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CURRICULUM VITAE

1975- Laurea in Scienze Biologiche presso l'Università di Roma "La Sapienza". 1981-1987- Ricercatore confermato presso la Facoltà si Scienze MM.FF.NN. dell'Università di Roma "La Sapienza". 1987-1994- Professore Associato di Fisiologia Vegetale presso l'Università di Roma "Tor Vergata". 1995-ad oggi- Professore Ordinario di Fisiologia Vegetale presso l'Università di Roma "Tor Vergata". 1995-2004- Direttore della Scuola di Specializzazione in Applicazioni Biotecnologiche dell'Università di Roma "Tor Vergata". 1997-2001- Presidente della Società Italiana di Fisiologia Vegetale. 1997-2005- Direttore del Consorzio Interuniversitario "Biologia Molecolare delle piante" 2001-2004- Presidente del corso di laurea I livello in Biotecnologie-Università di Roma "Tor Vergata" 2004-2013- Direttore del Dipartimento di Biologia-Università di Roma "Tor Vergata"

2004-2013- Membro della Conferenza dei Direttori di Dipartimento di Ateneo

2005-2013- Membro della Giunta della Conferenza dei Direttori di Dipartimento di Ateneo

2008-2011-Membro del Consiglio tecnico amministrativo del “Centro Congressi e Rappresentanza Villa Mondragone “-Università di Roma "Tor Vergata" 2007-2010 Membro del Comitato Nazionale Biosicurezza, Biotecnologie e Scienze della Vita 2009-2013 Delegata del Rettore alla realizzazione di un'anagrafe della Ricerca e al coordinamento e sviluppo dell'attività di Ricerca dell'Ateneo Premi: 2005- Medaglia Accademia Nazionale delle Scienze detta dei XL per le Scienze Fisiche e Naturali per il 2004.

 

INSEGNAMENTI

Biochimica e Fisiologia vegetale:Corso di Laurea a ciclo unico in Pharmacy

Pharmaceutical applications of plant metabolites: LM Industrial Biotechnology e Corso di Laurea a ciclo unico in Pharmacy

 

 

PRODUTTIVITÀ E IMPATTO SCIENTIFICO

La Prof Aducci ha svolto la sua attività di ricerca nell’ambito della biochimica e biologia molecolare delle piante e dei processi alla base della crescita delle cellule vegetali e della sua regolazione.

La  Prof.ssa Aducci è autore di 100 lavori pubblicati su riviste scientifiche “peer-reviewed” [h-index=19 (WOS) e 22 (Google Scholar)]  e 180 abstracts a Congressi Nazionali ed Internazionaliche investono le aree di ricerca sotto indicate

 

AREE DI RICERCA

a) ruolo della fusicoccina : una fitotossina, un  fitoregolatore e un nuovo potenziale farmaco;

b) trasduzione del segnale nelle piante. Proteine 14.3.3:ruolo e regolazione. Vie di trasduzione attivate da zuccheri ;

c)studi di interazione delle proteine 14-3-3 con i loro bersagli nelle piante e in altri organismi;

d) ruolo e regolazione delle isoforme delle proteine 14-3-3 nelle piante;

e) trasporto nelle piante: H+-ATPasi nella membrana plasmatica e sua regolazione;

f) MAP chinasi nelle piante: identificazione e caratterizzazione di ZmMPK6, una MAPchinasi da mais;

g) proteinasi vegetali: purificazione, localizzazione e caratterizzazione biochimica e cinetica di proteinasi da diverse specie di piante.

 

SELECTED PUBLICATIONS

1.   Camoni L, Marra M, Garufi A,  Visconti S , Aducci P 2006

The Maize Root Plasma Membrane H+-ATPase Is Regulated by a Sugar-Induced Transduction Pathway

      Plant Cell Physiol. 47, 743-747

 

2.   Sottocornola B, Visconti S, Orsi S, Gazzarrini S,Giacometti S, Olivari C, Camoni L, Aducci P, Marra M, Abenavoli A, Thiel G, Moroni A. 2006

The potassium channel KAT1 is activated by plant and animal 14-3-3 proteins.

J Biol Chem.281(47):35735-41.

 

3.   Garufi A, Visconti S, Camoni L, Aducci P. 2007

Polyamines as physiological regulators of 14-3-3 interaction with the plant plasma membrane H+-ATPase

Plant Cell Physiol.48,434-440

 

4.   Visconti S., Camoni L., Marra M.and Aducci P. 2008

Role of the 14-3-3 C-Terminal Region in the Interaction with the Plasma Membrane H+-ATPase

Plant Cell Physiol.49 (12),1887-1897

 

5.   Aducci P., and Visconti S. (2008). Organismi geneticamente modificati. In: Enciclopedia Medica Italiana (USES, Firenze, Italy), pp.2700-2707.

 

6.   Aducci, P., Camoni, L., and Visconti, S. (2010). La fusicoccina: da fitotossina a farmaco. Nutrirsi 8, 30-33.

 

7.   Visconti S., and Aducci, P. (2010). OGM: per saperne di più. Nutrirsi 6, 31-35.

 

8.   Camoni, L., Di Lucente, C., Visconti, S., and Aducci, P. (2011). The phytotoxin fusicoccin promotes platelet aggregation via 14-3-3-glycoprotein Ib-IX-V interaction. Biochem. J. 436, 429-436.

 

9.   Aducci, P., and Camoni, L. (2011). Fotosintesi. Nutrirsi 10, 6-9.

 

10.               Camoni, L., Di Lucente, C., Pallucca, R., Visconti, S., and Aducci, P. (2012). Binding of phosphatidic acid to 14-3-3 proteins hampers their ability to activate the plant plasma membrane H+-ATPase. IUBMB Life 64, 710-716.

 

11.               Aducci, P., and Ascenzi, P. (2013) Leucyl Endopeptidase. In: Handbook of Proteolytic Enzymes, Rawlings, N.D. and Salvesen, G.S. ed. (Oxford Academic Press, Oxford, U.K.), pp. 3258-3260.

 

12.               Camoni L., Visconti S. , Aducci P (2013)

Hypothesis Paper- The phytotoxin fusicoccin, a selective stabilizer of 14-3-3 interactions? IUBMB Life   65, 513-517

 

13.               Abdelahad, N., Aducci, P., Altamura, M.M., Berta, G., Castiglione, M., Colombo, P., et al. (a cura di). (2014). Botanica: fondamenti di biologia delle piante. Idelson-Gnocchi.Napoli, Italia,

 

14.               Paiardini A., Aducci P., Cervoni L., Cutruzzolà F., Di Lucente C., Janson G., Pascarella S., Rinaldo S., Visconti S., Camoni L. (2014)

The Phytotoxin Fusicoccin Differently Regulates 14-3-3 Proteins Association to Mode III Targets IUBMB Life, , 66(1), 52-62

 

15.               Pallucca, R., Visconti, S., Camoni, L., Cesareni, G., Melino, S., Panni, S., Torreri P., AducciP. (2014).

      Specificity of εand non-εisoforms of Arabidopsis 14-3-3 proteins towards the H+ATPase and other targets. PLoS ONE, 9(3), 90764

 

16.               Farace G., Visconti S., Marchive C., Aducci P., Marra M., Trossat-Magnin C (2015)

Characterization, functional validation and gene expression patterns of two 14-3-3 isoforms from Vitis vinifera , Vitis, 54, 33–40

 

17.               Cattaneo L, Cicconi R, Mignogna G, GiorgiA, Mattei M, Graziani G, , Ferracane R., Grosso A., Aducci P., SchininàM. E., Marra M. (2015) Anti-

Proliferative Effect of Rosmarinus officinalis L. Extract on Human Melanoma A375 Cells. PLoS ONE10(7): e0132439. doi:10.1371/journal.pone.0132439

 

18.               Carlo Muzi, Lorenzo Camoni, Sabina Visconti, Patrizia Aducci (2016)

Cold stress affects Hþ-ATPase and phospholipase D activity in

Arabidopsis Plant Physiology and Biochemistry 108 (2016) 328-336

 

19.               Rodolfo C, Rocco M, Cattaneo L, Tartaglia M, Sassi M, Aducci P, et al. (2016) Ophiobolin A Induces Autophagy and Activates the Mitochondrial Pathway of Apoptosis in Human Melanoma Cells. PLoS ONE11(12): e0167672. doi:10.1371/journal.pone.0167672Inserire qui il curriculum

CURRICULUM VITAE

1975 Degree in Biological Sciences- University of Rome "La Sapienza" 1981-1987 Research associate- University of Rome "La Sapienza"- Faculty Of Science 1982-1983 Teaching fellow "Biochemistry of nutrition" and "Physiology of nutrition" in the Advanced School of Nutrition Science- University of Rome "La Sapienza" 1987-1994 Associate professor of Plant Physiology- University of Rome "Tor Vergata" 1991-1992 Teaching contract in "Crop Physiology"- University of Basilicata, Potenza- Faculty of Agriculture  1994-present Full professor of Plant Physiology- University of Rome "Tor Vergata" 1995-2004 Director of the Advanced School of Biotechnology- University of Rome "Tor Vergata"    1997-2001 President of the Italian Society of Plant Physiology 1997-2005 Director of ConsorzioInteruniversitario “BiologiaMolecolare delle Piante” 2001-2004 President of the course of Biotechnology (I level degree)- University of Rome “Tor Vergata”     2004-2012 Head of Department of Biology-University of Rome “Tor Vergata” 2007-2010 Member of National Committee for Biosafety, Biotechnology and Life Science        2009-2013 vice-Rector for coordination and development of University Research Specialawards    2005 Medaglia Accademia Nazionale delle Scienze detta dei XL per le Scienze Fisiche e Naturali per il 2004    

TEACHING

Plant biochemistry and physiology: Degree Course in Pharmacy

Pharmaceutical applications of plant metabolites: Degree Course in Pharmacy Natural compound metabolism and officinal plants: Degree Course in Industrial Biotechnology (Second Level)      

 

SCIENTIFIC PRODUCTIVITY       Research activity of Prof Aducci  is on  the biochemistry and molecular biology of plants and on  the mechanism  of plant growth and its regulation.

She is author of 100 papers on high-ranking journals and  180 abstracts of International and National Congresseson the following researchtopics

 

 

 

 

RESEARCH TOPICS

a)role of fusicoccin: a phytotoxin, a plant regulator and a potential new therapeutic agent;

b) plant signal transduction.14-3-3 proteins: role and regulation. Sugar sensing pathways;

c) study of interaction of 14-3-3 proteins  with targets in plants and other organisms;

d) role and regulation of 14-3-3 isoforms in plants; 

e)plant transport: plasmalemma H+-ATPase and its regulation;

f) MAP kinases in plants: identification and characterization of ZmMPK6, a MAPkinase  from maize;

g)plant proteinases: purification, localization and biochemical and kinetic characterization of proteinases from different plants.

 

SELECTED PUBLICATIONS

C. Muzi, L. Camoni, S. Visconti, P. Aducci (2016)

Cold stress affects Hþ-ATPase and phospholipase D activity in

ArabidopsisPlant Physiology and Biochemistry 108 (2016) 328-336

 

Cattaneo L, Cicconi R, Mignogna G, GiorgiA, Mattei M, Graziani G, FerracaneR., GrossoA.,AducciP., SchininàM. E., MarraM.(2015)

Anti-Proliferative Effect of Rosmarinusofficinalis L. Extract on Human Melanoma A375 Cells. PLoS ONE10(7): e0132439. doi:10.1371/journal.pone.0132439

 

Pallucca R., Visconti S., Camoni L., Cesareni G.,Melino S., Panni S., TorreriP.,

AducciP. (2014).

Specificity of εand non-εisoforms of Arabidopsis 14-3-3 proteins towards the

H+-ATPase and other targets. PLoS ONE, 9(3), 90764.

 

A.Paiardini, P. Aducci, L. Cervoni, F.Cutruzzolà, C. Di Lucente, G.Janson,S.Pascarella,S. Rinaldo, S. Visconti, L. Camoni (2014)

The PhytotoxinFusicoccin Differently Regulates 14-3-3 Proteins Association to Mode III TargetsIUBMB Life,DOI 10.1002/iub.1239, Published online in Wiley Online Library

 

Camoni L., Visconti S. , Aducci P (2013)

Hypothesis Paper- The phytotoxinfusicoccin, a selective stabilizer of 14-3-3 interactions? IUBMB Life65, 513-517

 

Aducci, P., and Ascenzi, P. (2013) Leucyl Endopeptidase. In: Handbook of Proteolytic Enzymes, Rawlings, N.D. and Salvesen, G.S. ed. (Oxford Academic Press, Oxford, U.K.), pp. 3258-3260.

 

Camoni L,  Di Lucente C., Pallucca R., Visconti S , Aducci P (2012)

Binding of phosphatidic acid to 14-3-3 proteins hampers their

ability to activate the plant plasma membrane H+-ATPase

IUBMB Life64(8), 710–716, August 2012

 

Camoni L,  Di Lucente C., Visconti S , Aducci P (2011)

The phytotoxinfusicoccin promotes platelet aggregation via

14-3-3–glycoprotein Ib-IX-V interaction1

Biochem. J.436, 429–436

 

Visconti S, Camoni L, Marra M, Aducci P. (2008)

Role of the 14-3-3 C-terminal region in the interaction with the plasma membrane H+-ATPase.Plant Cell Physiol.49(12), 1887-97   Garufi A, Visconti S, Camoni L, Aducci P. 2007

Polyamines as physiological regulators of 14-3-3 interaction with the plant plasma membrane H+-ATPase Plant Cell Physiol.48,434-440

 

Camoni L, Marra M, Garufi A,  Visconti S , Aducci P 2006

The Maize Root Plasma Membrane H+-ATPase Is Regulated by a Sugar-Induced Transduction Pathway Plant Cell Physiol. 47,743-747

 

Sottocornola B, Visconti S, Orsi S, GazzarriniS,Giacometti S, Olivari C, Camoni L, Aducci P, Marra M, Abenavoli A, Thiel G, Moroni A. 2006

The potassium channel KAT1 is activated by plant and animal 14-3-3 proteins. J BiolChem.281(47), 35735-41.

 

Lalle M., Visconti S., Marra M., Camoni L., Velasco  R., Aducci P. 2005

ZmMPK6, a novel maize MAP kinase that interacts with 14-3-3 proteins

PlantMolecularBiology59, 713–722

 

Giacometti S., Camoni L., Albumi C., Visconti S., De Michelis M.I., Aducci P. 2004. Role of tyrosine phosphorylation of 14-3-3 proteins in plant plasma-membrane H+-ATPase regulation. PlantBiology, 6, 422-431.

 

Visconti S. Camoni L., Fullone M.R., Lalle M., Marra M., Aducci P. 2003. Mutational analysis of the interaction between 14-3-3 proteins and plant plasma membrane H+-ATPase. The Journal of Biological Chemistry, 278,  8172-8178

 

Aducci P., Camoni L., Marra M., Visconti S. 2002. From cytosol to organelles: 14-3-3 proteins as multifunctional regulators of plant cell. IUBMB Life, 53, 49-55

 

Camoni L., Visconti S., Marra M. and Aducci P. 2001. Adenosine 5’-monophosphate inhibits the association of 14-3-3 proteins with the plant plasma membrane H+-ATPase. The Journal of Biological Chemistry276, 31709-31712

 

Camoni L., Iori V., Marra M., Aducci P. (2000) “Phosphorylation-dependent interaction between plant plasma membrane H+-ATPase and 14.3.3 proteins.” The Journal of Biological Chemistry,275, 9919-9923

 

M. Marra, C. Olivari, S. Visconti, C. Albumi, P. Aducci, M.I. De Michelis (2000) “A phosphopeptide corresponding to the cytosolic stretch connecting transmembrane segments 8 and 9 of the plasma membrane H+‑ATPase binds 14‑3‑3  proteins and inhibits fusicoccin induced activation of the H+‑ATPase”Plant Biology, 2, 1-6.

 

Fuglsang A.T., Visconti S., Drumm K., Jahn T.,  Stensballe A., Mattei B., Jensen O.N.,  Aducci P., Palmgren M.G. (1999) 14-3-3 protein Binding to the Plasma Membrane H+-ATPase AHA2 Involves the Three C-terminal Residues Tyr946-Thr-Val and Requires Phosphorylation of Thr947” The Journal of Biological Chemistry,274, 36774-36780.

 

Fullone M.R., Visconti S.,  Marra M., Fogliano V. and Aducci P. (1998) Fusicoccin effect on the in vitro interaction between plant 14.3.3. proteins and plasma membrane H+-ATPase. The Journal of Biological Chemistry,273 (N.13), 7698-7702

 

Marra M.,  Ballio A., Battirossi P., Fogliano V., Fullone MR. , Slayman C.L. and Aducci P., (1995) The fungal H+-ATPase from Neurosporacrassa reconstituted with fusicoccin receptors senses fusicoccin signal. Proc.Natl.Acad.Sci. (USA), 92,1599-1603

 

Aducci P., Ballio A., Fogliano V., Fullone M.R., Marra M.,     Proietti N. (1993) Purification and photoaffinitylabeling of fusicoccin receptors from maize. European Journal of Biochemistry, 214, 339-445

 

Aducci P.,Ballio A.,Blein J.-P.,Fullone M.R.,Rossignol M.,  Scalla R. (1988)  Functional reconstitution of a proton-translocating system  responsive to fusicoccin. Proc.Natl.Acad.Sci.,85 (21),7849-7851.(Washington DC, USA).

 

Insert here the curriculum

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In the present study, 14-3-3ε and 14-3-3ω isoforms, which were representative of ε and non-ε phylogenetic groups, were overexpressed in Arabidopsis thaliana plants; the effect of their overexpression was investigated on H+-ATPase activation and plant response to cold stress. Results demonstrated that H+-ATPase activity was increased in 14-3-3ω-overexpressing plants, whereas overexpression of both 14-3-3 isoforms brought about cold stress tolerance, which was evaluated through ion leakage, lipid peroxidation, osmolyte synthesis, and ROS production assays. A dedicated tandem mass tag (TMT)-based proteomic analysis demonstrated that different proteins involved in the plant response to cold or oxidative stress were over-represented in 14-3-3ε-overexpressing plants.";s:9:"metadata5";s:130:"Overexpression of 14-3-3 proteins enhances cold tolerance and increases levels of stress-responsive proteins of Arabidopsis plants";s:9:"metadata6";s:114:"Visconti, S; D'Ambrosio, C; Fiorillo, A; Arena, S; Muzi, C; Zottini, M; Aducci, P; Marra, M; Scaloni, A; Camoni, L";s:9:"metadata7";s:30:"10.1016/j.plantsci.2019.110215";s:9:"metadata8";N;s:9:"metadata9";N;s:10:"metadata10";N;}i:1;a:14:{s:9:"citazione";s:149:"Camoni, L., Visconti, S., Aducci, P., & Marra, M. (2019). From plant physiology to pharmacology: fusicoccin leaves the leaves. 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Thereafter, FC became, and still is, a tool in plant physiology, due to its ability to influence a number of fundamental processes, which are dependent on the activation of the plasma membrane H+-ATPase. Molecular studies carried out in the last 20 years clarified details of the mechanism of proton pump stimulation, which involves the fusicoccin-mediated irreversible stabilization of the complex between the H+-ATPase and activatory 14-3-3 proteins. More recently, FC has been shown to influence cellular processes involving 14-3-3 binding to client proteins both in plants and animals. 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PLOS ONE, 10(7), e0132439.";s:4:"data";s:4:"2015";s:2:"id";s:20:"PUBBLICAZIONE_301034";s:6:"handle";s:11:"2108/171879";s:9:"metadata1";s:19:"Articolo su rivista";s:9:"metadata2";s:300:"Antineoplastic Agents, Phytogenic; Apigenin; Cell Cycle; Cell Line, Tumor; Cell Proliferation; Cell Survival; Diterpenes, Abietane; Drug Screening Assays, Antitumor; Glucuronates; Humans; Luteolin; Melanoma; Oxidative Stress; Plant Extracts; Protein Carbonylation; Reactive Oxygen Species; Rosmarinus";s:9:"metadata3";s:34:"Settore MED/05 - Patologia Clinica";s:9:"metadata4";s:1662:"Rosemary (Rosmarinus officinalis L.) has been used since ancient times in traditional medicine, while nowadays various rosemary formulations are increasingly exploited by alternative medicine to cure or prevent a wide range of health disorders. Rosemary's bioproperties have prompted scientific investigation, which allowed us to ascertain antioxidant, anti-inflammatory, cytostatic, and cytotoxic activities of crude extracts or of pure components. Although there is a growing body of experimental work, information about rosemary's anticancer properties, such as chemoprotective or anti-proliferative effects on cancer cells, is very poor, especially concerning the mechanism of action. Melanoma is a skin tumor whose diffusion is rapidly increasing in the world and whose malignancy is reinforced by its high resistance to cytotoxic agents; hence the availability of new cytotoxic drugs would be very helpful to improve melanoma prognosis. Here we report on the effect of a rosemary hydroalcoholic extract on the viability of the human melanoma A375 cell line. Main components of rosemary extract were identified by liquid chromatography coupled to tandem mass spectrometry (LC/ESI-MS/MS) and the effect of the crude extract or of pure components on the proliferation of cancer cells was tested by MTT and Trypan blue assays. The effect on cell cycle was investigated by using flow cytometry, and the alteration of the cellular redox state was evaluated by intracellular ROS levels and protein carbonylation analysis. 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USES Edizioni Scientifiche - UTET.";s:4:"data";s:4:"2008";s:2:"id";s:19:"PUBBLICAZIONE_49368";s:6:"handle";s:10:"2108/13395";s:9:"metadata1";s:19:"Contributo in libro";s:9:"metadata2";N;s:9:"metadata3";s:36:"Settore BIO/04 - Fisiologia Vegetale";s:9:"metadata4";N;s:9:"metadata5";s:34:"Organismi Geneticamente Modificati";s:9:"metadata6";s:22:"Aducci, P; Visconti, S";s:9:"metadata7";N;s:9:"metadata8";N;s:9:"metadata9";N;s:10:"metadata10";N;}i:25;a:14:{s:9:"citazione";s:195:"Visconti, S., Camoni, L., Marra, M., & Aducci, P. (2008). Role of the 14-3-3 C-terminal region in the interaction with the plasma membrane H+-ATPase. 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