There is a vast repository of knowledge regarding improving beer taste stability via wort boiling. However, as far as we are aware, there are few reports dealing with taste stability improvement in terms of quality characteristics by boiling, under proper conditions, the first wort and second worts separately. In this study, more than 50 brews in a pilot scale brewing facility were conducted to investigate suitable boiling conditions for first and second worts. When the second wort (i.e., the last 10% of the total filtered wort) was kept under a low heat load atmosphere (78°C), casted to the boiling first wort, and then re-boiled for 10 min, the produced beer exhibited no significant differences compared to that of the general beer in terms of taste stability. However, when an adsorbent (bentonite, silica gel, activated carbon or PVPP) was individually added to the second wort and the same boiling procedure was performed, the oxidized flavour of the forced aged beer, treated with activated carbon, significantly decreased, compared to that of the general brew (level of significance α = 0.01). The data from the chemical analysis and fermentation behavior are presented.

: Free amino nitrogen (FAN) and other low‐molecular‐weight nitrogen compounds (LNC) are highly important as nutrients for yeast. Many different types of low‐malt beer exist around the world, some of which are produced with barley as an adjunct. In these cases, inhibitors contained in barley are known to influence the amount of LNC in wort. Accordingly, it is important to investigate which proteinase class is key in producing these compounds. By investigating the relationship between the FAN contained in wort produced from malt and barley (barley adjunct wort) and malt proteinase activity, it was found that cysteine proteinase and 1,10‐orthophenanthroline (O‐Phen)‐inhibitable metallo proteinases had a significant correlation to the barley adjunct wort FAN levels. In addition, the relationship between malting conditions and these proteinase activities was investigated and the conditions defined for maximal production of proteinases as follows: steeping degree, 50%; germination temperature, 12°C; germination days, 6 days; water spray, 3 times and concentration of gibberellic acid, 10 mg/kg (barley).