Color perception and the limits of color constancy

Summary A summary of colorimetry is given and the limits of color constancy mechanism under changing illuminations are discussed.     

A new locus (leuK) affecting the regulation of branched-chain amino acid, histidine, and tryptophan biosynthetic enzymes.

A locus (leuK) affecting regulation of the leucine operon was selected by isolating a spontaneous Ara+ derivative of an Escherichia coli B/r strain carrying an ara-leu fusion in which the arabinose operon is under leucine control. Genetic analyses by P1 transduction demonstrated that the lesion is located to the right of the galactose operon. Regulation of the biosynthetic enzymes for leucine, isoleucine-valine, histidine, and tryptophan was altered in a strain carrying leuK16. High-level gene expression in the heterozygous merodiploid strain F' leuK+/leuK16) demonstrated the dominance of the mutant allele to the wild-type allele. No apparent effect was observed in the mutant on N-acetylornithinase, a biosynthetic enzyme in the arginine pathway, nor on any of the 18 aminoacyl-tRNA synthetases examined. However, compared with that of the parent strain, the extent of the charging of leucyl-, isoleucyl-, valyl-, histidyl-, and arginyl-tRNA was decreased in the mutant.     

Contributions to the theory of invariance of color under the condition of varying illumination

Any visual-processing algorithm aimed at attaining color constancy will in fact attain it only for restricted spectral classes of illuminants and reflectances. These classes constitute implicit heuristics for the physical world, in an artificial-intelligence sense. In the present work, physically reasonable spectral classes are presented which insure that von Kries's law of chromatic adaptation will — in its simplest form — restore object colors in human tristimulus space to illuminant-invariant positions in the space. Algebraic functions of the adapted tristimulus values are presented which are illuminant-invariant for some departures from the spectral heuristics. These functions, a hierarchy of invariants, may be useful in developing lighting and pigment standards for partially controlled viewing environments.     

Quantitation of fluorescence fading phenomena for identifying intracellular biopolymers.

The fading behavior of the 670 nm fluorescence emission band produced by unfixed rat mast cells stained with acridine orange (AO) has been found to be in excellent agreement with the behavior predicted by second order chemical kinetics. The reciprocal of fluorescence intensity plotted against time yields a straight line. When due account is taken of dye/cell ratio and the intensity of fluorescence-exciting radiation, Io (measured with the standard phosphor particle), the slope of this straight line is a constant, k', which is independent of dye/cell ratio and Io. k' differs from the second order photochemical rate constant by a constant factor. The fading of a given AO-biopolymer complex is described by a particular value of k'. Two values of k' have been found for rat mast cell granules, indicating the presence of two different AO-biopolymer complexes. Fading of fluorescence may serve to identify particular intracellular biopolymers in individual cells even when present in a heterogeneous population.     

Nutritional and physiological factors affecting germination of heterothallic Saccharomyces cerevisiae ascospores.

Saccharomyces cerevisiae strain AP-3 was examined with respect to those nutritional requirements and physiological conditions which influence its germination rate. It was found that glucose as a carbon source supported the most rapid rate of germination for this heterothallic strain. In contrast, strain AP-3 spore germination was supported the least by the carbon sources potassium acetate and lactose. Of the nitrogen sources tested in culture medium containing glucose, the complex nitrogen sources peptone and casein hydrolysate appeared to be capable of stimulating germination better than a control culture containing ammonium sulphate. None of the amino acids screened were found to stimulate strain AP-3 germination compared with ammonium sulphate. The optimal culture medium pH for ascospore germination was 4.5 although spore germination could still be initiated by glucose between pH 3.0 and pH 7.5. Germination initiation by glucose was observed over a temperature range from 25 degrees C to 50 degrees C, but the optimal temperature appeared to be 40 degrees C.     

Functional modulation of brain sodium channels by cAMP-dependent phosphorylation.

Voltage-gated Na+ channels, which are responsible for the generation of action potentials in brain, are phosphorylated by cAMP-dependent protein kinase in vitro and in intact neurons. Phosphorylation by cAMP-dependent protein kinase reduces peak Na+ currents 40%--50% in membrane patches excised from rat brain neurons or from CHO cells expressing type IIA Na+ channels. Inhibition of basal cAMP-dependent protein kinase activity by transfection with a plasmid encoding a dominant negative mutant regulatory subunit increases Na+ channel number and activity, indicating that even the basal level of kinase activity is sufficient to reduce Na+ channel activity significantly. Na+ currents in membrane patches from kinase-deficient cells were reduced up to 80% by phosphorylation by cAMP-dependent protein kinase. These effects could be blocked by a specific peptide inhibitor of cAMP-dependent protein kinase and reversed by phosphoprotein phosphatases. Convergent modulation of brain Na+ channels by neurotransmitters acting through the cAMP and protein kinase C signaling pathways may result in associative regulation of electrical activity by different synaptic inputs.     

Repression of cytosine deaminase by pyrimidines in Salmonella typhimurium.

The synthesis of cytosine deaminase in Salmonella typhimurium is repressed by pyrimidines. This repression is mediated by both a uridine and a cytidine compound, indicating a distinct difference in the regulation of synthesis of cytosine deaminase from the regulation of the de novo pyrimidine pathway enzymes. A salvage role for the enzyme in pyrimidine metabolism is postulated.     

Protein synthesis and degradation in cultured muscle is altered by a phorbol diester tumor promoter

The tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) was observed to influence the relative rates of synthesis and degradation of several polypeptides in cultured chick embryo myotubes. The direction of influence partially correlated with whether the polypeptide was uniquely expressed in myotubes or also expressed in its proliferating precursors. The synthesis of all but one of the eight myotube-unique polypeptides examined was inhibited and the degradation of all but two was stimulated. The exceptions were intermediate filament subunits. In contrast, the metabolism of several non-myotube-unique polypeptides was either unaffected or influenced in the opposite direction. A method involving saturation of the intracellular leucine precursor pool with extracellular radioactive leucine suggested that the absolute rate of protein synthesis was only minimally, if at all, affected by the promoter. The effects on protein synthesis were at least partially reversible following removal of the promoter. The changes in synthesis and degradation did not reflect normal maturational changes in cultured myotubes and thus they appeared to be induced by TPA. The data suggest that under some circumstances the rates of synthesis and degradation of several proteins are inversely coupled in the myotube. They also provide a partial explanation for earlier ultrastructural observations that TPA caused a loss of myofilaments and an accumulation of intermediate filaments. Since myotubes occupy the G₁ (or G₀) stage of the cell cycle, and the DNA content of the cultures was not affected by TPA, TPA's effects were not mediated through cell cycle-dependent mechanisms.