Lignocellulosic materials valorization in second generation biorefineries: an opportunity to produce fungal biopigments.

Second generation biorefineries play an important role in the production of renewable energy and fuels, utilizing forest and agro-industrial residues and by-products as raw materials. The integration of novel bioproducts, such as: xylitol, ß-carotene, xylooligosaccharides, and biopigments into the biorefinery's portfolio can offer economic benefits in the valorization of lignocellulosic materials, particularly cellulosic and hemicellulosic fractions. Fungal biopigments, known for their additional antioxidant and antimicrobial properties, are appealing to consumers and can have applications in various industrial sectors, including food and pharmaceuticals. The use of lignocellulosic materials as carbon and nutrient sources for the growth medium helps to reduce production costs, increasing the competitiveness of fungal biopigments in the market. In addition, the implementation of biopigment production in biorefineries allows the utilization of underutilized fractions, such as hemicellulose, for value-added bioproducts. This study deals with the potential of fungal biopigments production in second generation biorefineries in order to diversify the produced biomolecules together with energy generation. A comprehensive and critical review of the recent literature on this topic has been conducted, covering the major possible raw materials, general aspects of second generation biorefineries, the fungal biopigments and their potential for incorporation into biorefineries.

Generation of a triple-fluorescent mouse strain allows a dynamic and spatial visualization of different liver phagocytes in vivo.

Resident and circulating immune cells have been extensively studied due to their almost ubiquitous role in cell biology. Despite their classification under the "immune cell department", it is becoming increasingly clear that these cells are involved in many different non-immune related phenomena, including fetus development, vascular formation, memory, social behavior and many other phenotypes. There is a huge potential in combining high-throughput assays - including flow cytometry and gene analysis - with in vivo imaging. This can improve our knowledge in both basic and clinical cell biology, and accessing the expression of markers that are relevant in the context of both homeostasis and disease conditions might be instrumental. Here we describe how we generated a novel mouse strain that spontaneously express three different fluorescence markers under control of well-studied receptors (CX3CR1, CCR2 and CD11c) that are involved in a plethora of stages of cell ontogenesis, maturation, migration and behavior. Also, we assess the percentage of the expression and co-expression of each marker under homeostasis conditions, and how these cells behave when a local inflammation is induced in the liver applying a cutting-edge technology to image cells by confocal intravital microscopy.

Hydrodynamic cavitation-assisted acid pretreatment and fed-batch simultaneous saccharification and co-fermentation for ethanol production from sugarcane bagasse using immobilized cells of Scheffersomyces parashehatae.

A new alternative for hydrodynamic cavitation-assisted pretreatment of sugarcane bagasse was proposed, along with a simultaneous saccharification and co-fermentation (SSCF) process performed in interconnected columns. Influential variables in the pretreatment were evaluated using a statistical design, indicating that an ozone flow rate of 10 mg min-1 and a pH of 5.10 resulted in 86 % and 72 % glucan and xylan hydrolysis yields, respectively, in the subsequent enzymatic hydrolysis process. Under these optimized conditions, iron sulfate (15 mg L-1) was added to assess Fenton pretreatment, resulting in glucan and xylan hydrolysis yields of 92 % and 71 %, respectively, in a material pretreated for 10 min. In SSCF, ethanol volumetric productivities of 0.33 g L-1 h-1 and of 0.54 g L-1 h-1 were obtained in batch and fed-batch operation modes, achieving 26 g L-1 of ethanol in 48 h in the latter mode.

Ocorrência de aflatoxinas em amendoim e seus produtos comercializados no Estado da Bahia durante o ano de 2002 / Occurrence of Aflatoxins in peanut and peanut products commercialized in the state of Bahia during the year 2002

Este estudo teve como objetivo avaliar a contaminação por aflatoxinas (B1,B2,G1 e G2) em amostras de amendoim comercializadas em alguns municípios do estado da Bahia. Foram analisadas 100 amostras, sendo 33 de amendoim e 67 de produtos a base de amendoim. A coleta das amostras foi realizada aleatoriamente em diferentes estabelecimentos comerciais da cidade de Salvador (75 amostras) e em municípios do estado da Bahia (25 amostras) durante o período de janeiro a outubro de 2002. A extração foi realizada com acetonitrila:água (84:16, v/v), e a quantificação das aflatoxinas procedida pelo método de Cromatografia Líquida de Alta Eficiência (CLAE), empregando detecção por fluorescência. Das 31 amostras de amendoim analisadas, 29 (93,55 por cento) foram positivas, sendo que 17 (54,84 por cento), apresentaram teor de contaminação por B1 + B2 + G1+G2 superior a 20 ug/kg. Para as 69 amostras de derivados de amendoim, apenas 6 (8,7 por cento) apresentaram contaminação por aflatoxinas B1+B2+G1+G2 superior ao limite. Os resultados ainda revelaram que 20(80 por cento) do total de amostras coletadas nos municípios do Estado (25) e 38 (50,7 por cento) das 75 amostras procedentes de Salvador foram positivas. Os resultados ressaltam a necessidade de um controle eficaz dos níveis de aflatoxinas destes produtos na região