Accelerated design of bioconversion processes using automated microscale processing techniques

被引:106
作者
Lye, GJ [1 ]
Ayazi-Shamlou, P [1 ]
Baganz, F [1 ]
Dalby, PA [1 ]
Woodley, JM [1 ]
机构
[1] UCL, Adv Ctr Biochem Engn, Dept Biochem Engn, London WC1E 7JE, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1016/S0167-7799(02)00011-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Microscale processing techniques are rapidly emerging as a means to increase the speed of bioprocess design and reduce material requirements. Automation of these techniques can reduce labour intensity and enable a wider range of process variables to be examined. This article examines recent research on various individual microscale unit operations including microbial fermentation, bioconversion and product recovery techniques. It also explores the potential of automated whole process sequences operated in microwell formats. The power of the whole process approach is illustrated by reference to a particular bioconversion, namely the Baeyer-Villiger oxidation of bicyclo[3.2.0]hept-2-en-6-one for the production of optically pure lactones.
引用
收藏
页码:29 / 37
页数:9
相关论文
共 72 条
[1]   Device for sterile online measurement of the oxygen transfer rate in shaking flasks [J].
Anderlei, T ;
Büchs, J .
BIOCHEMICAL ENGINEERING JOURNAL, 2001, 7 (02) :157-162
[2]   Directed evolution: Creating biocatalysts for the future [J].
Arnold, FH .
CHEMICAL ENGINEERING SCIENCE, 1996, 51 (23) :5091-5102
[3]   Improved biocatalysts by directed evolution and rational protein design [J].
Bornscheuer, UT ;
Pohl, M .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2001, 5 (02) :137-143
[4]  
Büchs J, 2000, BIOTECHNOL BIOENG, V68, P589, DOI 10.1002/(SICI)1097-0290(20000620)68:6<589::AID-BIT1>3.0.CO
[5]  
2-J
[6]  
Büchs J, 2000, BIOTECHNOL BIOENG, V68, P594, DOI 10.1002/(SICI)1097-0290(20000620)68:6<594::AID-BIT2>3.0.CO
[7]  
2-U
[8]   Introduction to advantages and problems of shaken cultures [J].
Büchs, J .
BIOCHEMICAL ENGINEERING JOURNAL, 2001, 7 (02) :91-98
[9]   Metabolic engineering and directed evolution for the production of pharmaceuticals [J].
Chartrain, M ;
Salmon, PM ;
Robinson, DK ;
Buckland, BC .
CURRENT OPINION IN BIOTECHNOLOGY, 2000, 11 (02) :209-214
[10]   OXYGEN LIMITATION CAN INDUCE MICROBIAL SECONDARY METABOLITE FORMATION - INVESTIGATIONS WITH MINIATURE ELECTRODES IN SHAKER AND BIOREACTOR CULTURE [J].
CLARK, GJ ;
LANGLEY, D ;
BUSHELL, ME .
MICROBIOLOGY-UK, 1995, 141 :663-669