ライフサイエンスコーパス: mesophyll

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

2 olymers are allowed to diffuse back into the mesophyll.

3 bility of SCARECROW promoter activity in the mesophyll.

4 protoplasts from the veins but not from the mesophyll.

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

6 interaction between GI and FT repressors in mesophyll.

7 as allowed to wick between epidermis and the mesophyll.

8 concentration to a level higher than in the mesophyll.

9 efore they were transported into the cladode mesophyll.

10 erence signal-embedded within the plant leaf mesophyll.

11 ndle sheath cells, retrodiffuses back to the mesophyll.

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

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

14 in the opposite direction, from epidermis to mesophyll.

15 to the site of initial carboxylation in the mesophyll.

16 bute diffuse and direct light throughout the mesophyll.

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

18 ness of the abaxial epidermis and the spongy mesophyll.

19 the leaf layer underneath the epidermis, the mesophyll.

20 cially in the palisade parenchyma and spongy mesophyll.

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

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

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

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

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

26 In leaf tissues, mesophyll and bundle sheath cell fate is determined, and

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

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

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

30 by laser scanning confocal microscopy, leaf mesophyll and epidermal tissue of transgenic plants show

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

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

33 ting flagellins grew similarly, both in leaf mesophyll and in hydathode/vascular colonization assays.

34 the plasma membrane of cotyledon epidermal, mesophyll and petiole cells during blade expansion.

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

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

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

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

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

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

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

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

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

44 showed signals in the leaf vascular bundles, mesophyll, and epidermal cells as well as in epidermal b

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

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

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

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

49 cells, and high signal intensity in palisade mesophyll associated with vesicles near plastids.

50 n a defined direction, (2) the bundle sheath-mesophyll boundary serves as a novel regulatory point fo

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

52 ssay confirmed a large amount of activity in mesophyll, but not in bundle sheath membranes.

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

54 ellin when infiltrated into Arabidopsis leaf mesophyll, but this correlation was misleading.

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

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

57 that may coordinate stomatal behaviour with mesophyll carbon assimilation.

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

59 enhance photosynthetic capacity or increase mesophyll cell density.

60 nforcement of the hinge through differential mesophyll cell expansion.

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

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

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

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

65 rom Arabidopsis thaliana leaf guard cell and mesophyll cell protoplasts was studied using the patch c

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

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

68 Expression of ZmPPCK1 in leaves is mesophyll cell-specific and light-induced, indicating th

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

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

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

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

73 luding the route of sucrose efflux from leaf mesophyll cells and transport across vacuolar membranes.

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

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

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

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

78 nals in the leaf vasculature and surrounding mesophyll cells but low-intensity signals are also detec

79 re of barley plants to nitrate were large in mesophyll cells but small in epidermal cells.

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

81 defective in plastid division, and its leaf mesophyll cells contain only one or two grossly enlarged

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

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

84 nia, designated zIAA8, which is expressed by mesophyll cells differentiating as tracheary elements in

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

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

87 As a proof-of-concept approach, mesophyll cells from Arabidopsis thaliana were laser-mic

88 to study the physiology of ion transport in mesophyll cells from two Thlaspi spp. that differ signif

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

90 Expression was detected in mesophyll cells in leaves.

91 h a fluorescent dye can traffic between leaf mesophyll cells in microinjection assays.

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

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

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

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

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

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

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

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

100 reductase in sap samples from epidermal and mesophyll cells of barley (Hordeum vulgare L.) and Arabi

101 istance for diffusion of CO(2) to Rubisco in mesophyll cells of C(3) plants.

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

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

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

105 expressing a cytosolic GS1 isoenzyme in leaf mesophyll cells of tobacco.

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

107 the overexpression of cytosolic GS1 in leaf mesophyll cells seems to provide an alternate route to c

108 roplasts are more evenly distributed in leaf mesophyll cells than in the wild type.

109 ncluding an entirely symplastic pathway from mesophyll cells to sink tissues.

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

111 Chloroplasts in mesophyll cells typically contain five to seven granules

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

113 hosphoenolpyruvate carboxylase (PEPC) in the mesophyll cells was studied.

114 Highly pure preparations of guard cells and mesophyll cells were isolated in the presence of transcr

115 culent-like, have a second layer of palisade mesophyll cells, and are frequently shed during extreme

116 sma membrane region of leaf epidermal cells, mesophyll cells, and guard cells, where its distribution

117 otein indicated tonoplast location in spongy mesophyll cells, and high signal intensity in palisade m

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

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

120 altered leaf structure, a reduced number of mesophyll cells, and ultrastructural changes of the chlo

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

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

123 uced ZNT1 transcript abundance in the spongy mesophyll cells, but less in the other cell types.

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

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

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

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

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

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

130 ression profiles were compared with those of mesophyll cells, resulting in identification of 64 trans

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

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

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

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

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

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

141 while chloroplastic PPDK also accumulates in mesophyll cells.

142 ntially expressed in guard cells compared to mesophyll cells.

143 K proteins operate cell-autonomously in leaf mesophyll cells.

144 mary acceptor for fixation of bicarbonate in mesophyll cells.

145 development, but is also sugar-inducible in mesophyll cells.

146 ulated Se in their leaf vascular tissues and mesophyll cells.

147 of a subset of auxin response genes in leaf mesophyll cells.

148 n phloem have abundant plasmodesmata between mesophyll cells.

149 as detected in xylem parenchyma, phloem, and mesophyll cells.

150 3 are required for suppressing expression in mesophyll cells.

151 atterning with the development of underlying mesophyll cells.

152 fewer starch granules compared with control mesophyll cells.

153 distinguished in tobacco (Nicotiana tabacum) mesophyll cells; and (c) shown that interaction between

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

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

156 F.M. Bailey) Domin are exposed to dim light, mesophyll chloroplasts spread along the periclinal walls

157 ective agents on tobacco (Nicotiana tabacum) mesophyll chloroplasts was first examined by transmissio

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

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

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

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

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

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

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

165 of the leaf into the chloroplast, defined as mesophyll conductance (g(m)), is finite.

166 Mesophyll conductance (gm ) describes the movement of CO

167 Mesophyll conductance (gm ) is an important factor limit

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

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

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

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

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

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

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

175 As expected, mesophyll conductance is positively correlated with phot

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

177 Mesophyll conductance of C4 species was similar to that

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

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

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

181 Mesophyll conductance significantly, and variably, limit

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

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

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

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

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

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

188 boxylations alone, such that the dark period mesophyll conductance, g(i), was 0.044 mol m(-2) s(-1) b

189 dark but are also characterized by improved mesophyll conductance.

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

191 satory cell size enlargement, the underlying mesophyll/cortex layer kept normal cell numbers and resu

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

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

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

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

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

197 nism of symplastic loading, sucrose from the mesophyll diffuses into intermediary cells and is conver

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

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

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

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

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

203 is largely explained by photorespiratory and mesophyll effects.

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

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

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

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

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

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

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

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

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

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

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

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

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

217 ild type and becomes localized to the middle mesophyll in the expanding lamina.

218 that the movement of sugar alcohol from the mesophyll into the phloem in apple and A. scandens is sy

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

220 es as the ablation reaches the epidermal and mesophyll layers.

221 iple pulses were demonstrated to ablate some mesophyll layers.

222 uring maize (Zea mays) C(4) differentiation, mesophyll (M) and bundle sheath (BS) cells accumulate di

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

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

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

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

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

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

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

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

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

232 entiate into specific bundle sheath (BS) and mesophyll (M) types to accommodate C4 photosynthesis.

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

234 ized leaf cell types, bundle sheath (bs) and mesophyll (mp), which provide the foundation for this hi

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

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

237 Upon shift from CL to HL, mesophyll of expanded leaves of the triple mutant bleach

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

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

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

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

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

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

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

245 transport and carbon reduction either in the mesophyll or in guard cell chloroplasts.

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

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

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

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

250 sponse does not require a reduction in ci by mesophyll photosynthesis.

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

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

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

254 ent gene expression system using Arabidopsis mesophyll protoplasts has proven an important and versat

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

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

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

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

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

260 luorescent protein-tagged CHX20 expressed in mesophyll protoplasts was localized mainly to membranes

261 In mesophyll protoplasts, AtECA3-green fluorescent protein

262 and natural auxin response genes assayed in mesophyll protoplasts, suggesting that ARF7 plays a majo

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

264 transporters to the tonoplast in Arabidopsis mesophyll protoplasts.

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

266 vation in Arabidopsis (Arabidopsis thaliana) mesophyll protoplasts.

267 enes that were monitored in Arabidopsis leaf mesophyll protoplasts.

268 eaves and Arabidopsis (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 ades in the normal position, but the adaxial mesophyll shows disorganized patterns of cell division,

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

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

276 The mesophyll surface area exposed to intercellular air spac

277 ient trafficking from the bundle sheath into mesophyll that is vital to establishing systemic infecti

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

279 ngle polypeptide could be identified only in mesophyll thylakoids and derived PSII membranes, but not

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

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

282 5 domain moved into and infected nonvascular mesophyll tissue when the source-sink relationship of th

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

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

285 ing in the reverse direction (i.e., from the mesophyll to bundle sheath).

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

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

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

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

290 t for this motif to mediate bundle sheath-to-mesophyll trafficking is dependent on leaf developmental

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

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

293 Chloroplasts from spongy mesophyll, vascular and epidermal cells of Arabidopsis t

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

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

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

297 t impairments in photosynthesis in the upper mesophyll were associated with light-independent enzymat

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