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1.
Biotechnol Bioeng ; 75(3): 267-75, 2001 Nov 05.
Article in English | MEDLINE | ID: mdl-11590599

ABSTRACT

Steady-state culture characteristics are usually determined in chemostat cultivations, which are very time-consuming. In contrast, acceleration-stat (A-stat) cultivations in which the dilution rate is continuously changed with a constant acceleration rate are not so time-consuming, especially at high acceleration rates. Therefore, the A-stat could be advantageous to use instead of the chemostat. However, the highest acceleration rate, meaning the fastest A-stat that can be applied for estimating steady-state culture characteristics, is not known yet. Experimental results obtained with Zygosaccharomyces rouxii, an important yeast in soy sauce processes, showed that the culture characteristics during the A-stat with an acceleration rate of 0.001 h(-2) were roughly comparable to those of the chemostat. For higher acceleration rates the deviation between the culture characteristics in the A-stat and those in the chemostat obtained at the same dilution rate generally started to increase. The source of these deviations was examined by simulation for Saccharomyces cerevisiae. The simulations demonstrated that this deviation was not only dependent on the metabolic adaptation rate of the yeast, but also on the rate of change in environmental substrate concentrations during A-stats. From this work, it was concluded that an A-stat with an acceleration rate of 0.001 h(-2) is attractive to be used instead of chemostat whenever a rough estimation of steady-state culture characteristics is acceptable.


Subject(s)
Saccharomyces cerevisiae/metabolism , Zygosaccharomyces/metabolism , Adaptation, Physiological , Bioreactors , Fermentation , Reproducibility of Results , Saccharomyces cerevisiae/physiology , Zygosaccharomyces/physiology
2.
J Biotechnol ; 88(2): 129-39, 2001 Jun 15.
Article in English | MEDLINE | ID: mdl-11403847

ABSTRACT

Immobilization of salt-tolerant yeasts considerably decreases the total time required for the flavour development in soy-sauce processes. For immobilization of cells, alginate gel is mostly used as support material. However, alginate is not very suitable for use in soy-sauce processes because alginate is sensitive to abrasion and chemically unstable towards the high salt content of the soy-sauce medium. In contrast, a newly developed polyethylene-oxide gel seems to be more suitable, but this gel has not been used so far for flavour production in a bioreactor with a high salt content. Therefore, this gel was applied with immobilized salt-tolerant yeasts in a continuous stirred-tank reactor, containing more than 12.5% (w/v) salt. In this reactor, the polyethylene-oxide gel particles did not show any abrasion for several days, while alginate gel beads were already destroyed within 1 day. In addition, the polyethylene-oxide gel particles with immobilized salt-tolerant yeasts Candida versatilis and Zygosaccharomyces rouxii showed a good flavour production. From this work, it was concluded that the application of polyethylene-oxide gel in long-term soy-sauce processes is attractive in the case the sticking together of polyethylene-oxide gel particles can be controlled.


Subject(s)
Guaiacol/analogs & derivatives , Industrial Microbiology/methods , Polyethylene Glycols/chemistry , Yeasts/physiology , Alginates/chemistry , Bioreactors , Candida/physiology , Cells, Immobilized , Ethanol/metabolism , Gels , Glucuronic Acid , Guaiacol/metabolism , Hexuronic Acids , Industrial Microbiology/instrumentation , Salts/chemistry , Salts/metabolism , Zygosaccharomyces/physiology
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