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Structural and functional characterization of TraI from pKM101 reveals basis for DNA processing
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics. Umeå University, Faculty of Medicine, Wallenberg Centre for Molecular Medicine at Umeå University (WCMM).
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics. Umeå University, Faculty of Medicine, Wallenberg Centre for Molecular Medicine at Umeå University (WCMM).ORCID iD: 0000-0003-4165-9277
Umeå University, Faculty of Medicine, Wallenberg Centre for Molecular Medicine at Umeå University (WCMM). Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.ORCID iD: 0000-0001-6848-322x
2023 (English)In: Life Science Alliance, E-ISSN 2575-1077, Vol. 6, no 4, article id e202201775Article in journal (Refereed) Published
Abstract [en]

Type 4 secretion systems are large and versatile protein machineries that facilitate the spread of antibiotic resistance and other virulence factors via horizontal gene transfer. Conjugative type 4 secretion systems depend on relaxases to process the DNA in preparation for transport. TraI from the well-studied conjugative plasmid pKM101 is one such relaxase. Here, we report the crystal structure of the trans-esterase domain of TraI in complex with its substrate oriT DNA, highlighting the conserved DNA-binding mechanism of conjugative relaxases. In addition, we present an apo structure of the trans-esterase domain of TraI that includes most of the flexible thumb region. This allows us for the first time to visualize the large conformational change of the thumb subdomain upon DNA binding. We also characterize the DNA binding, nicking, and religation activity of the trans-esterase domain, helicase domain, and full-length TraI. Unlike previous indications in the literature, our results reveal that the TraI trans-esterase domain from pKM101 behaves in a conserved manner with its homologs from the R388 and F plasmids.

Place, publisher, year, edition, pages
Life Science Alliance, LLC , 2023. Vol. 6, no 4, article id e202201775
National Category
Structural Biology
Identifiers
URN: urn:nbn:se:umu:diva-204501DOI: 10.26508/lsa.202201775ISI: 000923931600001PubMedID: 36669792Scopus ID: 2-s2.0-85147045764OAI: oai:DiVA.org:umu-204501DiVA, id: diva2:1735014
Funder
Swedish Research Council, 2018-07152Vinnova, 2018-04969Swedish Research Council Formas, 2019-02496Swedish Research Council, 2016- 03599Knut and Alice Wallenberg FoundationThe Kempe Foundations, SMK-1762The Kempe Foundations, SMK-1869Available from: 2023-02-07 Created: 2023-02-07 Last updated: 2024-09-24Bibliographically approved
In thesis
1. Exploring the diversity of conjugative type IV secretion systems
Open this publication in new window or tab >>Exploring the diversity of conjugative type IV secretion systems
2024 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

The increase of antibiotic resistance is a major threat to human health. The spread of mobile genetic elements (MGEs) via conjugation is a major contributor to this problem, especially in hospital settings. Many MGEs encode Type IV Secretion Systems (T4SSs), which are multiprotein complexes that transfer the MGE from donor to recipient cells. T4SSs are versatile systems that exist in all prokaryotes. While most research has focused on T4SSs from Gram negative (G) bacteria, it is important to understand the similarities and differences with T4SSs from Gram positive (G+) bacteria, given their different cell envelopes. Additionally, there is also variability within G T4SSs, which is not yet fully understood.

The aim of this thesis was to explore the diversity of T4SSs, using pKM101 from E. coli (G) and pCF10 from E. faecalis (G+) as model systems, with a focus on DNA transfer and replication (Dtr) proteins.

We biochemically characterized the relaxase TraI from pKM101, which processes plasmid DNA prior to transfer through the T4SS. We also solved the crystal structure of its transesterase domain with and without its substrate oriT DNA, highlighting its conserved mechanism of action. We further explored the relationship between TraI and the accessory protein TraK, using AlphaFold to predict an interaction involving the TraI CTD. This was confirmed experimentally using in vivo BPA-crosslinking.

Many conjugative plasmids encode single-stranded DNA-binding proteins (SSBs), which are thought to protect DNA during transfer. pCF10 encodes the protein PrgE, which was proposed to be one such SSB. However, our biochemical studies and X-ray crystallography revealed that PrgE is an OB-fold protein with unexpected DNA-binding behavior. While its benefit for the plasmid remains unclear, our functional studies have shown that it does not play a role in conjugation.

Finally, we analyzed the structural diversity of conjugative T4SSs in G and G+ bacteria, using bioinformatics and structural modelling. This revealed unknown commonalities, which indicate that G+ T4SS mating channels are likely more similar in structure to G T4SSs than expected.

In summary, this thesis provides new insights into the Dtr proteins that play an integral role in T4SS mediated conjugation, knowledge that hopefully can be used in the fight against hospital acquired infections in the future.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2024. p. 60
Series
Umeå University medical dissertations, ISSN 0346-6612 ; 2325
Keywords
Antibiotic resistance, Horizontal gene transfer, Conjugation, Type IV Secretion Systems, Relaxases, Single-stranded DNA-binding proteins, Biochemistry, Structural Biology
National Category
Structural Biology Biochemistry Molecular Biology
Research subject
Biochemistry
Identifiers
urn:nbn:se:umu:diva-229972 (URN)978-91-8070-495-3 (ISBN)978-91-8070-496-0 (ISBN)
Public defence
2024-10-24, Carl Kempe salen (KBE303), KBC-huset, Linnaeus väg 6, Umeå, 09:00 (English)
Opponent
Supervisors
Available from: 2024-10-01 Created: 2024-09-24 Last updated: 2025-02-20Bibliographically approved

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Breidenstein, Annikater Beek, JosyBerntsson, Ronnie

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