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Catálogo Taxonômico da Fauna do Brasil: Setting the baseline knowledge on the animal diversity in Brazil Brasil
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Boeger, Walter A.
; Valim, Michel P.
; Zaher, Hussam
; Rafael, José A.
; Forzza, Rafaela C.
; Percequillo, Alexandre R.
; Serejo, Cristiana S.
; Garraffoni, André R.S.
; Santos, Adalberto J.
; Slipinski, Adam
; Linzmeier, Adelita M.
; Calor, Adolfo R.
; Garda, Adrian A.
; Kury, Adriano B.
; Fernandes, Agatha C.S.
; Agudo-Padrón, Aisur I.
; Akama, Alberto
; Silva Neto, Alberto M. da
; Burbano, Alejandro L.
; Menezes, Aleksandra
; Pereira-Colavite, Alessandre
; Anichtchenko, Alexander
; Lees, Alexander C.
; Bezerra, Alexandra M.R.
; Domahovski, Alexandre C.
; Pimenta, Alexandre D.
; Aleixo, Alexandre L.P.
; Marceniuk, Alexandre P.
; Paula, Alexandre S. de
; Somavilla, Alexandre
; Specht, Alexandre
; Camargo, Alexssandro
; Newton, Alfred F.
; Silva, Aline A.S. da
; Santos, Aline B. dos
; Tassi, Aline D.
; Aragão, Allan C.
; Santos, Allan P.M.
; Migotto, Alvaro E.
; Mendes, Amanda C.
; Cunha, Amanda
; Chagas Júnior, Amazonas
; Sousa, Ana A.T. de
; Pavan, Ana C.
; Almeida, Ana C.S.
; Peronti, Ana L.B.G.
; Henriques-Oliveira, Ana L.
; Prudente, Ana L.
; Tourinho, Ana L.
; Pes, Ana M.O.
; Carmignotto, Ana P.
; Wengrat, Ana P.G. da Silva
; Dornellas, Ana P.S.
; Molin, Anamaria Dal
; Puker, Anderson
; Morandini, André C.
; Ferreira, André da S.
; Martins, André L.
; Esteves, André M.
; Fernandes, André S.
; Roza, André S.
; Köhler, Andreas
; Paladini, Andressa
; Andrade, Andrey J. de
; Pinto, Ângelo P.
; Salles, Anna C. de A.
; Gondim, Anne I.
; Amaral, Antonia C.Z.
; Rondón, Antonio A.A.
; Brescovit, Antonio
; Lofego, Antônio C.
; Marques, Antonio C.
; Macedo, Antonio
; Andriolo, Artur
; Henriques, Augusto L.
; Ferreira Júnior, Augusto L.
; Lima, Aurino F. de
; Barros, Ávyla R. de A.
; Brito, Ayrton do R.
; Romera, Bárbara L.V.
; Vasconcelos, Beatriz M.C. de
; Frable, Benjamin W.
; Santos, Bernardo F.
; Ferraz, Bernardo R.
; Rosa, Brunno B.
; Sampaio, Brunno H.L.
; Bellini, Bruno C.
; Clarkson, Bruno
; Oliveira, Bruno G. de
; Corrêa, Caio C.D.
; Martins, Caleb C.
; Castro-Guedes, Camila F. de
; Souto, Camilla
; Bicho, Carla de L.
; Cunha, Carlo M.
; Barboza, Carlos A. de M.
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; Barreto, Carlos
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; Agne, Carlos E.Q.
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; Lamas, Carlos J.E.
; Rocha, Carlos
; Mascarenhas, Carolina S.
; Margaría, Cecilia B.
; Waichert, Cecilia
; Digiani, Celina
; Haddad, Célio F.B.
; Azevedo, Celso O.
; Benetti, Cesar J.
; Santos, Charles M.D. dos
; Bartlett, Charles R.
; Bonvicino, Cibele
; Ribeiro-Costa, Cibele S.
; Santos, Cinthya S.G.
; Justino, Cíntia E.L.
; Canedo, Clarissa
; Bonecker, Claudia C.
; Santos, Cláudia P.
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; Gonçalves, Clayton C.
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; Schwertner, Cristiano F.
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; Dias, Cristina de O.
; Lucena, Daercio A. de A.
; Manfio, Daiara
; Amorim, Dalton de S.
; Queiroz, Dalva L. de
; Queiroz, Dalva L. de
; Colpani, Daniara
; Abbate, Daniel
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; Takiya, Daniela M.
; Fernandes, Daniell R.R.
; Ament, Danilo C.
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; Silva, Darliane E.
; Pollock, Darren A.
; Muniz, David B.
; Gibson, David I.
; Nogueira, David S.
; Marques, Dayse W.A.
; Lucatelli, Débora
; Garcia, Deivys M.A.
; Baêta, Délio
; Ferreira, Denise N.M.
; Rueda-Ramírez, Diana
; Fachin, Diego A.
; Souza, Diego de S.
; Rodrigues, Diego F.
; Pádua, Diego G. de
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; Amaral, Diogo C.
; Chandler, Donald S.
; Maccagnan, Douglas H.B.
; Caron, Edilson
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; Shimbori, Eduardo M.
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; Lima, Élison F.B.
; Castro, Elizeu B. de
; Orlandin, Elton
; Nascimento, Elynton A. do
; Razzolini, Emanuel
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; Araujo, Enilma M. de
; Nishiyama, Eric Y.
; Spiessberger, Erich L.
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; Schunck, Fabio
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; Machado, Fabrizio M.
; Barbo, Fausto E.
; Agrain, Federico A.
; Ribeiro, Felipe B.
; Moreira, Felipe F.F.
; Barbosa, Felipe F.
; Silva, Fenanda S.
; Cavalcanti, Fernanda F.
; Straube, Fernando C.
; Carbayo, Fernando
; Carvalho Filho, Fernando
; Zanella, Fernando C.V.
; Jacinavicius, Fernando de C.
; Farache, Fernando H.A.
; Leivas, Fernando
; Dias, Fernando M.S.
; Mantellato, Fernando
; Vaz-de-Mello, Fernando Z.
; Gudin, Filipe M.
; Albuquerque, Flávio
; Molina, Flavio B.
; Passos, Flávio D.
; Shockley, Floyd W.
; Pinheiro, Francielly F.
; Mello, Francisco de A.G. de
; Nascimento, Francisco E. de L.
; Franco, Francisco L.
; Oliveira, Francisco L. de
; Melo, Francisco T. de V.
; Quijano, Freddy R.B.
; Salles, Frederico F.
; Biffi, Gabriel
; Queiroz, Gabriel C.
; Bizarro, Gabriel L.
; Hrycyna, Gabriela
; Leviski, Gabriela
; Powell, Gareth S.
; Santos, Geane B. dos
; Morse, Geoffrey E.
; Brown, George
; Mattox, George M.T.
; Zimbrão, Geraldo
; Carvalho, Gervásio S.
; Miranda, Gil F.G.
; Moraes, Gilberto J. de
; Lourido, Gilcélia M.
; Neves, Gilmar P.
; Moreira, Gilson R.P.
; Montingelli, Giovanna G.
; Maurício, Giovanni N.
; Marconato, Gláucia
; Lopez, Guilherme E.L.
; Silva, Guilherme L. da
; Muricy, Guilherme
; Brito, Guilherme R.R.
; Garbino, Guilherme S.T.
; Flores, Gustavo E.
; Graciolli, Gustavo
; Libardi, Gustavo S.
; Proctor, Heather C.
; Gil-Santana, Helcio R.
; Varella, Henrique R.
; Escalona, Hermes E.
; Schmitz, Hermes J.
; Rodrigues, Higor D.D.
; Galvão Filho, Hilton de C.
; Quintino, Hingrid Y.S.
; Pinto, Hudson A.
; Rainho, Hugo L.
; Miyahira, Igor C.
; Gonçalves, Igor de S.
; Martins, Inês X.
; Cardoso, Irene A.
; Oliveira, Ismael B. de
; Franz, Ismael
; Fernandes, Itanna O.
; Golfetti, Ivan F.
; S. Campos-Filho, Ivanklin
; Oliveira, Ivo de S.
; Delabie, Jacques H.C.
; Oliveira, Jader de
; Prando, Jadila S.
; Patton, James L.
; Bitencourt, Jamille de A.
; Silva, Janaina M.
; Santos, Jandir C.
; Arruda, Janine O.
; Valderrama, Jefferson S.
; Dalapicolla, Jeronymo
; Oliveira, Jéssica P.
; Hájek, Jiri
; Morselli, João P.
; Narita, João P.
; Martin, João P.I.
; Grazia, Jocélia
; McHugh, Joe
; Cherem, Jorge J.
; Farias Júnior, José A.S.
; Fernandes, Jose A.M.
; Pacheco, José F.
; Birindelli, José L.O.
; Rezende, José M.
; Avendaño, Jose M.
; Duarte, José M. Barbanti
; Ribeiro, José R. Inácio
; Mermudes, José R.M.
; Pujol-Luz, José R.
; Santos, Josenilson R. dos
; Câmara, Josenir T.
; Teixeira, Joyce A.
; Prado, Joyce R. do
; Botero, Juan P.
; Almeida, Julia C.
; Kohler, Julia
; Gonçalves, Julia P.
; Beneti, Julia S.
; Donahue, Julian P.
; Alvim, Juliana
; Almeida, Juliana C.
; Segadilha, Juliana L.
; Wingert, Juliana M.
; Barbosa, Julianna F.
; Ferrer, Juliano
; Santos, Juliano F. dos
; Kuabara, Kamila M.D.
; Nascimento, Karine B.
; Schoeninger, Karine
; Campião, Karla M.
; Soares, Karla
; Zilch, Kássia
; Barão, Kim R.
; Teixeira, Larissa
; Sousa, Laura D. do N.M. de
; Dumas, Leandro L.
; Vieira, Leandro M.
; Azevedo, Leonardo H.G.
; Carvalho, Leonardo S.
; Souza, Leonardo S. de
; Rocha, Leonardo S.G.
; Bernardi, Leopoldo F.O.
; Vieira, Letícia M.
; Johann, Liana
; Salvatierra, Lidianne
; Oliveira, Livia de M.
; Loureiro, Lourdes M.A. El-moor
; Barreto, Luana B.
; Barros, Luana M.
; Lecci, Lucas
; Camargos, Lucas M. de
; Lima, Lucas R.C.
; Almeida, Lucia M.
; Martins, Luciana R.
; Marinoni, Luciane
; Moura, Luciano de A.
; Lima, Luciano
; Naka, Luciano N.
; Miranda, Lucília S.
; Salik, Lucy M.
; Bezerra, Luis E.A.
; Silveira, Luis F.
; Campos, Luiz A.
; Castro, Luiz A.S. de
; Pinho, Luiz C.
; Silveira, Luiz F.L.
; Iniesta, Luiz F.M.
; Tencatt, Luiz F.C.
; Simone, Luiz R.L.
; Malabarba, Luiz R.
; Cruz, Luiza S. da
; Sekerka, Lukas
; Barros, Lurdiana D.
; Santos, Luziany Q.
; Skoracki, Maciej
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; Andrade, Manuella F.G.
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; Alvarenga, Thiago M.
; Carvalho, Thiago R. de
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; McElrath, Thomas C.
; Henry, Thomas
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; Sandoval-Gómez, Vivian E.
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; Mathis, Wayne N.
; Souza, Wesley de O.
; Colombo, Wesley D.
; Tomaszewska, Wioletta
; Wosiacki, Wolmar B.
; Ovando, Ximena M.C.
; Leite, Yuri L.R.
.
ABSTRACT The limited temporal completeness and taxonomic accuracy of species lists, made available in a traditional manner in scientific publications, has always represented a problem. These lists are invariably limited to a few taxonomic groups and do not represent up-to-date knowledge of all species and classifications. In this context, the Brazilian megadiverse fauna is no exception, and the Catálogo Taxonômico da Fauna do Brasil (CTFB) (http://fauna.jbrj.gov.br/), made public in 2015, represents a database on biodiversity anchored on a list of valid and expertly recognized scientific names of animals in Brazil. The CTFB is updated in near real time by a team of more than 800 specialists. By January 1, 2024, the CTFB compiled 133,691 nominal species, with 125,138 that were considered valid. Most of the valid species were arthropods (82.3%, with more than 102,000 species) and chordates (7.69%, with over 11,000 species). These taxa were followed by a cluster composed of Mollusca (3,567 species), Platyhelminthes (2,292 species), Annelida (1,833 species), and Nematoda (1,447 species). All remaining groups had less than 1,000 species reported in Brazil, with Cnidaria (831 species), Porifera (628 species), Rotifera (606 species), and Bryozoa (520 species) representing those with more than 500 species. Analysis of the CTFB database can facilitate and direct efforts towards the discovery of new species in Brazil, but it is also fundamental in providing the best available list of valid nominal species to users, including those in science, health, conservation efforts, and any initiative involving animals. The importance of the CTFB is evidenced by the elevated number of citations in the scientific literature in diverse areas of biology, law, anthropology, education, forensic science, and veterinary science, among others. publications problem uptodate up date classifications context exception (CTFB http//fauna.jbrj.gov.br/, httpfaunajbrjgovbr http //fauna.jbrj.gov.br/ , jbrj gov br (http://fauna.jbrj.gov.br/) 2015 Brazil 80 specialists 1 2024 133691 133 691 133,69 125138 125 138 125,13 82.3%, 823 82 3 (82.3% 102000 102 000 102,00 7.69%, 769 7 69 (7.69% 11000 11 11,00 . 3,567 3567 567 (3,56 2,292 2292 2 292 (2,29 1,833 1833 833 (1,83 1,447 1447 447 (1,44 1000 1,00 831 (83 628 (62 606 (60 520 (52 50 users science health biology law anthropology education others http//fauna.jbrj.gov.br/ faunajbrjgovbr //fauna.jbrj.gov.br (http://fauna.jbrj.gov.br/ 201 8 202 13369 13 133,6 12513 12 125,1 82.3% (82.3 10200 10 00 102,0 7.69% 76 6 (7.69 1100 11,0 3,56 356 56 (3,5 2,29 229 29 (2,2 1,83 183 83 (1,8 1,44 144 44 (1,4 100 1,0 (8 62 (6 60 52 (5 5 http//fauna.jbrj.gov.br (http://fauna.jbrj.gov.br 20 1336 133, 1251 125, 82.3 (82. 1020 0 102, 7.69 (7.6 110 11, 3,5 35 (3, 2,2 22 (2, 1,8 18 (1, 1,4 14 4 ( 82. (82 7.6 (7. 3, (3 2, (2 (1 7. (7
2.
Dereplication of Sclerotiorin-Like Azaphilones Produced by Penicillium meliponae Using LC-MS/MS Analysis and Molecular Networking SclerotiorinLike Sclerotiorin Like LCMS/MS LCMSMS LC MS/MS MS LCMS MSMS
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Peres, Eldrinei G.
; Souza, Mayane P.
; Sousa, Thiago F.
; Silva, Carlos V. A. da
; Barros, André L.
; Silva, Felipe M. A. da
; Costa, Emmanoel V.
; Medeiros, Lívia S. de
; Forim, Moacir R.
; Souza, Afonso D. L. de
; Paz, Weider H. P.
; Silva, Gilvan F. da
; Souza, Antonia Q. L. de
; Koolen, Hector H. F.
.
Journal of the Brazilian Chemical Society
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Penicillium meliponae, a recently described and rare species, was isolated as an endophytic fungus from the Amazonian plant Duguetia sthelechantha, and has been proven to be a pigment producer. Considering the high productivity of this species and the lack of data on its chemical composition, the present study aimed to characterize the chemical profile of P. meliponae and evaluate the influence of agitation and the use of different culture media. For this purpose, liquid chromatography coupled with mass spectrometry (LC-MS/MS) and molecular networking were used, allowing the identification of 17 azaphilone molecules with sclerotiorin-like skeletons, becoming the first chemical report of this species. In addition, the different production patterns in the tested culture media were indicative that this species is sensitive to changes in the composition of the carbon source and to the presence of agitation. Furthermore, this work contributes to the fragmentation mechanisms of the different possible structural arrangements for azaphilones of the sclerotiorin type and serves as a repository of information on the gas-phase behavior of this type of metabolite in mass spectrometry experiments and will assist future studies aimed at the discovery of azaphilones. sthelechantha producer P purpose LCMS/MS LCMSMS LC MS/MS MS (LC-MS/MS used 1 sclerotiorinlike like skeletons addition Furthermore gasphase gas phase LCMS MSMS
3.
Screening of Alkaloid-Producing Endophytic Penicillium Strains from Amazon Medicinal Plants by Electrospray Ionization Mass Spectrometry (ESI-MS) and Principal Component Analysis (PCA)
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Silva-Filho, Francinaldo A. da
; Souza, Marjory M. M. de
; Rezende, Gabriel O.
; Silva, Felipe M. A. da
; Cruz, Jeferson C. da
; Silva, Gilvan F. da
; Souza, Afonso D. L. de
; Souza, Antonia Q. L. de
.
Journal of the Brazilian Chemical Society
- Journal Metrics
The genus Penicillium is among the most promising alkaloid-producing fungal and therefore plays an important role in terms of producing molecules with biotechnological potential. Thus, in order to identify alkaloid-producing fungi, 25 endophytic Penicillium strains previously isolated from Amazon medicinal plants were subject to an integrative approach based on direct infusion positive electrospray ionization mass spectrometry (ESI-MS) and principal component analysis (PCA). The multivariate analysis pointed paxiline (1), glandicoline B (2), roquefortine C (3), and oxaline (5) as responsible for the segregation of three promising alkaloid-producing groups, been these groups constituted for P. chrysogenum, P. oxalicum, P. paxilli, and P. rubens strains. These alkaloids and the glandicoline A (4) were tentatively identified by multiple-stage mass spectrometry. In addition, compounds 1 and 2 were isolated and confirmed by using 1D and 2D nuclear magnetic resonance (NMR) spectroscopy. Overall, the chemical profile analysis by ESI-MS along with PCA provided a simple and effective approach to screening alkaloid-producing Penicillium strains for biotechnological applications.
https://doi.org/10.21577/0103-5053.20210074
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4.
Antifungal Polyketides and Other Compounds from Amazonian Endophytic Talaromyces Fungi
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Silva, Paulo H. F. da
; Souza, Mayane P. de
; Bianco, Eliana A.
; Silva, Sarah R. S. da
; Soares, Liviane N.
; Costa, Emmanoel V.
; Silva, Felipe M. A. da
; Barison, Andersson
; Forim, Moacir R.
; Cass, Quezia B.
; Souza, Afonso D. L. de
; Koolen, Hector H. F.
; Souza, Antonia Q. L. de
.
The continuous search for biologically active compound candidates pushes the pursuit of new substances produced by diverse organisms. Endophytic fungi are known as a promising source of metabolites with several biological activities. Based on the rich Amazonian biodiversity and the chemical potential of microbial sources, three Talaromyces strains, all major endophytes from their respective host plants, were studied aiming at the isolation of biologically active secondary metabolites. Through classical chromatographic approaches, 13 compounds were isolated from the antimicrobial extracts of the studied strains. From these, polyketides, steroids, anhydrides, and phenolic compounds were identified. Among them, two previously undescribed compounds were elucidated based on spectroscopic and spectrometric methods, a homodimer chromanone and a maleic anhydride methyl ester. The antimicrobial activity against a panel of pathogenic microorganisms from extracts, fractions, and isolated compounds was evaluated.
https://doi.org/10.21577/0103-5053.20170176
905 downloads
5.
Talaroxanthone, a novel xanthone dimer from the endophytic fungus Talaromyces sp. associated with Duguetia stelechantha (Diels) R. E. Fries
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Koolen, Hector H. F.
; Menezes, Laís S.
; Souza, Mayane P.
; Silva, Felipe M. A.
; Almeida, Fabiana G. O.
; Souza, Antonia Q. L. de
; Nepel, Angelita
; Barison, Andersson
; Silva, Flávio Henrique da
; Evangelista, Danilo Elton
; Souza, Afonso D. L. de
.
DgCr22.1b, um isolado endofítico de Talaromyces sp., foi coletado na Floresta Amazônica a partir da planta medicinal Duguetia stelechantha. Do fracionamento do extrato metanólico de sua massa micelial, foi isolada uma nova xantona dimérica talaroxantona. A estrutura deste novo composto foi elucidada com base em análises espectroscópicas incluindo experimentos de ressonância magnética nuclear (RMN) 2D.
DgCr22.1b, an endophytic isolate of Talaromyces sp., was collected in the Amazonian Rainforest from the medicinal plant Duguetia stelechantha. From the fractionation of the methanolic mycelial extract, a new xanthone dimer talaroxanthone was isolated. The structure of this new compound was elucidated based on spectroscopic analyses including 2D nuclear magnetic resonance (NMR) experiments.
https://doi.org/10.5935/0103-5053.20130104
1736 downloads
6.
Extraction and evaluation of fatty acid compositon of Orbignyaphalerata martius oils (arecaceae) from Maranhão State, Brazil
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Santos, Débora S.
; Silva, Ilna G. da
; Araújo, Bruno Q.
; Lopes Júnior, Cícero A.
; Monção, Nayana B. N.
; Citó, Antônia M. das G. L.
; Souza, Mércia H. S. L. de
; Nascimento, Maria do D. S. B.
; Costa, Maria Célia Pires
.
A composição de ácidos graxos de seis amostras de Orbignya phalerata de diferentes cidades do estado do Maranhão foi estudada. Os óleos foram extraídos utilizando extrator Soxhlet por duas metodologias e a composição de ácidos graxos foi avaliada por cromatografia gasosa-espectrometria de massas (CG-EM). O teor da fração de lipídios revelou que o solvente usado influencia na extração, sendo a maior porcentagem obtida com hexano. O teor de lipídios variou de 62,46-67,45%, com predominância de ácidos graxos saturados (80,32-87,80%), principalmente ácido láurico (C12:0) com percentual de 44,86-52,15%. A análise multivariada mostrou a distribuição das amostras de O. phalerata em três regiões distintas e sugere que a composição química dos óleos pode estar associada com a sua localização geográfica. Estes dados mostram o conhecimento da biodiversidade de ácidos graxos de O. phalerata entre as diferentes regiões do estado do Maranhão.
The fatty acid composition of six Orbignya phalerata samples of different cities from Maranhão State (Brazil) was studied. The oils were extracted by two methods using Soxhlet extractor and the fatty acid composition was evaluated by gas chromatography-mass spectrometry (GC-MS) analysis. The lipid fraction content showed that the solvent used influences lipid extraction, the highest percent was obtained with hexane. Lipid content ranged from 62.46-67.45%, with predominance of saturated fatty acids (80.32-87.80%), mainly lauric acid (C12:0) with 44.86 to 52.15%. Multivariate analysis showed the distribution of O. phalerata samples into three distinct regions and suggests that the oil chemical composition may be associated with their geographic location. These data show knowledge of the biodiversity of O. phalerata fatty acids among the different regions of the Maranhão State (Brazil).
https://doi.org/10.5935/0103-5053.20130045
3942 downloads
7.
Triterpenes and flavonoids from the roots of Mauritia flexuosa
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Koolen, Hector H. F.
; Soares, Elzalina R.
; Silva, Felipe M. A. da
; Souza, Antonia Q. L. de
; Rodrigues Filho, Edson
; Souza, Afonso D. L. de
.
Mauritia flexuosa L. f., Arecaceae, is an endemic species of South America. This species was studied with the intent to isolate the constituents of its roots. After the fractionation of the n-hexane and methanolic extracts from the roots of M. flexuosa, six triterpenes were obtained: friedelin, taraxerone, lupenyl acetate, lupenone, betulin and betulinic acid, along with three flavonoids: rutin, quercitrin and quercetin. All the compounds were identified by analysis of NMR and MS data and comparison with the literature. All those compounds are been reported for the first time in Mauritia, and the chemosystematic significance of the flavonoids isolated in this genus is discussed.
19684 downloads
8.
A new guaiane mannoside from a Eutypa-like fungus isolated from Murraya paniculata in Brazil
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Souza, Afonso D. L.
; Rodrigues-Filho, Edson
; Souza, Antonia Q. L.
; Henrique-Silva, Flavio
; Pereira, José O.
.
Um fungo semelhante aos do gênero Eutypa foi isolado da madeira do caule de Murraya paniculata. Cultivado em meio líquido, o fungo produziu o novo sesquiterpeno do tipo guaiano (1R,4S,5S,7R,10R)-10-hidroxiguaianol-10-O-β-manopiranosídeo e um diastereômero da harzialactona A, a 3-hidróxi-5-fenilmetil-(3S,5R)-tetraidrofuran-2-ona, obtida pela primeira vez como produto natural. As estruturas desses metabólitos foram elucidadas com base na análise dos seus respectivos dados espectroscópicos.
A Eutypa-like fungus was isolated from the stems of Murraya paniculata. The fungus was cultivated in liquid medium and produced the new guaiane-type sesquiterpenoid (1R,4S,5S,7R,10R)-10-hydroxyguaianol 10-O-β-mannopyranoside and the 3-hydroxy-5-phenylmethyl-(3S,5R)-tetrahydrofuran-2-one, a diastereomer of harzialactone A, obtained for the first time from a natural source. The structures of these metabolites were elucidated based on analysis of their spectroscopic data.
1883 downloads
9.
Eficiência de produtos vegetais no controle da lagarta-do-cartucho-do-milho Spodoptera frugiperda (J.E.Smith, 1797) (Lepidoptera: Noctuidae)
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O presente trabalho teve por objetivo avaliar a eficiência de produtos vegetais no controle de Spodoptera frugiperda (J.E.Smith, 1797) na cultura do milho. Os experimentos foram instalados, nos anos de 2002 e 2004, com a pulverização dos produtos vegetais em cinco tratamentos, e quatro repetições. No ano de 2002, os produtos testados foram: Azadirachta indica A. Juss. (extrato aquoso 2%), e óleo a 1%; Melia azedarach L. (extrato aquoso 2%); Quassia amara L. (extrato aquoso 2%); óleo de nim, Azadirachta indica 1 e 2%. No ano de 2004, os produtos testados foram: A. indica (extrato aquoso 5%), e óleo a 2%, M. azedarach (extrato aquoso 5%), Trichilia pallida Sw. (extrato aquoso 5%). As avaliações, porcentagem de infestação da lagarta-do-cartucho por parcela, foram efetuadas aos três, sete e dez dias após a pulverização dos extratos. Conclui-se que extratos aquosos das plantas A. indica 2%, T.pallida 5%, Q. amara 2% e M. azedarach 2% e 5% e óleo de A. indica 1% e 2% com adição de tenso ativo não iônico, não possuem eficiência necessária como único método de controle da largarta-do-cartucho S. frugiperda em condições de campo. Os produtos começam a afetar o desenvolvimento da lagarta após alguns dias da ingestão das folhas pulverizadas, observado na avaliação efetuada aos sete dias após a aplicação dos extratos.
The objective of this work was to study the efficiency of vegetable pesticides in the control of Spodoptera frugiperda (J.E.Smith, 1797) in corn culture. The experiments were installed, in the years of 2002 and 2004, with the spraying of the vegetable products in five treatments, and four repetitions. In the year of 2002 the tested products were: Azadirachta indica A. Juss (aqueous extract 2%), and oil at 1%; Melia azedarach L. (aqueous extract 2%); Quassia amara L. (aqueous extract 2%); nim oil, Azadirachta indica 1 and 2%. In the year of 2004 the tested products were: A. indica (aqueous extract 5%), and oil at 2%, M. azedarach (aqueous extract 5%), Trichilia pallida Sw. (aqueous extract 5%). The evaluations like percentage of infestation of the fall armyworm per plot, were made three, seven and ten days after the extracts application respectively. It was possible to verify that aqueous extracts of the plants A. indica 2%, T. pallida 5%, Q. amara 2% and M. azedarach 2% and 5% and A. indica oil 1% and 2% with addition of non ionic active tense, don't possess necessary efficiency as the only control method of the fall armyworm S. frugiperda in field conditions. The products begin to affect the development of fall armyworms some days after the ingestion of the powdered leaves, observed in the seven days after the extracts application.
4052 downloads
Cited 2 times in SciELO
10.
Diversidade de policetídeos produzidos por espécies de Penicillium isoladas de Melia azedarach e murraya paniculata
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Pastre, Renata
; Marinho, Andrey M. R.
; Rodrigues-Filho, Edson
; Souza, Antônia Q. L.
; Pereira, José Odair
.
Eight compounds comprising four groups of polyketides, the xanthone fusarindin, the mixed peptide alkaloid-polyketide GKK1032, the anthraquinones crisophanol, citreoveridin and janthinone, and the azaphylones dihydrocitrinone, citrinin and citrinin H-1, were identified in Penicillium species isolated as endophytic fungi from Melia azedarach and Murraya paniculata. The antibacterial activity of the azaphylones was tested and showed that citrinin H-1 is more active than citrinin.
13083 downloads
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