ライフサイエンスコーパス: Nicotiana

1 nduces systemic acquired resistance (SAR) in Nicotiana.

2 on of MYBL1 through stable transformation of Nicotiana.

3 s shaped the evolution of HAE-induced EDS in Nicotiana.

4 The walls of Nicotiana alata pollen tubes contain a linear arabinan c

5 We describe a thioredoxin (Trx) type h from Nicotiana alata, NaTrxh, which interacts with and reduce

6 show that element-specific dynamics in young Nicotiana allopolyploids reflect their dynamics in diplo

7 Prior studies with Nicotiana and Arabidopsis described failed assembly of t

8 pothesis, we compared three allotetraploids, Nicotiana arentsii, N. rustica and N. tabacum, which aro

9 Brassica rapa (extrastaminal nectaries) and Nicotiana attenuata (gynoecial nectaries).

10 Using lines of the wild tobacco Nicotiana attenuata genetically altered in specific well

11 we have planted the annual postfire tobacco Nicotiana attenuata into an experimental field plot in t

12 We use Nicotiana attenuata plants silenced in mitogen-activated

13 We demonstrate that jasmonate-deficient Nicotiana attenuata plants suffer more damage by arthrop

14 ns of IAA accumulation in herbivore-attacked Nicotiana attenuata plants to unravel its role in the re

15 Here, Nicotiana attenuata plants, in which floral volatiles ha

16 of AGOs in the interaction of wild tobacco (Nicotiana attenuata) with a naturally occurring hemibiot

17 Native populations of Nicotiana attenuata, a wild tobacco species, have been s

18 We used Nicotiana attenuata, an ecological model plant with well

19 ore tissue-level metabolic specialization in Nicotiana attenuata, an ecological model with rich secon

20 genetic mapping population of wild tobacco, Nicotiana attenuata, originating from a cross of 2 natur

21 In Nicotiana attenuata, specific RNA-directed RNA polymeras

22 Here, we used the desert annual, Nicotiana attenuata, to investigate the function of TOC1

23 ed transcriptomic responses in wild tobacco, Nicotiana attenuata, using a phylotranscriptomic approac

24 ble in native populations of coyote tobacco, Nicotiana attenuata, with some producing no nectar at al

25 ing GLS (SlGLS) and its homolog (NaGLS) from Nicotiana attenuata.

26 enses against herbivores of the wild tobacco Nicotiana attenuata; whether they also function as gener

27 RBO-sgRNA delivery platform to target GFP in Nicotiana benthamiana (16c) plants, and gene editing was

28 Nicotiana benthamiana (Nb) is a natural null mutant carr

29 out transgene integration is accomplished in Nicotiana benthamiana (Nb), Eruca sativa (arugula), Trit

30 DS1 functions in the model Solanaceous plant Nicotiana benthamiana (Nb).

31 andidate genes to combinatorially express in Nicotiana benthamiana (tobacco) and identified six pathw

32 Transient expression in Nicotiana benthamiana (tobacco) and particle bombardment

33 e ectopically expressed the OsPIP1;3 gene in Nicotiana benthamiana (tobacco).

34 n virus (CLCuMuV) V2 directly interacts with Nicotiana benthamiana AGO4 (NbAGO4) and that the L76S mu

35 Silencing of GCN4 in Nicotiana benthamiana and Arabidopsis thaliana compromis

36 y is transferable to the Solanaceous species Nicotiana benthamiana and cannot be substituted by AtEDS

37 the accumulation of antioxidant flavonols in Nicotiana benthamiana and confers tolerance to abiotic s

38 BAK1 was expressed transiently in Nicotiana benthamiana and immunopurified after treatment

39 tristeza virus (CTV) triggered ROS burst in Nicotiana benthamiana and in the natural citrus host, th

40 persensitive response in transient assays in Nicotiana benthamiana and in wheat demonstrated specific

41 e entire Asp aminotransferase gene family in Nicotiana benthamiana and isolated and cloned the genes

42 heat shock protein70-1 (HSP70-1) inserts in Nicotiana benthamiana and maize (Zea mays).

43 n from P. patens in the heterologous systems Nicotiana benthamiana and Nicotiana tabacum using transi

44 pendent and RPP1/ATR1Delta51-dependent HR in Nicotiana benthamiana and Nicotiana tabacum, respectivel

45 plant morphology by transient expression in Nicotiana benthamiana and overexpression in transgenic N

46 son with other UGTs in vegetative tissues of Nicotiana benthamiana and peppermint (Mentha x piperita)

47 owever, a functional Ptr1 ortholog exists in Nicotiana benthamiana and potato, and both mediate recog

48 small interfering RNA into the model plants Nicotiana benthamiana and tomato (Solanum lycopersicum).

49 of TurboID and miniTurbo in Arabidopsis and Nicotiana benthamiana and versatile vectors enable custo

50 lencing and recombinant expression assays in Nicotiana benthamiana and yeast cells to examine its fun

51 We sought to develop Nicotiana benthamiana as a system to study NHR against Z

52 e 25 successfully attacked a non-host plant, Nicotiana benthamiana as well as resistant soybean culti

53 mains are sufficient to induce cell death in Nicotiana benthamiana Autoactive CC domains and full-len

54 Transient expression of both variants in Nicotiana benthamiana by agroinfiltration enhanced P. pa

55 titatively analyzed GFP-labeled MT arrays in Nicotiana benthamiana cells transiently expressing GFP-I

56 nucleus and the cytoplasm, but in transgenic Nicotiana benthamiana cells, bimolecular fluorescence co

57 when expressed in Xenopus laevis oocytes and Nicotiana benthamiana cells, Ma1 mediates a malate-depen

58 vesiculation were observed in BBSV-infected Nicotiana benthamiana cells.

59 otinylated proteins expressed transiently in Nicotiana benthamiana coupled to untargeted LC-MS to ide

60 ric IgA1, IgA2m(1), and IgA2m(2) variants in Nicotiana benthamiana DeltaXT/FT plants lacking the enzy

61 H2O2 sensor, we show that in photosynthetic Nicotiana benthamiana epidermal cells, exposure to high

62 Ectopic, transient expression in Nicotiana benthamiana epidermal leaf cells demonstrated

63 AS) and Flavonoid 3_5 hydroxylase (C75A1) in Nicotiana benthamiana followed by efficacy analysis agai

64 onses in Marchantia and the model angiosperm Nicotiana benthamiana further reveal a shared set of ort

65 of the RNA Polymerase III in a model species Nicotiana benthamiana had pleiotropic effects, including

66 Nicotiana benthamiana has been extensively used as a mod

67 The plant Nicotiana benthamiana has been shown to be resistant to

68 the class II diTPSs, transient expression in Nicotiana benthamiana identified SdCPS1 as an ent-CPP sy

69 Our data reveal that Nicotiana benthamiana incorporates two different paralog

70 stance to P. syringae Expression of CRK28 in Nicotiana benthamiana induced cell death, which required

71 Here, we show that in leaves of Nicotiana benthamiana infected by potato spindle tuber v

72 Heterologous expression of OsSWEET13 in Nicotiana benthamiana leaf cells elevates sucrose concen

73 isoforms were imported into chloroplasts of Nicotiana benthamiana leaf cells, whereas N. munroi CA1a

74 reen fluorescent protein fusion construct in Nicotiana benthamiana leaf epidermal and mesophyll cells

75 ization in developing Arabidopsis plants and Nicotiana benthamiana leaf epidermal cells.

76 Using transient expression in Nicotiana benthamiana leaf, we demonstrated that the EXS

77 vage-dependent luciferase gene correction in Nicotiana benthamiana leaves (Johnson et al. in Plant Mo

78 orm homodimers when transiently expressed in Nicotiana benthamiana leaves and heterodimers when coexp

79 luorescence complementation (BiFC) assays in Nicotiana benthamiana leaves and the complex localized i

80 barley (Hordeum vulgare) CSLF6 and CSLH1 in Nicotiana benthamiana leaves and, consistent with our bi

81 Transient overexpression of DXS in Nicotiana benthamiana leaves elevated monoterpene synthe

82 expression of the AtCCT1 catalytic domain in Nicotiana benthamiana leaves increased PC content, and S

83 -mediated transient expression of ShMYB78 in Nicotiana benthamiana leaves induced the ectopic deposit

84 Co-expression of SnRK1alpha with PAL in Nicotiana benthamiana leaves resulted in the severe atte

85 of TcADH2 and TcALDH1 together with TcCDS in Nicotiana benthamiana leaves results in the production o

86 Here, we used heterologous expression in Nicotiana benthamiana leaves to identify a minimal set o

87 Nicotiana benthamiana leaves were exposed to a sucking i

88 ile puncta in L. japonicus root hairs and in Nicotiana benthamiana leaves.

89 g cDNAs led to increased oil biosynthesis in Nicotiana benthamiana leaves.

90 sion in Saccharomyces cerevisiae (yeast) and Nicotiana benthamiana leaves.

91 ng Protein 47 (RBP47) upon cotransfection of Nicotiana benthamiana leaves.

92 greater extent than individual expression in Nicotiana benthamiana leaves.

93 nduced by ShMYB78 heterologous expression in Nicotiana benthamiana leaves.

94 lized in the extracellular space of infected Nicotiana benthamiana leaves.

95 version of a Brassica napus MPK4 (BnMPK4) in Nicotiana benthamiana leaves.

96 nhance crocin accumulation when expressed in Nicotiana benthamiana leaves.plantcell;31/11/2789/FX1F1f

97 encing of the WRKY25/22 orthologous genes in Nicotiana benthamiana led to a delay in programmed cell

98 Silencing of Nicotiana benthamiana NbGPAT6a increased leaf susceptibi

99 e, by virus-induced gene silencing (VIGS) of Nicotiana benthamiana NHEJ genes, and by biochemical ass

100 mefaciens-mediated transient coexpression in Nicotiana benthamiana of an MtVAMP721e-RNAi construct (V

101 wed the host range of MYMIV not to extend to Nicotiana benthamiana or tomato.

102 were conducted in vegetative or reproductive Nicotiana benthamiana plants (i.e., before or after the

103 is of nuclear and cytoplasmic fractions from Nicotiana benthamiana plants coinfected with Q-satRNA an

104 Transgenic Nicotiana benthamiana plants expressing Rs-cps dsRNA wer

105 w that L2 is unable to suppress silencing in Nicotiana benthamiana plants that have undergone the veg

106 Arabidopsis and Nicotiana benthamiana plants with reduced expression of

107 display mutual exclusion/cross-protection in Nicotiana benthamiana plants.

108 and easily purified in large quantities from Nicotiana benthamiana plants.

109 08 and 09) were expressed in glycoengineered Nicotiana benthamiana plants.

110 odify N-glycans upon transient expression in Nicotiana benthamiana plants.

111 Transient expression of SGRL in leaves of Nicotiana benthamiana promoted the degradation of chloro

112 ant-secreted beta-galactosidase 1 (BGAL1) of Nicotiana benthamiana promotes hydrolytic elicitor relea

113 robacterium-mediated transient expression in Nicotiana benthamiana provided strong evidence that miR8

114 silencing of two importin-alpha paralogs in Nicotiana benthamiana resulted in significant reduction

115 Moreover, overexpression of PrCYP79D73 in Nicotiana benthamiana resulted in the emission of (E/Z)-

116 ts coagroinfiltrated with a reporter gene in Nicotiana benthamiana revealed that P1N-PISPO acts as an

117 erologous expression in Escherichia coli and Nicotiana benthamiana showed that all five AADC/AAS gene

118 Furthermore, silencing of a Nicotiana benthamiana SKP1 ortholog leads to the destabi

119 enzymes in total) to N-formyldemecolcine in Nicotiana benthamiana starting from the amino acids phen

120 ransient expression of WRI1 with OLEOSIN1 in Nicotiana benthamiana stimulates triacylglycerol accumul

121 lipid droplets is enhanced in the transient Nicotiana benthamiana system through ectopic production

122 y developed a transient expression system in Nicotiana benthamiana that allowed us to demonstrate tha

123 Here, we demonstrate in Nicotiana benthamiana that transient expression of the N

124 ficking of P20-defective satBaMV in infected Nicotiana benthamiana The transgene-derived satBaMV, unc

125 a sgRNA from a single virus-derived mRNA in Nicotiana benthamiana This vector yielded high levels of

126 accharomyces cerevisiae as well as the plant Nicotiana benthamiana through transgenic expression of R

127 st import assays and transient expression in Nicotiana benthamiana to address this.

128 d a luminescence-based AS reporter system in Nicotiana benthamiana to screen pathogen effectors modul

129 established a transient expression system in Nicotiana benthamiana to study detailed interactions amo

130 iens-mediated transient expression assays in Nicotiana benthamiana to test if NPQ kinetics could be m

131 interact specifically with PRK4 and PRK5 in Nicotiana benthamiana transient expression assays, and a

132 on experiments in these tomato plants and in Nicotiana benthamiana transiently expressing Mi-1.2 and

133 The expression host was Nicotiana benthamiana using a geminiviral vector for tra

134 tomato (Solanum lycopersicum cv 75 m82D) and Nicotiana benthamiana Using deep learning, we classified

135 Our goal is to metabolically engineer Nicotiana benthamiana using montbretia genes to achieve

136 elf" plant could be transferred to leaves of Nicotiana benthamiana via recombinant expression of PLA2

137 erent fungal species to induce cell death in Nicotiana benthamiana was tested following agroinfiltrat

138 osomal protein-encoding gene, RPL10 (QM), in Nicotiana benthamiana We analyzed the expression levels

139 sting of Agrobacterium-infiltrated leaves of Nicotiana benthamiana We observed that one of these pren

140 ls of Arabidopsis (Arabidopsis thaliana) and Nicotiana benthamiana We present transient expression of

141 ll-free extracts, in yeast, and in the plant Nicotiana benthamiana We propose that there are major di

142 Q1 (recognition of XopQ 1), an NLR native to Nicotiana benthamiana with a Toll-like interleukin-1 rec

143 , Capsella rubella, and Brassica oleracea in Nicotiana benthamiana yielded fungal-type sesterterpenes

144 ransient expression of the entire pathway in Nicotiana benthamiana yields brassinin, demonstrating th

145 uorescence complementation assay in tobacco (Nicotiana benthamiana) epidermal cells.

146 brane when expressed transiently in tobacco (Nicotiana benthamiana) leaves and Arabidopsis (Arabidops

147 er cell death when overexpressed in tobacco (Nicotiana benthamiana) leaves and does so in a manner th

148 onfirmed by transient expression in tobacco (Nicotiana benthamiana) leaves and grapevine plantlets.

149 its use in transiently transformed tobacco (Nicotiana benthamiana) leaves.

150 Transgenic tobacco (Nicotiana benthamiana) plants that overexpress three yea

151 ) SEIPIN deletion mutant strain and a plant (Nicotiana benthamiana) transient expression system were

152 sites on agroinfiltration of tobacco plants (Nicotiana benthamiana).

153 reduces recalcitrance in transgenic tobacco (Nicotiana benthamiana).

154 in the cells of expanded leaves in tobacco (Nicotiana benthamiana).

155 The recent discovery that GLRaV-3 can infect Nicotiana benthamiana, a plant model organism, makes new

156 ciates with heterologously expressed NFR5 in Nicotiana benthamiana, and directly binds and phosphoryl

157 Xa10 induces programmed cell death in rice, Nicotiana benthamiana, and mammalian HeLa cells.

158 encing suppression activity and infection in Nicotiana benthamiana, Arabidopsis and soybean.

159 s interactor FRATAXIN (FH), when silenced in Nicotiana benthamiana, compromised nonhost resistance to

160 me P450 TgCYP76AE2, transiently expressed in Nicotiana benthamiana, converts epikunzeaol into epidihy

161 iltration-based transient gene expression in Nicotiana benthamiana, functionality of the recombinant

162 ce of two homeologs of the AGO1-like gene in Nicotiana benthamiana, NbAGO1-1H and NbAGO1-1L.

163 as well as tomato (Solanum lycopersicum) and Nicotiana benthamiana, revealing that the link between P

164 monas vesicatoria effector protein AvrBsT in Nicotiana benthamiana, suggesting that it may be a broad

165 66 target mimic and three solanaceous hosts: Nicotiana benthamiana, tobacco (N. tabacum), and tomato

166 Using heterologous expression in Nicotiana benthamiana, we define multiple sites of N dom

167 ing a dual-luciferase based sensor system in Nicotiana benthamiana, we quantitatively assessed the re

168 etic enzymes in Saccharomyces cerevisiae and Nicotiana benthamiana, we reconstitute the complete path

169 nstrated that RBPG1 and PG form a complex in Nicotiana benthamiana, which also involves the Arabidops

170 3IP conferred resistance to RSV infection in Nicotiana benthamiana.

171 siently co-expressed with a GFPP synthase in Nicotiana benthamiana.

172 ) independent of their enzymatic activity in Nicotiana benthamiana.

173 RX17 was examined by transient expression in Nicotiana benthamiana.

174 uce significant cell death when expressed in Nicotiana benthamiana.

175 were obtained after transient expression in Nicotiana benthamiana.

176 n as demonstrated by transient expression in Nicotiana benthamiana.

177 onfer methylation of a transgene reporter in Nicotiana benthamiana.

178 nity in the non-host solanaceous model plant Nicotiana benthamiana.

179 ed with fluorescent protein and expressed in Nicotiana benthamiana.

180 tion-dependent cell death in Arabidopsis and Nicotiana benthamiana.

181 efense against Tobacco Mosaic Virus (TMV) in Nicotiana benthamiana.

182 era avenae and transiently expressed them in Nicotiana benthamiana.

183 N-glycosylated upon expression in transgenic Nicotiana benthamiana.

184 oactive NLRs when transiently coexpressed in Nicotiana benthamiana.

185 ized, fucose-free versions of PG9 and RSH in Nicotiana benthamiana.

186 omato, potato, pepper, eggplant, tobacco and Nicotiana benthamiana.

187 to elicit immunity-associated cell death in Nicotiana benthamiana.

188 n and colocalization assays in the CaMV host Nicotiana benthamiana.

189 r gene fusions when coexpressed in citrus or Nicotiana benthamiana.

190 g) VLPs and the model antigen GFP in vivo in Nicotiana benthamiana.

191 tive response when co-expressed with Pm1a in Nicotiana benthamiana.

192 nsensitive DELLA alleles when coexpressed in Nicotiana benthamiana.

193 gnaling domain when transiently expressed in Nicotiana benthamiana.

194 s effector XopJ4 was identified in the plant Nicotiana benthamiana.

195 ened for activity by transient expression in Nicotiana benthamiana.

196 rabidopsis accessions, and an nrg1 mutant in Nicotiana benthamiana.

197 essful reconstruction of MbA biosynthesis in Nicotiana benthamiana.

198 of specific PTI pathways in both potato and Nicotiana benthamiana.

199 ;22,23-dioxide when transiently expressed in Nicotiana bethamiana In contrast, in Lycopodium clavatum

200 1 orthologs appear to be present only in the Nicotiana genus.

201 virus)), but not in resistant host systems (Nicotiana glutinosa and Chenopodium quinoa with TMV).

202 expressed with these effectors in leaves of Nicotiana glutinosa.

203 Species of Nicotiana grow naturally in different parts of the world

204 Nicotiana is an excellent system in which to study allop

205 in Nicotiana suaveolens cineole synthase and Nicotiana langsdorffii terpineol synthase.

206 en fluorescent protein (GFP)-UVR8 fusions in Nicotiana leaves and transgenic Arabidopsis.

207 function, transient expression of CsGSTF1 in Nicotiana occurred in the nucleus, cytoplasm and membran

208 ollen rejection and rejection of pollen from Nicotiana plumbaginifolia.

209 Nicotiana species are frequently investigated for their

210 Flowers of Nicotiana species emit a characteristic blend including

211 logy, and medicinal application of different Nicotiana species growing around the globe presented in

212 ced leaf transcriptomes from closely-related Nicotiana species revealed a key gene co-expression netw

213 e protease inhibitors, is essential to SI in Nicotiana spp.

214 RNA interference suppression of NaSIPP in Nicotiana spp. pollen grains disrupts the SI by preventi

215 is detected specifically in mature pollen of Nicotiana spp.; however, in self-compatible plants, this

216 ne the different terpineol-cineole ratios in Nicotiana suaveolens cineole synthase and Nicotiana lang

217 t was only shared with the eponymous species Nicotiana suaveolens of the sister section Suaveolentes.

218 XopQ recognition in both the closely-related Nicotiana sylvestris and the distantly-related beet plan

219 STF), and its orthologs in Petunia, pea, and Nicotiana sylvestris are required for leaf blade outgrow

220 gned to select for chloroplast transfer from Nicotiana sylvestris into Nicotiana tabacum cells.

221 f blade outgrowth in Medicago truncatula and Nicotiana sylvestris, respectively.

222 F's ability to complement the lam1 mutant of Nicotiana sylvestris.

223 racterization of a Transposable Element from Nicotiana tabacum (Tnt1) insertional mutant line were ca

224 of a repeated cybrid between the solanaceae Nicotiana tabacum and Hyoscyamus niger.

225 We found that pollen tubes from Nicotiana tabacum and other plant species with a solid o

226 mature Eruca sativa, Nasturtium officinale, Nicotiana tabacum and Spinacia oleracea plants and in is

227 mes of N. tabacum The glandular trichomes of Nicotiana tabacum are highly productive in terms of seco

228 last transfer from Nicotiana sylvestris into Nicotiana tabacum cells.

229 aphy of this landscape in the ancestral host Nicotiana tabacum Comparing the topographies of the land

230 hosts: Capsicum annuum cv. Marengo (pepper), Nicotiana tabacum cv. Xanthi nc (tobacco), and Cucurbita

231 evaluated by gene overexpression in tobacco (Nicotiana tabacum cv. Xanthi).

232 nTag system with the catalytic domain of the Nicotiana tabacum DRM methyltransferase, which efficient

233 MD of Arabidopsis (Arabidopsis thaliana) and Nicotiana tabacum GnTI toward Golgi localization and n-g

234 More recently in our history, Nicotiana tabacum has attracted interest as one of the m

235 NtPDR1 from Nicotiana tabacum has been shown to be involved in the c

236 ted inactivation of the plastid PsaI gene in Nicotiana tabacum has no measurable effect on photosynth

237 Nicotiana tabacum L. plants expressing dsRNA homologous

238 sing nicotine content in cultivated tobacco (Nicotiana tabacum L.) may be of value for industrial pur

239 have developed nfsI transplastomic tobacco (Nicotiana tabacum L.) to reduce pollen-borne transgene f

240 y roles of five BRC gene members in tobacco (Nicotiana tabacum L.) using CRISPR site-directed mutagen

241 resulted in rapid chlorophyll degradation in Nicotiana tabacum leaves and led to accumulation of pheo

242 Using both transient assays in Nicotiana tabacum leaves or Actinidia arguta fruits and

243 ase (nCas9-Target-AID) systems to mutagenize Nicotiana tabacum protoplasts and to regenerate plants h

244 terologous systems Nicotiana benthamiana and Nicotiana tabacum using transient and stable nuclear tra

245 ore the RNA content of TAC preparations from Nicotiana tabacum was determined using whole genome tili

246 development in two susceptible host systems (Nicotiana tabacum with TMV (Tobacco mosaic virus), and A

247 Using tobacco (Nicotiana tabacum) 'Bright Yellow 2' cell suspension and

248 ases during cell plate expansion in tobacco (Nicotiana tabacum) 'Bright Yellow-2' cells: massive deli

249 of KAT1 and cocrystallized it with tobacco (Nicotiana tabacum) 14-3-3 proteins to describe the prote

250 tegy to the Clp protease complex of tobacco (Nicotiana tabacum) and identified a set of chloroplast p

251 chloroplast association in vivo in tobacco (Nicotiana tabacum) and observed weaker tethering to addi

252 e, miR159 function was inhibited in tobacco (Nicotiana tabacum) and rice (Oryza sativa) using miRNA M

253 utilized the highly synchronizable tobacco (Nicotiana tabacum) Bright yellow 2 (BY2) cell suspension

254 lastid transformation is routine in tobacco (Nicotiana tabacum) but 100-fold less frequent in Arabido

255 patens for transient expression and tobacco (Nicotiana tabacum) BY2 cells for stable transformation.

256 xysome linker protein CcmM35 within tobacco (Nicotiana tabacum) chloroplasts.

257 ization, and functional analysis of tobacco (Nicotiana tabacum) EXO70 isoforms.

258 inward-rectifying K(+) channels of tobacco (Nicotiana tabacum) guard cells and show its close parall

259 Recently, tobacco (Nicotiana tabacum) leaves were engineered to accumulate

260 When ectopically expressed in tobacco (Nicotiana tabacum) leaves, MtNPD1 colocalized with vacuo

261 Here we develop an RNAi-RbcS tobacco (Nicotiana tabacum) master-line, tobRrDeltaS, for produci

262 Here, by generating transplastomic tobacco (Nicotiana tabacum) mutants with point mutations in the a

263 ing high levels of botryococcene in tobacco (Nicotiana tabacum) plants by diverting carbon flux from

264 ation was explored using transgenic tobacco (Nicotiana tabacum) plants that have either high (PAO) or

265 enerated a series of transplastomic tobacco (Nicotiana tabacum) plants to alter tRNA(Glu) expression

266 struct expressing Hvt and lectin in tobacco (Nicotiana tabacum) plants under phloem specific promoter

267 photosynthetic capacity and growth, tobacco (Nicotiana tabacum) plants with increased levels of trans

268 isoprene-emitting and non-emitting tobacco (Nicotiana tabacum) plants, to examine: the response of i

269 nt monoclonal antibody expressed in tobacco (Nicotiana tabacum) plants.

270 diting site was introduced into the tobacco (Nicotiana tabacum) plastid genome.

271 gged transmembrane (TM) proteins in tobacco (Nicotiana tabacum) pollen tubes growing normally or trea

272 In steady-state growing tobacco (Nicotiana tabacum) pollen tubes, SEC3a displayed amino-t

273 In transient expression assays in tobacco (Nicotiana tabacum) protoplasts, TSAR1 and TSAR2 exhibit

274 Here, we show that the tobacco (Nicotiana tabacum) retrotransposon Tnt1 efficiently tran

275 Moreover, plants carrying a tobacco (Nicotiana tabacum) retrotransposon Tnt1 insertion in MtT

276 lation and translation in leaves of tobacco (Nicotiana tabacum) seedlings after transfer from moderat

277 fruits and seeds, and nicotine in tobacco ( Nicotiana tabacum) seedlings.

278 is of the cytochrome b6f complex in tobacco (Nicotiana tabacum) seems to be restricted to young leave

279 m in the dicotyledonous model plant tobacco (Nicotiana tabacum) that allows us to study the leaf deet

280 ted them by metabolite profiling of tobacco (Nicotiana tabacum) tissues.

281 Here, we show that tobacco (Nicotiana tabacum) trichomes contain a specific Rubisco

282 he angiosperms rice (Oryza sativa), tobacco (Nicotiana tabacum), and Arabidopsis (Arabidopsis thalian

283 Arabidopsis (Arabidopsis thaliana), tobacco (Nicotiana tabacum), and cultivated tomato under the cont

284 d in tomato (Solanum lycopersicum), tobacco (Nicotiana tabacum), Medicago truncatula, wheat (Triticum

285 eral species including A. thaliana, tobacco (Nicotiana tabacum), N. benthamiana, N. attenuata and tom

286 ighlighted, with a special focus on tobacco (Nicotiana tabacum).

287 nt species (Hordeum vulgare, Vicia faba, and Nicotiana tabacum).

288 xin (Hvt) and onion leaf lectin, in tobacco (Nicotiana tabacum).

289 ted in primary PD at cytokinesis in tobacco (Nicotiana tabacum).

290 expression of CsGSTF1 in transgenic tobacco (Nicotiana tabacum).

291 mical compounds in cell cultures of tobacco (Nicotiana tabacum); (2) confirmation of the identified h

292 51-dependent HR in Nicotiana benthamiana and Nicotiana tabacum, respectively.

293 benthamiana and overexpression in transgenic Nicotiana tabacum.

294 and abiotic stress tolerance in model plant Nicotiana tabacum.

295 lism operating in the glandular trichomes of Nicotiana tabacum.

296 ich was confirmed by localization studies in Nicotiana tabacum.

297 erated response to natural shading events in Nicotiana (tobacco), resulting in increased leaf carbon

298 was identified to be the target of miR395 in Nicotiana tobacum, which belongs to low affinity sulfate

299 alloplasmic N. tabacum line we used carries Nicotiana undulata cytoplasmic genomes, and its flowers

300 ts of allopolyploidy on floral morphology in Nicotiana, using corolla tube measurements and geometric