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Biomedical subjects

A Illanes

Publications and source records attributed to A Illanes.

At least 19 recordsLinked to original sources

Strategies for fed-batch cultivation of t-PA producing CHO cells: substitution of glucose and glutamine and rational design of culture medium.

A strategy for fed-batch cultivation of t-PA producing recombinant CHO cells is presented, based on the substitution of glucose and glutamine for slowly metabolized nutrients and in a rational design of the medium. Media for the batch and fed stages were based on the cell specific amino acid requirements, which allowed a more accurate determination of the initiation of the fed stage and the frequency of nutrient addition from then on. Salt concentration was also reduced in both media to avoid an increase in osmolality. As a consequence of this rational design, most amino acid did not accumulate significantly during the fed stage, as usually occurs when their supply is not based on cell requirements; also, lower amounts of by-products were obtained when osmolality level was kept low, that altogether increased viability, longevity and t-PA production when compared with a reference batch culture. Alternating glucose and galactose during the fed stage, allowed lactate detoxification of the cells through their own metabolism. This allowed an increase in cell growth and cell viability with respect to a fed-batch culture in which only glucose was used in the fed stage.

Animals↗

Temperature optimization for reactor operation with chitin-immobilized lactase under modulated inactivation.

Temperature effects on all kinetic and inactivation parameters have been determined for chitin immobilized lactase from Kluyveromyces marxianus var. marxianus, and proper temperature functions have been validated. Maximum reaction rate, Michaelis constant referred to lactose, inhibition constant for galactose and inactivation rates increased with temperature. Enzyme inactivation was adequately modelled by a two-stage series mechanism. The effect of galactose and lactose on enzyme inactivation was determined in terms of modulation factors that were positive for galactose and negative for lactose over the whole range of temperature studied. Modulation factors were mild functions of temperature in the first stage and strong functions in the second stage of CIL inactivation where galactose positive modulation factors increase with temperature and lactose negative modulation factors decrease with temperature. Temperature explicit functions for all kinetic and inactivation parameters were incorporated into a scheme to optimize the temperature of operation for a sequential batch reactor with chitin-immobilized lactase, based on an annual cost objective function for reactor operation. Software for temperature optimization was developed creating a friendly interface with user that allows the introduction of variations in all parameters and operational criteria to perform sensitivity analysis.

Journal Article↗

Evaluation of penicillin acylase production by two strains of Bacillus megaterium.

Penicillin acylase is a key enzyme for the production of semisynthetic beta-lactam antibiotics. The intracellular enzyme from Escherichia coli has been thoroughly studied and characterized. The extracellular enzyme from Bacillus megaterium, despite its potential advantages, has received less attention in the recent scientific literature. A comparative study is presented for the production of penicillin acylase with two strains of Bacillus megaterium in batch fermentation in previously optimized complex and defined media. The enzyme produced by the selected strain has been recovered, partially purified and its kinetic behaviour determined.

Bacillus megaterium↗

[Immobilization of microbial lactase].

Lactase (beta-D galactoside-galactohydrolase, E.C.3.2.1.23) is a relevant enzyme to the dairy industry as it modifies undesirable functional and nutritional properties derived from the lactose content in milk and dairies, and as a way of recovering or upgrading cheese whey. This latter aspect has been considered to develop an enzyme catalyst suitable for the continuous hydrolysis of whey permeate. The selection of enzyme and support and the immobilization procedure has been reported previously. Results obtained in the immobilization of fungal lactase on activated chitin have prompted us to scale-up the procedure, a system being developed in which the enzyme is immobilized within the reactor (in situ). Results are presented for the in situ immobilization of lactase with and without recirculation of the reagents. Previous procedure was reproduced, although moderate profiles of activity were generated through the catalyst bed which were not eliminated by recirculation. Packed bed reactors with immobilized lactase were operated at varying flowrates and lactose concentrations, results being compared, in terms of substrate conversion and reactor productivity, with a theoretical model based on the corresponding kinetic expression and ideal flow regime. Deviations are significant at high flowrates which is attributed to backmixing and channeling through the catalyst bed. The model fits reasonably well at low flowrates and high feed substrate concentration. Productivity was 58 g of glucose/l.h at 40 ml/h of 120 g/l of lactose. Stability of the immobilized lactase was assessed in long-term reactor operation with whey permeate (35 g/l of lactose) at 40 degrees C and pH 4.0. Operational half-life was 120 days.

Dairy Products↗

Internal potassium activity in ferret ventricular muscle.

Measurements of the K activity (aiK) in ferret ventricle were made using either single- or double-barrelled K-sensitive micro-electrodes. aiK was also estimated from the Nernst equation by measuring the membrane potential when changing the external K concentration. Micro-electrodes filled with the Corning K sensor gave unreliable results most probably due to interference from some substance(s) in the heart cells. Reproduceable measurements were obtained using a valinomycin cocktail as the K sensor. The mean value +/- S.D. for aiK from four experiments which met strict criteria for calibration, electrode penetration and drift was 104 mmol/l +/- 9 mmol/l. If all nine experiments were taken the value was 101 mmol/l +/- 8 mmol/l. Estimation from the Nernst equation gave values of aiK that were on average 20 mmol/l higher than the measured values with the valinomycin cocktail. It is recommended that a valinomycin cocktail be used to measure aiK.

Animals↗

[Protein enrichment of sugar beet bagasse for fermentation].

Leached beet pulp is a plentiful waste in the sugar beet industry in Chile, reaching 100.000 metric tons per year on a dry basis. It represents an interesting substrate for protein upgrading through fermentation by cellulolytic organisms, because of the high content of cellulose and hemicellulose, with small amounts of protein and lignin (Table 1). The fermentation of leached beet pulp by the cellulolytic fungus Trichoderma reesei QM 9414 was studied under carbon limitation, with the celluloses as the only carbon and energy source. Nitrogen was supplied as ammonium sulphate and the medium was supplemented with other mineral salts as required for growth. Results on the kinetics of cellulose and hemicellulose degradation, level of reducing sugars in the medium, mycelial growth and production of cellulolytic enzymes are presented. Mycelial growth and related parameters were evaluated by an indirect method, based on nitrogen balances during fermentation. A yield of 0.26 g. of dry cell/g. of cellulosic substrate consumed and productivity of 0.095 g. of dry cell per liter per hour were obtained and compared with reported results on similar systems. After 40 to 45 hours of fermentation, approximately 80% of the cellulose and 45% of the hemicellulose were degraded (Fig. 2). Both, exoglucanase and endoglucanase, were induced; endoglucanase was growth associated, while exoglucanase appeared later in the growth phase, reaching its maximum activity in the stationary phase (Fig. 3). The product obtained was 30% protein and only 40 to 45% residual fiber, mostly hemicellulose. Mild acid hydrolysis has been successful in degrading hemicellulose but not cellulose, in the leached beet pulp.(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Feed↗

Effects of lidocaine in rabbit atria.

Standard microelectrode recordings were obtained from rabbit right and left atria. Lidocaine (1 X 10(-5) M) had no effect on these, but 5 X 10(-5) M lidocaine significantly slowed rate and Vmax. This concentration had no effect on the duration of the action potential, a result clearly different from the effect of this drug in Purkinje tissue. Lidocaine had much less effect on the 'steady-state' relation of membrane potential to Vmax of phase 0 of the action potential than on the 'membrane responsiveness curve' obtained by the extra stimulus technique. We have demonstrated time-related recovery from sodium inactivation in rabbit left atria and have shown that lidocaine slows recovery in this tissue as it does in Purkinje fibres.

Action Potentials↗