Metabolic pathways for microalgal biohydrogen production: Current progress and future prospectives

被引:46
作者
El-Dalatony, Marwa M. [1 ,2 ]
Zheng, Yuanzhang [3 ]
Ji, Min-Kyu [4 ]
Li, Xiangkai [1 ]
Salama, El-Sayed [1 ]
机构
[1] Lanzhou Univ, Sch Publ Hlth, Dept Occupat & Environm Hlth, Lanzhou 730000, Gansu, Peoples R China
[2] Lanzhou Univ, Sch Life Sci, Lanzhou 730000, Gansu, Peoples R China
[3] Indiana Univ, Sch Med Biochem, Dept Mol Biol, Indianapolis, IN 46202 USA
[4] Korea Environm Inst, Environm Assessment Grp, Yeongi Gun 30147, South Korea
关键词
Microalgae; Biohydrogen; Hydrogenases; Pathways; Bioreactors; FERMENTATIVE HYDROGEN-PRODUCTION; VOLATILE FATTY-ACIDS; CHLAMYDOMONAS-REINHARDTII; H-2; PRODUCTION; CLOSTRIDIUM-BUTYRICUM; CURRENT LIMITATIONS; DARK FERMENTATION; ELECTROLYSIS CELL; LIGHT-INTENSITY; GREEN-ALGAE;
D O I
10.1016/j.biortech.2020.124253
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Microalgal biohydrogen (bioH(2)) has attracted global interest owing to its potential carbon-free source of sustainable renewable energy. Most of previous reviews which focused on microalgal bioH(2), have shown unclear differentiation among the metabolic pathways. In this review, investigation of all different metabolic pathways for microalgal bioH(2) production along with discussion on the recent research work of last 5-years have been considered. The major factors (such as light, vital nutrients, microalgal cell density, and substrate bioavailability) are highlighted. Moreover, effect of various pretreatment approaches on the constituent's bioaccessibility is reported. Microbial electrolysis cells as a new strategy for bioH(2) production is stated. Comparison between the operation conditions of various bioreactors and economic feasibility is also emphasized. Genetic, metabolic engineering, and synthetic biology as recent technologies improved the microalgal bioH(2) production through inactivation of uptake hydrogenase (H(2)ase), inhibition of the competing pathways in polysaccharide synthesis, and improving the O-2 tolerant H(2)ase.
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收藏
页数:14
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