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Unique nucleotide sequence-guided assembly of repetitive DNA parts for synthetic biology applications.

Nature protocols (2014-08-08)
Joseph P Torella, Florian Lienert, Christian R Boehm, Jan-Hung Chen, Jeffrey C Way, Pamela A Silver
ABSTRACT

Recombination-based DNA construction methods, such as Gibson assembly, have made it possible to easily and simultaneously assemble multiple DNA parts, and they hold promise for the development and optimization of metabolic pathways and functional genetic circuits. Over time, however, these pathways and circuits have become more complex, and the increasing need for standardization and insulation of genetic parts has resulted in sequence redundancies--for example, repeated terminator and insulator sequences--that complicate recombination-based assembly. We and others have recently developed DNA assembly methods, which we refer to collectively as unique nucleotide sequence (UNS)-guided assembly, in which individual DNA parts are flanked with UNSs to facilitate the ordered, recombination-based assembly of repetitive sequences. Here we present a detailed protocol for UNS-guided assembly that enables researchers to convert multiple DNA parts into sequenced, correctly assembled constructs, or into high-quality combinatorial libraries in only 2-3 d. If the DNA parts must be generated from scratch, an additional 2-5 d are necessary. This protocol requires no specialized equipment and can easily be implemented by a student with experience in basic cloning techniques.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
L-(+)-Arabinose, ≥99%
Sigma-Aldrich
Tris Acetate-EDTA buffer, 10× concentrate, BioReagent, for molecular biology, non-sterile; 0.2 μm filtered
Sigma-Aldrich
Ampicillin sodium salt
Sigma-Aldrich
Poly(ethylene glycol), average Mn 4,000, platelets