Strategies for Improved Docosahexaenoic Acid Synthesis in Microalgae.

IF 3.9 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Kunal Dutta, Mariia S Ashikhmina, Ekaterina V Skorb, Sergey Shityakov
{"title":"Strategies for Improved Docosahexaenoic Acid Synthesis in Microalgae.","authors":"Kunal Dutta, Mariia S Ashikhmina, Ekaterina V Skorb, Sergey Shityakov","doi":"10.1021/acssynbio.5c00294","DOIUrl":null,"url":null,"abstract":"<p><p>Docosahexaenoic acid (DHA) is an omega-3 fatty acid that is essential for optimal brain growth and development. Fish oil is the main dietary source of DHA. However, off-flavors and contamination with persistent organic pollutants are the main issues when DHA is sourced ethically from deep-sea fishes. Microalgae offer a sustainable, viable option for DHA production. However, optimization of the DHA yield using low-cost materials helps in reducing the fermentation cost. In this systematic review, we cover recent progress on enhanced DHA production during the last ten years, 2015-2025. We discuss how mutagenomics, genetic engineering, and numerous growth supplementations help in enhanced DHA production. ARTP mutagenesis significantly improves DHA yield up to 41.4 g/L. While overexpression/co-overexpression/manipulating selected genes linked to the central carbohydrate metabolism, lipid metabolism showed DHA yield up to 51.5 g/L. Furthermore, sustainable, low-cost carbon and nitrogen sources of fermentation media enhanced microalgal biomass and DHA yield. DHA yield was 20.7 g/L using maize starch hydrolysate as a carbon source and soybean meal hydrolysate as a nitrogen source. In addition, cane molasses as a nitrogen source along with overexpressed sucrose dehydrogenase in an adaptive laboratory evolution (ALE) optimized microalgal strain displayed a 162.86% increase in DHA yield (25.26 g/L). Differentially expressed genes (DEGs) revealed from transcriptomics are aligned with the metabolomics profile of DHA-producing microalgae. Enzymes linked to the central carbohydrate metabolism, fatty acid synthase (FAS), and polyketide synthase (PKS) pathways were upregulated along with high cellular demands of NADPH and acetyl-CoA. We believe this review may be useful for further advancement of high-yield DHA-producing microalgae.</p>","PeriodicalId":26,"journal":{"name":"ACS Synthetic Biology","volume":" ","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2025-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Synthetic Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1021/acssynbio.5c00294","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Docosahexaenoic acid (DHA) is an omega-3 fatty acid that is essential for optimal brain growth and development. Fish oil is the main dietary source of DHA. However, off-flavors and contamination with persistent organic pollutants are the main issues when DHA is sourced ethically from deep-sea fishes. Microalgae offer a sustainable, viable option for DHA production. However, optimization of the DHA yield using low-cost materials helps in reducing the fermentation cost. In this systematic review, we cover recent progress on enhanced DHA production during the last ten years, 2015-2025. We discuss how mutagenomics, genetic engineering, and numerous growth supplementations help in enhanced DHA production. ARTP mutagenesis significantly improves DHA yield up to 41.4 g/L. While overexpression/co-overexpression/manipulating selected genes linked to the central carbohydrate metabolism, lipid metabolism showed DHA yield up to 51.5 g/L. Furthermore, sustainable, low-cost carbon and nitrogen sources of fermentation media enhanced microalgal biomass and DHA yield. DHA yield was 20.7 g/L using maize starch hydrolysate as a carbon source and soybean meal hydrolysate as a nitrogen source. In addition, cane molasses as a nitrogen source along with overexpressed sucrose dehydrogenase in an adaptive laboratory evolution (ALE) optimized microalgal strain displayed a 162.86% increase in DHA yield (25.26 g/L). Differentially expressed genes (DEGs) revealed from transcriptomics are aligned with the metabolomics profile of DHA-producing microalgae. Enzymes linked to the central carbohydrate metabolism, fatty acid synthase (FAS), and polyketide synthase (PKS) pathways were upregulated along with high cellular demands of NADPH and acetyl-CoA. We believe this review may be useful for further advancement of high-yield DHA-producing microalgae.

微藻中改进二十二碳六烯酸合成的策略
二十二碳六烯酸(DHA)是一种omega-3脂肪酸,对大脑的最佳生长和发育至关重要。鱼油是DHA的主要膳食来源。然而,当DHA从深海鱼类中获得时,变质和持久性有机污染物的污染是主要问题。微藻为DHA生产提供了一种可持续的、可行的选择。然而,利用低成本材料优化DHA产量有助于降低发酵成本。在这篇系统综述中,我们介绍了过去十年(2015-2025)在提高DHA产量方面的最新进展。我们讨论了突变基因组学、基因工程和许多生长补充剂如何帮助提高DHA的产量。ARTP诱变显著提高DHA产量,最高可达41.4 g/L。当过表达/共过表达/操纵与中心碳水化合物代谢相关的选定基因时,脂质代谢显示DHA产量高达51.5 g/L。此外,可持续、低成本的发酵培养基碳氮源提高了微藻生物量和DHA产量。以玉米淀粉水解液为碳源,豆粕水解液为氮源,DHA产量为20.7 g/L。此外,在适应性实验室进化(ALE)优化的微藻菌株中,甘蔗糖蜜作为氮源并过度表达蔗糖脱氢酶,其DHA产量提高了162.86% (25.26 g/L)。转录组学显示的差异表达基因(DEGs)与产生dha的微藻的代谢组学特征一致。与中心碳水化合物代谢、脂肪酸合成酶(FAS)和聚酮合成酶(PKS)途径相关的酶随着NADPH和乙酰辅酶a的高细胞需求而上调。本文的研究对进一步开发高产dha微藻具有一定的参考价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信