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8, 603 (1969). 14 B. H. Davies, D. Jones and T. W. Goodwin, Biochem. J. 87, 326 (1963). 15 T. W. Goodwin, Biochem. J. 50, 550 (1952). 16 T. W. Goodwin, M. Jamikorn and J. S. Willmer, Biochem. J. 53, 531 (1953). 17 B. H. Davies, J. Villoutreix, R. J. H. Williams and T. W. Goodwin, Biochem. J. 89, 96P (1963). 18 R. J. H. Williams, B. H. Davies and T. W. Goodwin, Phytochem. 4, 79 (1965). 19 T. W. Goodwin and R. J. H. Williams, Biochem. J. 94, 5c (1965). 20 G. Meissner and M. Delbrück, Plant Physiol.
The pheno menon of the induction period is far from being clearly understood; there is no one unambiguous explanation. One plausible hypothesis considers the above mentioned facts as 'tails' of the processes of super-rapid interconversions of carotenoids observed by different authors 30-32 . Summing up all the facts known about the time dependence of the violaxathin-cycle reactions, we can say that it is a very complex function, its complexity being based on the fact that what we observe in our experiments may be a result of several different reactions with different velocity constants.
Nicotine inhibition of carotenoid biosynthesis in Rhodomicrobrium vannielii RECENT STUDIES OF CAROTENOID BIOSYNTHESIS IN BACTERIA J. C. B. McDERMOTT ET AL lycopene content at the expense of the total of other carotenoids also suggests that lycopene is the likely precursor of all the other carotenoids normally present in Rhodomicrobium vannielii. It is interesting that lycopene is apparently the key intermediate in carotenoid biosynthesis in Rhodomicrobium vannielii, whereas neurosporene is the key compound in the case of Rhodopseudomonas spheroides.