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  • American Society for Microbiology  (27)
  • 1970-1974  (27)
Type of Medium
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  • American Society for Microbiology  (27)
Language
Years
  • 1970-1974  (27)
Year
Subjects(RVK)
  • 1
    Online Resource
    Online Resource
    American Society for Microbiology ; 1972
    In:  Journal of Bacteriology Vol. 110, No. 1 ( 1972-04), p. 266-272
    In: Journal of Bacteriology, American Society for Microbiology, Vol. 110, No. 1 ( 1972-04), p. 266-272
    Abstract: Two direct methods are presented for estimating the average number of deoxyribonucleic acid (DNA) uptake sites in competent cells of Bacillus subtilis from measurement of 14 C- or 3 H-thymine-labeled DNA uptake by competent culture. Advantage is taken of two facts: (i) effective contact between competent cells and transforming DNA molecules is established within a short time after mixing them together, and (ii) DNA molecules enter the competent B. subtilis cells in a linear fashion at a finite speed. From the number of DNA molecules initially attached to competent cells by brief exposure to transforming DNA in the first method or from the rate of DNA uptake by competent culture in the second method, the average number of DNA uptake sites is calculated to be 20 to 53 per competent cell.
    Type of Medium: Online Resource
    ISSN: 0021-9193 , 1098-5530
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1972
    detail.hit.zdb_id: 1481988-0
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    American Society for Microbiology ; 1973
    In:  Infection and Immunity Vol. 7, No. 1 ( 1973-01), p. 46-52
    In: Infection and Immunity, American Society for Microbiology, Vol. 7, No. 1 ( 1973-01), p. 46-52
    Abstract: The ability of hamster lymphoid cells to become cytotoxic in vitro to xenogeneic human cells after stimulation with concanavalin A (ConA) was investigated by using the cell-mediated 51 Cr release test. Cytotoxicity developed by 12 to 16 hr with peak values acquired within 24 hr of stimulation with ConA. The cytotoxicity was found to be mediated by the lymphoid cells themselves rather than by soluble substances. Spleen cells were more efficient than lymph node cells in releasing radioactivity from human cells. The concentration of mitogen was found to be critical in the development of cytotoxicity. ConA concentrations of 12.5 μg or less per culture conferred upon the lymphoid cells the capacity to release 51 Cr from target cells whereas higher concentrations were ineffective and even inhibitory. The cell-mediated cytotoxicity could be reversed by methyl α- d -glucopyranoside, but only during the first 8 to 12 hr of stimulation. The lytic reaction did not require the presence of ConA.
    Type of Medium: Online Resource
    ISSN: 0019-9567 , 1098-5522
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1973
    detail.hit.zdb_id: 1483247-1
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  • 3
    Online Resource
    Online Resource
    American Society for Microbiology ; 1971
    In:  Applied Microbiology Vol. 22, No. 1 ( 1971-07), p. 131-132
    In: Applied Microbiology, American Society for Microbiology, Vol. 22, No. 1 ( 1971-07), p. 131-132
    Abstract: A simple growth medium is reported, in which Bacillus megaterium forms heat-stable spores, heat-labile spores, or only vegetative cells by changing the carbon and nitrogen source. Studies carried out in such media could be very useful in elucidating biochemical events which lead to bacterial sporulation.
    Type of Medium: Online Resource
    ISSN: 0003-6919
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1971
    detail.hit.zdb_id: 207801-6
    detail.hit.zdb_id: 1478346-0
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  • 4
    Online Resource
    Online Resource
    American Society for Microbiology ; 1972
    In:  Applied Microbiology Vol. 23, No. 1 ( 1972), p. 161-163
    In: Applied Microbiology, American Society for Microbiology, Vol. 23, No. 1 ( 1972), p. 161-163
    Type of Medium: Online Resource
    ISSN: 0003-6919
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1972
    detail.hit.zdb_id: 207801-6
    detail.hit.zdb_id: 1478346-0
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  • 5
    Online Resource
    Online Resource
    American Society for Microbiology ; 1970
    In:  Applied Microbiology Vol. 19, No. 6 ( 1970), p. 1017-1018
    In: Applied Microbiology, American Society for Microbiology, Vol. 19, No. 6 ( 1970), p. 1017-1018
    Type of Medium: Online Resource
    ISSN: 0003-6919
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1970
    detail.hit.zdb_id: 207801-6
    detail.hit.zdb_id: 1478346-0
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  • 6
    Online Resource
    Online Resource
    American Society for Microbiology ; 1973
    In:  Antimicrobial Agents and Chemotherapy Vol. 3, No. 3 ( 1973-03), p. 399-406
    In: Antimicrobial Agents and Chemotherapy, American Society for Microbiology, Vol. 3, No. 3 ( 1973-03), p. 399-406
    Abstract: Cells of Pseudomonas aeruginosa suspended in 0.2 M Mg 2+ , 20% sucrose, 0.01 M tris(hydroxymethyl)aminomethane, or water partially release lipopolysaccharide. The release of alkaline phosphatase from the periplasmic space and the ability to form spheroplasts on lysozyme treatment is directly related to the lipopolysaccharide released during treatment with 0.2 M Mg 2+ , 20% sucrose, or other agents. The synthesis of ribonucleic acid (RNA) by intact cells, magnesium-lysozyme spheroplasts, or 20% sucrose-lysozyme spheroplasts is not sensitive to actinomycin D, whereas RNA synthesis by intact cells or spheroplasts in the presence of ethylene-diaminetetraacetic acid (EDTA) is sensitive to actinomycin D. EDTA alone has an inhibitory effect on RNA synthesis by whole cell, by magnesium-lysozyme spheroplasts, and by 20% sucrose-lysozyme spheroplasts. The experimental data indicate that, although the cell wall is damaged by 0.2 M Mg 2+ or 20% sucrose treatment in the presence of lysozyme, the treated cells or spheroplasts are still resistant to actinomycin D. These results suggest that the cytoplasmic membrane should be considered as the final and determinative barrier to this antibiotic in this organism.
    Type of Medium: Online Resource
    ISSN: 0066-4804 , 1098-6596
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1973
    detail.hit.zdb_id: 1496156-8
    SSG: 12
    SSG: 15,3
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  • 7
    Online Resource
    Online Resource
    American Society for Microbiology ; 1972
    In:  Infection and Immunity Vol. 5, No. 3 ( 1972-03), p. 352-358
    In: Infection and Immunity, American Society for Microbiology, Vol. 5, No. 3 ( 1972-03), p. 352-358
    Abstract: The 51 Cr-release test was used to detect cytotoxic antibodies in adult rabbits bearing tumors induced by Shope fibroma virus. The following are the recommended experimental conditions: the infection of RK-13 cells with a multiplicity of 1 to 2 infectious units per cell for 48 hr, 51 Cr labeling of infected cells during the last 12 hr of incubation, sensitization of suspended labeled infected cells for 1 hr with immune serum, and quantitation of cell damage by the amount of 51 Cr released after 6 hr of incubation in the presence of complement. The immune sera reacted only with fibroma virus-infected cells but not with cells infected with vaccinia virus or herpesvirus type 1. Similarly, sera prepared against vaccinia virus and herpesvirus type 1 were not cytotoxic to fibroma virus-infected cells, although they were cytotoxic to cells infected with homologous viruses. The total antibody activity in sera of rabbits infected with Shope fibroma virus was detected first on day 7, gradually rose to its peak by day 23, and persisted at that level for at least 50 days. The 19 S antibody was detected on day 7, reached peak titers by day 13, and disappeared by day 17. The 7 S antibody was barely detectable on day 7, reached maximum titers on day 13, and remained high for at least 50 days. The tumors appeared on the 3rd day after virus inoculation, reached maximum size on day 13, and regressed completely by day 23.
    Type of Medium: Online Resource
    ISSN: 0019-9567 , 1098-5522
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1972
    detail.hit.zdb_id: 1483247-1
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  • 8
    Online Resource
    Online Resource
    American Society for Microbiology ; 1972
    In:  Journal of Bacteriology Vol. 112, No. 1 ( 1972-10), p. 188-194
    In: Journal of Bacteriology, American Society for Microbiology, Vol. 112, No. 1 ( 1972-10), p. 188-194
    Abstract: The biological activities of Bacillus subtilis ribosomes pretreated with 0.5, 1, or 2 m m p -chloromercuribenzoate (PCMB) were examined. The ribosomes treated with 1 or 2 m m PCMB lost their capacity to synthesize polyphenylalanine as well as the capacity to bind phenylalanyl-transfer ribonucleic acid. On the other hand, approximately 70% of the polyphenylalanine synthesis capacity was lost with ribosomes pretreated with 0.5 m m PCMB. This inhibition was found to be due to a specific inhibition of the translocation step. The effect of 0.5 m m PCMB was reversed by 20 m m Mg 2+ without the loss of PCMB bound to ribosomes, while β-mercaptoethanol partially reversed the inhibitory effect with concomitant loss of bound PCMB.
    Type of Medium: Online Resource
    ISSN: 0021-9193 , 1098-5530
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1972
    detail.hit.zdb_id: 1481988-0
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    American Society for Microbiology ; 1974
    In:  Journal of Bacteriology Vol. 118, No. 3 ( 1974-06), p. 911-918
    In: Journal of Bacteriology, American Society for Microbiology, Vol. 118, No. 3 ( 1974-06), p. 911-918
    Abstract: Approximately one-half of the mutants of Saccharomyces cerevisiae that are selected as resistant to methyl mercury are also found to require methionine. Eighty-four percent of these met mutations occur at the met 15 locus, and the remaining 16% occur at the met 2 locus. Surprisingly, the methionine-requiring mutants are recovered at a much higher frequency on methionineless media than on media supplemented with methionine. Growth patterns of the met mutants on media having a continuous concentration gradient of methionine and mercury compounds indicate that, at a critical concentration of the mercury compounds, the methionine requirement of certain met mutants is partially or completely alleviated. This was found for met 2, met 15, and to a lesser extent for met 6, but not for any other methionine mutants. This loss of methionine requirement is produced with methyl mercury, phenyl mercury, and mercuric chloride although met 2 and met 15 strains can be shown to be resistant only to methyl mercury. Other methionine auxotrophs are not resistant to any of the three mercury compounds. The met 2 and met 15 mutants, but not the other methionine auxotrophs, develop a sheen of an unidentified product when grown on media with mercuric chloride but not with methyl mercury or phenyl mercury. It is suggested that met 2 and met 15 mutants produce a simple diffusible substance, which detoxifies methyl mercury, which reacts with mercuric chloride to produce a sheen, and which is the cause of the methionine requirement.
    Type of Medium: Online Resource
    ISSN: 0021-9193 , 1098-5530
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1974
    detail.hit.zdb_id: 1481988-0
    SSG: 12
    Library Location Call Number Volume/Issue/Year Availability
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  • 10
    Online Resource
    Online Resource
    American Society for Microbiology ; 1974
    In:  Journal of Bacteriology Vol. 119, No. 1 ( 1974-07), p. 129-137
    In: Journal of Bacteriology, American Society for Microbiology, Vol. 119, No. 1 ( 1974-07), p. 129-137
    Abstract: The effects of N,N ′-dicyclohexylcarbodiimide (DCCD) on the growth of Streptococcus faecalis , and on the growth, β-galactosidase synthesis, and various membrane-mediated processes, were studied in wild-type Escherichia coli JE1011 and its lipopolysaccharide-defective mutant NS1. DCCD (0.1 mM) completely inhibited the growth of S. faecalis and E. coli NS1 but had little effect on strain JE1011. The same amount of DCCD with E. coli NS1, but not with E. coli JE1011, inhibited the induction of β-galactosidase, increased the permeability of the cells to o -nitrophenyl-β- d -galactoside without causing extensive cell lysis or release of ultraviolet-absorbing materials, and inhibited the oxidation of certain intermediates of the tricarboxylic acid cycle. Inhibition of the oxidation of malate, fumarate, and α-ketoglutarate by DCCD appeared to be at the level of the transport system for these compounds. Inhibition of the membrane-bound adenosine triphosphatase by DCCD was not entirely responsible for these effects, since oxidation of these substances, and transport of [ 14 C]succinate and [ 14 C]fumarate, was inhibited by DCCD in a mutant, N 144 , which lacked adenosine triphosphatase activity. It is concluded that lipopolysaccharide forms a barrier to DCCD in wild-type E. coli , and that DCCD can inhibit several processes in the cell.
    Type of Medium: Online Resource
    ISSN: 0021-9193 , 1098-5530
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 1974
    detail.hit.zdb_id: 1481988-0
    SSG: 12
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