Demonstrates sugar conversion optimization in brewers’ spent grains, indicating potential for sustainable biorefinery development.
This study presents an integrated biorefinery concept using brewers’ spent grains (BSG) processed via acidic enzymatic proteolysis and dilute nitric acid treatment for the production of protein-rich hydrolysates and poly(3-hydroxybutyrate) (PHB). After aqueous extraction of dextrins, acidic proteolysis of the remaining BSG solids (10% w/v, pH 3, 50 °C, 10 U/g) achieved a protein extraction efficiency of 66.9 ± 0.6%. The protein-rich hydrolysate contained, per 100 g protein, mainly glutamic acid and glutamine (29.8%), aspartic acid and asparagine (9.7%), leucine (8.1%), proline (7.2%) and valine (6.7%). Central composite design was employed for the optimization of dilute HNO 3 pretreatment of the remaining BSG solids to maximize the glucan and hemicellulose to sugar conversion yield, considering HNO 3 concentration (0-1% w/v) and temperature (70-120 °C) as process variables. The optimal BSG treatment was achieved at 0.29% (w/v) HNO 3 , 120 °C and 30 min reaction duration, resulting in 58.1% overall glucan and hemicellulose to sugar conversion yield. The hydrolysate contained 75.1% glucose, 20.7% xylose, 3.7% galactose and 1.5% arabinose. Fed-batch fermentation of Paraburkholderia sacchari using the optimal BSG hydrolysate resulted in 97.7 g/L PHB, 65.5% (w/w) intracellular PHB content, 0.31 g/g PHB yield and a productivity of 2.87 g/(L∙h). This biorefinery concept resulted in the production of 155.1 g PHB and 160.2 g protein-rich extract produced as hydrolysate from 1 kg BSG. • Optimal pretreatment (0.29% HNO 3 , 120 °C, 30 min) achieved 58.1% sugar yield. • Acidic proteolysis extracted efficiently 67% of BSG protein. • Biorefinery co-produced 155 g PHB and 160 g protein hydrolysate per kg BSG. • P. sacchari fermentation reached 97.7 g/L PHB with 2.87 g/(L∙h) productivity.
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Argeiti et al. (2026) studied this question.
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