A variety of prokaryotes produce a bacteriophage-like gene transfer agent (GTA), and the alphaproteobacterial RcGTA is a model GTA. Some environmental isolates of lack the ability to acquire genes transferred by the RcGTA (recipient capability). In this work, we investigated the reason why strain 37b4 lacks recipient capability. The RcGTA head spike fiber and tail fiber proteins have been proposed to bind extracellular oligosaccharide receptors, and strain 37b4 lacks a capsular polysaccharide (CPS). The reason why strain 37b4 lacks a CPS was unknown, as was whether the provision of a CPS to 37b4 would result in recipient capability. To address these questions, we sequenced and annotated the strain 37b4 genome and used BLAST interrogations of this genome sequence to search for homologs of genes known to be needed for recipient capability. We also created a cosmid-borne genome library from a wild-type strain, mobilized the library into 37b4, and used the cosmid-complemented strain 37b4 to identify genes needed for a gain of function, allowing for the acquisition of RcGTA-borne genes. The relative presence of CPS around a wild-type strain, 37b4, and cosmid-complemented 37b4 cells was visualized using light microscopy of stained cells. Fluorescently tagged head spike fiber and tail fiber proteins of the RcGTA particle were created and used to measure the relative binding to wild-type and 37b4 cells. We found that strain 37b4 lacks recipient capability because of an inability to bind RcGTA; the reason it is incapable of binding is that it lacks CPS, and the absence of CPS is due to the absence of genes previously shown to be needed for CPS production in another strain. In addition to the head spike fiber, we found that the tail fiber protein also binds to the CPS.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218006 | PMC |
http://dx.doi.org/10.3390/genes14051124 | DOI Listing |
Genes (Basel)
May 2023
Department of Microbiology & Immunology, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
A variety of prokaryotes produce a bacteriophage-like gene transfer agent (GTA), and the alphaproteobacterial RcGTA is a model GTA. Some environmental isolates of lack the ability to acquire genes transferred by the RcGTA (recipient capability). In this work, we investigated the reason why strain 37b4 lacks recipient capability.
View Article and Find Full Text PDFBioelectrochemistry
October 2013
Department of Biochemistry and Structural Biology, Lund University, P.O. Box 124, SE-22100 Lund, Sweden.
The metabolically versatile purple bacteria Rhodobacter capsulatus was investigated to check its possible applicability in biofuel cells and electrochemical microbial biosensors. The wild type strain ATCC 17015 and mutant strain 37b4 lacking the lipopolysaccharide capsule was compared for their ability to communicate with electrodes modified with an osmium redox polymer. In this work, aerobic heterotrophically grown R.
View Article and Find Full Text PDFGene
December 1996
Institute of Biology II/Microbiology, University of Freiburg, Germany.
The primary and atomic structures of the porin protein from Rhodobacter (Rb.) capsulatus strain 37b4 were determined several years ago by peptide sequencing and X-ray crystallography. In this work the gene encoding this porin (named porCa) was cloned and sequenced.
View Article and Find Full Text PDFMol Gen Genet
November 1996
Institut für Biologie II/Mikrobiologie, Universität, Freiburg, Germany.
The pore-forming outer-membrane protein from Rhodobacter (R.) capsulatus (wild-type B10 strain) was isolated and purified under non-denaturing conditions. The monomer unit of the isolated porin has a molecular mass of about 28 kDa, as judged by SDS-PAGE, whereas the native protein migrates at 75 kDa.
View Article and Find Full Text PDFMicrobiol Res
August 1996
Institut für Biologie II/Mikrobiologie, Freiburg, Germany.
Porin was isolated from Rhodobacter (Rb.) capsulatus wild type B10, as well as from Rb. capsulatus 37b4 as a control.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!