<?xml version="1.0" encoding="UTF-8"?>
<records>
<record>
<language>eng</language>
<publisher>Science and Education Publishing</publisher>
<journalTitle>Journal of Applied &amp; Environmental Microbiology</journalTitle>
<publicationDate>2014-06-16</publicationDate>
<volume>2</volume>
<issue>4</issue>
<startPage>185</startPage>
<endPage>193</endPage>
<doi>10.12691/jaem-2-4-12</doi>
<publisherRecordId>JAEM20142412</publisherRecordId>
<documentType>article</documentType>
<title language="eng">Exploring the Efficacy of Bioaugmentation Strategy in Microbial Degradation of Chloroaniline</title>
<authors>
<author>
<name>M. Shah</name>
<email>shahmp@uniphos.com</email>
<affiliationId>1</affiliationId>
</author>
</authors>
<affiliationsList>
<affiliationName affiliationId="1">Industrial Waste Water Research Laboratory, Division of Applied &amp; Environmental Microbiology, Enviro Technology Limited, Gujarat, India</affiliationName>

</affiliationsList>
<abstract language="eng">Pseudomonas spp. was isolated from activated-sludge and found to be able to mineralize 3-chloroaniline (3-CA). This strain was tested for its ability to clean wastewater containing 3-CA upon inoculation in activated-sludge. To monitor its survival, the strain was chromosomally marked with the gfp gene and designated Agfp. After inoculation into a lab-scale semi continuous activated-sludge (SCAS) system, the inoculated strain maintained itself in the sludge at least 45 days and was present in the sludge flocs. After an initial adaptation period of 6 days, complete degradation of 3-CA was obtained during two weeks, while no degradation at all occurred in the non-inoculated control reactors. Upon further operation of the SCAS system, only 50 % 3-CA removal was observed. Denaturing Gradient Gel Electrophoresis (DGGE) of 16S rRNA genes revealed a dynamic change in the microbial community structure of the activated-sludge. The DGGE patterns of the non inoculated and the inoculated reactors evolved after 7 days to different clusters, which suggests an effect of strain inoculation on the microbial community structure. The results indicate that bioaugmentation, even with a strain originating from that ecosystem and able to effectively grow on a selective substrate, is not permanent and will probably require regular resupplementation.</abstract>
<fullTextUrl format="pdf">http://pubs.sciepub.com/jaem/2/4/12/jaem-2-4-12.pdf</fullTextUrl>
<keywords language="eng"><keyword>Pseudomonas</keyword>
<keyword>gfp</keyword>
<keyword>chloroaniline</keyword>
<keyword>DGGE</keyword>
</keywords>
</record>
</records>
