Casa-Villegas Mary, Marín-Navarro Julia, Polaina Julio
Instituto de Agroquímica y Tecnología de Alimentos, CSIC, Valencia, Spain.
Departamento de Bioquímica, Facultad de Biología, Universidad de Valencia, Valencia, Spain.
World J Microbiol Biotechnol. 2017 Jul;33(7):140. doi: 10.1007/s11274-017-2308-4. Epub 2017 Jun 6.
We describe a procedure by which filter paper is digested with a cellulolytic enzyme preparation, obtained from Trichoderma reesei cultivated under solid state fermentation conditions and then fermented by a recombinant Saccharomyces cerevisiae strain. The yeast strain produces a β-glucosidase encoded by the BGL1 gene from Saccharomycopsis fibuligera that quantitatively and qualitatively complements the limitations that the Trichoderma enzyme complex shows for this particular activity. The supplemental β-glucosidase activity fuels the progression of cellulose hydrolysis and fermentation by decreasing the inhibitory effects caused by the accumulation of cellobiose and glucose. Fermentation of filter paper by this procedure yields ethanol concentrations above 70 g/L.
我们描述了一种方法,即先用纤维素分解酶制剂消化滤纸,该酶制剂从在固态发酵条件下培养的里氏木霉中获得,然后用重组酿酒酵母菌株进行发酵。该酵母菌株产生由扣囊复膜孢酵母的BGL1基因编码的β-葡萄糖苷酶,该酶在数量和质量上弥补了木霉酶复合物在这种特定活性方面所表现出的局限性。补充的β-葡萄糖苷酶活性通过降低纤维二糖和葡萄糖积累所引起的抑制作用,推动纤维素水解和发酵的进程。通过该方法对滤纸进行发酵,乙醇浓度可超过70 g/L。