ライフサイエンスコーパス: planta

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

2 ic fruiting bodies and GFP was detectable in planta.

3 ave a higher probability of being present in planta.

4 on strategy directly modulates T6P levels in planta.

5 he Bradi5g03300 UGT converts DON into D3G in planta.

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

7 state and explaining its weaker activity in planta.

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

9 an absolute requirement for all cysteines in planta.

10 OsSQE2 is the preferred partner of OsONS1 in planta.

11 iding with strongly reduced fungal growth in planta.

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

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

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

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

16 FUL) and ARF proteins directly associate in planta.

17 TP-binding protein that formed homodimers in planta.

18 ectopic expression of specific antibodies in planta.

19 s colonization when transiently expressed in planta.

20 3 confirmed the regulatory role of CIPK23 in planta.

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

22 ating lignin composition and/or structure in planta.

23 ole of a phenylpropanoid coupling product in planta.

24 PP2A constitutively associates with BAK1 in planta.

25 ly been investigated after overexpression in planta.

26 LS1 protein facilitates the movement of B in planta.

27 Specific interactions were verified in planta.

28 long-distance translocation of cytokinins in planta.

29 emely resistant to external H2O2 exposure ex planta.

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

31 the production of further glycoconjugates in planta.

32 endoplasmic reticulum and Golgi membranes in planta.

33 adly used to investigate effector biology in planta.

34 mutation reduced this enzymatic activity in planta.

35 esis of hundreds of different TAG species in planta.

36 onjugates that are used for lignification in planta.

37 ylation but not H3K23 acetylation of IDM1 in planta.

38 ically diverge in transcript distribution in planta.

39 bimolecular fluorescence complementation in planta.

40 icle induction to the BMV infection cycle in planta.

41 al control elements for genetic variation in planta.

42 nd reveal novel aspects of K(+) transport in planta.

43 genes that regulate stomatal development in planta.

44 strated that proteins interacted pairwise in planta.

45 are present in a complex with SOBIR1/EVR in planta.

46 r normal BRI1 signaling and tomato growth in planta.

47 ed HopQ1 protein showed reduced stability in planta.

48 In addition, XB25 associates with XA21 in planta.

49 the sealing function of lipidic polymers in planta.

50 ve and inducible over-expression of MYB46 in planta.

51 on and is required for starch degradation in planta.

52 itivity, and limit sphingolipid synthesis in planta.

53 for cell cycle release and proliferation in planta.

54 and amplification of transgene expression in planta.

55 iciency of these custom-designed proteins in planta.

56 be engineered and assembled successfully in planta.

57 zation and virulence-promoting activities in planta.

58 and the two proteins physically associate in planta.

59 nfirm FaEGSs as genuine eugenol synthases in planta.

60 he accumulation of glycosylated stilbenes in planta.

61 n comparison to the terpenes accumulating in planta.

62 pproach was used to study the role of SN1 in planta.

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

64 )-ATPase (ACA8) forms a complex with FLS2 in planta.

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

66 ed in tobacco leaves, which was confirmed in planta.

67 00, KatE can also provide some protection in planta.

68 Rx1 binds to NbGlk1 in vitro and in planta.

69 in VirE2 in a yeast two-hybrid system and in planta.

70 ecapitulated the trichome chemistry found in planta.

71 or difference in sensitivity in vitro and in planta.

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

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

74 a novel processing mechanism is occurring in planta.

75 e, indicative of increased TCE metabolism in planta.

76 C glucuronosylation could not be analyzed in planta.

77 en ER bodies and glucosinolate metabolism in planta.

78 fectors enabled direct effector detection in planta.

79 minearum is reorganized both in vitro and in planta.

80 emain incompletely understood, especially in planta.

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

82 easy platform for assessing gene function in planta.

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

84 d to investigate the RNA binding proteome in planta.

85 s integrated into the complex HSR network in planta.

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

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

88 OW transcriptional cascade were validated in planta.

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

90 or mediating the signal that triggers the in planta activation of the saprotrophic program.

91 ALMT1, is physiologically associated with in planta aluminum (Al) resistance.

92 Subsequent in planta analyses revealed SOC1 repression by several flor

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

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

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

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

97 these problems, we performed an extensive in planta analysis of published BiFC fragments used in meta

98 ylated forms of AtCPK5 were detected both in planta and after expression of AtCPK5 in a cell-free pla

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

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

101 festans infection on potato plants, using in planta and detached leaf assays.

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

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

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

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

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

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

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

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

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

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

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

113 d effectiveness of NAA and BTOA as auxins in planta and provides a tool for designing new and effecti

114 e for IAA in the regulation of abscission in planta and reveal, to our knowledge for the first time,

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

116 ots strongly stimulated biofilm formation ex planta and that an abundant small molecule in the exudat

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

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

119 ism consistent with reduced PXA1 activity in planta and that, based on the double mutant cgi-58 pxa1,

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

121 verely compromised in its ability to grow in planta, and its growth can be partially rescued by the e

122 e ubiquitin and a CEP12 peptide (GrCEP12) in planta, and that GrCEP12 suppresses resistance gene-medi

123 1 each physically interact with PLDalpha1 in planta, and that mutation of the so-called PLDalpha1 'DR

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

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

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

127 trate the potential of SRS for a range of in planta applications by presenting in situ chemical analy

128 ize (Zea mays; ZmNRH), using in vitro and in planta approaches.

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

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

131 In planta as in the moss Physcomitrella patens protoplasts,

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

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

134 ization of four CfTPSs using in vitro and in planta assays.

135 dopsis thaliana leads to dwarfism, making in planta assessment of SA effects difficult in this model

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

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

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

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

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

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

142 In planta bimolecular fluorescence complementation assays c

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

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

145 In planta binding assays show that GmRIN4a can associate wi

146 roader DNA structural features may define in planta binding.

147 In planta bioluminescence resonance energy transfer analysi

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

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

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

151 al or plant genomes, or by RNAi generated in planta by a plant virus infection.

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

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

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

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

156 two subunits contribute to K(+) transport in planta by forming heteromeric channels with other Shaker

157 l components of the BRL3 receptor complex in planta by immunoprecipitation and mass spectrometry anal

158 ions as an important structural regulator in planta by modulating the precise status of pectin acetyl

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

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

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

162 A comparison of the transcriptomes from in planta cells and from cells exposed to osmotic stress, o

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

164 e pull-down, in vitro ubiquitination, and in planta coimmunoprecipitation experiments.

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

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

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

168 In planta concentrations of these compounds strongly inhibi

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

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

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

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

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

174 Unexpectedly, in planta, E. coli CPS acts primarily on the sn-1 position

175 re uniquely relevant to rapid N signaling in planta, enriched in dynamic N-responsive genes, and regu

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

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

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

179 , avoiding the complexity inherent in the in planta experiments.

180 Here, we report that in planta expressed HopM1 suppresses two early PAMP-trigger

181 In planta expression of a thermophilic endoglucanase (AcCel

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

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

184 Enzyme kinetics, in planta expression, lignin structural analysis, and impro

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

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

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

188 We used in planta fluorescence lifetime imaging microscopy and fluo

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

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

191 The in planta function of PpORS, therefore, is probably related

192 In planta functional characterization of these TPS enzymes

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

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

195 his study demonstrates that BSMV-mediated in planta-generated RNAi is an effective strategy for funct

196 ents in this system can be used to obtain in planta-generated silencing of corresponding genes inside

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

198 Here we report the in planta generation of the functionally active monoclonal

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

200 old), enzyme activity level (7-fold), and in planta geranyl diphosphate and geranylgeranyl diphosphat

201 Moreover, extensive in planta glycoengineering allowed the generation of SM6 de

202 Differences between in vitro- versus in planta-grown embryos suggest that metabolic heterogeneit

203 e hyphae from primary hyphae, but further in planta growth was aborted.

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

205 Efficient in planta GT was achieved in Arabidopsis thaliana by expres

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

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

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

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

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

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

212 Overexpression of OST1 in planta in the absence of ABA application does not affect

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

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

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

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

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

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

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

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

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

222 chromatin immunoprecipitation (ChIP) and in planta microarrays.

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

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

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

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

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

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

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

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

231 Extension of the protocol to in planta plastid transformation depends on the development

232 metric and NMR analysis revealed that the in planta produced peptide differs from the synthetic versi

233 hibition of fungal growth correlated with in planta production of siRNAs corresponding to the targete

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

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

236 ted regulation of CSD activation pathways in planta relative to other known CCS-independent activatio

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

238 ybrid, chromatin immunoprecipitation, and in planta reporter gene experiments indicate that an L1-box

239 nsight into their capacity for moving Suc in planta, representative members of each clade were first

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

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

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

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

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

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

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

247 In planta, Rubisco deactivated at low irradiance except in

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

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

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

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

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

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

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

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

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

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

258 In planta, such monolignol-pCA conjugates become incorporat

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

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

261 l analysis of AtDEG15 deletion constructs in planta support the requirement of the CaM-binding domain

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

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

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

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

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

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

268 erting an accurate control of ME activity in planta, through changes in metabolite and substrate conc

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

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

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

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

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

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

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

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

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

278 In planta transient expression of NnCYP76B6 showed a signif

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

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

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

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

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

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

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

286 In planta, very limited information is available about how

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

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

289 Functional adherence in planta was mediated by the adhesin EcpD in combination w

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

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

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

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

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

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

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

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

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

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

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