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1 sids, chemosensory array, and photosynthetic chromatophore.
2 and LH2), which pack tightly together in the chromatophore.
3 ature of membranes caused by proteins in the chromatophore.
4 e often arranged in pseudo-organelles called chromatophores.
5 ions of the bacterial plasma membrane termed chromatophores.
6 f the bc(1) activity found in the complement chromatophores.
7 are affected by mutations in three types of chromatophores.
8 e carotenoid bandshift in both B187DN and WT chromatophores.
9 were similar (+/- 15%) in both WT and B187DN chromatophores.
10 bandshift of carotenoids in Rb. sphaeroides chromatophores.
11 ment of different types of pigment-producing chromatophores.
15 rane (intracytoplasmic membrane and air-aged chromatophore), and purified bc(1) complex was prepared
16 nthetic electron transfer in whole cells, in chromatophores, and with purified components to ascertai
18 The zebrafish has three different types of chromatophores: black melanophores, yellow xanthophores,
20 1 complex, purified from RS delta IV-adapted chromatophores containing a fraction of the wild type cy
25 lex, which has not been imaged yet in native chromatophores, did not induce a preferred membrane curv
26 using either purified or detergent dispersed chromatophore-embedded R. capsulatus bc(1) complex, we d
30 rane fragments derived from bacterial cells (chromatophores from Rhodopseudomonas sphaeroides) and ma
31 bandshift of carotenoids in Rb. sphaeroides chromatophores from wild type (WT) and mutant cells, in
32 e isolation intracytoplasmic (ICM) vesicles (chromatophores) from Rhodopseudomonas sphaeroides using
34 light-induced transcriptional regulation of chromatophore genes and most EGT-derived nuclear genes.
37 Several genes have been transferred from the chromatophore genome to the host nuclear genome through
39 csos4A) are encoded by both the nuclear and chromatophore genomes, suggesting that EGT in Paulinella
41 otein complexes, now known as ribosomes, and chromatophores in photosynthetic microorganisms attracte
42 concentration was identical in WT and B187DN chromatophores, indicating that covalent modification of
43 out chromatophores or in detergent-disrupted chromatophores, indicating that position 175 of cytochro
44 tergent disruption of the sealed, inside-out chromatophores, indicating that this position of cytochr
48 opositive cells are present in the posterior chromatophore lobe, the putative location of the chromat
49 Famide-immunopositive cells in the posterior chromatophore lobes also express glutamate-like immunore
50 g regions are on the cytoplasmic side of the chromatophore membrane and closed to the DE loop and hel
51 omplex formation was observed both in native chromatophore membrane and in chromatophores treated wit
55 onstructed by site-directed mutagenesis, and chromatophore membranes as well as purified bc1 complexe
57 sh activation through the reaction center in chromatophore membranes from Rhodobacter sphaeroides, ha
58 lex, the steady-state level of cyt cy in the chromatophore membranes obtained using cells grown in mi
59 -subunit cytochrome (cyt) b-c1 subcomplex in chromatophore membranes of Rhodobacter capsulatus mutant
60 In this study, CooC was purified from the chromatophore membranes of Rhodospirillum rubrum with a
61 entified and thought to be localized only to chromatophore membranes, is predominantly located in aci
66 situ hybridization shows that some putative chromatophore motoneurons express FaRP-like immunoreacti
69 Pharmacological studies demonstrate that the chromatophore muscles contain receptors blocked by gluta
70 gans, each of which is regulated by a set of chromatophore muscles directly innervated by centrally l
71 pplication causes a rapid contraction of the chromatophore muscles, resulting in chromatophore expans
73 FMRFamide application causes contraction of chromatophore muscles; however, the FMRFamide effect is
74 ty and function of the transmitter(s) at the chromatophore neuromuscular junction (NMJ) in the Europe
81 aleimide (NEM), either in sealed, inside-out chromatophores or in detergent-disrupted chromatophores,
82 the coordinated activity of millions of skin chromatophore organs, each of which is regulated by a se
84 y contracting muscles to reversibly activate chromatophores--pigment-containing cells under their ski
89 iated predominately ipsilateral expansion of chromatophores present on the mantle, but not on the hea
90 nd -LH2 complexes from digitonin-solubilized chromatophores revealed high levels of comigrating elect
94 key role in controlling the expansion of the chromatophores that generate these diverse body patterns
95 formance is further optimized by phototropic chromatophores that regulate the dose of illumination re
96 um-derived photosynthetic organelles termed 'chromatophores' that originated relatively recently (0.0
97 a, which contains photosynthetic organelles (chromatophores) that are only 60-200 million years old.
98 we have observed in Rhodobacter sphaeroides chromatophores, that when a fraction of heme b(H) is red
99 Binding of ligands (cytochrome c(2) for the chromatophores, the peptide agonists DAMGO and melanotan
100 both in native chromatophore membrane and in chromatophores treated with 0.5 M NaCl in the presence o
101 evel structural model of a low-light-adapted chromatophore vesicle from Rhodobacter sphaeroides, we i
102 An all-atom structural model for an entire chromatophore vesicle is presented, which improves upon
105 cteria is contained within organelles called chromatophores, which form as extensions of the cytoplas
106 ed by neural crest-derived pigment cells, or chromatophores, which include black melanophores, yellow
107 in) [9, 10], preserves dermal pigment cells (chromatophores)-xanthophores, iridophores, and melanopho
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