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Titlebook: Directed Evolution Library Creation; Methods and Protocol Frances H. Arnold,George Georgiou Book 2003 Humana Press 2003

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发表于 2025-3-21 19:28:33 | 显示全部楼层 |阅读模式
书目名称Directed Evolution Library Creation
副标题Methods and Protocol
编辑Frances H. Arnold,George Georgiou
视频video
概述Includes supplementary material:
丛书名称Methods in Molecular Biology
图书封面Titlebook: Directed Evolution Library Creation; Methods and Protocol Frances H. Arnold,George Georgiou Book 2003 Humana Press 2003
描述Biological systems are very special substrates for engineering—uniquely the products of evolution, they are easily redesigned by similar approaches. A simple algorithm of iterative cycles of diversification and selection, evolution works at all scales, from single molecules to whole ecosystems. In the little more than a decade since the first reported applications of evolutionary design to enzyme engineering, directed evolution has matured to the point where it now represents the centerpiece of industrial biocatalyst development and is being practiced by thousands of academic and industrial scientists in com- nies and universities around the world. The appeal of directed evolution is easy to understand: it is conceptually straightforward, it can be practiced without any special instrumentation and, most important, it frequently yields useful solutions, many of which are totally unanticipated. Directed evolution has r- dered protein engineering readily accessible to a broad audience of scientists and engineers who wish to tailor a myriad of protein properties, including th- mal and solvent stability, enzyme selectivity, specific activity, protease s- ceptibility, allosteric control
出版日期Book 2003
版次1
doihttps://doi.org/10.1385/159259395X
isbn_softcover978-1-61737-471-5
isbn_ebook978-1-59259-395-8Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2003
The information of publication is updating

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发表于 2025-3-21 22:49:45 | 显示全部楼层
Guglielmo Chiodi,Leonardo Dittaversity is generated entirely in vitro, and the protocol, involving two rounds of PCR with no gel purifications, can be accomplished easily in less than one day, followed by cloning as one would for a traditional PCR product.
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发表于 2025-3-22 06:49:37 | 显示全部楼层
Construction of Designed Protein Libraries Using Gene Assembly Mutagenesisversity is generated entirely in vitro, and the protocol, involving two rounds of PCR with no gel purifications, can be accomplished easily in less than one day, followed by cloning as one would for a traditional PCR product.
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Saturation Mutagenesisms, and study structure-function relationships. With saturation mutagenesis, it is possible to create a library of mutants containing all possible mutations at one or more pre-determined target positions in a gene sequence.
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DNA Shuffling annealing, and extension by a polymerase (..). Recombination occurs when fragments from different parents anneal at a region of high sequence identity. Following this reassembly reaction, PCR amplification with primers is used to generate full-length chimeras suitable for cloning into an expression vector.
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In Vitro DNA Recombination by Random Priminggical systems (.,.). As compared to random mutagenesis, recombination may be advantageous in combining beneficial mutations that have arisen independently and may be synergistic, while simultaneously removing deleterious mutations.
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Preparation of SCRATCHY Hybrid Protein Librariese identity between the original sequences (.). Such multi-crossover hybrids can be of interest to the studies of fundamental questions of protein evolution and folding, as well as to the tailoring of enzymes for therapeutic and industrial applications.
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