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Review
. 2019 Mar 27;19(6):463-470.
doi: 10.1002/elsc.201800133. eCollection 2019 Jun.

Lignin valorization meets synthetic biology

Affiliations
Review

Lignin valorization meets synthetic biology

Renkuan Zhang et al. Eng Life Sci. .

Abstract

Lignin, an abundant renewable resource in nature, is a highly heterogeneous biopolymer consisting of phenylpropanoid units. It is essential for sustainable utilization of biomass to convert lignin to value-added products. However, there are technical obstacles for lignin valorization due to intrinsic heterogeneity. The emerging of synthetic biology technologies brings new opportunities for lignin breakdown and utilization. In this review, we discussed the applications of synthetic biology on lignin conversion, especially the production of value-added products, such as aromatic chemicals, ring-cleaved chemicals from lignin-derived aromatics and bio-active substances. Synthetic biology will offer new potential strategies for lignin valorization by optimizing lignin degradation enzymes, building novel artificial converting pathways, and improving the chassis of model microorganisms.

Keywords: artificial pathway; bio‐degradation; lignin valorization; synthetic biology; value‐added products.

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Conflict of interest statement

The authors have declared no conflicts of interest.

Figures

Figure 1
Figure 1
The framework of synthetic biology applied in lignin valorization
Figure 2
Figure 2
The synthesis route of chemicals from lignin‐derived aromatic molecule. (A) The aromatic chemicals. (B) The ring‐cleaved chemicals. (C) The bio‐active substances. R‐groups for Flavonoids R1 = R2: Pinocembrin, R1 = OH, R2 = H: Naringenin, R= R= OH: Eriodictyol; for Coumarins R= R= OH: Esculetin, R= OCH3, R= OH: Scopoletin; For Stilbenoids R= R= H: Pinosylvin, R= OH, R= H: Resveratol; R= R= OH: Piceatannol

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