NaPMT1.1 Notes
- UniProt curates Q93XQ5 as Putrescine N-methyltransferase 1 and places it in nicotine biosynthesis with predominant root expression. [file:NICAT/NaPMT1.1/NaPMT1.1-uniprot.txt "DE RecName: Full=Putrescine N-methyltransferase 1"; "CC -!- PATHWAY: Alkaloid biosynthesis; nicotine biosynthesis."; "CC -!- TISSUE SPECIFICITY: Mainly expressed in roots."]
- PMT catalyzes S-adenosylmethionine-dependent methylation of putrescine to N-methylputrescine, the first specific metabolite on the route to nicotine. PMID:19651420
- TreeGrafter assignment to spermidine synthase reflects PMT's evolutionary origin from spermidine synthase rather than its present catalytic activity. PMID:19651420
- In N. attenuata, Winz and Baldwin cloned PMT1 and PMT2 and found that both root PMT transcripts rose after MeJA, wounding, and Manduca sexta herbivory, while ethylene suppressed this induction. PMID:11299398
- The 2017 Nicotiana genome paper places root nicotine biosynthesis in N. attenuata as a duplicated specialization of polyamine and NAD metabolism, consistent with PMT as a root defense-pathway enzyme. PMID:28536194
- The full glucosylation preprint keeps PMT in the minimal completed pathway by using ODC, PMT, and MPO to generate N-methylpyrrolinium for in planta nicotine reconstruction. [file:projects/NICOTINE_BIOSYNTHESIS/biorxiv-nicotine-glucosylation-notes.md "In N. benthamiana leaves, the in planta reconstruction uses ODC, PMT, and MPO to generate N-methylpyrrolinium, then depends on the glucosylation-late-pathway module to make labelled nicotine"; "ODC, PMT, and MPO remain part of the minimal upstream module needed to feed the completed pathway."]