Shikimic acid biosynthesis in microorganisms: Current status and future direction

ElsevierVolume 62, January–February 2023, 108073Biotechnology AdvancesAuthor links open overlay panelHighlights•

This review briefly introduced shikimic acid pathways and the application of shikimic acid.

This review systematically summarizes breeding strategies of shikimic acid-producing strains.

This review analyzes the disadvantages of current status and prospects for developing shikimic acid-producing strains.

Abstract

Shikimic acid (SA), a hydroaromatic natural product, is used as a chiral precursor for organic synthesis of oseltamivir (Tamiflu®, an antiviral drug). The process of microbial production of SA has recently undergone vigorous development. Particularly, the sustainable construction of recombinant Corynebacterium glutamicum (141.2 g/L) and Escherichia coli (87 g/L) laid a solid foundation for the microbial fermentation production of SA. However, its industrial application is restricted by limitations such as the lack of fermentation tests for industrial-scale and the requirement of growth-limiting factors, antibiotics, and inducers. Therefore, the development of SA biosensors and dynamic molecular switches, as well as genetic modification strategies and optimization of the fermentation process based on omics technology could improve the performance of SA-producing strains. In this review, recent advances in the development of SA-producing strains, including genetic modification strategies, metabolic pathway construction, and biosensor-assisted evolution, are discussed and critically reviewed. Finally, future challenges and perspectives for further reinforcing the development of robust SA-producing strains are predicted, providing theoretical guidance for the industrial production of SA.

Keywords

Natural product

Shikimic acid

Metabolic engineering

Genetic engineering

Biosensor

Fermentation

AbbreviationsDAHP

3-deoxy-D-arabino-heptulosonate-7-phosphate

PPP

pentose phosphate pathway

PTS

phosphoenolpyruvate: carbohydrate phosphotransferase system

E4P

d-erythrose 4-phosphate

EPSP

5-enolpyruvylshikimate-3-phosphate

L-DOPA

3,4-dihydroxy-l-phenylalanine

KDPG

2-keto-3-deoxy-6-phosphogalactonate

FACS

fluorescence-activated cell sorting

RFP

red fluorescence protein

GSMMs

genome-scale metabolic models

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