Literature DB >> 20201809

Random mutagenesis methods for in vitro directed enzyme evolution.

Nikolaos E Labrou1.   

Abstract

Random mutagenesis is a powerful tool for generating enzymes, proteins, entire metabolic pathways, or even entire genomes with desired or improved properties. This technology is used to evolve genes in vitro through an iterative process consisting of recombinant generation. Coupled with the development of powerful high-throughput screening or selection methods, this technique has been successfully used to solve problems in protein engineering. There are many methods to generate genetic diversity by random mutagenesis and to create combinatorial libraries. This can be achieved by treating DNA or whole bacteria with various chemical mutagens, by passing cloned genes through mutator strains, by "error-prone" PCR mutagenesis, by rolling circle error-prone PCR, or by saturation mutagenesis. The next sections of this review article focus on recent advances in techniques and methods used for in vitro directed evolution of enzymes using random mutagenesis. Selected examples, highlighting successful applications of these methods, are also presented and discussed.

Mesh:

Substances:

Year:  2010        PMID: 20201809     DOI: 10.2174/138920310790274617

Source DB:  PubMed          Journal:  Curr Protein Pept Sci        ISSN: 1389-2037            Impact factor:   3.272


  27 in total

1.  Uricases as therapeutic agents to treat refractory gout: Current states and future directions.

Authors:  Xiaolan Yang; Yonghua Yuan; Chang-Guo Zhan; Fei Liao
Journal:  Drug Dev Res       Date:  2011-12-29       Impact factor: 4.360

Review 2.  Molecular engineering of antibodies for therapeutic and diagnostic purposes.

Authors:  Frédéric Ducancel; Bruno H Muller
Journal:  MAbs       Date:  2012-07-01       Impact factor: 5.857

Review 3.  Technologies of directed protein evolution in vivo.

Authors:  Artem Blagodatski; Vladimir L Katanaev
Journal:  Cell Mol Life Sci       Date:  2010-12-29       Impact factor: 9.261

Review 4.  Biocatalyst development by directed evolution.

Authors:  Meng Wang; Tong Si; Huimin Zhao
Journal:  Bioresour Technol       Date:  2012-01-21       Impact factor: 9.642

Review 5.  Robotics for enzyme technology: innovations and technological perspectives.

Authors:  Mandeep Dixit; Kusum Panchal; Dharini Pandey; Nikolaos E Labrou; Pratyoosh Shukla
Journal:  Appl Microbiol Biotechnol       Date:  2021-05-10       Impact factor: 4.813

6.  The CDC50A extracellular domain is required for forming a functional complex with and chaperoning phospholipid flippases to the plasma membrane.

Authors:  Katsumori Segawa; Sachiko Kurata; Shigekazu Nagata
Journal:  J Biol Chem       Date:  2017-12-24       Impact factor: 5.157

Review 7.  Protein engineering for metabolic engineering: current and next-generation tools.

Authors:  Ryan J Marcheschi; Luisa S Gronenberg; James C Liao
Journal:  Biotechnol J       Date:  2013-04-16       Impact factor: 4.677

8.  In vitro evolution of enzymes.

Authors:  Misha V Golynskiy; John C Haugner; Aleardo Morelli; Dana Morrone; Burckhard Seelig
Journal:  Methods Mol Biol       Date:  2013

Review 9.  Pre-existing anti-adeno-associated virus antibodies as a challenge in AAV gene therapy.

Authors:  Vedell Louis Jeune; Jakob A Joergensen; Roger J Hajjar; Thomas Weber
Journal:  Hum Gene Ther Methods       Date:  2013-04-03       Impact factor: 2.396

10.  Improving Escherichia coli FucO for furfural tolerance by saturation mutagenesis of individual amino acid positions.

Authors:  Huabao Zheng; Xuan Wang; Lorraine P Yomano; Ryan D Geddes; Keelnatham T Shanmugam; Lonnie O Ingram
Journal:  Appl Environ Microbiol       Date:  2013-03-08       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.