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1 f specific cyanobacterial pigments, that is, phycocyanin.
2  are correlated with later concentrations of phycocyanin.
3 ortest for precipitation and the longest for phycocyanin.
4 ion of the light-harvesting phycobiliprotein phycocyanin.
5 on that encodes the light-harvesting protein phycocyanin.
6 he specific oligomeric structures found with phycocyanin.
7 ocyanobilin-bound, cysteine 153 of wild-type phycocyanin.
8 operties very similar to those of unmodified phycocyanin.
9 bearing core polypeptides, but no detectable phycocyanin.
10 ycobiliproteins (100mg/kg ig), (4) PB plus C-phycocyanin (100mg/kg ig), and four groups receiving HgC
11 ed pyrromethenone 6, the C,D-ring segment of phycocyanin (2).
12 ups receiving HgCl(2)+phycobiliproteins or C-phycocyanin (50, and 100mg/kg ig).
13            The two lowest-energy CD bands of phycocyanin 612 originated from paired bilins, and the t
14 lins as naturally occurring reporter groups, phycocyanin 612 was shown to undergo a reversible change
15                                          For phycocyanin 612, a major surprise was that a pair of bil
16 anization of three cryptomonad biliproteins (phycocyanins 612 and 645 and phycoerythrin 545) was exam
17                                  Two others (phycocyanin 630 and phycoerythrin 566) were studied less
18                                              Phycocyanin 645 and phycoerythrin 545 were suggested to
19                             At 45 degrees C, phycocyanin 645 maximally undergoes a reversible and sta
20                                              Phycocyanin 645 was found to have a 550-fs lifetime.
21                                              Phycocyanin, a natural product purified from Spirulina,
22 itation, discharge, phosphorus (P) load, and phycocyanin, a pigment of Cyanobacteria are clustered as
23 unctional high-value algae extracts, rich in phycocyanin, a protein-pigment complex derived from A. p
24 solated phycobilisomes caused a reduction in phycocyanin absorbance and a broadening and shifting of
25    CpcM exhibited lower activity on trimeric phycocyanin after complete chromophorylation and oligome
26                            Fluorescence from phycocyanin, allophycocyanin, allophycocyanin-B/terminal
27                  Genes for the apoprotein (C-phycocyanin alpha subunit; cpcA) and the heterodimeric l
28                           The ability of the phycocyanin alpha-subunit (CpcA) to bind alternative lin
29  that includes the subunits of the CpcE/CpcF phycocyanin alpha-subunit lyase of Synechococcus sp. str
30 02 was coexpressed in these strains with the phycocyanin alpha-subunit phycocyanobilin lyase, CpcE/Cp
31  phycocyanobilin by phycoerythrobilin on the phycocyanin alpha-subunit.
32  the total Microcystis population based on c-phycocyanin (alpha subunit; cpcA) gene equivalents (Adj.
33 tures are assembled from chromophore-bearing phycocyanin and allophycocyanin subunits, nonpigmented l
34                              Recombinant apo-phycocyanin and apo-allophycocyanin subunits were used a
35 a new approach for fast cleavage of PCB from phycocyanin and gave at 120 degrees C the same yield wit
36 orms of a major phycobilisome protein called phycocyanin and initiate the production of a third form
37       Overall, electrostatic complexation of phycocyanin and lambda-carrageenan is a promising techni
38 iptional regulation and that it co-ordinates phycocyanin and phycocyanobilin biosynthesis in red ligh
39 coloured phycobiliproteins, allophycocyanin, phycocyanin and phycoerythrin (PE).
40                                            C-Phycocyanin and sugar (C-PC/S) blended agar hydrocolloid
41 onated, circular helical (blue) structure of phycocyanin and the anionic SDS micelles.
42 lities to stabilise the blue conformation of phycocyanin and to apply the stabilised form in food pro
43 sophisticated antennae with rods composed of phycocyanin and two types of phycoerythrins (PEI and PEI
44              The total antioxidant activity, phycocyanins, and beta carotene content were quantified
45 red for all variates and those of P load and phycocyanin are most strongly clustered.
46                        Allophycocyanin and C-phycocyanin are prominent in providing a natural source
47                 Carotenoids, chlorophyll and phycocyanin are three types of photosynthetic pigments f
48                                              Phycocyanins are pigment-protein complexes with potentia
49 d autophagic cell death, thereby identifying phycocyanin as a promising anti-pancreatic cancer agent.
50  we investigate the therapeutic potential of phycocyanin as an anti-PDA agent in vivo and in vitro.
51 pplication of phycobiliproteins, e.g. blue C-phycocyanin, as natural water-soluble food colourants is
52 fied the chromophorylated (holo form) of the phycocyanin B-subunit (CpcB) as its target, while apo-Cp
53                Three peptides belonging to C-phycocyanin beta subunit (P72508) were designated as qua
54                                   His-tagged phycocyanin beta--BCCP114 constructs expressed in Anabae
55                                          The phycocyanin beta-subunit from the cpcT mutant has slight
56  peptide containing Cys-153 derived from the phycocyanin beta-subunit of the cpcT mutant.
57 y attaches phycocyanobilin to Cys-153 of the phycocyanin beta-subunit.
58 sing practical real-time measures of in vivo phycocyanin (by fluorometry) and secchi depth was constr
59              The spectra reveal the ratio of phycocyanin (C-PC) and allophycocyanin (APC) in the ante
60                                            C-Phycocyanin (C-PC) is a phycobiliprotein extracted from
61                                            C-Phycocyanin (C-PC) represents an alternative to artifici
62                                            C-Phycocyanin (C-PC), a blue phycobiliprotein from microal
63 resent single-molecule characterization of C-phycocyanin (C-PC), a three-pigment biliprotein that sel
64 anionic polysaccharide lambda-carrageenan on phycocyanins color appearance at pH 2.5-6.0, unheated an
65                        All cells have a high phycocyanin content whilst phycoerythrin is absent.
66 chromatographic method for purification of C-phycocyanin (CPC) from species of Oscillatoria tenuis.
67 recursors to gardenia (genipin) blue color), phycocyanins, curcuminoids, and chlorophylls.
68 activity of cytochrome-c-oxidase, and slower phycocyanin degradation.
69 hycocyanin (mixture of allophycocyanin and c-phycocyanin) disassembled and denatured between 50 and 7
70 he ends of the phycobilisome's rods to the C-phycocyanin disks along their length in <600 fs.
71                          In such recombinant phycocyanins equipped with stable trimerization domains,
72 between P load extremes and the next extreme phycocyanin event within the same year of observation.
73  In conclusion, our studies demonstrate that phycocyanin exerts anti-pancreatic cancer activity by in
74 a or beta subunits of Anabaena sp. PCC7120 C-phycocyanin formed stoichiometric complexes in vivo with
75 ture sensitivity of the natural blue pigment phycocyanin from Arthrospira platensis limits its applic
76                                              Phycocyanin from the cpcT mutant has an absorbance maxim
77 al structure of the light-harvesting protein phycocyanin from the cyanobacterium Cyanidium caldarium
78                                              Phycocyanins from cyanobacteria are possible sources for
79                                     Purified phycocyanins from the cpcT mutant and wild type were cle
80                                 We show that phycocyanin gene expression requires RcaC.
81 mplete loss of light regulation, measured by phycocyanin gene expression, only occurred in the triple
82                                              Phycocyanin has demonstrated to be more selective to cya
83  and all other cyanobacteria that synthesize phycocyanin have a gene, cpcT, that is paralogous to cpe
84 nclude linkers connecting two chains of five phycocyanin hexamers (CpcN) and two core subdomains (Apc
85                                              Phycocyanin hexamers dissociate to trimers with equilibr
86                                              Phycocyanin induces G2/M cell cycle arrest, apoptotic an
87                   These results suggest that phycocyanin instability in bilin-deletion mutants is a c
88                                              Phycocyanin is able to induce apoptosis of PANC-1 cell b
89       Mechanistically, cell death induced by phycocyanin is the result of cross-talk among the MAPK,
90 , which plays an important role in balancing phycocyanin-mediated apoptosis and autosis.
91 tion of both autophagy and apoptosis rescues phycocyanin-mediated cell death.
92   The altered genes were then expressed in a phycocyanin-minus mutant of the transformable Synechocys
93 time treatments, it was shown how a purified phycocyanin (mixture of allophycocyanin and c-phycocyani
94 ared to create the Gel/NL/Fe/P film (gelatin/phycocyanin nanoliposome/zero-valent iron nanoparticle/p
95                                   Initially, phycocyanin nanoliposomes were prepared to create the Ge
96 teractions around the zero surface charge of phycocyanin over a broad pH range (~4.1-6.4).
97 sent work aimed to prepare microparticles of phycocyanin (PC(MP)) and of an ultrasound-assisted phyco
98 cpcU mutants produced an altered form of the phycocyanin (PC) beta subunit, which had a mass approxim
99 core and six radiating rods, each with three phycocyanin (PC) discs.
100 ha and beta subunits of the phycobiliprotein phycocyanin (PC) in the filamentous cyanobacterium Fremy
101    In red light, cells produce red-absorbing phycocyanin (PC), whereas in green light, green-absorbin
102                     Our study used a ternary phycocyanin-podophyllotoxin-IDO1 self-assembled nanoplat
103          All doses of phycobiliproteins or C-phycocyanin prevented enhancement of oxidative markers a
104  shown to stabilise the blue conformation of phycocyanin, preventing formation of the green conformat
105 ts a high degree of wavelength-dependence in phycocyanin production, and this ability enables it to g
106                           On the other hand, phycocyanin promotes autophagic cell death by inhibiting
107                                 Furthermore, phycocyanin promotes the activation and nuclear transloc
108 lly, spectroscopic properties of recombinant phycocyanin R-PCIII, in which the CpcA subunits carry a
109 ment selection and the targeting of specific phycocyanin regions for stabilization, reducing the depe
110                                              Phycocyanin-rich Synechococcus-like cells were the most
111 of Synechocystis sp. PCC 6803 from the outer phycocyanin rods to the allophycocyanin core.
112 ontrast to sequential chemical denaturation, phycocyanin's chromophore and protein structure were sim
113 new role assigned to chromophore beta-155 in phycocyanin sheds light on the numerical relationships a
114  into protonated, partially unfolded (green) phycocyanin species.
115                                              Phycocyanin subunits from Synechocystis sp. 6701 that we
116 bacterium Anabaena sp. PCC7120 recombinant C-phycocyanin subunits with one or more different tags, in
117         A cpcT null mutant contains 40% less phycocyanin than wild type and produces smaller phycobil
118 cible variations in phycobilisome-associated phycocyanin that do not correlate with transcript levels
119 he mutants showed that tryptic peptides from phycocyanin that included Asn72 were also 14 Da lighter
120 s are offset rather than aligned as in other phycocyanins that have been crystallized to date.
121 imitation and exhibits an increased ratio of phycocyanin to chlorophyll during nutrient-replete growt
122                                              Phycocyanin trimers dissociate to monomers with equilibr
123                               In crystals of phycocyanin used in this study, the hexamers are offset
124                      The perceived colour of phycocyanins varies with pH, and a method to stabilise t
125  micelles on pH-induced colour variations of phycocyanin was examined.
126  chromophore bound by the alpha subunit of C-phycocyanin was probed in buffered binary solvent system
127 lative contents of phycoerythrin (PE) and/or phycocyanin when cells are shifted from red to green lig
128  cell growth inhibition and death induced by phycocyanin, whereas inhibition of both autophagy and ap
129 d initiate the production of a third form of phycocyanin, which possesses a minimal number of sulfur-
130 s indicated 80 % encapsulation efficiency of phycocyanin, with stable nanoliposomes of 100 nm and a z

 
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