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Komagataeibacter tool kit (KTK): a modular cloning system for multigene constructs and programmed protein secretion from cellulose producing bacteria
File | Description | Size | Format | |
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Manuscript File_Goosens_2021_ACS SB FINAL.docx | Accepted version | 1.88 MB | Microsoft Word | View/Open |
Title: | Komagataeibacter tool kit (KTK): a modular cloning system for multigene constructs and programmed protein secretion from cellulose producing bacteria |
Authors: | Goosens, V Walker, K Aragon, S Singh, A Senthivel, V Dekker, L Caro Astorga, J Buat, M Song, W Lee, KY Ellis, T |
Item Type: | Journal Article |
Abstract: | Bacteria proficient at producing cellulose are an attractive synthetic biology host for the emerging field of Engineered Living Materials (ELMs). Species from the Komagataeibacter genus produce high yields of pure cellulose materials in a short time with minimal resources, and pioneering work has shown that genetic engineering in these strains is possible and can be used to modify the material and its production. To accelerate synthetic biology progress in these bacteria, we introduce here the Komagataeibacter tool kit (KTK), a standardised modular cloning system based on Golden Gate DNA assembly that allows DNA parts to be combined to build complex multigene constructs expressed in bacteria from plasmids. Working in Komagataeibacter rhaeticus, we describe basic parts for this system, including promoters, fusion tags and reporter proteins, before showcasing how the assembly system enables more complex designs. Specifically, we use KTK cloning to reformat the Escherichia coli curli amyloid fibre system for functional expression in K. rhaeticus, and go on to modify it as a system for programming protein secretion from the cellulose producing bacteria. With this toolkit, we aim to accelerate modular synthetic biology in these bacteria, and enable more rapid progress in the emerging ELMs community. |
Issue Date: | 17-Dec-2021 |
Date of Acceptance: | 1-Nov-2021 |
URI: | http://hdl.handle.net/10044/1/92374 |
DOI: | 10.1021/acssynbio.1c00358 |
ISSN: | 2161-5063 |
Publisher: | American Chemical Society |
Start Page: | 3422 |
End Page: | 3434 |
Journal / Book Title: | ACS Synthetic Biology |
Volume: | 10 |
Issue: | 12 |
Copyright Statement: | © 2021 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Synth. Biol., after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acssynbio.1c00358 |
Sponsor/Funder: | Engineering & Physical Science Research Council (EPSRC) Engineering and Physical Sciences Research Council Engineering & Physical Science Research Council (EPSRC) Commission of the European Communities US Army (US) Engineering & Physical Science Research Council (EPSRC) |
Funder's Grant Number: | EP/M002306/1 EP/N026489/1 EP/N026489/1 820699 W911NF1810387 EP/S032215/1 |
Keywords: | 0304 Medicinal and Biomolecular Chemistry 0601 Biochemistry and Cell Biology 0903 Biomedical Engineering |
Publication Status: | Published |
Online Publication Date: | 2021-11-12 |
Appears in Collections: | Bioengineering Aeronautics Faculty of Engineering |