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1.
J Ind Microbiol Biotechnol ; 39(8): 1179-88, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22399240

RESUMO

Lasiodiplodan, an exopolysaccharide of the (1→6)-ß-D: -glucan type, is produced by Lasiodiplodia theobromae MMPI when grown under submerged culture on glucose. The objective of this study was to evaluate lasiodiplodan production by examining the effects of carbon (glucose, fructose, maltose, sucrose) and nitrogen sources (KNO(3), (NH(4))(2)SO(4), urea, yeast extract, peptone), its production in shake flasks compared to a stirred-tank bioreactor, and to study the rheology of lasiodiplodan, and lasiodiplodan's anti-proliferative effect on breast cancer MCF-7 cells. Although glucose (2.05 ± 0.05 g L(-1)), maltose (2.08 ± 0.04 g L(-1)) and yeast extract (2.46 ± 0.06 g L(-1)) produced the highest amounts of lasiodiplodan, urea as N source resulted in more lasiodiplodan per unit biomass than yeast extract (0.74 ± 0.006 vs. 0.22 ± 0.008 g g(-1)). A comparison of the fermentative parameters of L. theobromae MMPI in shake flasks and a stirred-tank bioreactor at 120 h on glucose as carbon source showed maximum lasiodiplodan production in agitated flasks (7.01 ± 0.07 g L(-1)) with a specific yield of 0.25 ± 0.57 g g(-1) and a volumetric productivity of 0.06 ± 0.001 g L(-1) h(-1). A factorial 2(2) statistical design developed to evaluate the effect of glucose concentration (20-60 g L(-1)) and impeller speed (100-200 rpm) on lasiodiplodan production in the bioreactor showed the highest production (6.32 g L(-1)) at 72 h. Lasiodiplodan presented pseudoplastic behaviour, and the apparent viscosity increased at 60°C in the presence of CaCl(2). Anti-proliferative activity of lasiodiplodan was demonstrated in MCF-7 cells, which was time- and dose-dependent with an IC(50) of 100 µg lasiodiplodan mL(-1).


Assuntos
Ascomicetos/metabolismo , Reatores Biológicos , Neoplasias da Mama/patologia , Glucanos/biossíntese , Glucanos/química , Glucose/metabolismo , Ascomicetos/química , Ascomicetos/efeitos dos fármacos , Biomassa , Neoplasias da Mama/tratamento farmacológico , Proliferação de Células/efeitos dos fármacos , Fermentação/efeitos dos fármacos , Glucanos/metabolismo , Glucose/farmacologia , Humanos , Cinética , Células MCF-7 , Maltose/metabolismo , Maltose/farmacologia , Nitrogênio/metabolismo , Reologia , Sacarose/metabolismo , Sacarose/farmacologia
2.
Molecules ; 17(12): 14298-309, 2012 Dec 03.
Artigo em Inglês | MEDLINE | ID: mdl-23208465

RESUMO

Studies evaluating the toxicity caused by fungal exopolysaccharides of the ß-(1-->6)-D-glucan type are rare. In this study, the toxicological effects of sub-chronic treatments with lasiodiplodan (ß-(1-->6)-D-glucan from Lasiodiplodia theobromae MMPI) were evaluated in mice through the assessment of biochemical, hematological, and histopathological alterations. Thirty-two mice (16 male, 16 female) were used in this study divided in two groups; one group received lasiodiplodan (50 mg/kg body weight) daily for 28 days via gavage, and another (control group) received saline during the same period. Blood samples were collected via cardiac puncture for hematological and biochemical analyses. Liver, heart, kidney, and spleen were collected for histopathological analysis. Statistical analysis was performed through one-way analysis of variance and only p < 0.05 F-values were presented. Significant reduction in blood glucose in the male group (35%; p < 0.01), transaminases activity in both sexes (AST and ALT; ~35%; p < 0.05), and urea (20%; p < 0.01) in the female group was observed with the lasiodiplodan treatment. The results showed that sub-chronic treatments with lasiodiplodan did not generate hematological and histopathological alterations leading to signs of toxicity in healthy mice, independent of gender.


Assuntos
Coração , Rim , Fígado , Baço , beta-Glucanas , Animais , Relação Dose-Resposta a Droga , Feminino , Coração/efeitos dos fármacos , Humanos , Intubação Gastrointestinal , Rim/efeitos dos fármacos , Rim/patologia , Fígado/efeitos dos fármacos , Fígado/patologia , Masculino , Camundongos , Baço/efeitos dos fármacos , Baço/patologia , beta-Glucanas/administração & dosagem , beta-Glucanas/toxicidade
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