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Dive into the research topics where Adriana M. Broussalis is active.

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Featured researches published by Adriana M. Broussalis.


Journal of Ethnopharmacology | 1999

Argentine plants as potential source of insecticidal compounds

Adriana M. Broussalis; Graciela Ferraro; Virginia S. Martino; Roberto Pinzón; Jorge D. Coussio; Jairo Calle Álvarez

CH2Cl2 and MeOH extracts of 15 Argentine plants used locally as insecticides, were evaluated for their insecticidal activity. Chenopodium multifidum L. (Chenopodiaceae); Flaveria bidentis (L.) O.K. (Compositae); Aristolochia argentina Gris. (Aristolochiaceae) and Tagetes erecta L. (Compositae) showed a significant activity against Sitophilus oryzae.


Phytochemistry | 2001

First cyclotide from Hybanthus (Violaceae)

Adriana M. Broussalis; Ulf Göransson; Jorge D. Coussio; Graciela Ferraro; Virginia S. Martino; Per Claeson

Hypa A, a novel macrocyclic polypeptide containing 30 amino acid residues, has been isolated from the n-butanol extract of the Argentine plant Hybanthus parviflorus. The sequence, cyclo-(SCVYIPCTITALLGCSCKNKVCYNGIPCAE), was determined by automated Edman degradation, quantitative amino acid analysis and nanospray MS/MS(2). Three intramolecular disulfide bridges stabilize the cyclic peptide backbone of hypa A. Using these structural features to classify the peptide as a cyclotide, we extended the distribution of that substance class to a new genus, and now propose a uniform nomenclature for cyclotides.


Analytical Biochemistry | 2003

Expression of Viola cyclotides by liquid chromatography-mass spectrometry and tandem mass spectrometry sequencing of intercysteine loops after introduction of charges and cleavage sites by aminoethylation

Ulf Göransson; Adriana M. Broussalis; Per Claeson

The expression of cyclotides-macrocyclic plant peptides-was profiled in six violets, Viola cotyledon, V. biflora, V. arvensis, V. tricolor, V. riviniana, and V. odorata, by LC-MS. All were found to express notably complex mixtures, with single species containing >50 cyclotides. To facilitate their sequencing by MS-MS, an analytical strategy is presented involving aminoethylation of cysteines. This overcomes a number of problems intimately associated with the cyclotide core structure-that is, their joined N and C termini, disulfide knot, and low or clustered content of positively charged amino acids and enzymatic cleavage sites. As a result, charges as well as cleavage sites are introduced at the most conserved part of their sequence, the cysteines. Combined with tryptic digestion, all intercysteine loops are then of suitable size and charge for MS-MS sequencing. The utility of this strategy is shown by the sequencing of two novel cyclotides isolated from V. cotyledon; vico A (cyclo-(AESCVYIPCFTGIAGCSCKNKVCYYNGSIPC)) and vico B (cyclo-(AESCVYIPCITGIAGCSCKNKVCYYNGSIPC)); their complete sequence could be determined by nanospray MS-MS. The strategy for converting conserved cysteines to enzymatic cleavage sites might also benefit the study of other peptides and proteins displaying similar structural problems for MS analysis.


Journal of Ethnopharmacology | 2002

In vitro antiplasmodial activity of extracts of Argentinian plants

S. Debenedetti; Liliana Muschietti; C. van Baren; M. Clavin; Adriana M. Broussalis; Virginia S. Martino; Peter J. Houghton; David C. Warhurst; Jonathan C. P. Steele

Fifteen extracts from nine selected Argentine medicinal plants were tested for their antiplasmodial activity in vitro by assessing their ability to inhibit the uptake of [3H]-hypoxanthine into the Plasmodium falciparum K1 pyrimethamine/chloroquine resistant strain. The methanol extract of Satureja parvifolia showed good antiplasmodial activity (IC(50) 3 microg/ml). Inhibition of the growth of P. falciparum was also observed with aqueous extracts of Buddleja globosa and S. parvifolia.


Journal of Thermal Analysis and Calorimetry | 2010

Thermal analysis of lipoic acid and evaluation of the compatibility with excipientes

María A. Moyano; Adriana M. Broussalis; Adriana Ines Segall


Crop Protection | 2010

Hybanthus parviflorus (Violaceae): insecticidal activity of a South American plant.

Adriana M. Broussalis; S. Clemente; Graciela Ferraro


Revista Latinoamericana de Química | 2000

1,8 cineol: responsible for the insecticide activity of lavandula spica Mill (lavender)

Romina Maga; Adriana M. Broussalis; Sandra V. Clemente; Graciela Mareggiani; Graciela Ferraro


Latin American and Caribbean Bulletin of Medicinal and Aromatic Plants | 2010

Estudio farmacobotánico de hojas, cortezas y leños de Simaroubaceae sensu lato de Argentina. Parte I. Alvaradoa subovata Cronquist, Picramnia parvifolia Engl., Picramnia sellowii Planch. y Castela coccinea Griseb

Adriana Cortadi; Luisina Andriolo; María N. Campagna; María Laura Martínez; Osvaldo Di Sapio; Adriana M. Broussalis; Martha Gattuso; Susana Gattuso


Latin American and Caribbean Bulletin of Medicinal and Aromatic Plants | 2011

Contribución al estudio de dos especies medicinales argentinas del género Hybanthus (Violaceae)

Jorge Miño; Anibal G. Amat; Graciela Ferraro; Adriana M. Broussalis


Archive | 2002

Peptide profiling by LC-MS and MS sequencing of intercysteine loops: Expression profiles of Viola cyclotides

Ulf Göransson; Adriana M. Broussalis; Per Claeson

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Graciela Ferraro

National Scientific and Technical Research Council

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Jorge D. Coussio

University of Buenos Aires

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Liliana Muschietti

National Scientific and Technical Research Council

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Anibal G. Amat

National University of Misiones

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C. van Baren

University of Buenos Aires

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