The search result changed since you submitted your search request. Documents might be displayed in a different sort order.
  • search hit 2 of 22
Back to Result List

AssemblX: a user-friendly toolkit for rapid and reliable multi-gene assemblies

  • The assembly of large DNA constructs coding for entire pathways poses a major challenge in the field of synthetic biology. Here, we present AssemblX, a novel, user-friendly and highly efficient multi-gene assembly strategy. The software-assisted AssemblX process allows even unexperienced users to rapidly design, build and test DNA constructs with currently up to 25 functional units, from 75 or more subunits. At the gene level, AssemblX uses scar-free, overlap-based and sequence-independent methods, allowing the unrestricted design of transcriptional units without laborious parts domestication. The assembly into multi-gene modules is enabled via a standardized, highly efficient, polymerase chain reaction-free and virtually sequence-independent scheme, which relies on rare cutting restriction enzymes and optimized adapter sequences. Selection and marker switching strategies render the whole process reliable, rapid and very effective. The assembly product can be easily transferred to any desired expression host, making AssemblX usefulThe assembly of large DNA constructs coding for entire pathways poses a major challenge in the field of synthetic biology. Here, we present AssemblX, a novel, user-friendly and highly efficient multi-gene assembly strategy. The software-assisted AssemblX process allows even unexperienced users to rapidly design, build and test DNA constructs with currently up to 25 functional units, from 75 or more subunits. At the gene level, AssemblX uses scar-free, overlap-based and sequence-independent methods, allowing the unrestricted design of transcriptional units without laborious parts domestication. The assembly into multi-gene modules is enabled via a standardized, highly efficient, polymerase chain reaction-free and virtually sequence-independent scheme, which relies on rare cutting restriction enzymes and optimized adapter sequences. Selection and marker switching strategies render the whole process reliable, rapid and very effective. The assembly product can be easily transferred to any desired expression host, making AssemblX useful for researchers from various fields.show moreshow less

Export metadata

Additional Services

Search Google Scholar Statistics
Metadaten
Author details:Lena HochreinORCiDGND, Fabian MachensORCiDGND, Juergen Gremmels, Karina Schulz, Katrin MesserschmidtORCiDGND, Bernd Mueller-RoeberORCiDGND
DOI:https://doi.org/10.1093/nar/gkx034
ISSN:0305-1048
ISSN:1362-4962
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/28130422
Title of parent work (English):Nucleic acids research
Publisher:Oxford Univ. Press
Place of publishing:Oxford
Publication type:Article
Language:English
Year of first publication:2017
Publication year:2017
Release date:2020/04/20
Volume:45
Number of pages:12
Funding institution:Federal Ministry of Education and Research of Germany (BMBF) [031A172]; BMBF [031A172]
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
Peer review:Referiert
Accept ✔
This website uses technically necessary session cookies. By continuing to use the website, you agree to this. You can find our privacy policy here.