Industrial Crop Research Centre, Agricultural Research Council, Bologna, Italy.
Enzyme Microb Technol. 2012 May 10;50(6-7):304-10. doi: 10.1016/j.enzmictec.2012.02.005. Epub 2012 Mar 7.
Bioconversion of lignocellulosic biomass to fuel requires a hydrolysis step to obtain fermentable sugars, generally accomplished by fungal enzymes. Large-scale screening of different microbial strains would provide optimal enzyme cocktails for any target feedstock. The aim of this study was to screen a large collection of Trichoderma sp. strains for the hydrolytic potential towards switchgrass (Panicum virgatum L.). Strains were cultivated in a small-scale system and assayed in micro-plates for xylanase and cellulase activities. The population distributions of these traits are reported after growth on switchgrass in comparison with cellulose. The distribution profiles suggest that the growth on switchgrass strongly promotes xylanase production. The IK4 strain displayed the highest xylanase activity after growth on switchgrass (133U/mL). Enzymes (10FPU/g substrate) from IK4 were compared with those from 2 cellulolytic Trichoderma strains and a commercial enzyme in saccharification time-course experiments on untreated and pretreated switchgrass and on an artificial substrate. Samples were analysed by DNS assay and by an oxygraphic method for sugar equivalent or glucose concentration. On the untreated substrate, IK4 enzymes even outperformed a 5-fold load of commercial enzyme, suggesting that xylanase or accessory enzymes are a limiting factor on this type of recalcitrant substrate. On the other substrates, IK4 preparations showed intermediate behaviour if compared with the commercial enzyme at 10FPU/g substrate and at 5-fold load. IK4 also nearly halved the time to release 50% of the hydrolysable sugar equivalents (T(50%)), with respect to the other preparations at the same enzymatic load. DNS assay and oxygraphic method gave highly correlated results for the 3 saccharified substrates. The study suggests that accessory enzymes like xylanase play a key role in improving the performance of cellulase preparations on herbaceous lignocellulosic feedstocks like switchgrass.
木质纤维素生物质转化为燃料需要水解步骤以获得可发酵糖,通常通过真菌酶完成。对不同微生物菌株进行大规模筛选将为任何目标原料提供最佳的酶混合物。本研究的目的是筛选大量木霉属菌株对柳枝稷(Panicum virgatum L.)的水解潜力。菌株在小规模系统中培养,并在微板中测定木聚糖酶和纤维素酶活性。与纤维素相比,报告了这些特性在柳枝稷上生长后的种群分布。分布曲线表明,柳枝稷的生长强烈促进木聚糖酶的产生。IK4 菌株在柳枝稷上生长后的木聚糖酶活性最高(133U/mL)。IK4 的酶(10FPU/g 底物)与来自 2 种纤维素分解木霉属菌株和一种商业酶的酶在未处理和预处理柳枝稷以及人工底物上的糖化时间过程实验中进行了比较。样品通过 DNS 测定法和用于糖当量或葡萄糖浓度的测氧法进行分析。在未处理的底物上,IK4 酶甚至超过了商业酶的 5 倍负荷,这表明木聚糖酶或辅助酶是这种类型的难处理底物的限制因素。在其他底物上,如果与商业酶相比,IK4 制剂在 10FPU/g 底物和 5 倍负荷下表现出中间行为。IK4 还将释放 50%可水解糖当量的时间(T(50%))缩短了近一半,与相同酶负荷下的其他制剂相比。DNS 测定法和测氧法对 3 种糖化底物的结果高度相关。该研究表明,辅助酶如木聚糖酶在提高纤维素酶制剂对柳枝稷等草本木质纤维素饲料的性能方面起着关键作用。