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Biomedical subjects

S Aronoff

Publications and source records attributed to S Aronoff.

At least 37 records · Page 2Linked to original sources

Boron in plants: a biochemical role.

Boron, as borate, appears to have a role in partitioning metabolism between the glycolytic and pentose-shunt pathways. This effect results from the association of borate with 6-phosphogluconic acid, forming a virtual substrate that inhibits the action of 6-phosphogluconate dehydrogenase. In the absence of borate, the inhibition of the enzyme is released, and excess phenolic acids are formed. These acids also associate strongly with borate and thus develop an autocatalytic system for production of excess phenolic acids which cause necrosis of tissue and eventual death of the plant.

Borates↗

Investigations on the Role of Boron in Plants III. Anatomical Observations.

Electron microscopic examination of leaf mesophyll cells of boron-deficient sunflower plant reveals that chloroplasts degenerate and cell walls undergo profound structural changes before any visual deficiency symptoms become apparent. Mitochondria, which increase in number as deficiency develops, frequently show myeline figures, while nuclei may develop dense rhombohedral structures.

Journal Article↗

Photosynthate transport using tritiated water.

The exchange of HTO with aerial portions of the soybean was studied under a variety of conditions. When fed to a lone leaf or leaflet in a saturated air atmosphere (all other leaves and the growing point having been excised), the HTO profile virtually ceases at a distance of 2 cm from the feeding chamber in the photosynthetic plant, but is greater and more extensive in the unilluminated plant. The differences are accentuated when roots are excised. Under these latter conditions the photosynthetic T-fixed gradient virtually disappears.HTO was exchanged with darkened petioles. When the rest of the shoot was kept in the light (the leaf being in a saturated H(2)O-vapor atmosphere) atmosphere) almost half the activity moves acropetally, and under these conditions (35 min, room temp) over 8% may be found in the leaf. Approximately one-tenth moves basipetally, with none being found in the stem. When the leaf is dark, no movement occurs out of the petiolar feeding chamber.An attempt was made to distinguish between sucrose transport by diffusion and mass flow of water by means of 2 mathematical models. In Model I, self-diffusion of HTO, Fick's Law was used, with the water and photosynthate moving independently. Model I consisted of an equilibrated, single pool of constant specific activity, generating a radioactive profile as a result of self-diffusion. In Model II, mass flow, water exchanged freely between the phloem and the surrounding tissues. The conducting bundle, 7790 micron(2), (0.25% of the total cross-section) was an average phloem. The numerical solution for the second model was obtained by Fortran programming on a digital computer and compared with experimental data. Comparison of these models with the experimental results suggest that mass flow is not a dominant process in soybean photosynthate translocation.

Journal Article↗

Apetiolar photosynthate translocation.

Apetiolar transport of photosynthate (-14)C has been studied by feeding of (14)CO(2) to soybean petioles. Translocation occurs in the absence of leaves, but both the rate and velocity are diminished. The effect of root excision is not as profound as that of leaves. It appears, in some instances, to inhibit transport partially, so that accumulation of photosynthate develops, giving a steeper isotopic gradient. The effect of leaf darkening is to diminish its uptake of photosynthate from the petiole, possibly as a result of decreased transpiration in the lowered temperature of the darkened leaf. The data suggest that neither mass flow nor active transport provide an adequate basis for normal photosynthate transport but that the leaves provide a direct force requiring structural continuity, or a translocation carrier.

Journal Article↗

Catalase: kinetics of photooxidation.

The kinetics of photooxidation of catalase is a four-step consecutive reaction, if each of the four porphyrin moieties acts independently. The rate of enzyme inactivation is a first-order reaction resulting from destruction of a single porphyrin. The kinetics of absorbancy is more complex, depending upon the absorption probabilities of each of the microspecies. With equal probabilities. the log of the sum of the normalized absorptivities is a linear function of time.

Catalase↗