scholarly journals INCREASE IN BACTERIOPHAGE AND GELATINASE CONCENTRATION IN CULTURES OF BACILLUS MEGATHERIUM

1939 ◽  
Vol 23 (1) ◽  
pp. 59-79 ◽  
Author(s):  
John H. Northrop

1. The increase in bacteria, phage concentration, and gelatinase concentration in cultures of B. megatherium has been determined. 2. With lysogenic cultures the phage concentration, gelatinase concentration, and bacteria concentration increase logarithmically at first. The phage and gelatinase concentration then decrease while the bacteria concentration increases to a maximum. 3. The results are the same with sensitive cultures if the ratio of phage to bacteria is small. If the ratio of phage to bacteria is large phage, gelatinase, and bacteria concentration all increase at first and then decrease. The maximum rate of increase coincides approximately with the maximum rate of oxygen consumption of the culture. 4. 60–90 per cent of the phage is free from the cells. 5. The amount of phage produced is determined by the combined phage and not by the total phage. 6. Phage is produced during growth of the cells and not during lysis. 7. In a very narrow range of pH near 5.55 no increase in bacteria occurs but large increases in phage may be obtained.

An investigation has been made of the oxidation of hexene-1 at 263°C. The unusual form of dependency of reaction rate on hydrocarbon pressure obtained when the maximum rate of pressure change is used as a measure of reaction rate is explained by the fact that much of the oxygen is consumed before the maximum rate of pressure change is attained. This, and the observation that the maximum rate of oxygen consumption exhibits a different dependence on hexene concentration compared with the maximum rate of pressure change confirm that maximum rate of pressure change is an invalid measure of reaction rate. Analyses have been made for certain intermediates and products throughout the course of the reaction, and it has been possible to explain many of the experimental features in terms of ideas previously propounded. A decrease in pressure which in many experiments precedes the rapid increase in pressure is attributed to polymerization reactions which predominated over oxidative degradations in the early stages of the reaction, particularly when the olefin is present in excess.


1981 ◽  
Vol 38 (11) ◽  
pp. 1309-1315 ◽  
Author(s):  
D. W. Rodgers ◽  
F. W. H. Beamish

Oxygen consumption and uptake of waterborne methylmercury were measured for rainbow trout (Salmo gairdneri) forced to swim at sustained swimming speeds at 10 and 20 °C. The concentrations of methylmercury used (< 8 μg Hg∙L−1) did not affect oxygen consumption. The log of mass specific oxygen consumption increased linearly with relative swimming speed. Standard metabolic rates were significantly different (P < 0.05) at 10 and 20 °C (111 and 192 mg O2∙kg−1∙h−1, respectively) but the rate of increase in oxygen consumption with swimming speed was not significantly different between temperatures. The rate of methylmercury uptake was positively correlated with both oxygen consumption and methylmercury concentration. Multiple linear regression equations relating the logs of rate of methylmercury uptake, rate of oxygen consumption, and methylmercury concentration at 10 and 20 °C were contiguous and a single equation described the relationship at both temperatures. The efficiency of methylmercury uptake relative to oxygen was ~0.25 at both temperatures. Assuming an oxygen percent utilization of 33%, the percent utilization of methylmercury from water was ~8%.Key words: methylmercury, uptake, respiration, oxygen consumption, rainbow trout, bioaccumulation, pollutant


2000 ◽  
Vol 48 (4) ◽  
pp. 369 ◽  
Author(s):  
David T. Booth

Incubation temperature influences embryonic development and the morphology of resultant hatchlings in many species of turtle but few studies have addressed its effect on oxygen consumption and total embryonic energy expenditure. Eggs of the Australian broad-shelled river turtle, Chelodina expansa, were incubated at constant temperatures of 24˚C and 28˚C to determine the effect of temperature on oxygen consumption, embryonic energy expenditure and hatchling morphology. All embryos at both incubation temperatures experienced a period of developmental diapause immediately after oviposition. Once this initial diapause was broken, embryos underwent a further period of developmental arrest when the embryo was still very small and had minimal oxygen consumption (<20 µL h–1). However, once rapid embryonic growth started, development appeared to be continuous. Rate of increase and peak rate of oxygen consumption were temperature dependent, both being highest at 28˚C. Net production efficiency (total oxygen consumed during incubation divided by yolk-free hatchling mass) was 120 mL O2 g–1 at 24˚C and 111 mL O2g–1 at 28˚C. Hatchling mass and yolk-free hatchling mass were independent of incubation temperature, but hatchlings from 28˚C had larger residual yolks and smaller head widths than hatchlings from 24˚C.


In a comparison of muscles poisoned with mono-iodo-acetic acid (IAA) in the presence and in the absence of oxygen respectively, Lundsgaard (1930) found:- (1) That the spontaneous breakdown of phosphagen in poisoned resting muscle is much more rapid under anaerobic conditions. (2) That the onset of the characteristic contracture produced by IAA is accompanied always by an increase in the rate of oxygen consumption.


1981 ◽  
Vol 51 (4) ◽  
pp. 858-863 ◽  
Author(s):  
D. L. Stokes ◽  
N. R. MacIntyre ◽  
J. A. Nadel

To study the effects of exercise on pulmonary diffusing capacity, we measured the lungs' diffusing capacity for carbon monoxide (DLCO) during exhalation from 30 to 45% exhaled vital capacity in eight healthy subjects at rest and during exercise while both sitting and supine. We found that DLCO at these lung volumes in resting subjects was 26.3 +/- 3.2% (mean +/- SE) higher in the supine than in the sitting position (P less than 0.001). We also found that, in both positions, DLCO at these lung volumes increased significantly (P less than 0.001) with increasing exercise and approached similar values at maximal exercise. The pattern of increase in DLCO with an increase in oxygen consumption in both positions was curvilinear in that the rate of increase in DLCO during mild exercise was greater than the rate of increase in DLCO during heavy exercise (P = 0.02). Furthermore, in the supine position during exercise, it appeared that DLCO reached a physiological maximum.


1996 ◽  
Vol 271 (3) ◽  
pp. F717-F722
Author(s):  
G. Bajaj ◽  
M. Baum

Intracellular cystine loading by use of cystine dimethyl ester (CDME) results in a generalized inhibition in proximal tubule transport due, in part, to a decrease in intracellular ATP. The present study examined the importance of phosphate and metabolic substrates in the proximal tubule dysfunction produced by cystine loading. Proximal tubule intracellular phosphorus was 1.8 +/- 0.1 in control tubules and 1.1 +/- 0.1 nmol/mg protein in proximal tubules incubated in vitro with CDME P < 0.001). Infusion of sodium phosphate in rabbits and subsequent incubation of proximal tubules with a high-phosphate medium attenuated the decrease in proximal tubule respiration and prevented the decrease in intracellular ATP with cystine loading. Tricarboxylic acid cycle intermediates have been shown to preserve oxidative metabolism in phosphate-depleted proximal tubules. In proximal tubules incubated with either 1 mM valerate or butyrate, there was a 42 and 34% reduction (both P < 0.05) in the rate of oxygen consumption with cystine loading. However, tubules incubated with 1 mM succinate or citrate had only a 13 and 14% P = NS) reduction in the rate of oxygen consumption, respectively. These data are consistent with a limitation of intracellular phosphate in the pathogenesis of the proximal tubule dysfunction with cystine loading.


1995 ◽  
Vol 41 (4-5) ◽  
pp. 372-377 ◽  
Author(s):  
João P. S. Cabral

Pseudomonas syringae cells starved in buffer released orcinol-reactive molecules and materials that absorbed ultraviolet light. The number of cells culturable in nutrient medium decreased more rapidly than the number of intact particles determined by microscopy. The results suggested that starvation resulted in the lysis of an increasing number of cells, and that a fraction of the intact particles were not culturable. Starvation also resulted in a decrease in the rate of oxygen consumption with acetate, glycerol, and succinate, but at different levels. Whereas the respiration of acetate and glycerol decreased concomitantly with culturability, the respiration of succinate decreased to levels similar to the concentration of intact cells, suggesting that all intact particles respired the succinate, but only the culturable cells respired the acetate and glycerol. The results suggest that measuring the activity of the electron-transport system can overestimate the viability of starved bacterial cells, and that complex metabolic activities such as the respiration of acetate and glycerol are probably better suited for the evaluation of this parameter.Key words: Pseudomonas syringae, starvation, culturability, viability, respiration.


1958 ◽  
Vol 41 (5) ◽  
pp. 959-988 ◽  
Author(s):  
W. P. Hurlbut

Azide (0.2 to 5.0 mM) and chloretone (2.0 to 15.0 mM) reversibly inhibited 20 to 90 per cent of the resting respiration of frog sciatic nerves, and caused a loss of potassium and a gain of sodium in this tissue. The changes in ionic contents that developed after 5 or 10 hours were roughly correlated with the degree of respiratory depression, but the time courses of these changes were different with the two reagents. In azide these changes appeared to begin immediately, while in chloretone, at concentrations between 3.0 and 5.0 mM, the ionic shifts developed after a delay of several hours. Fifteen millimolar chloretone produced immediate changes in ionic contents several times greater than those produced by anoxia. The changes in ionic distribution produced in 5 hours by anoxia, 5.0 mM azide, or 5.0 mM chloretone were at least partially reversible; those produced by 15.0 mM chloretone were irreversible. With the exception of 15.0 mM chloretone the ionic shifts produced by these reagents may be due primarily to the depression of the respiration, although there are indications that azide acts, in addition, by another pathway. Concentrations of azide or chloretone that depressed the resting rate of oxygen consumption more than 50 per cent produced a slow conduction block, while 15.0 mM chloretone blocked conduction within 15 minutes.


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