1. Using intact cells of
Chlorella, which had been pretreated with sodium azide (10
-4M to inhibit the activity of catalase, investigations were made-by the “pre-illumination” experiments using C
14O
2 according to Calvin and Benson-on the effect of H
2O
2, upon the photogenic capacity (reduc-ing agent) for CO
2-fixation.
2. It was demonstrated that the level of the C
14O
2-fixing capacity was markedly lowered in the presence of H
2O
2), indicating that the reducing agent was oxidized by H
2O
2. Based on the fact that the same oxidizing effect has been observed with oxygen and quinone, it was inferred that H
2O
2 shares with oxygen and quinone the property of acting as a Hi11 oxidant. The reactivity of these oxidants towards the reducing agent in question was found to be in the order:
quinone<H
2O
2<O
2.
Along the line of reasoning developed in a previous work it was discussed that (i) H
2O
2, is formed in green cells as a result of reaction of O
2, with the reducing agent; that (ii) in normal cells the H
2O
2 thus formed is immediately decomposed by catalase, and that (iii) the inhibitory effect of cyanide upon photosynthesis is due to the inhibition of catalase leading to the accumulation of H
2O
2 which consumes the reducing agent that plays the key role in reducing phosphoglyceric acid to triosephosphate in the mechanism of photosynthesis.
This study was aided by grants from the Nishina Memorial Foundation, the Rockefeller Foundation, and the Ministry of Education. To these bodies we extend our grateful thanks.
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