ライフサイエンスコーパス: photosynthate

1 bacterium Mesorhizobium loti in exchange for photosynthate.

2 n source (i.e. insects) with host plants for photosynthate.

3 among mats, originating from cyanobacterial photosynthate.

4 of cells, suggesting an increased supply of photosynthate.

5 urce and excluding contributions from recent photosynthate.

6 a for use by the plant in exchange for plant photosynthate.

7 ve of N-limited restraints on utilization of photosynthates.

8 e molecular dinitrogen in exchange for plant photosynthates.

9 ls simply respond to a diffusing gradient of photosynthate?

10 ositively correlated with photosynthesis and photosynthate accumulation.

11 trend in CUE implies that the proportion of photosynthate allocated to autotrophic respiration is no

12 ipping) to examine the impacts of rice plant photosynthate allocation on paddy N2O emissions.

13 Reducing photosynthate allocation to the grain by spikelet clippi

14 Our findings demonstrate that optimizing photosynthate allocation to the grain can reduce paddy N

15 Increasing photosynthate allocation to the grain in rice (Oryza sat

16 Photosynthate allocation to tree roots and their mycorrh

17 iotropic effect on how the plant distributes photosynthate among fruit.

18 To optimize the utilization of photosynthate and avoid damage that can result from the

19 ung leaves non-cellautonomously to available photosynthates and leads to organs constituted of a grea

20 synthesis and unraveling how plants allocate photosynthates and prioritize different carbohydrate syn

21 pattern for efficient distribution of water, photosynthates and signaling molecules.

22 e starch, which restrict the capacity to use photosynthate, and high CO(2), which increases the poten

23 lant vascular network also transports water, photosynthates, and signaling molecules and is essential

24 is conserved across plant species and sugars/photosynthates are crucial for P-deficiency signal trans

25 port tree metabolism and growth when current photosynthates are insufficient, offering resilience in

26 Moreover, we also show that sugars and photosynthates are integrally related to P-deficiency-in

27 tes against (13)CO(2) so that source sugars (photosynthates) are on average (13)C depleted by 20 per

28 also describe how meristems deal with extra photosynthate as a result of exposure to elevated CO2.

29 nscriptionally regulated by both nitrate and photosynthate availability.

30 These results are consistent with photosynthate being trapped within anthocyanin-accumulat

31 It also alters the allocation of photosynthates between ribulose 1,5-bisphosphate regener

32 The relative use of new photosynthate compared to stored carbon (C) for the prod

33 fold less than predicted for requirements of photosynthate delivery.

34 Besides photosynthates, dodder (Cuscuta spp.) acquires phloem-mo

35 se cortical cells are the first to intercept photosynthate exiting the vascular cylinder, transcript

36 Both (11)CO(2) fixation and (11)C-photosynthate export from the labeled source leaf increa

37 affected by the disrupted supply of current photosynthate for over 1 yr; however, carbohydrate conce

38 ns in regulating respiration of recent plant photosynthate from soil.

39 bacteria donated genes that allow export of photosynthate from the plastid and its polymerization in

40 oprene is made primarily from recently fixed photosynthate; however, alternate carbon sources play an

41 osystems and account for a large fraction of photosynthate in a wide range of ecosystems; they theref

42 dition to its role as a major translocatable photosynthate in Rosaceae species, sorbitol is a widespr

43 mRNA could be linked to the availability of photosynthate in the plant.

44 hange with the microsymbiont-obtaining plant photosynthates in exchange for mineral nutrients: enhanc

45 al minerals to their plant hosts and receive photosynthates in return.

46 Potential modules for dynamic photosynthate input, wetting-event inputs, freeze-thaw i

47 ate winter, after an extended period with no photosynthate input.

48 in mind, this study emphasizes the import of photosynthate into developing embryos, its conversion in

49 atalyzes a crucial step in the conversion of photosynthate into oil, suggesting a preferred plastid r

50 n nutrient deprivation, microalgae partition photosynthate into starch and lipids at the expense of p

51 urements of photosystem II), partitioning of photosynthate into sucrose and starch, and plant growth.

52 es play an important role, particularly when photosynthate is limiting.

53 If growth at night is fast, photosynthate is used for growth at the start of the day

54 from decomposition of surface-derived modern photosynthate, not catotelm C.

55 own to bring about short-term adjustments of photosynthate partitioning between starch and sucrose (S

56 f respiratory CO2 refixation and anaplerotic photosynthate partitioning in support of storage oil and

57 acteria, nematodes and insects intercept the photosynthate produced by plants, and viruses use replic

58 sistent with a defect in chloroplast-derived photosynthate production and are largely rescued by sucr

59 2), which increases the potential to produce photosynthate, provides conditions for strong down-regul

60 At the same time, (11)C-photosynthate remaining in the aboveground sink tissues

61 e-enhanced and up-/down-regulated in vivo by photosynthate supply from the shoots.

62 anscript (NE-PpcK) is markedly influenced by photosynthate supply from the shoots.

63 anoxic stress on soil microbes and decreased photosynthates supply.

64 ulation mechanisms: the symbiont shares only photosynthate that it cannot use itself, and the host de

65 The mobilization of photosynthate through myo-inositol translocation links r

66 ) C-CO2 was applied to trace (13) C-labelled photosynthate throughout plants, fungi, and soil microbe

67 re the primary recipients of (13) C-labelled photosynthate throughout the system, representing 60-70%

68 een aboveground production and allocation of photosynthate to belowground processes and the temporal

69 is a preferred route of carbon from imported photosynthate to seed oil in the embryo.

70 The conversion of photosynthate to seed storage reserves is crucial to pla

71 s closely coordinated with the production of photosynthate to supply nutrients for growth.

72 his is noteworthy since these leaves provide photosynthate to the developing grain.

73 on cycles as plant hosts divert up to 20% of photosynthate to the obligate biotrophic fungi.

74 to SUSIBA2 rice, favouring the allocation of photosynthates to aboveground biomass over allocation to

75 hat NTS and SSS can enhance translocation of photosynthates to grains during the post-anthesis stage.

76 cular mycorrhizal fungi (AMF) transfer plant photosynthate underground which can stimulate soil micro

77 ed quantifying the relative fractions of new photosynthate vs stored C used in root growth and root r

78 n Rsoil suggests that under eCO2, additional photosynthate was produced, transported belowground, and

79 m a closed network that transports essential photosynthates, water and signaling molecules to the dev

80 New fine-root growth was largely from recent photosynthate, while nearly one-quarter of respired C wa

81 Tomato fruit are sinks of photosynthate, yet unripe green fruit contribute signifi