Literature DB >> 18502530

Group-specific PCR-RFLP and real-time PCR methods for detection and tentative discrimination of strictly anaerobic beer-spoilage bacteria of the class Clostridia.

Riikka Juvonen1, Teija Koivula, Auli Haikara.   

Abstract

The strictly anaerobic brewery contaminants of the genera Pectinatus, Megasphaera, Selenomonas and Zymophilus in the class Clostridia constitute an important group of spoilage bacteria of unpasteurised, packaged beers. The aim of this study was to develop and evaluate group-specific PCR methods to detect and differentiate these bacteria in beer. A group-specific primer pair targeting a 342-bp variable region of the 16S rRNA gene was designed and evaluated in end-point PCR with gel electrophoresis and in real-time PCR with SYBR Green I dye. Significant cross-reactions with DNAs from any of the forty-two brewery-related, non-target microbes or from real brewery samples were not detected in either PCR system. The group-specific end-point and real-time PCR products could be differentiated according to species/genus and spoilage potential using restriction fragment length polymorphism (KpnI, XmnI, BssHII, ScaI) and melting point curve analysis, respectively. In combination with a rapid DNA extraction method, the PCR reactions detected ca 10(0)-10(3) CFU per 25 ml of beer depending on the strain and on the PCR system. The end-point and real-time PCR analysis took 6-7 h and 2-3 h, respectively. Pre-PCR enrichment of beer samples for 1-3 days ensured the detection of even a single cultivable cell. The PCR and cultivation results of real brewery samples were mostly congruent but the PCR methods were occasionally more sensitive. The PCR methods developed allow the detection of all the nine beer-spoilage Pectinatus, Megasphaera, Selenomonas and Zymophilus species in a single reaction and their differentiation below group level and reduce the analysis time for testing of their presence in beer samples by 1-2 days. The methods can be applied for brewery routine quality control and for studying occurrence, diversity and numbers of the strictly anaerobic beer spoilers in the brewing process.

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Year:  2008        PMID: 18502530     DOI: 10.1016/j.ijfoodmicro.2008.03.042

Source DB:  PubMed          Journal:  Int J Food Microbiol        ISSN: 0168-1605            Impact factor:   5.277


  5 in total

1.  Establishment of a nested-ASP-PCR method to determine the clarithromycin resistance of Helicobacter pylori.

Authors:  Xiao-Feng Luo; Jian-Hua Jiao; Wen-Yue Zhang; Han-Ming Pu; Bao-Jin Qu; Bing-Ya Yang; Min Hou; Min-Jun Ji
Journal:  World J Gastroenterol       Date:  2016-07-07       Impact factor: 5.742

2.  Identification of plasmalogen cardiolipins from Pectinatus by liquid chromatography-high resolution electrospray ionization tandem mass spectrometry.

Authors:  Tomáš Řezanka; Dagmar Matoulková; Lucie Kyselová; Karel Sigler
Journal:  Lipids       Date:  2013-10-10       Impact factor: 1.880

3.  Hydrophilic interaction liquid chromatography: ESI-MS/MS of plasmalogen phospholipids from Pectinatus bacterium.

Authors:  Tomáš Rezanka; Lucie Siristova; Dagmar Matoulková; Karel Sigler
Journal:  Lipids       Date:  2011-04-11       Impact factor: 1.880

4.  Application of high-resolution melting analysis for differentiation of spoilage yeasts.

Authors:  Mine Erdem; Zülal Kesmen; Esra Özbekar; Bülent Çetin; Hasan Yetim
Journal:  J Microbiol       Date:  2016-08-31       Impact factor: 3.422

5.  Growth of Dunaliella tertiolecta and associated bacteria in photobioreactors.

Authors:  Aino-Maija Lakaniemi; Veera M Intihar; Olli H Tuovinen; Jaakko A Puhakka
Journal:  J Ind Microbiol Biotechnol       Date:  2012-05-11       Impact factor: 3.346

  5 in total

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