TRFLP analysis reveals that fungi rather than bacteria are associated with premature yeast flocculation in brewing

Mandeep Kaur1, John P Bowman, Doug C Stewart

  • 1Food Safety Centre, Tasmanian Institute of Agriculture, University of Tasmania, Hobart, TAS, Australia. mandeepk@utas.edu.au

Insights

Premature yeast flocculation (PYF) in brewing is linked to fungal communities in barley malt. Molecular monitoring of barley malt offers a viable alternative for detecting PYF during fermentation.

Area of Science:

  • Brewing Science
  • Microbiology
  • Molecular Biology

Background:

  • Premature yeast flocculation (PYF) is a sporadic issue in brewing, leading to incomplete sugar utilization.
  • Identifying the microbial causes of PYF is crucial for the brewing industry.

Purpose of the Study:

  • To investigate the association between barley malt microbial communities and PYF occurrence.
  • To differentiate microbial profiles in barley malt linked to PYF positive (PYF +ve) and negative (PYF -ve) fermentations.

Main Methods:

  • Culture-independent, PCR-based fingerprinting techniques were employed.
  • Terminal restriction fragment length polymorphism (TRFLP) was used to analyze fungal and bacterial DNA from barley malt.

Main Results:

  • Significant differences in fungal DNA fingerprint patterns were observed between PYF +ve and PYF -ve barley malts.
  • Specific fungal terminal restriction fragments (TRFs) in the 360-460 bp range (HaeIII enzyme) varied between sample groups.
  • Bacterial communities did not show significant variation, suggesting they are unlikely to cause PYF.

Conclusions:

  • Fungal communities in barley malt are strongly associated with PYF occurrence.
  • Molecular analysis of barley malt offers a potential method for early detection and management of PYF.
  • The source of barley malt did not influence the fungal taxa implicated in PYF.

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