IJRET
  • CrossRef
  • Google Scholar
  • ischolar
  • Index Copernicus
  • IJRET
  • Alternate Text
  • IJRET
  • IJRET
  • IJRET
  • Alternate Text
  • IJRET
  • IJRET
  • IJRET
  • IJRET
  • IJRET
  • IJRET
  • IJRET
Authors will receive one hard copy of full paper, individual print certificates and digital certificates, Submit Manuscript

CALL FOR PAPERS : DEC-2018

Submission Last Date :  30-Dec-2018
Acceptance Notification :  in 15 days
Publication Date :  in 5 days
Submit Manuscript Online

FOR AUTHORS

FOR REVIEWERS

IJRET® PUBLICATIONS

DOWNLOADS

CONTACT US

NEWS & UPDATES

Call for Paper Vol-7 Iss-02 Feb-2018

IJRET invites papers from various engineering disciplines for Volume-07 Issue-02, Feb-2018.

Submit Manuscript

Published Vol-07 Iss-01 Jan-18

IJRET Volume-07 Issue-01, Jan-2018 is published now.

Browse Papers

MICROBIAL COMMUNITY ANALYSIS IN ANAEROBIC PALM OIL MILL EFFLUENT (POME) WASTEWATER BY DENATURING GRADIENT GEL ELECTROPHORESIS (DGGE)

Husna Ahmad Tajuddin, Luqman Chuah Abdullah, Thomas S.Y.Choong

Abstract: Microorganisms play a key role in wastewater bio-treatment processes and understanding the microbial community structure is of great importance to improve treatment performance. Denaturing gradient gel electrophoresis (DGGE) was used to monitor succession of the microbial community and thus predominant bands were sequenced to reveal the microbial community composition inside palm oil mill effluent (POME) wastewater.DNA bands from DGGE gels were excised with a sterile blade and placed in 1.5 ml eppendorf tube containing 50 µl deionized water (ddH2O). Tubes were incubated overnight at 4?C to elute the DNA. Eluted DNA was purified using QIAquick gel extraction kits (QIAGEN, Inc., Valencia, CA) and was frozen and thawed three times.Microbial DNA successfully excised and purified from DGGE was amplified using polymerase chain reaction (PCR).Five micro liters of the supernatant were used as a template to re-amplify the DNA using 16s rDNA primers,341f (with no GC-clamp) (5- cct-acg-gga-ggc-agc-ag-3) and reverse(r) primers 907r (5-ccc-cgt-caa-ttc-att-tga-gtt-t-3). Amplification was repeated referring to the steps in ‘PCR amplification of 16s rDNA’. PCR products from agarose gels were cut and purified using QIAquick Gel Extraction Kit (QIAGEN, Inc., Valencia, CA), which were similar to the purification steps after recovery of DNA from DGGE, and sequenced in both directions with the same primers (with no GC-clamp) as used in PCR. Moreover, start-up is an important step in establishing proper community structure in all kinds of biological treatment processes. In anaerobic POME wastewater, 6 sequences of Firmicutes, 5 sequence of Proteobacterium and 2 sequences of Bacteroidetes were found through denaturing gradient gel electrophoresis (DGGE) results. Sequence closely related to Rummeliibacillus suwonensis strain G20 was detected grows at band BE10, BE11, BE12, BE15, BE16, BE17 and BE18. Meanwhile BE25 and BE26 were found at band after treatment process done.Rummeliibacillus suwonensis is an aerobic, Gram-positive, rod shaped, round-spore-forming bacteria which were isolated from aerobic condition.

Keywords: Palm oil mill effluent (POME), anaerobic POME, Denaturing gradient gel electrophoresis (DGGE), and microbial community.

DOI: https://doi.org/10.15623/ijret.2015.0408001

Home | Publication Ethics | Privacy Policy | Terms & Conditions | Refund Policy | Feedback | Contact Us
Copyright © 2012-2018 IJRET Journal All rights reserved