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Eddy BP (1956) The suitability of some algae for mass cultivation for food, with special reference to Dunaliella bioculata. Journal of Experimental Botany 21: 372-380.
Javed Q & Merrett MJ (1986) Properties and immunochemical characterization of NADPH-specific glutamate dehydrogenase from Euglena gracilis. New Phytologist 104: 407-413.
DOI: none
Lang I, Hodac L, Friedl T & Feussner I (2011) Fatty acid profiles and their distribution patterns in microalgae: a comprehensive analysis of more than 2000 strains from the SAG culture collection BMC Plant Biology 11: 124.
Rennis DS & Ford TW (1992) A survey of antigenic differences between phycoerythrins of various red algal (Rhodophyta) species Phycologia 31: 192-204.
Abomohra AE, Wagner M, El-Sheekh M & Hanelt D (2012) Lipid and total fatty acid productivity in photoautotrophic fresh water microalgae: Screening studies towards biodiesel production. Journal of Applied Phycology 25: 931-936.
Maberly SC, Courcelle C, Groben R & Gontero B (2010) Phylogenetically-based variation in the regulation of the Calvin cycle enzymes, phophoribulokinase and glyceraldehyde-3-phosphate dehydrogenase, in algae. Journal of Experimental Botany 61: 735-745.
Zaib M, Saeed A, Hussain I, Athar MM & Iqbal M (2014) Voltammetric detection of As(III) with Porphyridium cruentum based modified carbon paste electrode biosensor. Biosensors and Bioelectronics 62: 242-248.
Rennis DS (1991) Differences in antigenic reactivity of six types of phycoerythrin to monoclonal anti-R-phycoerythrin. Phycologia 30: 329-338.
Roussel M, Villay A, Delbac F, Michaud P, Laroche C, Roriz D, El Alaoui H & Diogon M (2015) Antimicrosporidian activity of sulphated polysaccharides from algae and their potential to control honeybee nosemosis. Carbohydrate Polymers 133: 213-220.
Slocombe SP, Zhang QY, Ross M, Anderson A, Thomas NJ, Lapresa A, Rad Menéndez C, Campbell CN, Black KD, Stanley MS & Day JG (2015) Unlocking nature's treasure-chest: Screening for oleaginous algae. Scientific Reports 5: 09844.
Zaib M, Athar MM, Saeed A, Farooq U, Salman M & Makshoof MN (2016) Equilibrium, kinetic and thermodynamic biosorption studies of Hg(II) on red algal biomass of Porphyridium cruentum. Green Chemistry Letters and Reviews 9: 179-189.
Division/Phylum: Rhodophyta Class: Porphyridiophyceae Order: Porphyridiales

Note: for strains where we have DNA barcodes we can be reasonably confident of identity, however for those not yet sequenced we rely on morphology and the original identification, usually made by the depositor. Although CCAP makes every effort to ensure the correct taxonomic identity of strains, we cannot guarantee that a strain is correctly identified at the species, genus or class levels. On this basis users are responsible for confirming the identity of the strain(s) they receive from us on arrival before starting experiments.
For strain taxonomy we generally use AlgaeBase for algae and Adl et al. (2019) for protists.

Culture media, purity and growth conditions:
Medium: f/2 Quad or ASW with 12.5ml l-1 soil extract; Bacteria present; maintained by serial subculture;
Attributes
Authority(Bory de Saint-Vincent) Drew & Ross 1965
IsolatorVischer (1947)
Collection Sitewet shaded tuff Basel, Switzerland
Notes Deposited as P. cruentum
Axenicity Status Bacteria present
Area Europe
Country Switzerland
Environment Brackish
GMO No
In Scope of Nagoya Protocol No
ABS Note Collected pre Nagoya Protocol. No known Nagoya Protocol restrictions for this strain.
Collection Date c 1947
Original Designation V No. 107.ON 1204
Pathogen Not pathogenic: Hazard Class 1
Strain Maintenance Sheet SM_Porphyridiumpurpureum.pdf
Toxin Producer Not Toxic / No Data
Type Culture No
Taxonomy WoRMS ID 145788
Equivalent StrainsSAG 1380-1a,UTEX 161
Synonyms Porphyridium cruentum

CCAP 1380/1A

Porphyridium purpureum