Microbial engineering for shikimate biosynthesis

被引:1
|
作者
Ding, Qiang [1 ,3 ,4 ]
Ye, Chao [2 ]
机构
[1] Anhui Univ, Sch Life Sci, Hefei 230601, Peoples R China
[2] Nanjing Normal Univ, Sch Food Sci & Pharmaceut Engn, Nanjing 210023, Peoples R China
[3] Anhui Univ, Anhui Higher Educ Inst, Key Lab Human Microenvironm & Precis Med, Hefei 230601, Peoples R China
[4] Anhui Key Lab Modern Biomfg, Hefei 230601, Anhui, Peoples R China
关键词
Shikimate biosynthesis; Chassis construction; Biochemical strategy; Pathway remold; Global regulation; ESCHERICHIA-COLI; DYNAMIC REGULATION; ACID PRODUCTION; CORYNEBACTERIUM-GLUTAMICUM; SACCHAROMYCES-CEREVISIAE; METABOLIC FLUX; GENES IMPROVES; SYSTEMS; EXPRESSION; BIOSENSORS;
D O I
10.1016/j.enzmictec.2023.110306
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
Shikimate, a precursor to the antiviral drug oseltamivir (Tamiflu & REG;), can influence aromatic metabolites and finds extensive use in antimicrobial, antitumor, and cardiovascular applications. Consequently, various strategies have been developed for chemical synthesis and plant extraction to enhance shikimate biosynthesis, potentially impacting environmental conditions, economic sustainability, and separation and purification processes. Mi-crobial engineering has been developed as an environmentally friendly approach for shikimate biosynthesis. In this review, we provide a comprehensive summary of microbial strategies for shikimate biosynthesis. These strategies primarily include chassis construction, biochemical optimization, pathway remodelling, and global regulation. Furthermore, we discuss future perspectives on shikimate biosynthesis and emphasize the importance of utilizing advanced metabolic engineering tools to regulate microbial networks for constructing robust mi-crobial cell factories.
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页数:11
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