Guan Di, Zhao Rui, Li Yuan, Sakakibara Yoshikiyo, Ike Masakazu, Tokuyasu Ken
1 Food Research Institute, National Agriculture and Food Research Organization.
J Appl Glycosci (1999). 2019 Feb 20;66(1):21-28. doi: 10.5458/jag.jag.JAG-2018_0006. eCollection 2019.
Novel bioreactor beads for simultaneous saccharification and fermentation (SSF) of lime-pretreated rice straw (RS) into ethanol were prepared. Genetically modified cells expressing genes encoding xylose reductase, xylitol dehydrogenase, and xylulokinase were immobilized in calcium alginate beads containing inorganic lightweight filler particles to reduce specific gravity. For SSF experiments, the beads were floated in slurry composed of lime-pretreated RS and enzymes and incubated under CO atmosphere to reduce the pH for saccharification and fermentation. Following this reaction, beads were readily picked up from the upper part of the slurry and were directly transferred to the next vessel with slurry. After 240 h of incubation, ethanol production by the beads was equivalent to that by free cells, a trend that was repeated in nine additional runs, with slightly improved ethanol yields. Slurry with pre-saccharified lime-pretreated RS was subjected to SSF with floating beads for 168 h. Although higher cell concentrations in beads resulted in more rapid initial ethanol production rates, with negligible diauxic behavior for glucose and xylose utilization, no improvement in the ethanol yield was observed. A fermentor-scale SSF experiment with floating beads was successfully performed twice, with repeated use of the beads, resulting in the production of 40.0 and 39.7 g/L ethanol. There was no decomposition of the beads during agitation at 60 rpm. Thus, this bioreactor enables reuse of yeast cells for efficient ethanol production by SSF of lignocellulosic feedstock, without the need for instruments for centrifugation or filtration of whole slurry.
制备了用于将石灰预处理稻草(RS)同步糖化发酵(SSF)为乙醇的新型生物反应器珠粒。将表达编码木糖还原酶、木糖醇脱氢酶和木酮糖激酶基因的转基因细胞固定在含有无机轻质填料颗粒的海藻酸钙珠粒中以降低比重。对于SSF实验,将珠粒漂浮在由石灰预处理的RS和酶组成的浆液中,并在CO气氛下孵育以降低pH值用于糖化和发酵。反应后,珠粒很容易从浆液上部取出并直接转移到装有浆液的下一个容器中。孵育240小时后,珠粒产生的乙醇量与游离细胞产生的乙醇量相当,在另外九次运行中也重复出现了这种趋势,乙醇产量略有提高。将预糖化的石灰预处理RS的浆液与漂浮珠粒进行168小时的SSF。尽管珠粒中较高的细胞浓度导致初始乙醇产生速率更快,葡萄糖和木糖利用的双相生长行为可忽略不计,但未观察到乙醇产量的提高。成功进行了两次使用漂浮珠粒的发酵罐规模的SSF实验,珠粒可重复使用,产生了40.0和39.7 g/L的乙醇。在60 rpm搅拌过程中珠粒没有分解。因此,这种生物反应器能够通过木质纤维素原料的SSF重复使用酵母细胞以高效生产乙醇,而无需用于整个浆液离心或过滤的仪器。