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1  encode proteins destined for the developing chromoplast.
2 vity and the transition from chloroplasts to chromoplasts.
3 ower OR mutant have only one or two enlarged chromoplasts.
4 , etioplasts, chloroplasts, amyloplasts, and chromoplasts.
5  the carotenoids and their entrapment within chromoplasts.
6 fferentiate into photosynthetically inactive chromoplasts.
7 ibility decreased upon thermal processing of chromoplasts.
8 umulation of lycopene or beta-carotenoids in chromoplasts.
9 esult of the conversion of chloroplasts into chromoplasts.
10 ments for chloroplasts to differentiate into chromoplasts.
11 tor was also an integral membrane protein of chromoplasts.
12 n to be present on the surface of fibrils in chromoplasts.
13 noids is required for the differentiation of chromoplasts, a process that involves a concurrent repro
14 ul expression of foreign genes in transgenic chromoplasts and availability of marker-free chloroplast
15 hickening, preventing the differentiation of chromoplasts and eventually repressing the expression of
16 ts in the mesocarp tissue differentiate into chromoplasts and undergo major shifts in morphology.
17  non-green edible parts (carrots) containing chromoplasts, and 53% in proplastids of cultured cells w
18 ition of leaves, nor does it alter color and chromoplast appearance in flower petals.
19 and oxidative stress defense, whereas PGs in chromoplasts are also an active site for carotenoid conv
20                                              Chromoplasts are colored plastids that synthesize and st
21 a demonstrate that the internal membranes of chromoplasts are functional with respect to protein tran
22 red fruit beta-carotene levels with impaired chromoplast biogenesis.
23 ating and heating only was observed; (ii) in chromoplasts, both beta-carotene and lycopene bioaccessi
24         It was recently reported that tomato chromoplasts can synthesize ATP through a respiratory pr
25   In contrast to the situation prevailing in chromoplasts, capsanthin was not esterified and its incr
26 inones, alpha-tocopherol, and lipids and, in chromoplasts, carotenoids as well.
27 s the conclusion that the differentiation of chromoplasts coincides with carotenoid accumulation duri
28 t isolated red bell pepper (Capsicum annuum) chromoplasts contain the 75-kD component of the chloropl
29                          The red crystalline chromoplasts contained lycopene as a dominant carotenoid
30                                              Chromoplasts contained the thylakoid Sec component prote
31 s the first demonstration of ferredoxin in a chromoplast-containing tissue.
32  fruit ripening in tomato and indicates that chromoplast development in fruit does not depend on func
33                               Chloroplast to chromoplast development involves new synthesis and plast
34 tic pathway, and ORANGE (OR), a regulator of chromoplast differentiation and enhancer of carotenoid b
35 romote carotenoid accumulation by activating chromoplast differentiation and increasing carotenoid bi
36 nthesis and accumulation can directly affect chromoplast differentiation and structure.
37 athway, elicits an artificial chloroplast-to-chromoplast differentiation in leaves.
38 gether, the data provide new insights on the chromoplast differentiation process while enriching our
39 ule length and frequency are correlated with chromoplast differentiation, but only in one plastid pop
40 n, integrated into the internal membranes of chromoplasts during in vitro assays, and immunoblot anal
41 functional types (chloroplasts, leucoplasts, chromoplasts, etc.) that have distinct proteomes dependi
42 roplastids or other noncolored plastids into chromoplasts for carotenoid accumulation.
43  Moreover, Cmor-lowbeta was found to inhibit chromoplast formation and chloroplast disintegration in
44 particularly abundant in carotenoid-enriched chromoplasts found in ripe fruits and flowers.
45                        Further, we show that chromoplasts from specific cultivars vary in shape and s
46 t, we have introduced several genes into the chromoplast genome.
47 f CsCCD2 with the developmental state of the chromoplast in the developing stigma.
48 on and unique development of red crystalline chromoplasts in Cara Cara are discussed.
49 on and induced occurrence of red crystalline chromoplasts in cultured Newhall juice vesicles, indicat
50 ties of the morphology of pigment-containing chromoplasts in nutritionally important carotenoid sourc
51                      Given the importance of chromoplasts in the deposition of carotenoids in plants
52 were identified in the PG proteome of pepper chromoplasts, including four enzymes of carotenoid biosy
53            Structural differentiation of the chromoplast is characterized by a sharp and continuous d
54  show here that controlling the formation of chromoplasts is an important mechanism by which caroteno
55 sical form of carotenoid deposition in plant chromoplasts is suggested to have major impact on their
56 tments on carotenoid bioaccessibility at the chromoplast level was obtained.
57 tosyl diacylglycerols, which are part of the chromoplasts lipid machinery of enzymes involved in the
58 essibility was attributed to modification in chromoplasts membrane and carotenoids-protein complexes.
59 rophyll a/b protein failed to associate with chromoplast membranes and instead accumulated in the str
60 E. coli is the same as previously shown with chromoplast membranes.
61 stic insights into the machinery controlling chromoplast number and highlight a potential new strateg
62                                              Chromoplast number and size define the sink strength for
63 ter carotenoid levels via their influence on chromoplast number and/or size.
64 s) allele, and found that it also constrains chromoplast number in Arabidopsis calli.
65 ng is known about the mechanisms controlling chromoplast number.
66 g with PARC6 for binding to ARC3 to restrict chromoplast number.
67 ne is a carotenoid found in chloroplasts and chromoplasts of tomatoes, providing the familiar red col
68 t it may cleave carotenoids localized in the chromoplast outer envelope.
69                            Here we show that chromoplast oxygen consumption is stimulated by the elec
70 ftf (plastid fusion/translocation factor), a chromoplast protein, integrated into the internal membra
71 ar, the differentiation of chloroplasts into chromoplasts results in an enhanced storage capacity for
72 der fbn mutants displayed altered isoprenoid chromoplast sequestration patterns, notably with a signi
73  bio-encapsulation (carotenoid-enriched oil, chromoplasts, small cell clusters, and large cell cluste
74           We found an increased abundance of chromoplast-specific carotenoid-associated protein (CHRC
75 ce of mRNAs from phytoene synthase (PSY) and chromoplast-specific lycopene beta-cyclase (CYCB) allele
76 A probe of the tomato (Solanum lycopersicum) chromoplast-specific lycopene beta-cyclase, CYC-b.
77 to the synthesis of capsanthin, a non-native chromoplast-specific xanthophyll, using an RNA viral vec
78        Differences in cell wall material and chromoplast substructure between matrices influenced car
79 oid bioaccessibility while, in tomatoes, the chromoplast substructure represented the most important
80                  For carrots, cell walls and chromoplast substructure were important barriers for car
81 fic role of the natural structural barriers (chromoplast substructure/cell wall) and of the phases (s
82                               Cell walls and chromoplast substructures constitute natural structural
83 e oil phase, a system lacking cell walls and chromoplast substructures that could hamper carotenoid r
84  of natural structural barriers (cell walls, chromoplast substructures) on carotenoid bioaccessibilit
85 nate from a system not capable of developing chromoplasts, this indicates that the poly-cis pathway o
86               Therefore, the contribution of chromoplasts to total fruit respiration appears to incre
87 2 expression and could acts as a mediator of chromoplast-to-nucleus signalling, coordinating the expr
88 mong the main features of the chloroplast-to-chromoplast transition revealed by the study, chromoplas
89 sting that CmOr regulates the chloroplast-to-chromoplast transition.
90 uid-crystalline state within the nano-scaled chromoplast tubules.
91 n of one of its components (cytochrome f) in chromoplasts using immunoblot and immunocytochemical tec
92  well as from pepper (Capsicum annuum) fruit chromoplasts using mass spectrometry.
93 were found in Cara Cara but only one type of chromoplast was present in each cell.
94 ed transformation of chloroplasts to tubular chromoplasts was accompanied by an accumulation of up to
95           The ATP synthesis rate of isolated chromoplasts was dependent on the supply of NAD(P)H and
96  (in chloroplasts) and chromorespiration (in chromoplasts), we suggest that they define a respiratory
97          Using bell pepper (Capsicum annuum) chromoplasts, we establish that phyllobilin hydroxylatio
98                                 The isolated chromoplasts were able to further localize the 33- and 1
99 ellow globular and red elongated crystalline chromoplasts were found in Cara Cara but only one type o
100                         Only yellow globular chromoplasts were observed in Newhall flesh.
101 lar and tubular elements in papaya and mango chromoplasts, where carotenoids accumulate in a lipid-di
102  decrease stromule formation on tomato fruit chromoplasts, whereas preventing chloroplast development

 
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