Abstract/Details

Identification and characterization of a cryptic D-serine deaminase (DSD) gene from Burkholderia cepacia


1998 1998

Other formats: Order a copy

Abstract (summary)

Isolates of Burkholderia cepacia differed in their ability to utilize D-serine as a carbon and energy source. Strain 17616 is one of the strains which ordinarily fails to utilize D-serine. D-serine also inhibited the growth of this strain on alternative carbon sources such as mannitol. D-serine resistant (Dsd$\sp+$) mutants of strain 17616 were isolated which formed high constitutive levels of a D-serine deaminase not present in the wild type. The majority of such mutants also utilized D-serine as sole carbon source. A 5.5-kb fragment of B. cepacia DNA containing the dsd gene was cloned into the DsdA$\sp-$ strain E. coli AC6082. Introduction of recombinant plasmids carrying the dsd gene into strains 17616 or AC6082 resulted in high levels of constitutive D-serine deaminase activity as well as expression of a new peptide with the predicted size (45 kDa) of the the dsd gene product.

Efforts were made to define the mechanism of activation of the cryptic dsd gene in strain 17616. Comparison of PCR products of the region upstream of the dsd gene in the wild type and Dsd$\sp+$ strains indicated that dsd gene expression was not a consequence of insertion of tranposable-gene-activating elements upstream of the cryptic gene as had been observed for activation of foreign bla and lac genes in this strain. Furthermore, no other alterations were detected in this upstream region that would account for dsd gene activation.

Analysis the region downstream of the dsd gene revealed the presence of a marR-like repressor gene and adjacent multi-drug resistance transporter gene. The orientation of the latter two genes was opposite to that of the dsd gene. We were interested in the possibility that the marR (multiple antibiotic resistance/multiple adaptive response) protein might control dsd gene expression. To explore this possibility, I compared the nucleotide sequences of the marR gene from the representative Dsd$\sp+$ strain 249-50 with the corresponding wild type gene. The wild type and mutant sequences were identical.

Indexing (details)


Subject
Microbiology;
Molecular biology
Classification
0410: Microbiology
0307: Molecular biology
Identifier / keyword
Biological sciences, Burkholderia cepacia, D-serine deaminase, Serine deaminase
Title
Identification and characterization of a cryptic D-serine deaminase (DSD) gene from Burkholderia cepacia
Author
Montgomery, Stacy O.
Number of pages
184
Publication year
1998
Degree date
1998
School code
0118
Source
DAI-B 59/10, Dissertation Abstracts International
Place of publication
Ann Arbor
Country of publication
United States
ISBN
9780599073548, 0599073543
Advisor
Lessie, Thomas G.
University/institution
University of Massachusetts Amherst
University location
United States -- Massachusetts
Degree
Ph.D.
Source type
Dissertations & Theses
Language
English
Document type
Dissertation/Thesis
Dissertation/thesis number
9909192
ProQuest document ID
304439248
Copyright
Database copyright ProQuest LLC; ProQuest does not claim copyright in the individual underlying works.
Document URL
http://search.proquest.com/docview/304439248
Access the complete full text

You can get the full text of this document if it is part of your institution's ProQuest subscription.

Try one of the following:

  • Connect to ProQuest through your library network and search for the document from there.
  • Request the document from your library.
  • Go to the ProQuest login page and enter a ProQuest or My Research username / password.