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P R Córdoba

Publications and source records attributed to P R Córdoba.

4 recordsLinked to original sources

Continuous production of L(+)-lactic acid by Lactobacillus casei in two-stage systems.

A two-stage two-stream chemostat system and a two-stage two-stream immobilized upflow packed-bed reactor system were used for the study of lactic acid production by Lactobacillus casei subsp casei. A mixing ratio of D12/D2 = 0.5 (D = dilution rate) resulted in optimum production, making it possible to generate continuously a broth with high lactic acid concentration (48 g l-1) and with a lowered overall content of initial yeast extract (5 g l-1), half the concentration supplied in the one-step process. In the two-stage chemostat system, with the first stage at pH 5.5 and 37 degrees C and a second stage at pH 6.0, a temperature change from 40 degrees C to 45 degrees C in the second stage resulted in a 100% substrate consumption at an overall dilution rate of 0.05 h-1. To increase the cell mass in the system, an adhesive strain of L. casei was used to inoculate two packed-bed reactors, which operated with two mixed feedstock streams at the optimal conditions found above. Lactic acid fermentation started after a lag period of cell growth over foam glass particles. No significant amount of free cells, compared with those adhering to the glass foam, was observed during continuous lactic acid production. The extreme values, 57.5 g l-1 for lactic acid concentration and 9.72 g l-1 h-1 for the volumetric productivity, in upflow packed-bed reactors were higher than those obtained for free cells (48 g l-1 and 2.42 g l-1 h-1) respectively and the highest overall L(+)-lactic acid purity (96.8%) was obtained in the two-chemostat system as compared with the immobilized-cell reactors (93%).

Biomass↗

Fluidized bed design parameters affecting novel lactic Acid downstream processing.

Lactic acid purification was directly done from fermentation utilizing a fluidized bed column refilled with a strong anionic exchange resin. The purpose of this work was to study the influence of two important design parameters, bed-diameter (D) and bed-height (H), in the lactic acid binding and elution capacity of the matrix. By changing the settled bed height from 2.5 to 5 cm for each diameter of column analyzed it was possible to obtain an 50% increase in the binding capacity of the resin in all experiments. This fact was attributed to a higher contact time between the culture broth and the anionic resin produced by the increase of back mixing and lactic acid residence time.

Adsorption↗

[Beta-galactosidase activity of strains of Kluyveromyces spp. and production of ethanol from lactose].

We investigated the behavior of yeast of the genus Kluyveromyces (K. fragilis 507, K. lactis 29 and K. lactis 10), which grow on lactose as sole carbon source, since they possess an enzyme system for the utilization of this sugar. We determined the beta-galactosidase activity of these strains, grown in the logarithmic phase in media containing glucose and lactose. On addition of 0 to 12% v/v ethanol to cells treated with toluene, we did not observe inhibition of the enzyme in strain 10 of Kluyveromyces lactis, which showed the greatest activity (704.4 Units). Since there exist the possibility of industrial utilization of concentrated whey (4 times), we performed fermentation tests of the three strains, at 30 C, in media containing initial lactose concentrations of 16.5 and 24.5%. After 48 h the residual lactose concentration was practically zero, and the ethanol concentrations had reached 7.60 and 10.10% v/v. It might be expected that the rate of fermentation of a disaccharide such as lactose would be related to the rate of hydrolysis of the sugar, so that strains having a higher rate of enzymatic hydrolysis should show a higher fermentation rate. However, we did not observe such behavior, as strains of Kluyveromyces having enzymatic activities as different as K. lactis 10 (704.4 U) and K. lactis 29 (189.7 U) did not show any great difference in the production of ethanol from lactose.

Ethanol↗

[The biomass in upflow anaerobic filters].

A cylindrical upflow filter packed with non-reticulated polyurethane foam, seeded with anaerobic sewage sludge and geared to biological treatment of dairy industrial wastewater, was used to determine the biomass content of the biofilm and suspended flora. This microflora is responsible for the conversion to methane and carbon dioxide of most of organic matter in wastewater. The methanogenic process reduces the COD of liquid wastes in more than 83% when operate at organic loading rate of 6 Kg COD/m3/d. Sequential sampling showed that biomass could be determined by measurement of volatile solids of each filter section. Those solids are related to filter geometry an produce accumulation of flocs (0.7g/l) in the bottom zone corresponding to liquid inlet.

Bacteria, Anaerobic↗