ライフサイエンスコーパス: mesophyll

1 undle sheath) and linear electron transport (mesophyll).

2 nse to photosynthesis occurring within plant mesophyll.

3 TOR (EPF) family altered cell density in the mesophyll.

4 y than NtRbcS-M, an isoform expressed in the mesophyll.

5 to the site of initial carboxylation in the mesophyll.

6 bute diffuse and direct light throughout the mesophyll.

7 e expression of cell cycle genes in the leaf mesophyll.

8 ness of the abaxial epidermis and the spongy mesophyll.

9 the leaf layer underneath the epidermis, the mesophyll.

10 response to red light in the absence of the mesophyll.

11 cially in the palisade parenchyma and spongy mesophyll.

12 bility of SCARECROW promoter activity in the mesophyll.

13 protoplasts from the veins but not from the mesophyll.

14 dian rhythms of [Ca(2+)]i only in the spongy mesophyll.

15 interaction between GI and FT repressors in mesophyll.

16 as allowed to wick between epidermis and the mesophyll.

17 efore they were transported into the cladode mesophyll.

18 a function of depth, peaking deep within the mesophyll.

19 olymers are allowed to diffuse back into the mesophyll.

20 concentration to a level higher than in the mesophyll.

21 erence signal-embedded within the plant leaf mesophyll.

22 t of ABA on photosynthesis and the effect of mesophyll ABA on yield under both well-watered and droug

23 y, but how this relates to the regulation of mesophyll airspace configuration is poorly understood.

24 lines of wheat and Arabidopsis to show that mesophyll airspace formation is linked to stomatal funct

25 luences the degree and spatial patterning of mesophyll airspace formation, and indicate that this rel

26 The formation of stomata and leaf mesophyll airspace must be coordinated to establish an e

27 propose that the coordination of stomata and mesophyll airspace pattern underpins water use efficienc

28 and (8) Kox is strongly influenced by spongy mesophyll anatomy, decreasing with protoplast size and i

29 ribution of functional stomata on underlying mesophyll anatomy.

30 port for a given concentration of Suc in the mesophyll and (2) segregation of oligomers and the inver

31 d the formation of a glycine shuttle between mesophyll and BS cells that characterizes C2 photosynthe

32 transcript and protein levels and decreased mesophyll and BS osmotic water permeability (P(f)), meso

33 ARECROW:microRNA plants) exhibited decreased mesophyll and BS Pf and decreased K(leaf) but no decreas

34 ynthesis genes is partitioned such that leaf mesophyll and bundle sheath cells accumulate different c

35 that differences in light perception between mesophyll and bundle sheath cells facilitate differentia

36 y network differentially accumulated between mesophyll and bundle sheath cells, indicative of differe

37 that its reactions are compartmented between mesophyll and bundle sheath cells.

38 pecies B. sinuspersici function analogous to mesophyll and bundle sheath chloroplasts of Kranz-type C

39 we demonstrate that 61% of all light-induced mesophyll and bundle sheath genes were induced only by b

40 sis gene expression is compartmented between mesophyll and bundle-sheath cells.

41 a vapor-phase signal that originates in the mesophyll and causes stomata to open in the light.

42 d with a thin hydrophobic filter between the mesophyll and epidermis stomata responded normally to li

43 in response to extracellular ATP and of leaf mesophyll and guard cell chloroplasts during light-to-lo

44 ave limited numbers of plasmodesmata between mesophyll and phloem, displayed typical symptoms of load

45 ed on the abundance of plasmodesmata between mesophyll and phloem.

46 t least seven cell border interfaces between mesophyll and sieve elements.

47 tively, but the TAM-GFP signal levels in the mesophyll and stomata in the 35S:TAM-GFP lines only diff

48 Furthermore, the GFP signals in the mesophyll and stomata in the TAM:TAM-GFP and 35S:TAM-GFP

49 g roles for these metabolites within the CAM mesophyll and stomatal complex.

50 wever, a strong positive correlation between mesophyll and stomatal conductance among cultivars appar

51 tations due to CO(2) diffusivity through the mesophyll and supply of CO(2) to photosynthetic reaction

52 es form a crucial interface between the leaf mesophyll and the atmosphere, controlling water and carb

53 uces oscillatory [Ca(2+)]i signals in spongy mesophyll and vascular bundle cells, but not other cell

54 f deformation induced by desiccation in both mesophyll and xylem suggest that cell wall collapse is u

55 f evaporation accounted for by the vascular, mesophyll, and epidermal regions.

56 te gene expression across the bundle sheath, mesophyll, and guard cells in the C4 leaf.

57 inal tissues, fewer cells in the interveinal mesophyll, and normal perivascular bundle sheath cells.

58 hat phyB expression in the stomatal lineage, mesophyll, and phloem is sufficient to restore wild-type

59 all aerial tissues including the epidermis, mesophyll, and vascular bundle, its tissue-specific func

60 r, by the cell layer in which they operate - mesophyll at a two-cell distance from leaf veins versus

61 owed an increase of total As in the vein and mesophyll but not in the epidermis of young mature leave

62 U lineage were present in both epidermis and mesophyll, but oleosin occurred only in epidermis.

63 co is primarily found in the chloroplasts of mesophyll (C3 plants), bundle-sheath (C4 plants), and gu

64 ansients showed that minor vein collapse and mesophyll capacitance could effectively buffer major vei

65 s that may coordinate stomatal behavior with mesophyll carbon assimilation and explore stomatal kinet

66 that may coordinate stomatal behaviour with mesophyll carbon assimilation.

67 leaves triggered significant enlargement of mesophyll cell area per transverse section width (S/W),

68 af surface while inducing both epidermal and mesophyll cell death.

69 enhance photosynthetic capacity or increase mesophyll cell density.

70 he mutant defects are unified by compromised mesophyll cell development.

71 hetic biochemistry inside a typical C3-plant mesophyll cell geometry.

72 er major vein allocation, greater numbers of mesophyll cell layers and higher cell mass densities.

73 as 3 days after germination in epidermal and mesophyll cell layers, which undergo endoreplication to

74 different ABA responses in guard cell versus mesophyll cell metabolomes.

75 Changes in S/W associated with mesophyll cell morphology occurred earlier than changes

76 oted starch synthesis, restoring granules in mesophyll cell plastids.

77 JUB1 transactivates DREB2A expression in mesophyll cell protoplasts and transgenic plants and bin

78 NAP transactivated the promoter of AAO3 in mesophyll cell protoplasts, and electrophoretic mobility

79 L2-5 and IL4-3 in detail and found increased mesophyll cell size and leaf ploidy levels, suggesting t

80 Increased mesophyll cell size and palisade tissue thickness, in K-

81 to abaxial stomatal densities (SD(aba) ) and mesophyll cell wall thickness (T(CW) ).

82 ust above the ligule into highly specialized mesophyll cells (MCs) and bundle sheath cells (BSCs) at

83 n in guard cells but are starch deficient in mesophyll cells (plastidial phosphoglucose isomerase [pP

84 edominantly as sucrose, which is produced in mesophyll cells and imported into phloem cells for trans

85 nnels, linking it with Na(+) accumulation in mesophyll cells and salt bladders as well as leaf photos

86 minantly in the intracellular compartment of mesophyll cells and was enriched in chloroplasts where i

87 leaves have dramatically elongated palisade mesophyll cells and, in some cases, increased leaf ploid

88 of photosynthesis in C4 plants, whereas the mesophyll cells are only involved in CO2 fixation.

89 ls, whereas BAM3 is the dominant activity in mesophyll cells at night.

90 educing resistance to CO(2) diffusion inside mesophyll cells by facilitating CO(2) transfer in both g

91 late biosynthetic steps occur in specialized mesophyll cells called idioblasts.

92 Furthermore, rapidly after transfer to Suc, mesophyll cells contained fewer and smaller plastids, wh

93 evealed by transmission electron microscopy, mesophyll cells degrade chloroplasts, but degradation is

94 ing of subcellular compartments within plant mesophyll cells during haustoria ontogenesis.

95 GFP-fusion experiments in tobacco mesophyll cells established that the plant protein is ta

96 undance in guard cell-enriched epidermis and mesophyll cells from leaves of K. fedtschenkoi.

97 d classical Kranz anatomy with lightly lobed mesophyll cells having low chloroplast coverage.

98 cient to activate photosystem II assembly in mesophyll cells in etiolated maize.

99 re readily detected in conducting as well as mesophyll cells in stems and source leaves.

100 hnique to isolated vacuoles from Arabidopsis mesophyll cells in the whole-vacuole mode, we studied th

101 mechanism divided between bundle sheath and mesophyll cells increases photosynthetic efficiency.

102 leaf migrates from photosynthetically active mesophyll cells into the phloem down its concentration g

103 igrates passively through plasmodesmata from mesophyll cells into the sieve elements.

104 ated from Arabidopsis (Arabidopsis thaliana) mesophyll cells is mediated by two distinct membrane tra

105 er starch biosynthesis in guard cells and/or mesophyll cells is rate limiting for high CO2-induced st

106 mented transcriptional repression of RBCS in mesophyll cells is responsible for repressing LS synthes

107 Most mesophyll cells of harlequin flowers showed extremely hi

108 The chloroplast organelle in mesophyll cells of higher plants represents a sunlight-d

109 suberin-like lamellae in both epidermal and mesophyll cells of leaves.

110 Notably, the mesophyll cells of pgi1-2 leaves accumulated exceptional

111 Photosynthesis occurs in mesophyll cells of specialized organs such as leaves.

112 Furthermore, dtx50 mutant mesophyll cells preloaded with ABA released less ABA com

113 Following excitation, mesophyll cells recovered their prestimulus potential no

114 nergy is used to transfer sucrose (Suc) from mesophyll cells to the phloem of leaf minor veins agains

115 Chloroplasts in mesophyll cells typically contain five to seven granules

116 retention of substantial amounts of ptDNA in mesophyll cells until leaf necrosis.

117 ng cells such as guard cells, trichomes, and mesophyll cells, and in vascular tissue.

118 The coordinated positioning of veins, mesophyll cells, and stomata across a leaf is crucial fo

119 ls were found to originate primarily in leaf mesophyll cells, as detected by aniline blue staining.

120 in Nicotiana benthamiana leaf epidermal and mesophyll cells, but did not possess AO activity, as sho

121 ts, photosynthesis occurs in both the BS and mesophyll cells, but the BS cells are the major sites of

122 While the function of mesophyll cells, guard cells, phloem companion cells and

123 ell-specific metabolism, including guard and mesophyll cells, in order to elucidate mesophyll-derived

124 d for the three-dimensional (3D) geometry of mesophyll cells, leading to potential differences betwee

125 dles (perivascular), from the photosynthetic mesophyll cells, or within the vicinity of the stomatal

126 ental gradient and between bundle sheath and mesophyll cells, respectively.

127 ue-dependent stimulations of ChR2 expressing mesophyll cells, resting around -160 to -180 mV, reprodu

128 ealed significant accumulation of Rubisco in mesophyll cells, suggesting a continuing cell type-speci

129 rated in the cytosol than in the vacuoles of mesophyll cells, thus increasing the driving force for p

130 tion; we also observed severe alterations in mesophyll cells, which lack oil bodies and normal plasti

131 accumulates primarily phytoglycogen in leaf mesophyll cells, with only small amounts of starch in ot

132 atterning with the development of underlying mesophyll cells.

133 fewer starch granules compared with control mesophyll cells.

134 parallel pathways for CO(2) diffusion inside mesophyll cells.

135 e interactions between the bundle sheath and mesophyll cells.

136 itrogen metabolism between bundle sheath and mesophyll cells.

137 esistant membranes from Arabidopsis thaliana mesophyll cells.

138 gene was expressed in both bundle sheath and mesophyll cells.

139 tal gradient and in mature bundle sheath and mesophyll cells.

140 while chloroplastic PPDK also accumulates in mesophyll cells.

141 ntially expressed in guard cells compared to mesophyll cells.

142 S) to the first site of carboxylation in the mesophyll cells.

143 s, higher ploidy levels, and larger palisade mesophyll cells.

144 e sclerenchyma above and/or below instead of mesophyll cells; and supernumerary bundle sheath cells d

145 t veins are separated by one rather than two mesophyll cells; many veins have sclerenchyma above and/

146 maize (Zea mays) MET1 homolog is enriched in mesophyll chloroplasts compared with bundle sheath chlor

147 When grown in a light-dark regime, mesophyll chloroplasts of dpe2-1xphs1a contain a single

148 s responsible for repressing LS synthesis in mesophyll chloroplasts, a ubiquitin promoter-driven RBCS

149 Rubisco accumulates in bundle sheath but not mesophyll chloroplasts, but the mechanisms that underlie

150 showed that AtCPT7 resides in the stroma of mesophyll chloroplasts.

151 f tissues, and show that the vasculature and mesophyll clocks asymmetrically regulate each other in A

152 (i) and WUE(plant) , by addressing potential mesophyll CO(2) conductance (g(m) ) and biochemical limi

153 elerate stomatal movements in synchrony with mesophyll CO(2) demand and to improve water use efficien

154 te mesophyll-derived signals that coordinate mesophyll CO2 demands with stomatal behaviour, in order

155 In the second, expression was maximal in the mesophyll compared with both guard cells and bundle shea

156 giosperm taxa displayed significantly higher mesophyll conductance (g (m)), yet their stomatal conduc

157 3)C and (18)O) are commonly used to estimate mesophyll conductance (g (m)).

158 also developed a new formulation to estimate mesophyll conductance (g(m) ) based on actual hydration

159 Mesophyll conductance (g(m) ) is the diffusion of CO(2)

160 The internal CO(2) gradient imposed by mesophyll conductance (g(m) ) reduces substrate availabi

161 g(c) ) that maximizes A while accounting for mesophyll conductance (g(m) ) was used to interpret new

162 The cold acclimations of mesophyll conductance (g(m) ), bundle-sheath conductance

163 Mesophyll conductance (gm ) describes the movement of CO

164 Mesophyll conductance (gm ) is an important factor limit

165 Enhancing mesophyll conductance (i.e. the rate of carbon dioxide d

166 t steady state, in vivo Rubisco activity and mesophyll conductance accounted for 84% of the limitatio

167 Mesophyll conductance and g(bs) responded strongly to me

168 to increase our fundamental understanding of mesophyll conductance and leaf function and, consequentl

169 iod 1915-1995, and including corrections for mesophyll conductance and photorespiration, dW/dc(a) for

170 apparently impedes positive scaling between mesophyll conductance and water use efficiency in soybea

171 ry to expectations, photosynthetic rates and mesophyll conductance both increased with increasing lea

172 is potential to increase photosynthesis and mesophyll conductance by selecting for greater leaf mass

173 iques, may provide additional information on mesophyll conductance in C3 plants.

174 que was developed to allow quantification of mesophyll conductance in C4 plants and to provide an alt

175 ygen isotope technique allowed estimation of mesophyll conductance in C4 plants and, when combined wi

176 As expected, mesophyll conductance is positively correlated with phot

177 tially independent variation in stomatal and mesophyll conductance may allow a plant to improve water

178 Mesophyll conductance of C4 species was similar to that

179 ll and BS osmotic water permeability (P(f)), mesophyll conductance of CO2, photosynthesis, K(leaf), t

180 hyll exhibited reduced P(f), but not reduced mesophyll conductance of CO2, suggests that the BS-mesop

181 h sets the initial boundaries of a number of mesophyll conductance parameters, incorporating an overv

182 To improve water use efficiency, mesophyll conductance should be increased without concom

183 Mesophyll conductance significantly, and variably, limit

184 The presence of genetic variation for mesophyll conductance suggests that there is potential t

185 Here, we partition the variance in mesophyll conductance to within- and among-cultivar comp

186 We demonstrate that mesophyll conductance varies more than 2-fold and that 3

187 ld conditions and examine the covariation of mesophyll conductance with photosynthetic rate, stomatal

188 ulation at flow junctions (e.g. stomatal and mesophyll conductance, and malic acid transport across t

189 meters included net CO(2) assimilation rate, mesophyll conductance, and mitochondrial respiration at

190 2) transfer conductance within plant leaves (mesophyll conductance, g(m) ) is currently not considere

191 e of flow of the gas within the leaf, termed mesophyll conductance.

192 dark but are also characterized by improved mesophyll conductance.

193 WUE, including photosynthesis, stomatal and mesophyll conductances, and canopy structure.

194 low light and moderate humidity but that the mesophyll contributes substantially when the leaf center

195 We show that the mesophyll crystals of pigweed (Amaranthus hybridus) exhi

196 e synchrony of stomatal behavior relative to mesophyll demands for CO(2).

197 e chlorophyll concentration as a function of mesophyll depth for 57 plant taxa.

198 d and mesophyll cells, in order to elucidate mesophyll-derived signals that coordinate mesophyll CO2

199 work concurrently to coordinate stomatal and mesophyll development for optimal leaf gas exchange, and

200 A delay in mesophyll differentiation apparent both in the leaf anat

201 vestigation identifies a new role for RBR in mesophyll differentiation that affects tissue porosity a

202 An explicit consideration of mesophyll diffusion increases the modeled cumulative CO2

203 , CO2 concentrations drop considerably along mesophyll diffusion pathways from substomatal cavities t

204 pressing or reducing TEM specifically in the mesophyll, display lower or higher trichome numbers, res

205 It has been suggested that a mesophyll-driven signal coordinates A and stomatal condu

206 review we evaluate the current literature on mesophyll-driven signals that may coordinate stomatal be

207 We also evaluate the current literature on mesophyll-driven signals that may coordinate stomatal be

208 is largely explained by photorespiratory and mesophyll effects.

209 y expressed in the evening, whereas rhythmic mesophyll-enriched genes tend to be expressed in the mor

210 heories of trichome formation as they reveal mesophyll essential during epidermal trichome initiation

211 epending on internal leaf architecture, with mesophyll evaporation a subordinate component.

212 Hence, the fact that SCARECROW:microRNA mesophyll exhibited reduced P(f), but not reduced mesoph

213 rm PPDK, whereas pdk1 specifies the abundant mesophyll form.

214 of ecosystem-scale stomatal conductance and mesophyll function, without relying on measures of soil

215 t starch biosynthesis in guard cells but not mesophyll functions in CO2-induced stomatal closing.

216 r due to an internal conductance in the leaf mesophyll (g(m) ) that is variable and seldom computed.

217 net photosynthesis (A) and stomatal (gs) and mesophyll (gm) conductances, alongside the 53 data profi

218 Epidermis-mesophyll grafts for T. pallida were created by placing

219 When epidermis-mesophyll grafts were constructed with a thin hydrophobi

220 yll conductance of CO2, suggests that the BS-mesophyll hydraulic continuum acts as a feed-forward con

221 from the leaf epidermis to specialized leaf mesophyll idioblast and laticifer cells to complete the

222 rafficking from palisade mesophyll to spongy mesophyll in Nicotiana benthamiana leaves.

223 gers ectopic stomatal differentiation in the mesophyll layer and atml1 mutation enhances the stomatal

224 ate the diel pattern of carbon fluxes within mesophyll layers.

225 low rates of photosynthesis, largely due to mesophyll limitation.

226 zed by a CO2-concentrating mechanism between mesophyll (M) and bundle sheath (BS) cells of leaves.

227 y and functional differentiation between the mesophyll (M) and bundle sheath (BS) cells of maize (Zea

228 tion of SQDG and PG molecular species, among mesophyll (M) and bundle sheath (BS) cells, are compared

229 d reduction are typically coordinated across mesophyll (M) and bundle sheath (BS) cells, respectively

230 ate the reactions of photosynthesis into the mesophyll (M) and bundle sheath (BS).

231 ural features, leaf thickness (Thick(leaf)), mesophyll (M) cell surface area exposed to intercellular

232 sts in differentiated bundle sheath (BS) and mesophyll (M) cells of maize (Zea mays) leaves are speci

233 ruvate regeneration also vary between BS and mesophyll (M) cells.

234 d with C3 relatives and become restricted to mesophyll (M) or bundle sheath (BS) cells.

235 tmentalization of key C(4) enzymes either to mesophyll (M) or bundle sheath cells is considered a cru

236 to meet the high lipoate requirement of leaf mesophyll mitochondria.

237 ted to more MS mitochondria and less GLDP in mesophyll mitochondria.

238 g the epidermis of one leaf onto the exposed mesophyll of another leaf.

239 , we show that increased cell density in the mesophyll of Arabidopsis can be used to increase leaf ph

240 e-specific localization in the epidermis and mesophyll of isozymes implicated in starch and malate tu

241 The epidermis but not mesophyll of leaves of vanilla (Vanilla planifolia) and

242 y labeled GA3 accumulates exclusively in the mesophyll of leaves, but not in the epidermis, and that

243 accumulation in secondary phloem and in the mesophyll of needles, where we also observed increasing

244 tion of diffuse versus direct light into the mesophyll of sun-grown sunflower leaves led to a more he

245 f unbound arsenite increased in the vein and mesophyll of young mature leaves.

246 duction, or cell type-specific expression in mesophyll or bundle sheath cells.

247 lly characterized RbcS isoforms expressed in mesophyll or bundle-sheath cells.

248 We found that GI expressed in either mesophyll or vascular bundles rescues the late-flowering

249 Interestingly, GI expressed in mesophyll or vascular tissues increases FT expression wi

250 of photosynthetic bundle sheath (inner) and mesophyll (outer) cells.

251 iation due to differences in leaf thickness, mesophyll palisade fraction, and presence of large inter

252 Genomes of the rice (Oryza sativa) xylem and mesophyll pathogens Xanthomonas oryzae pv. oryzae (Xoo)

253 a reduction of hydraulic conductance of the mesophyll pathways outside the xylem would cause a stron

254 onses as a result of red light influences on mesophyll photosynthesis.

255 e that stomata-specific regulators can alter mesophyll properties, which provides insight into how mo

256 lifetime microscopy in Arabidopsis thaliana mesophyll protoplasts and bimolecular fluorescence compl

257 ed Nicotiana benthamiana leaves, Arabidopsis mesophyll protoplasts and tobacco BY-2 protoplasts, rega

258 assays in Arabidopsis (Arabidopsis thaliana) mesophyll protoplasts indicated that a combination of th

259 nescence-associated vacuoles are detected in mesophyll protoplasts of des1 mutants.

260 Our functional results in Zea mays mesophyll protoplasts on ABA-inducible expression effect

261 minant-negative SYP121-Sp2 fragment in maize mesophyll protoplasts or epidermal cells leads to a decr

262 a transient expression system in Arabidopsis mesophyll protoplasts that is highly amenable for the di

263 Targeting assays in Arabidopsis thaliana mesophyll protoplasts using green fluorescent protein fu

264 When expressed alone in mesophyll protoplasts, ZmPIP2s are efficiently targeted

265 eaves and Arabidopsis (Arabidopsis thaliana) mesophyll protoplasts.

266 transporters to the tonoplast in Arabidopsis mesophyll protoplasts.

267 iRNAs) in Arabidopsis (Arabidopsis thaliana) mesophyll protoplasts.

268 plants and in isolated Arabidopsis thaliana mesophyll protoplasts.

269 ntrasting behavior when expressed in tobacco mesophyll protoplasts: KAT2 forms homotetrameric channel

270 By 72 h, rare invasion by PsyB728a to the mesophyll region of host leaves occurs, but endophytic a

271 undle sheath (BS) surface area; (2) palisade mesophyll remains well hydrated in hypostomatous species

272 em into leaf tissues, they accumulate in the mesophyll, resulting in relative changes in emission int

273 bcS operons that either encoded one of three mesophyll small subunits (pS1, pS2, and pS3) or the pota

274 of genes was misregulated in plants lacking mesophyll-specific phytochromes relative to constitutive

275 A-signaling inhibitor under the control of a mesophyll-specific promoter (FBPase::abi1-1, abbreviated

276 did not lead to Rubisco accumulation in the mesophyll, suggesting that LS synthesis is impeded even

277 l densities (SD(ada) ), stomatal ratio (SR), mesophyll surface area exposed to IAS (S(mes) ) and leaf

278 The mesophyll surface area exposed to intercellular air spac

279 As K stress increased, decreased mesophyll surface exposed to intercellular space and chl

280 d 3 (cgr2/3) resulted in thin but dense leaf mesophyll that limited CO2 diffusion to chloroplasts.

281 he epidermis and airspaces in the underlying mesophyll tissue is vital for efficient gas exchange in

282 e on large series of consecutive sections of mesophyll tissue obtained by focused ion beam-scanning e

283 ola strain BLS256, pathogens that infect the mesophyll tissue of the leading models for plant biology

284 nfers differentiation of stomata in internal mesophyll tissues and occasional multiple epidermal laye

285 er lead to coupled changes in the underlying mesophyll tissues.

286 ) species, CAM stomata open at night for the mesophyll to fix CO(2) into malate (Mal) and store it in

287 decreasing expression from bundle sheath to mesophyll to guard cells.

288 STVd) required for trafficking from palisade mesophyll to spongy mesophyll in Nicotiana benthamiana l

289 rose migrates from sites of synthesis in the mesophyll to the phloem, or which cells mediate efflux i

290 ans of passive symplastic diffusion from the mesophyll to the phloem.

291 that accumulate during the day assisting in mesophyll turgor maintenance or being converted to starc

292 Here, we show that mesophyll vacuoles from Arabidopsis sense and control th

293 that TIAs are actively taken up by C. roseus mesophyll vacuoles through a specific H(+) antiport syst

294 almost exclusively on Na(+) sequestration to mesophyll vacuoles.

295 ines in which GI is expressed exclusively in mesophyll, vascular bundles, epidermis, shoot apical mer

296 leaf isotopic enrichment, the maintenance of mesophyll water status, stomatal regulation, and the int

297 As external (capillary) water, and then mesophyll water, evaporated from moss tissue, assimilati

298 t that water is optimally distributed in the mesophyll when the lateral distance between veins (dx) i

299 ut also in regulating GA distribution in the mesophyll, which in turn directs epidermal trichome form

300 Leaf veins supply the mesophyll with water that evaporates when stomata are op