ライフサイエンスコーパス: etioplast

1 oplasts) versus the yellow base of the leaf (etioplasts).

2 cis-carotenes and restored PLB formation in etioplasts.

3 s localized to the prolamellar bodies within etioplasts.

4 f large amounts of Pchlide b in the isolated etioplasts.

5 es, including chloroplasts, amyloplasts, and etioplasts.

6 in abundance regulates lipid biosynthesis in etioplasts.

7 component of metabolism and redox sensing in etioplasts.

8 ytochrome f, and in protein targeting in the etioplast, a nonphotosynthetic plastid type.

9 Mutant seedlings also display defects in etioplast and amyloplast development.

10 4VCR is a membrane-bound enzyme, embedded in etioplast and etiochloroplast membranes.

11 aracterized by smaller prolamellar bodies in etioplasts and decreased thylakoid stacking in chloropla

12 -kDa immunoreactive protein were detected in etioplasts, and no immunoreactive proteins were observed

13 (Pchlide) b is an abundant pigment in barley etioplasts but is rather unstable, as it is rapidly conv

14 on of the PsbE apoprotein can be achieved in etioplasts by suitable manipulations of the promoter and

15 mediating the transcriptional output during etioplast-chloroplast transition.

16 in various types, which include proplastids, etioplasts, chloroplasts, amyloplasts, and chromoplasts.

17 n the cue mutants, which correlates with the etioplast defect.

18 ishes a quantitative requirement for PORA in etioplast development by demonstrating significant membr

19 rtant for skotomorphogenesis by assisting in etioplast development, and normal photomorphogenic devel

20 l chloroplast differentiation and absence of etioplast development.

21 nase activity restored PLB formation in ccr2 etioplasts during skotomorphogenesis.

22 oprotective activities required to poise the etioplast for light development.

23 0-fold purification of P Phi B synthase from etioplasts from dark-grown oat (Avena sativa L. cv Garry

24 Moreover, the high pleomorphy of etioplasts from dark-grown seedlings, leucoplasts from r

25 rexpression also promotes the development of etioplasts from proplastids in dark-grown seedlings, sub

26 ght-induced development of chloroplasts from etioplasts in Arabidopsis (Arabidopsis thaliana).

27 amellar bodies (PLBs) and the development of etioplasts in darkness.

28 photosynthetic competence by converting pale etioplasts into green chloroplasts.

29 o green seedlings involves the conversion of etioplasts into mature chloroplasts via a multifaceted,

30 n etiolated barley leaves or isolated barley etioplasts irrespective of the extraction protocol.

31 ot the cytochrome has a specific function in etioplasts is unknown.

32 lles, and that it plays an essential role in etioplast metabolism by participating in the desaturatio

33 show that the redox state of the PQ pool in etioplasts might control chlorophyll biosynthesis, perha

34 uses striking ultrastructural alterations in etioplasts; most notably, it causes a condensed prolamel

35 to gain insight into the function of PTOX in etioplasts of dark-grown seedlings.

36 cialized plastid types, such as proplastids, etioplasts, or amyloplasts.

37 st that they define a respiratory process in etioplasts that we have termed "etiorespiration".

38 rs to the light-dependent differentiation of etioplasts to chloroplasts in angiosperms.

39 RNA accumulation, and the differentiation of etioplasts to chloroplasts, are retarded in their abilit

40 Etioplast-to-chloroplast differentiation involves massiv

41 tructural membrane transformation during the etioplast-to-chloroplast transition in runner bean (Phas

42 trastructural changes characteristic for the etioplast-to-chloroplast transition.

43 gers chloroplast differentiation whereby the etioplast transforms into a photosynthesizing chloroplas

44 also been claimed that extraction of barley etioplasts with 100% acetone containing 0.1% diethyl pyr

45 The mutants have underdeveloped etioplasts, with increasing impairments in cue6, cue8 an