β-Amylase is important to the malting and brewing industry because it is one of four main enzymes involved in fermentable sugar production during mashing. There are two functional barley β-amylases encoded by the Bmy1 and Bmy2 genes. Mashing is commonly performed at high temperatures and β-amylase1 (Bmy1) is vulnerable to thermal inactivation at these temperatures. Unlike Bmy1, Bmy2 is not stored at useful levels in the mature grain but Bmy2 encodes a more thermostable β-amylase. Expression of β-amylase is not thought to occur during malting but, interestingly, de novo expression of Bmy2 is seen in other Triticeae tribe members during germination. Therefore, this research was conducted to determine if barley Bmy2 is de novo expressed during micromalting. De novo expression of Bmy2 is observed in both a two- and six-row malting cultivar (Conrad and Legacy, respectively). Legacy Bmy2 transcript levels significantly increased (40-fold) between 0 and 4 Days of Germination (DoG) and Conrad Bmy2 transcript levels significantly increased (20-fold) between 0 and 3 DoG. Legacy had significantly (1.9-fold) more Bmy2 transcript levels than Conrad by the end of micromalting. The β-amylase activity and protein immunoblots corroborated the gene expression data thus reliably demonstrating the de novo expression of Bmy2 during micromalting.
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