Cellulose-containing raw materials are currently considered to be among the most promising types of raw materials for the production of value-added bio-products. However, for the implementation of the developed process, the application of universal pre-processing methods is a prerequisite. In the present paper, a study into the bioconversion of oat hull and miscanthus cellulose samples by enzymatic hydrolysis into glucose solutions is presented. The substrates were obtained by two-stage processing of raw materials with dilute solutions of nitric acid and sodium hydroxide. Enzymatic hydrolysis was carried out using the Cellolux-A and Ultraflo Core enzyme preparations at an initial substrate concentration of 40 g/L. At the first stage, the reactivity of the substrates to enzymatic hydrolysis in an acetate buffer solution was studied over a period of 72 hours. Cellulose samples from both types of raw materials were established to possess equally high reactivity in terms of the reducing substances. Glucose obtained from the substrate yielded 94–95 % and 88–91 %, respectively. This indicates the universality of the pre-treatment method used for raw materials having a cellulose content of 35–45 %. At the second stage, hydrolysis of the substrates was carried out using a pilot fermenter in an aqueous medium with an excess of enzyme preparations. Over a period of 32 hours, aqueous hydrolysates were obtained with a concentration of reducing substances and glucose equal to 42 g/L (94 % yield from the substrate) and 33–35 g/L (74–78 % yield from the substrate), respectively. The glucose (79–83 %) and pentose (1–2 %) content of the reducing substances indicates glucose to predominate in the composition of the resulting solutions. The high bioconversion efficiency rate is additionally demonstrated by a comparative analysis of scanning electron spectroscopy results for substrates and residues following hydrolysis in a pilot fermenter. Glucose solutions obtained in an aqueous medium are emerging as promising materials for the preparation of culture media and the synthesis of valuable metabolites. The authors declare no conflict of interests regarding the publication of this article.