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Genome Mining Enabled by Biosynthetic Characterization Uncovers a Class of Benzoxazolinate‐Containing Natural Products in Diverse Bacteria.

Authors :
Shi, Yi‐Ming
Crames, Jan J.
Czech, Laura
Bozhüyük, Kenan A. J.
Shi, Yan‐Ni
Hirschmann, Merle
Lamberth, Stefanie
Claus, Peter
Paczia, Nicole
Rückert, Christian
Kalinowski, Jörn
Bange, Gert
Bode, Helge B.
Source :
Angewandte Chemie; 12/19/2022, Vol. 134 Issue 51, p1-11, 11p
Publication Year :
2022

Abstract

Benzoxazolinate is a rare bis‐heterocyclic moiety that interacts with proteins and DNA and confers extraordinary bioactivities on natural products, such as C‐1027. However, the biosynthetic gene responsible for the key cyclization step of benzoxazolinate remains unclear. Herein, we show a putative acyl AMP‐ligase responsible for the last cyclization step. We used the enzyme as a probe for genome mining and discovered that the orphan benzobactin gene cluster in entomopathogenic bacteria prevails across Proteobacteria and Firmicutes. It turns out that Pseudomonas chlororaphis produces various benzobactins, whose biosynthesis is highlighted by a synergistic effect of two unclustered genes encoding enzymes on boosting benzobactin production; the formation of non‐proteinogenic 2‐hydroxymethylserine by a serine hydroxymethyltransferase; and the types I and II NRPS architecture for structural diversity. Our findings reveal the biosynthetic potential of a widespread benzobactin gene cluster. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00448249
Volume :
134
Issue :
51
Database :
Complementary Index
Journal :
Angewandte Chemie
Publication Type :
Academic Journal
Accession number :
160736593
Full Text :
https://doi.org/10.1002/ange.202206106