Yeast systems biotechnology for the production of heterologous proteins

被引:50
作者
Graf, Alexandra [1 ,2 ]
Dragosits, Martin [1 ]
Gasser, Brigitte [1 ]
Mattanovich, Diethard [1 ,2 ]
机构
[1] Univ Nat Resources & Appl Life Sci, Inst Appl Microbiol, Dept Biotechnol, A-1190 Vienna, Austria
[2] Univ Appl Sci, Sch Bioengn, Vienna, Austria
基金
奥地利科学基金会;
关键词
systems biotechnology; heterologous protein; yeast; Pichia pastoris; systems biology; metabolic engineering; SACCHAROMYCES-CEREVISIAE; RECOMBINANT PROTEIN; ESCHERICHIA-COLI; PICHIA-PASTORIS; ASPERGILLUS-NIGER; METABOLIC-FLUX; TRANSCRIPTIONAL RESPONSES; KLUYVEROMYCES-LACTIS; BACILLUS-MEGATERIUM; SECRETION STRESS;
D O I
10.1111/j.1567-1364.2009.00507.x
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
Systems biotechnology has been established as a highly potent tool for bioprocess development in recent years. The applicability to complex metabolic processes such as protein synthesis and secretion, however, is still in its infancy. While yeasts are frequently applied for heterologous protein production, more progress in this field has been achieved for bacterial and mammalian cell culture systems than for yeasts. A critical comparison between different protein production systems, as provided in this review, can aid in assessing the potentials and pitfalls of applying systems biotechnology concepts to heterologous protein producing yeasts. Apart from modelling, the methodological basis of systems biology strongly relies on postgenomic methods. However, this methodology is rapidly moving so that more global data with much higher sensitivity will be achieved in near future. The development of next generation sequencing technology enables an unexpected revival of genomic approaches, providing new potential for evolutionary engineering and inverse metabolic engineering.
引用
收藏
页码:335 / 348
页数:14
相关论文
共 101 条
[61]   Engineering HlyA hypersecretion in Escherichia coli based on proteomic and microarray analyses [J].
Lee, PS ;
Lee, KH .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 89 (02) :195-205
[62]   Systems biotechnology for strain improvement [J].
Lee, SY ;
Lee, DY ;
Kim, TY .
TRENDS IN BIOTECHNOLOGY, 2005, 23 (07) :349-358
[63]   Low-temperature increases the yield of biologically active herring antifreeze protein in Pichia pastoris [J].
Li, ZJ ;
Xiong, F ;
Lin, QS ;
d'Anjou, M ;
Daugulis, AJ ;
Yang, DSC ;
Hew, CL .
PROTEIN EXPRESSION AND PURIFICATION, 2001, 21 (03) :438-445
[64]   The impact of next-generation sequencing technology on genetics [J].
Mardis, Elaine R. .
TRENDS IN GENETICS, 2008, 24 (03) :133-141
[65]   Applications of cell sorting in biotechnology [J].
Mattanovich, D ;
Borth, N .
MICROBIAL CELL FACTORIES, 2006, 5 (1)
[66]   Stress in recombinant protein producing yeasts [J].
Mattanovich, D ;
Gasser, B ;
Hohenblum, H ;
Sauer, M .
JOURNAL OF BIOTECHNOLOGY, 2004, 113 (1-3) :121-135
[67]   Importance of systems biology in engineering microbes for biofuel production [J].
Mukhopadhyay, Aindrila ;
Redding, Alyssa M. ;
Rutherford, Becky J. ;
Keasling, Jay D. .
CURRENT OPINION IN BIOTECHNOLOGY, 2008, 19 (03) :228-234
[68]   Design of transcriptional fusions of stress sensitive promoters and GFP to monitor the overburden of Escherichia coli hosts during recombinant protein production [J].
Nemecek, S. ;
Marisch, K. ;
Juric, R. ;
Bayer, K. .
BIOPROCESS AND BIOSYSTEMS ENGINEERING, 2008, 31 (01) :47-53
[69]   Analysis and validation of proteomic data generated by tandem mass spectrometry [J].
Nesvizhskii, Alexey I. ;
Vitek, Olga ;
Aebersold, Ruedi .
NATURE METHODS, 2007, 4 (10) :787-797
[70]   Metabolic engineering [J].
Nielsen, J .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2001, 55 (03) :263-283