1,592 research outputs found
Cultivation and Fractionation of Leguminous Biomass for Lactic Acid Production
Chemical industries are set to increase the proportion of renewable feedstock in their production in the decades ahead. Green Biorefineries that divide fresh green biomass into cakes and juice deliver valuable products for various industrial uses. Press juice can be used to produce lactic acid (LA), a promising building blok for the future. In this study, optimal cultivation and fractionation processes for generating a fermentation medium from legumes for lactic acid production by Bacillus coagulans are analyzed. The contents of press juices from alfalfa cultivated on arable land at three different sites and from a clover-grass mixture on a grassland site taken on different sampling dates are compared. In addition, fresh biomass yields from the different biomass samples are examined. This paper focuses on the methods applied, and provides initial results. Yield differences of up to 40 % and 60 % were recorded between different study sites and sampling dates, respectively. Fermentation analysis of the different samples revealed that press juices can supplement the main parts of nutrients for lactic acid bacteria, producing economically interesting amounts of lactic acid. These findings could increase the use of lactic acid in chemical industries and bring about a shift towards a higher proportion of renewables, namely legumes, in the processing chain
Valorising pasta industry wastes by the scale up and integration of solid-state and liquid-submerged fermentations
Pasta waste has previously been studied in a process to obtain lactic acid through a sequential hydrolysis and fermentation. The process was improved by using enzymes produced via solid-state fermentation of wheat bran in shake flasks. However, the scale-up of the solid-state fermentation is a complex task. In this study, amylase was produced in a home-designed tray bioreactor which allowed to carry out the hydrolysis and fermentation steps at the pilot scale. Due to the efficiency of the solid-state fermentation and the activity of the enzyme, only a small amount (100 g) of wheat bran was required to achieve high yields in a hydrolysis in a 72 L bioreactor (50 L working volume). Overall, the lactic acid yield was 0.68 gLA/gdS, and after the purification, the lactic acid recovered was 55 %, with a total ion concentration of 500 mg/L and an enantiomeric purity of 98.1 % L-LA.11 pĂĄgina
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Production and purification of L-lactic acid in lab and pilot scales using sweet sorghum juice
Sweet sorghum juice (SSJ) was evaluated as fermentation substrate for the production of l-lactic acid. A thermophilic Bacillus coagulans isolate was selected for batch fermentations without the use of additional nutrients. The first batch of SSJ (Batch A) resulted on higher lactic acid concentration, yield and productivity with values of 78.75 g·Lâ1, 0.78 g·gâ1 and 1.77 g·Lâ1 hâ1, respectively. Similar results were obtained when the process was transferred into the pilot scale (50 L), with corresponding values of 73 g·Lâ1, 0.70 g·gâ1 and 1.47 g·Lâ1 hâ1. A complete downstream process scheme was developed in order to separate lactic acid from the fermentation components. Coarse and ultra-filtration were employed as preliminary separation steps. Mono- and bipolar electrodialysis, followed by chromatography and vacuum evaporation were subsequently carried out leading to a solution containing 905.8 g·Lâ1 lactic acid, with an optical purity of 98.9%. The results of this study highlight the importance of the downstream process with respect to using SSJ for lactic acid production. The proposed downstream process constitutes a more environmentally benign approach to conventional precipitation methods
Counteractive effects of antenatal glucocorticoid treatment on D1 receptor modulation of spatial working memory.
RATIONALE: Antenatal exposure to the glucocorticoid dexamethasone dramatically increases the number of mesencephalic dopaminergic neurons in rat offspring. However, the consequences of this expansion in midbrain dopamine (DA) neurons for behavioural processes in adulthood are poorly understood, including working memory that depends on DA transmission in the prefrontal cortex (PFC). OBJECTIVES: We therefore investigated the influence of antenatal glucocorticoid treatment (AGT) on the modulation of spatial working memory by a D1 receptor agonist and on D1 receptor binding and DA content in the PFC and striatum. METHODS: Pregnant rats received AGT on gestational days 16-19 by adding dexamethasone to their drinking water. Male offspring reared to adulthood were trained on a delayed alternation spatial working memory task and administered the partial D1 agonist SKF38393 (0.3-3Â mg/kg) by systemic injection. In separate groups of control and AGT animals, D1 receptor binding and DA content were measured post-mortem in the PFC and striatum. RESULTS: SKF38393 impaired spatial working memory performance in control rats but had no effect in AGT rats. D1 binding was significantly reduced in the anterior cingulate cortex, prelimbic cortex, dorsal striatum and ventral pallidum of AGT rats compared with control animals. However, AGT had no significant effect on brain monoamine levels. CONCLUSIONS: These findings demonstrate that D1 receptors in corticostriatal circuitry down-regulate in response to AGT. This compensatory effect in D1 receptors may result from increased DA-ergic tone in AGT rats and underlie the resilience of these animals to the disruptive effects of D1 receptor activation on spatial working memory.The authorsâ research is funded by the Wellcome
Trust (grant number 086871/Z/08/Z), the MRC (G0701500), a joint
award from the MRC (G1000183) and Wellcome Trust (093875/Z/10/
Z) in support of the Behavioral and Clinical Neuroscience Institute at
Cambridge University, and an MRC strategic award to the Imperial
College-Cambridge University-Manchester University (ICCAM) addiction
cluster (G1000018).This is the final version of the article. It first appeared from Springer at http://dx.doi.org/10.1007/s00213-016-4405-8
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