Acronym MarSynth
Category
Marine Biotechnology
Title Marine DNA modifying enzymes for synthetic biology Programme National Programme
Instrument (FP6)
Contact Type (FP7)
Strand (Interreg)
NA
Theme (FP7)
Activity Area (FP6)
Regional Area (Interreg)
Action (COST)
NA
Specific Programme (FP7)
NA
Funding source National Coordinator Atle Noralf Larsen Coordinator email NA
Coordinator institution
UiT - The Arctic University of Norway (Norway)
Institutions involved
NA - Norinnova Technology Transfer AS (Norway) ,
Start year 2017 End year 2021 Funding (€) € 831,579 Website https://prosjektbanken.forskningsradet.no/en/project/FORISS/267396?Kilde=FORISS&distribution=Ar&chart=bar&calcType=funding&Sprak=no&sortBy=date&sortOrder=desc&resultCount=30&offset=0&TemaEmne.2=Energi+-+Politikk+og+forvaltning Summary Synthetic biology is a rapidly evolving field, and is heralded as a possible solution for the challenges in future bioeconomy and bioenergy. The ultimate vision of synthetic biology is to create new biological operating systems of cells that predictably are able to carry out useful tasks. One of the key steps in a synthetic biology pipeline is the assembly of DNA fragments into larger functional constructs often involving multiple assemblies. A current bottleneck is however the lack of a robust room-temperature method to do multiple DNA assemblies without time-consuming manual treatment steps. A new DNA assembly method able to bypass the current hurdles is therefore highly desired.
The background for this project is the large marine bioprospecting efforts in the Arctic, coupled with knowledge based and innovative efforts in a previous Biotek2021 project (OptiZyme, 2013-2016), leading to identification and characterization of several marine heat-labile DNA-modifying enzymes with a high potential for industrial and biotechnological purposes. The proposed project aims at developing enzymes specialized for performing multiple DNA fragment assembly at room temperature. Through Proof of Principle (PoP) studies, protocols and formulations of the engineered enzymes will be optimized to ensure a quick, efficient and reliable DNA assembly platform. The best enzyme composition will be selected for Proof of Concept (PoC) and a User Case study, where the complete lactose operon will be assembled using the developed technology thus enabling the synthetic engineered bacterium to grow and utilize lactose as a carbon source. An important part of this project is to continuously engage with end users to ensure that our assembly platform meets customers’s need. Key elements of responsible research and innovation will be integrated throughout the project.
Keywords
Genetic;
Genomic;
Marine enzymes;
Engineering;
Bioproduct;
Bioprospecting;
Marine Region
76
Not associated to marine areas
0
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