Literature DB >> 30748

Enchancement of streptococcal transformation yield by proteolytic enzymes.

P G Fuchs, W T Dobrzański.   

Abstract

Trypsin and other proteolytic enzymes, added together with transforming DNA or during cell-DNA contact to competent cultures of several streptococcal strains, enchanced (10 to 600%) the yield of genetic transformation (stimulation). With few exceptions, the level of stimulation was high (over 100%) when competence was low (below 2%). Stimulation was caused by the action of an enzyme on competent cells and not on any other component of transformation mixture. The phenomenon occurred when the enzyme was added to the culture not earlier than 7 min before and not later than 5 min after the period of cell-DNA contact. The presence of trypsin during cell-DNA contact caused: (i) the alterations at cell surface, demonstrated by electron microscopy, increased release of 3H-amino acid-labeled material, and higher cell susceptibility to autolysis; (ii) the increase of both total and irreversible binding of DNA by the cells; and (iii) the decrease of early nucleolytic degradation of DNA by cells. These and other data point to the importance of a delicate balance of recipient cell's surface nuclease activities in the effectiveness of transformation process. It is also possible that trypsin eliminates an unknown cellular factor which obstructs DNA-cell receptors interaction.

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Year:  1978        PMID: 30748      PMCID: PMC218660          DOI: 10.1128/jb.136.1.295-303.1978

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  20 in total

1.  Nuclease content of group H Streptococcus strain Challis cell surface extracts inactivating transforming deoxyribonucleic acid.

Authors:  B J Starościak; P Ceglowski; W T Dobrzański
Journal:  J Bacteriol       Date:  1975-07       Impact factor: 3.490

2.  PREPARATION OF TRANSFORMING DEOXYRIBONUCLEIC ACID BY PHENOL TREATMENT.

Authors:  H SAITO; K I MIURA
Journal:  Biochim Biophys Acta       Date:  1963-08-20

3.  [Research on the kinetics of bacterial transformations].

Authors:  R Thomas
Journal:  Biochim Biophys Acta       Date:  1955-12

4.  Identification of a deoxyribonuclease implicated in genetic transformation of Diplococcus pneumoniae.

Authors:  S Lacks; B Greenberg; M Neuberger
Journal:  J Bacteriol       Date:  1975-07       Impact factor: 3.490

5.  Nucleolytic degradation of homologous and heterologous deoxyribonucleic acid molecules at the surface of competent pneumococci.

Authors:  H Seto; R Lopez; O Garrigan; A Tomasz
Journal:  J Bacteriol       Date:  1975-05       Impact factor: 3.490

6.  Cell surface-located deoxyribonucleic acid receptors in transformable pneumococci.

Authors:  H Seto; R Lopez; A Tomasz
Journal:  J Bacteriol       Date:  1975-06       Impact factor: 3.490

7.  Transformation and DNA size. I. Activity of fragments of defined size and a fit to a random double cross-over model.

Authors:  A Cato; W R Guild
Journal:  J Mol Biol       Date:  1968-10-14       Impact factor: 5.469

8.  Physical and genetic hybrids formed in bacterial transformation.

Authors:  T Gurney; M S Fox
Journal:  J Mol Biol       Date:  1968-02-28       Impact factor: 5.469

9.  Competence for deoxyribonucleic acid uptake and deoxyribonuclease action external to cells in the genetic transformation of Diplococcus pneumoniae.

Authors:  S Lacks; B Greenberg
Journal:  J Bacteriol       Date:  1973-04       Impact factor: 3.490

10.  Breakage prior to entry of donor DNA in Pneumococcus transformation.

Authors:  D A Morrison; W R Guild
Journal:  Biochim Biophys Acta       Date:  1973-04-11
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  1 in total

1.  Role of Streptococcus sanguis (strain Wicky) cell surface-located deoxyribonucleic acid-binding factor in transformation of a homologous strain.

Authors:  P Cegłowski; M Kawczyński; W T Dobrzański
Journal:  J Bacteriol       Date:  1981-04       Impact factor: 3.490

  1 in total

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