In vitro assay of MpnS activity. (A) Crude cell extract from an E. coli MpnS overexpression strain was incubated aerobically with 1-¹³C-HEP in the presence of Fe(II) and the phosphorus-containing products were examined using ³¹P NMR spectroscopy. After incubation for 1 hour a single product was observed as a doublet centered at 23.5 ppm. The mass and retention time of this product determined by LC-MS is consistent with this product being 1-¹³CMPn (Fig. S3). (B) Spiking of this reaction with the substrate, 1-¹³C-HEP produced a second doublet centered at 19 ppm, showing that the substrate was completely consumed in the initial reaction. (C) The identity of the reaction products was determined using ¹³C NMR after repeating the assay in a sealed vial using purified MpnS with a mixture of 1-¹³C-HEP and 2-¹³C-HEP as substrates. The C-2 labeled carbon of HEP is converted to ¹³C bicarbonate (H¹³CO ^-₃), while the C-1-labelled carbon is converted to 1-¹³C-MPn. Bonding to phosphorus splits the ¹³C peak in the NMR spectrum. Thus, the C-1 peak is split and the C-2 peak is not. Glycerol, a component of the assay mixture, is also observed in the ¹³C spectrum. The ¹³C label is indicated by a red asterisk.

(A) The evolutionary relationships of biochemically characterized MpnS, HepD and HppE proteins (shown in bold) and homologs recovered from Genbank and the GOS metagenomic dataset was inferred using maximum likelihood analysis as described. Bootstrap values from 100 replicates are shown at the nodes. Robust bootstrap support for the tree shows that the method clearly differentiates MpnS (green), HepD (blue) and HppE (red) proteins. The full tree with all individual homologs shown is presented in Fig S9. (B) The gene content of large scaffolds containing the GOS MpnS homologs is compared to the mpnS locus of N. maritimus. The grey boxes represent sequencing gaps between paired-end reads.

In vivo production of methylphosphonate esters by N. maritimus. (A) A cell extract of N. maritimus was prepared by sonication of whole cells as described. After removal of the cell debris by centrifugation, the supernatant was examined by ³¹P NMR spectroscopy revealing at least two compounds with chemical shifts in the range typical of phosphonic acids. (B) The two-dimensional HMBC NMR spectrum of N. maritimus cell extract. Comparison of the proton splitting patterns (shown in the insets) to those of model compounds (Figs S6 & S7) clearly shows that the P compound at 28 ppm in the ³¹P dimension is a methylphosphonate ester. The doublet of the proton at 1.4 ppm coupled to the phosphorus is diagnostic for a methyl group bonded directly to phosphorus, i.e. a methylphosphonate moiety. (C) High resolution LC-MS analysis showing the presence of free methylphosphonate after strong acid hydrolysis of N. maritimus cell debris. The extracted ion chromatogram centered around m/z 94.99035 (exact monoisotopic mass of methylphosphonate [M-H]^-) with Fourier-transform mass spectrum and ion structure is shown in the inset. The chromatographic and MS fragmentation pattern is identical to an authentic MPn standard (Fig S8).