The structure of syringomycins A1, E and G.

By a combination of 1D and 2D 1H- and 13C-NMR, FAB-MS, and chemical and enzymatic reactions carried out at the milligram level, it has been demonstrated that syringomycin E, the major phytotoxic antibiotic produced by Pseudomonas syringae pv. syringae, is a new lipodepsipeptide. Its amino acid sequence is Ser-Ser-Dab-Dab-Arg-Phe-Dhb-4(Cl)Thr-3(OH)Asp with the beta-carboxy group of the C-terminal residue closing a macrocyclic ring on the OH group of the N-terminal Ser, which in turn is N-acylated by 3-hydroxydodecanoic acid. Syringomycins A1 and G, two other metabolites of the same bacterium, differ from syringomycin E only in their fatty acid moieties corresponding, respectively, to 3-hydroxydecanoic and 3-hydroxytetradecanoic acid.

Membrane topography of the photosynthetic reaction center polypeptides of Rhodopseudomonas sphaeroides.

The topography of the photosynthetic reaction center (RC) polypeptides (H, M, and L) was investigated by proteolysis and radioiodination of membrane vesicles isolated from Rhodopseudomonas sphaeroides. Chromatophores, obtained from French-pressed cell lysates, are closed vesicles' and oriented inside out with respect to the cytoplasmic membrane (cytoplasmic side out). Spheroplast-derived vesicles (SDVs), obtained after osmotic lysis of lysozyme-treated cells, are oriented right side in (periplasmic side out). Alpha-Chymotrypsin treatment of chromatophores and trypsin treatment of SDVs resulted in cleavage of H. Alpha-Chymotrypsin treatment of SDVs did not cleave H, and trypsin treatment of chromatophores did not consistently cleave this polypeptide. M and L of both vesicles were apparently not affected by these proteases. The SDV trypsin cleavage product of H was identified by alpha-chymotryptic (125)I-labeled peptide mapping and had a molecular weight of 26 000. Membrane surface radioiodination with chloroglycoluril coated on glass tubes resulted in preferential labeling of H and M of SDVs and chromatophores. The radiospecific activities of H, M, and L were higher with labeling of SDVs as compared to labeling of chromatophores. Alpha-Chymotryptic (125)I-labeled peptide maps of H, M, and L from surface-radioiodinated SDVs differed from the corresponding maps of these polypeptides from surface-radioiodinated chromatophores. The results indicate the asymmetric exposure of H, M, and L on opposite surfaces of the R. sphaeroides membrane. Exposed iodination sites of these polypeptides are more abundant on the periplasmic surface than on the cytoplasmic surface of this membrane.

Mechanism of Action of Pseudomonas syringae Phytotoxin, Syringomycin : Stimulation of Red Beet Plasma Membrane ATPase Activity.

Syringomycin, a peptide toxin produced by the phytopathogen Pseudomonas syringae pv syringae preferentially stimulated (2-fold) the vanadate-sensitive ATPase activity associated with the plasma membrane of red beet storage tissue. The toxin had a very slight effect on the tonoplast ATPase and had no detectable effect on the mitochondrial ATPase. Optimal stimulation was achieved with 10 to 50 micrograms of syringomycin per 25 micrograms of membrane protein. Treatment of membranes with 0.1% (weight/volume) deoxycholate eliminated the activation effect, and enzyme solubilized with Zwittergent 3-14 was not affected by syringomycin. ATPase activity was activated to the same extent at KCl concentrations ranging from 0 to 50 millimolar. Valinomycin, nigericin, carbonylcyanide p-trifluoromethoxyphenylhydrazone, and gramicidin did not increase the plasma membrane ATPase activity. However, these ionophores did not hinder the ability of syringomycin to stimulate the activity. We suggest that syringomycin does not increase ATPase activity by altering membrane ion gradients nor directly interacting with the enzyme, but possibly through regulatory effectors or covalent modification of the enzyme.