Association of NADP- and NAD-linked malic enzyme activities in Zea mays: Relation to C4 pathway photosynthesis

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Abstract

Two of the three metabolic subtypes of species utilizing C4-pathway photosynthesis are defined by high activities of either NADP malic enzyme (NADP malic enzyme type) or a coenzyme A (CoA)- and acetyl-CoA-activated NAD malic enzyme (NAD malic enzyme type). These enzymes function to decarboxylate malate as an integral part of the photosynthetic process. Leaves of NADP malic enzyme-type species also contain significant NAD-dependent malic enzyme activity. The purpose of the present study was to examine the nature and photosynthetic role of this activity. With Zea mays, this NAD-dependent activity was found to vary widely in fresh leaf extracts. Incubating extracts at 25 °C resulted in a disproportionate increase in NAD activity so that the final ratio of NADP to NAD activity was always about 5. Strong evidence was provided that the NADP and NAD malic enzyme activities in Z. mays extracts were catalyzed by the same enzyme. These activities remained associated during purification and were coincident after polyacrylamide gel electrophoresis. The pH optimum for NAD-dependent activity was about 7.1, compared with 8.3 for NADP malic enzyme activity. Other properties of the NAD-dependent activity are described, a particularly notable feature being the inhibition of this activity by less than 1 μm NADP and NADPH. Evidence is provided that the NADP malic enzyme of several other NADP malic enzyme-type C4 species also has associated activity toward NAD. We concluded that the NAD-dependent malic enzyme activity would have no significant function in photosynthesis.

References (17)

  • M.D. Hatch et al.

    Arch. Biochem. Biophys

    (1973)
  • C.K.M. Rathnam et al.

    Arch. Biochem. Biophys

    (1975)
  • M.D. Hatch et al.

    Arch. Biochem. Biophys

    (1974)
  • T. Kagawa et al.

    Arch. Biochem. Biophys

    (1975)
  • D.D. Davies et al.

    Phytochemistry

    (1974)
  • I. Ziegler

    Biochim. Biophys. Acta

    (1974)
  • T. Nishikido et al.

    Biochem. Biophys. Res. Commun

    (1974)
  • U. Heber et al.

    Biochim. Biophys. Acta

    (1965)
There are more references available in the full text version of this article.

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