Literature DB >> 29779651

The Biochemistry and Structural Biology of Cyanobactin Pathways: Enabling Combinatorial Biosynthesis.

Wenjia Gu1, Shi-Hui Dong2, Snigdha Sarkar1, Satish K Nair3, Eric W Schmidt4.   

Abstract

Cyanobactin biosynthetic enzymes have exceptional versatility in the synthesis of natural and unnatural products. Cyanobactins are ribosomally synthesized and posttranslationally modified peptides synthesized by multistep pathways involving a broad suite of enzymes, including heterocyclases/cyclodehydratases, macrocyclases, proteases, prenyltransferases, methyltransferases, and others. Here, we describe the enzymology and structural biology of cyanobactin biosynthetic enzymes, aiming at the twin goals of understanding biochemical mechanisms and biosynthetic plasticity. We highlight how this common suite of enzymes may be utilized to generate a large array or structurally and chemically diverse compounds.
© 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Combinatorial biosynthesis; Cyanobactins; Cyclic peptide; Natural products; RiPP biosynthesis; Synthetic biology

Mesh:

Substances:

Year:  2018        PMID: 29779651      PMCID: PMC6463883          DOI: 10.1016/bs.mie.2018.03.002

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  88 in total

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Journal:  Biochemistry       Date:  1999-11-23       Impact factor: 3.162

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  17 in total

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7.  Genome-Mining-Based Discovery of the Cyclic Peptide Tolypamide and TolF, a Ser/Thr Forward O-Prenyltransferase.

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