A third purine biosynthetic pathway encoded by aminoadenine-based viral DNA genomes

Cells have two purine pathways that synthesize adenine and guanine ribonucleotides from phosphoribose via inosylate. A chemical hybrid between adenine and guanine, 2-aminoadenine (Z), replaces adenine in the DNA of the cyanobacterial virus S-2L. We show that S-2L and Vibrio phage PhiVC8 encode a third purine pathway catalyzed by PurZ, a distant paralog of succinoadenylate synthase (PurA), the enzyme condensing aspartate and inosylate in the adenine pathway. PurZ condenses aspartate with deoxyguanylate into dSMP (N6-succino-2-amino-2'-deoxyadenylate), which undergoes defumarylation and phosphorylation to give dZTP (2-amino-2'-deoxyadenosine-5'-triphosphate), a substrate for the phage DNA polymerase. Crystallography and phylogenetics analyses indicate a close relationship between phage PurZ and archaeal PurA enzymes. Our work elucidates the biocatalytic innovation that remodeled a DNA building block beyond canonical molecular biology.

Automated summary

This study reveals a third purine pathway encoded by cyanobacterial virus S-2L and Vibrio phage PhiVC8, catalyzed by PurZ, which synthesizes 2-amino-2'-deoxyadenosine-5'-triphosphate. Crystallography and phylogenetics analyses show a close relationship between phage PurZ and archaeal PurA enzymes. This work elucidates a biocatalytic innovation beyond canonical molecular biology, remodeling a DNA building block.