Production of arachidonic acid by Mortierella alpina using wastes from potato chips industry.

AIMS: This research aimed to determine the potential use of wastes from the potato chips industry as a carbon source to develop an economical culture medium for the production of biomass, lipids and arachidonic acid (ARA) by Mortierella alpina. METHODS AND RESULTS: A synthetic culture medium was optimized using a Plackett-Burman and central composite rotatable design, and used as a base to evaluate and characterize the potential use of wastes from the potato chips industry as carbon sources for the production of biomass, lipids and ARA by M. alpina. The waste was selected among other solid and liquid hydrolysed residues/by-products, and local low-cost alternatives for nitrogen sources were also evaluated. After 6 days of fermentation, the biomass concentration reached 20 g l-1 with 40% of total lipids, and a 35% ARA content in the lipids fraction. Savings in production were calculated using a sensitivity analysis for the alternative culture medium in different scenarios. CONCLUSIONS: This study showed a 7% savings in culture media expenses in the production of ARA-enriched biomass of M. alpina, compared to the conventional synthetic culture medium, when waste from the potato chips industry was used as an alternative source of carbon and macro/microelements, supplemented with a low-cost yeast extract alternative. SIGNIFICANCE AND IMPACT OF THE STUDY: The demonstration of the use of potato chips wastes as a low-cost carbon source for the biomass, lipids and ARA production, suggesting an eco-friendly alternative for the use of agri-food wastes for valuable metabolites production.

Technological mapping and trends in photobioreactors for the production of microalgae.

Photobioreactors (PBRs) are equipment of central importance for the massive cultivation of microalgae, providing controlled conditions for high cell productivity. There are a few popular PBR designs, with contrasting advantages and limitations, such as poor light distribution, mass transfer, or hydrodynamic behavior. Due to the environmental concerns in recent decades and the discovery of new, useful microalgal metabolites, the interest in finding alternatives to solve technological bottlenecks of PBRs has intensified. In this process, new geometries, materials, and modes of light supply were developed, generating a significant scientific and technological output, reported in papers and patents. We present a technological landscape analysis of photobioreactor design, focusing on improvements of the classical geometries and trends in industrial photobioreactors. The analysis of 412 patent documents showed a surge in innovation filing since 2005 and a reduction in the number of new documents along the last decade. The recent efforts in design improvement, the leading countries, institutes and companies that innovate, and the trends in PBR technology are presented and discussed.

Isolation, selection and evaluation of antagonistic yeasts and lactic acid bacteria against ochratoxigenic fungus Aspergillus westerdijkiae on coffee beans.

UNLABELLED: In this study, yeasts and lactic acid bacteria (LAB) were isolated from coffee fruits and identified via biochemical and molecular approaches. The isolates represented the Pichia, Debaryomyces, Candida, Clavispora, Yarrowia, Sporobolomyces, Klyveromyces, Torulaspora and Lactobacillus genera. Four isolates, namely Pichia fermentans LPBYB13, Sporobolomyces roseus LPBY7E, Candida sp. LPBY11B and Lactobacillus brevis LPBB03, were found to have the greatest antagonist activity against an ochratoxigenic strain of Aspergillus westerdijkiae on agar tests and were selected for further characterization. Applications of P. fermentans LPBYB13 in coffee cherries artificially contaminated with A. westerdijkiae showed efficacy in reducing ochratoxin A (OTA) content up to 88%. These results highlight that P. fermentans LPBYB13 fulfils the principle requirements of an efficient biological control of aflatoxigenic fungi in coffee beans and may be seen as a reliable candidate for further validation in field conditions. SIGNIFICANCE AND IMPACT OF THE STUDY: Studies based on microbial ecology and antagonistic interactions are important for the development of new strategies in controlling aflatoxin contamination of crops and are relevant to further biotechnological applications. This study shows that coffee fruit is a potential source for the isolation of microbial strains with antifungal ability. A new yeast strain, Pichia fermentans LPBYB13, showed efficacy in reducing growth and ochratoxin A production of Aspergillus westerdijkiae in coffee beans. Our results should encourage the use of this yeast strain on a large scale for biocontrol of aflatoxigenic fungi in coffee beans.

Effect of different compounds on the induction of laccase production by Agaricus blazei.

Laccases are polyphenol oxidases produced by many fungi and have many applications in textile, food and beverage, and pulp and paper industries. Laccase production can be induced using aromatic or phenolic compounds that mostly affect the transcription of laccase-encoding genes. In this study, we analyzed laccase and biomass production by Agaricus blazei in the presence of different concentrations of nitrogen, copper, and inducers such as pyrogallol, veratryl alcohol, xylidine, vanillin, guaiacol, and ethanol. Laccase production by A. blazei U2-4 reached 43.8 U/mL in the presence of 2.8 g/L nitrogen and 150 µM copper. However, addition of copper to the cultivation medium decreased biomass production. Different compounds differentially induced laccase production by A. blazei. Moreover, different concentrations of these inducers exerted different effects on laccase activity. Ethanol (1.0 mM), guaiacol (0.5 mM), and vanillin (0.5 mM) were the best inducers and increased laccase activity by 120% (A. blazei U2-2), 30% (A. blazei U2-3), and 9% (A. blazei U2-4), respectively. In contrast, pyrogallol and xylidine decreased laccase activity but increased biomass production.

Optimum conditions for inducing laccase production in Lentinus crinitus.

Laccases are environmentally friendly alternatives in many important applications such as in bioremediation, biopulping, textile, and the food industry. They have wide substrate specificity, can oxidize a broad range of compounds, and show potential for use in various industrial processes. Therefore, developing methods to increase laccase production is important. In the current study, we aimed to identify optimum conditions for inducing laccase production in the basidiomycete Lentinus crinitus cultivated under varying nitrogen concentrations and in the presence of potential inducers of laccase production, including copper and phenolic compounds. Peak enzymatic activity (11,977 U/L) occurred at higher nitrogen concentrations (2.8 g/L nitrogen). Regardless of the nitrogen concentration, addition of copper increased the laccase activity and decreased mycelial growth, with maximum laccase activity (14,320 U/L) observed at the highest nitrogen concentration combined with 150 mM CuSO4. In addition, ethanol (0.5 or 1.0 mM) and guaiacol (1.5 mM) increased laccase production to 15,000, 14,800, and 14,850 U/L, respectively. Our findings highlighted the optimum conditions for producing L. crinitusderived laccase as potential alternatives to the conventional production and application of the enzyme.

Influence of airflow intensity on phytase production by solid-state fermentation.

Phytase production by Aspergillus niger F3 by solid state fermentation (SSF) on citrus peel was evaluated at pilot scale under different aeration conditions. The best airflow intensity was 1 VkgM (Lair kg medium(-1) min(-1)), which allowed to produce 65 units of phytases per gram in dry basis (65 Ug(-1) d.b.) as it removed the metabolic heat generated by the microorganism, Agitation did not improve heat removal. Airflow intensity was considered as scale-up criterion. When the airflow intensity was maintained at 1 VkgM for SSF with 2 and 20 kg of medium, the kinetics parameters for biomass and enzyme concentration at the end of fermentation differed by less than 2. The air flow intensity was required to maintain the temperature and cool the SSF and to provide oxygen for microbial growth. Air flow intensity is a key a factor that must be considered when scale-up of SSF is attempted.

Co-culture of microalgae, cyanobacteria, and macromycetes for exopolysaccharides production: process preliminary optimization and partial characterization.

In this study, the biomass and exopolysaccharides (EPS) production in co-cultures of microalgae/cyanobacteria and macromycetes was evaluated as a technology for producing new polysaccharides for medical and/or industrial application. Based on biomass and EPS productivity of monocultures, two algae and two fungi were selected and cultured in different co-culture arrangements. The hydrosoluble EPS fractions from mono- and co-cultures were characterized by ¹³C NMR spectroscopy and gas chromatography coupled to mass spectrometry and compared. It was found that co-cultures resulted in the production of an EPS different from those produced by monocultures, showing fungal predominance with microalgal/cyanobacterial traces. Co-cultures conditions were screened (temperature, agitation speed, fungal and microalgae inoculation rate, initial pH, illumination rate, and glucose concentration) in order to achieve maximum biomass and EPS production, resulting in an increase of 33 and 61% in exopolysaccharides and biomass productions, respectively (patent pending).

The behavior of kinetic parameters in production of pectinase and xylanase by solid-state fermentation.

Solid-state fermentation (SSF) is defined as the growth of microbes without a free-flowing aqueous phase. The feasibility of using a citrus peel for producing pectinase and xylanase via the SSF process by Aspergillus niger F3 was evaluated in a 2 kg bioreactor. Different aeration conditions were tested to optimize the pectinase and xylanase production. The best air flow intensity was 1 V kg M (volumetric air flow per kilogram of medium), which allowed a sufficient amount of O2 for the microorganism growth producing 265 U/g and 65 U/g pectinases and xylanases, respectively. A mathematical model was applied to determine the different kinetic parameters related to SSF. The specific growth rate and biomass oxygen yield decreased during fermentation, whereas an increase in the maintenance coefficient for the different employed carbon sources was concurrently observed.

Influence of drying methods over in vitro antitumoral effects of exopolysaccharides produced by Agaricus blazei LPB 03 on submerged fermentation.

Agaricus blazei is a mushroom that belongs to the Brazilian biodiversity and is considered as an important producer of bioactive compounds beneficial to human health. Studies have demonstrated that these compounds present immuno-modulatory, antioxidant and antitumor properties. In order to compare the most used method for fungal polysaccharide drying, lyophilization with other industrial-scale methods, the aim of this work was to submit A. blazei LPB 03 polysaccharide extracts to vaucum, spray and freeze drying, and evaluate the maintenance of its antitumoral effects in vitro. Exopolysaccharides produced by A. blazei LPB 03 on submerged fermentation were extracted with ethanol and submitted to drying processes. The efficiency represents the water content that was removed during the drying process. The resultant dried products showed water content around 3% and water activity less than 0.380, preventing therefore the growth of microorganisms and reactions of chemical degradation. Exopolysaccharide extracts dried by vacuum and spray dryer did not showed any significant cytotoxic effect on cell viability of Wistar mice macrophages. Content of total sugars and protein decrease after drying, nevertheless, 20 mg/ml of exopolysaccharides dried by spray dryer reached 33% of inhibition rate over Ehrlich tumor cells in vitro.

Efeito do extrato bruto enzimático de Streptomyces Viridosporus T7A sobre a digestibilidade de matéria seca in vitro para ruminantes / Effect of the Streptomyces Viridosporus T7A crude fermentation extract on the in vitro digestibility of dry matter for ruminants / Effeito do extrato bruto enzimático de streptoniyces viridosporus T7A sobre a digestibilidade de matéria seca in vitro para ruminantes

As forragens de um modo geral possuem boa digestibilidade para os animais ruminantes, mas os resíduos das agroindústrias, tais como palhas e bagaços, têm aproveitamento limitado, devido ao alto teor em lignina. A cepa Streptomyces viridosporus T7A é capaz de produzir, em substrato lignocelulósico enzimas de interesse agroindustrial como a lignina peroxidase, xilanase, esterase e celulase. Neste trabalho, estudou-se o efeito da adição do extrato bruto enzimático de Streptomyces viridosporus T7A sobre a digestibilidade da fibra em ruminantes, pelo método de digestibilidade in vitro. O extrato foi adicionado na proporção de 0,2; 0,5; 2,0 e 5,0 por cento durante 48 horas, em conteúdo ruminal colhido de um búfalo cirurgicamente fistulado. Não houve diferença estatística com o controle na digestibilidade in vitro da matéria seca, quando o extrato bruto foi adicionado nos níveis de 0,2; 0,5; 2,0 e 5,0 por cento. No entanto, observou-se maior digestibidade no nível de 0,2 por cento.

Forages generally have good digestibilility in ruminant animals, but the use of agro-industrial wastes such as straws and bagasses is limited by their high proportion of lignin. In lignocellulosic substrate, the Streptomyces viridosporus T7A strain is capable to produce interesting enzymes as lignin peroxydase, xylanase, esterase, and cellulase. We studied the in vitro effect of the addition of the Streptomyces viridosporus T7A crude fermentation enzymatic extract on digestibility of fibers in ruminants. The extract was added to filtered ruminal fluid obtained from a surgically fistulated Asian buffalo, 0.2 percent, 0.5 percent, 2.0 percent, and 5.0 percent proportions. After 48 hours there was found no statistic difference in dry matter digestibility in vitro among control and the crude extract levels of 0.2, 0.5, 2.0, and 5.0 percent levels. Higher digestibility, however, was observed when it was added at 0.2 percent level.

Las forrajes generalmente tienen buena digestibilidad para los animales rumiantes, pero el uso de residuos agro-industriales como pajas y bagazos es limitados por su alta proporción de lignina. En substrato lignocelulósico, el Streptomyces viridosporus T7A es capaz de producir enzimas de interés industrial, como lignina peroxidase, xilanase, esterase y celulase. En este trabajo se estudió el efecto in vitro de la adición del extracto enzimático bruto de Streptomyces viridosporus T7A sobre la digestibilidad de fibras en rumiantes. El extracto se agregó a fluido rumial filtrado, obtenido de un búfalo quirúrgicamente fistulado, en proporciones de 0,2, 0,5, 2,0 y 5,0. Después de 48 horas, no se encontró ninguna diferencia estadística en la digestibilidad de la materia seca in vitro entre el control y los niveles de 0,2, 0,5, 2,0 y 5,0 del extracto bruto. Sin embargo, se observó digestibilidad más grande con el nivel fue de 0,2.

Avaliação do potencial de uso do extrato bruto da fermentação por Streptomyces Viridosporus T7 A em medicinaveterinária / Evaluation of the potential applicability of Streptomyces Viridosporus T7 A crude fermentation extract in veterinary medicine / Evaluación del potencial de uso del extracto bruto de la fermentación por Streptomyces viridosporus T7A en medicina veterinaria

Desde a sua descoberta como produtoras de antibióticos, as bactérias do gênero Streptomyces têm sido muito estudadas, em função de seu grande interesse para a indústria. A maioria das cepas de Streptomyces sintetiza substâncias antibacterianas, antifúngicas, antitumorais, antiparasitárias, herbicidas e enzimas, que têm empregos em medicina e agricultura, bem como em vários processos biotecnológicos. Neste trabalho estudou-se a aplicação do extrato bruto enzimático obtido da fermentação por Streptomyces viridosporus T7A para uso veterinário. O extrato bruto enzimático foi submetido a testes de atividade antimicrobiana e de inocuidade, em cultivo celular e em camundongos. Observou-se efeito inibidor sobre cepas patogênicas Gram positivas (Staphylococcus aureus), porém não sobre bactérias Gram negativas (Salmonella sp., Pseudomonas sp. e Escherichia coli). Em cultivo celular, o extrato mostrou ausência de toxicidade e efeito citoprotetor, e em camundongos foi inócuo, e teve influência positiva no peso final nos grupos tratados.

Since discovered as antibiotics producers, Streptomyces genus bacteria had been studied to a great extent, because their great industrial interest. Most of the Streptomyces strains synthesize antibacterial, antifungal, antineoplastic, antiparasitic, and herbicide substances, as well as enzymes, which are used in medicine, agriculture and other biotechnological processes. We studied the potential applicability of Streptomyces viridosporus T7A crude fermentation extract in veterinary medicine. The antimicrobial properties of enzymatic crude extract were tested against pathogenic bacteria strains, and its innocuity was tested both in cellular cultives and mice. It was observed inhibitory effect against pathogenic Gram positive bacteria (Staphylococcus aureus), but not against pathogenic Gram negative bacteria (Salmonella sp., Pseudomonas sp., and Escherichia coli). In cellular cultives, the extract showed citoprotector effect and absence of toxicity. In mice, it was innocuous and had positive influence on the final weight in the treated groups.

Desde que fueran descubiertas como productoras de antibióticos, las bacterias del género Streptomyces vienen siendo muy estudiadas, por tener gran interés para la industria. La mayoría de las variedades de Streptomyces sintetiza substancias antibacterianas, antifúngicas, antitumorales, antiparasitarias y herbicidas, así como enzimas que se usan en medicina, agricultura y otros procesos biotecnológicos. En este trabajo, se estudió el potencial de uso del extracto bruto de la fermentación por Streptomyces viridosporus T7A en medicina veterinaria. Las propiedades antimicrobianas del extracto bruto enzimático fueran testadas contra bacterias patogénicas, así como se testó su inocuidad tanto en cultivos celulares cuanto en ratones. Se observó efecto inhibitorio sobre bacterias patogénicas Gram positivas (Staphylococcus aureus), pero no sobre bacterias Gram negativas (Salmonella sp., Pseudomonas sp. y Escherichia coli). En cultivo celular, el extracto mostró ausencia de toxicidad y efecto citoprotector, y en ratones fue inocuo, y ha influenciado positivamente el peso final de los grupos tratados.

Continuous aerobic phenol degradation by defined mixed immobilized culture in packed bed reactors.

A defined mixed culture of Pseudomonas putida, Commamonas testosteroni and Candida tropicalis was immobilized by adsorption on polyurethane foam, cocoa-fibers, expanded slate and sintered glass. Packed bed reactors were used for long-term continuous phenol biodegradations. Loading experiments were done to study the impact of the following parameters: (1) hydraulic retention time, (2) dissolved oxygen concentration, and (3) elimination of the oxygen limitation. After the acclimation period (approximately 10 d), the loading test with the individual packings showed the following maximum degradation rates: sintered glass 34, polyurethane foam 12, expanded slate 11.5, and cocoa-fibers 7.7 kg m(-3) d(-1). All these values were reached at a removal efficiency >99 % and with oxygen in excess. Under these conditions, the pH of the diluted unbuffered medium in the reactor effluent was 3.2-4.0 and no incompletely oxidized metabolic intermediates were found. The free cell concentration in the effluent increased after the phenol overloading time period.

Conidia production of Beauveria sp. by solid-state fermentation for biocontrol of Ilex paraguariensis caterpillars.

Conidia production of Beauveria sp. strain LAG by solid-state fermentation (SSF) using blends of agro-industrial residues (residual potatoes and sugar-cane bagasse) was optimized with respect to cultivation conditions and the composition of substrate mixture in Erlenmeyer flasks and column-type bioreactor. With a blend of 60 % residual potatoes and 40 % sugar-cane bagasse the optimum conditions achieved were: incubation temperature 26 degrees C, initial substrate pH 6, inoculum concentration 10(7) conidia per g substrate; optimal initial moisture of the substrate was 70 % for Erlenmeyer flasks, in column-type bioreactor (with forced aeration) the optimal initial moisture of the substrate was 65 % with airflow of 60 mL/min. The highest production (1.07 x 10(10) conidia per g dry substrate) was achieved after a 10-d fermentation. The conidia were used in laboratory assays against Thelosia camina and Hylesia sp., caterpillars that are serious pests of mate plants. The mortality of T. camina was >90 % 10 d after spraying caterpillars with 1 mL conidia suspension at a concentration 10(5)-10(8)/mL. For Hylesia sp., the mortality was 70 %, 7 d after immersion in the conidia suspension containing 108 conidia per mL. Therefore, the Beauveria sp. LAG can be considered to be an important biocontrol instrument in the prospect of the Integrated Pest Management for mate plants.

Packed bed column fermenter and kinetic modeling for upgrading the nutritional quality of coffee husk in solid-state fermentation.

Studies were carried out to evaluate solid-state fermentation (SSF) for the upgradation of the nutritional quality of coffee husk by degrading the caffeine and tannins present in it. SSF was carried out by Aspergillus niger LPBx in a glass column fermenter using factorial design experiments and surface response methodology to optimize bioprocess parameters such as the substrate pH and moisture content and aeration rate. The first factorial design showed that the moisture content of the substrate and aeration rate were significant factors for the degradation of toxic compounds, which was confirmed by the second factorial design too. The kinetic study showed that the degradation of toxic compounds was related to the development of the mold and its respiration and also to the consumption of the reducing sugars present in coffee husk. From the values obtained experimentally for the oxygen uptake rate and CO(2) evolved, the system determined a biomass yield (Y(x/o)) of 3.811 (g of biomass).(g of consumed O(2))(-1) and a maintenance coefficient (m) of 0.0031 (g of consumed O(2)).(g biomass of biomass)(-1).h(-1). The best results on the degradation of caffeine (90%) and tannins (57%) were achieved when SSF was carried out with a 30 mL.min(-1) aeration rate using coffee husk having a 55% initial moisture content. The inoculation rate did not affect the metabolization of the toxic compounds by the fungal culture. After SSF, the protein content of the husk was increased to 10.6%, which was more than double that of the unfermented husk (5.2%).

Production, purification and properties of microbial phytases.

Phytases (myo-inositol hexakisphosphate phosphohydrolase, EC 3.1.3.8) catalyse the release of phosphate from phytate (mycoinositol hexakiphosphate). Several cereal grains, legumes and oilseeds, etc., store phosphorus as phytate. Environmental pollution due to the high-phosphate manure, resulting in the accumulation of P at various locations has raised serious concerns. Phytases appear of significant value in effectively controlling P pollution. They can be produced from a host of sources including plants, animals and micro-organisms. Microbial sources, however, are promising for their commercial exploitations. Strains of Aspergillus sp., chiefly A. ficuum and A. niger have most commonly been employed for industrial purposes. Phytases are considered as a monomeric protein, generally possessing a molecular weight between 40 and 100 kDa. They show broad substrate specificity and have generally pH and temperature optima around 4.5-6.0 and 45-60 degrees C. The crystal structure of phytase has been determined at 2.5 A resolution. Immobilization of phytase has been found to enhance its thermostability. This article reviews recent trends on the production, purification and properties of microbial phytases.

Solid state cultivation--an efficient method to use toxic agro-industrial residues.

Studies were carried out to screen twelve strains of Lentinus edodes for their efficiency to grow on toxic agro-industrial residues of coffee industry in solid state cultivation (SSC). Based on best mycelial growth (7.57 mm/day) and biomass production (48.78 mg/plate in 12 days at 24 degrees C) in coffee husk extract medium, a strain, L. edodes LPB 02 was selected for mushroom cultivation in SSC on coffee husk (treated and untreated), coffee spent ground, and a mixed-substrate comprising coffee husk and coffee spent ground (1:1). SSC was carried out under different conditions of moisture and spawn rate. Spawn rate of 10% and moisture level of 55-60% was found suitable for all the substrates. Treatment of the coffee husk with hot water was found useful for its utilization by the fungus. Results showed that there was an increase in the protein content and decrease in the fibre content of the substrates after SSC. Fruiting bodies were obtained from the treated coffee husk, spent ground and mixed-substrate, and the biological efficiency achieved was 85.8, 88.6 and 78.4% for these substrates, respectively. However, no fruiting body was obtained with raw coffee husk was used as the substrate. Results showed that after SSC, there was a decrease of about 27, 40 and 24% in caffeine and about 18, 49 and 12% in tannin contents in the treated coffee husk, coffee spent ground and mixed substrate, respectively. No caffeine or, tannins were found in fruiting body indicating their degradation by the fungal strain.

Lactobacillus plantarum amylase acting on crude starch granules. Native isoforms and activity changes after limited proteolysis.

The microheterogeneous native amylolytic complex secreted by the isolate A6 of Lactobacillus plantarum revealed a selective enzyme specificity loss when submitted to a limited proteolysis under a suboptimum pH condition. A clear electrophoretic profile change toward just one shorter, more acidic, and equally active polypeptide fragment resulted from the pronase E pretreatment. Although the whole enzyme activity remained apparently unaffected for soluble starch, the native parallel activity on intact and non-gelatinized starch granules either from cereals or tubers was dramatically reduced. This phenomenon was more clearly documented by scanning electron microscopy using the easiest accessible native substrate: wheat starch granules. The anion-exchange-purified native enzymes from L. plantarum displayed a different optimum pH curve when compared with the thermotolerant alpha-amylase from Bacillus licheniformis. The alpha-amylases from the lactic-acid-producing A6 isolate presented an electrophoretic profile easily distinguishable from those from B. liqueniformis and B. subtilis species.

Advances in microbial amylases.

This review makes a comprehensive survey of microbial amylases, i.e. alpha-amylase, beta-amylase and glucoamylase. Amylases are among the most important enzymes and are of great significance in present-day biotechnology. Although they can be derived from several sources, such as plants, animals and micro-organisms, the enzymes from microbial sources generally meet industrial demands. Microbial amylases could be potentially useful in the pharmaceutical and fine-chemical industries if enzymes with suitable properties could be prepared. With the advent of new frontiers in biotechnology, the spectrum of amylase application has widened in many other fields, such as clinical, medicinal and analytical chemistries, as well as their widespread application in starch saccharification and in the textile, food, brewing and distilling industries. In this review, after a brief description of the sources of amylases, we discuss the molecular biology of amylases, describing structures, cloning, sequences, and protoplast fusion and mutagenesis. This is followed by sections on their production and finally the properties of various amylases.

Production and shelf-life studies of low cost beverage with soymilk, buffalo cheese whey and cow milk fermented by mixed cultures of Lactobacillus casei ssp. shirota and Bifidobacterium adolescentis.

A study was performed to develop a fermented milk beverage with the aim to increase the potential application of buffalo cheese whey and soymilk. A mixed substrate was prepared by selective combination, which contained buffalo cheese whey 35%, soymilk 30% and cow milk 35%. The substrate mixture was fermented by a mixed culture of Lactobacillus casei shirota and Bifidobacterium adolescentis at 37 degrees C for 8 h keeping a 1:1.5 proportion between the lactic and bifidobacteria within a 5% (v/v) inoculum size. The fermented beverage was lightly extra-flavoured with vanilla essence and subjected to chemical, microbiological and sensory evaluations during storage for 28 days at 4 degrees C. Except a slight variation in the acidity, no other properties changed even after 28 days. There were no contaminating organisms (Salmonella and coliforms), which indicated the sanitary and hygienic conditions of the processing and the viable cells of the bacterial strains was well within recommended limits (6.8 x 10(8) cells for L. casei and 2.3 x 10(7) cells for Bifidobacterium). No negative changes were found in the sensory characteristics of the beverage allowing its good acceptability in all during the storage period.

Recent developments in microbial inulinases. Its production, properties, and industrial applications.

Microbial inulinases are an important class of industrial enzymes that have gained much attention recently. Inulinases can be produced by a host of microorganisms, including fungi, yeast, and bacteria. Among them, however, Aspergillus sp. (filamentous fungus) and Kluyveromyces sp. (diploid yeast) are apparently the preferred choices for commercial applications. Among various substrates (carbon source) employed for their production, inulin-containing plant materials offer advantages in comparison to pure substrates. Although submerged fermentation has been universally used as the technique of fermentation, attempts are being made to develop solid-state fermentation technology also. Inulinases catalyze the hydrolysis of inulin to D-fructose (fructose syrup), which has gained an important place in human diets today. In addition, inulinases are finding other newer applications. This article reviews more recent developments, especially those made in the past decade, on microbial inulinases--its production using various microorganisms and substrates. It also describes the characteristics of various forms of inulinases produced as well as their applications.