Transcriptomic Signature of Lipid Production in Australian Aurantiochytrium sp. TC20.

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Hauptverfasser: Lee Chang, Kim Jye, Gorron Gomez, Eduardo, Ebrahimie, Esmaeil, Dehcheshmeh, Manijeh Mohammadi, Frampton, Dion M F, Zhou, Xue-Rong
Format: Artículo científico
Sprache:en
Veröffentlicht: Marine biotechnology (New York, N.Y.) 2025
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author Lee Chang, Kim Jye
Gorron Gomez, Eduardo
Ebrahimie, Esmaeil
Dehcheshmeh, Manijeh Mohammadi
Frampton, Dion M F
Zhou, Xue-Rong
author_facet Lee Chang, Kim Jye
Gorron Gomez, Eduardo
Ebrahimie, Esmaeil
Dehcheshmeh, Manijeh Mohammadi
Frampton, Dion M F
Zhou, Xue-Rong
Lee Chang, Kim Jye
Gorron Gomez, Eduardo
Ebrahimie, Esmaeil
Dehcheshmeh, Manijeh Mohammadi
Frampton, Dion M F
Zhou, Xue-Rong
collection PubMed - marine biology
contents Transcriptomic Signature of Lipid Production in Australian Aurantiochytrium sp. TC20. Lee Chang, Kim Jye Gorron Gomez, Eduardo Ebrahimie, Esmaeil Dehcheshmeh, Manijeh Mohammadi Frampton, Dion M F Zhou, Xue-Rong Stramenopiles Transcriptome Lipid Metabolism Australia Fatty Acids Gene Expression Profiling Aurantiochytrium not only excels in producing long-chain polyunsaturated fatty acids such as docosahexaenoic acid for humans, but it is also a source of essential fatty acids with minimal impacts on wild fisheries and is vital in the transfer of atmospheric carbon to oceanic carbon sinks and cycles. This study aims to unveil the systems biology of lipid production in the Australian Aurantiochytrium sp. TC20 by comparing the transcriptomic profiles under optimal growth conditions with increased fatty acid production from the early (Day 1) to late exponential growth phase (Day 3). Particular attention was paid to 227 manually annotated genes involved in lipid metabolism, such as FAS (fatty acid synthetase) and subunits of polyunsaturated fatty acids (PUFA) synthase. PCA analysis showed that differentially expressed genes, related to lipid metabolism, efficiently discriminated Day 3 samples from Day 1, highlighting the key robustness of the developed lipid-biosynthesis signature. Highly significant (pFDR
format Artículo científico
id pubmed_39912956
institution PubMed
language en
publishDate 2025
publisher Marine biotechnology (New York, N.Y.)
record_format pubmed
spellingShingle Transcriptomic Signature of Lipid Production in Australian Aurantiochytrium sp. TC20.
Lee Chang, Kim Jye
Gorron Gomez, Eduardo
Ebrahimie, Esmaeil
Dehcheshmeh, Manijeh Mohammadi
Frampton, Dion M F
Zhou, Xue-Rong
Stramenopiles
Transcriptome
Lipid Metabolism
Australia
Fatty Acids
Gene Expression Profiling
Transcriptomic Signature of Lipid Production in Australian Aurantiochytrium sp. TC20. Lee Chang, Kim Jye Gorron Gomez, Eduardo Ebrahimie, Esmaeil Dehcheshmeh, Manijeh Mohammadi Frampton, Dion M F Zhou, Xue-Rong Stramenopiles Transcriptome Lipid Metabolism Australia Fatty Acids Gene Expression Profiling Aurantiochytrium not only excels in producing long-chain polyunsaturated fatty acids such as docosahexaenoic acid for humans, but it is also a source of essential fatty acids with minimal impacts on wild fisheries and is vital in the transfer of atmospheric carbon to oceanic carbon sinks and cycles. This study aims to unveil the systems biology of lipid production in the Australian Aurantiochytrium sp. TC20 by comparing the transcriptomic profiles under optimal growth conditions with increased fatty acid production from the early (Day 1) to late exponential growth phase (Day 3). Particular attention was paid to 227 manually annotated genes involved in lipid metabolism, such as FAS (fatty acid synthetase) and subunits of polyunsaturated fatty acids (PUFA) synthase. PCA analysis showed that differentially expressed genes, related to lipid metabolism, efficiently discriminated Day 3 samples from Day 1, highlighting the key robustness of the developed lipid-biosynthesis signature. Highly significant (pFDR
title Transcriptomic Signature of Lipid Production in Australian Aurantiochytrium sp. TC20.
topic Stramenopiles
Transcriptome
Lipid Metabolism
Australia
Fatty Acids
Gene Expression Profiling
url https://pubmed.ncbi.nlm.nih.gov/39912956/