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<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran/Springer</PublisherName>
				<JournalTitle>International Journal of Environmental Research</JournalTitle>
				<Issn>1735-6865</Issn>
				<Volume>9</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>01</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>MicrobiologicalAssessment of the BiofilterMatrixWithin a Biofiltration systemTreating Borehole water in KwaZulu-Natal (SouthAfrica)</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>263</FirstPage>
			<LastPage>272</LastPage>
			<ELocationID EIdType="pii">896</ELocationID>
			
<ELocationID EIdType="doi">10.22059/ijer.2015.896</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>L.S.</FirstName>
					<LastName>Beukes</LastName>
<Affiliation>Discipline of Microbiology, School of Life Sciences, University of KwaZulu-Natal, Private
Bag X01, Pietermaritzburg 3209, South Africa</Affiliation>

</Author>
<Author>
					<FirstName>S.</FirstName>
					<LastName>Schmidt</LastName>
<Affiliation>Discipline of Microbiology, School of Life Sciences, University of KwaZulu-Natal, Private
Bag X01, Pietermaritzburg 3209, South Africa</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>31</Day>
				</PubDate>
			</History>
		<Abstract>To assess the microbiological status of a biofiltration system used to treat borehole water, filter&lt;br /&gt;matrix samples were analyzed after staining for the presence of active biofilms using confocal laser scanning&lt;br /&gt;microscopy (CLSM). CLSM revealed the presence of biofilms on the filter matrix with actively metabolizing&lt;br /&gt;microbial cells present. Thereafter, heterotrophs,manganese oxidizing bacteria (MOB) and iron oxidizing bacteria&lt;br /&gt;(IOB) present in the biofilms were quantified. For heterotrophs a count of 2.9×107 cfu/g was established using&lt;br /&gt;R2A agar while counts for presumptive MOB and IOB were established as 2.4×107 cfu/g and 3.1×107 cfu/g&lt;br /&gt;respectively. In addition, a clone library was established using DNAextracted from a pooled filter matrix sample&lt;br /&gt;to assess the diversity of bacteria present within the biofilter matrix. A total of 100 randomly selected clones&lt;br /&gt;were separated into 14 unique operational taxonomic unit (OTU’s) based upon restriction patterns of amplified&lt;br /&gt;partial 16S rRNA genes. Overall, 38% of the clones were assigned to the phylum Proteobacteria, 13% to the&lt;br /&gt;phylum Actinobacteria, 24% to the phylum Firmicutes, 21% to the phylum Nitrospirae and 4% to the phylum&lt;br /&gt;Verrucomicrobia.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Biofiltration system/ biofilm / CLSM/microbial counts/16S rRNA gene clone library</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijer.ut.ac.ir/article_896_061412e4a03c02f9902576ec55ebbe77.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
