Synthetic ligation reassembly in directed evolution

Abstract

A directed evolution process for rapid and facilitated production from a progenitor polynucleotide template, of a library of mutagenized progeny polynucleotides wherein each of the 20 naturally encoded amino acids is encoded at each original codon position. This method, termed site-saturation mutagenesis, or simply saturation mutagenesis, is preferably based on the use of the degenerate N,N,G/T sequence. Also, a method of non-stochastically producing a library of chimeric nucleic acid molecules having an overall assembly order that is chosen by design. Accordingly, a set of progenitor templates, such as genes (e.g. a family of esterase genes) or genes pathways (e.g. encoding antibiotics) can be shuffled to generate a sizable library of distinct progeny polynucleotide molecules (e.g. 10 100 ) and correspondingly encoded polypeptides.

What is claimed is: 
     
         1 . A method of non-stochastically producing a library of chimeric nucleic acid molecules having an overall assembly order that is non-random comprising:
 (a) non-randomly generating a plurality of nucleic acid building blocks having mutually compatible ligatable ends; and   (b) assembling the nucleic acid building blocks, such that a designed overall assembly order is achieved;   whereby a set of progenitor templates can be shuffled to generate a library of progeny polynucleotide molecules and correspondingly encoded polypeptides, and   whereby screening of the progeny polynucleotide library provides a means to identify a desirable species that have a desirable property.   
     
     
         2 . A method of non-stochastically producing a library comprised of a defined number of groupings comprised of one or more groupings of chimeric nucleic acid molecules having an overall assembly order that is chosen by design, said method comprised of:
 (a) generating by design for each grouping a set of specific nucleic acid building blocks having serviceable mutually compatible ligatable ends, and   (b) assembling these nucleic acid building blocks according to said groupings, such that a designed overall assembly order is achieved;   whereby a set of progenitor templates can be shuffled to generate a library of progeny polynucleotide molecules and correspondingly encoded polypeptides, and   whereby the expression screening of the progeny polynucleotide library provides a means to identify a desirable species that has a desirable property.