Fat metabolism in higher plants: Properties of a soluble stearyl-acyl carrier protein desaturase from maturing Carthamus tinctorius,☆☆

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Abstract

A soluble extract from maturing safflower seeds (Carthamus tinctorius) synthesized [14C]oleic acid from [14C]malonate, or [14C]stearyl-acyl carrier protein. Stearyl-acyl carrier protein was generated from [14C]malonate by the seed extract. The desaturase had only a trace of activity when stearyl-CoA was the substrate. The stearyl-acyl carrier protein desaturase had a specific requirement for ferredoxin which was only partially replaced by flavodoxin. While NADPH was an effective reductant, NADH was ineffective. However, the most effective reductant was a system composed of ferredoxin, grana lamellae, ascorbic acid, dichlorophenolindophenol, and light. No NADPH requirement was observed when this reducing system was employed. Stearylacyl carrier protein desaturase activity was enhanced by dithiothreitol and reduced glutathione, but was partially inhibited by β-mercaptoethanol. The desaturase activity was inhibited by 1 mm potassium cyanide but insensitive to carbon monoxide. No lipid micelle requirement could be demonstrated.

References (27)

  • D.K. Bloomfield et al.

    J. Biol. Chem

    (1960)
  • J.B. Marsh et al.

    Biochim. Biophys. Acta

    (1962)
  • J. Nagai et al.

    J. Biol. Chem

    (1968)
  • V. McMahon et al.

    Biochim. Biophys. Acta

    (1964)
  • I.K. Vijay et al.

    J. Biol. Chem

    (1971)
  • I.K. Vijay et al.

    J. Biol. Chem

    (1972)
  • C.H. Birge et al.

    Biochem. Biophys. Res. Commun

    (1967)
  • J. Jaworski et al.

    Arch. Biochem. Biophys

    (1974)
  • L.E. Mortenson

    Biochim. Biophys. Acta

    (1964)
  • W.R. Morrison et al.

    J. Lipid Res

    (1964)
  • P. Harris et al.

    Biochim. Biophys. Acta

    (1969)
  • N. Oshino et al.

    Biochim. Biophys. Acta

    (1966)
  • N. Baker et al.

    Eur. J. Biochem

    (1971)
  • Cited by (0)

    This is paper LIX in a series. Paper LVIII is the preceding paper (Arch. Biochem. Biophys., 161, 147–157, 1974). Paper LX is the following paper (Arch. Biochem. Biophys., 161, 166–173, 1974).

    ☆☆

    Suported in part by NIH Grant GM 19213-01.

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