Production of recombinant proteins by filamentous fungi

被引:172
作者
Ward, Owen P. [1 ]
机构
[1] Univ Waterloo, Dept Biol, Waterloo, ON N2L 3G1, Canada
基金
美国国家科学基金会;
关键词
Aspergillus; Trichoderma; Penicillium; Recombinant protein; Heterologous; Protease; Genome; Filamentous; Fungi; Pathogenesis; N-ACETYLGLUCOSAMINYLTRANSFERASE-I; HETEROLOGOUS GENE-EXPRESSION; FATTY-ACID DESATURASES; CELL WALL DEGRADATION; SOLID-STATE CULTURE; EGG-WHITE LYSOZYME; ASPERGILLUS-NIGER; TRICHODERMA-REESEI; PENICILLIUM-CHRYSOGENUM; POLYKETIDE SYNTHASE;
D O I
10.1016/j.biotechadv.2011.09.012
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
The initial focus of recombinant protein production by filamentous fungi related to exploiting the extraordinary extracellular enzyme synthesis and secretion machinery of industrial strains, including Aspergillus, Trichoderma, Penicillium and Rhizopus species, was to produce single recombinant protein products. An early recognized disadvantage of filamentous fungi as hosts of recombinant proteins was their common ability to produce homologous proteases which could degrade the heterologous protein product and strategies to prevent proteolysis have met with some limited success. It was also recognized that the protein glycosylation patterns in filamentous fungi and in mammals were quite different, such that filamentous fungi are likely not to be the most suitable microbial hosts for production of recombinant human glycoproteins for therapeutic use. By combining the experience gained from production of single recombinant proteins with new scientific information being generated through genomics and proteomics research, biotechnologists are now poised to extend the biomanufacturing capabilities of recombinant filamentous fungi by enabling them to express genes encoding multiple proteins, including, for example, new biosynthetic pathways for production of new primary or secondary metabolites. It is recognized that filamentous fungi, most species of which have not yet been isolated, represent an enormously diverse source of novel biosynthetic pathways, and that the natural fungal host harboring a valuable biosynthesis pathway may often not be the most suitable organism for biomanufacture purposes. Hence it is expected that substantial effort will be directed to transforming other fungal hosts, non-fungal microbial hosts and indeed non microbial hosts to express some of these novel biosynthetic pathways. But future applications of recombinant expression of proteins will not be confined to biomanufacturing. Opportunities to exploit recombinant technology to unravel the causes of the deleterious impacts of fungi, for example as human, mammalian and plant pathogens, and then to bring forward solutions, is expected to represent a very important future focus of fungal recombinant protein technology. Crown Copyright (C) 2011 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1119 / 1139
页数:21
相关论文
共 289 条
[1]  
Abianova A R, 2010, Prikl Biokhim Mikrobiol, V46, P342
[2]   Changes in nitrogen assimilation, metabolism, and growth in transgenic rice plants expressing a fungal NADP(H)-dependent glutamate dehydrogenase (gdhA) [J].
Abiko, Tomomi ;
Wakayama, Masataka ;
Kawakami, Akira ;
Obara, Mitsuhiro ;
Kisaka, Hiroaki ;
Miwa, Tetsuya ;
Aoki, Naohiro ;
Ohsugi, Ryu .
PLANTA, 2010, 232 (02) :299-311
[3]   Quantitative iTRAQ Secretome Analysis of Aspergillus niger Reveals Novel Hydrolytic Enzymes [J].
Adav, Sunil S. ;
Li, An A. ;
Manavalan, Arulmani ;
Punt, Peter ;
Sze, Siu Kwan .
JOURNAL OF PROTEOME RESEARCH, 2010, 9 (08) :3932-3940
[4]   Culture-based strategies for reduction of protease activity in filtrates from Aspergillus niger NRRL-3 [J].
Ahamed, A ;
Singh, A ;
Ward, OP .
WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 2005, 21 (8-9) :1577-1583
[5]   DELTA-(L-ALPHA-AMINOADIPYL)-L-CYSTEINYL-D-VALINE SYNTHETASE, THE MULTIENZYME INTEGRATING THE 4 PRIMARY REACTIONS IN BETA-LACTAM BIOSYNTHESIS, AS A MODEL PEPTIDE SYNTHETASE [J].
AHARONOWITZ, Y ;
BERGMEYER, J ;
CANTORAL, JM ;
COHEN, G ;
DEMAIN, AL ;
FINK, U ;
KINGHORN, J ;
KLEINKAUF, H ;
MACCABE, A ;
PALISSA, H ;
PFEIFER, E ;
SCHWECKE, T ;
VANLIEMPT, H ;
VONDOHREN, H ;
WOLFE, S ;
ZHANG, JY .
BIO-TECHNOLOGY, 1993, 11 (07) :807-810
[6]   Subtractive cloning of cDNA from Aspergillus oryzae differentially regulated between solid-state culture and liquid (submerged) culture [J].
Akao, T ;
Gomi, K ;
Goto, K ;
Okazaki, N ;
Akita, O .
CURRENT GENETICS, 2002, 41 (04) :275-281
[7]  
Akin AR, 2003, United States Patent Application, Patent No. 20030045697
[8]   Vaccine production in Neurospora crassa [J].
Allgaier, Silke ;
Taylor, Rebecca D. ;
Brudnaya, Yuliya ;
Jacobson, David J. ;
Cambareri, Edward ;
Stuart, W. Dorsey .
BIOLOGICALS, 2009, 37 (03) :128-132
[9]   From genomics to post-genomics in Aspergillus [J].
Archer, DB ;
Dyer, PS .
CURRENT OPINION IN MICROBIOLOGY, 2004, 7 (05) :499-504
[10]   HEN EGG-WHITE LYSOZYME EXPRESSED IN, AND SECRETED FROM, ASPERGILLUS-NIGER IS CORRECTLY PROCESSED AND FOLDED [J].
ARCHER, DB ;
JEENES, DJ ;
MACKENZIE, DA ;
BRIGHTWELL, G ;
LAMBERT, N ;
LOWE, G ;
RADFORD, SE ;
DOBSON, CM .
BIO-TECHNOLOGY, 1990, 8 (08) :741-745