ライフサイエンスコーパス: photoassimilate

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1 rts its role in the systemic distribution of photoassimilate.

2 ntirely, inhibited exudation of radiolabeled photoassimilate.

3 controlled primarily by the availability of photoassimilates.

4 ght requirement and the hyperaccumulation of photoassimilates.

5 crucial roles played by uridine salvage for photoassimilate allocation and partitioning.

6 Mannitol is an important photoassimilate, as well as providing plants with resist

7 effect of light intensity on the quantity of photoassimilates available to the fruits without a clear

8 otosynthesis is dependent on partitioning of photoassimilate between starch and sucrose, and varies i

9 leaves, Tre6P influences the partitioning of photoassimilates between Suc, organic acids, and amino a

10 ow that the only vital function of AtSUC2 in photoassimilate distribution is phloem loading.

11 Phloem loading is the initial step in photoassimilate export and the one that creates the driv

12 ild type, vte1 and vte2 had reduced rates of photoassimilate export as early as 6 h into low-temperat

13 nt of transfer cell walls and maintenance of photoassimilate export capacity during low-temperature (

14 The rapid reduction in photoassimilate export in vte2 coincides with callose de

15 ng impacts on LT-induced sugar accumulation, photoassimilate export reduction and vascular-specific c

16 d facilitate greater yields through enhanced photoassimilate export to sink tissues.

17 rrelated with their extent of suppression of photoassimilate export.

18 istance is likely not caused by diversion of photoassimilates from growth to defense but rather by a

19 Transport of photoassimilates from leaf tissues (source regions) to t

20 potential of regulating the translocation of photoassimilates from source to sink tissues represents

21 ocities and volume flow to supply sinks with photoassimilates greatly depend on the geometry of the m

22 Leaves are the primary source of photoassimilate in crop plants, and understanding the ge

23 r veins for transport rather than loading of photoassimilates in source tissue does not preclude viru

24 Conversion of photoassimilate into mannitol and glycerol for carbon se

25 hesis, but exhibit increased partitioning of photoassimilate into sucrose and have delayed photosynth

26 Uptake of photoassimilates into the leaf phloem is the key step in

27 ty of Fru-2,6-P2 to modulate partitioning of photoassimilate is an important determinant of growth an

28 ally devoid of P-protein structures and lost photoassimilates more rapidly after injury than control

29 expressed can be predicted by a knowledge of photoassimilate movement patterns in vivo.

30 Photoassimilates play crucial roles during plant-pathoge

31 (35S::AVP1 cassette) enhanced shoot biomass, photoassimilate production and transport, rhizosphere ac

32 ccharides is an adaptive strategy to improve photoassimilate retention, and consequently translocatio

33 Photoassimilates such as sugars are transported through

34 te uptake is potentiated by increased carbon photoassimilate (sucrose) levels.

35 number of loading strategies for the primary photoassimilates, sucrose and sugar alcohols.

36 associated with a concentration gradient of photoassimilates (the non-mobile solutes) that exists in

37 eferential allocation by the fungus of plant photoassimilate to weather grains of limestone and silic

38 mature seeds indicated reduced conversion of photoassimilates to oil.

39 ective in transfer cell wall development and photoassimilate transport at low temperature (LT).

40 Sucrose is the photoassimilate transported from the leaves to the fruit

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