Moramarco, Filippo
(2019)
Atypical LONELY GUY protein in Bordetella pertussis synthetizes a cytokinin-like compound negatively related to oxidative stress, [Dissertation thesis], Alma Mater Studiorum Università di Bologna.
Dottorato di ricerca in
Biologia cellulare e molecolare, 31 Ciclo. DOI 10.6092/unibo/amsdottorato/8793.
Documenti full-text disponibili:
|
Documento PDF (English)
- Richiede un lettore di PDF come Xpdf o Adobe Acrobat Reader
Disponibile con Licenza: Salvo eventuali più ampie autorizzazioni dell'autore, la tesi può essere liberamente consultata e può essere effettuato il salvataggio e la stampa di una copia per fini strettamente personali di studio, di ricerca e di insegnamento, con espresso divieto di qualunque utilizzo direttamente o indirettamente commerciale. Ogni altro diritto sul materiale è riservato.
Download (2MB)
|
Abstract
The Gram-negative bacterium Bordetella pertussis (Bp) is the causative agent of whooping cough. This infection is re-emerging and new features related to Bordetella pathogenesis and microbiology could be relevant to defeat it. BP1253 from Bp is a predicted exported protein erroneously classified as lysine decarboxylase, presenting sequence homology with some newly structurally characterized “LONELY GUY” proteins. These cytokinin-activating enzymes share with BP1253 the highly conserved motif PGGxGTxxE and the amino acid residues of the catalytic core. SEC and MALS analysis revealed a dimeric form as functional unit. Surface plasmon resonance studies showed that BP1253 selectively binds monophosphate nucleotides and dinucleotides such as AMP, GMP and NAD, NADP. Applying an enzymatic assay in the presence of nucleotides as substrates, we clearly showed that BP1253 is able to cleave the N-glycosidic linkage between the base and the ribose, leading to the formation of free bases. This phosphoribohydrolase activity, time- and dose- dependent, is the crucial reaction in producing active cytokinins, which are phytormones in plants. Moreover, the enzymatic assay with site-specific mutants confirmed the amino acids 120R and 143D as the catalytic residues and the positive charge in position 121 crucial for the reaction. Through LC-MS/MS we identified in growth medium of Tohama strain the 6-O-Methylguanine as physiological product of the BP1253, in agreement with the higher activity of the enzyme towards GMP. Although 6-O-Methylguanine resulted to be toxic for the same bacteria in oxidative stress conditions, BP1253 turned out to be also prevalently expressed in clinical isolates. Overall, the data presented show for the first time the presence of a cytokinin-activating enzyme in Bordetella pertussis.
Abstract
The Gram-negative bacterium Bordetella pertussis (Bp) is the causative agent of whooping cough. This infection is re-emerging and new features related to Bordetella pathogenesis and microbiology could be relevant to defeat it. BP1253 from Bp is a predicted exported protein erroneously classified as lysine decarboxylase, presenting sequence homology with some newly structurally characterized “LONELY GUY” proteins. These cytokinin-activating enzymes share with BP1253 the highly conserved motif PGGxGTxxE and the amino acid residues of the catalytic core. SEC and MALS analysis revealed a dimeric form as functional unit. Surface plasmon resonance studies showed that BP1253 selectively binds monophosphate nucleotides and dinucleotides such as AMP, GMP and NAD, NADP. Applying an enzymatic assay in the presence of nucleotides as substrates, we clearly showed that BP1253 is able to cleave the N-glycosidic linkage between the base and the ribose, leading to the formation of free bases. This phosphoribohydrolase activity, time- and dose- dependent, is the crucial reaction in producing active cytokinins, which are phytormones in plants. Moreover, the enzymatic assay with site-specific mutants confirmed the amino acids 120R and 143D as the catalytic residues and the positive charge in position 121 crucial for the reaction. Through LC-MS/MS we identified in growth medium of Tohama strain the 6-O-Methylguanine as physiological product of the BP1253, in agreement with the higher activity of the enzyme towards GMP. Although 6-O-Methylguanine resulted to be toxic for the same bacteria in oxidative stress conditions, BP1253 turned out to be also prevalently expressed in clinical isolates. Overall, the data presented show for the first time the presence of a cytokinin-activating enzyme in Bordetella pertussis.
Tipologia del documento
Tesi di dottorato
Autore
Moramarco, Filippo
Supervisore
Co-supervisore
Dottorato di ricerca
Ciclo
31
Coordinatore
Settore disciplinare
Settore concorsuale
Parole chiave
Bordetella pertussis, BP1253, LONELY GUY, LOGs, phosphoribohydrolase activity, BpLOG, cytokinin, 6-O-methylguanine, oxidative stress
URN:NBN
DOI
10.6092/unibo/amsdottorato/8793
Data di discussione
2 Aprile 2019
URI
Altri metadati
Tipologia del documento
Tesi di dottorato
Autore
Moramarco, Filippo
Supervisore
Co-supervisore
Dottorato di ricerca
Ciclo
31
Coordinatore
Settore disciplinare
Settore concorsuale
Parole chiave
Bordetella pertussis, BP1253, LONELY GUY, LOGs, phosphoribohydrolase activity, BpLOG, cytokinin, 6-O-methylguanine, oxidative stress
URN:NBN
DOI
10.6092/unibo/amsdottorato/8793
Data di discussione
2 Aprile 2019
URI
Statistica sui download
Gestione del documento: