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Formation of NADPH-nitrate reductase activity in vitro from Aspergillus nidulans niaD and cnx mutants

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Summary

Mutants of A. nidulans at several loci lack detectable NADPH-nitrate reductase activity. These loci include niaD, the structural gene for the nitrate reductase polypeptide, and five other loci termed cnxABC, E, F, G and H which are presumed to be involved in the formation of a molybdenum-containing component (MCC) necessary for nitrate reductase activity. When frozen mycelia from A. nidulans deletion mutant niaD26 were homogenized in a Ten Broeck homogenizer together with frozen mycelia from either enzA6, cnxE29, cnxF12, enxG4 or cnxH3 strains grown on urea+nitrate as the nitrogen source, nitrate reductase activity was detectable in the extract. Similar results were obtained by co-homogenizing niaD mycelia with Neurospora crassa nit-1 mycelia induced on nitrate. Thus, all A. nidulans cnx mutants are similar to the N. crassa nit-1 strain in their capacity to yield NADPH-nitrate reductase in the presence of the presumed MCC. As judged by the amounts of nitrate reductase formed, niaD26 mycelia grown on urea±nitrate contained much more available MCC than ammonium-grown mycelia. No NADPH-nitrate reductase activity was found in extracts prepared by co-homogenizing mycelia from all five A. nidulans cnx strains. Wild-type A. nidulans NADPH-nitrate reductase acid dissociated by adjustment to pH 2.0–2.5 and re-adjusted to pH 7 could itself re-assemble to form active nitrate reductase and thus was not a sueful source of MCC for these experiments. These results are consistent with the conclusion that the active nitrate reductase complex is composed of polypeptide components which are the niaD gene product, plus the MCC which is formed through the combined action of the cnx gene products. Further, the production of MCC may be regulated in response to the nitrogen nutrition available to the organism.

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References

  • Clutterbuck, A.J., Cove, D.J.: The genetic loci of Aspergillus nidulans. In: CRC handbook of microbiology, Vol. IV (A.I. Laskin and H. Lechevalier, eds.), Cleveland, Ohio: Chemical Rubber Publishing Co. 1973

    Google Scholar 

  • Coddington, A.: Biochemical studies on the nit mutants of Neurospora crassa. Molec. gen. Genet. 145, 195–206 (1976)

    Google Scholar 

  • Cove, D.J.: The induction and repression of nitrate reductase in the fungus Aspergillus nidulans. Biochim. biophys. Acta (Amst.) 113, 51–56 (1966)

    Google Scholar 

  • Cove, D.J.: Control of gene action in Aspergillus nidulans. Proc. roy. Soc. B 176, 267–275 (1970)

    Google Scholar 

  • Cove, D.J.: The control of catabolism in Aspergillus nidulans. In: Second International Symposium on the Genetics of Industrial Microorganisms (K.D. McDonald, ed.)., London: Academic Press, Ltd. 1976a

    Google Scholar 

  • Cove, D.J.: Chlorate toxicity in Aspergillus nidulans. Studies of mutants altered in nitrate assimilation. Molec. gen. Genet. 146, 147–159 (1976b)

    Google Scholar 

  • Cove, D.J., Pateman, J.A.: Independently segregating genetic loci concerned with nitrate reductase activity in Aspergillus nidulans. Nature (Lond.) 198, 262–263 (1963)

    Google Scholar 

  • Cove, D.J., Pateman, J.A.: Autoregulation of the synthesis of nitrate reductase in Aspergillus nidulans. J. Bact. 97, 1374–1378 (1969)

    Google Scholar 

  • Downey, R.J.: The multimeric nature of NADPH-nitrate reductase from Aspergillus nidulans. Microbios 7, 53–60 (1973)

    Google Scholar 

  • Downey, R.J., Focht, W.J.: Subunit character of the NADPH-nitrate reductase from Aspergillus nidulans. Microbios 11A, 61–70 (1974)

    Google Scholar 

  • Garrett, R.H.: The induction of nitrate reductase in Neurospora crassa. Biochim. biophys. Acta (Amst.) 264, 481–489 (1972)

    Google Scholar 

  • Garrett, R.H., Nason, A.: Involvement of a b-type cytochrome in the assimilatory nitrate reductase of Neurospora crassa. Proc. nat. Acad. Sci. (Wash.) 58, 1603–1610 (1967)

    Google Scholar 

  • Garrett, R.H. Nason, A.: Further purification and properties of Neurospora nitrate reductase. J. biol. Chem. 244, 2870–2882 (1969)

    Google Scholar 

  • Garrett, R.H. Cove, D.J.: In vitro formation of NADPH-nitrate reductase activity from Aspergillus nidulans niaD and cnx mutants. Amer. Soc. Microbiol. Conf. on Nitrification and Reduction of Nitrogen Oxides, Athens, Ga., U.S.A., 7–10 Sept., 1976

  • Ketchum, P.A.: In vitro formation of assimilatory nitrate reductase: presence of the constitutive component in bacteria. Biochem. biophys. Res. Comm. 52, 1450–1456 (1973)

    Google Scholar 

  • Ketchum, P.A. Cambier, H.Y., Frazier, W.A. III, Madansky, C.H., Nason, A.: In vitro assembly of Neurospora assimilatory nitrate reductase from protein subunits of a Neurospora mutant and the xanthine oxidizing or aldehyde oxidase systems of higher animals. Proc. nat. Acad. Sci. (Wash.) 66, 1016–1023 (1970)

    Google Scholar 

  • Ketchum, P.A., Downey, R.J.: In vitro restoration of nitrate reductase: investigation of Aspergillus nidulans and Neurospora crassa nitrate reductase mutants. Biochim. biophys. Acta (Amst.) 385, 354–361 (1975)

    Google Scholar 

  • Layne, E.: Spectrophotometric and turbidometric methods for measuring proteins. In: Methods in enzymology, Vol. III (S.P.Colowick and N.O. Kaplan, eds.). New York: Academic Press, Inc. 1957

    Google Scholar 

  • Lee, K.-Y., Pan, S.-S., Erickson, R., and Nason, A.: Involvement of molybdenum and iron in the in vitro assembly of assimilatory nitrate reductase utilizing Neurospora mutant nit-1. J. biol. Chem. 249, 3941–3952 (1974)

    Google Scholar 

  • MacDonald, D.W., Cove, D.J.: Studies on temperature-sensitive mutations affecting the assimilatory nitrate reductase of Aspergillus nidulans. Europ. J. Biochem. 47, 107–110 (1974)

    Google Scholar 

  • MacDonald, D.W., Cove, D.J., Coddington, A.: Cytochrome-c reductases from wild-type and mutant strains of Aspergillus nidulans Molec. gen. Genet. 128, 187–199 (1974)

    Google Scholar 

  • MacDonald, D.W., Cove, D.J., Coddington A.: Cytochrome-c reductases from wild-type and mutant strains of Aspergillus nidulans. Molec. gen. Genet. 128, 187–199 (1970)

    Google Scholar 

  • Nason, A., Antoine, A.D., Ketchum, P.A., Frazier, W.A., III, Lee, D.K.: Formation of assimilatory nitrate reductase by in vitro inter-cistronic complementation in Neurospora crassa. Proc. nat. Acad. Sci. (Wash.) 65, 133–144 (1970)

    Google Scholar 

  • Nason, A., Lee, K.-Y., Pan, S.-S., Ketchum, P.A., Lambert, A., De Vries, J.: In vitro formation of assimilatory reduced nicotinamide adenine dinucleotide phosphate: nitrate reductase from a Neurospora mutant and a component of molybdenumenzymes. Proc. nat. Acad. Sci. (Wash.) 68, 3242–3246 (1971)

    Google Scholar 

  • Pan, S.-S., Nason, A.: Further characterization of purified assimilatory NADPH: nitrate reductase from Neurospora crassa. Proc. Fed. Amer. Soc. exptl. Biol. 35, 1530 (1976)

    Google Scholar 

  • Pateman, J.A., Cove, D.J., Rever, B.M., Roberts, D.B.: A common co-factor for nitrate reductase and xanthine dehydrogenase which also regulates the synthesis of nitrate reductase. Nature (Lond.) 201, 58–60 (1964)

    Google Scholar 

  • Pateman, J.A., Rever, B.M., Cove, D.J.: Genetic and biochemical studies of nitrate reduction in Aspergillus nidulans. Biochem. J. 104, 103–111 (1967)

    Google Scholar 

  • Rucklidge, G., Notton, B., Hewitt, E.: Reconstitution in vitro of nitrate reductase from apoprotein of molybdenum-deficient spinach. Biochem. Soc. Trans. 4, 77–80 (1976)

    Google Scholar 

  • Scazzocchio, C.: The genetic control of molybdoflavoproteins in Aspergillus nidulans. Use of the NADPH-dehydrogenase activity associated with xanthine-dehydrogenase to investigate substrate and product induction. Molec. gen. Genet. 125, 147–155 (1973)

    Google Scholar 

  • Scazzocchio, C.: The genetic determination of molybdoflavoenzymes in Aspergillus nidulans. J. Less-Common Metals 36, 461–464 (1974)

    Google Scholar 

  • Scazzocchio, C., Holl, F.B., Foguelman, A.I.: The genetic control of molybdoflavoproteins in Aspergillus nidulans. Allopurinolresistant mutants constituitive for xanthine-dehydrogenase. Europ. J. Biochem. 36, 428–445 (1973)

    Google Scholar 

  • Solomonson, L.P., Lorimer, G.H., Hall, R.L., Borchers, R., Bailey, J.L.: Reduced nicotinamide adenine dinucleotide-nitrate reductase of Chlorella vulgaris. Purification, prosthetic groups, and molecular properties. J. biol. Chem. 250, 4120–4127 (1975)

    Google Scholar 

  • Sorger, G.J.: Nitrate reductase electron transport systems in mutant and in wild-type strains of Neurospora. Biochim. biophys. Acta (Amst.) 118, 484–494 (1966)

    Google Scholar 

  • Vega, J.M., Greenbaum, P., Garrett, R.H.: Studies on the in vitro inactivation of the Neurospora crassa assimilatory nitrite reductase in the presence of reduced pyridine nucleotides plus flavin. Biochim. biophys. Acta (Amst.) 377, 251–257 (1975)

    Google Scholar 

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Communicated by W. Gajewski

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Garrett, R.H., Cove, D.J. Formation of NADPH-nitrate reductase activity in vitro from Aspergillus nidulans niaD and cnx mutants. Molec. gen. Genet. 149, 179–186 (1976). https://doi.org/10.1007/BF00332887

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