Morphological Change and Cell Disruption of Haematococcus pluvialis Cyst during High-Pressure Homogenization for Astaxanthin Recovery

被引:25
|
作者
Praveenkumar, Ramasamy [1 ,2 ]
Lee, Jiye [3 ]
Vijayan, Durairaj [3 ]
Lee, Soo Youn [3 ]
Lee, Kyubock [4 ]
Sim, Sang Jun [5 ]
Hong, Min Eui [5 ]
Kim, Young-Eun [6 ]
Oh, You-Kwan [6 ]
机构
[1] Roskilde Univ, Dept Sci & Environm, DK-4000 Roskilde, Denmark
[2] Roskilde Univ, Ctr Virtual Learning Technol, DK-4000 Roskilde, Denmark
[3] Korea Inst Energy Res, Climate Change Res Div, Daejeon 34129, South Korea
[4] Chungnam Natl Univ, Grad Sch Energy Sci & Technol, Daejeon 34134, South Korea
[5] Korea Univ, Dept Chem & Biol Engn, Seoul 02841, South Korea
[6] Pusan Natl Univ, Sch Chem & Biomol Engn, Busan 46241, South Korea
来源
APPLIED SCIENCES-BASEL | 2020年 / 10卷 / 02期
基金
新加坡国家研究基金会;
关键词
Haematococcus pluvialis; high-pressure homogenization; astaxanthin; cyst; cell disruption; MICROALGAE CHLORELLA; EXTRACTION; WALL; RELEASE; MILD;
D O I
10.3390/app10020513
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Haematococcus pluvialis accumulates astaxanthin, which is a high-value antioxidant, during the red cyst stage of its lifecycle. The development of a rigid cell wall in the cysts hinders the recovery of astaxanthin. We investigated morphological changes and cell disruption of mature H. pluvialis cyst cells while using high-pressure homogenization for astaxanthin extraction. When treated with French-press-cell (pressure, 10,000-30,000 psi; passage, 1-3), the intact cyst cells were significantly broken or fully ruptured, releasing cytoplasmic components, thereby facilitating the separation of astaxanthin by ethyl acetate. Fluorescence microscopy observations using three different fluorescent dyes revealed that a greater degree of cell breakage caused greater external dispersion of astaxanthin, chlorophyll, lipids, proteins, and carbohydrates. The mechanical treatment resulted in a high cell disruption rate of up to 91% based on microscopic cell typing and Coulter methods. After the ethyl acetate extraction, the astaxanthin concentration significantly increased by 15.2 mg/L in proportion to the increase in cell disruption rate, which indicates that cell disruption is a critical factor for solvent-based astaxanthin recovery. Furthermore, this study recommends a synergistic combination of the fast instrumental particle-volume-distribution analysis and microscope-based morphologic phenotyping for the development of practical H. pluvialis biorefinery processes that co-produce various biological products, including lipids, proteins, carbohydrates, chlorophyll, and astaxanthin.
引用
收藏
页数:10
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