Lignocellulosic wastes such as straw are attractive resources for biofuel production when subjected to biological treatment (hydrolysis). However, their complex lignocellulosic structure can hinder saccharification. The urgent need for microbial groups with high levels of straw saccharifying activities is therefore a key step in the bioconversion of lignocellulosic straw into fermentable monosaccharides. Existing traditional methods of qualitative and quantitative screening of lignocellulolytic microbial isolates are costly, time consuming and largely not environmentally friendly. In this study, a Biolog (MT2) microplate-based assay was evaluated for potential use as an alternative screening method. This was carried out using three commercially available substrates (cellulose, xylan and lignin) and four native lignocellulosic straws (wheat, rice, sugarcane, and pea ball-milled straws). Selected bacterial isolates from soil, compost and straws were screened quantitatively using both traditional crude enzyme and Biolog (MT2) microplate methods. Positive correlations (R2 values up to 0.86) between Biolog and the traditional enzyme methodologies were observed with respect to these isolates and their lignocellulosic activities. Quantitative assays were less labor intensive and faster (3–7 days) in Biolog microplates than in traditional assays which lasted for 12–15 days. Ball-milled rice and sugarcane straws were bio-converted to monosaccharaides more readily than wheat and pea straws and the commercially available substrates (cellulose, xylan and lignin). Environmental scanning electron microscopy (ESEM) analysis of ball-milled rice and sugarcane straws suggested that this was due to their higher silica content. Overall, the Biolog (MT2) microplate system was shown to be an effective, time saving and inexpensive alternative method for the screening of both lignocellulose-degrading bacteria and different substrates for saccharification. |
