Lignocellulose Biotechnology Laboratory, Department of Microbiology, University of Delhi South Campus, New Delhi 110021, India.
Biotechnol Biofuels. 2012 Mar 20;5:16. doi: 10.1186/1754-6834-5-16.
Enzymatic hydrolysis, the rate limiting step in the process development for biofuel, is always hampered by its low sugar concentration. High solid enzymatic saccharification could solve this problem but has several other drawbacks such as low rate of reaction. In the present study we have attempted to enhance the concentration of sugars in enzymatic hydrolysate of delignified Prosopis juliflora, using a fed-batch enzymatic hydrolysis approach.
The enzymatic hydrolysis was carried out at elevated solid loading up to 20% (w/v) and a comparison kinetics of batch and fed-batch enzymatic hydrolysis was carried out using kinetic regimes. Under batch mode, the actual sugar concentration values at 20% initial substrate consistency were found deviated from the predicted values and the maximum sugar concentration obtained was 80.78 g/L. Fed-batch strategy was implemented to enhance the final sugar concentration to 127 g/L. The batch and fed-batch enzymatic hydrolysates were fermented with Saccharomyces cerevisiae and ethanol production of 34.78 g/L and 52.83 g/L, respectively, were achieved. Furthermore, model simulations showed that higher insoluble solids in the feed resulted in both smaller reactor volume and shorter residence time.
Fed-batch enzymatic hydrolysis is an efficient procedure for enhancing the sugar concentration in the hydrolysate. Restricting the process to suitable kinetic regimes could result in higher conversion rates.
酶解是生物燃料生产过程中的限速步骤,但由于糖浓度低,其一直受到阻碍。高固体酶糖化可以解决这个问题,但也有其他几个缺点,例如反应速率低。在本研究中,我们试图通过分批酶水解的方法来提高酶解木质素去除后的刺槐中糖的浓度。
在 20%(w/v)的高固体负荷下进行了酶水解,使用动力学模型比较了分批和分批补料酶水解的动力学。在分批模式下,在 20%初始底物浓度下,实际糖浓度值与预测值存在偏差,获得的最大糖浓度为 80.78g/L。采用分批补料策略将最终糖浓度提高到 127g/L。分批和分批补料酶解液分别用酿酒酵母发酵,乙醇产量分别为 34.78g/L 和 52.83g/L。此外,模型模拟表明,进料中较高的不溶性固体含量会导致反应器体积更小和停留时间更短。
分批酶水解是提高水解液中糖浓度的有效方法。将过程限制在合适的动力学模型中可以获得更高的转化率。