Donato Giovannelli

Dr. Donato Giovannelli


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 April 2019 in Frontiers in Microbiology
Verified
Journal Article
Open access
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NMNancy Merino
Nancy Merino
HAHeidi S. Aronson
Heidi S. Aronson
DBDiana P. Bojanova
Diana P. Bojanova
JFJayme Feyhl-Buska
Jayme Feyhl-Buska
MWMichael L. Wong
Michael L. Wong
DGDonato Giovannelli
Donato Giovannelli
Prokaryotic life has dominated most of the evolutionary history of our planet, evolving to occupy virtually all available environmental niches. Extremophiles, especially those thriving under multiple extremes, represent a key area of research for multiple disciplines, spanning from the study of adaptations to harsh conditions, to the biogeochemical cycling of elements. Extremophile research also has implications for origin of life studies and the search for life on other planetary and celestial bodies. In this article, we will review the current state of knowledge for the biospace in which life operates on Earth and will discuss it in a planetary context, highlighting knowledge gaps and areas of opportunity.

1 April 2008 in Environmental Health Perspectives
Verified
Journal Article
Open access
Roberto DanovaroRoberto Danovaro
Roberto Danovaro
LBLucia Bongiorni
Lucia Bongiorni
CCCinzia Corinaldesi
Cinzia Corinaldesi
DGDonato Giovannelli
Donato Giovannelli
Elisabetta DamianiElisabetta Damiani
Elisabetta Damiani
APAntonio Pusceddu
Antonio Pusceddu
Coral bleaching (i.e., the release of coral symbiotic zooxanthellae) has negative impacts on biodiversity and functioning of reef ecosystems and their production of goods and services. This increasing world-wide phenomenon is associated with temperature ...

16 January 2014 in The ISME Journal
Verified
Journal Article
Closed access
CVCostantino Vetriani
Costantino Vetriani
JVJames W Voordeckers
James W Voordeckers
MCMelitza Crespo-Medina
Melitza Crespo-Medina
COCharles E O’bRien
Charles E O’bRien
DGDonato Giovannelli
Donato Giovannelli
RLRichard A Lutz
Richard A Lutz
Despite the frequent isolation of nitrate-respiring Epsilonproteobacteria from deep-sea hydrothermal vents, the genes coding for the nitrate reduction pathway in these organisms have not been investigated in depth. In this study we have shown that the gene cluster coding for the periplasmic nitrate reductase complex (nap) is highly conserved in chemolithoautotrophic, nitrate-reducing Epsilonproteobacteria from deep-sea hydrothermal vents. Furthermore, we have shown that the napA gene is expressed in pure cultures of vent Epsilonproteobacteria and it is highly conserved in microbial communities collected from deep-sea vents characterized by different temperature and redox regimes. The diversity of nitrate-reducing Epsilonproteobacteria was found to be higher in moderate temperature, diffuse flow vents than in high temperature black smokers or in low temperatures, substrate-associated communities. As NapA has a high affinity for nitrate compared with the membrane-bound enzyme, its occurrence in vent Epsilonproteobacteria may represent an adaptation of these organisms to the low nitrate concentrations typically found in vent fluids. Taken together, our findings indicate that nitrate reduction is widespread in vent Epsilonproteobacteria and provide insight on alternative energy metabolism in vent microorganisms. The occurrence of the nap cluster in vent, commensal and pathogenic Epsilonproteobacteria suggests that the ability of these bacteria to respire nitrate is important in habitats as different as the deep-sea vents and the human body.

8 September 2016 in Annual Review of Microbiology
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Journal Article
Closed access
BJBenjamin I. Jelen
Benjamin I. Jelen
DGDonato Giovannelli
Donato Giovannelli
PFPaul G. Falkowski
Paul G. Falkowski
All life on Earth is dependent on biologically mediated electron transfer (i.e., redox) reactions that are far from thermodynamic equilibrium. Biological redox reactions originally evolved in prokaryotes and ultimately, over the first ∼2.5 billion years of Earth's history, formed a global electronic circuit. To maintain the circuit on a global scale requires that oxidants and reductants be transported; the two major planetary wires that connect global metabolism are geophysical fluids—the atmosphere and the oceans. Because all organisms exchange gases with the environment, the evolution of redox reactions has been a major force in modifying the chemistry at Earth's surface. Here we briefly review the discovery and consequences of redox reactions in microbes with a specific focus on the coevolution of life and geochemical phenomena.

27 September 2014 in Marine Ecology
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Journal Article
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FPFrancesca Pasotti
Francesca Pasotti
EMElena Manini
Elena Manini
DGDonato Giovannelli
Donato Giovannelli
AWAnne‐Cathrin Wölfl
Anne‐Cathrin Wölfl
DMDonata Monien
Donata Monien
AVAnn Vanreusel
Ann Vanreusel
The West Antarctic Peninsula is one of the fastest warming regions on Earth. Faster glacier retreat and related calving events lead to more frequent iceberg scouring, fresh water input and higher sediment loads, which in turn affect shallow water benthic marine assemblages in coastal regions. In addition, ice retreat creates new benthic substrates for colonization. We investigated three size classes of benthic biota (microbenthos, meiofauna and macrofauna) at three sites in Potter Cove (King George Island, West Antarctic Peninsula) situated at similar water depths but experiencing different disturbance regimes related to glacier retreat. Our results revealed the presence of a patchy distribution of highly divergent benthic assemblages within a relatively small area (about 1 km2). In areas with frequent ice scouring and higher sediment accumulation rates, an assemblage mainly dominated by macrobenthic scavengers (such as the polychaete Barrukia cristata), vagile organisms and younger individuals of sessile species (such as the bivalve Yoldia eightsi) was found. Macrofauna were low in abundance and very patchily distributed in recently ice‐free areas close to the glacier, whereas the pioneer nematode genus Microlaimus reached a higher relative abundance in these newly exposed sites. The most diverse and abundant macrofaunal assemblage was found in areas most remote from recent glacier influence. By contrast, the meiofauna showed relatively low densities in these areas. The three benthic size classes appeared to respond in different ways to disturbances likely related to ice retreat, suggesting that the capacity to adapt and colonize habitats is dependent on both body size and specific life traits. We predict that, under continued deglaciation, more diverse, but less patchy, benthic assemblages will become established in areas out of reach of glacier‐related disturbance.

1 July 2016 in International Journal of Systematic and Evolutionary Microbiology
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Journal Article
Closed access
DGDonato Giovannelli
Donato Giovannelli
MCMatthew Chung
Matthew Chung
JSJustin Staley
Justin Staley
VSValentin Starovoytov
Valentin Starovoytov
NBNadine Le Bris
Nadine Le Bris
CVCostantino Vetriani
Costantino Vetriani
An anaerobic, nitrate-reducing, sulfur- and thiosulfate-oxidizing bacterium, designated strain 1812ET, was isolated from the vent polychaete Riftia pachyptila, which was collected from a deep-sea hydrothermal vent on the East Pacific Rise. Cells were Gram-stain-negative rods, measuring approximately 1.05±0.11 µm by 0.40±0.05 µm. Strain 1812ET grew at 25 – –45 °C (optimum 35 °C), with 1.5–4.0 % (w/v) NaCl (optimum 3.0 %) and at pH 5.0–8.0 (optimum pH 6.0). The generation time under optimal conditions was 3 h. Strain 1812ET was an anaerobic chemolithotroph that grew with either sulfur or thiosulfate as the energy source and carbon dioxide as the sole carbon source. Nitrate was used as a sole terminal electron acceptor. The predominant fatty acids were C16 : 1 ω7c, C18 : 1 ω7c and C16 : 0. The major polar lipids were phosphatidylethanolamine, diphosphatidylglycerol and phosphatidylglycerol. The major respiratory quinone was menaquinone MK-6 and the G+C content of the genomic DNA was 47.4 mol%. Phylogenetic analysis of the 16S rRNA gene of strain 1812ET showed that the isolate belonged to the Epsilonproteobacteria , and its closest relatives were Sulfurovum lithotrophicum 42BKTT and Sulfurovum aggregans Monchim 33T (98.3 and 95.7 % sequence similarity, respectively). DNA–DNA relatedness between strain 1812ET and the type strain of S. lithotrophicum was 29.7 %, demonstrating that the two strains are not members of the same species. Based on the phylogenetic, molecular, chemotaxonomic and physiological evidence, strain 1812ET represents a novel species within the genus Sulfurovum , for which the name Sulfurovum riftiae sp. nov. is proposed. The type strain is 1812ET (=DSM 101780T=JCM 30810T).