Cargando…

Comparative Transcriptomic Analysis Uncovers Genes Responsible for the DHA Enhancement in the Mutant Aurantiochytrium sp.

Docosahexaenoic acid (DHA), a n-3 long-chain polyunsaturated fatty acid, is critical for physiological activities of the human body. Marine eukaryote Aurantiochytrium sp. is considered a promising source for DHA production. Mutational studies have shown that ultraviolet (UV) irradiation (50 W, 30 s)...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Liangxu, Hu, Zhangli, Li, Shuangfei, Yang, Hao, Li, Siting, Lv, Chuhan, Zaynab, Madiha, Cheng, Christopher H. K., Chen, Huapu, Yang, Xuewei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232246/
https://www.ncbi.nlm.nih.gov/pubmed/32272666
http://dx.doi.org/10.3390/microorganisms8040529
_version_ 1783535343231827968
author Liu, Liangxu
Hu, Zhangli
Li, Shuangfei
Yang, Hao
Li, Siting
Lv, Chuhan
Zaynab, Madiha
Cheng, Christopher H. K.
Chen, Huapu
Yang, Xuewei
author_facet Liu, Liangxu
Hu, Zhangli
Li, Shuangfei
Yang, Hao
Li, Siting
Lv, Chuhan
Zaynab, Madiha
Cheng, Christopher H. K.
Chen, Huapu
Yang, Xuewei
author_sort Liu, Liangxu
collection PubMed
description Docosahexaenoic acid (DHA), a n-3 long-chain polyunsaturated fatty acid, is critical for physiological activities of the human body. Marine eukaryote Aurantiochytrium sp. is considered a promising source for DHA production. Mutational studies have shown that ultraviolet (UV) irradiation (50 W, 30 s) could be utilized as a breeding strategy for obtaining high-yield DHA-producing Aurantiochytrium sp. After UV irradiation (50 W, 30 s), the mutant strain X2 which shows enhanced lipid (1.79-fold, 1417.37 mg/L) and DHA (1.90-fold, 624.93 mg/L) production, was selected from the wild Aurantiochytrium sp. Instead of eicosapentaenoic acid (EPA), 9.07% of docosapentaenoic acid (DPA) was observed in the mutant strain X2. The comparative transcriptomic analysis showed that in both wild type and mutant strain, the fatty acid synthesis (FAS) pathway was incomplete with key desaturases, but genes related to the polyketide synthase (PKS) pathway were observed. Results presented that mRNA expression levels of CoAT, AT, ER, DH, and MT down-regulated in wild type but up-regulated in mutant strain X2, corresponding to the increased intercellular DHA accumulation. These findings indicated that CoAT, AT, ER, DH, and MT can be exploited for high DHA yields in Aurantiochytrium.
format Online
Article
Text
id pubmed-7232246
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-72322462020-05-22 Comparative Transcriptomic Analysis Uncovers Genes Responsible for the DHA Enhancement in the Mutant Aurantiochytrium sp. Liu, Liangxu Hu, Zhangli Li, Shuangfei Yang, Hao Li, Siting Lv, Chuhan Zaynab, Madiha Cheng, Christopher H. K. Chen, Huapu Yang, Xuewei Microorganisms Article Docosahexaenoic acid (DHA), a n-3 long-chain polyunsaturated fatty acid, is critical for physiological activities of the human body. Marine eukaryote Aurantiochytrium sp. is considered a promising source for DHA production. Mutational studies have shown that ultraviolet (UV) irradiation (50 W, 30 s) could be utilized as a breeding strategy for obtaining high-yield DHA-producing Aurantiochytrium sp. After UV irradiation (50 W, 30 s), the mutant strain X2 which shows enhanced lipid (1.79-fold, 1417.37 mg/L) and DHA (1.90-fold, 624.93 mg/L) production, was selected from the wild Aurantiochytrium sp. Instead of eicosapentaenoic acid (EPA), 9.07% of docosapentaenoic acid (DPA) was observed in the mutant strain X2. The comparative transcriptomic analysis showed that in both wild type and mutant strain, the fatty acid synthesis (FAS) pathway was incomplete with key desaturases, but genes related to the polyketide synthase (PKS) pathway were observed. Results presented that mRNA expression levels of CoAT, AT, ER, DH, and MT down-regulated in wild type but up-regulated in mutant strain X2, corresponding to the increased intercellular DHA accumulation. These findings indicated that CoAT, AT, ER, DH, and MT can be exploited for high DHA yields in Aurantiochytrium. MDPI 2020-04-07 /pmc/articles/PMC7232246/ /pubmed/32272666 http://dx.doi.org/10.3390/microorganisms8040529 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Liangxu
Hu, Zhangli
Li, Shuangfei
Yang, Hao
Li, Siting
Lv, Chuhan
Zaynab, Madiha
Cheng, Christopher H. K.
Chen, Huapu
Yang, Xuewei
Comparative Transcriptomic Analysis Uncovers Genes Responsible for the DHA Enhancement in the Mutant Aurantiochytrium sp.
title Comparative Transcriptomic Analysis Uncovers Genes Responsible for the DHA Enhancement in the Mutant Aurantiochytrium sp.
title_full Comparative Transcriptomic Analysis Uncovers Genes Responsible for the DHA Enhancement in the Mutant Aurantiochytrium sp.
title_fullStr Comparative Transcriptomic Analysis Uncovers Genes Responsible for the DHA Enhancement in the Mutant Aurantiochytrium sp.
title_full_unstemmed Comparative Transcriptomic Analysis Uncovers Genes Responsible for the DHA Enhancement in the Mutant Aurantiochytrium sp.
title_short Comparative Transcriptomic Analysis Uncovers Genes Responsible for the DHA Enhancement in the Mutant Aurantiochytrium sp.
title_sort comparative transcriptomic analysis uncovers genes responsible for the dha enhancement in the mutant aurantiochytrium sp.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232246/
https://www.ncbi.nlm.nih.gov/pubmed/32272666
http://dx.doi.org/10.3390/microorganisms8040529
work_keys_str_mv AT liuliangxu comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp
AT huzhangli comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp
AT lishuangfei comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp
AT yanghao comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp
AT lisiting comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp
AT lvchuhan comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp
AT zaynabmadiha comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp
AT chengchristopherhk comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp
AT chenhuapu comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp
AT yangxuewei comparativetranscriptomicanalysisuncoversgenesresponsibleforthedhaenhancementinthemutantaurantiochytriumsp