Literature DB >> 3141569

Preferential uptake of restriction fragments from a gonococcal cryptic plasmid by competent Neisseria gonorrhoeae.

K L Burnstein1, D W Dyer, P F Sparling.   

Abstract

Factors involved in the specificity of DNA uptake by competent Neisseria gonorrhoeae were examined. Host-controlled modification did not affect uptake. Certain restriction fragments of the 4.2 kb gonococcal cryptic plasmid pFA1 and of the replicative form of the bacteriophage M13 were taken up in preference to others, independent of differences in fragment size. A 600 bp fragment from the 4.2 kb plasmid was cloned into pLES2, a gonococcal-Escherichia coli shuttle vector; the 600 bp fragment was taken up into a DNAase-I-resistant state in preference to the vector fragment. A second 370 bp fragment in pFA1 was also taken up preferentially. The 600 bp and 370 bp fragments share a 10 bp sequence, which is found in pFA1 only on fragments that were taken up readily. However, a fragment from M13 which was efficiently taken up did not contain this 10 bp sequence. In addition, this sequence was not sufficient to direct preferential DNA uptake by gonococci, since a recombinant plasmid containing this 10 bp sequence was not taken up appreciably better than the vector plasmid or another recombinant plasmid containing an unrelated 10 bp sequence. Sequence comparisons of the three restriction fragments which were preferentially taken up did not yield any consensus sequences greater than 7 bp. Although it is likely that efficient uptake of DNA by gonococci is determined by DNA structure, a single short sequence could not be found that accounted for specific uptake.

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Year:  1988        PMID: 3141569     DOI: 10.1099/00221287-134-3-547

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  9 in total

1.  Determination of surface-exposed, functional domains of gonococcal transferrin-binding protein A.

Authors:  Mary Kate Yost-Daljev; Cynthia Nau Cornelissen
Journal:  Infect Immun       Date:  2004-03       Impact factor: 3.441

2.  Cloning and characterization of the catalase gene of Neisseria gonorrhoeae: use of the gonococcus as a host organism for recombinant DNA.

Authors:  S R Johnson; B M Steiner; G H Perkins
Journal:  Infect Immun       Date:  1996-07       Impact factor: 3.441

3.  Species-specific uptake of DNA by gonococci is mediated by a 10-base-pair sequence.

Authors:  C Elkins; C E Thomas; H S Seifert; P F Sparling
Journal:  J Bacteriol       Date:  1991-06       Impact factor: 3.490

4.  Transformation-deficient mutants of piliated Neisseria gonorrhoeae.

Authors:  G D Biswas; S A Lacks; P F Sparling
Journal:  J Bacteriol       Date:  1989-02       Impact factor: 3.490

Review 5.  Gene transfer in Neisseria gonorrhoeae.

Authors:  G D Biswas; S A Thompson; P F Sparling
Journal:  Clin Microbiol Rev       Date:  1989-04       Impact factor: 26.132

Review 6.  Virulence functions and antigen variation in pathogenic Neisseriae.

Authors:  T F Meyer; M Frosch; C P Gibbs; R Haas; R Halter; J Pohlner; J P van Putten
Journal:  Antonie Van Leeuwenhoek       Date:  1988       Impact factor: 2.271

7.  Factors influencing the specific interaction of Neisseria gonorrhoeae with transforming DNA.

Authors:  S D Goodman; J J Scocca
Journal:  J Bacteriol       Date:  1991-09       Impact factor: 3.490

8.  Identification and arrangement of the DNA sequence recognized in specific transformation of Neisseria gonorrhoeae.

Authors:  S D Goodman; J J Scocca
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

9.  Variations in gene organization and DNA uptake signal sequence in the folP region between commensal and pathogenic Neisseria species.

Authors:  Yvonne Qvarnstrom; Gote Swedberg
Journal:  BMC Microbiol       Date:  2006-02-17       Impact factor: 3.605

  9 in total

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