Conversion of saturated fatty acid to unsaturated one: Whole-cell catalysis of Saccharomyces cerevisiae

被引:4
|
作者
Wang, Yu [1 ]
Ji, Xiaotong [2 ,3 ]
Chen, Lin [2 ,4 ,5 ]
Yang, Guanpin [6 ]
Zhou, Wenjun [2 ,4 ,5 ,7 ]
Huang, Xinhe [1 ,7 ]
Liu, Tianzhong [2 ,4 ,5 ]
机构
[1] Southwest Jiaotong Univ, Sch Life Sci & Engn, Chengdu 610031, Peoples R China
[2] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Key Lab Biofuels, Key Lab Shandong Energy Biol Genet Resources, Qingdao 266101, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Shandong Energy Inst, Qingdao 266101, Peoples R China
[5] Qingdao New Energy Shandong Lab, Qingdao 266101, Peoples R China
[6] Ocean Univ China, Coll Marine Life Sci, Qingdao 266071, Peoples R China
[7] 189 Songling Rd, Qingdao, Peoples R China
基金
中国国家自然科学基金;
关键词
Value-increment; Whole-cell catalysis; Lipids; Palmitoleic acid; Saccharomyces cerevisiae; ELONGATION; MICROALGAE; YEAST;
D O I
10.1016/j.bej.2023.108960
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
New production technology for functional unsaturated fatty acids such as DHA, EPA, ARA, and POA (palmitoleic acid) is urgently required. Here we developed a whole-cell catalysis method to convert low-value fatty acids to high-value one by using Saccharomyces cerevisiae as whole-cell biocatalyst. Results showed that palmitic acid was the most appropriate substrate for the bioconversion, and it increased the production of POA by 17.0% in comparison with de novo synthesis by fermentation only. A thorough investigation on the primary bioconversion conditions was performed. Under the optimum parameters, the substrate utilization rate reached 96.1%, which resulted in the production of POA increased to 5.9 g L-1, 90.3% higher than that of fermentation only. Stable isotope analysis showed that up to 61.7% of substrate was catalyzed to POA. Transcriptomic analysis revealed a repression from glucose to lipid but an acceleration from lipidic substrate to POA in S. cerevisiae during wholecell catalysis.
引用
收藏
页数:11
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