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The effect of the new antibiotic myxothiazol on the respiration of Paracoccus denitrificans

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Abstract

Myxothiazol inhibited the electron transport in the cytochrome b-c 1segment of membrane particles from Paracoccus denitrificans. There remained, however, a residual NADH oxidation of about 10% which was probably due to the presence of an alternative respiratory pathway via cytochrome o. This may also explain why in presence of myxothiazol growth of P. denitrificans is resumed, at a reduced rate, after an adaption period of 1 h.

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References

  • Asano A, Brodie AF (1964) Oxidative phosphorylation in fractionated bacterial systems. XIV. Respiratory chains of Mycobacterium phlei. J Biol Chem 239:4280–4291

    PubMed  Google Scholar 

  • Becker WF, Jagow G von, Anke T, Steglich W (1981) Oudemansin, strobilurin A, strobilurin B and myxothiazol: new inhibitors of the bc 1segment of the respiratory chain with an E-β-methoxyacrylate system as common structural element. FEBS Lett 132:329–333

    PubMed  Google Scholar 

  • Chang JP, Morris JG (1962) Studies on the utilization of nitrate by Micrococcus denitrificans. J Gen Microbiol 29:301–310

    PubMed  Google Scholar 

  • Gerth K, Irschik H, Reichenbach H, Trowitzsch W (1980) Myxothiazol, an antibiotic from Myxococcus fulvus (Myxobacterales). I. Cultivation, isolation, physico-chemical and biological properties. J Antibiotics 33:1474–1479

    Google Scholar 

  • Henry MF, Vignais PM (1979) Induction by cyanide of cytochrome d in the plasma membrane of Paracoccus denitrificans. FEBS Lett 100:41–46

    PubMed  Google Scholar 

  • Jagow G von, Engel WD (1981) Complete inhibition of electron transfer from ubiquinol to cytochrome b by the combined action of antimycin and myxothiazol. FEBS Lett 136:19–24

    PubMed  Google Scholar 

  • John P, Whatley FR (1975) Paracoccus denitrificans and the evolutionary origin of the mitochrondrion. Nature 254:495–498

    PubMed  Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275

    PubMed  Google Scholar 

  • Müller W, Schewe T, Rapoport S (1977) Elektronentransportpartikel aus Rinderherzmitochondrien als Testsystem auf Hemmstoffe der Atmungskette. Acta Biol Med Ger 36:941–960

    PubMed  Google Scholar 

  • Riccio P, Schägger H, Engel WD, Jagow G von (1977) bc 1-Complex from beef-heart. One-step purification by hydroxyapatite chromatography in Triton X-100, polypeptide pattern and respiratory chain characteristics. Biochim Biophys Acta 459:250–262

    PubMed  Google Scholar 

  • Sapshead LM, Wimpenny JWT (1972) The influence of oxygen and nitrate on the formation of cytochrome pigments of the aerobic and anaerobic respiratory chain of Micrococcus denitrificans. Biochim Biophys Acta 267:388–397

    PubMed  Google Scholar 

  • Scholes PB, Smith L (1968) Composition and properties of the membrane-bound respiratory chain system of Micrococcus denitrificans. Biochim Biophys Acta 153:363–375

    PubMed  Google Scholar 

  • Stouthamer AH (1980) Bioenergetic studies on Paracoccus denitrificans. Trends Biochem Sci 5:164–166

    Google Scholar 

  • Thierbach G, Reichenbach H (1981a) Myxothiazol, a new antibiotic interfering with respiration. Antimicrob Agents Chemother 19:504–507

    PubMed  Google Scholar 

  • Thierbach G, Reichenbach H (1981b) Myxothiazol, a new inhibitor of the cytochrome b-c 1segment of the respiratory chain. Biochim Biophys Acta 638:282–289

    PubMed  Google Scholar 

  • Thierbach G, Michaelis G (1982) Mitochondrial and nuclear myxothiazol resistance in Saccharomyces cerevisiae. Mol Gen Genet 186:501–506

    PubMed  Google Scholar 

  • Trowitzsch W, Reifenstahl G, Wray V, Gerth K (1980) Myxothiazol, an antibiotic from Myxococcus fulvus (Myxobacterales). II. Structure elucidation. J Antibiotics 33:1480–1490

    Google Scholar 

  • Van Verseveld HW, Stouthamer AH (1978) Electron-transport chain and coupled oxidative phosphorylation in methanol-grown Paracoccus denitrificans. Arch Microbiol 118:13–20

    PubMed  Google Scholar 

  • Vignais PM, Henry MF, Sim E, Kell DB (1981) The electron transport system and hydrogenase of Paracoccus denitrificans. Curr Top Bioenerg 12:115–196

    Google Scholar 

  • Willison JC, John P (1979) Mutants of Paracoccus dentrificans deficient in c-type cytochromes. J Gen Microbiol 115:443–450

    Google Scholar 

  • Willison JC, Haddock BA, Boxer DH (1981) A mutant of Paracoccus denitrificans deficient in cytochrome a+a 3. FEMS Microbiol Lett 10:249–255

    Google Scholar 

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Article No. 12 on antibiotics from gliding bacteria. For article No. 11 see: G. Thierbach and G. Michaelis, Mol Gen Genet 1986:501–506, 1982

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Thierbach, G., Reichenbach, H. The effect of the new antibiotic myxothiazol on the respiration of Paracoccus denitrificans . Arch. Microbiol. 134, 104–107 (1983). https://doi.org/10.1007/BF00407940

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  • DOI: https://doi.org/10.1007/BF00407940

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