ライフサイエンスコーパス: epicotyl

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1 that adds this residue was purified from pea epicotyls.

2 applied to one side of a carborundum-abraded epicotyls.

3 ts from homogenates of green leaf, etiolated epicotyl and cotyledon, and root tissues of pea were poo

4 d to cotyledons were transferred through the epicotyl and into the collection medium.

5 The initial rate H+/ATP coupling ratios of epicotyl and the nitrate-sensitive fruit proton pumping

6 uples H+ pumping from ATP hydrolysis both in epicotyls and in nitrate-sensitive fruit V-ATPases.

7 US expression was limited to the cotyledons, epicotyl, and root elongation zone.

8 abundant in the apical region of hypocotyls, epicotyls, and roots.

9 n fruit tonoplasts, unlike those of seedling epicotyls, contain nitrate-insensitive H+-ATPase activit

10 Substantial vascular exudation from pea epicotyls could be obtained without tissue damage at 0.5

11 s mutant the temperature-dependent arrest of epicotyl development is due to a failure of normal leaf

12 d, reconstituted V-ATPases of both fruit and epicotyl exhibited similar inhibitor profiles, except th

13 XET activity from epicotyl extracts used nonfucosylated seed amyloid xylog

14 with a structural role of the former during epicotyl growth where efficient association with cellulo

15 Unlike the epicotyl H(+)-ATPase, the fruit H(+)-ATPase activity was

16 In addition, the epicotyl H+ pumping activity was inactivated by oxidatio

17 Unlike the epicotyl inhibitors, and resistant to oxidation.

18 We conclude that the 45Ca2+ fed to pea epicotyls occurs largely in the cell wall, and that auxi

19 displaced through the elongation zone of the epicotyl of etiolated pea (Pisum sativum L. var Alaska)

20 rapid growth and most abundant in elongating epicotyls of etiolated seedlings.

21 Protein extracts from epicotyls or germinating cotyledons, in which XET1 or NX

22 isolated from nasturtium (Tropaeolum majus) epicotyl RNA.

23 We show for pea (Pisum sativum L.) epicotyl sections that this hypothesis is incorrect.

24 When epicotyl segments (6 mm long, 4 mm from the apical hook)

25 te H+ efflux, increase Ca2+ release from pea epicotyl segments, whereas cycloheximide, which inhibits

26 Hypocotyls and epicotyls show higher accumulation of pmeu1 transcripts

27 on in all vegetative tissues examined (root, epicotyl, stem, and leaf) except in germinating cotyledo

28 onset of curvature, on the upper side of the epicotyl, there was a conspicuous transient increase in

29 Cold inactivation of the epicotyl V-ATPase by nitrate ( > or = 100 mM) was correl

30 H+-leakage indicated that the reconstituted epicotyl V-ATPase exhibited twice as much intrinsic unco

31 sac V-ATPases appeared thicker than those of epicotyl V-ATPases in electron micrographs.

32 is lower than that of nitrate-sensitive and epicotyl V-ATPases.

33 e of intact pea (Pisum sativum L. cv Alaska) epicotyls was examined by gel-filtration chromatography.

34 ly, Agrobacterium-mediated transformation of epicotyls was unsuccessful when a constitutive promoter

35 by tonoplast vesicles from lemon fruits and epicotyls were compared.

36 r H+-ATPases (V-ATPases) of lemon fruits and epicotyls were detergent-solubilized, purified by column

37 Seven day old etiolated pea epicotyls were loaded symmetrically with 3H-indole 3-ace

38 d etiolated pea (Pisum sativum L. cv Alaska) epicotyls with 3 molar LiCl.

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