Abstract
An enzymic build-up of an antisporulant during a wet light period and its enzymic decay over a dry dark period may explain the inhibitory effect of light upon sporulation and its reversal by darkness. Fluorescent blue light of relatively low photon flux density (3.7 .mu.E [einstein] m-2 s-1) inhibited sporulation by 99% at 20.degree. C. Light level and temperature during the sporulation period determined spore yield of the pathogen: at high temperatures (in the range 8-24.degree. C) sporulation was inhibited at low light level, while no inhibition occurred at much higher light levels at low temperatures. Preceding dry dark treatments given at 20.degree. C considerably diminished the inhibitory effect of light, but not if given at 10.degree. C. The diffusion of an inhibitory compound from irradiated to unirradiated areas of detached leaves was demonstrated. The continuing photosynthetic activity of the host in the light at 20.degree. C and the lack of sucrose following dark periods at 10.degree. C were not associated with the inhibitory effect of light. The similarity between the role of light in the present system and the role of light in activation and decay of phenylalanine ammonia-lyase is discussed.

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