Ricardo Alves

Dr. Ricardo Alves

orcid

Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

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

Representative Publications

View All Publications
19 September 2017 in Microbial Cell Factories
Verified
Journal Article
Open access
PDF file
IMI. M. C. Morais
I. M. C. Morais
ACA. L. Cordeiro
A. L. Cordeiro
GTG. S. Teixeira
G. S. Teixeira
VDVitor Sousa Domingues
Vitor Sousa Domingues
RNR. M. D. Nardi
R. M. D. Nardi
VSVera Lúcia Santos
Vera Lúcia Santos
Lactobacillus species produce biosurfactants that can contribute to the bacteria’s ability to prevent microbial infections associated with urogenital and gastrointestinal tracts and the skin. Here, we described the biological and physicochemical properties of biosurfactants produced by Lactobacillus jensenii P6A and Lactobacillus gasseri P65. The biosurfactants produced by L. jensenii P6A and L. gasseri P65 reduced the water surface tension from 72 to 43.2 mN m−1 and 42.5 mN m−1 as their concentration increased up to the critical micelle concentration (CMC) values of 7.1 and 8.58 mg mL−1, respectively. Maximum emulsifying activity was obtained at concentrations of 1 and 5 mg mL−1 for the P6A and P65 strains, respectively. The Fourier transform infrared spectroscopy data revealed that the biomolecules consist of a mixture of carbohydrates, lipids and proteins. The gas chromatography-mass spectrum analysis of L. jensenii P6A biosurfactant showed a major peak for 14-methypentadecanoic acid, which was the main fatty acid present in the biomolecule; conversely, eicosanoic acid dominated the biosurfactant produced by L. gasseri P65. Although both biosurfactants contain different percentages of the sugars galactose, glucose and ribose; rhamnose was only detected in the biomolecule produced by L. jensenii P6A. Emulsifying activities were stable after a 60-min incubation at 100 °C, at pH 2–10, and after the addition of potassium chloride and sodium bicarbonate, but not in the presence of sodium chloride. The biomolecules showed antimicrobial activity against clinical isolates of Escherichia coli and Candida albicans, with MIC values of 16 µg mL−1, and against Staphylococcus saprophyticus, Enterobacter aerogenes and Klebsiella pneumoniae at 128 µg mL−1. The biosurfactants also disrupted preformed biofilms of microorganisms at varying concentrations, being more efficient against E. aerogenes (64%) (P6A biosurfactant), and E. coli (46.4%) and S. saprophyticus (39%) (P65 biosurfactant). Both strains of lactobacilli could also co-aggregate pathogens. This report presents the first characterization of biosurfactants produced by L. jensenii P6A and L. gasseri P65. The antimicrobial properties and stability of these biomolecules indicate their potential use as alternative antimicrobial agents in the medical field for applications against pathogens that are responsible for infections in the gastrointestinal and urogenital tracts and the skin.

16 May 2017 in Molecules
Verified
Journal Article
Open access
PDF file
ASAudrey R. S. T. Silva
Audrey R. S. T. Silva
RSRicardo Scher
Ricardo Scher
FSFlaviane V. Santos
Flaviane V. Santos
SFSebastião R. Ferreira
Sebastião R. Ferreira
SCSócrates C. H. Cavalcanti
Sócrates C. H. Cavalcanti
SDSilvio Dolabella
Silvio Dolabella
Several constituents of essential oils have been shown to be active against pathogens such as bacteria, fungi, and protozoa. This study demonstrated the in vitro action of ten compounds present in essential oils against Leishmania amazonensis promastigotes. With the exception of p-cymene, all evaluated compounds presented leishmanicidal activity, exhibiting IC50 between 25.4 and 568.1 μg mL−1. Compounds with the best leishmanicidal activity presented a phenolic moiety (IC50 between 25.4 and 82.9 μg mL−1). Alicyclic alcohols ((−)-menthol and isoborneol) and ketones ((−)-carvone) promoted similar activity against the parasite (IC50 between 190.2 and 198.9 μg mL−1). Most of the compounds showed low cytotoxicity in L929 fibroblasts. Analysis of the structure-activity relationship of these compounds showed the importance of the phenolic structure for the biological action against the promastigote forms of the parasite.

1 January 2020 in Bioorganic & Medicinal Chemistry Letters
Verified
Journal Article
Closed access
FOFlaviano M. Ottoni
Flaviano M. Ottoni
EGEliza R. Gomes
Eliza R. Gomes
RPRodrigo M. Pádua
Rodrigo M. Pádua
MOMônica C. Oliveira
Mônica C. Oliveira
Izabella Thaís SilvaIzabella Thaís Silva
Izabella Thaís Silva
RARicardo Alves
Ricardo Alves

1 May 2009 in Bioorganic & Medicinal Chemistry Letters
Verified
Journal Article
Closed access
ABAndre Luis Branco de Barros
Andre Luis Branco de Barros
VCValbert Nascimento Cardoso
Valbert Nascimento Cardoso
LMLuciene das Graças Mota
Luciene das Graças Mota
ELElaine Amaral Leite
Elaine Amaral Leite
BOBruno Oliveira
Bruno Oliveira
RARicardo Alves
Ricardo Alves

1 July 2017 in Nanomedicine: Nanotechnology, Biology and Medicine
Verified
Journal Article
Closed access
DFDiego dos Santos Ferreira
Diego dos Santos Ferreira
BOBruno Oliveira
Bruno Oliveira
VKVidhya Kumar
Vidhya Kumar
VCValbert Nascimento Cardoso
Valbert Nascimento Cardoso
SFSimone Odília Fernandes
Simone Odília Fernandes
PCPeter Caravan
Peter Caravan

1 September 2017 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
SASaulo Fernandes de Andrade
Saulo Fernandes de Andrade
BOBárbara G. Oliveira
Bárbara G. Oliveira
LPLarissa C. Pereira
Larissa C. Pereira
JRJonas P. Ramos
Jonas P. Ramos
AJAngélica R. Joaquim
Angélica R. Joaquim
RARicardo Alves
Ricardo Alves