Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10231589 | Biotechnology Advances | 2013 | 15 Pages |
Abstract
Genetic diversity creation is a core technology in directed evolution where a high quality mutant library is crucial to its success. Owing to its importance, the technology in genetic diversity creation has seen rapid development over the years and its application has diversified into other fields of scientific research. The advances in molecular cloning and mutagenesis since 2008 were reviewed. Specifically, new cloning techniques were classified based on their principles of complementary overhangs, homologous sequences, overlapping PCR and megaprimers and the advantages, drawbacks and performances of these methods were highlighted. New mutagenesis methods developed for random mutagenesis, focused mutagenesis and DNA recombination were surveyed. The technical requirements of these methods and the mutational spectra were compared and discussed with references to commonly used techniques. The trends of mutant library preparation were summarised. Challenges in genetic diversity creation were discussed with emphases on creating “smart” libraries, controlling the mutagenesis spectrum and specific challenges in each group of mutagenesis methods. An outline of the wider applications of genetic diversity creation includes genome engineering, viral evolution, metagenomics and a study of protein functions. The review ends with an outlook for genetic diversity creation and the prospective developments that can have future impact in this field.
Keywords
TALENsNRREMPEMSRESAAVdNTPMGSTIMNEBRestriction-free cloningZFNssDNA8-oxo-dGTPUDGpBpaSESAMdITPepPCRdPTPCPECNew England Biolabsp-benzoylphenylalanineEnoyl ACP reductasedsDNAPPCPGSTInDelRCASingle-stranded DNAdouble-stranded DNADNARandom mutagenesisSite-directed mutagenesisRestriction enzymesEthyl methane sulfonatedeoxyribonucleic acidTransversionsGoITAMdeoxyribonucleotide triphosphateRolling circle amplificationGenetic diversityDirected evolutionSlicebase pairserror-prone polymerase chain reactioninsertion and deletionEnoyl-acyl carrier protein reductasetranscription activator-like effector nucleasesSynthetic biologyStaggered extension processPhosphorothioateCASTKlenow fragmentSDMMetabolic engineeringGenome engineeringmapDNA recombinationNucleotidezinc finger nucleasepolymerase chain reactionPCRAdeno-associated virusCRPcAMP receptor proteingene of interestSTEPTransitionsglutathione-S-transferaseUracil-DNA glycosylase
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Kang Lan Tee, Tuck Seng Wong,