Modeling bacterial growth responses

Summary The main steps of modeling bacterial growth responses are summarized and a new model for growth curves is shown. Its advantages are analyzed from some theoretical and practical points of view. The new model fits better and has more advantageous statistical properties than the Gompertz curve.     

Infrared analysis of lecithin/sphingomyelin ratios

A clinical evaluation of a quantitative infrared method for lecithin and sphingomyelin is described. The method incorporates techniques of computer-assisted infrared spectroscopy for both control of the microprocessor-based infrared spectrophotometer and for evaluation of the data. An advanced software package for quantitative infrared analysis, which can operate on a microcomputer, provides the possibility of complete automation of the analysis. Results of the analyses of amniotic fluids from 20 patients are presented. In general, the results of the analysis of the lecithin/sphingomyelin ratio by the infrared method correspond closely to those obtained by two-dimensional thin-layer chromatography on the same respective samples.     

Isolation and photosynthetic characteristics of mesophyll cells from developing leaves of soybean

Mesophyll cells were isolated from developing sink leaves (25 to 30 mm in length) of soybean, Glycine max (L.) Merr. cv. Will. Leaf strips were incubated for two h in a buffered medium containing osmoticum and 0.2% Pectolyase Y-23. Gently stirring the leaf strips released from 7 to 16% of the total leaf mesophyll cells. Other pectinase enzymes, effective in releasing cells from mature source leaves (70 to 75 mm in length), did not release cells from sink leaves. Sink and source cell preparations were about 50 and 95% intact, respectively, based on the exclusion of Evans Blue dye. Intact cells could not be separated from broken cells on Ficoll or metrizamide density gradients. Total protein and catalase, glyceraldehyde-3-phosphate dehydrogenase, glycolate oxidase, phosphoenolpyruvate carboxylase, and ribulose 1,5-bisphosphate carboxylase activities on a chlorophyll basis were about 50% lower in sink mesophyll cells than in sink leaf homogenates indicating that broken sink cells lost soluble protein to the medium. Source cells and source leaf homogenates had comparable amounts of protein and enzymatic activities. Enzymatic activities on a chlorophyll basis were similar in source and sink leaves with the exception of phosphenolpyruvate carboxylase, which was two times higher in sink leaves. This enzyme was also exceptionally low in source and sink cells being only 61 and 23%, respectively, of whole leaf activities. Sink cell rates of ¹⁴CO₂ fixation were only 7% of source cell rates and sink cells did not show light-dependent O₂ evolution. Both cell preparations had photosystem II activiteis which were comparable to rates of ¹⁴CO₂ fixation at satuarating light and CO₂ concentration. It was concluded that the reduced photosynthetic rate of sink cells was limited by the low photochemical capacity rather than a limitation of Calvin cycle enzymes.     

A comparison of the effects of aspirin and histamine on fluid balance in the recruited lung

Salicylate administration has been reported to increase the flow of protein-rich lymph from lungs of animals, however, the mechanism of this response is unclear. In the present study we measured pulmonary hemodynamics and lung fluid and lung fluid and protein flux in anesthetized sheep, surgically prepared for the collection of lung lymph, in order to examine the possible effect of aspirin (ASP) on lung vascular permeability. ASP was given during recruitment of pulmonary microvascular surface area induced by sustained elevation of left atrial pressure (Pla) (Group 1) or continuous infusion of adenosine triphosphate (ATP) (Group 2). We compared the results of ASP administration to those found in similarly prepared animals given histamine (H) during like periods of increased Pla (Group 3) or ATP infusion (Group 4). ASP administration resulted in increased lymphatic protein clearance (Cp) in both Groups 1 and 2. In Group 1, following the characteristic increase in lung lymph flow (Q1) and fall in the ratio of lung lymph to plasma protein concentration (L/P) produced by Pla elevation, ASP administration resulted in a further increase in Q1 and a significant increase in L/P. The results found in ASP animals are qualitatively similar to those observed in Groups 3 and 4 after H. While we cannot specifically rule out a hemodynamic effect of the drug, our results suggest the increased protein flux observed following ASP administration was mediated at least in part through and increase in lung microvascular permeability.