The fate of newly made DNA in Escherichia coli mutants thermosensitive in DNA synthesis

Summary E. coli mutants exist in which DNA synthesis is thermosensitive. In one class of these mutants DNA synthesis stops immediately if a critical temperature (42°C) is reached. When DNA replication in such mutants is followed by ³H thymidine incorporation at 33°C, it is found that 1. only the newly made DNA is degraded at 42°C, 2. the discontinuously replicated DNA is lost predominantly at 42°C, 3. 1–3% of the chromosomal DNA is rendered acid soluble at 42°C without concomitant loss of viability of the cells at 33°C.Replication of phage DNA is inhibited in the same mutant at 42°C. However, when DNA synthesis is followed in infected cells at 33°C it is found that 1. no degradation of specific DNA seems to occur at 42°C in the early phase of infection, 2. replicating DNA molecules in the late phase of infection are completed at 42°C before DNA synthesis comes to a halt.     

The Relationship between Cell Membrane Potassium Ion Transport and Glycolysis : The effect of ethacrynic acid

Cell membrane transport of K⁺ stimulates the rate of glycolysis in Ehrlich ascites tumor cells. A study of the characteristics of this relationship indicates that the stimulation occurs under anaerobic as well as under aerobic conditions. The data suggest that glycolysis is stimulated by a K⁺ transport mechanism that is coupled to Na⁺ transport because the effect is blunted or abolished when the principal intracellular ion is lithium or choline. This stimulus to glycolysis is blocked by ouabain and ethacrynic acid, agents that have been shown to inhibit monovalent cation transport in erythrocytes. In contrast to the action of ouabain, glycolysis is inhibited by ethacrynic acid in Ehrlich ascites tumor cells in the absence of cell membrane K⁺ transport. In studies with ghost-free hemolysates of human erythrocytes and with cytosol prepared from Ehrlich ascites tumor cells, ethacrynic acid significantly blocks lactate formation from fructose diphosphate demonstrating the direct inhibitory effect of this agent on one or more enzymes of the Embden-Meyerhof pathway. Since ethacrynic acid has no influence on lactate formation in intact erythrocytes utilizing an endogenous substrate, the presumptive site of inhibition is proximal to the 3-phosphoglycerate level.     

Effects of nitrogen,phosphorus and potassium fertilizers on the assimilation capacity ofBeta vulgaris chloroplasts (I)

Summary Aspects of non-cyclic photophosphorylation and NADP photoreduction,viz (a) the effects produced on these processes by the three fertilizer elements: nitrogen, phosphorus and potassium; (b) variations in the catalase activity of reaction mixtures following fertilizer application, and (c) correlations between photosynthesis as measured on leaf-tissue discs and the assimilation capacity of chloroplast suspension, were studied. The role of catalase in the non-cyclic photophosphorylation processes was also studied.While photophosphorylation is influenced chiefly by the level of available soil phosphorus, NADP reduction is affected by all three nutrients. In addition, there was a greater degree of significance, for diagnostic and application purposes, in the values obtained if these two activities were referred to the chloroplast count rather than to the chlorophyll content.Catalase activity, in addition to responding in a different way to the respective fertilizer treatments and, in particular to available soil nitrogen, was governed by the principal constituents of the reaction mixture and in a manner contrary to that of non-cyclic photophosphorylation as measured in terms of oxygen evolution.Experimental findings further showed that photosynthesis is correlated chiefly with NADP-reduction capacity.     

Die wachstumsfördernde Wirkung von Tannin auf Getreidekoleoptilen

Zusammenfassung Schwach konzentrierte Tanninlösungen (5·10^–5 bis 5·10^–8 molar) vermochten das Wachstum 10 mm langer Koleoptilabschnitte von 15 Kulturformen vonAvena sativa, Hordeum distichon, Hordeum vulgare, Zea mays, Triticum aestivum undSecale cereale um etwa 6–25% zu fördern. Die mögliche Beteiligung von Gerbstoffen am Streckungswachstum höherer Pflanzen wurde diskutiert.

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Summary The growth of 10 mm coleoptile sections of 15 cultivars ofAvena sativa, Hordeum distichon, Hordeum vulgare, Zea mays, Triticum aestivum andSecale cereale was stimulated by dilute tannin-solutions (5·10^–5 to 5·10^–8 molar) from 6 up to 25%. The possible role of tannins in elongation growth of higher plants was discussed.

     

Reduction of a Tetrazolium Salt in Determining Growth Activity of Yeast-Phase Histoplasma capsulatum

A colorimetric method using a tetrazolium compound, 3,4,5-dimethylthiozalil-(1 or 2),2,5-diphenyltetrazolium bromide (TTBr), was developed for studying the growth activity of yeast-phase Histoplasma capsulatum. Materials extracted in phosphate buffer, pH 7.0, from cells at different stages of growth reduced TTBr. Colorimetric changes were correlated with enzymatic activity. Under standardized conditions specified herein, the optical density of the reduced tetrazole was an index of the growth activity of the organism.     

About phoma liliana Chandra & Tandon

Summary In vitro,Phoma liliana could not be distinguished from the later-describedP. ehretiae and two incidental isolates fromMangifera andChrysanthemum. Starting from the principle of the classification in the Deuteromycetes, our conclusion is that we must speak of one and the same form-species, which can be found on different plants.     

Studies on several genetic hematological traits of the Mexican population. XII. Distribution of blood group antigens in twelve Indian tribes

Blood samples from 1090 Mexican Indians belonging to the Chol, Chontal, Totonac, Huastec, Mixe, Mazatec, Zapotec, Mixtec, Chinantec, Nahua, Cora and Huichol linguistic groups, were obtained and examined in regard to the following blood group antigens: A, B. M, N, P, C, c, D, E, e, Fy(a), K and Di(a). The gene frequencies were similar to what has been described for other Amerindians; high values for O, M, CDe, cDE and Duffy; low to absent Kell and presence of Diego in variable amounts. The frequency of chromosomes CDE and cDe/cde was somewhat higher than usual and some of the tribes had relatively high frequencies of the A and B antigens. It was felt that variable degrees of non-Indian admixture was at least partially responsible for this situation. A previous study dealing with the distribution of abnormal hemoglobins and glucose-6-phosphate dehydrogenase deficiency in these same tribes, had strongly suggested the possibility of some Negro admixture in the Chontal, Nahua and Cora tribes. However, this was not specifically reflected in their blood group distribution. This served to emphasize the need of investigating as many markers as possible when trying to characterize a population.     

Die Wirkungsweise von Cercosporella herpotricboides Fron, dem Erreger der Halmbruchkrankheit des Getreides

In halt: 1. Einleitung und Aufgabenstellung.—2. Art und Ausmaß der Scnäden im Feld-versuch.—3. Wirkungen des Krankheitserregers auf Sommergetreide.—4. Bekämpfungsmöglichkeiten.—5. Besprechung der Ergebnisse.—Zusammenfassung.—Summary. —Literaturverzeichnis.     

Effect of Drying on Unexposed Autoradiographic Emulsion in Relation to Background

Unexposed blanks prepared from Kodak AR 10 stripping film were dried by 3 methods: (1) fast, open drying with a fan for 25 min, (2) slow drying in a desiccator for 6 hr, and (3) very slow drying in a desiccator for 24 hr. The number of background grains depended on the mode of drying. Fast drying (method 1) gave 0.7 grain per 100 μ², slow drying (method 2) gave 0.33 grain; very slow drying (method 3), only 0.17 grain. The increase of background after fast drying is assumed to be caused by the rapid shrinkage of wet emulsion. This causes an increase in the intraemulsion pressure which, in turn, sensitizes the silver bromide crystals to cause an increase in the number of developable grains.     

The pectinolytic enzyme of Selenomonas ruminantium

A cell-bound pectinolytic enzyme was isolated from cells of Selenomonas ruminantium and purified about 360-fold. The optimum pH and temperature for enzyme activity was 7.0 and 40°. The enzyme degraded polymeric substrates by hydrolysis of digalacturonic acid units from the non-reducing end; the best substrate was nona-galacturonic acid. Unsaturated trigalacturonate was also degraded, but 30% slower than the saturated analogue. The enzyme was classified as a poly (1,4-aP-D-galactosiduronate) digalacturono-hydrolase; EC 3.2.1.82. Another enzyme, hydrolysing digalacturonic acid to monomers, was also produced in a very small amount by this organism.