AWWA WQTC62571 PDF

AWWA WQTC62571 PDF

Name:
AWWA WQTC62571 PDF

Published Date:
11/01/2005

Status:
Active

Description:

The Influence of Disinfectant Regime on the Microbial Composition of Downstream Drinking Water Biofilms

Publisher:
American Water Works Association

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Russian version):
200 business days

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Biofilms occur throughout drinking water distribution systems, and their composition is highly dependent on the water matrix as well as the material and condition of the pipes. Many utilities are considering changes in their disinfection regimes to improve the microbial quality of the water and to limit the formation of disinfection byproducts in plant effluent. These changes often involve the addition of upstream ultraviolet (UV) treatment and/or the use of monochloramine instead of chlorine to provide the disinfectant residual. There is little information about what effect such changes in disinfection regime will have on distribution biofilms. Using a flow-through laboratory model, the study used molecular techniques to examine the bacterial composition of biofilms formed from the same water source on different pipe materials, under different disinfection regimes (chlorine and monochloramine at appropriate concentrations) with and without upstream UV treatment. Source water was a soft surface water source in Halifax, Canada. Controls were also included without any additional disinfectant residual. Two substrates, cast iron and polycarbonate coupons in annular reactors, were used to represent pipe materials. The biofilm samples were removed from the coupons at defined intervals and total DNA was extracted from the samples. The samples were also cultured on R2A medium for heterotrophic plate count, and R2A plates were harvested to extract DNA from cultivable bacteria. The DNA samples from both sources were then used to assess the composition of the biofilm bacterial community by PCR-DGGE (denaturing gradient gel electrophoresis). Primers for a variable region of the 16 S rRNA gene were used to amplify bacterial DNA. These fragments were then separated on a DGGE gel which separates same size fragments on the basis of their sequence. Identification is achieved by carefully excising bands from the gel, cloning, sequencing and comparing sequences with libraries from online databases (BLAST and Ribosomal Database Project II). Differences were clearly seen in the gels for each of the treatments examined so far; full characterization of the biofilms is ongoing and it is anticipated that definite differences will emerge between different disinfectants as well as the coupon materials. The significance of such differences remains to be determined. Includes figures.
Edition : Vol. - No.
File Size : 1 file , 2.4 MB
Note : This product is unavailable in Ukraine, Russia, Belarus
Number of Pages : 7
Published : 11/01/2005

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