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The effect of illumination on the electrical conductance of rhodopsin solutions.

An apparatus was constructed in order to record continuously and simultaneously changes in extinction and electrical conductance of rhodopsin solutions. With this apparatus, changes in electrical conductance on exposing rhodopsin to light were investigated. On illumination solutions of rhodopsin revealed a conductance change so long as they preserved their photosensitivity. The conductance change begins almost immediately upon illumination and is almost proportional to the amount of rhodopsin decomposed, continuing until rhodopsin is converted to indicator yellow. Near pH 7 the conductance is apt to increase slightly, while it decreases considerably outside the range of pH 6-9, being accompanied by a pH change towards neutrality. The conductance change is regarded as an essential property of rhodopsin, because it occurs in aqueous suspension as well as in digitonin solution; it may be caused by hydrogen or hydroxyl ions and some other conductive substances. It is also noteworthy that the petroleum ether-soluble component of the rod outer segments-presumably the lipide-tends to increase the conductance change. In suspensions of rod outer segments and retinal homogenates, the conductance increases on illumination irrespective of pH: this may be due to secondary reactions following the photic reaction of rhodopsin. We shall discuss the significance of the conductance change in relation to the initiation of visual excitation.

Electric Conductivity↗

Endogenous photosensitization in a carotenoidless mutant of Rhodopseudomonas speroides.

Endogenous photosensitization in a carotenoidless mutant of Rhodopseudomonas spheroides has been studied. When this mutant is exposed to visible light and oxygen there is a short lag period followed by exponential killing of the cells. The killing process obeys the Bunsen-Roscoe law of reciprocity and is temperature-independent. The chlorophyll content of the cells does not affect the rate of killing until a certain low threshold has been reached. Exposure of photosynthetically grown cells to air in the dark induces a temporary desensitization to the killing. A certain proportion of the population is invariably resistant to the photokilling. Evidence is presented to show that the resistance of these cells is probably a result of their abnormally low chlorophyll content. One consequence of the irradiation is the appearance of abnormally small colonies upon plating the survivors. This is interpreted in terms of a multi-hit theory. The photosensitizing pigment itself (the intracellular bacteriochlorophyll) is destroyed. The process is zero order, temperature-dependent, and does not follow the reciprocity law. It is suggested that the death of the cell results from a disruption of the cell membrane.

Chlorophyll↗

Light-induced efficiency and pigment alterations in red algae.

The low photosynthetic efficiency of chlorophyll in freshly collected red algae, can, in the case of Porphyra perforata, P. nereocystis, and Porphyridium cruentum, be increased by growing the algae for 10 days in red or blue light. Exposure to darkness or to green light maintains the algae in their originally low efficiency with respect to chlorophyll, while retaining the high efficiency of phycobilins. Red- or blue-adapted algae are rapidly reversed by exposure to green light, the chlorophyll efficiency dropping to low values again in a few hours. This is assumed to account for the action spectrum of freshly gathered plants. Some pigment changes were observed, but not in the direction of "chromatic adaptation;" and the carotenoid pigments were not activated, even by blue light, but remained as photosynthetically inactive shading filters. The higher red algae (Florideae) did not show activation of chlorophyll by red or blue light.

Chlorophyll↗

Photo-reactions in Phycomyces; growth and tropic responses to the stimulation of narrow test areas.

Sporangiophores of Phycomyces in stage IV b have been stimulated by parallel light in test areas 0.2 mm. wide. The growth responses to large stimuli are very large, owing probably to light scattered within the specimen. For medium stimuli the sensitive zone coincides with the growth response zone obtained previously and excludes the region of maximum stretch. Sustained stimulations were used to elicit tropic responses. The bends formed travel away from the sporangium at a speed equal to the growth speed. Thus they remain very close to the stimulus when this is held at a constant level relative to ground but separate from it for stimuli programmed differently. The existence of a protoplasmic structure, the "inner wall," with the following properties is postulated: it is attached to the lower, non-growing part of the sporangiophore and grows by addition above the sensitive zone. It neither stretches nor twists in the sensitive zone. It is the seat of the light receptors and gives growth and tropic responses. The cell wall follows its bends by elastic stretch.

Cytoplasm↗

Growth distribution in the light-growth response of Phycomyces.

Elongation of sporangiophores marked with numerous starch grains was photographically recorded in the steady state and during the light-growth response when the rate is more than doubled. From these records the spatial distribution of growth within the cell's growth zone was derived. Stimulation by a single saturating flash of light speeds growth proportionally in all parts of the growing zone, maintaining the same pattern of growth distribution as in the steady state. This finding implies that light is absorbed and acts locally throughout the length of the cell's growth zone. Cohen and Delbrück's proposal of a partial spatial separation of light reception and growth is discussed.

Fungi↗

Photodynamic response in bacteria.

The photodynamic lethal response of Gram negative bacteria was found to be a one event phenomenon as previously reported. However, the kinetics of the lethal response in Gram-positive microorganisms was found to be more complex. The survivor response of the latter was dividable into at least two distinct parts, each of which could be influenced by various environmental and genetic factors. Some correlation was found between sensitivity or resistance to x-ray and ultraviolet radiations and sensitivity or resistance to photodynamic action.

Bacteria↗