<?xml version='1.0' encoding='utf-8'?>
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>K.N. Timmis</dc:contributor>
  <dc:contributor>D.F. Dwyer</dc:contributor>
  <dc:creator>M.L. Krumme</dc:creator>
  <dc:date>1993</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;&lt;i&gt;Pseudomonas cepacia&lt;/i&gt; G4 degrades trichloroethylene (TCE) via a degradation pathway for aromatic compounds which is induced by substrates such as phenol and tryptophan. &lt;i&gt;P. cepacia&lt;/i&gt; G4 5223 PR1 (PR1) is a Tn5 insertion mutant which constitutively expresses the toluene &lt;i&gt;ortho&lt;/i&gt;-monooxygenase responsible for TCE degradation. In groundwater microcosms, phenol-induced strain G4 and noninduced strain PR1 degraded TCE (20 and 50 μM) to nondetectable levels (&amp;lt; 0.1 μM) within 24 h at densities of 10&lt;sup&gt;8&lt;/sup&gt; cells per ml; at lower densities, degradation of TCE was not observed after 48 h. In aquifer sediment microcosms, TCE was reduced from 60 to &amp;lt; 0.1 μM within 24 h at 5 x 10&lt;sup&gt;8&lt;/sup&gt; PR1 organisms per g (wet weight) of sediment and from 60 to 26 μM over a period of 10 weeks at 5 x 10&lt;sup&gt;7&lt;/sup&gt; PR1 organisms per g. Viable G4 and PR1 cells decreased from approximately 10&lt;sup&gt;7&lt;/sup&gt; to 10&lt;sup&gt;4&lt;/sup&gt; per g over the 10-week period.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1128/aem.59.8.2746-2749.1993</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>American Society for Microbiology</dc:publisher>
  <dc:title>Degradation of trichloroethylene by Pseudomonas cepacia G4 and the constitutive mutant strain G4 5223 PR1 in aquifer microcosms</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>