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Dive into the research topics where Giuliana d'Ippolito is active.

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Featured researches published by Giuliana d'Ippolito.


ChemBioChem | 2007

LOX-Induced Lipid Peroxidation Mechanism Responsible for the Detrimental Effect of Marine Diatoms on Zooplankton Grazers

Angelo Fontana; Giuliana d'Ippolito; Adele Cutignano; Giovanna Romano; Nadia Lamari; Alexia Massa Gallucci; Guido Cimino; Antonio Miralto; Adrianna Ianora

Some marine diatoms negatively affect the reproduction of dominant zooplankton grazers such as copepods, thus compromising the transfer of energy through the marine food chains. In this paper, the metabolic mechanism that leads to diatom‐induced toxicity is investigated in three bloom‐forming microalgae. We show that copepod dysfunctions can be induced by highly reactive oxygen species (hROS) and a blended mixture of diatom products, including fatty acid hydroperoxides (FAHs); these compounds display teratogenic and proapoptotic properties. The process is triggered by the early onset of lipoxygenase activities that elicit the synthesis of species‐specific products, the basic structures of which were established (1–20); these compounds boost oxidative stress by massive lipid peroxidation. Our study might explain past laboratory and field results showing how diatoms damage zooplankton grazers even in the absence of polyunsaturated aldehydes, a class of molecules that has been formerly implicated in mediating the toxic activity of diatoms on copepods.


Tetrahedron Letters | 2002

New birth-control aldehydes from the marine diatom Skeletonema costatum: characterization and biogenesis

Giuliana d'Ippolito; Giovanna Romano; Olimpia Iadicicco; Antonio Miralto; Adrianna Ianora; Guido Cimino; Angelo Fontana

Abstract The paper describes the identification of short-chain aldehydes ( 4 – 7 ) from the marine diatom Skeletonema costatum , and their effects on copepod egg viability and sea urchin cell division. Compounds 4 – 7 were isolated as carboethoxyethylidene (CET) derivatives and their characterization was performed by NMR and GCMS analyses. Evidence is presented to support the defensive role and biosynthetic origin of these compounds in S. costatum .


Pure and Applied Chemistry | 2007

Chemistry of oxylipin pathways in marine diatoms

Angelo Fontana; Giuliana d'Ippolito; Adele Cutignano; Antonio Miralto; Adrianna Ianora; Giovanna Romano; Guido Cimino

Oxylipins are important signal transduction molecules widely distributed in animals and plants where they regulate a variety of events associated with physiological and pathological processes. The family embraces several different metabolites that share a common origin from the oxygenase-catalyzed oxidation of polyunsaturated fatty acids. The biological role of these compounds has been especially studied in mammalians and higher plants, although a varied and very high concentration of these products has also been reported from marine macroalgae. This article gives a summary of our results concerning the oxylipin chemistry of marine diatoms, a major class of planktonic microalgae that discourage predation from their natural grazers, zooplanktonic copepods, using chemical warfare. These apparently harmless microscopic cells produce a plethora of oxylipins, including short-chain unsaturated aldehydes, hydroxyl-, keto-, and epoxyhydroxy fatty acid derivatives, that induce reproductive failure in copepods through abortions, congenital malformations, and reduced larval growth. The biochemical process involved in the production of these compounds shows a simple regulation based on decompartmentation and mixing of preexisting enzymes and requires hydrolysis of chloroplast-derived glycolipids to feed the downstream activities of C16 and C20 lipoxygenases.


Tetrahedron Letters | 2002

Detection of short-chain aldehydes in marine organisms: the diatom Thalassiosira rotula

Giuliana d'Ippolito; Olimpia Iadicicco; Giovanna Romano; Angelo Fontana

Abstract Short-chain aldehydes are analysed by GC–MS and NMR after their transformation into the corresponding carboxyethylethylidene (CET) derivatives via Wittig reaction. The procedure implies the treatment of the aldehyde with (carbetoxyethylidene)-triphenylphosphorane under very mild conditions. The method is suitable for the detection of short and medium chain aldehydes. CET derivatives are easily prepared and can be utilised for the analysis of raw biological samples. The efficacy of the method has been tested in the identification of biologically active aldehydes in the marine diatom Thalassiosira rotula . At least two compounds, trans , trans -octadienal and 2- trans -4- trans -2,4,7-octatrienal, that have not been revealed in previous papers are unambiguously identified in the microalga.


Light-Science & Applications | 2017

Tomographic flow cytometry by digital holography

Francesco Merola; Pasquale Memmolo; Lisa Miccio; Roberto Savoia; Martina Mugnano; Angelo Fontana; Giuliana d'Ippolito; Angela Sardo; Achille Iolascon; Antonella Gambale; Pietro Ferraro

High-throughput single-cell analysis is a challenging task. Label-free tomographic phase microscopy is an excellent candidate to perform this task. However, in-line tomography is very difficult to implement in practice because it requires a complex set-up for rotating the sample and examining the cell along several directions. We demonstrate that by exploiting the random rolling of cells while they are flowing along a microfluidic channel, it is possible to obtain in-line phase-contrast tomography, if smart strategies for wavefront analysis are adopted. In fact, surprisingly, a priori knowledge of the three-dimensional position and orientation of rotating cells is no longer needed because this information can be completely retrieved through digital holography wavefront numerical analysis. This approach makes continuous-flow cytotomography suitable for practical operation in real-world, single-cell analysis and with a substantial simplification of the optical system; that is, no mechanical scanning or multi-direction probing is required. A demonstration is given for two completely different classes of biosamples: red blood cells and diatom algae. An accurate characterization of both types of cells is reported, despite their very different nature and material content, thus showing that the proposed method can be extended by adopting two alternate strategies of wavefront analysis to many classes of cells.


ChemBioChem | 2006

Chloroplastic glycolipids fuel aldehyde biosynthesis in the marine diatom Thalassiosira rotula.

Adele Cutignano; Giuliana d'Ippolito; Giovanna Romano; Nadia Lamari; Guido Cimino; Ferdinando Febbraio; Roberto Nucci; Angelo Fontana

Enzymatic preparations and specialized analytical tools have shown that chloroplast‐derived glycolipids are the main substrates for the biosynthetic pathway that produces antiproliferative polyunsaturated aldehydes in broken cells of the marine diatom Thalassiosira rotula. This process, which is associated with the formation of free fatty acids and lyso compounds from polar lipids but not triglycerides, is largely dependent on glycolipid hydrolytic activity, rather than phospholipase A2 as previously suggested. Preliminary characterization of lipolytic enzymes has revealed protein bands of 40–45 kDa. Under native conditions these proteins seem to be associated with soluble aggregates that have an apparent molecular weight of approximately 200 kDa. The biochemical process, which is similar to that described in the algal‐bloom forming diatom Skeletonema costatum, suggests a mechanism based on decompartmentalization and mixing of preexisting enzymes and substrates.


Marine Drugs | 2013

Composition and Quantitation of Microalgal Lipids by ERETIC 1H NMR Method

Genoveffa Nuzzo; Carmela Gallo; Giuliana d'Ippolito; Adele Cutignano; Angela Sardo; Angelo Fontana

Accurate characterization of biomass constituents is a crucial aspect of research in the biotechnological application of natural products. Here we report an efficient, fast and reproducible method for the identification and quantitation of fatty acids and complex lipids (triacylglycerols, glycolipids, phospholipids) in microalgae under investigation for the development of functional health products (probiotics, food ingredients, drugs, etc.) or third generation biofuels. The procedure consists of extraction of the biological matrix by modified Folch method and direct analysis of the resulting material by proton nuclear magnetic resonance (1H NMR). The protocol uses a reference electronic signal as external standard (ERETIC method) and allows assessment of total lipid content, saturation degree and class distribution in both high throughput screening of algal collection and metabolic analysis during genetic or culturing studies. As proof of concept, the methodology was applied to the analysis of three microalgal species (Thalassiosira weissflogii, Cyclotella cryptica and Nannochloropsis salina) which drastically differ for the qualitative and quantitative composition of their fatty acid-based lipids.


International Journal of Molecular Sciences | 2015

Hydrogen Production by the Thermophilic Bacterium Thermotoga neapolitana

Nirakar Pradhan; Laura Dipasquale; Giuliana d'Ippolito; Antonio Panico; Piet N.L. Lens; Giovanni Esposito; Angelo Fontana

As the only fuel that is not chemically bound to carbon, hydrogen has gained interest as an energy carrier to face the current environmental issues of greenhouse gas emissions and to substitute the depleting non-renewable reserves. In the last years, there has been a significant increase in the number of publications about the bacterium Thermotoga neapolitana that is responsible for production yields of H2 that are among the highest achievements reported in the literature. Here we present an extensive overview of the most recent studies on this hyperthermophilic bacterium together with a critical discussion of the potential of fermentative production by this bacterium. The review article is organized into sections focused on biochemical, microbiological and technical issues, including the effect of substrate, reactor type, gas sparging, temperature, pH, hydraulic retention time and organic loading parameters on rate and yield of gas production.


Organic and Biomolecular Chemistry | 2004

Lipase-mediated production of defensive toxins in the marine mollusc Oxynoe olivacea

Adele Cutignano; Valentina Notti; Giuliana d'Ippolito; Anna Domènech Coll; Guido Cimino; Angelo Fontana

Metabolites related to caulerpenyne (1), a toxic sesquiterpene featured by two enol-acetate residues, play a major role in the chemical defence of both algae of the genus Caulerpa and a few molluscs of the order Sacoglossa. Here we report the direct evidence that cell-free preparations of Oxynoe olivacea, a Mediterranean sacoglossan, transform efficiently the algal metabolite 1 to oxytoxin-2 (3), the main defensive metabolite of the mollusc. The process implies two distinct hydrolytic activities, here named LIP-1 and LIP-2, able to operate either hydrolysis of the acetyl residue at C-1 or concerted elimination of the acetyl groups at C-4 and C-13. Incubation experiments with tissue homogenates of O. olivacea or with commercially available lipases suggest a two-step mechanism that involves, in vitro, an unstable metabolite characterized as preoxytoxin-2 (4). The course of the entire process can be easily monitored by reverse phase HPLC/ESI-MS, as well as by NMR measurements, which provides direct evidence of the enzymatic mechanism leading to the formation of this last compound (4). In agreement with the literature, both fresh and frozen tissues of Mediterranean Caulerpa prolifera also have the capability to transform 1 into aldehydic derivatives, namely oxytoxin-1 (2) and oxytoxin-2 (3), through hydrolysis of the acetyl groups. However, differently from experiments with mollusc homogenates, the conversion is not complete and caulerpenyne (1) can be detected in the algal suspension for a few hours. HPLC/ESI-MS monitoring of this transformation suggests that the hydrolytic route involves different activities in the mollusc and seaweed.


Marine Drugs | 2014

Oxylipin Diversity in the Diatom Family Leptocylindraceae Reveals DHA Derivatives in Marine Diatoms

Deepak Nanjappa; Giuliana d'Ippolito; Carmela Gallo; Adriana Zingone; Angelo Fontana

Marine planktonic organisms, such as diatoms, are prospective sources of novel bioactive metabolites. Oxygenated derivatives of fatty acids, generally referred to as oxylipins, in diatoms comprise a highly diverse and complex family of secondary metabolites. These molecules have recently been implicated in several biological processes including intra- and inter-cellular signaling as well as in defense against biotic stressors and grazers. Here, we analyze the production and diversity of C20 and C22 non-volatile oxylipins in five species of the family Leptocylindraceae, which constitute a basal clade in the diatom phylogeny. We report the presence of species-specific lipoxygenase activity and oxylipin patterns, providing the first demonstration of enzymatic production of docosahexaenoic acid derivatives in marine diatoms. The differences observed in lipoxygenase pathways among the species investigated broadly reflected the relationships observed with phylogenetic markers, thus providing functional support to the taxonomic diversity of the individual species.

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Angelo Fontana

National Research Council

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Adele Cutignano

National Research Council

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Giovanna Romano

Stazione Zoologica Anton Dohrn

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Antonio Miralto

Stazione Zoologica Anton Dohrn

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Adrianna Ianora

Stazione Zoologica Anton Dohrn

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Carmela Gallo

National Research Council

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Angela Sardo

National Research Council

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Antonio Panico

University of Naples Federico II

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