TY - CHAP
T1 - Modular Golden Gate Assembly of Linear DNA Templates for Cell-Free Prototyping
AU - Lehr, François Xavier
AU - Gaizauskaite, Aukse
AU - Lipińska, Katarzyna Elżbieta
AU - Gilles, Sara
AU - Sahoo, Arpita
AU - Inckemann, René
AU - Niederholtmeyer, Henrike
N1 - Publisher Copyright:
© The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature 2025.
PY - 2025
Y1 - 2025
N2 - Cell-free transcription and translation (TXTL) systems have emerged as a powerful tool for testing genetic regulatory elements and circuits. Cell-free prototyping can dramatically accelerate the design-build-test-learn cycle of new functions in synthetic biology, in particular when quick-to-assemble linear DNA templates are used. Here, we describe a Golden-Gate-assisted, cloning-free workflow to rapidly produce linear DNA templates for TXTL reactions by assembling transcription units from basic genetic parts of a modular cloning toolbox. Functional DNA templates composed of multiple parts such as promoter, ribosomal binding site (RBS), coding sequence, and terminator are produced in vitro in a one-pot Golden Gate assembly reaction followed by polymerase chain reaction (PCR) amplification. We demonstrate assembly, cell-free testing of promoter and RBS combinations, as well as characterization of a repressor–promoter pair. By eliminating time-consuming transformation and cloning steps in cells and by taking advantage of modular cloning toolboxes, our cell-free prototyping workflow can produce data for large numbers of new assembled constructs within a single day.
AB - Cell-free transcription and translation (TXTL) systems have emerged as a powerful tool for testing genetic regulatory elements and circuits. Cell-free prototyping can dramatically accelerate the design-build-test-learn cycle of new functions in synthetic biology, in particular when quick-to-assemble linear DNA templates are used. Here, we describe a Golden-Gate-assisted, cloning-free workflow to rapidly produce linear DNA templates for TXTL reactions by assembling transcription units from basic genetic parts of a modular cloning toolbox. Functional DNA templates composed of multiple parts such as promoter, ribosomal binding site (RBS), coding sequence, and terminator are produced in vitro in a one-pot Golden Gate assembly reaction followed by polymerase chain reaction (PCR) amplification. We demonstrate assembly, cell-free testing of promoter and RBS combinations, as well as characterization of a repressor–promoter pair. By eliminating time-consuming transformation and cloning steps in cells and by taking advantage of modular cloning toolboxes, our cell-free prototyping workflow can produce data for large numbers of new assembled constructs within a single day.
KW - DNA assembly
KW - E. coli cell-free systems
KW - Golden Gate cloning
KW - In vitro transcription translation
KW - Linear DNA
KW - Rapid prototyping
UR - http://www.scopus.com/inward/record.url?scp=85205605391&partnerID=8YFLogxK
U2 - 10.1007/978-1-0716-4220-7_11
DO - 10.1007/978-1-0716-4220-7_11
M3 - Chapter
C2 - 39363073
AN - SCOPUS:85205605391
T3 - Methods in Molecular Biology
SP - 197
EP - 217
BT - Methods in Molecular Biology
PB - Humana Press Inc.
ER -