Phycocyanin
Phycocyanin is a pigment-protein complex from the light-harvesting phycobiliprotein family, along with allophycocyanin and phycoerythrin. It is an accessory pigment to chlorophyll. All phycobiliproteins are water-soluble, so they cannot exist within the membrane like carotenoids can. Instead, phycobiliproteins aggregate to form clusters that adhere to the membrane called phycobilisomes. Phycocyanin is a characteristic light blue color, absorbing orange and red light, particularly near 620 nm, and emits fluorescence at about 650 nm. Allophycocyanin absorbs and emits at longer wavelengths than phycocyanin C or phycocyanin R. Phycocyanins are found in Cyanobacteria. Phycobiliproteins have fluorescent properties that are used in immunoassay kits. Phycocyanin is from the Greek phyco meaning “algae” and cyanin is from the English word “cyan", which conventionally means a shade of blue-green and is derived from the Greek “kyanos" which means a somewhat different color: "dark blue". The product phycocyanin, produced by Aphanizomenon flos-aquae and Spirulina, is for example used in the food and beverage industry as the natural coloring agent 'Lina Blue' or 'EXBERRY Shade Blue' and is found in sweets and ice cream. In addition, fluorescence detection of phycocyanin pigments in water samples is a useful method to monitor cyanobacteria biomass.
The phycobiliproteins are made of two subunits having a protein backbone to which 1-2 linear tetrapyrrole chromophores are covalently bound.
C-phycocyanin is often found in cyanobacteria which thrive around hot springs, as it can be stable up to around 70 °C, with identical spectroscopic behaviours at 20 and 70 °C. Thermophiles contain slightly different amino acid sequences making it stable under these higher conditions. Molecular weight is around 30,000 Da.
Stability of this protein invitro at these temperatures has been shown to be substantially lower. Photo-spectral analysis of the protein after 1 min exposure to 65 °C conditions in a purified state demonstrated a 50% loss of tertiary structure.
Structure
Phycocyanin shares a common structural theme with all phycobiliproteins. The structure begins with the assembly of phycobiliprotein monomers, which are heterodimers composed of α and β subunits, and their respective chromophores linked via thioether bond.Each subunit is typically composed of eight α-helices. Monomers spontaneously aggregate to form ring-shaped trimers 3, which have rotational symmetry and a central channel. Trimers aggregate in pairs to form hexamers 6, sometimes assisted with additional linker proteins. Each phycobilisome rod generally has two or more phycocyanin hexamers. Despite the overall similarity in structure and assembly of phycobiliproteins, there is a large diversity in hexamer and rod conformations, even when only considering phycocyanins. On a larger scale phycocyanins also vary in crystal structure, although the biological relevance of this is debatable.
As an example, the structure of C-phycocyanin from Synechococcus vulcanus has been refined to 1.6 Angstrom resolution. The monomer consists of 332 amino acids and 3 thio-linked phycocyanobilin cofactor molecules. Both the α- and β-subunits have a PCB at amino acid 84, but the β-subunit has an additional PCB at position 155 as well. This additional PCB faces the exterior of the trimeric ring and is therefore implicated in inter-rod energy transfer in the phycobilisome complex. In addition to cofactors, there are many predictable non-covalent interactions with the surrounding solvent that are hypothesized to contribute to structural stability.
R-phycocyanin II is found in some Synechococcus species. R-PC II is said to be the first PEB containing phycocyanin that originates in cyanobacteria. Its purified protein is composed of alpha and beta subunits in equal quantities. R-PC II has PCB at beta-84 and the phycoerythrobillin at alpha-84 and beta-155.
As of March 7, 2018, there are 44 crystal structures of phycocyanin deposited in the Protein Data Bank.
Spectral characteristics
C-phycocyanin has a single absorption peak at ~621 nm, varying slightly depending on the organism and conditions such as temperature, pH, and protein concentration in vitro. Its emission maximum is ~642 nm. This means that the pigment absorbs orange light, and emits reddish light. R-phycocyanin has an absorption maxima at 533 and 544 nm. The fluorescence emission maximum of R-phycocyanin is 646 nm.Property | C-Phycocyanin | R-Phycocyanin |
Absorption maximum | 621 | 533, 544 |
Emission maximum | 642 | 646 |
Extinction Coefficient | 1.54x106 M−1cm−1 | - |
Quantum Yield | 0.81 | - |
Ecological Relevance
Phycocyanin is produced by many photoautotrophic cyanobacteria. Even if cyanobacteria have large concentrations of phycocyanin, productivity in the ocean is still limited due to light conditions.Phycocyanin has ecological significance in indicating cyanobacteria bloom. Normally chlorophyll a is used to indicate cyanobacteria numbers, however since it is present in a large number of phytoplankton groups, it is not an ideal measure. For instance a study in the Baltic Sea used phycocyanin as a marker for filamentous cyanobacteria during toxic summer blooms. Some filamentous organisms in the Baltic Sea include Nodularia spumigena and Aphanizomenon flosaquae.
An important cyanobacteria named spirulina is a micro algae that produces C-PC.
There are many different methods of phycocyanin production including photoautotrophic, mixotrophic and heterotrophic and recombinant production. Photoautotrophic production of phycocyanin is where cultures of cyanobacteria are grown in open ponds in either subtropical or tropical regions. Mixotrophic production of algae is where the algae are grown on cultures that have an organic carbon source like glucose. Using mixotrophic production produces higher growth rates and higher biomass compared to simply using a photoautotrophic culture. In the mixotrophic culture, the sum of heterotrophic and autotrophic growth separately was equal to the mixotrophic growth. Heterotrophic production of phycocyanin is not light limited, as per its definition. Galdieria sulphuraria is a unicellular rhodophyte that contains a large amount of C-PC and a small amount of allophycocyanin. G. sulphuraria is an example of the heterotrophic production of C-PC because its habitat is hot, acidic springs and uses a number of carbon sources for growth. Recombinant production of C-PC is another heterotrophic method and involves gene engineering.
Lichen-forming fungi and cyanobacteria often have a symbiotic relationship and thus phycocyanin markers can be used to show the ecological distribution of fungi-associated cyanobacteria. As shown in the highly specific association between Lichina species and Rivularia strains, phycocyanin has enough phylogenetic resolution to resolve the evolutionary history of the group across the northwestern Atlantic Ocean coastal margin.
Biosynthesis
The two genes cpcA and cpcB, located in the cpc operon and translated from the same mRNA transcript, encode for the C-PC α- and β-chains respectively. Additional elements such as linker proteins, and enzymes involved in phycobilin synthesis and the phycobiliproteins are often encoded by genes in adjacent gene clusters, and the cpc operon of Arthrospira platensis also encodes a linker protein assisting in the assembly of C-PC complexes. In red algae, the phycobiliprotein and linker protein genes are located on the plastid genome.Phycocyanobilin is synthesised from heme and inserted into the C-PC apo-protein by three enzymatic steps. Cyclic heme is oxidised to linear biliverdin IXα by heme oxygenase and further converted to 3Z-phycocyanobilin, the dominant phycocyanobilin isomer, by 3Z-phycocyanobilin:ferredoxin oxidoreductase. Insertion of 3Z-phycocyanobilin into the C-PC apo-protein via thioether bond formation is catalysed by phycocyanobilin lyase.
The promoter for the cpc operon is located within the 427-bp upstream region of the cpcB gene. In A. platensis, 6 putative promoter sequences have been identified in the region, with four of them showing expression of green fluorescent protein when transformed into E. coli. The presence of other positive elements such as light-response elements in the same region have also been demonstrated.
The multiple promoter and response element sequences in the cpc operon enable cyanobacteria and red algae to adjust its expression in response to multiple environmental conditions. Expression of the cpcA and cpcB genes is regulated by light. Low light intensities stimulate synthesis of CPC and other pigments, while pigment synthesis is repressed at high light intensities. Temperature has also been shown to affect synthesis, with specific pigment concentrations showing a clear maximum at 36 °C in Arthronema africanum, a cyanobacterium with particular high C-PC and APC contents.
Nitrogen and also iron limitation induce phycobiliprotein degradation. Organic carbon sources stimulate C-PC synthesis in Anabaena spp., but seem to have almost no effector negative effect in A. platensis. In the rhodophytes Cyanidium caldarium and Galdieria sulphuraria, C-PC production is repressed by glucose but stimulated by heme.
Biotechnology
Pure phycocyanin extractions can be isolated from algae. The basic segregation order is as follows. The rupturing of the cell wall, with mechanical forces or chemical agents. Then, C-PC is isolated with centrifugation and purified with ammonium sulfate precipitation or chromatography -either ion or gel-filtration. After, the sample gets frozen and dried..