Creating multiple-crossover DNA libraries independent of sequence identity.
about
On the conservative nature of intragenic recombinationDirected evolution of protein enzymes using nonhomologous random recombinationExploring protein fitness landscapes by directed evolutionTo get what we aim for--progress in diversity generation methodsDirected evolution: tailoring biocatalysts for industrial applicationsIdentifying residue-residue clashes in protein hybrids by using a second-order mean-field approach.Chemical and biochemical strategies for the randomization of protein encoding DNA sequences: library construction methods for directed evolution.Evolution of highly active enzymes by homology-independent recombination.Library analysis of SCHEMA-guided protein recombination.Enhanced crossover SCRATCHY: construction and high-throughput screening of a combinatorial library containing multiple non-homologous crossovers.eCodonOpt: a systematic computational framework for optimizing codon usage in directed evolution experimentsOn the structural and functional modularity of glycinamide ribonucleotide formyltransferases.FamClash: a method for ranking the activity of engineered enzymes.Laboratory-directed protein evolutionDirected evolution: an approach to engineer enzymes.Non-homologous recombination of deoxyribonucleoside kinases from human and Drosophila melanogaster yields human-like enzymes with novel activities.Steering directed protein evolution: strategies to manage combinatorial complexity of mutant libraries.Combinatorial recombination of gene fragments to construct a library of chimeras.Nucleic acid evolution and minimization by nonhomologous random recombination.Prospecting metagenomic enzyme subfamily genes for DNA family shuffling by a novel PCR-based approachEngineering Kinases to Phosphorylate Nucleoside Analogs for Antiviral and Cancer Therapy.Restriction enzyme-free construction of random gene mutagenesis libraries in Escherichia coli.Mixed oligonucleotides for random mutagenesis: best way of making them.Protein engineering 20 years on.Combinatorial engineering of 1-deoxy-D-xylulose 5-phosphate pathway using cross-lapping in vitro assembly (CLIVA) method.Assessing directed evolution methods for the generation of biosynthetic enzymes with potential in drug biosynthesis.The enzymatic basis for pesticide bioremediation.Directed evolution 2.0: improving and deciphering enzyme properties.Sex in a test tube: testing the benefits of in vitro recombination.Biomolecular engineering for nanobio/bionanotechnology.Combinatorial recombination of gene fragments to construct a library of chimerasCreating protein biocatalysts as tools for future industrial applicationsEnzyme engineering toolbox – a ‘catalyst’ for changeA highly stable laccase obtained by swapping the second cupredoxin domain
P2860
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P2860
Creating multiple-crossover DNA libraries independent of sequence identity.
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Creating multiple-crossover DNA libraries independent of sequence identity.
@ast
Creating multiple-crossover DNA libraries independent of sequence identity.
@en
type
label
Creating multiple-crossover DNA libraries independent of sequence identity.
@ast
Creating multiple-crossover DNA libraries independent of sequence identity.
@en
prefLabel
Creating multiple-crossover DNA libraries independent of sequence identity.
@ast
Creating multiple-crossover DNA libraries independent of sequence identity.
@en
P2093
P2860
P356
P1476
Creating multiple-crossover DNA libraries independent of sequence identity.
@en
P2093
P2860
P304
11248-11253
P356
10.1073/PNAS.201413698
P407
P577
2001-09-18T00:00:00Z