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Titlebook: Directed Enzyme Evolution; Screening and Select Frances H. Arnold,George Georgiou Book 2003 Humana Press 2003

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書目名稱Directed Enzyme Evolution
副標題Screening and Select
編輯Frances H. Arnold,George Georgiou
視頻videohttp://file.papertrans.cn/281/280660/280660.mp4
概述Includes supplementary material:
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Directed Enzyme Evolution; Screening and Select Frances H. Arnold,George Georgiou Book 2003 Humana Press 2003
描述Directed evolution comprises two distinct steps that are typically applied in an iterative fashion: (1) generating molecular diversity and (2) finding among the ensemble of mutant sequences those proteins that perform the desired fu- tion according to the specified criteria. In many ways, the second step is the most challenging. No matter how cleverly designed or diverse the starting library, without an effective screening strategy the ability to isolate useful clones is severely diminished. The best screens are (1) high throughput, to increase the likelihood that useful clones will be found; (2) sufficiently sen- tive (i. e. , good signal to noise) to allow the isolation of lower activity clones early in evolution; (3) sufficiently reproducible to allow one to find small improvements; (4) robust, which means that the signal afforded by active clones is not dependent on difficult-to-control environmental variables; and, most importantly, (5) sensitive to the desired function. Regarding this last point, almost anyone who has attempted a directed evolution experiment has learned firsthand the truth of the dictum “you get what you screen for. ” The protocols in Directed Enzyme Evoluti
出版日期Book 2003
版次1
doihttps://doi.org/10.1385/1592593968
isbn_softcover978-1-61737-472-2
isbn_ebook978-1-59259-396-5Series 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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Planung, Entscheidung und Kontrolle, can be implemented in high-throughput and thus are useful for biocatalyst discovery and engineering by directed evolution. These include assays employing Gibbs’ reagent, 4-aminoantipyrine (4-AAP) and Fast Violet B (FVB) (.). These methods should enable the optimization of oxygenases to industrially
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Book 2003rol environmental variables; and, most importantly, (5) sensitive to the desired function. Regarding this last point, almost anyone who has attempted a directed evolution experiment has learned firsthand the truth of the dictum “you get what you screen for. ” The protocols in Directed Enzyme Evoluti
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