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Biomedical subjects
Publications and source records attributed to J C Munday.
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The fluorescence transient of Chlorella pyrenoidosa, excited by saturating light absorbed mainly by system II, has a dip D between the peak I at 75 msec and the large peak P at 400 msec (the times depend on light intensity). This dip is observed in aerobic cells and in anaerobic cells where it is prominent. In anaerobic cells, the I-D decline is hastened almost equally by absorption of either 705 or 650 nm background light. In anaerobic cells, supplementary 700 and 710 nm light given during the transient slightly hastens and heightens P. Methyl viologen, an exogenous system I electron acceptor, eliminates P. Results suggest that system I action causes D, and that P is due to reduction of Q (fluorescence quencher) and intersystem intermediates caused by development of a block in oxidation of XH (X being the primary electron acceptor of light reaction I). Mathematical analysis suggests that if only two forms of Q participate beyond I, then system I action is required for D. If three forms participate, then the system Q --> QH --> Q' (see text) may explain D. The Malkin model (14), in its present form, does not allow D.
The fluorescence transient of Chlorella pyrenoidosa, excited by saturating blue light, has a base level O, hump I, dip D, peak P, and at 1.5 sec a quasi-steady level S (12). With 2 sec exciting exposures and 4 min dark periods, preillumination-1 (lambda >/= 690 nm, intensities 1-750 ergs/sec-cm(2) incident), replacing the dark periods, lowers I more effectively than preillumination-2 (650 nm </= lambda </= 680 nm) in both aerobic and anaerobic cells. Results indicate that the intersystem electron transport pool A as well as the primary electron acceptor of pigment system II Q (fluorescence quencher) is normally being reduced at I. Preillumination-1 lowers and delays P. Preillumination-2 (absorbed by both pigment systems) also lowers P, but delays P only at low intensity; at high intensity it hastens P. Preillumination-1 raises S while preillumination-2 lowers S. With 30 instead of 2 sec exciting light exposures, preillumination-1 causes a large S increase, and at low intensity a P increase. The S effects seem to be of a long-term nature (26-29) rather than rapid changes in the redox state of Q. As exciting light intensity increases, fluorescence yield at P increases three-fold maximally. The ratio of P (anaerobic) to O (aerobic) is 5.5. These high ratios restrict the Franck-Rosenberg model of photosynthesis (13), which is based on fluorescence yield doubling.
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