Skotnicki M L, Warr R G, Goodman A E, Lee K J, Rogers P L
Biochem Soc Symp. 1983;48:53-86.
A process is under development at the University of New South Wales to produce fermentation ethanol faster and more efficiently. The process is based on the micro-organism Zymomonas mobilis, which has higher specific rates of ethanol production and higher yields when compared with the traditionally used yeasts. By using hollow fibre membranes for cell recycle, high productivity continuous processes have been studied at laboratory-scale. Pilot scale evaluations (500 litres) are now in progress through Licence Agreements between the University and industry. Genetic manipulation and recombinant DNA techniques are being used to increase the ethanol tolerance and broaden the substrate range. Most recently glucoamylase genes from Aspergillus niger have been cloned into Escherichia coli K12 as part of a programme to enable direct fermentation of starch to ethanol by Z. mobilis.
新南威尔士大学正在研发一种能更快、更高效地生产发酵乙醇的工艺。该工艺基于运动发酵单胞菌这种微生物,与传统使用的酵母相比,它具有更高的乙醇生产比速率和更高的产量。通过使用中空纤维膜进行细胞循环,已在实验室规模上研究了高生产率的连续工艺。目前,通过大学与企业之间的许可协议正在进行中试规模评估(500升)。正在使用基因操作和重组DNA技术来提高乙醇耐受性并拓宽底物范围。最近,作为使运动发酵单胞菌能够将淀粉直接发酵为乙醇的计划的一部分,来自黑曲霉的葡糖淀粉酶基因已被克隆到大肠杆菌K12中。