<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>DSpace Collection: Flinders' staff research in Microbiology, reportable as part of ERA, 2001-</title>
  <link rel="alternate" href="http://hdl.handle.net/2328/8390" />
  <subtitle>Flinders' staff research in Microbiology, reportable as part of ERA, 2001-</subtitle>
  <id>http://hdl.handle.net/2328/8390</id>
  <updated>2013-05-22T13:51:21Z</updated>
  <dc:date>2013-05-22T13:51:21Z</dc:date>
  <entry>
    <title>The staphylococcal QacR multidrug regulator binds a correctly spaced operator as a pair of dimers</title>
    <link rel="alternate" href="http://hdl.handle.net/2328/25947" />
    <author>
      <name>Grkovic, Steve</name>
    </author>
    <author>
      <name>Brown, Melissa Hackett</name>
    </author>
    <author>
      <name>Schumacher, Maria A</name>
    </author>
    <author>
      <name>Brennan, Richard G</name>
    </author>
    <author>
      <name>Skurray, Ronald Anthony</name>
    </author>
    <id>http://hdl.handle.net/2328/25947</id>
    <updated>2013-05-13T02:07:45Z</updated>
    <published>2001-01-01T00:00:00Z</published>
    <summary type="text">Title: The staphylococcal QacR multidrug regulator binds a correctly spaced operator as a pair of dimers
Authors: Grkovic, Steve; Brown, Melissa Hackett; Schumacher, Maria A; Brennan, Richard G; Skurray, Ronald Anthony
Abstract: Expression of the Staphylococcus aureusplasmid-encoded QacA multidrug transporter is regulated by the divergently encoded QacR repressor protein. To circumvent the formation of disulfide-bonded degradation products, site-directed mutagenesis to replace the two cysteine residues in wild-type QacR was undertaken. Analysis of a resultant cysteineless QacR derivative indicated that it retained full DNA-binding activities in vivo and in vitro and continued to be fully proficient for the mediation of induction ofqacA expression in response to a range of structurally dissimilar multidrug transporter substrates. The cysteineless QacR protein was used in cross-linking and dynamic light-scattering experiments to show that its native form was a dimer, whereas gel filtration indicated that four QacR molecules bound per DNA operator site. The addition of inducing compounds led to the dissociation of the four operator-bound QacR molecules from the DNA as dimers. Binding of QacR dimers to DNA was found to be dependent on the correct spacing of the operator half-sites. A revised model proposed for the regulation ofqacA expression by QacR features the unusual characteristic of one dimer of the regulatory protein binding to each operator half-site by a process that does not appear to require the prior self-assembly of QacR into tetramers.</summary>
    <dc:date>2001-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Stable low-copy-number Staphylococcus aureus&#xD;
            shuttle vectors</title>
    <link rel="alternate" href="http://hdl.handle.net/2328/9352" />
    <author>
      <name>Grkovic, Steve</name>
    </author>
    <author>
      <name>Brown, Melissa Hackett</name>
    </author>
    <author>
      <name>Hardie, Kate M</name>
    </author>
    <author>
      <name>Firth, Neville</name>
    </author>
    <author>
      <name>Skurray, Ronald Anthony</name>
    </author>
    <id>http://hdl.handle.net/2328/9352</id>
    <updated>2010-10-25T01:00:12Z</updated>
    <published>2003-01-01T00:00:00Z</published>
    <summary type="text">Title: Stable low-copy-number Staphylococcus aureus&#xD;
            shuttle vectors
Authors: Grkovic, Steve; Brown, Melissa Hackett; Hardie, Kate M; Firth, Neville; Skurray, Ronald Anthony</summary>
    <dc:date>2003-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Comparison of enrichment methods for the isolation
            of pyrene-degrading bacteria</title>
    <link rel="alternate" href="http://hdl.handle.net/2328/9353" />
    <author>
      <name>Gaskin, Sharyn Elizabeth</name>
    </author>
    <author>
      <name>Bentham, Richard Henry</name>
    </author>
    <id>http://hdl.handle.net/2328/9353</id>
    <updated>2010-07-27T05:54:02Z</updated>
    <published>2005-01-01T00:00:00Z</published>
    <summary type="text">Title: Comparison of enrichment methods for the isolation
            of pyrene-degrading bacteria
Authors: Gaskin, Sharyn Elizabeth; Bentham, Richard Henry</summary>
    <dc:date>2005-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Actinoalloteichus hymeniacidonis sp. nov., an
            actincomycete isolated from the marine sponge Hymeniacidon perleve</title>
    <link rel="alternate" href="http://hdl.handle.net/2328/9351" />
    <author>
      <name>Huang, Jianyu</name>
    </author>
    <author>
      <name>Zhang, Haitao</name>
    </author>
    <author>
      <name>Zheng, Wen</name>
    </author>
    <author>
      <name>Luo, Hongli</name>
    </author>
    <author>
      <name>Jin, Yan</name>
    </author>
    <author>
      <name>Huang, Ying</name>
    </author>
    <author>
      <name>Liu, Zhiheng</name>
    </author>
    <author>
      <name>Zhang, Wei</name>
    </author>
    <id>http://hdl.handle.net/2328/9351</id>
    <updated>2010-07-27T05:54:01Z</updated>
    <published>2006-01-01T00:00:00Z</published>
    <summary type="text">Title: Actinoalloteichus hymeniacidonis sp. nov., an
            actincomycete isolated from the marine sponge Hymeniacidon perleve
Authors: Huang, Jianyu; Zhang, Haitao; Zheng, Wen; Luo, Hongli; Jin, Yan; Huang, Ying; Liu, Zhiheng; Zhang, Wei</summary>
    <dc:date>2006-01-01T00:00:00Z</dc:date>
  </entry>
</feed>

