the first time for in planta quantitation of biopharmaceuticals, is especia

236 icated regulation of CSD activation pathways in planta relative to other known CCS-independent activa

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

238 e-hybrid, chromatin immunoprecipitation, and in planta reporter gene experiments indicate that an L1-

239 n insight into their capacity for moving Suc in planta, representative members of each clade were fir

240 )-independent ABA-signaling branches and the in planta requirement of simultaneous phosphorylation at

241 Our in planta results show that OPT3 is important for leaf p

242 nal analysis of selected effector candidates in planta revealed that HaRxL17 enhances plant susceptib

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

244 To evaluate the effect of in planta RNAi on the control of this nematode, a specif

245 ss III peroxidases (PRXs) in plants, but the in planta role of most members of this family still rema

246 However, the in planta role of thioredoxins in the regulation of SI s

247 In planta, Rubisco deactivated at low irradiance except

248 Using a specifically designed in planta sampler, field sampling was conducted at a sit

249 To assess this variability, we developed an in planta sampling method to obtain high-frequency measu

250 an be determined, the role of these proteins in planta should be deciphered.

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

252 ction than wild-type plants, and vice versa, in planta silencing of MjTTL5 substantially increased pl

253 ted by treatment with catharanthine, and its in planta silencing redistributes catharanthine to incre

254 election of TT2 and PAP4, thereby converting in planta specificity of the PA towards the anthocyanin

255 ere confirmed at a rate of 32% in orthogonal in planta split-green flourescent protein interaction as

256 Cell-free degradation and in planta stabilization assays in the presence of MG132,

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

258 In planta, such monolignol-pCA conjugates become incorpo

259 ased when co-expressed with a functional KEG in planta, suggesting that KEG contributes to FDH degrad

260 ly interacts with Arabidopsis thaliana DDB1A in planta, suggesting that WDR55 may be a novel substrat

261 ical analysis of AtDEG15 deletion constructs in planta support the requirement of the CaM-binding dom

262 Nevertheless, bioassays using an in Planta System showed that the Asian citrus psyllid wa

263 e three proteins may be present in a complex in planta that is required to coordinate a correct photo

264 uggests direct interaction of IQD1 and KLCR1 in planta that is supported by GFP approximately IQD1-de

265 s and resulted in a dominant-negative allele in planta that was phenotypically similar to sob3-6.

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

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

268 exerting an accurate control of ME activity in planta, through changes in metabolite and substrate c

269 We show that expressing the created enzyme in planta, thus etherifying the para-hydroxyls of lignin

270 ochemical assays and heterologous expression in planta to demonstrate that TcADH2 encodes an enzyme t

271 ng seed development, indicate that PDCT acts in planta to enhance the fluxes of fatty acids through P

272 of PCBER is to reduce phenylpropanoid dimers in planta to form antioxidants that protect the plant ag

273 ates the auxin-responsive PIN3 transcription in planta to steer the early steps of lateral root forma

274 bunit Regulatory Particle AAA-ATPase6 (RPT6) in planta to suppress proteasome activity, resulting in

275 tudy, particularly rhizosphere interactions, in planta transformations, and physicochemical propertie

276 ining mechanisms of uptake and accumulation, in planta transformations, the effects of PPCPs on plant

277 g a Tobacco rattle virus-derived plasmid for in planta transient expression of double stranded RNA (d

278 In planta transient expression of NnCYP76B6 showed a sig

279 Furthermore, the in planta transient expression of these three selected n

280 with NbGlk1 and prevents its assembly on DNA in planta unless activated by PVX.

281 f possible co-evolution with host plants and in-planta up-regulation in particular, aided identificat

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

283 ysis of three PLRV-interacting host proteins in planta using a reverse-genetics approach revealed a c

284 tion between HopQ1 and 14-3-3a was confirmed in planta using the fluorescence resonance energy transf

285 of SOMT1, SOMT2, and SOMT3 were investigated in planta using virus-induced gene silencing.

286 In planta, very limited information is available about h

287 pHapo was monitored in planta via microscopy-based ratio imaging, and the le

288 on, length, motility, biofilm formation, and in planta virulence.

289 Functional adherence in planta was mediated by the adhesin EcpD in combinatio

290 m Arabidopsis and rice transiently expressed in planta, we demonstrate that a urease-UreD-UreF-UreG c

291 To explore these processes in planta, we developed a chemical genetic toolbox of ph

292 In yeast (Saccharomyces cerevisiae) and in planta, we further demonstrated by both coimmunopreci

293 Here, through a forward genetic screen in planta, we identify a conserved amino acid residue th

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

295 function, but not for localization, of HMA4 in planta, whereas the Glu residue is important but not

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

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

298 As can physically interact both in vitro and in planta with all secondary CESAs.

299 log S. lycopersicum (Sl)SOBIR1-like interact in planta with both Cf-4 and Ve1 and are required for th

300 Furthermore, DKM can interact in yeast and in planta with proteins involved in shoot apical meriste