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University of Texas Health Science Center at Houston

Characterization of The Role of The Pkm101-Encoded T4Ss Outer Membrane Core Complex In Substrate Transfer, Pilus Biogenesis, and Recipient Cell Contact

Abstract

dc:description.abstract

<p>The bacterial type IV secretion systems (T4SS) encoded on the <em>Escherichia coli</em> pKM101 and R388 conjugative plasmids and the <em>Agrobacterium tumefaciens</em> <em>virB</em> operon are composed of 12 subunits arranged in an architecturally similar fashion. Structural studies of the T4SS from R388 (Trw<sub>R388</sub>) highlighted the presence of a distinct outer membrane core complex (OMCC) and inner membrane complex (IMC) joined together by a central stalk. This thesis is focused on the development of the pKM101 model system and the role of an OMCC cap region formed by alpha helical antenna projections (AP) found in VirB10 and TraF<sub>pKM101</sub>. I introduced various internal deletions, truncations, and substitutions between TraF<sub>pKM101</sub> and VirB10 to study the role of the AP cap in (i) substrate transfer to recipient plant or bacterial cells, (ii) pilus biogenesis and donor-specific bacteriophage sensitivity, and (iii) recipient cell contact. My results demonstrate that the C-terminal tails of VirB10 and TraF<sub>pKM101</sub> are essential for DNA transfer and pilus biogenesis, whereas the AP domains are only important for pilus biogenesis. Neither of these domains is critical for recipient cell contact as monitored by sensitivity to <em>Pseudomonas aeruginosa</em> containing a functional type VI secretion system. Finally, I demonstrated that the IMC of pKM101 is able to functionally pair with the OMCCs from either VirB/VirD4, Trw<sub>R388</sub>, or the Ptl T4SS of <em>Bordetella pertussis</em> restoring recipient cell contact and plasmid transfer. These results highlight the common ancestry between these functionally distinct machines and support a model where functionally independent IMCs and OMCCs have co-evolved to form the T4SS in Gram-negative bacteria.</p>

Degree

thesis:*
Name thesis:degree_name
Doctor of Philosophy (PhD)
Level thesis:degree_level
Dissertation (PhD)
Year dc:date.available
2017

Author and committee

dc:creator, dc:contributor.*
Authors dc:creator
  • Gordon, Jay E
  • <p>http://www.orcid.org/0000-0001-7692-5569</p>
Contributors dc:contributor
  • Peter J. Christie, Ph.D.
  • Mikhail Bogdanov, Ph.D.
  • Heidi B. Kaplan, Ph.D.

Subjects

dc:subject × 12

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:digitalcommons.library.tmc.edu:utgsbs_dissertations-1821

Chain of custody

source
Harvested from
University of Texas Health Science Center at Houston
Base URL
digitalcommons.library.tmc.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Gordon, Jay E; <p>http://www.orcid.org/0000-0001-7692-5569</p>. Characterization of The Role of The Pkm101-Encoded T4Ss Outer Membrane Core Complex In Substrate Transfer, Pilus Biogenesis, and Recipient Cell Contact. Dissertation (PhD) thesis, 2017. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/779