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African Journal of Biotechnology

     
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  Afr. J. Biotechnol.

  Vol. 9 No. 10

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  Search Pubmed for articles by:

  Bakar AF

  Abdulamir AS
 

 
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African Journal of Biotechnology Vol. 9 (10), pp. 1481-1492 8 March, 2010

ISSN 1684-5315  © 2010 Academic Journals  

 

 

Full Length Research Paper

 

Detection and quantification of probiotic bacteria using optimized DNA extraction, traditional and real-time PCR methods in complex microbial communities

 

Abdulamir A. S.1,2, Yoke T. S.3, Nordin N.3 and Abu Bakar F.1,3*

 

1Institute of Bioscience, University Putra Malaysia, 43400 Serdang, Selangor, Malaysia.

2Microbiology department, College of Medicine, Al-nahrain University, 14222, Baghdad, Iraq.

3Faculty of Food Science and Technology, University Putra Malaysia, 43400 Serdang, Selangor, Malaysia.

 

*Corresponding author. E-mail: fatimah_upm_fst@yahoo.com. Tel: 00-60-389468375.  Fax: 00-60-89423552.

 

Accepted 26 November, 2009

 

   Abstract

 

The aim of this study is to optimize molecular detection and quantification methods of probiotic bacteria in complex microbial communities that have long been difficult for traditional culture-based methods. Traditional and real-time PCR were optimized to detect and quantify Lactobacillus spp. and Bifidobacterium spp. in complex microbial community. Fish and shrimp sauce were used as a model for complex microbial community. Directly form samples, 4 DNA extraction methods, primers specificity, PCR, and real-time PCR procedures were optimized, tested in comparison with samples, enriched bacteria and related standard bacterial strains, E. coli, Bacteroides, Enterococcus and Salmonella. Results showed that extracted genomic DNA using Wizard® Genomic DNA Purification Kit showed the highest yield, quality and performance. Moreover, the specificity of the primer set specific for Lactobacillus spp. and Bifidobacterium spp. was checked and found highly specific. The sensitivity of real-time PCR was higher than the conventional PCR and its quantifying potential is very precise for the detection and quantification of Lactobacillus spp. but not Bifidobacterium spp. which was absent in the tested samples. In conclusion, PCR and real-time PCR assays could be used very efficiently in quantifying and detecting Lactobacillus spp. that are present in very PCR-suppressive and complex microbial environment.

 

Key words: PCR, real-time PCR, DNA extraction, Bifidobacterium spp., Lactobacillus spp., fermentation, probiotic.

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