The Effect of the Plant Growth Retardants Amo 1618 and CCC on Gibberellin Production in Fusarium monili‐forme: Light Stimulated Biosynthesis of Gibberellins

Through the use of a single gene dwarf mutant of Zea mays L., dwarf‐1, the interaction of growth retardants with gibberellin biosynthesis was studied in Fusarium monitiforme . It was demonstrated that the growth retardants 2‐isopropyl‐4‐dimcthylamine‐5‐methyphenyl‐1‐piperidine‐cai'boxylate methyl chloride (Amo 1618) and (2‐chloroethyl) trimethylammonium chloride (CCC) are more effective inhibitors of gibberellin biosynthesis in cultures maintained under continuous illumination. Light grown cultures produced significantly more biologically active gibberellin‐like materials than dark grown cultures. Stock cultures exposed to light also promoted the subsequent biosynthesis of gibberellins in the dark. Chromatographical analysis of the soluble gibberellins extracted from the culture medium revealed that large amounts of chromatographically detectable A 3 and A 7 were produced in light cultures with only A 7 produced in the dark. Light also induced a greater incorporation of acelate‐2‐ 14 C into the gibberellins A 7 , A 3 and an unidentified gibberellin. Growth returdants occasionally caused a complete disappearance of chromatographically detectable gibberellins in the dark; however, in the light at no concentration tested was it possible to detect the complete disappearance of gibberellin‐like material. A 3 was always detectable. Like higher plants, different strains of F. moniliforme exhibit variation which makes them more or less sensitive to the growth retardants. This variation is interpreted to mean that there may be more than one pathway leading to the synthesis of the gibberellins.