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An overview on reconstructing the biosynthetic system of actinomycetes for polyketides production
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Huang XIE1, 2, Yilei ZHENG1, 2, Yiting SU1, 2, Jingyi RUAN1, 2, Yongquan LI1, 2
Synthetic Biology Journal | 2024, 5(3) : 612 - 630
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Synthetic Biology Journal | 2024, 5(3): 612-630
Invited Review
An overview on reconstructing the biosynthetic system of actinomycetes for polyketides production
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Huang XIE1, 2, Yilei ZHENG1, 2, Yiting SU1, 2, Jingyi RUAN1, 2, Yongquan LI1, 2
Affiliations
  • 1 Institute of Pharmaceutical Biotechnology,Zhejiang University,Hangzhou 310058,Zhejiang,China
  • 2 Zhejiang Provincial Key Laboratory for Microbial Biochemistry and Metabolic Engineering,Hangzhou 310058,Zhejiang,China
Published: 2024-06-30 doi: 10.12211/2096-8280.2023-087
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Actinomycetes, enriched with secondary metabolites, have emerged as a resource for drug discovery. These organisms predominantly harbor bioactive compounds such as polyketides, non-ribosomal peptides, aminoglycosides, and terpenes, with polyketides representing the most diverse class. Polyketides are divided into three major categories based on polyketide synthase: type Ⅰ, type Ⅱ, and type Ⅲ, in which type Ⅰ polyketides are most widely distributed and abundant, with macrocyclic lactone compounds serving as their archetypal representatives. Macrocyclic lactone compounds, frequently utilized as antibiotics, anti-cancer agents, immunosuppressants, and antiparasitic agents, hold immense biological significance. This review comments the biosynthetic process of macrolides, and strategies for biosynthesizing actinomycete polyketides are proposed, which encompass genome remodeling, regulatory pathway recombination, combinatorial metabolic engineering, and the modifications of polyketide structures. By knocking out competing gene clusters and superfluous genomic islands, augmenting the supply of precursors, and enhancing precursor supply and lipid stream processing, researchers can obtain genome-minimized and optimized industrial chassis, followed with manipulations such as promoter engineering, regulatory factor engineering, overexpression of the rate-limiting enzyme genes, enhanced substrate transport and tolerance, targeted modifications of the key enzymes, rational design of polyketides, etc. Furthermore, the optimized chassis and biosynthetic gene clusters are integrated to develop robust strains for multi-omics analyses and fermentation process optimization, which can be guided by rapidly developed synthetic biology enabling technologies and artificial intelligence, to develop a high-quality, efficient polyketides biosynthesis system. These advancements can offer robust technical support for the large-scale production of polyketides pharmaceuticals and their derivatives.

actinomycetes  /  polyketide  /  strain reconstruction  /  production  /  metabolic engineering  /  synthetic biology
Huang XIE, Yilei ZHENG, Yiting SU, Jingyi RUAN, Yongquan LI. An overview on reconstructing the biosynthetic system of actinomycetes for polyketides production[J]. Synthetic Biology Journal, 2024 , 5 (3) : 612 -630 . DOI: 10.12211/2096-8280.2023-087
Year 2024 volume 5 Issue 3
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Article Info
doi: 10.12211/2096-8280.2023-087
  • Receive Date:2023-11-28
  • Online Date:2025-07-07
  • Published:2024-06-30
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  • Received:2023-11-28
  • Revised:2024-01-16
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Affiliations
    1 Institute of Pharmaceutical Biotechnology,Zhejiang University,Hangzhou 310058,Zhejiang,China
    2 Zhejiang Provincial Key Laboratory for Microbial Biochemistry and Metabolic Engineering,Hangzhou 310058,Zhejiang,China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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