Consolidated bioprocessing of cellulosic biomass: an update

被引:925
作者
Lynd, LR [1 ]
van Zyl, WH
McBride, JE
Laser, M
机构
[1] Dartmouth Coll, Thayer Sch Engn, Hanover, NH 03755 USA
[2] Univ Stellenbosch, Dept Microbiol, ZA-7602 Matieland, South Africa
关键词
D O I
10.1016/j.copbio.2005.08.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Biologically mediated processes seem promising for energy conversion, in particular for the conversion of lignocellulosic biomass into fuels. Although processes featuring a step dedicated to the production of cellulase enzymes have been the focus of most research efforts to date, consolidated bioprocessing (CBP) - featuring cellulase production, cellulose hydrolysis and fermentation in one step - is an alternative approach with outstanding potential. Progress in developing CBP-enabling microorganisms is being made through two strategies: engineering naturally occurring cellulolytic microorganisms to improve product-related properties, such as yield and titer, and engineering non-cellulolytic organisms that exhibit high product yields and titers to express a heterologous cellulase system enabling cellulose utilization. Recent studies of the fundamental principles of microbial cellulose utilization support the feasibility of CBP.
引用
收藏
页码:577 / 583
页数:7
相关论文
共 60 条
[41]   EFFICIENT SECRETION OF 2 FUNGAL CELLOBIOHYDROLASES BY SACCHAROMYCES-CEREVISIAE [J].
PENTTILA, ME ;
ANDRE, L ;
LEHTOVAARA, P ;
BAILEY, M ;
TEERI, TT ;
KNOWLES, JKC .
GENE, 1988, 63 (01) :103-112
[42]   ENZYMATIC HYDROLYSIS OF CELLULOSE [J].
REESE, ET .
APPLIED MICROBIOLOGY, 1956, 4 (01) :39-45
[43]   EXPRESSION OF TETANUS TOXIN FRAGMENT-C IN YEAST - GENE SYNTHESIS IS REQUIRED TO ELIMINATE FORTUITOUS POLYADENYLATION SITES IN AT-RICH DNA [J].
ROMANOS, MA ;
MAKOFF, AJ ;
FAIRWEATHER, NF ;
BEESLEY, KM ;
SLATER, DE ;
RAYMENT, FB ;
PAYNE, MM ;
CLARE, JJ .
NUCLEIC ACIDS RESEARCH, 1991, 19 (07) :1461-1467
[44]   Direct production of ethanol from raw corn starch via fermentation by use of a novel surface-engineered yeast strain codisplaying glucoamylase and α-amylase [J].
Shigechi, H ;
Koh, J ;
Fujita, Y ;
Matsumoto, T ;
Bito, Y ;
Ueda, M ;
Satoh, E ;
Fukuda, H ;
Kondo, A .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (08) :5037-5040
[45]  
Strobel HP, 2004, P NAT M AM SOC MICR
[46]   Expression of Aspergillus aculeatus no. F-50 cellobiohydrolase I (cbhI) and β-glucosidase 1 (bgl1) genes by Saccharomyces cerevisiae [J].
Takada, G ;
Kawaguchi, T ;
Sumitani, J ;
Arai, M .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1998, 62 (08) :1615-1618
[47]  
TARDIF C, 2001, J IND MICROBIOL BIOT, V16, P1
[48]   Electrotransformation of Clostridium thermocellum [J].
Tyurin, MV ;
Desai, SG ;
Lynd, LR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (02) :883-890
[49]  
van Walsum GP, 1998, BIOTECHNOL BIOENG, V58, P316, DOI 10.1002/(SICI)1097-0290(19980420)58:2/3<316::AID-BIT31>3.0.CO
[50]  
2-7