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Dive into the research topics where Gerardo Della Sala is active.

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Featured researches published by Gerardo Della Sala.


Marine Drugs | 2015

Isolation and assessment of the in vitro anti-tumor activity of smenothiazole A and B, chlorinated thiazole-containing peptide/polyketides from the Caribbean sponge, Smenospongia aurea.

Germana Esposito; Roberta Teta; Roberta Miceli; Luca S. Ceccarelli; Gerardo Della Sala; Rosa Camerlingo; Elena Irollo; Alfonso Mangoni; Giuseppe Pirozzi; Valeria Costantino

The study of the secondary metabolites contained in the organic extract of Caribbean sponge Smenospongia aurea led to the isolation of smenothiazole A (3) and B (4), hybrid peptide/polyketide compounds. Assays performed using four solid tumor cell lines showed that smenothiazoles exert a potent cytotoxic activity at nanomolar levels, with selectivity over ovarian cancer cells and a pro-apoptotic mechanism.


Marine Drugs | 2013

Smenamides A and B, Chlorinated Peptide/Polyketide Hybrids Containing a Dolapyrrolidinone Unit from the Caribbean Sponge Smenospongia aurea. Evaluation of Their Role as Leads in Antitumor Drug Research

Roberta Teta; Elena Irollo; Gerardo Della Sala; Giuseppe Pirozzi; Alfonso Mangoni; Valeria Costantino

An in-depth study of the secondary metabolites contained in the Caribbean sponge Smenospongia aurea led to the isolation of smenamide A (1) and B (2), hybrid peptide/polyketide compounds containing a dolapyrrolidinone unit. Their structures were elucidated using high-resolution ESI-MS/MS and homo- and heteronuclear 2D NMR experiments. Structures of smenamides suggested that they are products of the cyanobacterial metabolism, and 16S rRNA metagenomic analysis detected Synechococcus spongiarum as the only cyanobacterium present in S. aurea. Smenamides showed potent cytotoxic activity at nanomolar levels on lung cancer Calu-1 cells, which for compound 1 is exerted through a clear pro-apoptotic mechanism. This makes smenamides promising leads for antitumor drug design.


Marine Drugs | 2014

Polyketide Synthases in the Microbiome of the Marine Sponge Plakortis halichondrioides: A Metagenomic Update

Gerardo Della Sala; Thomas Hochmuth; Roberta Teta; Valeria Costantino; Alfonso Mangoni

Sponge-associated microorganisms are able to assemble the complex machinery for the production of secondary metabolites such as polyketides, the most important class of marine natural products from a drug discovery perspective. A comprehensive overview of polyketide biosynthetic genes of the sponge Plakortis halichondrioides and its symbionts was obtained in the present study by massively parallel 454 pyrosequencing of complex and heterogeneous PCR (Polymerase Chain Reaction) products amplified from the metagenomic DNA of a specimen of P. halichondrioides collected in the Caribbean Sea. This was accompanied by a survey of the bacterial diversity within the sponge. In line with previous studies, sequences belonging to supA and swfA, two widespread sponge-specific groups of polyketide synthase (PKS) genes were dominant. While they have been previously reported as belonging to Poribacteria (a novel bacterial phylum found exclusively in sponges), re-examination of current genomic sequencing data showed supA and swfA not to be present in the poribacterial genome. Several non-supA, non-swfA type-I PKS fragments were also identified. A significant portion of these fragments resembled type-I PKSs from protists, suggesting that bacteria may not be the only source of polyketides from P. halichondrioides, and that protistan PKSs should receive further investigation as a source of novel polyketides.


Environmental Microbiology Reports | 2013

Polyketide genes in the marine sponge Plakortis simplex: a new group of mono-modular type I polyketide synthases from sponge symbionts.

Gerardo Della Sala; Thomas Hochmuth; Valeria Costantino; Roberta Teta; William H. Gerwick; Lena Gerwick; Jörn Piel; Alfonso Mangoni

Summary Sponge symbionts are a largely unexplored source of new and unusual metabolic pathways. Insights into the distribution and function of metabolic genes of sponge symbionts are crucial to dissect and exploit their biotechnological potential. Screening of the metagenome of the marine sponge Plakortis simplex led to the discovery of the swf family, a new group of mono-modular type I polyketide synthase/fatty acid synthase (PKS/FAS) specifically associated with sponge symbionts. Two different examples of the swf cluster were present in the metagenome of P. simplex. A third example of the cluster is present in the previously sequenced genome of a poribacterium from the sponge Aplysina aerophoba but was formerly considered orthologous to the wcb/rkp cluster. The swf cluster was also found in six additional species of sponges. Therefore, the swf cluster represents the second group of mono-modular PKS, after the supA family, to be widespread in marine sponges. The putative swf operon consists of swfA (type I PKS/FAS), swfB (reductase and sulphotransferase domains) and swfC (radical S-adenosylmethionine, or radical SAM). Activation of the acyl carrier protein (ACP) domain of the SwfA protein to its holo-form by co-expression with Svp is the first functional proof of swf type genes in marine sponges. However, the precise biosynthetic role of the swf clusters remains unknown.


Environmental Science & Technology | 2015

Combined LC-MS/MS and Molecular Networking Approach Reveals New Cyanotoxins from the 2014 Cyanobacterial Bloom in Green Lake, Seattle.

Roberta Teta; Gerardo Della Sala; Evgenia Glukhov; Lena Gerwick; William H. Gerwick; Alfonso Mangoni; Valeria Costantino

Cyanotoxins obtained from a freshwater cyanobacterial collection at Green Lake, Seattle during a cyanobacterial harmful algal bloom in the summer of 2014 were studied using a new approach based on molecular networking analysis of liquid chromatography tandem mass spectrometry (LC-MS/MS) data. This MS networking approach is particularly well-suited for the detection of new cyanotoxin variants and resulted in the discovery of three new cyclic peptides, namely microcystin-MhtyR (6), which comprised about half of the total microcystin content in the bloom, and ferintoic acids C (12) and D (13). Structure elucidation of 6 was aided by a new microscale methylation procedure. Metagenomic analysis of the bloom using the 16S-ITS rRNA region identified Microcystis aeruginosa as the predominant cyanobacterium in the sample. Fragments of the putative biosynthetic genes for the new cyanotoxins were also identified, and their sequences correlated to the structure of the isolated cyanotoxins.


Marine Drugs | 2017

Plakofuranolactone as a Quorum Quenching Agent from the Indonesian Sponge Plakortis cf. lita

Valeria Costantino; Gerardo Della Sala; Kumar Saurav; Roberta Teta; Rinat Bar-Shalom; Alfonso Mangoni; Laura Steindler

There is an urgent need for novel strategies to fight drug resistance and multi-drug resistance. As an alternative to the classic antibiotic therapy, attenuation of the bacteria virulence affecting their Quorum sensing (QS) system is a promising approach. Quorum sensing (QS) is a genetic regulation system that allows bacteria to communicate with each other and coordinate group behaviors. A new γ-lactone that is capable of inhibiting the LasI/R QS system, plakofuranolactone (1), was discovered in the extract of the marine sponge Plakortis cf. lita, and its structure, including absolute configuration, was determined by NMR spectroscopy, MS spectrometry, and quantum-mechanical prediction of optical rotation. The quorum quenching activity of plakofuranolactone was evaluated using reporter gene assays for long- and short-chain signals (E. coli pSB1075, E. coli pSB401, and C. violeaceum CV026) and was confirmed by measuring the total protease activity (a virulence factor which is under control of the LasI/R system) of the wild-type P. aeruginosa PAO1. Further research will be pursued to assess the potential of plakofuranolactone as a new antivirulence lead compound and a chemical tool to increase the knowledge in this field.


Marine Drugs | 2012

Chalinulasterol, a Chlorinated Steroid Disulfate from the Caribbean Sponge Chalinula molitba. Evaluation of Its Role as PXR Receptor Modulator

Roberta Teta; Gerardo Della Sala; Barbara Renga; Alfonso Mangoni; Stefano Fiorucci; Valeria Costantino

Chalinulasterol (1) a new chlorinated sterol disulfate was isolated from the Caribbean sponge Chalinula molitba. Its structure was elucidated using mass spectrometry and NMR experiments. The possible role of chalinulasterol as modulator of the PXR nuclear receptor was investigated but, in spite of the close structural relationship with the PXR agonist solomonsterol A (2), it showed no activity. The structural requirements for the PXR nuclear receptor activity were discussed.


Marine Drugs | 2017

Cytotoxicity of Endoperoxides from the Caribbean Sponge Plakortis halichondrioides towards Sensitive and Multidrug-Resistant Leukemia Cells: Acids vs. Esters Activity Evaluation

Tanja Schirmeister; Swarna Oli; Hongmei Wu; Gerardo Della Sala; Valeria Costantino; Ean-Jeong Seo; Thomas Efferth

The 6-epimer of the plakortide H acid (1), along with the endoperoxides plakortide E (2), plakortin (3), and dihydroplakortin (4) have been isolated from a sample of the Caribbean sponge Plakortis halichondrioides. To perform a comparative study on the cytotoxicity towards the drug-sensitive leukemia CCRF-CEM cell line and its multi-drug resistant subline CEM/ADR5000, the acid of plakortin, namely plakortic acid (5), as well as the esters plakortide E methyl ester (6) and 6-epi-plakortide H (7) were synthesized by hydrolysis and Steglich esterification, respectively. The data obtained showed that the acids (1, 2, 5) exhibited potent cytotoxicity towards both cell lines, whereas the esters showed no activity (6, 7) or weaker activity (3, 4) compared to their corresponding acids. Plakortic acid (5) was the most promising derivative with half maximal inhibitory concentration (IC50) values of ca. 0.20 µM for both cell lines.


International Journal of Sustainable Development and Planning | 2016

Tracing Cyanobacterial Blooms To Assess The Impact Of Wastewaters Discharges On Coastal Areas And Lakes

Roberta Teta; Gerardo Della Sala; Alfonso Mangoni; Massimiliano Lega; Valeria Costantino

The rapid detection of cyanobacterial blooms has become an emerging and urgent need during the last years due to the increasing number of cyanobacterial harmful blooms (CHABs) all over the world. The main responsibility of this phenomenon is attributable to the nutrient enrichment, resulting from eutrophication processes of anthropogenic origin. The blooms deplete oxygen in surface waters through excessive bacterial respiration and decomposition and often release toxic substances (cyanotoxins) causing fish mortality and risks for public health. We have initiated a worldwide program for the early detection of cyanobacterial blooms using combined techniques based on chemical/biochemical analyses of samples collected on specific sites identified with remote/proximal sensing tools. Here we report our results obtained from the analysis of cyanobacterial blooms using a new powerful approach based on the combined use of LCMS/MS (Liquid Chromatography Tandem Mass Spectrometry) and Molecular Networking to detect the presence of known and novel cyanotoxins. In addition, we report the most recent results from our case studies on specific coastal areas and lakes, where the presence of cyanobacteria was confirmed to be related to the excess nutrient input of anthropogenic origin, resulting from wastewater discharges or runoff from fertilisers and manure spread on agricultural areas. The monitoring of bloom occurrence, composition, frequency and chemistry can provide important indicators of degraded water quality, supporting the Government Bodies in the evaluation of effectiveness of wastewater plans that insist on a specific coastal area.


Natural Product Reports | 2018

Challenges in the configuration assignment of natural products. A case-selective perspective

Marialuisa Menna; Concetta Imperatore; Alfonso Mangoni; Gerardo Della Sala; Orazio Taglialatela-Scafati

Covering: up to 2018 Even today, when planar structures of natural products can be determined with microgram samples, the configurational assignment continues to be a challenge. The relative and absolute configurations of natural products can be assigned by devising original approaches, relying on carefully acquired data on a case-by-case basis. In this review, the most widely available methods and techniques for the absolute configuration determination of novel natural products are concisely discussed. Selected illustrative examples (case studies) are presented, where original approaches integrating different chemical, spectroscopic, and/or computational methods have been devised to solve intriguing stereochemistry issues of natural small molecules.

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Valeria Costantino

University of Naples Federico II

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Alfonso Mangoni

University of Naples Federico II

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Roberta Teta

University of Naples Federico II

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Germana Esposito

University of Naples Federico II

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Giuseppe Pirozzi

Seconda Università degli Studi di Napoli

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Massimiliano Lega

University of Naples Federico II

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Joseph R. Pawlik

University of North Carolina at Wilmington

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Lena Gerwick

University of California

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