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T D Brock

Publications and source records attributed to T D Brock.

90 records · Page 5Linked to original sources

Measurement of steady-state growth rates of a thermophilic alga directly in nature.

Steady-state growth rates of thermophilic algae can be determined directly in nature in the flowing waters of a hot spring channel by measuring the rate of loss of algal cells when the channel is darkened. The half time of the loss rate in the steady state is identical to the generation time. We studied the unicellular blue-green alga Synechococcus in Yellowstone National Park. Temperature and flow rate remained relatively constant throughout the experiment. Quantitative cores were taken and homogenized; the algal cells were then counted by use of a Petroff-Hausser counting chamber. After ascertaining that the algal population was in a steady state, the channel was darkened in such a way that neither flow rate nor temperature was altered. The population began to decrease within 1 day; the loss rate was exponential with time for 2 to 3 decades. Half times were then calculated from these loss rates. The growth rates found were considerably lower than those for the same organism in laboratory culture. The results suggest that in nature the organism may be an obligate phototroph. In two cases, after the algal populations decreased to an undetectable level, the dark covers were removed and the rate of recolonization was measured. The kinetics of recolonization were different from the kinetics of washout.

Cell Division↗

Bacterial growth rate in the sea: direct analysis by thymidine autoradiography.

Autoradiography with tritiated thymidine was used to study microbial growth directly in nature. The epiphyte Leucothrix mucor was used since it is a large filamentous bacterium with a characteristic morphology making it recognizable in natural collections. The technique was developed initially with pure cultures. The relation between growth rate and the rate of accumulation of radioactive cells permitted derivation of a constant for use in calculating growth rate in natural material and in two-membered cultures of L. mucor growing epiphytically on pure cultures of marine algae. The growth rate (generation time) in two-membered cultures with the red alga Antithamnion sarniense was 94 minutes under the conditions used. In nature the growth rate of a sample from Iceland was 685 minutes; that of a sample from Long Island Sound was 660 minutes. There was no evidence of preferential growth in the basal portion of bacterial filaments nearest the algal surface. However, filamentous growth in nature, but not in pure or two-membered culture, was nonrandom, growth being clustered in some regions.

Autoradiography↗

Life at high temperatures. Evolutionary, ecological, and biochemical significance of organisms living in hot springs is discussed.

The time is now ripe for a concerted attack on the evolutionary, ecological, and molecular aspects of life at high temperatures. Hot springs provide nearly ideal ecosystems for such study, since they are natural environments of great antiquity and relative constancy, where organisms have evolved to meet the environmental challenges of high temperatures. Even from our present limited knowledge, we can draw a number of conclusions.

Adaptation, Physiological↗

Mode of filamentous growth of Leucothrix mucor in pure culture and in nature, as studied by tritiated thymidine autoradiography.

Mode of growth of Leucothrix mucor filaments was measured by autoradiography with tritiated thymidine. Studies were performed on L. mucor in pure cultures in free suspension, as an epiphyte of pure cultures of the red alga Antithamnion sarniense, and as an epiphyte of red algae in the sea. Statistical analyses of the distribution of growing cells was done by use of the nonparametric One-Sample Runs Test and a Cluster analysis adapted from quadrat analyses of plant ecologists. No evidence of preferential growth at base or tip of L. mucor filaments was obtained in any of these studies. However, in nature, but not in the laboratory, there were regions of L. mucor filaments which were nongrowing or dormant. Such nongrowing regions could incorporate tritiated glucose.

Autoradiography↗

Action of streptolysin S, the group D hemolysin, and phospholipase C on whole cells and spheroplasts.

Davie, Joseph M. (Indiana University, Bloomington), and Thomas D. Brock. Action of streptolysin S, the group D hemolysin, and phospholipase C on whole cells and spheroplasts. J. Bacteriol. 91:595-600. 1966.-The effect of streptolysin S, the group D hemolysin, and phospholipase C (the alpha toxin of Clostridium perfringens) on whole cells and spheroplasts or protoplasts of three strains of streptococci and Micrococcus lysodeikticus was tested. Viability, C(14)-glycine uptake, and lysis were measured. The group D hemolysin and phospholipase C were active against whole bacteria; streptolysin S was not. All three substances were active on spheroplasts. A partially resistant mutant derived from a strain sensitive to the group D hemolysin was also partially resistant to streptolysin S and phospholipase C. Antimycin A protected spheroplasts from streptolysin S but not from the group D hemolysin.

Antimycin A↗

Effect of teichoic acid on resistance to the membrane-lytic agent of Streptococcus zymogenes.

Davie, Joseph M. (Indiana University, Bloomington), and Thomas D. Brock. Effect of teichoic acid on resistance to the membrane-lytic agent of Streptococcus zymogenes. J. Bacteriol. 92:1623-1631. 1966.-The resistance of Streptococcus zymogenes to its own lytic agent has been shown to be due to the production of a specific, inhibitory teichoic acid. A survey of streptococcal strains showed that only strains resistant to the lytic agent produced the specific inhibitor. In addition, the inhibitor can be removed from spheroplasts of resistant strains, thereby making them sensitive to the lysin. Throughout the early part of the growth cycle, the inhibitor is associated with the cell and cannot be found in the medium. During late logarithmic phase, however, the inhibitor is released into the medium by the cells, and therefore is a contributing factor to the apparent lability of the lytic agent. The purified, inhibitory teichoic acid contains ribitol, phosphate, glucose, and d-alanine. The alkaline lability of the biological activity of the teichoic acid was correlated with the hydrolysis of the d-alanine. A streptococcal strain which is sensitive to the membrane-lytic agent produced an inactive ribitol teichoic acid which lacks the ester-linked d-alanine, whereas a lysin-resistant mutant of this strain produces a teichoic acid which contains d-alanine and which has inhibitory activity.

Acids↗

Biochemical and cellular changes occuring during conjugation in Hansenula wingei.

Brock, Thomas D. (Indiana University, Bloomington). Biochemical and cellular changes occurring during conjugation in Hansenula wingei. J. Bacteriol. 90:1019-1025. 1954.-A technique has been devised for deagglutinating mixed populations of conjugating cells so as to be able to visualize microscopically early stages of the conjugation process. A cell can form a conjugation tube only when in contact with a cell of opposite mating type, but may do so even if the mate is unresponsive or ultraviolet-inactivated. Cell fusion occurs, however, only when both cells are able to form conjugation tubes in a region of contact. Fusion begins almost as soon as the two cells begin to form protuberances, and long before any dissolution of cell-wall material between the cells occurs. A cell which has conjugated in one region of its cell wall is still able to conjugate with another cell in another region, so that triply and quadruply conjugated cells are occasionally formed. There is no significant net increase in deoxyribonucleic acid, ribonucleic acid, protein, or carbohydrate which might be related to the conjugation process, because any minor changes that occur in these components are also detected when cells of only one mating type are incubated or when the conjugation process is inhibited with the antibiotic cycloheximide. Changes in activity of beta-1,3-glucanase (with laminarin as substrate) and beta-1,6-glucanase (with pustulan as substrate) have been measured during the conjugation process, in addition to changes in the activity of several control enzymes which would not be expected to be related to the conjugation process. Significant increases in invertase (sucrase), laminarinase, and pustulanase were detected, and minimal increases occurred in beta-glucosidase and acid phosphatase. However, these same increases were also observed in controls involving only one mating type; thus, these increases are probably not related to the conjugation process, but may be a result of other processes which probably occur during incubation in the conjugation medium.

Ascomycota↗

CHLORAMPHENICOL.

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Journal Article↗