High-value bioproducts from microalgae: Strategies and progress

被引:91
作者
Liang, Ming-Hua [1 ]
Wang, Ling [2 ]
Wang, Qiming [3 ]
Zhu, Jianhua [2 ,3 ,4 ]
Jiang, Jian-Guo [1 ]
机构
[1] South China Univ Technol, Coll Food Sci & Engn, Guangzhou 510640, Guangdong, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Biotechnol, Zhenjiang, Jiangsu, Peoples R China
[3] Hunan Agr Univ, Coll Biosci & Biotechnol, Changsha, Hunan, Peoples R China
[4] Univ Maryland, Dept Plant Sci & Landscape Architecture, College Pk, MD 20742 USA
基金
美国国家科学基金会; 中国博士后科学基金;
关键词
Microalgae; high-value bioproducts; omics; abiotic stress; metabolic engineering; gene knockout; carotenoid; lipid; LC-PUFA; ALGA HAEMATOCOCCUS-PLUVIALIS; FATTY-ACID BIOSYNTHESIS; TYPE-2 DIACYLGLYCEROL ACYLTRANSFERASE; ENHANCE ASTAXANTHIN FORMATION; SYNTHASE GENE-EXPRESSION; BETA-CAROTENE KETOLASE; CHLAMYDOMONAS-REINHARDTII; LIPID PRODUCTION; DUNALIELLA-SALINA; GREEN MICROALGA;
D O I
10.1080/10408398.2018.1455030
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Microalgae have been considered as alternative sustainable resources for high-value bioproducts such as lipids (especially triacylglycerides [TAGs]), polyunsaturated fatty acids (PUFAs), and carotenoids, due to their relatively high photosynthetic efficiency, no arable land requirement, and ease of scale-up. It is of great significance to exploit microalgae for the production of high-value bioproducts. How to improve the content or productivity of specific bioproducts has become one of the most urgent challenges. In this review, we will describe high-value bioproducts from microalgae and their biosynthetic pathways (mainly for lipids, PUFAs, and carotenoids). Recent progress and strategies for the enhanced production of bioproducts from microalgae are also described in detail, and these strategies take advantages of optimized cultivation conditions with abiotic stress, chemical stress (addition of metabolic precursors, phytohormones, chemical inhibitors, and chemicals inducing oxidative stress response), and molecular approaches such as metabolic engineering, transcriptional engineering, and gene disruption strategies (mainly RNAi, antisense RNA, miRNA-based knockdown, and CRISPR/Cas9).
引用
收藏
页码:2423 / 2441
页数:19
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