2). These spots from the SH treatment were excised, digested with trypsin and subjected to MS analysis. A mascot search identified spot 195 as GlnK, and spot 196 as a mixture of both GlnB and GlnK (these proteins have the same predicted pI and MW; Table 2). Several predicted peptides of both GlnB and GlnK have the same mass, as these proteins are 79% identical in sequence. DAPT order We identified two peptides that are characteristic for each protein in the mass spectrum of spot 196 (Table 2) and MS/MS analysis of these particular peptides confirmed that this spot is a mixture of GlnB and GlnK. The peptide

of m/z of 1359.76, which is predicted to derive from GlnB only, was also observed in the mass spectrum of spot 195 (Fig. 3). Although we could not obtain good MS/MS data for this particular peptide, its presence suggests that spot 195 might also be a mixture of GlnB and GlnK. The experimental

pI for spot 195 (pI=5.58) was 0.55 units different from the predicted pI of GlnB and GlnK (pI=6.13). It is known that the PII proteins from H. seropedicae are subject to uridylylation (Benelli et al., 2001) and, by analogy with the E. coli PII proteins, it is assumed that uridylylation occurs at the conserved Opaganib datasheet Y51 residue. A signal of m/z of 1543.67 was observed in the mass spectrum of spot 195 but was absent in that of spot 196 (Fig. 3). This signal matches the expected increment of mass for the addition of a UMP group (monoisotopic mass of 306.03) in the peptide of m/z 1237.64, which carries the Y51 uridylylation site of both GlnB and

GlnK. Thus, spot 195 represents uridylylated monomers of GlnK and probably also of GlnB. We conclude that very low amounts of deuridylylated PII proteins are associated with the cell membrane in both +N and −N conditions and that more deuridylylated PII becomes membrane-associated after an ammonium shock (Fig. 2, compare signals of spot 196 in +N, −N and SH). To verify whether the membrane association of PII proteins occurs via interaction with AmtB we prepared membrane fractions from wild-type and amtB mutant strains collected before and after the ammonium shock. As attempts to localize the PII proteins in these Dichloromethane dehalogenase fractions by Western blot using polyclonal anti-PII antibodies from both E. coli and A. brasilense were unsuccessful, we decided to use a MS-based approach instead. These extracts were separated in a regular 12% SDS-PAGE and stained with Coomassie blue. A 1 cm region of molecular mass below the 14-kDa marker was excised from each lane, digested with trypsin and analyzed by MALDI-TOF MS/MS (Fig. S2A). The MS1 mass spectra indicate the presence of peaks with m/z of 1237.64 and 1330.78 in the samples from wild-type cell membrane extract collected both before and after the ammonium shock. These peaks match the expected peptide mass of 1237.64 and 1330.77 of GlnB and GlnK.