1975
DOI: 10.1042/bj1470063
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Physical-chemical properties of C-phycocyanin isolated from an acido-thermophilic eukaryote, Cyanidium caldarium

Abstract: C-Phycocyanin from an acido-thermophilic eukaryotic alga, Cyanidium caldarium, was characterized with respect to subunit structure, absorption spectrum and fluorescence properties and was found to be similar to C-phycocyanins from mesophilic sources. The pH-dependence of fluorescence polarization and the changes in sedimentation velocity as a function of pH, concentration and temperature indicate the presence of extremely large amounts of unusually stable 19S aggregates. It was not possible to disaggregate thi… Show more

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Cited by 42 publications
(22 citation statements)
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“…was found to degrade more than 80 % at higher temperatures ranging from 26 to 74°C (Chaiklahan et al 2012). Structurally, the conformation of PC has been reported to change into 23 % hexameric form at pH 5.5-6.0, while it persists up to 82 % in trimeric form at pH 7.0 (Kao et al 1975;Adams et al 1979;Chaiklahan et al 2012). This indicates that the trimeric form of PC is more stable at neutral pH which is mostly preferred for extraction of PBPs.…”
Section: Discussionmentioning
confidence: 89%
“…was found to degrade more than 80 % at higher temperatures ranging from 26 to 74°C (Chaiklahan et al 2012). Structurally, the conformation of PC has been reported to change into 23 % hexameric form at pH 5.5-6.0, while it persists up to 82 % in trimeric form at pH 7.0 (Kao et al 1975;Adams et al 1979;Chaiklahan et al 2012). This indicates that the trimeric form of PC is more stable at neutral pH which is mostly preferred for extraction of PBPs.…”
Section: Discussionmentioning
confidence: 89%
“…Kao et al (1975) have demonstrated that this C-phycocyanin is not colddissociated. Its properties remain unchanged from 10 to 50°C (Eisele et al 2000), and it can be considered a temperature-resistant protein.…”
Section: Cyanidium Caldariummentioning
confidence: 96%
“…Freeze thawing in distilled water (Padgett and Krogmann 1987) 100 mM phosphate buffer, 200 mM NaCl,10 mM EDTA, 0.02% Triton X-100 & 1 mg/ml lysozyme (Vernet et al 1990) DEAE -Cellulose (Bennett and Bogarad 1971) Using mechanical tissue homogenizers (Kao et al 1975) 1 M Tris (pH 8.0), 0.5 M EDTA, 20% sucrose (w/v) with 5 mg/ml lysozyme (Bhaskar et al 2005) DEAE-sepharose CL-6B (Zhang and Chen 1999) Extraction of dried bio mass at 4°C (Doker 2005) 1% rivanol (Minkova et al 2003) Streamline -DEAE (Bremjo 2006) Q-Sepharose (Sajilata and Singhal 2006) products to be manufactured as well as improvements in bioprocess engineering.…”
Section: Resultsmentioning
confidence: 99%