Magnetic field dependence of radical-pair decay kinetics and molecular triplet quantum yield in quinone-depleted reaction centers

Radical-pair decay kinetics and molecular triplet quantum yields at various magnetic fields are reported for quinone-depleted reaction centers from the photosynthetic bacterium Rhodopseudomonas sphaeroides R26. The radical-pair decay is observed by picosecond absorption spectroscopy to be a single exponential to within the experimental uncertainty at all fields. The decay time increases from 13 ns at zero field to 17 ns at 1 kG, and decreases to 9 ns at 50 kG. The orientation averaged quantum yield of formation of the molecular triplet of the primary electron donor, ³P, drops to 47% of its zero-field value at 1 kG and rises to 126% at 50 kG. Combined analysis of these data gives a singlet radical-pair decay rate constant of 5 · 10⁷s^?1, a lower limit for the triplet radical-pair decay rate constant of 1 · 10⁸s^?1 and a lower limit for the quantum yield of radical-pair decay by the triplet channel of 38% at zero field. The upper limit of the quantum yield of ³P formation at zero field is measured to be 32%. In order to explain this apparent discrepancy, decay of the radical pair by the triplet channel must lead to some rapid ground state formation as well as some ³P formation. It is proposed that the triplet radical pair decays to a triplet charge-transfer state which is strongly coupled to the ground state by spin-orbit interactions. Several possibilities for this charge-transfer state are discussed.     

Cell and cubitus interruptus dominant: two segment polarity genes on the fourth chromosome in Drosophila

The cubitus interruptus Dominant 4-O [ciD] locus is a member of a class of genes required for the proper formation of the repeating segmental pattern of the embryo. We have found a second locus on the fourth chromosome, Cell (Ce), which is also required for proper segmentation. Mutations in Ce cause the elimination of the posterior half and anterior margin of each segment. The complementation pattern of ciD and Ce alleles is complicated; certain alleles complement fully while others do not. We have isolated a series of translocations which have breakpoints within the ciD gene. These mutations also disrupt Ce2 function, indicating that ciD and Ce2 are intimately associated. We have also studied the maternal contribution of the wild-type gene product of the ciD and Ce genes by pole cell transplants. These experiments suggest that there is no maternal contribution of the ciD+ and Ce+ gene products, and that they are not required for oogenesis. Thus, it appears that the ciD and Ce loci may represent a gene complex that is activated during zygotic development and is required for the proper formation of segments.