ライフサイエンスコーパス: Spinacia oleracea

1 s in grana thylakoid membranes from spinach (Spinacia oleracea).

2 re distinct from a plastidic PGM of spinach (Spinacia oleracea).

3 n intact chloroplasts isolated from spinach (Spinacia oleracea).

4 s in grana thylakoid membranes isolated from Spinacia oleracea.

5 na benthamiana, Nicotiana tabacum MD609, and Spinacia oleracea.

6 report the draft genome sequence of spinach (Spinacia oleracea, 2n=12), which contains 25,495 protein

7 of TeA on the PM H(+)-ATPases from spinach (Spinacia oleracea) and A. thaliana (AHA2) by examining P

8 on of dynamic thylakoid stacking in spinach (Spinacia oleracea) and Arabidopsis (Arabidopsis thaliana

9 oris, a methylotrophic yeast, using spinach (Spinacia oleracea) and corn (Zea maize) cDNAs.

10 In contrast, the rrn operon in spinach (Spinacia oleracea) and mustard chloroplasts is transcrib

11 (Cd), zinc (Zn), and nickel (Ni) by spinach (Spinacia oleracea) and tomato (Lycopersicon esculentum)

12 feminization pathway in cultivated spinach (Spinacia oleracea), and investigated how this pathway ma

13 ng complex II (LHCII; isolated from spinach [Spinacia oleracea]) and the plant lipids monogalcatosyld

14 ensis (Portulacaceae) with Silene dioica and Spinacia oleracea as the outgroups.

15 gly, only some of them, such as the spinach (Spinacia oleracea) betaine aldehyde dehydrogenase (SoBAD

16 and edible portions of selected vegetables (Spinacia oleracea, Brassica campestris, Coriandrum sativ

17 , we demonstrate that living spinach plants (Spinacia oleracea) can be engineered to serve as self-po

18 angiosperms and in isolated intact spinach (Spinacia oleracea) chloroplasts undergoes light-/dark-in

19 ), soybean (Glycine max Merr.), and spinach (Spinacia oleracea) contained only a single polypeptide c

20 Expression of six Hsp70s in spinach (Spinacia oleracea cv Longstanding Bloomsdale) leaves gro

21 abelled palmitoyl-ACP prepared from spinach (Spinacia oleracea), delta(4)-acyl-ACP desaturase activit

22 dominant in the long-day (LD) plant spinach (Spinacia oleracea; GA53, GA44, GA19, GA20, GA1, GA8, and

23 iated with photosystem II (PSII) on spinach (Spinacia oleracea) grana membranes were examined using c

24 Previous work with spinach (Spinacia oleracea) has shown that the level of gibberell

25 Cultivated spinach (Spinacia oleracea) is a dioecious species.

26 degrees C) on nutrient retention of Spinach (Spinacia oleracea) juice, spray-dried in the absence of

27 ll proteins between grana in intact spinach (Spinacia oleracea L.) and Arabidopsis chloroplasts.

28 The extremely labile recombinant spinach (Spinacia oleracea L.) enzyme was stabilized by DL-alpha-

29 Spinach (Spinacia oleracea L.) is a dioecious species with an XY

30 Spinach (Spinacia oleracea L.) is a long-day (LD) rosette plant i

31 Spinach (Spinacia oleracea L.) is an economically important green

32 Spinach (Spinacia oleracea L.) is often used as a base vegetable

33 ation by osmotic stress in darkened spinach (Spinacia oleracea L.) leaves.

34 concentrations were determined for spinach (Spinacia oleracea L.) over a 24 h period to determine if

35 e investigated in the rosette plant spinach (Spinacia oleracea L.) under long-day (LD) conditions.

36 curcas was analysed and compared to spinach (Spinacia oleracea L.) using a ICP-AES.

37 ypes of common vegetables including spinach (Spinacia oleracea L.), lettuce (Lactuca sativa), carrot

38 sly linked with cold acclimation in spinach (Spinacia oleracea L.), was characterized and found to en

39 astic in pea (Pisum sativum L.) and spinach (Spinacia oleracea L.), which lack DMSP.

40 racterization of Dof gene family in spinach (Spinacia oleracea L.).

41 e stresses affect CMO expression, a spinach (Spinacia oleracea L., Chenopodiaceae) probe was used to

42 ctose-2,6-bisphosphatase was isolated from a Spinacia oleracea leaf library and used to express a rec

43 vidence on the in vivo Cl(-) distribution in Spinacia oleracea leaves and chloroplasts shows that suf

44 (18)O(2)]Acetate was incubated with spinach (Spinacia oleracea) leaves and the (18)O content in fatty

45 th reduced thioredoxin f and m from spinach (Spinacia oleracea) leaves reduced and activated the enzy

46 Nasturtium officinale, Nicotiana tabacum and Spinacia oleracea plants and in isolated Arabidopsis tha

47 Previously, the spinach (Spinacia oleracea) psbF-26 editing site was introduced i

48 atural pigments were extracted from spinach (Spinacia oleracea), red radish (Raphanus sativus L), win

49 os), leads to substantial losses in spinach (Spinacia oleracea) seed production in the only region of

50 ower meal (Tagetes erectus, TE) and spinach (Spinacia oleracea, SO) as carotenoid sources (mixture of

51 n (ACP) synthase III (KAS III) from spinach (Spinacia oleracea; So KAS III) was used to isolate two c

52 Structural comparison with SoPIP2;1 from Spinacia oleracea species provides new insights into the

53 Circular dichroism studies of Cab and the Spinacia oleracea (spinach) beta-class carbonic anhydras

54 ed and compared to the leafy green vegetable Spinacia oleracea (Spinach).

55 Spinach (Spinacia oleracea) TRX f has an apparent dissociation co

56 ive chromosome from chloroplasts of spinach (Spinacia oleracea) was analyzed by two-dimensional gel e

57 tween cerium oxide NPs with spinach plants ( Spinacia oleracea) was investigated by integrating pheno

58 lworm (Tenebrio molitor) larvae fed spinach (Spinacia oleracea), which is rich in iron.

59 ), tobacco (Nicotiana tabacum), and spinach (Spinacia oleracea) with a resolution of approximately 7

60 , we compared genome sequences of cultivated Spinacia oleracea, with a small Y-linked region on Chr4,