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Biomedical subjects

J B Callis

Publications and source records attributed to J B Callis.

16 recordsLinked to original sources
PubMed1994

In vivo imaging of the interior of Tradescantia zebrina leaves by optical cross-correlation interferometry.

Using optical correlation interferometry, a novel method for plant sciences, we in imaged in vivo the z-direction, perpendicular to the leaf surface, through Tradescantia zebrina leaves. Non-invasively we determined number of major cell layers, followed the time sequence of decrease in cell z-axis after exposure of tissues to high salt, and observed disruption of cells caused by freezing and thawing.

Interferometry↗
PubMed1990

Noninvasive method for monitoring ethanol in fermentation processes using fiber-optic near-infrared spectroscopy.

Short-wavelength near-infrared (SW-near-IR) spectroscopy (700-1100 nm) is used for the determination of ethanol during the time course of a fermentation. Measurements are performed noninvasively by means of a photodiode array spectrometer equipped with a fiber-optic probe placed on the outside of the glass-wall fermentation vessel. Pure ethanol/water and ethanol/yeast/water mixtures are studied to establish the spectral features that characterize ethanol and to show that determination of ethanol is independent of the yeast concentration. Analysis of the second-derivative data is accomplished with multilinear regression (MLR). The standard error of prediction (SEP) of ethanol in ethanol/water solutions is approximately 0.2% over a range of 0-15%; the SEP of ethanol in ethanol/yeast/water solutions is 0.27% (w/w). Results from the mixture experiments are then applied to actual yeast fermentations of glucose to ethanol. By use of a gas chromatographic method for validation, a good correlation is found between the intensity of backscattered light at 905 nm and the actual ethanol. Additional experiments show that a calibration model created for one fermentation can be used to predict ethanol production during the time course of others with a prediction error of 0.4%.

Ethanol↗
PubMed1989

Observation of individual DNA molecules undergoing gel electrophoresis.

Individual DNA molecules undergoing agarose gel electrophoresis were viewed with the aid of a fluorescence microscope. Molecular shape and orientation were studied in both steady and pulsed electric fields. It was observed that (i) DNA macromolecules advanced lengthwise through the gel in an extended configuration, (ii) the molecules alternately contracted and lengthened as they moved, (iii) the molecules often became hooked around obstacles in a U-shape for extended periods, and (iv) the molecules displayed elasticity as they extended from both ends at once. A computer model has been developed that simulates the migration of the molecules in a rotating-field gel electrophoresis experiment.

Computer Simulation↗
PubMed1981

Flow-cytogenetics. II. High-resolution ploidy measurements in human fibroblast cultures.

high-resolution flow-cytometric measurements of ethidium bromide/mithramycin-stained human fibroblast cultures reveal discrepancies between fluorescence pulse-height distributions and genome size as a function of cell strain, culture conditions, culture age, and proliferative stage. These discrepancies were quantitatively assessed by (1) evaluation of the variation of the widths of the 2c fluorescence pulse-height histogram peaks, (2) comparisons between sample to standard fluorescence ratios of 45,XO and 49,XXXXY cell strains, and (3) comparison of fluorescence intensities among cell populations of identical genome size but differing degrees of chromatin condensation (mitotic vs. nonmitotic cells of diploid and tetraploid cell strains). As in our previous studies with lymphocytes, our results suggest caution in equating fluorescence intensity with "DNA content" in flow measurements of nonhomogeneous cell populations. Conditions of cell culture and sample preparation must be standardized in order to compare "DNA content" differences by flow techniques. Remaining sources of variation presently limit detection to differences in DNA content of greater than 2%.

Cell Line↗
PubMed1979

No evidence for chromosomal mosaicism in multiple tissues of 10 patients with 45, XO Turner syndrome.

Why the frequency of spontaneous abortions among monosomy X conceptuses is 98% while the postnatal course of Turner syndrome is relatively benign has not been understood. One explanation could be that mosaicism for a euploid cell line confers viability and that those 2% of 45,XO zygotes surviving in utero have some degree of mosaicism. We thus reasoned that if the non-mosaic 45,XO karyotype is lethal, a thorough study of living Turner syndrome patients might reveal a much higher frequency of mosaicism than the 30--40% reported. Ten adult women with a 45,XO leukocyte karyotype were investigated, looking at five tissue types from all three germ layers: buccal mucosa and hair from ectoderm, urinary epithelium from endoderm and ectoderm, and lymphocytes and skin fibroblasts from mesoderm. We were unable to confirm mosaicism in these patients, although in 2 out of 10 there was the suggestion of a small percentage of euploid cells in skin and blood karyotypes.

Abortion, Spontaneous↗
PubMed1976

Multicomponent analysis in clinical chemistry by use of rapid scanning fluorescence spectroscopy.

To be useful in the clinical laboratory, multicomponent fluorescence analysis requires both the rapid measurement of the fluorescence intensity at a variety of excitation and emission wavelengths and the unambiguous reduction of the data by efficient algorithms. The Video Fluorometer, which exploits the multi-channel capability of a low-light-level television sensor to simultaneously acquire excitation and emission spectra, can meet the first requirement. For example, a complete set of emission and excitation spectra for perylene can be obtained in less than 2 s at concentrations of 10(-10) mol/liter. To meet the second need, we present two types of data-reduction strategies: (a)a least-squares fit to the data, with use of the spectra of previously determined compounds likely to be present; and (b)a determination of the eigenvalues and eigenvectors fo the fluorescence matrix, from which the number of components and the possible spectra of each can be estimated. Computer simulations of the least-squares fitting algorithms show that five strongly overlapping components can be determined in the presence of noise with an accuracy of better than 5%. Also, a fluorescent sample containing two species with very similar but unknown spectral properties can be resolved to obtain the spectrum of each.

Anthracenes↗