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Metabolic Pathway Rerouting in Paraburkholderia rhizoxinica Evolved Long-Overlooked Derivatives of Coenzyme F 420 .

Authors :
Braga D
Last D
Hasan M
Guo H
Leichnitz D
Uzum Z
Richter I
Schalk F
Beemelmanns C
Hertweck C
Lackner G
Source :
ACS chemical biology [ACS Chem Biol] 2019 Sep 20; Vol. 14 (9), pp. 2088-2094. Date of Electronic Publication: 2019 Sep 11.
Publication Year :
2019

Abstract

Coenzyme F <subscript>420</subscript> is a specialized redox cofactor with a negative redox potential. It supports biochemical processes like methanogenesis, degradation of xenobiotics, and the biosynthesis of antibiotics. Although well-studied in methanogenic archaea and actinobacteria, not much is known about F <subscript>420</subscript> in Gram-negative bacteria. Genome sequencing revealed F <subscript>420</subscript> biosynthetic genes in the Gram-negative, endofungal bacterium Paraburkholderia rhizoxinica , a symbiont of phytopathogenic fungi. Fluorescence microscopy, high-resolution LC-MS, and structure elucidation by NMR demonstrated that the encoded pathway is active and yields unexpected derivatives of F <subscript>420</subscript> (3PG-F <subscript>420</subscript> ). Further analyses of a biogas-producing microbial community showed that these derivatives are more widespread in nature. Genetic and biochemical studies of their biosynthesis established that a specificity switch in the guanylyltransferase CofC reprogrammed the pathway to start from 3-phospho-d-glycerate, suggesting a rerouting event during the evolution of F <subscript>420</subscript> biosynthesis. Furthermore, the cofactor activity of 3PG-F <subscript>420</subscript> was validated, thus opening up perspectives for its use in biocatalysis. The 3PG-F <subscript>420</subscript> biosynthetic gene cluster is fully functional in Escherichia coli , enabling convenient production of the cofactor by fermentation.

Details

Language :
English
ISSN :
1554-8937
Volume :
14
Issue :
9
Database :
MEDLINE
Journal :
ACS chemical biology
Publication Type :
Academic Journal
Accession number :
31469543
Full Text :
https://doi.org/10.1021/acschembio.9b00605