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1 Yu Peng -- 137 2026-09-24 08:18:42

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Peng, Y. Biosynthetic Pathways. Encyclopedia. Available online: https://encyclopedia.pub/entry/60458 (accessed on 26 September 2026).
Peng Y. Biosynthetic Pathways. Encyclopedia. Available at: https://encyclopedia.pub/entry/60458. Accessed September 26, 2026.
Peng, Yu. "Biosynthetic Pathways" Encyclopedia, https://encyclopedia.pub/entry/60458 (accessed September 26, 2026).
Peng, Y. (2026, September 24). Biosynthetic Pathways. In Encyclopedia. https://encyclopedia.pub/entry/60458
Peng, Yu. "Biosynthetic Pathways." Encyclopedia. Web. 24 September, 2026.
Biosynthetic Pathways
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Biosynthetic pathways are organized sequences of enzyme-catalyzed biochemical reactions through which microorganisms convert primary metabolic precursors into natural products and their structural derivatives. Within microbial natural-product biosynthesis, a pathway comprises the participating substrates, intermediates, cofactors, enzymes, regulatory elements, and transport or resistance functions that collectively determine the assembly and chemical maturation of a metabolite [1][2]. Core biosynthetic enzymes generate characteristic molecular scaffolds through reactions such as condensation, carbon–carbon bond formation, cyclization, and chain extension, while tailoring enzymes introduce structural features through oxidation, reduction, methylation, glycosylation, halogenation, acylation, or related transformations [1][3]. The pathway therefore encompasses the full biochemical route from precursor recruitment and scaffold formation to enzymatic modification, product release, and, where encoded, intracellular handling of the resulting natural product [2][3].

microbial natural products specialized metabolism biosynthetic enzymes metabolic intermediates

References

  1. Christopher T. Walsh; Polyketide and Nonribosomal Peptide Antibiotics: Modularity and Versatility. Science 2004, 303, 1805-1810. [CrossRef]
  2. Michael A. Fischbach; Christopher T. Walsh; Assembly-Line Enzymology for Polyketide and Nonribosomal Peptide Antibiotics: Logic, Machinery, and Mechanisms. Chem. Rev. 2006, 106, 3468-3496. [CrossRef]
  3. Marnix H Medema; Michael A Fischbach; Computational approaches to natural product discovery. Nat. Chem. Biol. 2015, 11, 639-648. [CrossRef]
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