A bioactive molecule made by unusual salvage of radical SAM enzyme byproduct 5-deoxyadenosine blurs the boundary of primary and secondary metabolism

• Published in: The Journal of biological chemistry 2021-01, Vol.296, p.100621, Article 100621
• Main Authors: Rapp, Johanna, Rath, Pascal, Kilian, Joachim, Brilisauer, Klaus, Grond, Stephanie, Forchhammer, Karl
• Format: Article
• Language: English
• Subjects: 5-deoxyadenosine salvage; 5-deoxyribose; 7-deoxysedoheptulose biosynthesis; carbohydrate biosynthesis; cyanobacteria; enzyme promiscuity; GC–MS; radical SAM enzymes; S-adenosylmethionine; secondary metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/j.jbc.2021.100621

5-Deoxyadenosine (5dAdo) is the byproduct of many radical S-adenosyl-l-methionine enzyme reactions in all domains of life. 5dAdo is also an inhibitor of the radical S-adenosyl-l-methionine enzymes themselves, making it necessary for cells to construct pathways to recycle or dispose of this toxic metabolite. However, the specific pathways involved have long remained unexplored. Recent research demonstrated a growth advantage in certain organisms by using 5dAdo or intermediates as a sole carbon source and elucidated the corresponding salvage pathway. We now provide evidence using supernatant analysis by GC–MS for another 5dAdo recycling route. Specifically, in the unicellular cyanobacterium Synechococcus elongatus PCC 7942 (S. elongatus), the activity of promiscuous enzymes leads to the synthesis and excretion first of 5-deoxyribose and subsequently of 7-deoxysedoheptulose. 7-Deoxysedoheptulose is an unusual deoxy-sugar, which acts as an antimetabolite of the shikimate pathway, thereby exhibiting antimicrobial and herbicidal activity. This strategy enables organisms with small genomes and lacking canonical gene clusters for the synthesis of secondary metabolites, like S. elongatus, to produce antimicrobial compounds from primary metabolism and enzymatic promiscuity. Our findings challenge the view of bioactive molecules as sole products of secondary metabolite gene clusters and expand the range of compounds that microorganisms can deploy to compete for their ecological niche.