Literature DB >> 22878384

Molecular basis for the maintenance of envelope integrity in Selenomonas ruminantium: cadaverine biosynthesis and covalent modification into the peptidoglycan play a major role.

Seiji Kojima1, Yoshiyuki Kamio.   

Abstract

Polyamine is a small organic polycation composed of a hydrocarbon backbone with multiple amino groups which ubiquitously exists in all living organisms from bacteria to higher animals. The critical step of polyamine biosynthesis generally includes the amino acid-decarboxylating reaction to produce the primary diamines, such as a synthesis of putrescine (NH(3)(+)·(CH(2))(4)·NH(3)(+)) from ornithine, and cadaverine (NH(3)(+)·(CH(2))(5)·NH(3)(+)) from lysine, which are catalyzed by pyridoxal-5'-phosphate (PLP; vitamin B(6))-dependent decarboxylases. Synthesized polyamines are implicated in a wide variety of cytoplasmic reactions such as DNA replication and protein synthesis, and are essential for proper growth of the organisms. However, in Selenomonas ruminantium, a strictly anaerobic Gram-negative bacterium dominant in sheep rumen, cadaverine displays its function in a quite distinctive scheme compared to the general bacteria reported. It serves as an essential constituent of the peptidoglycan for the maintenance of envelope integrity through an interaction with the periplasm-exposed SLH domain of Mep45, the outer membrane protein of this bacterium. Furthermore, cytoplasmic biosynthesis of cadaverine occurs totally in a eukaryotic-like manner rather than in a conventional way of bacteria. Lysine/ornithine decarboxylase (LDC/ODC), a PLP-dependent enzyme responsible for cadaverine synthesis in this bacterium, displays significant homology to the eukaryotic ODC but not to the general bacterial LDC nor ODC, and its activity is tightly regulated by antizyme-mediated proteolysis, a regulatory process generally found in eukaryotes. These findings represent the biological diversity of this bacterium beyond the preexisting knowledge related to the polyamine-physiology, cell envelope-architecture, and the regulatory system for the enzyme. In this review we will describe (i) the cadaverine-containing peptidoglycan of S. ruminantium: its chemical structure, biosynthesis, and biological function, and (ii) cellular biosynthesis of cadaverine by LDC/ODC and its antizyme-mediated regulation. In addition, we will briefly refer to (iii) the phylogenetic position and characteristics of S. ruminantium and its unique cadaverine-physiology.

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Year:  2012        PMID: 22878384     DOI: 10.3177/jnsv.58.153

Source DB:  PubMed          Journal:  J Nutr Sci Vitaminol (Tokyo)        ISSN: 0301-4800            Impact factor:   2.000


  4 in total

1.  An ancient divide in outer membrane tethering systems in bacteria suggests a mechanism for the diderm-to-monoderm transition.

Authors:  Anna Sartori-Rupp; Najwa Taib; Jerzy Witwinowski; Nika Pende; To Nam Tham; Daniel Poppleton; Jean-Marc Ghigo; Christophe Beloin; Simonetta Gribaldo
Journal:  Nat Microbiol       Date:  2022-03-04       Impact factor: 30.964

2.  Outer Membrane Proteome of Veillonella parvula: A Diderm Firmicute of the Human Microbiome.

Authors:  Daniel I Poppleton; Magalie Duchateau; Véronique Hourdel; Mariette Matondo; Jennifer Flechsler; Andreas Klingl; Christophe Beloin; Simonetta Gribaldo
Journal:  Front Microbiol       Date:  2017-06-30       Impact factor: 5.640

3.  A multidomain connector links the outer membrane and cell wall in phylogenetically deep-branching bacteria.

Authors:  Andriko von Kügelgen; Sofie van Dorst; Vikram Alva; Tanmay A M Bharat
Journal:  Proc Natl Acad Sci U S A       Date:  2022-08-09       Impact factor: 12.779

4.  Peptidoglycan-associated outer membrane protein Mep45 of rumen anaerobe Selenomonas ruminantium forms a non-specific diffusion pore via its C-terminal transmembrane domain.

Authors:  Seiji Kojima; Kanako Hayashi; Saeko Tochigi; Tomonobu Kusano; Jun Kaneko; Yoshiyuki Kamio
Journal:  Biosci Biotechnol Biochem       Date:  2016-06-07       Impact factor: 2.043

  4 in total

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