Literature DB >> 16226285

Cryptophyceae and rhodophyceae; chemotaxonomy, phylogeny, and application.

Graeme A Dunstan1, Malcolm R Brown, John K Volkman.   

Abstract

The biochemical compositions of seven strains of marine cryptomonad and a rhodophyte were determined in logarithmic phase batch (1.4 L flask) and semi-continuous (10 L carboy) culture. Lipid ranged from 13% to 28%, protein ranged from 53% to 68%, and carbohydrate ranged from 9% to 24% of the organic weight. The major lipid classes in the species examined were polar lipids (78-88% of total lipid). The major sterol in the Cryptophyceae and the Rhodophyceae was 24-methylcholesta-5,22E-dien-3beta-ol (62-99% of total sterols); which is also the major sterol in some diatoms and haptophytes. Smaller proportions of cholest-5-en-3beta-ol (1-17.7%) were also found in the Cryptophyceae. Most cryptomonads contained high proportions of the n-3 polyunsaturated fatty acids (PUFA), 18:3n-3 (20.7-29.9% of the total fatty acids), 18:4n-3 (12.5-30.2%), 20:5n-3 (7.6-13.2%) and 22:6n-3 (6.4-10.8%). However, the blue-green cryptomonad Chroomonas placoidea was characterized by a low proportion of 22:6n-3 (0.2% of total fatty acids), and a significant proportion of 22:5n-6 (4.5%), and the presence of 24-ethylcholesta-5,22E-dien-3beta-ol (35.5% of total sterols). The fatty acid composition of the rhodophyte Rhodosorus sp. was similar to those of the Cryptophyceae except for lower proportions of 18:4n-3 and lack of C21 and C22 PUFA. It is postulated that the primary endosymbiosis of a photosynthetic n-3 C18 PUFA-producing prokaryote and a eukaryotic host capable of chain elongation and desaturation of exogenous PUFA, resulted in the Rhodophyceae capable of producing n-3 C20 PUFA. The secondary endosymbiosis of a photosynthetic n-3 C20 PUFA-producing eukaryote (such as a Rhodosorus sp. like-rhodophyte) and a eukaryotic host capable of further chain elongation and desaturation, resulted in the Cryptophyceae being capable of producing n-3 C20 and C22 PUFA de novo. Selected isolates were examined further in feeding trials with juvenile Pacific oysters (Crassostrea gigas). Rhodomonas salina CS-24(containing elevated 22:6n-3) produced high growth rates in oysters; equivalent to the microalga commonly used in aquaculture, Isochrysis sp. (T.ISO).

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Year:  2005        PMID: 16226285     DOI: 10.1016/j.phytochem.2005.08.015

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  6 in total

1.  Application of fatty acids for chemotaxonomy of reef-building corals.

Authors:  Andrey B Imbs; Darja A Demidkova; Yurii Y Latypov; Long Q Pham
Journal:  Lipids       Date:  2007-08-21       Impact factor: 1.880

2.  Common and Species-Specific Effects of Phosphate on Marine Microalgae Fatty Acids Shape Their Function in Phytoplankton Trophic Ecology.

Authors:  José Pedro Cañavate; Isabel Armada; Ismael Hachero-Cruzado
Journal:  Microb Ecol       Date:  2017-04-14       Impact factor: 4.552

3.  Two unusual conjugated fatty acids, parinaric acid and α-eleostearic acid, are present in several Impatiens species, but not in congener Hydrocera triflora.

Authors:  Renu Puri; Ashish Kumar Choudhary; Paramananda Barman; Girish Mishra; R Geeta
Journal:  Physiol Mol Biol Plants       Date:  2022-06-01

4.  Fatty acid profiles and their distribution patterns in microalgae: a comprehensive analysis of more than 2000 strains from the SAG culture collection.

Authors:  Imke Lang; Ladislav Hodac; Thomas Friedl; Ivo Feussner
Journal:  BMC Plant Biol       Date:  2011-09-06       Impact factor: 4.215

5.  Marine Cryptophytes Are Great Sources of EPA and DHA.

Authors:  Elina Peltomaa; Matthew D Johnson; Sami J Taipale
Journal:  Mar Drugs       Date:  2017-12-26       Impact factor: 5.118

Review 6.  Fatty Acids of Marine Mollusks: Impact of Diet, Bacterial Symbiosis and Biosynthetic Potential.

Authors:  Natalia V Zhukova
Journal:  Biomolecules       Date:  2019-12-11
  6 in total

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