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Characterisation of a capsular polysaccharide from Moraxella nonliquefaciens CCUG 348T.
Ravikumaran, Kosala S; Armiento, Samantha; De Castro, Cristina; Molinaro, Antonio; Wilson, Jennifer C; Grice, I Darren; Peak, Ian R.
Affiliation
  • Ravikumaran KS; School of Pharmacy and Medical Science, Griffith University, Gold Coast Campus, Queensland, 4222, Australia.
  • Armiento S; Dipartimento di Scienze Chimiche, Università di Napoli Federico II, Complesso Universitario Monte S. Angelo, Via Cintia 4, 80126, Napoli, Italy.
  • De Castro C; Dipartimento di Scienze Chimiche, Università di Napoli Federico II, Complesso Universitario Monte S. Angelo, Via Cintia 4, 80126, Napoli, Italy.
  • Molinaro A; Dipartimento di Scienze Chimiche, Università di Napoli Federico II, Complesso Universitario Monte S. Angelo, Via Cintia 4, 80126, Napoli, Italy.
  • Wilson JC; School of Pharmacy and Medical Science, Griffith University, Gold Coast Campus, Queensland, 4222, Australia.
  • Grice ID; School of Pharmacy and Medical Science, Griffith University, Gold Coast Campus, Queensland, 4222, Australia; Institute for Glycomics, Griffith University, Gold Coast Campus, Queensland, 4222, Australia. Electronic address: d.grice@griffith.edu.au.
  • Peak IR; School of Pharmacy and Medical Science, Griffith University, Gold Coast Campus, Queensland, 4222, Australia; Institute for Glycomics, Griffith University, Gold Coast Campus, Queensland, 4222, Australia. Electronic address: i.peak@griffith.edu.au.
Carbohydr Res ; 538: 109095, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38507941
ABSTRACT
Moraxella nonliquefaciens is a commensal of the human upper respiratory tract (URT) but on rare occasions is recovered in cases of ocular, septic and pulmonary infections. Hence there is interest in the pathogenic determinants of M. nonliquefaciens, of which outer membrane (OM) structures such as fimbriae and two capsular polysaccharide (CPS) structures, →3)-ß-D-GalpNAc-(1→5)-ß-Kdop-(2→ and →8)-α-NeuAc-(2→, have been reported in the literature. To further characterise its surface virulence factors, we isolated a novel CPS from M. nonliquefaciens type strain CCUG 348T. This structure was elucidated using NMR data obtained from CPS samples that were subjected to various degrees of mild acid hydrolysis. Together with GLC-MS data, the structure was resolved as a linear polymer composed of two GalfNAc residues consecutively added to Kdo, →3)-ß-D-GalfNAc-(1→3)-α-D-GalfNAc-(1→5)-α-(8-OAc)Kdop-(2→. Supporting evidence for this material being CPS was drawn from the proposed CPS biosynthetic locus which encoded a potential GalfNAc transferase, a UDP-GalpNAc mutase for UDP-GalfNAc production and a putative CPS polymerase with predicted GalfNAc and Kdo transferase domains. This study describes a unique CPS composition reported in Moraxella spp. and offers genetic insights into the synthesis and expression of GalfNAc residues, which are rare in bacterial OM glycans.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Moraxella Limits: Humans Language: En Journal: Carbohydr Res / Carbohydr. res / Carbohydrate research Year: 2024 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Moraxella Limits: Humans Language: En Journal: Carbohydr Res / Carbohydr. res / Carbohydrate research Year: 2024 Type: Article Affiliation country: Australia