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Effect of sodium chloride and potassium chloride on growth response of yeasts Saccharomyces uvarum and Kloeckera brevis to free vitamin B6.

Acid hydrolysis is the most commonly used extraction procedure for the microbiological assay of vitamin B6 in food samples. Because NaCl or KCl is formed as a result of the extraction procedure, these 2 salts were tested as possible agents that may influence the growth response of the yeasts Saccharomyces uvarum and Kloeckera brevis. Results indicate that NaCl and KCl do effect the growth response of these 2 yeasts, depending on the salt concentration and the B6 vitamer present.

Food Microbiology↗

Mercury chloride--and methyl mercury chloride--induced inhibition in NOR activity.

Previous work has raised the question of whether mercury compounds inhibit the activity of the nucleolar organizing genes. For that reason we performed a cytophotodensitometric analysis on silver-stained interphase nuclei from human peripheral blood lymphocytes exposed to various concentrations of HgCl2 (0-150 X 10(-6) M), CH3HgCl (0-50 X 10(-6) M), and actinomycin D (0-0.1 microgram/ml). The last compound was used as a positive control. The cells were exposed to the compounds either during G1-early S phase, allowing recovery after the exposure, or from G1 until harvest; thus no recovery was allowed in this case. Like actinomycin D, both mercury compounds were shown to inhibit the NOR activity. This inhibition was furthermore more evident during the short exposure experiment. Our results do confirm that mercury compounds may, to a certain extent, influence some factors regulating the nucleolus-organizing activity.

Adult↗

The sodium and chloride dependence of chloride secretion by the opercular epithelium.

The effects of ion substitutions on the Cl- secretion rate and tissue conductance of isolated short-circuited opercular epithelia from sea-water-adapted Fundulus heteroclitus were investigated. Serosal Na+ substitution had the same effect on the Cl- secretion rate that serosal Cl- substitution had on the active component of the Cl- efflux. This similarity indicated a 1:1 Na-Cl requirement for active Cl- secretion across this epithelium, which supports the proposal of a coupled NaCl uptake mechanism at the serosal membrane of Cl- secretory epithelia. Mucosal Na+ and Cl- substitutions appeared to inhibit completely the active Cl- secretory flux. The reductions in the tissue conductance with mucosal ion substitutions suggested that this effect can be attributed to a blocking of the apical membrane Cl- conductance. These mucosal ion effects suggested a possible direct regulatory influence of the external salinity on the Cl- secretion rate and tissue conductance, which provide alternative explanations for observations with the teleost gill epithelium.

Animals↗

The role of chloride ion in photosystem II. I. Effects of chloride ion on photosystem II electron transport and on hydroxylamine inhibition.

1. Chloroplasts washed with Cl--free, low-salt media (pH 8) containing EDTA, show virtually no DCMU-insensitive silicomolybdate reduction. The activity is readily restored when 10 mM Cl- is added to the reaction mixture. Very similar results were obtained with the other Photosystem II electron acceptor 2,5-dimethylquinone (with dibromothymoquinone), with the Photosystem I electron acceptor FMN, and also with ferricyanide which accepts electrons from both photosystems. 2. Strong Cl--dependence of Hill activity was observed invariably at all pH values tested (5.5--8.3) and in chloroplasts from three different plants: spinach, tobacco and corn (mesophyll). 3. In the absence of added Cl- the functionally Cl--depleted chloroplasts are able to oxidize, through Photosystem II, artificial reductants such as catechol, diphenylcarbazide, ascorbate and H2O2 at rates which are 4--12 times faster than the rate of the residual Hill reaction. 4. The Cl--concentration dependence of Hill activity with dimethylquinone as an electron acceptor is kinetically consistent with the typical enzyme activation mechanism: E(inactive) + Cl- in equilibrium E . Cl- (active), and the apparent activation constant (0.9 mM at pH 7.2) is unchanged by chloroplast fragmentation. 5. The initial phase of the development of inhibition of water oxidation in Cl--depleted chloroplasts during the dark incubation with NH2OH (1/2 H2SO4) is 5 times slower when the incubation medium contains Cl- than when the medium contains NH2OH alone or NH2OH plus acetate ion. (Acetate is shown to be ineffective in stimulating O2 evolution).

Anions↗