RESUMO

The maintenance of the symbiosis between leaf-cutting ants and their mutualistic fungus Leucoagaricus gongylophorus Singer (Moller) is vital for the survival of both species. The specialist fungal parasite Escovopsis weberi Muchovej & Della Lucia is a threat to this symbiosis, causing severe damage to the fungal garden. Mycelial pellets are resistant fungal structures that can be produced under laboratory conditions. These structures were studied for use in biological pest control, but the production of mycelial pellets has not previously been documented in Escovopsis. One of the aims of this study was to induce Escovopsis weberi to produce mycelial pellets and investigate the potential of these pellets for the control of leaf-cutting ants. We compared the pathogenicity of Escovopsis weberi mycelial pellets and conidia against mini-colonies of Acromyrmex subterraneus subterraneus Forel when applied in the form of baits. Worker ants were able to distinguish mycelial pellets from conidia, as baits with mycelial pellets were more attractive to workers than those with conidia, causing a greater negative impact on colony health. All types of baits containing Escovopsis weberi influenced the foraging activity but only treatments with viable fungal propagules resulted in an increase in the quantity of waste material, with a significant negative impact on the fungal garden biomass. The results provided novel information regarding Escovopsis recognition by worker ants and differences between conidia and mycelial pellet dynamics in leaf-cutting ant colonies, with new perspectives for the biological control of these important pests.

RESUMO

Bacillus thuringiensis (Bt) (Bacillales:Bacillaceae) is a gram-positive bacterium that produces spores, several virulence factors and insecticidal toxins, making this microorganism the most used biopesticide worldwide. The use of inert supports such as polyurethane foam (PUF) in solid cultures has been a great alternative to produce various metabolites, including those produced by Bt. In this study we compared the yields, productivity and quality of the spores by two wild strains of Bt, (Y15 and EA3), grown in media with high substrate concentration in both culture systems: liquid and solid (PUF as solid inert support). Both strains showed 2.5- to 30-fold increases in spore production and productivity in solid culture, which showed an even greater increase when considering the spores retained in the PUF observed by scanning electron microscopy. Moreover, spore produced in solid culture showed up to sevenfold higher survival after a heat-shock treatment, relative to spores from liquid culture. The infectivity against larvae of Galleria mellonella (Lepidoptera:Pyralidae) improved also in spores from solid cultures. This comparison showed that the culture of Bt on solid support has clear advantages over liquid culture in terms of the production and quality of spores, and that those advantages can be attributed only to the culture system, as the same media composition was used in both systems.

Assuntos

RESUMO

The fungal genus Metarhizium comprises entomopathogenic species capable of producing overwintering structures known as microsclerotia. These structures offer many advantages in pest control due to the formation of infective conidia in situ and their persistence in the environment under adverse conditions. In addition, the in vitro production of Metarhizium microsclerotia under controlled liquid fermentation is faster and with greater process control than the production of aerial conidia. However, the potential of Metarhizium microsclerotia to control pests from the orders Lepidoptera and Hemiptera is unexplored. In this study, we examined the ability of Metarhizium spp. microsclerotia to promote corn growth and to provide plant protection against Spodoptera frugiperda (Lepidoptera: Noctuidae) and Dalbulus maidis (Hemiptera: Cicadellidae), through seed coating using microsclerotial granules. A screening to find higher microsclerotia producers was conducted by culturing 48 native Brazilian isolates of Metarhizium spp. (Metarhizium anisopliae, Metarhizium robertsii, Metarhizium humberi and Metarhizium sp. indeterminate). The best microsclerotia producers, M. anisopliae ESALQ1814, M. robertsii ESALQ2450 and M. humberi ESALQ1638 improved the leaf area, plant height, root length, and dry weight of plants compared to un-inoculated plants. Significant reduction in S. frugiperda survival (mortality > 55% after 7 days) was observed when larvae were fed on corn plants treated with any of the three Metarhizium species. Conversely, survival of D. maidis adults were unaffected by feeding on fungus-inoculated plants. Our results suggest that microsclerotia of Metarhizium spp. may act as biostimulants and to provide protection against S. frugiperda in corn through seed coating, thus adding an innovative strategy into the integrated management of this major worldwide pest.

Assuntos

RESUMO

A OMS, em 2007, recomendou a implementação da cultura líquida para o diagnóstico da tuberculose (TB) e teste de sensibilidade para países de baixa e média renda. Neste estudo foi avaliado odesempenho da cultura líquida MGIT em condição de rotina após dois anos de implantação em uma rede de laboratórios públicos. Foi efetuada análise retrospectiva de dados da cultura líquida,realizadas em dez laboratórios regionais do Instituto Adolfo Lutz, de janeiro a março de 2010. Foram incluídas amostras submetidas a baciloscopia, cultura líquida MGIT automatizada ou manual eidentificação presuntiva do complexo Mycobacterium tuberculosis (CMTB). Foram detectadas 1.159 culturas positivas. Destas, 113 (9,7%) contaminaram, e 1.046 foram analisadas, sendo 850 (81,3%) CMTB, 116 (11,1%) micobactérias não tuberculosas e 6 (0,6%) Nocardia sp. A taxa de contaminação foi de 2,2% e o acréscimo da cultura para o diagnóstico da TB foi de 29,9%. A média do tempo de detecção da cultura foi de 14,7 dias (DP+/- 11,7 dias). A acurácia da identificação presuntiva foide 91,3%. A cultura líquida MGIT demonstrou ser excelente alternativa para efetuar diagnóstico da TB e das micobacterioses, em razão da rapidez possibilitando uma intervenção rápida e eficaz no tratamento.

In 2007, WHO recommended the implementation of liquid culture for tuberculosis (TB) diagnosis anddrug-susceptibility test in low and middle-income countries. This study evaluated the performanceof MGIT culture in routine condition after two years of its implementation in a public laboratoriesnetwork. This is a retrospective study, which analyzed the data on the liquid culture performed in ten regional laboratories of the Institute Adolfo Lutz, from January to March 2010. The data included clinical samples submitted to microscopy, automated or manual MGIT culture and presumptive M. tuberculosis complex (MTBC) identification by analyzing the cord formation. Culture waspositive in 1,159 samples. Of these, 113 (9.7%) contaminated, and 1,046 were analyzed, of which 850 (81.3%) were identified as MTBC, 116 (11.1%) as non-tuberculous mycobacteria and 6 (0.6%)as Nocardia sp. Contamination rate was 2.2% and the contribution of culture to the TB diagnosis was 29.9%. The detection mean time was 14.7 days (SD+/-11.7 days). The accuracy of the presumptive identification of MTBC was 91.3%. MGIT liquid culture demonstrated to be an excellent alternative for diagnosing TB and mycobacterioses, because of the rapidity of diagnosis, thus allowing an immediate and effective treatment.

Assuntos

RESUMO

A OMS, em 2007, recomendou a implementação da cultura líquida para o diagnóstico da tuberculose (TB) e teste de sensibilidade para países de baixa e média renda. Neste estudo foi avaliado o desempenho da cultura líquida MGIT em condição de rotina após dois anosde implantação em uma rede de laboratórios públicos. Foi efetuada análise retrospectiva de dados da cultura líquida, realizadas em dez laboratórios regionais do Instituto Adolfo Lutz, de janeiro a março de 2010. Foram incluídas amostras submetidas a baciloscopia, cultura líquida MGIT automatizada ou manual e identificação presuntiva do complexo Mycobacterium tuberculosis (CMTB). Foram detectadas 1.159 culturas positivas. Destas, 113 (9,7%) contaminaram, e 1.046 foram analisadas, sendo 850 (81,3%) CMTB, 116 (11,1%) micobactérias não tuberculosas e 6 (0,6%) Nocardia sp A taxa de contaminação foi de 2,2% e o acréscimo da cultura para o diagnóstico da TB foi de 29,9%. A média do tempo de detecção da cultura foi de 14,7 dias (DP+/- 11,7 dias). A acurácia da identificação presuntiva foi de 91,3%. A cultura líquida MGIT demonstrou ser excelente alternativa para efetuar diagnóstico da TB e das micobacterioses, em razão da rapidez possibilitando uma intervenção rápida e eficaz no tratamento.

In 2007, WHO recommended the implementation of liquid culture for tuberculosis (TB) diagnosis and drug-susceptibility test in low and middle-income countries. This study evaluated the performance of MGIT culture in routine condition after two years of its implementation in a public laboratories network.This is a retrospective study, which analyzed the data on the liquid culture performed in ten regional laboratories of the Institute Adolfo Lutz, from January to March 2010. The data included clinical samples submitted to microscopy, automated or manual MGIT culture and presumptive M. tuberculosis complex (MTBC) identification by analyzing the cord formation. Culture was positive in 1,159 samples. Of these, 113 (9.7%) contaminated, and 1,046 were analyzed, of which 850 (81.3%) were identified as MTBC, 116 (11.1%) as non-tuberculous mycobacteria and 6 (0.6%) as Nocardia sp. Contamination rate was 2.2% and the contribution of culture to the TB diagnosis was 29.9%. The detection mean time was 14.7 days (SD+/-11.7 days). The accuracy of the presumptive identification of MTBC was 91.3%. MGIT liquid culture demonstrated to be an excellent alternative for diagnosing TB and mycobacterioses, because of the rapidity of diagnosis, thus allowing an immediate and effective treatment.

Assuntos

RESUMO

A OMS, em 2007, recomendou a implementação da cultura líquida para o diagnóstico da tuberculose (TB) e teste de sensibilidade para países de baixa e média renda. Neste estudo foi avaliado o desempenho da cultura líquida MGIT em condição de rotina após dois anosde implantação em uma rede de laboratórios públicos. Foi efetuada análise retrospectiva de dados da cultura líquida, realizadas em dez laboratórios regionais do Instituto Adolfo Lutz, de janeiro a março de 2010. Foram incluídas amostras submetidas a baciloscopia, cultura líquida MGIT automatizada ou manual e identificação presuntiva do complexo Mycobacterium tuberculosis (CMTB). Foram detectadas 1.159 culturas positivas. Destas, 113 (9,7%) contaminaram, e 1.046 foram analisadas, sendo 850 (81,3%) CMTB, 116 (11,1%) micobactérias não tuberculosas e 6 (0,6%) Nocardia sp A taxa de contaminação foi de 2,2% e o acréscimo da cultura para o diagnóstico da TB foi de 29,9%. A média do tempo de detecção da cultura foi de 14,7 dias (DP+/- 11,7 dias). A acurácia da identificação presuntiva foi de 91,3%. A cultura líquida MGIT demonstrou ser excelente alternativa para efetuar diagnóstico da TB e das micobacterioses, em razão da rapidez possibilitando uma intervenção rápida e eficaz no tratamento.(AU)

In 2007, WHO recommended the implementation of liquid culture for tuberculosis (TB) diagnosis and drug-susceptibility test in low and middle-income countries. This study evaluated the performance of MGIT culture in routine condition after two years of its implementation in a public laboratories network.This is a retrospective study, which analyzed the data on the liquid culture performed in ten regional laboratories of the Institute Adolfo Lutz, from January to March 2010. The data included clinical samples submitted to microscopy, automated or manual MGIT culture and presumptive M. tuberculosis complex (MTBC) identification by analyzing the cord formation. Culture was positive in 1,159 samples. Of these, 113 (9.7%) contaminated, and 1,046 were analyzed, of which 850 (81.3%) were identified as MTBC, 116 (11.1%) as non-tuberculous mycobacteria and 6 (0.6%) as Nocardia sp. Contamination rate was 2.2% and the contribution of culture to the TB diagnosis was 29.9%. The detection mean time was 14.7 days (SD+/-11.7 days). The accuracy of the presumptive identification of MTBC was 91.3%. MGIT liquid culture demonstrated to be an excellent alternative for diagnosing TB and mycobacterioses, because of the rapidity of diagnosis, thus allowing an immediate and effective treatment.(AU)

Assuntos

RESUMO

La introducción de nuevos cultivares de guayabo (Psidium guajava L.) amerita su propagación masiva, lo cual solo puede ser satisfecho mediante la micropropagación. Sin embargo la micropropagación convencional dejó de ser económicamente eficiente, debido al uso de agentes gelificantes y el elevado número de operaciones manuales, por esta razón se planteó en esta investigación, generar una metodología que permita disminuir los costos de producción por la exclusión del gelificante en los medios de cultivo, evaluando los sistemas de inmersión temporal (SIT) en la multiplicación in vitro de guayabo. Para lo cual, se evaluó el efecto del cultivo en SIT, se comparó los SIT tipo BIT® y RITA® y se evaluó el tiempo (1 y 2 min) y frecuencia (3 y 4 veces/día) de inmersión. Luego de seis semanas de cultivo se evaluó: número de brotes (NB), numero de nudos (NN), longitud de brote (LB) y coeficiente de multiplicación (CM). Con el empleo de SIT se logró valores superiores para NB (2,17), NN (3,5), LB (10,7 mm) y CM (2,8). En la comparación entre SIT tipo RITA y BIT, valores superiores se obtuvieron con el RITA® para NB (3,8), NN (3,8), LB (16,6 mm) y CM (10,4). Se determinó que con 2 min de inmersión se logró los mayores valores de NB (3,7), NN (13,4), LB (15,3 mm) y con 2 min de inmersión 3-4 veces/día el mayor CM (9,4 y 10,4). Se concluye que el cultivo en RITA® en la multiplicación favoreció crecimiento y la proliferación de brotes de guayabo.

The introduction of new cultivars of guava (Psidium guajava L.) deserves its mass propagation, which can only be satisfied by micropropagation. However conventional micropropagation stopped being economically efficient due to the use of gelling agents and the high number of manual operations. For this reason was considered in this research, generate a methodology to reduce production costs by exclusion of gelling in culture media, assessing temporary immersion systems (TIS) in the in vitro multiplication of guava. For which, the effect of the culture way was evaluated in TIS, type TIB® and RITA® compared the TIS and was evaluated the time (1 and 2 min) and frequency (3 and 4 times / day) of immersions. After six weeks of culture were evaluated: shoots number (NS), nodes number (NN), shoot length (SL) and multiplication rate (MR). With the use of TIS higher values for NS (2.17), NN (3.5), SL (10.7 mm) and MC (2.8) was achieved. When comparing RITA® and TIB, higher values were obtained with the RITA® for NS (3.8), NN (3.8), SL (16.6 mm) and MC (10.4). It was determined that 2 min of immersion with the highest values of NS (3.7), NN (13.4), SL (15.3 mm) and 2 min immersion 3-4 times/day achieved the highest MC (9.4 and 10.4). We conclude that the RITA® culture favored the multiplication in growth and proliferation of shoots of guava.

RESUMO

Background: Berkleasmium sp. Dzf12, an endophytic fungus from Dioscorea zingiberensis, was a high producer of palmarumycin C13 with various bioactivities. In the present study, the experimental designs based on statistics were employed to evaluate and optimize the medium for palmarumycin C13 production in mycelia liquid culture of Berkleasmium sp. Dzf12. Results: Among various carbon and nitrogen sources, glucose, peptone and yeast extract were found to be the most favourable for palmarumycin C13 production based on the one-factor-at-a-time experiments. After Plackett-Burman test on the medium, glucose, peptone and yeast extract were further verified to be the most significant factors to stimulate palmarumycin C13 accumulation. These three factors (i.e., glucose, peptone and yeast extract) were then optimized through the experiments of central composite design (CCD) and analysis of response surface methodology (RSM). The optimized medium compositions for palmarumycin C13 production were determined as 42.5 g/l of glucose, 6.5 g/l of peptone, 11.0 g/l of yeast extract, 1.0 g/l of KH2PO4, 0.5 g/l of MgSO4 x 7H2O, 0.05 g/l of FeSO4 x 7H2O, and pH 6.5. Under the optimal culture conditions, the maximum palmarumycin C13 yield of Berkleasmium sp. Dzf12 was increased to 318.63 mg/l, which was about 2.5-fold in comparison with that (130.44 mg/l) in the basal medium. Conclusions: The results indicate that the optimum production of palmarumycin C13 in Berkleasmium sp. Dzf12 liquid culture can be achieved by addition of glucose, peptone and yeast extract with their appropriate concentrations in the modified Sabouraud medium.

Assuntos

RESUMO

The fungi strains were tested in Bioscreen automated system to select the best nutritional source. Following, shaking submserse cultures were studied in media containing sole carbon or nitrogen source. The growth of these strains improved in media containing vegetable oil, with high concentration of lipids. The high concentration of γ-linolenic acid was obtained with M. circinelloides in culture containing sesame oil.

Linhagens de fungos foram testadas em sistema automatizado Bioscreen para selecionar melhor fonte nutricional. Em seguida, foram estudadas culturas submersas em meios contendo uma única fonte de carbono e de nitrogênio. As linhagens contendo alta concentração de lipídeos tiveram melhor crescimento em meio contendo óleos de gergelim ou de dendê. Maior concentração de ácido γ-linolênico foi obtida com M. circinelloides nas culturas em óleo de gergelim.

Assuntos

RESUMO

The fungi strains were tested in Bioscreen automated system to select the best nutritional source. Following, shaking submserse cultures were studied in media containing sole carbon or nitrogen source. The growth of these strains improved in media containing vegetable oil, with high concentration of lipids. The high concentration of -linolenic acid was obtained with M. circinelloides in culture containing sesame oil.

Linhagens de fungos foram testadas em sistema automatizado Bioscreen para selecionar melhor fonte nutricional. Em seguida, foram estudadas culturas submersas em meios contendo uma única fonte de carbono e de nitrogênio. As linhagens contendo alta concentração de lipídeos tiveram melhor crescimento em meio contendo óleos de gergelim ou de dendê. Maior concentração de ácido -linolênico foi obtida com M. circinelloides nas culturas em óleo de gergelim.

RESUMO

Production of baicalein, baicalin and wogonin by liquid culture of Scutellaria baicalensis cells derived from the plant root was studied. The maximum production obtained were 119 mg/L of baicalein at two week, 1372 mg/L of baicalin at eight week, and 14 mg/L of wogonin at two week. In addition, the production of baicalin was drastically increased to 1000 mg/L level at 3-week culture, and the extremely high production rate (339 mg/L•week) was obtained. In the comparison of total antioxidative activities among baicalein, baicalin and wogonin, evaluated by thiocyanate method, it was suggested that the location of hydroxyl groups both at 5- and 6-position contributed to enhancement of radical scavenging activity, and/or methoxylation at 8-position diminished the activity. The possibility of utilizing these flavonoids for natural antioxidants and medicine is also discussed.

RESUMO

The fungi strains were tested in Bioscreen automated system to select the best nutritional source. Following, shaking submserse cultures were studied in media containing sole carbon or nitrogen source. The growth of these strains improved in media containing vegetable oil, with high concentration of lipids. The high concentration of γ-linolenic acid was obtained with M. circinelloides in culture containing sesame oil.

RESUMO

Fusarium verticillioides Sacc. Niremberg (= F. moniliforme Sheldon) is a primary corn pathogen and the main fumonisin producer. Considering that the nutrient quality and its concentration in the culture medium have an important role in fumonisin production, the aim of this study was to evaluate fumonisin B1 (FB1 ) production by F. verticillioides in a liquid culture medium with different carbon and nitrogen sources. Three strains (103F, 113B and 103BR) were inoculated in nine liquid culture media with different carbon sources (glucose, fructose and maltose) at the concentration of 20 g/L and nitrogen (leucine, alanine and valine) at the concentration of 1 g/L. After selecting the strain (103F) and carbon/nitrogen sources (maltose/leucine) that provided the highest FB1 production, culture media with different maltose and leucine concentrations were evaluated. Keeping the leucine concentration at 1 g/L and increasing the maltose concentration from 20 g/L to 40 g/L, the FB1 production increased from 3.9 ?g/mL to 4.7 ?g/mL (p 0.05). On the other hand, keeping the maltose concentration at 40 g/L and decreasing the leucine concentration to 50% (from 2 g/L to 1 g/L) the FB1 production increased from 2.3 ?g/mL to 4.7 ?g/mL (p 0.05). FB1 production varied according to the F. verticillioides strain, concentration and carbon/nitrogen source in the liquid culture medium and the i

Fusarium verticillioides Sacc. Niremberg (= F. moniliforme Sheldon) é um patógeno primário de milho e principal produtor de fumonisinas. Considerando que a qualidade e a concentração de nutrientes no substrato apresentam papel importante na produção de fumonisinas, este trabalho teve como objetivo avaliar a produção de fumonisina B1 (FB1) por F. verticillioides em cultivo líquido com diferentes fontes de carbono e nitrogênio. Três cepas (103F, 113B e 103BR) foram inoculadas em nove meios de cultivo líquido com diferentes fontes de carbono (glucose, frutose e maltose) na concentração de 20 g/L e nitrogênio (leucina, alanina e valina) na concentração de 1 g/L. Após a seleção da cepa (103F) e fonte de carbono/nitrogênio (maltose/leucina) que proporcionaram maior produção de FB1, foram avaliados meios variando as concentrações de maltose e leucina. Fixando a concentração de leucina em 1 g/L e aumentando a concentração de maltose de 20 g/L para 40 g/L ocorreu um aumento na produção de FB1 de 3,9 ?g/mL para 4,7 ?g/mL (p 0,05). Por outro lado, fixando a concentração de maltose em 40 g/L e diminuindo a concentração de leucina em 50% (de 2 g/L para 1 g/L) ocorreu um aumento na produção de FB1 de 2,3 ?g/mL para 4,7 ?g/mL (p 0,05). A produção de FB1 variou de acordo com a cepa de F. verticillioides, concentração e fonte de carbono/nitrogênio no meio líquido, sendo que o aumento

RESUMO

The fungi strains were tested in Bioscreen automated system to select the best nutritional source. Following, shaking submserse cultures were studied in media containing sole carbon or nitrogen source. The growth of these strains improved in media containing vegetable oil, with high concentration of lipids. The high concentration of -linolenic acid was obtained with M. circinelloides in culture containing sesame oil.

Linhagens de fungos foram testadas em sistema automatizado Bioscreen para selecionar melhor fonte nutricional. Em seguida, foram estudadas culturas submersas em meios contendo uma única fonte de carbono e de nitrogênio. As linhagens contendo alta concentração de lipídeos tiveram melhor crescimento em meio contendo óleos de gergelim ou de dendê. Maior concentração de ácido -linolênico foi obtida com M. circinelloides nas culturas em óleo de gergelim.

RESUMO

Fusarium verticillioides Sacc. Niremberg (= F. moniliforme Sheldon) is a primary corn pathogen and the main fumonisin producer. Considering that the nutrient quality and its concentration in the culture medium have an important role in fumonisin production, the aim of this study was to evaluate fumonisin B1 (FB1 ) production by F. verticillioides in a liquid culture medium with different carbon and nitrogen sources. Three strains (103F, 113B and 103BR) were inoculated in nine liquid culture media with different carbon sources (glucose, fructose and maltose) at the concentration of 20 g/L and nitrogen (leucine, alanine and valine) at the concentration of 1 g/L. After selecting the strain (103F) and carbon/nitrogen sources (maltose/leucine) that provided the highest FB1 production, culture media with different maltose and leucine concentrations were evaluated. Keeping the leucine concentration at 1 g/L and increasing the maltose concentration from 20 g/L to 40 g/L, the FB1 production increased from 3.9 ?g/mL to 4.7 ?g/mL (p 0.05). On the other hand, keeping the maltose concentration at 40 g/L and decreasing the leucine concentration to 50% (from 2 g/L to 1 g/L) the FB1 production increased from 2.3 ?g/mL to 4.7 ?g/mL (p 0.05). FB1 production varied according to the F. verticillioides strain, concentration and carbon/nitrogen source in the liquid culture medium and the i

Fusarium verticillioides Sacc. Niremberg (= F. moniliforme Sheldon) é um patógeno primário de milho e principal produtor de fumonisinas. Considerando que a qualidade e a concentração de nutrientes no substrato apresentam papel importante na produção de fumonisinas, este trabalho teve como objetivo avaliar a produção de fumonisina B1 (FB1) por F. verticillioides em cultivo líquido com diferentes fontes de carbono e nitrogênio. Três cepas (103F, 113B e 103BR) foram inoculadas em nove meios de cultivo líquido com diferentes fontes de carbono (glucose, frutose e maltose) na concentração de 20 g/L e nitrogênio (leucina, alanina e valina) na concentração de 1 g/L. Após a seleção da cepa (103F) e fonte de carbono/nitrogênio (maltose/leucina) que proporcionaram maior produção de FB1, foram avaliados meios variando as concentrações de maltose e leucina. Fixando a concentração de leucina em 1 g/L e aumentando a concentração de maltose de 20 g/L para 40 g/L ocorreu um aumento na produção de FB1 de 3,9 ?g/mL para 4,7 ?g/mL (p 0,05). Por outro lado, fixando a concentração de maltose em 40 g/L e diminuindo a concentração de leucina em 50% (de 2 g/L para 1 g/L) ocorreu um aumento na produção de FB1 de 2,3 ?g/mL para 4,7 ?g/mL (p 0,05). A produção de FB1 variou de acordo com a cepa de F. verticillioides, concentração e fonte de carbono/nitrogênio no meio líquido, sendo que o aumento

RESUMO

ABSTRACT Six Penicillium strains were isolated from soil at a depth of 0 15 cm in the Juréia-Itatins Ecology Station (JIES), in the São Paulo State, Brazil. They were evaluated for xylanase production under different temperatures and carbon sources. The best carbon source and temperature were first determined in an automated Bioscreen C system, verifying the growth of microorganisms. Liquid media containing tap water with 2% carbohydrate and/or 1% nitrogen sources were used. Afterwards, Penicillium citrinum, P. fellutanum, P. rugulosum and P. decumbens were cultivated in 250 mL Erlenmeyer flasks with 50 mL of culture medium containing tap water sole 2% carbon source (fructose, glucose, mannitol, sucrose or xylose) and 1% yeast extract as a nitrogen source at pH 5.0 and 28o C, with agitation of 150 rpm for 72 hours. These same strains, except P. decumbens, and P. purpurogenum were cultivated in solid substrate with wheat bran under the same environmental conditions to study the potential of xylanase activity. Maximum xylanase activity was observed in cultures with wheat bran, without the addition of any other carbon source, using inocula containing 1 x 107 spores.mL-1 (28o C, pH 5.0, 72 h). It can be concluded that P. fellutanum and P. citrinumare a good xylanase producers under the conditions of 28º C. The results of xylanase activity were 54% less at 28º C in liquid cultures media cultures than in solid substrate.

RESUMO Seis linhagens de Penicillium foram isoladas do solo, na profundidade de 0 15 cm, na Estação Ecológica de Juréia-Itatins (EEJI), Estado de São Paulo, Brasil. Elas foram analisadas quanto a produção de xilanase sob diferentes temperaturas e fontes de carbono e de nitrogênio. Foi utilizado meio contendo água de torneira com 2% de carboidrato e/ou 1% de fonte de nitrogênio. A melhor fonte de carbono e temperatura foram obtidas no sistema automatizado de crescimento tipo Bioscreen C. Posteriormente, Penicillium citrinum, P. fellutanum, P. rugulosum e P. decumbens foram cultivadas em frascos agitados em 150 rpm, contendo meio líquido contendo água de torneira com uma única fonte de carbono 2% e/ou 1% de fonte de nitrogênio, pH 5.0, a 25o C, por 72 horas. Estas mesmas linhagens, exceto P. decumbens, e P. purpurogenum foram cultivadas em substrato sólido contendo farelo de trigo sob as mesmas condições ambientais anteriores de cultivo. Maior atividade de xilanase foi observada em culturas contendo farelo de trigo, sem adição de qualquer outra fonte de carbono, usando inoculo com 1.107 esporos mL-1 (25o C, pH 5.0, 72 h). Pode ser concluído que P. fellutanum e P. citrinum são bons produtores de xilanase a 28º C. Os resultados da atividade da xilanase foram 54% menores a 28º C em cultura líquida em relação aos resultados observados em substrato sólido.

RESUMO

In vitro suspension culture procedures for erythroid progenitor cells make it possible for us to obtain large cultures of erythrocyte populations for the investigation of globin gene switching. In this study we aimed to establish optimized culture systems for neonatal and adult erythroblasts and to explore the globin expression patterns in these culture systems. To culture CD34+ cells purified from human umbilical cord blood (CB) and adult bone marrow (BM), we respectively replaced the fetal bovine serum (FBS) with human cord serum and human adult serum. These CD34+ cells were then induced to erythroid differentiation. All the globin mRNA (including alfa-, xi-, vita-, gama-and epsilón-globin), the hemoglobin (Hb)-producing erythroid cells and the cellular distribution of fetal hemoglobin (Hb F) were identified during the culture process. The results showed that the globin expression pattern during erythroid differentiation in our culture systems closely recapitulated neonatal and adult patterns of globin expression in vivo, suggesting that our specially optimized culture systems not only overcame the higher Hb F levels in the BM-derived CD34+ culture in FBS-containing medium but also eliminated the disadvantages of low cell proliferation rate and low globin mRNA levels in serum-free medium.

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