Document Detail

Biodiscovery of new Australian thraustochytrids for production of biodiesel and long-chain omega-3 oils.
MedLine Citation:
PMID:  22252264     Owner:  NLM     Status:  Publisher    
Heterotrophic growth of thraustochytrids has potential in co-producing a feedstock for biodiesel and long-chain (LC, ≥C(20)) omega-3 oils. Biodiscovery of thraustochytrids from Tasmania (temperate) and Queensland (tropical), Australia, covered a biogeographic range of habitats including fresh, brackish, and marine waters. A total of 36 thraustochytrid strains were isolated and separated into eight chemotaxonomic groups (A-H) based on fatty acid (FA) and sterol composition which clustered closely with four different genera obtained by 18S rDNA molecular identification. Differences in the relative proportions (%FA) of long-chain C(20), C(22), omega-3, and omega-6 polyunsaturated fatty acids (PUFA), including docosahexaenoic acid (DHA), docosapentaenoic acid, arachidonic acid, eicosapentaenoic acid (EPA), and saturated FA, as well as the presence of odd-chain PUFA (OC-PUFA) were the major factors influencing the separation of these groups. OC-PUFA were detected in temperate strains of groups A, B, and C (Schizochytrium and Thraustochytrium). Group D (Ulkenia) had high omega-3 LC-PUFA (53% total fatty acids (TFA)) and EPA up to 11.2% TFA. Strains from groups E and F (Aurantiochytrium) contained DHA levels of 50-61% TFA after 7 days of growth in basal medium at 20 °C. Groups G and H (Aurantiochytrium) strains had high levels of 15:0 (20-30% TFA) and the sum of saturated FA was in the range of 32-51%. β,β-Carotene, canthaxanthin, and astaxanthin were identified in selected strains. Phylogenetic and chemotaxonomic groupings demonstrated similar patterns for the majority of strains. Our results demonstrate the potential of these new Australian thraustochytrids for the production of biodiesel in addition to omega-3 LC-PUFA-rich oils.
Kim Jye Lee Chang; Graeme A Dunstan; Guy C J Abell; Lesley A Clementson; Susan I Blackburn; Peter D Nichols; Anthony Koutoulis
Related Documents :
21767494 - Reengineering rate-limiting, millisecond enzyme motions by introduction of an unnatural...
15760164 - Transition metal-catalyzed synthesis and reactivity of n-alkenyl aziridines.
18570294 - 'naked-eye' enantioselective chemosensors for n-protected amino acid anions bearing thi...
16097794 - Nitrosative cytosine deamination. an exploration of the chemistry emanating from deamin...
425004 - The effect of prostaglandin e2, 15-methyl prostaglandin e2, and metiamide on establishe...
1206484 - Solid-state decomposition of para-substituted salicylic acids.
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-1-18
Journal Detail:
Title:  Applied microbiology and biotechnology     Volume:  -     ISSN:  1432-0614     ISO Abbreviation:  -     Publication Date:  2012 Jan 
Date Detail:
Created Date:  2012-1-18     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8406612     Medline TA:  Appl Microbiol Biotechnol     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Energy Transformed National Research Flagship, CSIRO, GPO Box 1538, Hobart, TAS 7001, Australia,
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Bioconjugated silicon quantum dots from one-step green synthesis.
Next Document:  Comparison and characterization of ?-amylase inducers in Aspergillus nidulans based on nuclear local...