Literature DB >> 13035070

Growth and phage production of B. megatherium. I. Growth of cells after infection with C phage. II. Rate of growth, phage yield, and RNA content of cells. III. Effect of various substances on growth rate and phage production.

J H NORTHROP.   

Abstract

I. Lysogenic B. megatherium 899a (de Jong, 1931) produces two types of phage (Gratia, 1936 c) T and C. The T phage forms cloudy plaques and gives rise to fresh lysogenic strains (Gratia, 1936 b) when added to the sensitive strain of megatherium. It may or may not cause lysis, depending on the media (Northrop, 1951). The C phage occurs very rarely) forms clear plaques, does not give rise to lysogenic strains, and causes complete lysis of the sensitive strain under all conditions tested, provided infection occurs. If C phage is added to the sensitive strain, and the mixture allowed to stand, or made into a hanging drop preparation, the infected cells stop growing and lyse completely after 60 to 80 minutes with the liberation of from 50 to 200 phage particles per cell. If, however, C phage is added to a rapidly growing culture of B. megatherium and the suspension shaken at 34 degrees , the cells continue to grow and divide for 50 to 60 minutes, after infection has occurred. They then lyse, with the liberation of from 1000 to 2500 phage particles per cell. II. The following determinations have been made on megatherium sensitive cells growing in 5 per cent peptone at different stages of growth. (1) Growth rate of infected and uninfected cells; (2) RNA, DNA, and protein content; (3) volume of the cell; (4) phage yield per cell by plaque count; (5) phage yield per cell by cell and plaque count; (6) lysis time. The growth rate decreases as the cell concentration increases. The lysis time and the protein N per cell are nearly independent of the growth rate; all the other values increase as the growth rate increases. The ratio See PDF for Equation is nearly constant. RNA and DNA per cell increase less rapidly than the volume, so that NA per unit volume is not constant, but decreases as the size of the cell increases. The phage yield measured under conditions in which the infected cells do not grow (by plaque count) is very nearly proportional to the size of the cell. The phage yield per cell, under conditions in which the infected cells do grow, increases more rapidly than the size of the cells. The phage yield per cell under these conditions may be calculated by the equation See PDF for Equation The determining factor for the variation in phage yield is the growth rate of the cells. This, in turn, is determined by the composition of the medium. III. The growth and phage production of megatherium 899a have been determined in the presence of the following substances: aureomycin, bacitracin, chloromycetin, gramicidin, Merck AB631, Merck AB191, Merck AB624, penicillin, streptomycin, terramycin, tyrothricin, usnic acid, acetone, chloroform, ethyl alcohol, formaldehyde, gentian violet, glycerin, maleic hydrazide, methyl alcohol, phenyl mercuric acetate, sodium fluoride, sulfanilamide, toluene, and urethane. In every case, the lowest concentration of the substance which completely inhibits growth, is also the lowest concentration which completely inhibits phage production. One antibiotic, Merck AB81, causes increased phage production in concentrations which partially inhibit growth, and low phage production in concentrations which completely inhibit growth (as determined by turbidity). Short exposure to ultraviolet light also decreases the growth rate, with increase in phage production. Longer exposure, which completely inhibits growth (as determined by turbidity) results in lysis and phage liberation.

Keywords:  BACILLUS; BACTERIOPHAGE

Mesh:

Substances:

Year:  1953        PMID: 13035070      PMCID: PMC2147375          DOI: 10.1085/jgp.36.4.581

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  14 in total

1.  Substrate Stabilization of Enzyme-Forming Capacity During the Segregation of a Heterozygote.

Authors:  S Spiegelman; W F Delorenzo
Journal:  Proc Natl Acad Sci U S A       Date:  1952-07       Impact factor: 11.205

2.  THE DEMONSTRATION OF PHAGE PRECURSOR IN THE BACTERIAL CELL.

Authors:  A P Krueger; J H Mundell
Journal:  Science       Date:  1938-12-09       Impact factor: 47.728

3.  [Anderson's lytic factor].

Authors:  L QUERSIN; J DIRKX
Journal:  Ann Inst Pasteur (Paris)       Date:  1951-04

4.  Biochemical studies on multiplication of bacterial viruses.

Authors:  S S COHEN
Journal:  Fed Proc       Date:  1951-06

5.  Mechanism of bacteriophage reproduction.

Authors:  S E LURIA
Journal:  Fed Proc       Date:  1951-06

6.  [Research on the lysogenic Bacillus megatherium].

Authors:  A LWOFF; A GUTMANN
Journal:  Ann Inst Pasteur (Paris)       Date:  1950-06

7.  THE MECHANISM OF BACTERIOPHAGE PRODUCTION.

Authors:  A P Krueger
Journal:  Science       Date:  1937-10-22       Impact factor: 47.728

8.  Growth and phage production of lysogenic B. megatherium.

Authors:  J H NORTHROP
Journal:  J Gen Physiol       Date:  1951-05       Impact factor: 4.086

9.  Phage formation in Staphylococcus muscae cultures. X. The relationship between virus synthesis, the release of bacterial ribonucleic acid, virus liberation, and cellular lysis.

Authors:  W H PRICE
Journal:  J Gen Physiol       Date:  1952-01       Impact factor: 4.086

10.  Phage formation in Staphylococcus muscae cultures; further observations on the relationship between virus release and cellular lysis.

Authors:  W H PRICE
Journal:  J Gen Physiol       Date:  1949-03-20       Impact factor: 4.086

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  10 in total

1.  The assimilation of amino acids by bacteria. 21. The effect of nucleic acids on the development of certain enzymic activities in disrupted staphylococcal cells.

Authors:  E F GALE; J P FOLKES
Journal:  Biochem J       Date:  1955-04       Impact factor: 3.857

2.  Induction of bacterial lysis by penicillin.

Authors:  L S PRESTIDGE; A B PARDEE
Journal:  J Bacteriol       Date:  1957-07       Impact factor: 3.490

3.  Phage-host relationships in nontoxigenic and toxigenic diphtheria bacilli.

Authors:  W L BARDSDALE; A M PAPPENHEIMER
Journal:  J Bacteriol       Date:  1954-02       Impact factor: 3.490

4.  Synthesis of protein in the pancreas. II. The role of ribonucleoprotein in protein synthesis.

Authors:  V ALLFREY; M M DALY; A E MIRSKY
Journal:  J Gen Physiol       Date:  1953-11-20       Impact factor: 4.086

5.  The effect of ultraviolet and white light on growth rate, lysis, and phage production of Bacillus megatherium.

Authors:  J H NORTHROP
Journal:  J Gen Physiol       Date:  1957-05-20       Impact factor: 4.086

6.  Studies on the origin of bacterial viruses. I-IV.

Authors:  J H NORTHROP
Journal:  J Gen Physiol       Date:  1958-09-20       Impact factor: 4.086

7.  Appearance of new phage types and new lysogenic strains after adaptation of lysogenic B. megatherium to ammonium sulfate culture medium.

Authors:  J H NORTHROP; J S MURPHY
Journal:  J Gen Physiol       Date:  1956-03-20       Impact factor: 4.086

8.  The proportion of terramycin-resistant mutants in B. megatherium cultures.

Authors:  J H NORTHROP
Journal:  J Gen Physiol       Date:  1957-09-20       Impact factor: 4.086

9.  Adaptation of Bacillus megatherium to terramycin (oxytetracycline).

Authors:  J H NORTHROP
Journal:  J Gen Physiol       Date:  1957-03-20       Impact factor: 4.086

Review 10.  Bacteriophage-based therapy in cystic fibrosis-associated Pseudomonas aeruginosa infections: rationale and current status.

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  10 in total

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