Discovering genetic determinants for cell-to-cell adhesion in two prevalent conjugative lactococcal plasmids
•Two predicted peptidoglycan-hydrolases as potential adhesins in lactococcal conjugation.•Overexpression of Tra11 and Trs15 cause a cell clumping phenotype in Lactococcus.•Both proteins cross-complement each other, supporting interchangeable function. Plasmids pNP40 and pUC11B encode two prevalent y...
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Published in | Current research in microbial sciences Vol. 6; p. 100239 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
2024
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | •Two predicted peptidoglycan-hydrolases as potential adhesins in lactococcal conjugation.•Overexpression of Tra11 and Trs15 cause a cell clumping phenotype in Lactococcus.•Both proteins cross-complement each other, supporting interchangeable function.
Plasmids pNP40 and pUC11B encode two prevalent yet divergent conjugation systems, which have been characterized in detail recently. Here, we report the elucidation of the putative adhesins of the pNP40 and pUC11B conjugation systems, encoded by traAd and trsAd, respectively. Despite their significant sequence divergence, TraAd and TrsAd represent the most conserved component between the pNP40- and the pUC11B-encoded conjugation systems and share similar peptidoglycan-hydrolase domains. Protein structure prediction using AlphaFold2 highlighted the structural similarities between their predicted domains, as well as the potential homo-dimeric state of both proteins. Expression of the putative surface adhesins resulted in a cell clumping phenotype not only among cells expressing these surface adhesins but also between adhesin-expressing and non-producing cells. Furthermore, mutant derivatives of plasmids pNP40 or pUC11B carrying a mutation in traAd or trsAd, respectively, were shown to act as efficient donors provided the corresponding recipient expresses either traAd or trsAd, thus demonstrating in trans reciprocal complementarity of these proteins in conjugation systems.
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2666-5174 2666-5174 |
DOI: | 10.1016/j.crmicr.2024.100239 |