Economical analysis of saturation mutagenesis experiments

被引:39
作者
Acevedo-Rocha, Carlos G. [1 ,2 ,4 ,5 ]
Reetz, Manfred T. [1 ,2 ]
Nov, Yuval [3 ]
机构
[1] Max Planck Inst Kohlenforsch, Dept Organ Synth, D-45470 Mulheim, Germany
[2] Univ Marburg, Dept Chem, D-35032 Marburg, Germany
[3] Univ Haifa, Dept Stat, IL-31905 Haifa, Israel
[4] Max Planck Inst Terr Mikrobiol, Prokaryot Small RNA Biol Grp, D-35043 Marburg, Germany
[5] Univ Marburg, Landes Offens Entwicklung Wissensch Okon Exzellen, D-35032 Marburg, Germany
关键词
DIRECTED EVOLUTION; SYNTHETIC BIOLOGY; REGULATORY ELEMENTS; GENE SYNTHESIS; CONSTRUCTION; LIBRARIES; DESIGN; DNA; STEREOSELECTIVITY; RANDOMIZATION;
D O I
10.1038/srep10654
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Saturation mutagenesis is a powerful technique for engineering proteins, metabolic pathways and genomes. In spite of its numerous applications, creating high-quality saturation mutagenesis libraries remains a challenge, as various experimental parameters influence in a complex manner the resulting diversity. We explore from the economical perspective various aspects of saturation mutagenesis library preparation: We introduce a cheaper and faster control for assessing library quality based on liquid media; analyze the role of primer purity and supplier in libraries with and without redundancy; compare library quality, yield, randomization efficiency, and annealing bias using traditional and emergent randomization schemes based on mixtures of mutagenic primers; and establish a methodology for choosing the most cost-effective randomization scheme given the screening costs and other experimental parameters. We show that by carefully considering these parameters, laboratory expenses can be significantly reduced.
引用
收藏
页数:12
相关论文
共 60 条
[1]   Expanding the metabolic engineering toolbox with directed evolution [J].
Abatemarco, Joseph ;
Hill, Andrew ;
Alper, Hal S. .
BIOTECHNOLOGY JOURNAL, 2013, 8 (12) :1397-1410
[2]   Directed evolution of stereoselective enzymes based on genetic selection as opposed to screening systems [J].
Acevedo-Rocha, Carlos G. ;
Agudo, Ruben ;
Reetz, Manfred T. .
JOURNAL OF BIOTECHNOLOGY, 2014, 191 :3-10
[3]  
Acevedo-Rocha CG, 2014, METHODS MOL BIOL, V1179, P189, DOI 10.1007/978-1-4939-1053-3_13
[4]  
Acevedo-Rocha CG, 2014, METHODS MOL BIOL, V1179, P103, DOI 10.1007/978-1-4939-1053-3_7
[5]   Achieving Regio- and Enantioselectivity of P450-Catalyzed Oxidative CH Activation of Small Functionalized Molecules by Structure-Guided Directed Evolution [J].
Agudo, Ruben ;
Roiban, Gheorghe-Doru ;
Reetz, Manfred T. .
CHEMBIOCHEM, 2012, 13 (10) :1465-1473
[6]   Modified base compositions at degenerate positions of a mutagenic oligonucleotide enhance randomness in site-saturation mutagenesis [J].
Airaksinen, A ;
Hovi, T .
NUCLEIC ACIDS RESEARCH, 1998, 26 (02) :576-581
[7]   ProxiMAX randomization: a new technology for non-degenerate saturation mutagenesis of contiguous codons [J].
Ashraf, Mohammed ;
Frigotto, Laura ;
Smith, Matthew E. ;
Patel, Seema ;
Hughes, Marcus D. ;
Poole, Andrew J. ;
Hebaishi, Husam R. M. ;
Ullman, Christopher G. ;
Hine, Anna V. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2013, 41 :1189-U250
[8]   All-codon scanning identifies p53 cancer rescue mutations [J].
Baronio, Roberta ;
Danziger, Samuel A. ;
Hall, Linda V. ;
Salmon, Kirsty ;
Hatfield, G. Wesley ;
Lathrop, Richard H. ;
Kaiser, Peter .
NUCLEIC ACIDS RESEARCH, 2010, 38 (20) :7079-7088
[9]   Stereoselective Oxidation of Aryl-Substituted Vicinal Diols into Chiral α-Hydroxy Aldehydes by Re-Engineered Propanediol Oxidoreductase [J].
Blikstad, Cecilia ;
Dahlstrom, Kathe M. ;
Salminen, Tiina A. ;
Widersten, Mikael .
ACS CATALYSIS, 2013, 3 (12) :3016-3025
[10]   Precision is essential for efficient catalysis in an evolved Kemp eliminase [J].
Blomberg, Rebecca ;
Kries, Hajo ;
Pinkas, Daniel M. ;
Mittl, Peer R. E. ;
Gruetter, Markus G. ;
Privett, Heidi K. ;
Mayo, Stephen L. ;
Hilvert, Donald .
NATURE, 2013, 503 (7476) :418-+